Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey : Identification of a Putative Locus on Chromosome 9q32-33
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-05-01
著者
-
BIANCHI Amedeo
European Consortium on the Genetics of Idiopathic Generalized Epilepsy
-
BEBEK Nerses
Department of Neurology, Istanbul faculty of Medicine
-
GOKYIGIT Aysen
Department of Neurology, Istanbul faculty of Medicine
-
BAYKAN Betul
Department of Neurology, Instanbul faculty of Medicine
-
MADIA Francesca
Laboratory of Human Genetics, E. O.
-
GIANOTTI Stefania
Laboratory of Human Genetics, E. O.
-
GUNEY Ahment
Department of Medical Biology and Genetics, Marmara University Medical Faculty
-
CINE Naci
Institute for Experimental Medicine (DETAE), Istanbul University
-
BIANCHI Amedeo
Unit of Neurology, Ospedale S. Donato
-
ZARA Federico
Laboratory of Neurogenetics, Unit of Neuromuscular Disease, Gaslini Institute and University of Geno
-
Cine Naci
Institute For Experimental Medicine (detae) Istanbul University
-
Guney A.
Department Of Medical Biology And Genetics Marmara University School Of Medicine
-
Madia Francesca
Laboratory Of Human Genetics E.o. Ospedali Galliera
-
Gianotti Stefania
Laboratory Of Human Genetics E. O.
-
Bebek Nerses
Department Of Neurology Istanbul Faculty Of Medicine
-
Bebek Nerses
Department Of Applied Physiology University Of Ulm
-
Zara Federico
Unit Of Neuromuscular Disorders Department Of Pediatrics Gaslini Institute University Of Genova
-
Zara Federico
Laboratory Of Neurogenetics Department Of Muscular And Neurodegenerative Disease "g. Gaslini&qu
-
Gokyigit Aysen
Department Of Neurology Istanbul University Istanbul Faculty Of Medicine
-
Zara Federico
Laboratory Of Neurogenetics Unit Of Neuromuscular Disease Gaslini Institute And University Of Genova
-
Bianchi Amedeo
Unit Of Neurology Ospedale S. Donato
-
Baykan Betul
Department Of Neurology Instanbul Faculty Of Medicine
-
Gokyigit Aysen
Department Of Neurology Istanbul Faculty Of Medicine
関連論文
- Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12
- Hot Water Epilepsy: Clinical and Electrophysiologic Findings Based on 21 Cases
- Autosomal Recessive Idiopathic Epilepsy in an Inbred Family from Turkey : Identification of a Putative Locus on Chromosome 9q32-33
- Lack of SCN1A Mutations in Familial Febrile Seizures
- No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12-q13.1
- Generalized Epilepsy with Febrile Seizures Plus (GEFS^+) : Clinical Spectrum in Seven Italian Families Unrelated to SCN1A, SCN1B, and GABRG2 Gene Mutations
- Dravet syndrome : Early clinical manifestations and cognitive outcome in 37 Italian patients
- Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy
- Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
- Benign Familial Infantile Convulsions : Linkage to Chromosome 16p12-q12 in 14 Families
- A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms
- Typical Absence Seizures Triggered by Photosensitivity
- Epileptic Seizures in Behcet Disease
- Ictal EEG patterns in epilepsy with centro-temporal spikes
- Diffuse Spike-Wave Status of 9-Year Duration Without Behavioral Change or Intellectual Decline