Novel mutations in MVK associated with hyperimmunoglobulinemia D with periodic fever syndrome phenotype (2014)
- Authors:
- USP affiliated authors: DUARTE, ALBERTO JOSE DA SILVA - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM ; JACOB, CRISTINA MIUKI ABE - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; IMUNOGLOBULINAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Clinical Immunology
- Volume/Número/Paginação/Ano: v. 34, supl 2, p. S197, 2014
- Conference titles: Biennal Meeting of the European Society for Immunodeficiencies/ ESID
-
ABNT
VASCONCELOS, D. Moraes et al. Novel mutations in MVK associated with hyperimmunoglobulinemia D with periodic fever syndrome phenotype. Journal of Clinical Immunology. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 11 maio 2024. , 2014 -
APA
Vasconcelos, D. M., Fujihira, E., Oliveira, J. B., Jesus, A. A., Silva, C., Castro, A. P. M., et al. (2014). Novel mutations in MVK associated with hyperimmunoglobulinemia D with periodic fever syndrome phenotype. Journal of Clinical Immunology. New York: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Vasconcelos DM, Fujihira E, Oliveira JB, Jesus AA, Silva C, Castro APM, Dorna MB, Pontillo A, Chuffi-Barros N, Jacob CMA, Carneiro-Sampaio MMS, Duarte AJ. Novel mutations in MVK associated with hyperimmunoglobulinemia D with periodic fever syndrome phenotype. Journal of Clinical Immunology. 2014 ; 34 S197.[citado 2024 maio 11 ] -
Vancouver
Vasconcelos DM, Fujihira E, Oliveira JB, Jesus AA, Silva C, Castro APM, Dorna MB, Pontillo A, Chuffi-Barros N, Jacob CMA, Carneiro-Sampaio MMS, Duarte AJ. Novel mutations in MVK associated with hyperimmunoglobulinemia D with periodic fever syndrome phenotype. Journal of Clinical Immunology. 2014 ; 34 S197.[citado 2024 maio 11 ] - Transient hypogamaglobulinemia of infancy: a review of clinical findings and evolution of patients
- Hemophagocytic syndrome associated to NK cells deficiency: a case report
- Restricted T-cell repertoire in four immunodysregulation polyendocrinopathy X-linked (IPEX) infants
- Chronic mucocutaneous candidiasis and its different faces
- Avaliação da função tímica em pacientes com síndrome de DiGeorge
- A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrome
- A new activation induced cytidine deaminase (AID) mutation in a brazilian family
- GH deficiency as the first endocrinopathy in a brazilian patient with an AIRE gene homozygous p326l mutation causing the APECED syndrome
- Neutropenia in antibody-deficient patients under IVIG replacement therapy
- Chronic granulomatous disease and infectious profile
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas