Detalhe da pesquisa
1.
Loss of hypothalamic MCH decreases food intake in amyotrophic lateral sclerosis.
Acta Neuropathol
; 145(6): 773-791, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37058170
2.
H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating.
Int J Mol Sci
; 22(17)2021 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502138
3.
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss.
EMBO J
; 35(10): 1077-97, 2016 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26951610
4.
Degeneration of serotonin neurons triggers spasticity in amyotrophic lateral sclerosis.
Ann Neurol
; 82(3): 444-456, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28856708
5.
Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.
Hum Mol Genet
; 24(8): 2228-40, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25552654
6.
Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis.
Acta Neuropathol
; 133(6): 887-906, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28243725
7.
Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis.
Brain
; 139(Pt 4): 1106-22, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26984187
8.
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis.
Acta Neuropathol
; 131(3): 465-80, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26744351
9.
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
Hum Mol Genet
; 22(12): 2350-60, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23446633
10.
Cortical hyperexcitability in mouse models and patients with amyotrophic lateral sclerosis is linked to noradrenaline deficiency.
Sci Transl Med
; 16(738): eadg3665, 2024 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38478631
11.
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
Neurobiol Dis
; 58: 220-30, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23742762