A. Miyamoto

发表

Hemidystonia, Hemichorea, and Motor Aphasia Associated With Bilateral Ischemic Lesions in the Striatum: Regional Cerebral Blood Flow Studies To Clarify the Pathophysiology

Satoru Takahashi, J. Oki, A. Miyamoto, 1998, Journal of child neurology.

The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome

Y. Makita, J. Oki, A. Miyamoto, 2001, Brain and Development.

Cerebellar hypoperfusion and developmental dysphasia in a male.

J. Oki, A. Miyamoto, S. Takahashi, 1999, Pediatric neurology.

Proton magnetic resonance spectroscopy to study the metabolic changes in the brain of a patient with Leigh syndrome

J. Oki, A. Miyamoto, A. Okuno, 1999, Brain and Development.

Wisconsin syndrome with brain volume laterality: a case report and review of the literature

Y. Makita, Hajime Tanaka, A. Miyamoto, 2022, Journal of Medical Case Reports.

Clinical and genetic features of acute encephalopathy in children taking theophylline

M. Mizuguchi, K. Kikuchi, M. Kubota, 2015, Brain and Development.

Nationwide survey (incidence, clinical course, prognosis) of Rasmussen’s encephalitis

H. Osaka, S. Nabatame, H. Oguni, 2010, Brain and Development.

Severe gastrointestinal symptoms caused by a novel DDX3X variant.

Y. Makita, T. Kaname, K. Yanagi, 2020, European journal of medical genetics.

Encephalopathy associated with haemophagocytic lymphohistiocytosis following rotavirus infection

H. Azuma, J. Oki, A. Miyamoto, 1999, European Journal of Pediatrics.

Autopsy Findings in Pyruvate Dehydrogenase E1α Deficiency: Case Report

Y. Tokusashi, M. Obata, J. Oki, 1997, Journal of child neurology.

Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome

J. Oki, A. Miyamoto, A. Okuno, 1999, Brain and Development.

Neuroradiological assessment of visuoperceptual disturbance in children with spina bifida and hydrocephalus

Hajime Tanaka, A. Miyamoto, A. Araki, 1997, Developmental medicine and child neurology.

Effects of neonatal hypoxia on brainstem cholinergic neurons-pedunculopontine nucleus and laterodorsal tegmental nucleus

J. Oki, Hajime Tanaka, A. Miyamoto, 1995, Brain and Development.

Kabuki make-up syndrome is not caused by microdeletion close to the van der Woude syndrome critical region at 1q32-q41.

N. Niikawa, Y. Makita, K. Yamada, 1999, American journal of medical genetics.

Beta-2-microglobulin and ferritin in cerebrospinal fluid for evaluation of patients with meningitis of different etiologies

Satoru Takahashi, J. Oki, A. Miyamoto, 1999, Brain and Development.

Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features

N. Matsumoto, K. Ogata, Y. Makita, 2012, Journal of Human Genetics.

FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome

K. Okajima, A. Miyamoto, A. Araki, 2012, Clinical genetics.

Serial neuroimages of acute necrotizing encephalopathy associated with human herpesvirus 6 infection

J. Oki, A. Miyamoto, H. Yoshida, 1995, Brain and Development.

Cyclic vomiting and elevation of creatine kinase associated with bitemporal hypoperfusion and EEG abnormalities: a migraine equivalent?

Satoru Takahashi, J. Oki, A. Miyamoto, 1998, Brain and Development.

Acute transverse myelitis caused by ECHO virus type 18 infection

H. Azuma, J. Oki, A. Miyamoto, 1995, European Journal of Pediatrics.

Improvement of hypertonus after treatment for sleep disturbances in three patients with severe brain damage

Hajime Tanaka, A. Miyamoto, A. Araki, 1997, Brain and Development.

CTG trinucleotide repeat length and clinical expression in a family with myotonic dystrophy

J. Oki, A. Miyamoto, A. Okuno, 1996, Brain and Development.

Pyruvate dehydrogenase complex deficiency with multiple minor anomalies

J. Oki, Hajime Tanaka, A. Miyamoto, 1997, Acta paediatrica Japonica : Overseas edition.

Genitopatellar syndrome: the first reported case in Japan

Y. Makita, Y. Matsubara, T. Kaname, 2018, Human Genome Variation.

PCDH19 mutation in Japanese females with epilepsy

H. Shiraishi, Y. Makita, N. Higurashi, 2012, Epilepsy Research.

ASSESSMENT OF VISUOPERCEPTUAL DISTURBANCE IN CHILDREN WITH SPASTIC DIPLEGIA USING MEASUREMENTS OF THE LATERAL VENTRICLES ON CEREBRAL MRI

Hajime Tanaka, A. Miyamoto, A. Araki, 1996, Developmental medicine and child neurology.

Theophylline-induced seizures in a 6-month-old girl Serum and cerebrospinal fluid levels

J. Oki, A. Miyamoto, Michio Yamamoto, 1994, Brain and Development.

Serial imaging in MELAS

J. Oki, A. Miyamoto, S. Takahashi, 1997, Neuroradiology.

De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome.

Y. Makita, J. Oki, A. Miyamoto, 1998, American journal of human genetics.

L1CAM mutation in a Japanese family with X-linked hydrocephalus: a study for genetic counseling

Y. Makita, N. Okamoto, J. Oki, 1997, Brain and Development.

Alobar holoprosencephaly with diabetes insipidus and neuronal migration disorder.

T. Saino, J. Oki, A. Miyamoto, 1995, Pediatric neurology.

[Effects of tizanidine for refractory sleep disturbance in disabled children with spastic quadriplegia].

K. Fujieda, Hajime Tanaka, A. Miyamoto, 2004, No to hattatsu = Brain and development.

GRIA3 p.Met661Thr variant in a female with developmental epileptic encephalopathy

Y. Makita, T. Kaname, K. Yanagi, 2023, Human Genome Variation.

Urine stone formation during treatment with zonisamide

J. Oki, A. Miyamoto, T. Okamoto, 2000, Brain and Development.

A Japanese boy with apparent Bohring‐Opitz or “C‐like” syndrome

Y. Makita, A. Miyamoto, Satoko Noguchi, 2006, American Journal of Medical Genetics. Part A.

Questionnaire survey on sleep habits of 3-year-old children in Asahikawa City: Comparison between 2005 and 2020

Hajime Tanaka, A. Miyamoto, Ikue Fukuda, 2023, Brain and Development.

Ictal HMPAO‐Single Photon Emission Computed Tomography Findings in Reading Epilepsy in a Japanese Boy

Satoru Takahashi, J. Oki, A. Miyamoto, 1995, Epilepsia.