A case of parietal lobe epilepsy with distinctive clinical and neuroradiological features
スポンサーリンク
概要
著者
-
OKA Akira
Department of Child Neurology, Institute of Neurological Sciences, Tottori University Faculty of Med
-
KUBOTA Masaya
Department of Internal Medicine, Gifu University Graduate School of Medicine
-
Kubota Masaya
Department Of Pediatrics Faculty Of Medicine The University Of Tokyo
-
Kubota Masaya
Department Of Internal Medicine Gifu University Graduate School Of Medicine
-
SAKAKIHARA Yoichi
Department of Pediatrics, Faculty of Medicine, The University of Tokyo
-
YANAGISAWA Masayoshi
Department of Pediatrics, The University of Tokyo
-
Yanagisawa Masayoshi
Department Of Pediatrics The University Of Todyo
-
Yanagisawa Masayoshi
Department Of Clinical Pathology Jichi Medical School
-
Oka Akira
Department Of Pediatrics Faculty Of Medicine The University Of Tokyo
-
Oka Akira
Department Of Child Neurology Institute Of Neurological Sciences Tottori University Faculty Of Medic
-
Oka Akira
Department Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Univers
-
Sakakihara Yoichi
Department Of Pediatrics Faculty Of Medicine The University Of Tokyo
関連論文
- A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI
- Pitavastatin inhibits azoxymethane-induced colonic preneoplastic lesions in C57BL/KsJ-db/db obese mice
- Serum and cerebrospinal fluid levels of cytokines in acute encephalopathy associated with human herpesvirus-6 infection
- Serum and CSF levels of cytokines in acute encephalopathy following prolonged febrile seizures
- Long-term ventilator support in patients with Werdnig-Hoffmann
- A case of parietal lobe epilepsy with distinctive clinical and neuroradiological features
- Temporary improvement of neurological symptoms with gammaglobulin therapy in a boy with adrenoleukodystrophy
- Reduction of seizure frequency with clomipramine in patients with complex partial seizures
- The gene copy ratios of SMN1/SMN2 in Japanese carriers with type I spinal muscular atrophy
- Varicella-associated acute necrotizing encephalopathy with a good prognosis
- Zonisamide-induced urinary lithiasis in patients with intractable epilepsy
- 良性 ローランドてんかんの患者の体性感覚誘発高周波振動の持続は長い
- Moebius syndrome, pituitary dwarfism and hypoplastic optic disc REPLY
- Infantile neuronal ceroid lipofuscinosis : The first reported case in Japan diagnosed by palmitoyl-protein thioesterase enzyme activity deficiency
- A Japanese girl with leukoencephalopathy with vanishing white matter
- STUDY OF ISOVOLUMIC CONTRACTION PHASE BLOOD FLOW PATTERN (a) IN LEFT VENTRICULAR OUTFLOW WITH DOPPLER ECHOCARDIOGRAPHY : Electrophysiology : 46th Annual Scientific Meeting, Japanese Circulation Society
- CLINICAL SIGNIFICANCE OF THE BLOOD FLOW PATTERN IN THE LEFT AND RIGHT VENTRICULAR OUTFLOW TRACT WITH THE DOPPLER ECHOCARDIOGRAPHY : Echocardiography : FREE COMMUNICATIONS (Abstract) : 45 Annual Scientific Meeting, Japanese Circulation Society
- Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus
- Transcranial magnetic stimulation in an adrenoleukodystrophy patient
- Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications
- The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusion
- Optimal dosage and differences in therapeutic efficacy of IGIV in Kawasaki disease
- Olivopontocerebellar atrophy of neonatal onset with muscle hypertonia in two siblings
- Beneficial effect of L-arginine for stroke-like episode in MELAS
- High-dose lorazepam for convulsive status epilepticus in an infant with holoprosencephaly
- Subependymal Giant Cell Astrocytoma With Positive Tuberin Expression : Case Report
- Ras シグナル伝達系の遺伝子変異による重複症候群の遺伝子解析
- Developmental expression of monocyte chemoattractant protein-1 in the human cerebellum and brainstem
- Severe gastrointestinal dysmotility in a patient with congenital myopathy : causal relationship to decrease of interstitial cells of Cajal
- Reply to the letter : "Arima syndrome and bilateral retinoblastoma in interstitial deletion of 13q14.13-q32.3" : Where is the molar tooth sign?
- Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma
- Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases
- Ethical attitudes of Japanese physicians regarding life-sustaining treatment for children with severe neurological disabilities
- Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers
- Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes
- Cross-Sectional Echocardiographic Findings of Left Ventricular Thrombi in a Ten-Year-Old Patient with Cardiomyopathy