S. Okada

发表

Gene therapy in Duchenne muscular dystrophy

K. Inui, S. Okada, G. Dickson, 1996, Brain and Development.

Review article Gene therapy in Duchenne muscular dystrophy

K. Inui, S. Okada, G. Dickson, 1996 .

The effect of pentylenetetrazole-kindling on the extracellular glutamate and taurine levels in the frontal cortex of rats

J. Ono, A. Yamatodani, S. Okada, 2000, Neuroscience Letters.

Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

M. Taniike, S. Nakajima, S. Okada, 1998 .

Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence

Yusuke Nakamura, H. Kurahashi, J. Ono, 2000, Journal of Human Genetics.

Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndrome

Yusuke Nakamura, H. Kurahashi, J. Ono, 1998, Human Genetics.

GM1 gangliosidosis in adults: Clinical and molecular analysis of 16 Japanese patients

Yoshiyuki Suzuki, N. Yanagisawa, Kunihiro Yoshida, 1992, Annals of neurology.

Tay-Sachs Disease: Generalized Absence of a Beta-D-N-Acetylhexosaminidase Component

J. O'brien, S. Okada, 1969, Science.

Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia

T. Okamura, K. Ozono, S. Okada, 2000, Journal of Bone and Mineral Metabolism.

Differentiation between dysmyelination and demyelination using magnetic resonance diffusional anisotropy

Koushi Harada, J. Ono, K. Harada, 1995, Brain Research.

Unverricht-Lundborg disease with cystatin B gene abnormalities.

K. Kagitani-Shimono, N. Okamoto, J. Ono, 2002, Pediatric neurology.

INSULIN AND GLUCAGON SECRETION IN HEPATIC GLYCOGENOSES

Y. Seino, H. Kodama, Y. Seino, 1979, Acta Paediatrica Scandinavica.

Characteristic MR features of encephalitis caused by Epstein-Barr virus: a case report

J. Ono, K. Harada, S. Okada, 1998, Pediatric Radiology.

The Silver‐Russell Syndrome: A Case with Hypergonadotropic Hypogonadism

S. Okada, H. Yabuuchi, T. Harada, 1980 .

NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C

K. Higaki, E. Nanba, T. Takeshima, 1999, Human Genetics.

Increased Serum IL-10 and Endothelin Levels in Hemolytic Uremic Syndrome Caused by Escherichia coli O157

T. Honda, S. Okada, Takehisa Yamamoto, 2000, Nephron.

Difficulty in differential diagnosis of atypical absence seizures and complex partial seizures in childhood

Yasuhiro Suzuki, H. Arai, J. Ono, 1995, Psychiatry and clinical neurosciences.

Interstitial Deletion of 14q, 46, XY, del (14) (q24.3q32.1) Associated With Status Nonepileptic Myoclonia and Delayed Myelination

J. Ono, K. Inui, S. Okada, 1999, Journal of child neurology.

I‐cell disease: clinical studies of 21 Japanese cases

M. Owada, S. Okada, T. Sakiyama, 1985, Clinical genetics.

The effects of sucrose loading on lysosomal hydrolases

S. Okada, H. Yabuuchi, Tomochika Kato, 2004, Molecular and Cellular Biochemistry.

The Role of Cytokines for the Pathogenesis of Hemolytic Uremic Syndrome Caused by Escherichia coli O 157:H7 Infections.

M. Monden, T. Shimazu, T. Honda, 1998 .

Enhancement of immunity against VZV by giving live varicella vaccine to the elderly assessed by VZV skin test and IAHA, gpELISA antibody assay.

H. Asada, K. Yoshikawa, K. Yamanishi, 2003, Vaccine.

Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157

K. Ozono, S. Okada, Takehisa Yamamoto, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets

K. Ozono, T. Michigami, S. Okada, 2005, Journal of Bone and Mineral Metabolism.

Hypophosphatemic rickets accompanying McCune–Albright syndrome: evidence that a humoral factor causes hypophosphatemia

H. Yoshikawa, K. Ozono, E. Takeda, 2001, Journal of Bone and Mineral Metabolism.

Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome

Yusuke Nakamura, Toshihiro Tanaka, Y. Yazaki, 2001, Journal of Human Genetics.

Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome

Yusuke Nakamura, H. Kurahashi, S. Ida, 1999, Journal of Human Genetics.

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease

M. Taniike, K. Inui, H. Tsukamoto, 1990, Journal of the Neurological Sciences.

A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

K. Ozono, T. Michigami, A. Miyauchi, 2001, Journal of Human Genetics.

Accumulation of Lysosphingolipids in Tissues from Patients with GM1 and GM2 Gangliosidoses

Takurou Kobayashi, I. Goto, K. Ohno, 1992, Journal of neurochemistry.

The Effects of Anticonvulsants on Liver and Bone Metabolism

Y. Seino, S. Okada, H. Yabuuchi, 1977 .

A Case of Vitamin D Dependency Type I

K. Ozono, Y. Seino, S. Nakajima, 1992 .

Bilateral intracranial granulomas as a complication of infected subdural peritoneal shunt

J. Ono, S. Okada, K. Morimoto, 1983, Brain and Development.

Effect of Pentylentetrazol (PTZ) Kindling on GABAergic System: A Histochemical Study by Staining for GABA‐Transaminase (GABA‐T)

J. Ono, K. Imai, S. Okada, 1993, The Japanese journal of psychiatry and neurology.

Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

H. Yoshikawa, K. Ozono, S. Okada, 2002, Journal of Bone and Mineral Metabolism.

Tay-Sachs Disease: Prenatal Diagnosis

J. Leroy, J. O'brien, S. Okada, 1971, Science.

Properties of sulfatases in cultured skin fibroblasts of multiple sulfatase deficient patients

K. Inui, S. Okada, H. Yabuuchi, 1981, Clinical genetics.

Generalized Gangliosidosis: Beta-Galactosidase Deficiency

J. O'brien, S. Okada, S. Okada, 1968, Science.

Electron microscopic examination of skin and conjunctival biopsy specimens in neuronal storage diseases

S. Okada, M. Shimada, T. Yamano, 1979, Brain and Development.

Generalized Gangliosidosis: Impaired Cleavage of Galactose from a Mucopolysaccharide and a Glycoprotein

S. Okada, M. Ho, Monica C. MacBrinn, 1969, Science.

Molecular Cloning and Expression of cDNA for Murine Galactocerebrosidase and Mutation Analysis of the Twitcher Mouse, a Model of Krabbe's Disease

M. Taniike, K. Ozono, K. Inui, 1996, Journal of neurochemistry.

Mucolipidosis with β‐Galactosidase Deficiency: a Type of Sialidosis

J. Furuyama, K. Inui, K. Yamashita, 1981 .

Hypothalamic-pituitary functions in patients with idiopathic pituitary dwarfism

K. Miyai, S. Okada, H. Yabuuchi, 1978, European Journal of Pediatrics.

Neuronal depletion of cerebellum in late infantile metachromatic leulcodystrophy

S. Okada, S. Ohta, M. Shimada, 1980, Brain and Development.

Ultrastructural pathology of rectum and skin biopsy specimens in lysosomal storage diseases

M. Taniike, T. Yamano, K. Inui, 1990 .

A case of giant axonal neuropathy showing focal aggregation and hypophosphorylation of intermediate filaments

I. Mohri, M. Taniike, S. Itami, 1998, Brain and Development.

Early-onset facioscapulohumeral muscular dystrophy: two case reports 1 A summary of this article was presented at the 37th Annual Meeting of the Japanese Society of Neurology in Omiya, Japan, on May 16, 1996. 1

K. Inui, I. Yanagihara, S. Okada, 1997, Brain and Development.

Ictal Video‐EEG Recording of Three Partial Seizures in a Patient with the Benign Infantile Convulsions Associated with Mild Gastroenteritis

