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Filtros : "Finzi, Simone" Removido: "Estados Unidos" Limpar

Filtros

USP affiliated authors
- betinjane, alberto jorge (~1)
- ferraz, victor evangelista de faria (~1)
- paula, jayter silva de (~1)
- susanna junior, remo (~1)
Date published
- 2017 (~1)
- 2015 (~1)
Subjects
- brasil (1)
- degeneração macular (1)
- desenvolvimento infantil (1)
- estudos de coortes (1)
- genes recessivos (1)

Artigo de periodico
Hypotrichosis with juvenile macular distrophy: a case report with molecular study (2017)
Kara Junior, Newton; Finzi, Simone; Susanna Júnior, Remo; Young, Terri L.
Source: Arquivos brasileiros de oftalmologia. Unidade: FM
Subjects: HIPOTRICOSE, DEGENERAÇÃO MACULAR, MUTAÇÃO GENÉTICA, GENES RECESSIVOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KARA JUNIOR, Newton et al. Hypotrichosis with juvenile macular distrophy: a case report with molecular study. Arquivos brasileiros de oftalmologia, n. 01, p. 49-51, 2017Tradução . . Disponível em: https://doi.org/10.5935/0004-2749.20170013. Acesso em: 05 nov. 2024.
APA
Kara Junior, N., Finzi, S., Susanna Júnior, R., & Young, T. L. (2017). Hypotrichosis with juvenile macular distrophy: a case report with molecular study. Arquivos brasileiros de oftalmologia, ( 01), 49-51. doi:10.5935/0004-2749.20170013
NLM
Kara Junior N, Finzi S, Susanna Júnior R, Young TL. Hypotrichosis with juvenile macular distrophy: a case report with molecular study [Internet]. Arquivos brasileiros de oftalmologia. 2017 ;( 01): 49-51.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5935/0004-2749.20170013
Vancouver
Kara Junior N, Finzi S, Susanna Júnior R, Young TL. Hypotrichosis with juvenile macular distrophy: a case report with molecular study [Internet]. Arquivos brasileiros de oftalmologia. 2017 ;( 01): 49-51.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5935/0004-2749.20170013
Artigo de periodico
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil (2015)
Melo, Mônica Barbosa de; Mandal, Anil K.; Tavares, Ivan M.; Ali, Mohammed Hasnat; Kabra, Meha; Vasconcellos, José Paulo Cabral de; Senthil, Sirisha; Sallum, Juliana M. F.; Kaur, Inderjeet; Betinjane, Alberto J.; Moura, Christiane R.; Paula, Jayter Silva de; Costa, Karita A.; Sarfarazi, Mansoor; Paolera, Mauricio Della; Finzi, Simone; Ferraz, Victor Evangelista de Faria; Costa, Vital P.; Belfort, Rubens; Chakrabarti, Subhabrata
Source: Plos One. Unidades: FM, FMRP
Subjects: DESENVOLVIMENTO INFANTIL, ESTUDOS DE COORTES, GLAUCOMA, BRASIL, ÍNDIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Mônica Barbosa de et al. Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil. Plos One, v. 10, n. 5, p. 11 art. e0127147, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0127147. Acesso em: 05 nov. 2024.
APA
Melo, M. B. de, Mandal, A. K., Tavares, I. M., Ali, M. H., Kabra, M., Vasconcellos, J. P. C. de, et al. (2015). Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil. Plos One, 10( 5), 11 art. e0127147. doi:10.1371/journal.pone.0127147
NLM
Melo MB de, Mandal AK, Tavares IM, Ali MH, Kabra M, Vasconcellos JPC de, Senthil S, Sallum JMF, Kaur I, Betinjane AJ, Moura CR, Paula JS de, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE de F, Costa VP, Belfort R, Chakrabarti S. Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil [Internet]. Plos One. 2015 ; 10( 5): 11 art. e0127147.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1371/journal.pone.0127147
Vancouver
Melo MB de, Mandal AK, Tavares IM, Ali MH, Kabra M, Vasconcellos JPC de, Senthil S, Sallum JMF, Kaur I, Betinjane AJ, Moura CR, Paula JS de, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE de F, Costa VP, Belfort R, Chakrabarti S. Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil [Internet]. Plos One. 2015 ; 10( 5): 11 art. e0127147.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1371/journal.pone.0127147

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