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Vici's syndrome associated to cleft palate:: clinical report on a brazilian boy (2013)
Siemann, M. E.; Zechi-Ceide, Roseli Maria; Kokitsu-Nakata, Nancy Mizue; Vendramini, Siulan; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Maximino, Luciana Paula
Source: Anais. Conference title: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRAC, FOB
Subjects: FISSURA LÁBIOPALATINA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIEMANN, M. E.; ZECHI-CEIDE, Roseli Maria; KOKITSU-NAKATA, Nancy Mizue; et al. Vici's syndrome associated to cleft palate:: clinical report on a brazilian boy. Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013.
APA
Siemann, M. E., Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Vendramini, S., Guion-Almeida, M. L., Richieri-Costa, A., & Maximino, L. P. (2013). Vici's syndrome associated to cleft palate:: clinical report on a brazilian boy. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais.
NLM
Siemann ME, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini S, Guion-Almeida ML, Richieri-Costa A, Maximino LP. Vici's syndrome associated to cleft palate:: clinical report on a brazilian boy. Anais. 2013 ;
Vancouver
Siemann ME, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini S, Guion-Almeida ML, Richieri-Costa A, Maximino LP. Vici's syndrome associated to cleft palate:: clinical report on a brazilian boy. Anais. 2013 ;
Artigo de periodico
Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature (2007)
Vendramini, Siulan; Richieri-Costa, Antonio; Guion-Almeida, Maria Leine
Source: European Journal of Human Genetics. Unidade: HRAC
Subjects: SÍNDROME DE GOLDENHAR, PERDA AUDITIVA NEUROSSENSORIAL, OUVIDO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VENDRAMINI, Siulan; RICHIERI-COSTA, Antonio; GUION-ALMEIDA, Maria Leine. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature. European Journal of Human Genetics, London, v. 15, n. 4, p. 411-421, 2007. Disponível em: < http://www.nature.com/ejhg/journal/v15/n4/pdf/5201770a.pdf > DOI: 10.1038/sj.ejhg.5201770.
APA
Vendramini, S., Richieri-Costa, A., & Guion-Almeida, M. L. (2007). Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature. European Journal of Human Genetics, 15( 4), 411-421. doi:10.1038/sj.ejhg.5201770
NLM
Vendramini S, Richieri-Costa A, Guion-Almeida ML. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature [Internet]. European Journal of Human Genetics. 2007 ; 15( 4): 411-421.Available from: http://www.nature.com/ejhg/journal/v15/n4/pdf/5201770a.pdf
Vancouver
Vendramini S, Richieri-Costa A, Guion-Almeida ML. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature [Internet]. European Journal of Human Genetics. 2007 ; 15( 4): 411-421.Available from: http://www.nature.com/ejhg/journal/v15/n4/pdf/5201770a.pdf
Dissertação (Mestrado)
Avaliação genética-clínica e audiológica de indivíduos com anomalias de 1º e 2º arcos branquiais associadas à anomalia radial (2006)
Vendramini, Siulan; Guion-Almeida, Maria Leine (Orientador)
Unidade: HRAC
Subjects: ARCOS BRANQUIAIS, GENÉTICA MÉDICA, SÍNDROME DE GOLDENHAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VENDRAMINI, Siulan; GUION-ALMEIDA, Maria Leine. Avaliação genética-clínica e audiológica de indivíduos com anomalias de 1º e 2º arcos branquiais associadas à anomalia radial. 2006.Universidade de São Paulo, Bauru, 2006. Disponível em: < http://www.teses.usp.br/teses/disponiveis/61/61131/tde-02102006-154900/ >.
APA
Vendramini, S., & Guion-Almeida, M. L. (2006). Avaliação genética-clínica e audiológica de indivíduos com anomalias de 1º e 2º arcos branquiais associadas à anomalia radial. Universidade de São Paulo, Bauru. Recuperado de http://www.teses.usp.br/teses/disponiveis/61/61131/tde-02102006-154900/
NLM
Vendramini S, Guion-Almeida ML. Avaliação genética-clínica e audiológica de indivíduos com anomalias de 1º e 2º arcos branquiais associadas à anomalia radial [Internet]. 2006 ;Available from: http://www.teses.usp.br/teses/disponiveis/61/61131/tde-02102006-154900/
Vancouver
Vendramini S, Guion-Almeida ML. Avaliação genética-clínica e audiológica de indivíduos com anomalias de 1º e 2º arcos branquiais associadas à anomalia radial [Internet]. 2006 ;Available from: http://www.teses.usp.br/teses/disponiveis/61/61131/tde-02102006-154900/
Artigo de periodico
A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate (2006)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Tabith Junior, Alfredo
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA PALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine; CEIDE, Roseli Maria Zechi; VENDRAMINI, Siulan; TABITH JUNIOR, Alfredo. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, London, v. 15, n. 3, p. 171-174, 2006. DOI: 10.1097/01.mcd.0000220603.09661.7e.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Tabith Junior, A. (2006). A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, 15( 3), 171-174. doi:10.1097/01.mcd.0000220603.09661.7e
NLM
Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.
Vancouver
Guion-Almeida ML, Ceide RMZ, Vendramini S, Tabith Junior A. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.
Artigo de periodico
Encephalocraniocutaneous lipomatosis: report on a brazilian girl (2004)
Nakata, Nancy Mizue Kokitsu; Vendramini, Siulan; Versiani, Beatriz R.; Ramos, Ester Silveira; Guion-Almeida, Maria Leine
Source: Arquivos de Ciências da Saúde. Unidades: FMRP, HRAC
Subjects: CÉREBRO, ANORMALIDADES DO SISTEMA NERVOSO, CONVULSÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu; VENDRAMINI, Siulan; VERSIANI, Beatriz R.; RAMOS, Ester Silveira; GUION-ALMEIDA, Maria Leine. Encephalocraniocutaneous lipomatosis: report on a brazilian girl. Arquivos de Ciências da Saúde, São José do Rio Preto, v. 11, n. 3, p. 192-194, 2004.
APA
Nakata, N. M. K., Vendramini, S., Versiani, B. R., Ramos, E. S., & Guion-Almeida, M. L. (2004). Encephalocraniocutaneous lipomatosis: report on a brazilian girl. Arquivos de Ciências da Saúde, 11( 3), 192-194.
NLM
Nakata NMK, Vendramini S, Versiani BR, Ramos ES, Guion-Almeida ML. Encephalocraniocutaneous lipomatosis: report on a brazilian girl. Arquivos de Ciências da Saúde. 2004 ; 11( 3): 192-194.
Vancouver
Nakata NMK, Vendramini S, Versiani BR, Ramos ES, Guion-Almeida ML. Encephalocraniocutaneous lipomatosis: report on a brazilian girl. Arquivos de Ciências da Saúde. 2004 ; 11( 3): 192-194.
Artigo de periodico
Auriculo-condylar syndrome: additional patients (2002)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Nakata, Nancy Mizue Kokitsu
Source: American Journal of Medical Genetics. Unidade: HRAC
Subject: SÍNDROMES OROFACIODIGITAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine; CEIDE, Roseli Maria Zechi; VENDRAMINI, Siulan; NAKATA, Nancy Mizue Kokitsu. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, New York, v. 112, n. 2, p. 209-214, 2002. DOI: 10.1002/ajmg.10631.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., Vendramini, S., & Nakata, N. M. K. (2002). Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics, 112( 2), 209-214. doi:10.1002/ajmg.10631
NLM
Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.
Vancouver
Guion-Almeida ML, Ceide RMZ, Vendramini S, Nakata NMK. Auriculo-condylar syndrome: additional patients. American Journal of Medical Genetics. 2002 ; 112( 2): 209-214.
Artigo de periodico
A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss (2000)
Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Vendramini, Siulan; Guerini, Rita de Cássia Mecca; Salmen, Isabel Cristina Drago Marquezine; Amaral, Natalie Camillo de Oliveira
Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, SURDEZ
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine; NAKATA, Nancy Mizue Kokitsu; CEIDE, Roseli Maria Zechi; et al. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, Bauru, v. 3, n. Ja, p. 23-26, 2000.
APA
Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., Vendramini, S., Guerini, R. de C. M., Salmen, I. C. D. M., & Amaral, N. C. de O. (2000). A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 3( Ja), 23-26.
NLM
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S, Guerini R de CM, Salmen ICDM, Amaral NC de O. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 23-26.
Vancouver
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S, Guerini R de CM, Salmen ICDM, Amaral NC de O. A brazilian boy with aural atresia, microtia, complex heart defect, and hearing loss. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 23-26.
Artigo de periodico
C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects (2000)
Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Vendramini, Siulan
Source: The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. Unidade: HRAC
Subjects: RETARDO MENTAL, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine; NAKATA, Nancy Mizue Kokitsu; VENDRAMINI, Siulan. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, Bauru, v. 3, n. Ja, p. 5-10, 2000.
APA
Guion-Almeida, M. L., Nakata, N. M. K., & Vendramini, S. (2000). C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders, 3( Ja), 5-10.
NLM
Guion-Almeida ML, Nakata NMK, Vendramini S. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 5-10.
Vancouver
Guion-Almeida ML, Nakata NMK, Vendramini S. C syndrome: report on a brazilian child with midline brain anomalies and terminal transverse limb defects. The Brazilian Journal of Dysmorphology and Speech-Hearing Disorders. 2000 ; 3( Ja): 5-10.
Artigo de periodico
Auriculo-condylar syndrome: further evidence for a new disorder (1999)
Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Vendramini, Siulan
Source: American Journal of Medical Genetics. Unidade: HRAC
Subject: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine; NAKATA, Nancy Mizue Kokitsu; CEIDE, Roseli Maria Zechi; VENDRAMINI, Siulan. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, New York, v. 86, n. 2, p. 130-133, 1999. DOI: 10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f.
APA
Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., & Vendramini, S. (1999). Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, 86( 2), 130-133. doi:10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f
NLM
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.
Vancouver
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.
Artigo de periodico
Lower lip pits and anorectal anomalies in Kabuki syndrome (1999)
Nakata, Nancy Mizue Kokitsu; Vendramini, Siulan; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Subject: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu; VENDRAMINI, Siulan; GUION-ALMEIDA, Maria Leine. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, New York, v. 86, n. 3, p. 282-284, 1999. DOI: 10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h.
APA
Nakata, N. M. K., Vendramini, S., & Guion-Almeida, M. L. (1999). Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, 86( 3), 282-284. doi:10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
NLM
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.
Vancouver
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.

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