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Artigo de periodico
Induced sputum abnormalities in gas station attendants (2022)
Silva, Tiago Henrique Garcia da; Gastaldi, Ada Clarice ; Santos, Marcel Koenigkam ; Martinis, Bruno Spinosa de ; Martinez, José Antônio Baddini
Source: International Archives of Occupational and Environmental Health. Unidades: FMRP, HRAC, FFCLRP
Subjects: INFLAMAÇÃO, PULMÃO, TRABALHADORES, RISCO AMBIENTAL, RISCOS OCUPACIONAIS, PNEUMOPATIAS
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ABNT
SILVA, Tiago Henrique Garcia da et al. Induced sputum abnormalities in gas station attendants. International Archives of Occupational and Environmental Health, v. 95, n. 2, p. 341-349, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00420-021-01755-2. Acesso em: 17 nov. 2024.
APA
Silva, T. H. G. da, Gastaldi, A. C., Santos, M. K., Martinis, B. S. de, & Martinez, J. A. B. (2022). Induced sputum abnormalities in gas station attendants. International Archives of Occupational and Environmental Health, 95( 2), 341-349. doi:10.1007/s00420-021-01755-2
NLM
Silva THG da, Gastaldi AC, Santos MK, Martinis BS de, Martinez JAB. Induced sputum abnormalities in gas station attendants [Internet]. International Archives of Occupational and Environmental Health. 2022 ; 95( 2): 341-349.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00420-021-01755-2
Vancouver
Silva THG da, Gastaldi AC, Santos MK, Martinis BS de, Martinez JAB. Induced sputum abnormalities in gas station attendants [Internet]. International Archives of Occupational and Environmental Health. 2022 ; 95( 2): 341-349.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s00420-021-01755-2
Artigo de periodico
Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome (2016)
Hong, Sungkook; Hu, Ping; Marino, Juliana; Hufnagel, Sophia B.; Hopkin, Robert J.; Toromanovic, Alma; Richieri-Costa, Antonio; Bicudo, Lucilene A. Ribeiro; Kruszka, Paul; Roessler, Erich; Muenke, Maximilian
Source: Human Molecular Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, HOLOPROSENCEFALIA, FENÓTIPOS
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ABNT
HONG, Sungkook et al. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome. Human Molecular Genetics, v. 25, n. 10, 2016Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddw064. Acesso em: 17 nov. 2024.
APA
Hong, S., Hu, P., Marino, J., Hufnagel, S. B., Hopkin, R. J., Toromanovic, A., et al. (2016). Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome. Human Molecular Genetics, 25( 10). doi:10.1093/hmg/ddw064
NLM
Hong S, Hu P, Marino J, Hufnagel SB, Hopkin RJ, Toromanovic A, Richieri-Costa A, Bicudo LAR, Kruszka P, Roessler E, Muenke M. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome [Internet]. Human Molecular Genetics. 2016 ; 25( 10):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1093/hmg/ddw064
Vancouver
Hong S, Hu P, Marino J, Hufnagel SB, Hopkin RJ, Toromanovic A, Richieri-Costa A, Bicudo LAR, Kruszka P, Roessler E, Muenke M. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome [Internet]. Human Molecular Genetics. 2016 ; 25( 10):[citado 2024 nov. 17 ] Available from: https://doi.org/10.1093/hmg/ddw064
Artigo de periodico
Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers (2010)
Lamônica, Dionísia Aparecida Cusin; Maximino, Luciana Paula; Abramides, Dagma Venturini Marques; Souza, Deise H.; Richieri-Costa, Antonio
Source: Clinical Dysmorphology. Unidades: FOB, HRAC
Subjects: RETARDO MENTAL (PATOLOGIA), TRANSTORNOS DA LINGUAGEM INFANTIL, DOENÇAS HEREDITÁRIAS, DOENÇAS CEREBRAIS
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ABNT
LAMÔNICA, Dionísia Aparecida Cusin et al. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers. Clinical Dysmorphology, v. 19, n. 2, p. 76-78, 2010Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e32833034fc. Acesso em: 17 nov. 2024.
APA
Lamônica, D. A. C., Maximino, L. P., Abramides, D. V. M., Souza, D. H., & Richieri-Costa, A. (2010). Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers. Clinical Dysmorphology, 19( 2), 76-78. doi:10.1097/mcd.0b013e32833034fc
NLM
Lamônica DAC, Maximino LP, Abramides DVM, Souza DH, Richieri-Costa A. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers [Internet]. Clinical Dysmorphology. 2010 ; 19( 2): 76-78.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/mcd.0b013e32833034fc
Vancouver
Lamônica DAC, Maximino LP, Abramides DVM, Souza DH, Richieri-Costa A. Nonprogressive congenital cerebellar ataxia, iris heterochromia, mental retardation and language impairment in two brothers [Internet]. Clinical Dysmorphology. 2010 ; 19( 2): 76-78.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/mcd.0b013e32833034fc
Artigo de periodico
Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? (2009)
Guion-Almeida, Maria Leine; Vendramini-Pittoli, Siulan; Passos-Bueno, Maria Rita ; Zechi-Ceide, Roseli Maria
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, IB
Assunto: ANOMALIA CRANIOFACIAL
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ABNT
GUION-ALMEIDA, Maria Leine et al. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?. American Journal of Medical Genetics. Part A, v. 149A, p. 2762-2764, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32816. Acesso em: 17 nov. 2024.
APA
Guion-Almeida, M. L., Vendramini-Pittoli, S., Passos-Bueno, M. R., & Zechi-Ceide, R. M. (2009). Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? American Journal of Medical Genetics. Part A, 149A, 2762-2764. doi:10.1002/ajmg.a.32816
NLM
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Vancouver
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Artigo de periodico
Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases (2008)
Marques, Ilza Lazarini; Bettiol, Heloisa; Souza, Luiz de; Barbieri, Marco Antonio; Bachega, Maria Irene
Source: Acta Paediatrica. Unidades: HRAC, FMRP
Assunto: SÍNDROME DE PIERRE ROBIN
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ABNT
MARQUES, Ilza Lazarini et al. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases. Acta Paediatrica, v. 97, n. 3, p. 371-375, 2008Tradução . . Disponível em: https://doi.org/10.1111/j.1651-2227.2008.00664.x. Acesso em: 17 nov. 2024.
APA
Marques, I. L., Bettiol, H., Souza, L. de, Barbieri, M. A., & Bachega, M. I. (2008). Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases. Acta Paediatrica, 97( 3), 371-375. doi:10.1111/j.1651-2227.2008.00664.x
NLM
Marques IL, Bettiol H, Souza L de, Barbieri MA, Bachega MI. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases [Internet]. Acta Paediatrica. 2008 ; 97( 3): 371-375.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1111/j.1651-2227.2008.00664.x
Vancouver
Marques IL, Bettiol H, Souza L de, Barbieri MA, Bachega MI. Longitudinal study of the growth of infants with isolated Robin sequence considered being severe cases [Internet]. Acta Paediatrica. 2008 ; 97( 3): 371-375.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1111/j.1651-2227.2008.00664.x
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
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ABNT
VENDRAMINI, Siulan e RICHIERI-COSTA, Antonio e 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, v. 15, n. 4, p. 411-421, 2007Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201770. Acesso em: 17 nov. 2024.
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.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/sj.ejhg.5201770
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.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1038/sj.ejhg.5201770
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
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ABNT
GUION-ALMEIDA, Maria Leine et al. A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate. Clinical Dysmorphology, v. 15, n. 3, p. 171-174, 2006Tradução . . Disponível em: https://doi.org/10.1097/01.mcd.0000220603.09661.7e. Acesso em: 17 nov. 2024.
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 [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e
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 [Internet]. Clinical Dysmorphology. 2006 ; 15( 3): 171-174.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/01.mcd.0000220603.09661.7e
Artigo de periodico
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis (2004)
Nishimura, Agnes Lumi; Mitne Neto, Miguel; Silva, Helga Cristina Almeida da; Richieri-Costa, Antonio; Middleton, Susan; Cascio, Duilio; Kok, Fernando; Oliveira, João Ricardo Mendes de; Gillingwater, T.; Webb, Jeanette; Skehel, Paul; Zatz, Mayana
Source: American Journal of Human Genetics. Unidades: HRAC, IB
Subjects: DOENÇAS NEURODEGENERATIVAS, MUTAÇÃO GENÉTICA
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ABNT
NISHIMURA, Agnes Lumi et al. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. American Journal of Human Genetics, v. 75, n. 5, p. 822-831, 2004Tradução . . Disponível em: http://www.journals.uchicago.edu/AJHG/journal/issues/v75n5/41577/41577.web.pdf. Acesso em: 17 nov. 2024.
APA
Nishimura, A. L., Mitne Neto, M., Silva, H. C. A. da, Richieri-Costa, A., Middleton, S., Cascio, D., et al. (2004). A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. American Journal of Human Genetics, 75( 5), 822-831. Recuperado de http://www.journals.uchicago.edu/AJHG/journal/issues/v75n5/41577/41577.web.pdf
NLM
Nishimura AL, Mitne Neto M, Silva HCA da, Richieri-Costa A, Middleton S, Cascio D, Kok F, Oliveira JRM de, Gillingwater T, Webb J, Skehel P, Zatz M. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis [Internet]. American Journal of Human Genetics. 2004 ; 75( 5): 822-831.[citado 2024 nov. 17 ] Available from: http://www.journals.uchicago.edu/AJHG/journal/issues/v75n5/41577/41577.web.pdf
Vancouver
Nishimura AL, Mitne Neto M, Silva HCA da, Richieri-Costa A, Middleton S, Cascio D, Kok F, Oliveira JRM de, Gillingwater T, Webb J, Skehel P, Zatz M. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis [Internet]. American Journal of Human Genetics. 2004 ; 75( 5): 822-831.[citado 2024 nov. 17 ] Available from: http://www.journals.uchicago.edu/AJHG/journal/issues/v75n5/41577/41577.web.pdf
Artigo de periodico
Sample preparation for atomic spectroscopy: evolution and future trends (2003)
Oliveira, Elisabeth de
Source: Journal of the Brazilian Chemical Society. Unidade: HRAC
Subjects: ESPECTROSCOPIA ATÔMICA, ENERGIA TÉRMICA, QUÍMICA ANALÍTICA
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ABNT
OLIVEIRA, Elisabeth de. Sample preparation for atomic spectroscopy: evolution and future trends. Journal of the Brazilian Chemical Society, v. 14, n. 2, p. 174-182, 2003Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532003000200004. Acesso em: 17 nov. 2024.
APA
Oliveira, E. de. (2003). Sample preparation for atomic spectroscopy: evolution and future trends. Journal of the Brazilian Chemical Society, 14( 2), 174-182. doi:10.1590/s0103-50532003000200004
NLM
Oliveira E de. Sample preparation for atomic spectroscopy: evolution and future trends [Internet]. Journal of the Brazilian Chemical Society. 2003 ; 14( 2): 174-182.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1590/s0103-50532003000200004
Vancouver
Oliveira E de. Sample preparation for atomic spectroscopy: evolution and future trends [Internet]. Journal of the Brazilian Chemical Society. 2003 ; 14( 2): 174-182.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1590/s0103-50532003000200004

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