Detalhe da pesquisa
1.
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder.
Clin Genet
; 100(4): 396-404, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34176129
2.
Brandalise syndrome: a rare inclusion cell disease.
Blood
; 136(11): 1373, 2020 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32957120
3.
Monoclonal gammopathy of clinical significance: in vivo demonstration of the anti-thrombotic effect of an acquired anti-thrombin antibody.
Haematologica
; 106(1): 316-319, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32817284
4.
Myelodysplastic Syndrome associated TET2 mutations affect NK cell function and genome methylation.
Nat Commun
; 14(1): 588, 2023 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36737440
5.
UBA1 Variations in Neutrophilic Dermatosis Skin Lesions of Patients With VEXAS Syndrome.
JAMA Dermatol
; 157(11): 1349-1354, 2021 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34495287
6.
Prevalence of UBA1 mutations in MDS/CMML patients with systemic inflammatory and auto-immune disease.
Leukemia
; 35(9): 2731-2733, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34344988
7.
[Abstracts of the 4th CoBioMe Congress]. / Résumés du 4e congrès CoBioMe.
Ann Biol Clin (Paris)
; : 265-275, 2021 Jun 25.
Artigo
em Francês
| MEDLINE | ID: mdl-34170254
8.
[Second edition of the CoBioMe congress]. / Deuxième édition du CoBioMe.
Ann Biol Clin (Paris)
; 77(2): 233-240, 2019 04 01.
Artigo
em Francês
| MEDLINE | ID: mdl-30998203
9.
[First edition of the CoBioMe congress]. / Première édition du CoBioMe Congrès des internes de biologie médicale.
Ann Biol Clin (Paris)
; 76(2): 205-216, 2018 04 01.
Artigo
em Francês
| MEDLINE | ID: mdl-29623891