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Artigo de periodico
Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome (2018)
Pinto, Rayane de Oliveira; Peixoto, Adriano Porto; Pinto, Ary dos Santos; Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi; Ozawa, Terumi Okada; Dalben, Gisele da Silva
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, HRACF
Subjects: ANORMALIDADES CRANIOFACIAIS, MICROGNATISMO, DISOSTOSE CRÂNIOFACIAL, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, Rayane de Oliveira et al. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome. The Journal of Craniofacial Surgery, v. 29, n. 6, p. 1596-1600, 2018Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000004588. Acesso em: 18 out. 2024.
APA
Pinto, R. de O., Peixoto, A. P., Pinto, A. dos S., Richieri-Costa, A., Ceide, R. M. Z., Ozawa, T. O., & Dalben, G. da S. (2018). Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome. The Journal of Craniofacial Surgery, 29( 6), 1596-1600. doi:10.1097/SCS.0000000000004588
NLM
Pinto R de O, Peixoto AP, Pinto A dos S, Richieri-Costa A, Ceide RMZ, Ozawa TO, Dalben G da S. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome [Internet]. The Journal of Craniofacial Surgery. 2018 ; 29( 6): 1596-1600.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/SCS.0000000000004588
Vancouver
Pinto R de O, Peixoto AP, Pinto A dos S, Richieri-Costa A, Ceide RMZ, Ozawa TO, Dalben G da S. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome [Internet]. The Journal of Craniofacial Surgery. 2018 ; 29( 6): 1596-1600.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/SCS.0000000000004588
Artigo de periodico
A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia (2013)
Zechi-Ceide, Roseli Maria ; Moura, Priscila Padilha; Raskin, Salmo; Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, HRACF
Subjects: SÍNDROME DE PIERRE ROBIN, MUTAÇÃO, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia. American Journal of Medical Genetics. Part A, v. 161, n. 8, p. 2088-2094, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36057. Acesso em: 18 out. 2024.
APA
Zechi-Ceide, R. M., Moura, P. P., Raskin, S., Richieri-Costa, A., & Guion-Almeida, M. L. (2013). A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia. American Journal of Medical Genetics. Part A, 161( 8), 2088-2094. doi:10.1002/ajmg.a.36057
NLM
Zechi-Ceide RM, Moura PP, Raskin S, Richieri-Costa A, Guion-Almeida ML. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 8): 2088-2094.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.36057
Vancouver
Zechi-Ceide RM, Moura PP, Raskin S, Richieri-Costa A, Guion-Almeida ML. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 8): 2088-2094.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.36057
Artigo de periodico
Birth defects in newborns and stillborns: an example of the Brazilian reality (2011)
Oliveira, Camila Ive Ferreira; Richieri-Costa, Antonio ; Ferrarese, Valéria Cristina Carvalho; Vaz, Denise Cristina Móz; Fett-Conte, Agnes Cristina
Source: BMC Research Notes. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, FETO, RECÉM-NASCIDO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Camila Ive Ferreira et al. Birth defects in newborns and stillborns: an example of the Brazilian reality. BMC Research Notes, v. 4, p. 343, 2011Tradução . . Disponível em: https://doi.org/10.1186/1756-0500-4-343. Acesso em: 18 out. 2024.
APA
Oliveira, C. I. F., Richieri-Costa, A., Ferrarese, V. C. C., Vaz, D. C. M., & Fett-Conte, A. C. (2011). Birth defects in newborns and stillborns: an example of the Brazilian reality. BMC Research Notes, 4, 343. doi:10.1186/1756-0500-4-343
NLM
Oliveira CIF, Richieri-Costa A, Ferrarese VCC, Vaz DCM, Fett-Conte AC. Birth defects in newborns and stillborns: an example of the Brazilian reality [Internet]. BMC Research Notes. 2011 ; 4 343.[citado 2024 out. 18 ] Available from: https://doi.org/10.1186/1756-0500-4-343
Vancouver
Oliveira CIF, Richieri-Costa A, Ferrarese VCC, Vaz DCM, Fett-Conte AC. Birth defects in newborns and stillborns: an example of the Brazilian reality [Internet]. BMC Research Notes. 2011 ; 4 343.[citado 2024 out. 18 ] Available from: https://doi.org/10.1186/1756-0500-4-343
Artigo de periodico
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes (2009)
Zechi-Ceide, Roseli Maria; Ribeiro, Lucilene Arilho; Raskin, Salmo; Bertolacini, Claudia Danielli Pereira; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA BILATERAL, GENES, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, v. 149A, n. 6, p. 1277-1279, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32844. Acesso em: 18 out. 2024.
APA
Zechi-Ceide, R. M., Ribeiro, L. A., Raskin, S., Bertolacini, C. D. P., Guion-Almeida, M. L., & Richieri-Costa, A. (2009). Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, 149A( 6), 1277-1279. doi:10.1002/ajmg.a.32844
NLM
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Vancouver
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Artigo de periodico
Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? (2008)
Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, TERATOMA, ANORMALIDADES CARDIOVASCULARES, NEOPLASIAS BUCAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?. Clinical Dysmorphology, v. 17, n. 2, p. 149-150, 2008Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e3282f254b7. Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., Ceide, R. M. Z., & Guion-Almeida, M. L. (2008). Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? Clinical Dysmorphology, 17( 2), 149-150. doi:10.1097/MCD.0b013e3282f254b7
NLM
Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7
Vancouver
Richieri-Costa A, Ceide RMZ, Guion-Almeida ML. Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity? [Internet]. Clinical Dysmorphology. 2008 ; 17( 2): 149-150.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/MCD.0b013e3282f254b7
Artigo de periodico
Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene (2008)
Ceide, Roseli Maria Zechi; Oliveira, Nélio Alessandro de Jesus; Guion-Almeida, Maria Leine; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita
Source: Clinical Dysmorphology. Unidades: HRAC, IB
Subjects: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi et al. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, v. 17, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3282fe1b8e. Acesso em: 18 out. 2024.
APA
Ceide, R. M. Z., Oliveira, N. A. de J., Guion-Almeida, M. L., Antunes, L. F. B. B., Richieri-Costa, A., & Passos-Bueno, M. R. (2008). Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, 17( 3), 225-226. doi:10.1097/mcd.0b013e3282fe1b8e
NLM
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Vancouver
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Artigo de periodico
Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome? (2006)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, LÁBIO FISSURADO, ANORMALIDADES DO SISTEMA NERVOSO, ANORMALIDADES CRANIOFACIAIS, GENÉTICA APLICADA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome?. American Journal of Medical Genetics. Part A, v. No 2006, n. 22, p. 2478-2481, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31518. Acesso em: 18 out. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2006). Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome? American Journal of Medical Genetics. Part A, No 2006( 22), 2478-2481. doi:10.1002/ajmg.a.31518
NLM
Guion-Almeida ML, Richieri-Costa A. Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2006 ; No 2006( 22): 2478-2481.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31518
Vancouver
Guion-Almeida ML, Richieri-Costa A. Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2006 ; No 2006( 22): 2478-2481.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31518
Artigo de periodico
PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI (2006)
Ribeiro, Lucilene Arilho; Murray, Jeffrey C.; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA, MUTAÇÃO, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e MURRAY, Jeffrey C. e RICHIERI-COSTA, Antonio. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2584-2586, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31369. Acesso em: 18 out. 2024.
APA
Ribeiro, L. A., Murray, J. C., & Richieri-Costa, A. (2006). PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI. American Journal of Medical Genetics Part A, 140A( 23), 2584-2586. doi:10.1002/ajmg.a.31369
NLM
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31369
Vancouver
Ribeiro LA, Murray JC, Richieri-Costa A. PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2584-2586.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31369
Artigo de periodico
Holoprosencephaly-like phenotype: clinical and genetic perspectives (2006)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: American Journal of Medical Genetics Part A. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, ANORMALIDADES MÚLTIPLAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Holoprosencephaly-like phenotype: clinical and genetic perspectives. American Journal of Medical Genetics Part A, v. 140A, n. 23, p. 2587-2593, 2006Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31378. Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2006). Holoprosencephaly-like phenotype: clinical and genetic perspectives. American Journal of Medical Genetics Part A, 140A( 23), 2587-2593. doi:10.1002/ajmg.a.31378
NLM
Richieri-Costa A, Ribeiro LA. Holoprosencephaly-like phenotype: clinical and genetic perspectives [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2587-2593.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31378
Vancouver
Richieri-Costa A, Ribeiro LA. Holoprosencephaly-like phenotype: clinical and genetic perspectives [Internet]. American Journal of Medical Genetics Part A. 2006 ; 140A( 23): 2587-2593.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.31378
Artigo de periodico
Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? (2005)
Castro, Carlos Henrique Bettoni Cruz de; Freitas, Patricia Zambonato ; Antoneli, Melissa Zattoni; Santiago, Giselda; Ribeiro, Lucilene Arilho ; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidades: HRAC, FOB, HRACF
Subjects: SÍNDROMES OROFACIODIGITAIS, VENTRÍCULOS CEREBRAIS, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Carlos Henrique Bettoni Cruz de et al. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome?. Clinical Dysmorphology, v. 14, n. 4, p. 197-201, 2005Tradução . . Disponível em: https://doi.org/10.1097/00019605-200510000-00006. Acesso em: 18 out. 2024.
