Detalhe da pesquisa
1.
Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations.
J Allergy Clin Immunol
; 140(4): 1112-1119, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28115216
2.
Poikiloderma with Neutropenia in Morocco: a Report of Four Cases.
J Clin Immunol
; 37(4): 357-362, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28353165
3.
Inherited biallelic CSF3R mutations in severe congenital neutropenia.
Blood
; 123(24): 3811-7, 2014 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24753537
4.
Very early onset inflammatory bowel disease associated with aberrant trafficking of IL-10R1 and cure by T cell replete haploidentical bone marrow transplantation.
J Clin Immunol
; 34(3): 331-9, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24519095
5.
Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.
J Clin Immunol
; 37(3): 282-286, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28353164
6.
Evidence-based interventions for children and adolescents with fetal alcohol spectrum disorders - A systematic review.
Eur J Paediatr Neurol
; 33: 50-60, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34058625
7.
ABCB1 protects kidney proximal tubule cells against cadmium-induced apoptosis: roles of cadmium and ceramide transport.
Toxicol Sci
; 121(2): 343-56, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21436125