Muscle CT scans in preclinical cases of Duchenne and Becker muscular dystrophy
スポンサーリンク
概要
著者
-
Fukuyama Yukio
Department Of Pediatrics Tokyo Women's Medical College
-
Osawa Makiko
Department of Pediatrics, Tokyo Women's Medical University
-
Osawa Makiko
Department Of Pediatrics Tokyo Women's Medical College
-
Arai Yumi
Department Of Pediatrics Tokyo Women's Medical College
-
Osawa Makiko
Department Of Pediatrics Faculty Of Medicine Tokyo Women's Medical University
-
Arai Yumi
Department Of Agricultural Chemistry Faculty Of Agriculture Meiji University
関連論文
- A Case of a Type 1 Diabetes Child with a Type 1 Diabetic Mother
- PJ-442 Fukutin Gene Mutations Cause Dilated Cardiomyopathy with Minimal Muscle Weakness(Cardiomyopathy, basic/clinical-6, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Wisconsin card sorting test in children with temporal lobe epilepsy
- Rasmussen Syndrome : Multifocal Spread of Inflammation Suggested from MRI and PET Findings
- Agranulocytosis following phenytoin-induced hypersensitivity syndrome
- Modified Atkins diet therapy for a case with glucose transporter type 1 deficiency syndrome
- Focal epileptic spasms, involving one leg, manifesting during the clinical course of west syndrome (WS)
- Extremely low-dose ACTH step-up protocol for West syndrome : Maximum therapeutic effect with minimal side effects
- Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in Japan
- Zonisamide for West syndrome : a comparison of clinical responses among different titration rate
- Effect of ACTH Therapy for Epileptic Spasms without Hypsarrhythmia
- EEG in Children with Early-onset Benign Occipital Seizure Susceptibility Syndrome : Panayiotopoulos Syndrome
- Clinical and EEG analysis of initial status epilipticus during infancy in patients with mesial temporal lobe epilepsy
- Myoclonic-astatic epilepsy of early childhood - clinical and EEG analysis of myoclonic-astatic seizures, and discussions on the nosology of the syndrome
- Severe myoclonic epilepsy in infants - a review based on the Tokyo Women's Medical University series of 84 cases
- Acquired epileptiform opercular syndrome: a case report and results of single photon emission computed tomography and computer-assisted electroencephalographic analysis
- A Study of the Effect of Color Photostimulation from a Cathode-rat Tube (CRT) Display on Photosensitive Patients : The Effect of Alternating Red-Cyan Flicker Stimulation
- Surgical Indication for Refractory Childhood Epilepsy
- Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy
- Study on surgical treatment of intractable childhood epilepsy
- Atonic Epileptic Drop Attacks Associated with Generalized Spike-and-Slow Wave Complexes: Video-Polygraphic Study in Two Patients
- Long*Term Prognosis of Lennox-Gastaut Syndrome
- Neuropsychological study of localization-related epilepsy in children
- Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
- Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus
- Benefits of FK 506 for refractory eye symptoms in a young child with ocular myasthenia gravis
- Pathological study of bronchospasms/tracheomalasia in patients with severe motor and intellectual disabilities
- Thalamic lesions in a long-surviving child with spinal muscular atrophy type I : MRI and EEG findings
- A 1-year-old infant with McArdle disease associated with hyper-creatine kinase-emia during febrile episodes
- Study on Photo-Pattern Sensitivity in Patients with Electronic Screen Game : Induced Seizures (ESGS): Effects of Spatial Resolution, Brightness, and Pattern Movement
- Familial antiphospholipid antibody in a child with involuntary movement and deterioration
- Electrophysiological study of myoclonic seizures in children
- Creatine monohydrate therapy in a Leigh syndrome patient with A8344G mutation
- Beta-Blocker Therapy for Cardiac Dysfunction in Patients With Muscular Dystrophy
- Long-term effect of flunarizine on patients with alternating hemiplegia of childhood in Japan
- Discharge diagnoses in infants with apparent life-threatening event
- A comparative study of high-dose and low-dose ACTH therapy for West syndrome
- Study on the Early-Onset Variant of Benign Childhood Epilepsy with Occipital Paroxysms Otherwise Described as Early-Onset Benign Occipital Seizure Susceptibility Syndrome
- Startle Epilepsy with Infantile Hemiplegia: Report of Two Cases Improved by Surgery
- Activity of neurons in ventrolateral respiratory groups during swallowing in decerebrate rats
- Polymorphism analysis of Fukuyama type congenital muscular dystrophy(FCMD) siblings with different phenotypes
- Roles of Fukutin, the Gene Responsible for Fukuyama-Type Congenital Muscular Dystrophy, in Neurons: Possible Involvement in Synaptic Function and Neuronal Migration
- 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
- Benign Familial Infantile Convulsions : Linkage to Chromosome 16p12-q12 in 14 Families
- Muscle CT scans in preclinical cases of Duchenne and Becker muscular dystrophy
- Effect of medical treatments on psychiatric symptoms in children with anorexia nervosa
- Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis
- Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
- Identification and Determination of α-Dicarbonyl Compounds Formed in the Degradation of Sugars
- 最適条件下高速液体クロマトグラフィーにより測定した、けいれん重積症例のミダゾラム血中濃度
- Morphometric study of the corpus callosum in Fukuyama type congenital muscular dystrophy by magnetic resonance imaging
- Prospective study of nesidioblastosis in newborns and infants: Hypoglycemic seizures, epileptogenesis and the significance of the C-peptide suppression test in pancreatectomy
- Marine necklace-chain Fragilariaceae (Bacillariophyceae) from Guam, including descriptions of Koernerella and Perideraion, genera nova
- Severe Peters Plus syndrome-like phenotype with anterior eye staphyloma and hypoplastic left heart syndrome : Proposal of a new syndrome
- New insights into the pathogenesis of spinal muscular atrophy
- A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish
- High-density CT of muscle and liver may allow early diagnosis of childhood-onset Pompe disease
- Close monitoring of initial enzyme replacement therapy in a patient with childhood-onset Pompe disease
- Lesions in the central tegmental tract in autopsy cases of developmental brain disorders
- Profile of Professor Yukio Fukuyama
- Severe muscle damage following viral infection in patients with Fukuyama congenital muscular dystrophy
- Two Cases of Precocious Puberty Associated with Hypothalamic Hamartoma