A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor δ2
スポンサーリンク
概要
- 論文の詳細を見る
- 2007-05-01
著者
-
Takahashi Yukitoshi
Department of Pediatrics, Gifu University School of Medicine
-
HAYASAKA KIYOSHI
Department of Pediatrics, Yamagata University School of Medicine
-
KATO Mitsuhiro
Department of Pediatrics, Yamagata University of School of Medicine
-
Hayasaka Kiyoshi
Department Of Pediatrics Yamagata University Faculty Of Medicine
-
Takahashi Yukitoshi
Department Of Pediatrics National Epilepsy Center
-
Takahashi Yukitoshi
Department Of Information And Computer Science Kagoshima University
-
Kato Mitsuhiro
Department Of Pediatrics Yamagata University School Of Medicine
-
SHIMOKAZE Tomoyuki
Department of Pediatrics, Yamagata Prefectural Shinjo Hospital
-
YOSHIMURA Yozo
Department of Pediatrics, Yamagata Prefectural Shinjo Hospital
-
Yoshimura Yozo
Department Of Pediatrics Yamagata Prefectural Shinjo Hospital
-
Shimokaze Tomoyuki
Department Of Pediatrics Yamagata Prefectural Shinjo Hospital
-
Kato Mitsuhiro
Department Of Pediatrics Yamagata University Hospital
-
Kato Mitsuhiro
Department Of Applied Chemistry Aichi Institute Of Technology
-
KATO Mitsuhiro
Department of Pediatrics, Yamagata University School of Medicine
-
Takahashi Yukitoshi
Department of Clinical Research, National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders
関連論文
- III C1 Probable molecular dysfunction by autoantibodies against NMDA receptor GluRe2 in epilepsies after acute encephalitis
- Epileptic seizures and structural abnormalities in a patient with holoprosencephaly
- Epilepsy in Peroxisomal Diseases
- Genetic Analysis of Shwachman-Diamond Syndrome : Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
- Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
- Analysis of the hypothalamus in a case of X-linked lissencephaly with abnormal genitalia (XLAG)
- A case of acute encephalitis with refractory, repetitive partial seizures, presenting autoantibody to glutamate receptor Gluε2
- Human CD4^+ central and effector memory T cells produce IL-21 : effect on cytokine-driven proliferation of CD4^+ T cell subsets
- MR imaging and ^1H-MR spectroscopy of a case of van der Knaap disease
- Mutation analysis of phenylketonuria in Yamagata prefecture, Japan
- De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
- Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
- Congenital Central Hypoventilation Syndrome : A Novel Mutation of the RET Gene in an Isolated Case
- Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
- Prader-Willi syndrome in a child with XYY
- Mild immunoglobulin A nephropathy in a patient with a marked increase in serum immunoglobulin A
- Successful Unrelated Donor Bone Marrow Transplantation for Shwachman-Diamond Syndrome with Leukemia
- CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen
- Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter
- Reflex Seizures in Patients with Malformations of Cortical Development and Refractory Epilepsy
- Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility
- Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease
- Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
- Deletion and Nonsense Mutations of the Connexin 32 Gene Associated with Charcot-Marie-Tooth Disease
- Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor δ2 autoantibody
- A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor δ2
- Mechamical and Kinetic Properties of PVA Hydrogel Immobilizing β-Galactosidase
- Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy
- Variational Study of Vacuum Wave Function for Lattice Gauge Theory in 2+1 Dimension
- Beraprost sodium for pulmonary hypertension with congenital heart disease
- Management of Functional Pulmonary Atresia with Isoproterenol in a Neonate with Ebstein's Anomaly
- Microangiopathic Hemolytic Anemia and Thrombocytopenia in a Child with Atrial Septal Defect and Pulmonary Hypertension
- Neural Crest and Central Nervous System Malformation
- Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency
- A case of Baraitser-Winter syndrome with unusual brain MRI findings : Pachygyria, subcortical-band heterotopia, and periventricular heterotopia
- Human Face Extraction and Recognition Using Radial Basis Function Networks
- Serial MR imaging and ^1H-MR spectroscopy of unidentified bright objects in a case of neurofibromatosis type 1
- IN VITRO FERTILIZATION USING EPIDIDYMAL SPERMATOZOA FOR THE PATIENTS WITH OBSTRUCTIVE AZOOSPERMIA
- A Case of Glycogen Storage Disease Type III (Glycogen Debranching Enzyme Deficiency) with Liver Cirrhosis and Hypertrophic Cardiomyopathy
- Mean Field Method for the Finite Temperature Lattice Gauge Theory : Particles and Fields
- Simultaneous Spectrophotometric Analysis of Aliphatic Amines Utilizing Thermochromism of Charge-Transfer Complexes with Tetrabromophenolphthalein Ethyl Ester
- Detection of DNA of six human herpesviruses in the cerebrospinal fluid of immunocompetent non-herpetic acute limbic encephalitis patients
- A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1
- Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
- Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan
- An Elderly Japanese Patient with Adult-onset Type II Citrullinemia with a Novel D493G Mutation in the SLC25A13 Gene
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype
- Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome
- Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion
- Influence of Concomitant Antiepileptic Drugs on Plasma Lamotrigine Concentration in Adult Japanese Epilepsy Patients
- Phenotypic variability in a family with Townes-Brocks syndrome
- The GARS gene is rarely mutated in Japanese patients with Charcot-Marie-Tooth neuropathy
- Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
- Focal encephalopathy with recurrent episodes of epileptic status and cluster mimicking hemiconvulsion-hemiplegia-epilepsy syndrome
- Ophthalmoplegia and Flaccid Paraplegia in a Patient with Anti-NMDA Receptor Encephalitis: A Case Report and Literature Review
- Going BAC or oligo microarray to the well : A commentary on Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- Evaluation of serum cytokine levels in toxic epidermal necrolysis and Stevens-Johnson syndrome compared with other delayed-type adverse drug reactions
- Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children
- Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms : 211G>A (G71R) mutation becomes a risk factor under inadequate feeding
- A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy
- Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan