Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability : Coexistence of auditory neuropathy and cochlear hearing loss
スポンサーリンク
概要
著者
-
Kimura Masahiko
島根大学 医学部小児科学
-
Kimura M
Department Of Pediatrics Shimane University School Of Medicine
-
KAGA Makiko
Department of Developmental Disorders, National Institute of Mental Health, National Center of Neuro
-
Sugai Kenji
国立精神・神経センター病院 小児神経科
-
Sugai Kenji
Department Of Child Neurology National Center Hospital Of Neurology And Psychiatry National Center O
-
Sugai Kenji
Department Of Neuropediatrics National Center Of Neurology And Psychiatry
-
Kaga Makiko
Department Of Development Disorders National Institute Of Mental Health National Centre Of Neurology
-
Sugai Kenji
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
SASAKI Masayuki
Department of Health Sciences, School of Medicine, Kyushu University
-
Hanaoka Shigeru
Department of Neuropediatrics, National Center of Neurology and Psychiatry
-
Sasaki Masayuki
Department Of Child Neurology National Center Hospital Of Neurology And Psychiatry National Center O
-
Hanaoka S
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
Hanaoka Shigeru
Department Of Child Neurology National Center Hospital For Mental Nerbous And Muscular Disorders Ncn
-
FUKUMIZU Michio
Department of Child Neurology, National Center Hospital for Mental, Nervous and Muscular Disorders,
-
NOBUTOKI Tatsuro
Department of Child Neurology, National Center Hospital for Mental, Nervous and Muscular Disorders,
-
ANZAI Yuki
Department of Pediatrics, St Luke's International Hospital
-
Anzai Yuki
Department Of Pediatrics St Luke's International Hospital
-
Fukumizu Michio
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
Nobutoki Tatsuro
Department Of Child Neurology National Center Hospital For Mental Nervous And Muscular Disorders Nat
-
Sasaki Masayuki
National Center Hospital For Mental Nervous Muscular Disorders National Center Of Neurology And Psyc
-
Kaga Makiko
National Center Hospital For Mental Nervous Muscular Disorders National Center Of Neurology And Psyc
-
Kimura Masahiko
National Center Hospital For Mental Nervous Muscular Disorders National Center Of Neurology And Psyc
-
Sasaki Masayuki
Department Of Anesthesiology Gunma University Graduate School Of Medicine
-
Sasaki Masayuki
Departments Of Child Neurology National Center Hospital For Neurology And Psychiatry National Center
-
Kimura Masahiko
Department Of Pediatrics Faculty Of Medicine Shimane University
-
Anzai Yuki
Department Of Clinical Neuropathology Tokyo Metropolitan Institute For Neuroscience
-
Sasaki Masayuki
Department of Child Neurology, National Center of Neurology and Psychiatry
関連論文
- Event-related potentials of self-face recognition in children with pervasive developmental disorders
- Pilot study on neonatal mass screening for inborn errors of metabolism by gas chromatography-mass spectrometry : eighteen months experience in Shimane Area
- Urinary organic acids in peroxisomal disorders : a simple screening method
- A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata
- Epilepsy in Peroxisomal Diseases
- Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouse
- Extraosseous accumulation of ^Tc-HMDP to radiation nephropathy, mimicking recurrent neuroblastoma
- Alterations of tumor suppressor genes (Rb, p16, p27 and p53) and an increased FDG uptake in lung cancer
- Comparison of ^FDG-PET with ^Tc-HMDP scintigraphy for the detection of bone metastases in patients with breast cancer
- PET evaluation of the relationship between D_2 receptor binding and glucose metabolism in patients with parkinsonism
- Lesion detectability of a gamma camera based coincidence system with FDG in patients with malignant tumors : A comparison with dedicated positron emission tomography
- An analysis of the physiological FDG uptake pattern in the stomach
- Differential FDG accumulation associated with GLUT-1 expression in a patient with lymphoma
- Clinical impact of whole body FDG-PET on the staging and therapeutic decision making for malignant lymphoma
- ^C-methionine uptake in cerebrovascular disease : A comparison with ^F-FDG PET and ^Tc-HMPAO SPECT
- The usefulness of dipyridamole thallium-201 single photon emission computed tomography for predicting perioperative cardiac events in patients undergoing non-cardiac vascular surgery
- Comparison of MET-PET and FDG-PET for differentiation between benign lesions and malignant tumors of the lung
- Molecular analysis of AVPR2 gene in a Japanese patient With X-linked nephrogenic diabetes insipidus, congenital heart disease and mental retardation
- Gas chromatographic-mass spectrometric screening for organic acidemias using dried urine filter paper : determination of α-ketoacids
- Gas chromatography-mass spectrometry with tert.-butyldimethylsilyl derivatization : use of the simplified sample preparations and the automated data system to screen for organic acidemias
- Gas chromatography-mass spectrometry with tert. -butyldimethylsilyl derivatization : use of the simplified sample preparations and the automated data system to screen for organic acidemias
- Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry
- A survey of Japanese patients with mitochondrial fatty acid β-oxidation and related disorders as detected from 1985 to 2000
- Rapid, simplified and sensitive method for screening fructose-1, 6-diphosphatase deficiency by analyzing urinary metabolites in urease/direct preparations and gas chromatography-mass spectrometry in the selected-ion monitoring mode
- Clinical and biochemical studies on Chinese patients with methylmalonic acidumia
- Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening
- Practical Assay Method of Cytosolic Acetoacetyl-CoA Thiolase by Rapid Release of Cytosolic Enzymes from Cultured Lymphocytes Using Digitonin
- Distal myopathy with rimmed vacuoles in a case of opercular syndrome
- Two Japanese families with hyperekplexia who have a Arg271Gln mutation in the glycine receptor alpha 1 subunit gene
- Enzymatic diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by detecting 2-octenoyl-CoA production using high-performance liquid chromatography : A practical confirmatory test for tandem mass spectrometry newborn screening in Japan
- Serial magnetic resonance angiography in cerebral infarction after varicella infection
- A Variant case of congenital bilateral perisylvian syndrome with asymmetric findings on neuroimaging and septum pellucidum defect
- A case of West syndrome well controlled by very short and low-does ACTH therapy
- Prenatal and postnatal evaluation of Dandy-Walker malformation : a case report
- Brain holding spells in early infancy
- Clinical study of partial epilepsies occurring before two years of life
- Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms
- Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
- Surgical treatment of early-infantile epileptic encephalopathy with suppression-bursts associated with focal cortical dysplasia
- Surgical Treatment of a Case of Early Infantile Epileptic Encephalopathy with Suppression-Bursts Associated with Focal Cortical Dysplasia
- Tremor and seizures associated with chronic manganese intoxication
- III B11 Infantile spasms treated by peri-insular hemispherotomy : a Case report
- Early onset distal muscular dystrophy
- SPECT evaluation of cerebral blood flow during arm exercise in patients with subclavian steal
- Early neuropsychological signs of childhood adrenoleukodystrophy (ALD)
- Oral etodolac, a COX-2 inhibitor, reduces postoperative pain immediately after fast-track cardiac surgery
- Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
- Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria
- Fluctuating hearing loss, episodic headache, and stroke with platelet hyperaggregability : Coexistence of auditory neuropathy and cochlear hearing loss
- Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
- II C12 Treatment of intractable epilepsies with supratherapeutic levels of phenobarbital
- Mechanical ventilation care in severe childhood neurological disorders
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
- A severely brain-damaged case of 3-hydroxyisobutyric aciduria
- Paroxysmal discharges on EEG in young autistic patients are frequent in frontal regions
- Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings
- Otoacoustic emission in patients with neurological disorders who have auditory brainstem response abnormality
- Transient seizure disappearance due to bilateral striatal necrosis in a patient with intractable epilepsy
- Panic Disorder in Irritable Bowel Syndrome
- Cerebral blood flow and vascular response to hypercapnia in hypertensive patients with leukoaraiosis
- Long-term effect of flunarizine on patients with alternating hemiplegia of childhood in Japan
- Hypoxic Effects on Cholesterol Metabolism of Cultured Rat Aortic and Brain Microvascular Endothelial Cells, and Aortic Vascular Smooth Muscle Cells
- Magnetic resonance imaging in congenital facial palsy
- Familial reducing body myopathy
- Neuropathology of early-infantile epileptic encephalopathy with suppression-bursts ; comparison with those of early myoclonic encephalopathy and West syndrome
- Fabrication and Characterization of Nb-(Nb Nanoconstrictions)-NbN Short Weak Links
- Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum
- Abnormal cerebral glucose metabolism in alternating hemiplegia of childhood
- Biodistribution and breast tumor uptake of 16α-[^F]-fluoro-17β-estradiol in rat
- Different neuroradiological findings during two stroke-like episodes in a patient with a congenital disorder of glycosylation type Ia
- Relapse patterns of localized non-Hodgkin's lymphoma of the head and neck after clinical remission: results of a strict follow-up procedure
- New Year's Greetings for 2007
- III B9 Resective epilepsy surgery in children : comparison between younger and older age groups
- Effective immunoglobulin therapy for brief tonic seizures in methylmalonic acidemia
- Mismatch negativity of the color modality during a selective attention task to auditory stimuli in children with mental retardation
- Non-convulsive status epilepticus and audiogenic seizures complicating a patient with asymmetrical epileptic spasms
- Thiamine-deficient encephalopathy due to excessive intake of isotonic drink or overstrict diet therapy in Japanese children
- Postnatal evolution of cortical malformation in the "non-affected" hemisphere of hemimegalencephaly
- Tourette's syndrome in Taiwan : an epidemiological study of tic disorders in an elementary school at Taipei County
- Hemifacial seizures due to ganglioglioma of cerebellum
- Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis
- Brain perfusion SPECT and EEG findings in children with autism spectrum disorders and medically intractable epilepsy
- Auditory perception in auditory neuropathy : Clinical similarity with auditory verbal agnosia
- Developmental changes of distortion product and transient evoked otoacoustic emissions in different age groups
- Current management of febrile seizures in Japan : An overview
- Founders of child neurology in Japan-Masaki Suzuki
- Self-face recognition in children with autism spectrum disorders : A near-infrared spectroscopy study
- Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome
- Augmented startle responses in opsoclonus-myoclonus syndrome
- Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination
- CD4^+ CD25^ regulatory T cell in childhood ocular myasthenia gravis
- Effects of low-dose hydrochlorothiazide on urolithiasis and bone metabolism in severely disabled individuals : A pilot study
- Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
- Greetings from the new Editor-in-Chief
- SISCOM technique with a variable Z score improves detectability of focal cortical dysplasia : a comparative study with MRI
- Decreased resting energy expenditure in patients with Duchenne muscular dystrophy
- Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
- A case of congenital axonal neuropathy associated with West syndrome
- Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia:—Three Case Reports—
- Posterior Disconnection in Early Infancy to Treat Intractable Epilepsy With Multilobar Cortical Dysplasia -Three Case Reports-