Detalhe da pesquisa
1.
Antinuclear antibody-associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus.
Blood
; 143(16): 1576-1585, 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38227934
2.
DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.
Blood
; 141(22): 2713-2726, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36952639
3.
Homozygous variant in TKFC abolishing triokinase activities is associated with isolated immunodeficiency.
J Med Genet
; 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38697782
4.
Severe adult hemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants.
J Allergy Clin Immunol
; 153(1): 256-264, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37678575
5.
Mendelian Causes of Autoimmunity: the Lupus Phenotype.
J Clin Immunol
; 44(4): 99, 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38619739
6.
Proteomic Profiling of Antimalarial Plasmodione Using 3-Benz(o)ylmenadione Affinity-Based Probes.
Chembiochem
; : e202400187, 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38639212
7.
Early systemic inflammation induces neurodevelopmental disorders: results from ARTEMIS, a French multicenter study of juvenile rheumatisms and systemic autoimmune and auto-inflammatory disorders and meta-analysis.
Mol Psychiatry
; 28(4): 1516-1526, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36747095
8.
Juvenile neuropsychiatric systemic lupus erythematosus: A specific clinical phenotype and proposal of a probability score.
Lupus
; 33(4): 328-339, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38315109
9.
Bi-allelic Variants in TKFC Encoding Triokinase/FMN Cyclase Are Associated with Cataracts and Multisystem Disease.
Am J Hum Genet
; 106(2): 256-263, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32004446
10.
Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers.
J Clin Immunol
; 43(3): 615-624, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36469191
11.
JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study.
J Clin Immunol
; 43(6): 1436-1447, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37171742
12.
Rcf2 revealed in cryo-EM structures of hypoxic isoforms of mature mitochondrial III-IV supercomplexes.
Proc Natl Acad Sci U S A
; 117(17): 9329-9337, 2020 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32291341
13.
A common coupling mechanism for A-type heme-copper oxidases from bacteria to mitochondria.
Proc Natl Acad Sci U S A
; 117(17): 9349-9355, 2020 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32291342
14.
Characterization of mutants with single and combined Qi and Qo site mutations in Saccharomyces cerevisiae reveals interactions between the picolinamide fungicide CAS-649 and azoxystrobin.
Pestic Biochem Physiol
; 189: 105313, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36549825
15.
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity.
J Allergy Clin Immunol
; 149(1): 369-378, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33991581
16.
Directed evolution predicts cytochrome b G37V target site modification as probable adaptive mechanism towards the QiI fungicide fenpicoxamid in Zymoseptoria tritici.
Environ Microbiol
; 24(3): 1117-1132, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34490974
17.
Saliva for molecular detection of SARS-CoV-2 in pre-school and school-age children.
Environ Microbiol
; 24(10): 4725-4737, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36065993
18.
Efficacy and tolerance of corticosteroids and methotrexate in patients with juvenile dermatomyositis: a retrospective cohort study.
Rheumatology (Oxford)
; 61(11): 4514-4520, 2022 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35199139
19.
Long-term efficacy and safety of canakinumab in patients with mevalonate kinase deficiency: results from the randomised Phase 3 CLUSTER trial.
Rheumatology (Oxford)
; 61(5): 2088-2094, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34554243
20.
Systemic inflammatory syndrome in children with FARSA deficiency.
Clin Genet
; 101(5-6): 552-558, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35132614