Y. Futagi, J. Ono, K. Imai, 1999, Epilepsia.

Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms

J. Ono, K. Imai, S. Okada, 1997, Epilepsia.

Inhibitory effect of theophylline on recombinant GABAA receptor

T. Mashimo, S. Okada, I. Uchida, 2001, Neuroreport.

Allele frequencies of intragenic, and 5′ and 3′ markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy

K. Inui, H. Tsukamoto, S. Okada, 1996, Japanese Journal of Human Genetics.

Sialidosis type 2 in Japan Clinical study in two siblings' cases and review of literature

S. Okada, Masaru Watanabe, Kyoko Yamamoto, 1983, Journal of the Neurological Sciences.

Mutation analysis of a Japanese patient with fucosidosis

H. Kurahashi, L. Fu, K. Inui, 1999, Journal of Human Genetics.

Shift of Serum Osteocalcin Components between Cord Blood and Blood at Day 5 of Life

S. Nakajima, S. Okada, K. Yamaoka, 2002, Pediatric Research.

Intracranial lipoma of the quadrigeminal region associated with complex partial seizures

J. Ono, K. Imai, S. Okada, 1998, Pediatric Radiology.

Metabolism: Enzymatic Diagnosis of Mucopolysaccharidosis and Lipidosis

S. Okada, H. Yabuuchi, Tohru Yutaka, 1985 .

A case of late variant form of infantile krabbe disease with a partial deficiency of galactocerebrosidase

S. Okada, H. Tanaka, Tomochika Kato, 1988, Brain and Development.

A case of chronic infantile type of fucosidosis: clinical and magnetic resonance image findings

K. Inui, T. Nishigaki, H. Tsukamoto, 2000, Brain and Development.

Outcome of Patients with West Syndrome: A Multicenter Cooperative Study.

Yasuhiro Suzuki, A. Yasuhara, H. Tamai, 1996 .

Immunohistochemistry of Neurotransmitters and Their Receptors in Hemimegalencephaly.

H. Kimura, H. Arai, M. Nakayama, 1996 .

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome

K. Inui, T. Nishigaki, H. Tsukamoto, 2000, Journal of Human Genetics.

Molecular cloning of the chromosomal breakpoint in the LIS1 gene of a patient with isolated lissencephaly and balanced t(8;17)

Yusuke Nakamura, H. Kurahashi, J. Ono, 1998, Human Genetics.

Partial deletion of the long arm of chromosome 11: ten Japanese children

J. Ono, H. Tsukamoto, S. Ohdo, 1996, Clinical genetics.

Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome

J. Ono, K. Inui, H. Tsukamoto, 2001, Brain and Development.

Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B1 and B2

I. Nonaka, H. Arai, K. Inui, 1997, Brain and Development.

Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNAIle 4269 mutation): histochemical, immunohistochemical, and ultrastructural study

T. Yanagihara, S. Yorifuji, M. Taniike, 1995, Journal of Neurological Sciences.

Efficacy and Side Effects of Short‐Term Alternate‐Day Adrenocorticotropic Hormone Therapy for Epileptic Spasms in Symptomatic Epilepsy

Y. Futagi, Yasuhiro Suzuki, K. Imai, 1996 .

Efficacy of bromide for intractable epilepsy in childhood.

J. Ono, K. Imai, S. Okada, 1990 .

Identification of Amino Acid Sequence in the Hinge Region of Human Vitamin D Receptor That Transfers a Cytosolic Protein to the Nucleus*

K. Ozono, T. Michigami, Chika Shimizu, 1999, The Journal of Biological Chemistry.

Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome

J. Dumanski, H. Kurahashi, S. Takai, 1994, Human Genetics.

Refined mapping of eight cosmid markers on human chromosome 22

G. Thomas, O. Delattre, T. Melot, 1994, Japanese Journal of Human Genetics.

The effect of spermine on the disaccharidase activities in suckling rats of different age.

