Bilateral opercular syndrome: an unusyal complication of perinatal difficulties
スポンサーリンク
概要
著者
-
Koeda Tatsuya
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
Koeda Tatsuya
Division Of Child Neurological Institute Of Neurology Sciences Faculty Of Medicine Tottori Universit
-
Takeshita Kenzo
Division Of Child Neurological Institute Of Neurology Sciences Faculty Of Medicine Tottori Universit
-
Takeshita Kenzo
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
-
KISA Toshiro
Department of Pediatrics,Shimane Prefectural Central Hospital
-
Kisa Toshiro
Department Of Pediatrics Shimane Prefectural Central Hospital
関連論文
- Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
- Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case
- Intracraninal calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report
- Sensorineural deafness in siblings with adenosine deaminase deficiency
- A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
- IgA and IgG2 Deficiency Associated with Zonisamide Therapy: A Case Report
- A functional magnetic resonance imaging study during sentence reading in Japanese dyslexic children
- Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan
- Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
- Cognitive and neurophysiological evaluation of Japanese dyslexia
- Frequency of the Prader-Willi syndrome in the San-in district, Japan
- Cellular senescence of angiofibroma stroma cells from patients with tuberous sclerosis
- Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion
- Slowly progressive cystic leukoencephalopathy with megalencephaly in a Japanese boy
- Carbohydrate-deficient glycoprotein syndrome : electrophoretic study of multiple serum glycoproteins
- Pontine hypoplasia in a child with sensorineural deafiness
- Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
- Unilateral occlusion of the middle cerebral artery after varicella-zoster virus infection
- A patient with cerebral palsy whose mother had a traffic accident during pregnancy : a diffuse axonal injury?
- Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
- Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
- A case report of remarkable improvement of motor disturbances with _L-dopa in a patient with post-diffuse axonal injury
- Bilateral opercular syndrome: an unusyal complication of perinatal difficulties
- 一過性 Extreme Spindle を示した亜急性マイコプラスマ脳炎の一例