GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome (2008)
- Authors:
- USP affiliated authors: JACOB, CRISTINA MIUKI ABE - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; GENES; DOENÇAS IMUNOLÓGICAS; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical and Experimental Immunology
- Volume/Número/Paginação/Ano: v. 154, suppl. 1, p. 29, res. P007, 2008
- Conference titles: Meeting of The European Society for Immunodeficiency
-
ABNT
CARNEIRO-SAMPAIO, M. et al. GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 23 abr. 2024. , 2008 -
APA
Carneiro-Sampaio, M., Jacob, C. M. A., Leone, C. R., Dorna, M. B., Pieri, P. C., Oliveira, J. B., et al. (2008). GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome. Clinical and Experimental Immunology. London: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Carneiro-Sampaio M, Jacob CMA, Leone CR, Dorna MB, Pieri PC, Oliveira JB, Pastorino AC, Della Manna T. GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome. Clinical and Experimental Immunology. 2008 ; 154 29.[citado 2024 abr. 23 ] -
Vancouver
Carneiro-Sampaio M, Jacob CMA, Leone CR, Dorna MB, Pieri PC, Oliveira JB, Pastorino AC, Della Manna T. GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome. Clinical and Experimental Immunology. 2008 ; 154 29.[citado 2024 abr. 23 ] - Transient hypogamaglobulinemia of infancy: a review of clinical findings and evolution of patients
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