Prognosis of occlusive disease of the circle of Willis (moyamoya disease) in children

T Kurokawa, S Tomita, K Ueda, O Narazaki, T Hanai… - Pediatric …, 1985 - Elsevier
The prognosis of 27 patients with moyamoya disease was studied. The ages at onset
ranged from 11 months to 4–11/12 years. Follow-up study was performed within 4 years …

Treatment of infantile spasms with zonisamide

S Yanai, T Hanai, O Narazaki - Brain and Development, 1999 - Elsevier
We determined the efficacy of and tolerability to zonisamide (ZNS) in newly diagnosed
patients with infantile spasms. ZNS, 4–20 mg/kg per day, was introduced as an add-on …

Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome

S Saitoh, N Oiso, T Wada, O Narazaki… - Journal of Medical …, 2000 - jmg.bmj.com
EDITOR—Deficiency of phosphorylase kinase (Phk), a regulatory protein kinase in glycogen
metabolism, is the most frequent cause of hepatic glycogen storage disease (GSD). Patients …

Hypogammaglobulinaemia in a patient with ring chromosome 21

S Ohga, F Nakao, O Narazaki, N Fusazaki… - Archives of disease in …, 1997 - adc.bmj.com
An 8 year old boy with ring chromosome 21 who was susceptible to sinorespiratory
infections due to hypogammaglobulinaemia is reported. He presented with the characteristic …

Central nervous system disorders and possible brain type carnitine palmitoyltransferase II deficiency

Y Ohtani, A Tomoda, T Miike, M Matsukura… - Brain and …, 1994 - Elsevier
We describe two male infants with central nervous system disorders, ie infantile spasms in
one and athetotic quadriplegia in the other, and with recurrent attacks of high plasma …

Menkes disease: is vitamin C treatment effective?

Y Ueki, O Narazaki, T Hanai - Brain and Development, 1985 - Elsevier
The pathogenesis of Menkes disease seems to be linked to metallothionein which binds to
copper trapped within cells in some tissues. The only known therapy for this disease is …

A case of hereditary motor and sensory neuropathy type III with a decrease in unmyelinated fibers.

O Narazaki, T Hanai, K Sakamoto, A Ohnishi - Brain & development, 1986 - europepmc.org
We report a 3-year-old girl with hereditary motor and sensory neuropathy type III with a
decrease in unmyelinated fibers. There have been few reports of such cases. The present …

[CITATION][C] An epidemiological study on shuffling babies at health check-up at 18 months of age.

O NARAZAKI, A NARAZAKI - 脳と発達, 1986 - jglobal.jst.go.jp
An epidemiological study on shuffling babies at health check-up at 18 months of age. |
Article Information | J-GLOBAL Art J-GLOBAL ID:200902012425712179 Reference number:87A0147141 …

[CITATION][C] A Case of Hereditary Motor and Sensory Neu-ropathy (HMSN) Type III with a Decrease in Unmyelinated Fibers

O Narazaki, T Hanai, K Sakamoto, A Ohnishi - Brain & Development, 1986

[CITATION][C] Intracranial Germinoma with Hemispherical Cerebral Atrophy: Report of a Case and a Suggestive Case.

YJ Chen, T Kurokawa, I Kitamoto, A Mitsudome… - Brain & Development, 1986