Detalhe da pesquisa
1.
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia.
N Engl J Med
; 388(2): 128-141, 2023 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36516086
2.
A KLHL40 3' UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism.
Hum Mol Genet
; 32(7): 1127-1136, 2023 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322148
3.
De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features.
Brain
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753057
4.
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease.
Brain
; 147(5): 1887-1898, 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38193360
5.
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards.
J Neurol Neurosurg Psychiatry
; 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38744462
6.
Ablation of the carboxy-terminal end of MAMDC2 causes a distinct muscular dystrophy.
Brain
; 146(12): 5235-5248, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37503746
7.
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure.
Acta Neuropathol
; 145(1): 127-143, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36264506
8.
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Brain
; 145(11): 3985-3998, 2022 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34957489
9.
FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum.
J Med Genet
; 59(11): 1069-1074, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35393337
10.
Partial loss-of-function variant in neuregulin 1 identified in family with heritable peripheral neuropathy.
Hum Mutat
; 43(9): 1216-1223, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35485770
11.
Systemic AAV8-mediated delivery of a functional copy of muscle glycogen phosphorylase (Pygm) ameliorates disease in a murine model of McArdle disease.
Hum Mol Genet
; 29(1): 20-30, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31511858
12.
Recent advances in our understanding of genetic rhabdomyolysis.
Curr Opin Neurol
; 35(5): 651-657, 2022 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35942668
13.
Identification of a novel heterozygous DYSF variant in a large family with a dominantly-inherited dysferlinopathy.
Neuropathol Appl Neurobiol
; 48(7): e12846, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35962550
14.
A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia-Support for the role of LAP1 in NMJ function and disease.
Neuropathol Appl Neurobiol
; 48(1): e12743, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34164833
15.
Biallelic hypomorphic variants in ALDH1A2 cause a novel lethal human multiple congenital anomaly syndrome encompassing diaphragmatic, pulmonary, and cardiovascular defects.
Hum Mutat
; 42(5): 506-519, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33565183
16.
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2.
Am J Hum Genet
; 102(3): 505-514, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29499166
17.
A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families.
Brain
; 143(10): 2904-2910, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33103729
18.
A Maori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele.
Brain
; 143(9): 2673-2680, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32851396
19.
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion.
Brain
; 143(2): 480-490, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32040566
20.
Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence.
PLoS Genet
; 14(12): e1007845, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30543681