Detalhe da pesquisa
1.
Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature.
Neurocase
; 24(1): 68-71, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29355451
2.
TARDBP mutation associated with semantic variant primary progressive aphasia, case report and review of the literature.
Neurocase
; 24(5-6): 301-305, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30773994
3.
[SOD1-N196 mutation in a family with amyotrophic lateral sclerosis]. / Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica.
Neurologia
; 27(1): 11-5, 2012 Jan.
Artigo
em Espanhol
| MEDLINE | ID: mdl-21549454
4.
Síndrome de Poland. Presentacíon de un caso. [Poland's syndrome. A case report].
Rev Med Univ Navarra
; 34(1): 21-3, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2096446
5.
The role of cyclooxygenase (COX)-2 derived prostanoids on vasoconstrictor responses to phenylephrine is increased by exposure to low mercury concentration.
J Physiol Pharmacol
; 61(1): 29-36, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20228412
6.
Serum levels of coenzyme Q10 in patients with Parkinson's disease.
J Neural Transm (Vienna)
; 107(2): 177-81, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10847558
7.
Serum levels of coenzyme Q10 in patients with Alzheimer's disease.
J Neural Transm (Vienna)
; 107(2): 233-9, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10847562
8.
Serum levels of coenzyme Q10 in patients with amyotrophic lateral sclerosis.
J Neural Transm (Vienna)
; 107(8-9): 1021-6, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11041280
9.
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.
Ann Neurol
; 50(3): 409-13, 2001 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-11558799
10.
Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
Muscle Nerve
; 26(2): 274-8, 2002 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12210393