H. Iwamoto

发表

A Clinical and EEG Study of Predominantly Unilateral Seizures in Children–Comparison with Severe Myoclonic Epilepsy in Infancy

S. Yamashita, S. Miyake, M. Yamada, 1987, The Japanese journal of psychiatry and neurology.

Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome

Yukichi Tanaka, S. Kimura, M. Hara, 1993, Brain and Development.

Are Down syndrome patients predisposed to Moyamoya disease?

Y. Fukushima, Y. Kuroki, Y. Kondo, 1986, European Journal of Pediatrics.

Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation

K. Yamakawa, N. Yasui-Furukori, H. Osaka, 2007, Epilepsy Research.

Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation

Y. Kuroiwa, Y. Inayama, Tatsuya Takahashi, 2005, Neuropathology : official journal of the Japanese Society of Neuropathology.

Concomitant administration of sodium dichloroacetate and vitamin B1 for lactic acidemia in children with MELAS syndrome.

I. Yokota, J. Matsuda, T. Saijo, 1997, The Journal of pediatrics.

Effect of a new H2-blocker, famotidine, in reflux esophagitis among severely handicapped children.

S. Yamashita, M. Yamada, H. Iwamoto, 1987, Clinical Therapeutics.

Molecular identification of adrenal inner zone antigen as a heme‐binding protein

G. Vinson, H. Hori, M. Okamoto, 2005, The FEBS journal.

Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation

H. Osaka, K. Kurosawa, J. Nagai, 2010, Brain and Development.

Epilepsy in childhood down syndrome

Y. Kuroki, Yasuyuki Suzuki, H. Iwamoto, 1984, Brain and Development.

Rapidly growing calcified cerebellar astrocytoma in infants

I. Yamamoto, T. Shuto, H. Iwamoto, 1996, Child's Nervous System.

Laryngeal dystonia in xeroderma pigmentosum

Yoshiaki Saito, S. Kimura, H. Iwamoto, 2005, Brain and Development.

[Unilateral hemispheric neoplasm and infantile spasms].

S. Yamashita, M. Hara, M. Yamada, 1986, No to hattatsu = Brain and development.

[Three Japanese children with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X)].

M. Masuno, Y. Kuroki, Y. Matsushita, 1998, No to hattatsu = Brain and development.

Infantile spongiform leukoencephalopathy: clinical and neuropathologic findings.

N. Arai, S. Yamashita, M. Hara, 2002, Pediatric Neurology.

Neonatal Asphyxia and Subsequent Epilepsy

S. Yamashita, M. Yamada, H. Iwamoto, 1987 .

Schoolchildren with Epilepsy: Epidemiological and Longitudinal Studies on Questionnaire for Teachers at Intervals of 12 Years

S. Yamashita, S. Miyake, M. Yamada, 1991, The Japanese journal of psychiatry and neurology.

A Long‐Term Follow‐Up Study of First Episodes of Idiopathic Status Convulsivus in Childhood: In Relation to Subsequent Epilepsy (Second Report)

Y. Fukuyama, H. Iwamoto, Y. Awaya, 1992, The Japanese journal of psychiatry and neurology.

Brain MRI findings of older patients with Pallister–Killian syndrome

Y. Kuroki, K. Kurosawa, N. Aida, 2006, Brain and Development.

Multicenter study of paroxysmal dyskinesias in Japan—Clinical and pedigree analysis

T. Matsuishi, M. Mizuguchi, S. Saitoh, 1999, Movement disorders : official journal of the Movement Disorder Society.

[A patient with alternating hemiplegia in childhood].

N. Sakuragawa, H. Tada, M. Yamada, 1989, No to hattatsu = Brain and development.

Congenital polyneuropathy in Walker-Warburg syndrome.

S. Kimura, H. Iwamoto, Y. Sasaki, 1992, Neuropediatrics.

[Mortality patterns of children with epilepsies in a children's medical center].

S. Yamashita, T. Miyagawa, M. Yamada, 1991, No to hattatsu = Brain and development.

Brain MR in Fukuyama congenital muscular dystrophy.

N. Aida, N. Kobayashi, K. Takada, 1996, AJNR. American journal of neuroradiology.