Detalhe da pesquisa
1.
De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity.
Genet Med
; 26(5): 101087, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38288683
2.
New insights into CC2D2A-related Joubert syndrome.
J Med Genet
; 60(6): 578-586, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36319078
3.
A Retrospective Multicentric Study of 34 Patients with Niemann-Pick Type C Disease and Early Liver Involvement in France.
J Pediatr
; 254: 75-82.e4, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36265573
4.
Characterization of novel CACNA1A splice variants by RNA-sequencing in patients with episodic or congenital ataxia.
Clin Genet
; 104(3): 365-370, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37177896
5.
Natural history of GM1 gangliosidosis-Retrospective cohort study of 61 French patients from 1998 to 2019.
J Inherit Metab Dis
; 46(5): 972-981, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37381921
6.
Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency.
J Med Genet
; 59(4): 377-384, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33737400
7.
An observational, prospective, multicenter, natural history study of patients with mucopolysaccharidosis type IIIA.
Mol Genet Metab
; 135(2): 133-142, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34991944
8.
Phenotypic characterization of seven individuals with Marbach-Schaaf neurodevelopmental syndrome.
Am J Med Genet A
; 188(9): 2627-2636, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35789103
9.
The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy.
Epilepsia
; 62(2): 325-334, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33410528
10.
Efficacy and safety of arimoclomol in Niemann-Pick disease type C: Results from a double-blind, randomised, placebo-controlled, multinational phase 2/3 trial of a novel treatment.
J Inherit Metab Dis
; 44(6): 1463-1480, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34418116
11.
Genetic and phenotypic spectrum associated with IFIH1 gain-of-function.
Hum Mutat
; 41(4): 837-849, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31898846
12.
Long-term survival outcomes of patients with Niemann-Pick disease type C receiving miglustat treatment: A large retrospective observational study.
J Inherit Metab Dis
; 43(5): 1060-1069, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32324281
13.
AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.
J Inherit Metab Dis
; 43(6): 1254-1264, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32557644
14.
Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome.
Am J Hum Genet
; 98(5): 971-980, 2016 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27108797
15.
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies.
Genet Med
; 21(3): 553-563, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29997391
16.
Hearing impairment as an early sign of alpha-mannosidosis in children with a mild phenotype: Report of seven new cases.
Am J Med Genet A
; 179(9): 1756-1763, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31241255
17.
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.
Am J Med Genet A
; 179(7): 1276-1286, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31124279
18.
Unveiling metabolic remodeling in mucopolysaccharidosis type III through integrative metabolomics and pathway analysis.
J Transl Med
; 16(1): 248, 2018 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30180851
19.
Efficacy and safety of Velmanase alfa in the treatment of patients with alpha-mannosidosis: results from the core and extension phase analysis of a phase III multicentre, double-blind, randomised, placebo-controlled trial.
J Inherit Metab Dis
; 41(6): 1215-1223, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29846843
20.
Comprehensive long-term efficacy and safety of recombinant human alpha-mannosidase (velmanase alfa) treatment in patients with alpha-mannosidosis.
J Inherit Metab Dis
; 41(6): 1225-1233, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29725868