APA
Castro, C. H. B. C. de, Freitas, P. Z., Antoneli, M. Z., Santiago, G., Ribeiro, L. A., & Richieri-Costa, A. (2005). Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? Clinical Dysmorphology, 14( 4), 197-201. doi:10.1097/00019605-200510000-00006
NLM
Castro CHBC de, Freitas PZ, Antoneli MZ, Santiago G, Ribeiro LA, Richieri-Costa A. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? [Internet]. Clinical Dysmorphology. 2005 ; 14( 4): 197-201.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200510000-00006
Vancouver
Castro CHBC de, Freitas PZ, Antoneli MZ, Santiago G, Ribeiro LA, Richieri-Costa A. Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrome? [Internet]. Clinical Dysmorphology. 2005 ; 14( 4): 197-201.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200510000-00006
Artigo de periodico
Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia (2005)
De Vitto, Luciana Paula Maximino; Abramides, Dagma Venturini Marques; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidades: FOB, HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, RETARDO MENTAL, OBESIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DE VITTO, Luciana Paula Maximino e ABRAMIDES, Dagma Venturini Marques e RICHIERI-COSTA, Antonio. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia. American Journal of Medical Genetics. Part A, v. 136, n. 2, p. 219-220, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30753. Acesso em: 18 out. 2024.
APA
De Vitto, L. P. M., Abramides, D. V. M., & Richieri-Costa, A. (2005). Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia. American Journal of Medical Genetics. Part A, 136( 2), 219-220. doi:10.1002/ajmg.a.30753
NLM
De Vitto LPM, Abramides DVM, Richieri-Costa A. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 2): 219-220.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30753
Vancouver
De Vitto LPM, Abramides DVM, Richieri-Costa A. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 2): 219-220.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30753
Artigo de periodico
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases (2005)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 352-353, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30628. Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2005). Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, 136( 4), 352-353. doi:10.1002/ajmg.a.30628
NLM
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30628
Vancouver
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30628
Artigo de periodico
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation (2005)
Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, DESENVOLVIMENTO FÍSICO, MAXILA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 346-347, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30625. Acesso em: 18 out. 2024.
APA
Ribeiro, L. A., & Richieri-Costa, A. (2005). Single median maxillary central incisor, hypophyseal tumor, and SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 346-347. doi:10.1002/ajmg.a.30625
NLM
Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30625
Vancouver
Ribeiro LA, Richieri-Costa A. Single median maxillary central incisor, hypophyseal tumor, and SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 346-347.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30625
Artigo de periodico
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation (2005)
Ribeiro, Lucilene Arilho; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 348-349, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30626. Acesso em: 18 out. 2024.
APA
Ribeiro, L. A., & Richieri-Costa, A. (2005). Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation. American Journal of Medical Genetics. Part A, 136( 4), 348-349. doi:10.1002/ajmg.a.30626
NLM
Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30626
Vancouver
Ribeiro LA, Richieri-Costa A. Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 348-349.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30626
Artigo de periodico
Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures (2005)
Guerra, Dania; Sanchez, Otto; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERRA, Dania e SANCHEZ, Otto e RICHIERI-COSTA, Antonio. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 377-380, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30665. Acesso em: 18 out. 2024.
APA
Guerra, D., Sanchez, O., & Richieri-Costa, A. (2005). Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures. American Journal of Medical Genetics. Part A, 136( 4), 377-380. doi:10.1002/ajmg.a.30665
NLM
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Vancouver
Guerra D, Sanchez O, Richieri-Costa A. Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 377-380.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30665
Artigo de periodico
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects (2005)
Ribeiro, Lucilene Arilho; Guerini, Rita de Cássia Mecca; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES MÚLTIPLAS, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e GUERINI, Rita de Cássia Mecca e RICHIERI-COSTA, Antonio. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 350-351, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30627. Acesso em: 18 out. 2024.
APA
Ribeiro, L. A., Guerini, R. de C. M., & Richieri-Costa, A. (2005). Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, 136( 4), 350-351. doi:10.1002/ajmg.a.30627
NLM
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30627
Vancouver
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30627
Artigo de periodico
Arachnoidal cyst, orofacial dysplasia, poor motor control, and severe language delay (2005)
Richieri-Costa, Antonio; Giacheti, Célia Maria; Abramides, Dagma Venturini Marques; Feniman, Mariza Ribeiro; Baldelin, C. G. R.
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, FOB
Subjects: ANORMALIDADES MÚLTIPLAS, RETARDO NO DESENVOLVIMENTO DA FALA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Arachnoidal cyst, orofacial dysplasia, poor motor control, and severe language delay. American Journal of Medical Genetics. Part A, v. 137, n. 1, p. 110-111, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30798. Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., Giacheti, C. M., Abramides, D. V. M., Feniman, M. R., & Baldelin, C. G. R. (2005). Arachnoidal cyst, orofacial dysplasia, poor motor control, and severe language delay. American Journal of Medical Genetics. Part A, 137( 1), 110-111. doi:10.1002/ajmg.a.30798
NLM
Richieri-Costa A, Giacheti CM, Abramides DVM, Feniman MR, Baldelin CGR. Arachnoidal cyst, orofacial dysplasia, poor motor control, and severe language delay [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 137( 1): 110-111.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30798
Vancouver
Richieri-Costa A, Giacheti CM, Abramides DVM, Feniman MR, Baldelin CGR. Arachnoidal cyst, orofacial dysplasia, poor motor control, and severe language delay [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 137( 1): 110-111.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30798
Artigo de periodico
The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: phenotypic and aetiological considerations (2004)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine
Source: International Journal of Medical Sciences. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine. The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: phenotypic and aetiological considerations. International Journal of Medical Sciences, v. 1, n. 1, p. 34-42, 2004Tradução . . Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (2004). The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: phenotypic and aetiological considerations. International Journal of Medical Sciences, 1( 1), 34-42.
NLM
Richieri-Costa A, Guion-Almeida ML. The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: phenotypic and aetiological considerations. International Journal of Medical Sciences. 2004 ; 1( 1): 34-42.[citado 2024 out. 18 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML. The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies: phenotypic and aetiological considerations. International Journal of Medical Sciences. 2004 ; 1( 1): 34-42.[citado 2024 out. 18 ]
Artigo de periodico
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? (2004)
Guion-Almeida, Maria Leine; Paula, Ligiane Alves Machado; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30153. Acesso em: 18 out. 2024.
APA
Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
NLM
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Vancouver
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2024 out. 18 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Artigo de periodico
Guadalajara camptodactyly syndrome type I: report on a new case (2002)
Ceide, Roseli Maria Zechi; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Guadalajara camptodactyly syndrome type I: report on a new case. Clinical Dysmorphology, v. 11, n. 2, p. 129-132, 2002Tradução . . Disponível em: https://doi.org/10.1097/00019605-200204000-00011. Acesso em: 18 out. 2024.
APA
Ceide, R. M. Z., Guion-Almeida, M. L., & Richieri-Costa, A. (2002). Guadalajara camptodactyly syndrome type I: report on a new case. Clinical Dysmorphology, 11( 2), 129-132. doi:10.1097/00019605-200204000-00011
NLM
Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Guadalajara camptodactyly syndrome type I: report on a new case [Internet]. Clinical Dysmorphology. 2002 ; 11( 2): 129-132.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200204000-00011
Vancouver
Ceide RMZ, Guion-Almeida ML, Richieri-Costa A. Guadalajara camptodactyly syndrome type I: report on a new case [Internet]. Clinical Dysmorphology. 2002 ; 11( 2): 129-132.[citado 2024 out. 18 ] Available from: https://doi.org/10.1097/00019605-200204000-00011

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