Hemophagocytic syndrome due to perforin-deficiency in three brazilian infants: Immunization could be the trigger? (2014)
- Authors:
- USP affiliated authors: JACOB, CRISTINA MIUKI ABE - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM
- Unidade: FM
- Subjects: DOENÇAS AUTOIMUNES; DOENÇAS DO RECÉM-NASCIDO
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Clinical Immunology
- ISSN: 0271-9142
- Volume/Número/Paginação/Ano: v. 34, n. 3, p. 350, 2014
- Conference titles: CIS Annual Meeting: Primary Immune Deficiency Diseases North American Conference
-
ABNT
JACOB, Cristina Miuki Abe et al. Hemophagocytic syndrome due to perforin-deficiency in three brazilian infants: Immunization could be the trigger?. Journal of Clinical Immunology. New York: Springer. . Acesso em: 08 abr. 2026. , 2014 -
APA
Jacob, C. M. A., Santos, C. de J. N. dos, Gomes, M. C., Carneiro-Sampaio, M., Pastorino, A. C., Dorna, M. de B., et al. (2014). Hemophagocytic syndrome due to perforin-deficiency in three brazilian infants: Immunization could be the trigger? Journal of Clinical Immunology. New York: Springer. -
NLM
Jacob CMA, Santos C de JN dos, Gomes MC, Carneiro-Sampaio M, Pastorino AC, Dorna M de B, Fernandes JF, Castro APC, Rocha V, Hamerschlak N, Saint-Basile G de. Hemophagocytic syndrome due to perforin-deficiency in three brazilian infants: Immunization could be the trigger? Journal of Clinical Immunology. 2014 ; 34( 3): 350.[citado 2026 abr. 08 ] -
Vancouver
Jacob CMA, Santos C de JN dos, Gomes MC, Carneiro-Sampaio M, Pastorino AC, Dorna M de B, Fernandes JF, Castro APC, Rocha V, Hamerschlak N, Saint-Basile G de. Hemophagocytic syndrome due to perforin-deficiency in three brazilian infants: Immunization could be the trigger? Journal of Clinical Immunology. 2014 ; 34( 3): 350.[citado 2026 abr. 08 ] - 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
- A new activation induced cytidine deaminase (AID) mutation in a brazilian family
- Avaliação da função tímica em pacientes com síndrome de DiGeorge
- Restricted T-cell repertoire in four immunodysregulation polyendocrinopathy X-linked (IPEX) infants
- Chronic mucocutaneous candidiasis and its different faces
- DiGeorge Syndrome: a not so rare disease
- Laboratory and clinical description of DiGeorge syndrome patients followed at a reference center: preliminary data
- Chédiak-Higashi syndrome: Experience from a brazilian reference center for primary immunodeficiency
- Chronic granulomatous disease and infectious profile
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas