Detalhe da pesquisa
1.
Insights into the expanding intestinal phenotypic spectrum of SOCS1 haploinsufficiency and therapeutic options.
J Clin Immunol
; 43(6): 1403-1413, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37156989
2.
Systemic inflammatory syndrome in children with FARSA deficiency.
Clin Genet
; 101(5-6): 552-558, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35132614
3.
Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy.
Clin Gastroenterol Hepatol
; 21(5): 1368-1371.e2, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35944833
4.
Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A.
Stem Cell Res
; 68: 103057, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36868038
5.
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
J Clin Invest
; 132(10)2022 05 16.
Artigo
Inglês
| MEDLINE | ID: mdl-35575086
6.
[Recent immunological literature under scrutiny by master students]. / L'actualité immunologique sous l'oeil critique des étudiants de Master 2.
Med Sci (Paris)
; 34(3): 219-222, 2018 Mar.
Artigo
Francês
| MEDLINE | ID: mdl-29547107