TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-03-01
著者
-
Artuch Rafael
Clinical Biochemistry Department Hospital Sant Joan De Deu
-
Ormazabal Aida
Clinical Biochemistry Department Hospital Sant Joan De Deu Barcelona And Centre For Biomedical Resea
-
GARCIA-CAZORLA Angels
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
-
FONS Carmen
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
-
RIZZU Patrizia
Clinical Genetics Department, VU Medisch Centrum
-
MARTORELL Loreto
Molecular Genetics Department, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
-
CAMPISTOL Jaume
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
-
FERNANDEZ-ALVAREZ Emilio
Department of Pediatric Neurology, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
-
ARTUCH Rafael
Clinical Biochemistry Department, Hospital Sant Joan de Deu, Barcelona University, CIBER-ER, Biomedical Network Research Centre on Rare Diseases, Instituto de Salud Carlos III
関連論文
- Cerebrospinal fluid pterins and neurotransmitters in early severe epileptic encephalopathies
- Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation
- TITF-1 gene mutation in a case of sporadic non-progressive chorea. Response to levodopa treatment