Norikazu Yoshimura, S. Mushiake, S. Okada, 1993, Cell biology international.

A case of mucolipidosis II: Biochemical, nutritional, and immunological studies

Masahiro Kato, S. Okada, S. Kojima, 1979, Brain and Development.

Ontogenesis of neurons immunoreactive for nitric oxide synthase in rat forebrain and midbrain.

H. Kimura, K. Kitahama, T. Nagai, 2001, Brain research. Developmental brain research.

Distribution of nitric oxide synthase-immunoreactive neurons in fetal rat brains at embryonic day 15 and day 19

H. Kimura, K. Kitahama, T. Nagai, 1996, Journal of Chemical Neuroanatomy.

A case of Hallervorden-Spatz disease: Progressive and intractable dystonia controlled by bilateral thalamotomy

T. Yoshimine, A. Kato, M. Taniike, 1992, Brain and Development.

Isolated lissencephaly sequence with balanced chromosome translocation involving 17p13.3

H. Kurahashi, J. Ono, S. Okada, 1998, Brain and Development.

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

Yusuke Nakamura, Toshihiro Tanaka, Y. Yazaki, 1998, Human Genetics.

MR diffusion imaging in Pelizaeus-Merzbacher disease

J. Ono, K. Harada, S. Okada, 1994, Brain and Development.

Vitamin D metabolites in human milk from mothers of preterm and full-term infants

Y. Seino, S. Okada, M. Zheng, 1990, Journal of Bone and Mineral Metabolism.

Lysosulfatide (Sulfogalactosylsphingosine) Accumulation in Tissues from Patients with Metachromatic Leukodystrophy

Y. Eto, Takurou Kobayashi, K. Inui, 1990, Journal of neurochemistry.

Structure of serum transferrin in carbohydrate-deficient glycoprotein syndrome.

Y. Wada, N. Taniguchi, N. Okamoto, 1992, Biochemical and biophysical research communications.

Electronmicroscopy of COnjunctival biopsy in mannosidosis

A. Mitsudome, S. Okada, M. Shimada, 1981, Neurology.

Evaluation of myelination by means of the T2 value on magnetic resonance imaging

J. Ono, K. Inui, Jiro Ono, 1993, Brain and Development.

Liposome-mediated gene transfer.

Y. Kaneda, K. Inui, S. Okada, 1995, Molecular and cell biology of human diseases series.

CORRELATION OF SUBCELLULAR LOCALIZATION OF DISEASE-SPECIFIC INCLUSIONS AND SPHINGOLIPID ACTIVATOR PROTEIN-1 (SAP-1) IN SULFATIDE SULFATASE-DEFICIENT FIBROBLASTS

M. Taniike, K. Shinoda, K. Inui, 1988 .

Synergistic effect of 1,25-dihydroxyvitamin D3 and retinoic acid in inducing U937 cell differentiation.

Y. Seino, S. Okada, K. Yamaoka, 1992, Journal of nutritional science and vitaminology.

Differentiation of dys- and demyelination using diffusional anisotropy.

K Sakurai, J. Ono, K. Harada, 1997, Pediatric neurology.

Biallelic inactivation of the APC gene in hepatoblastoma.

H. Kurahashi, K. Takami, I. Nishisho, 1995, Cancer research.

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

M. Taniike, K. Inui, T. Nishigaki, 1992, The Journal of pediatrics.

Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes.

Y. Kagawa, J. Hayashi, S. Ohta, 1994, The Journal of biological chemistry.

A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome

I. Nonaka, K. Inui, H. Tsukamoto, 2002, Neuromuscular Disorders.

An apoptotic depletion of oligodendrocytes in the twitcher, a murine model of globoid cell leukodystrophy.

Y. Urade, I. Mohri, M. Taniike, 1999, Journal of neuropathology and experimental neurology.

Manganese deposition in the brain during long-term total parenteral nutrition.

J. Ono, K. Harada, S. Okada, 1995, JPEN. Journal of parenteral and enteral nutrition.

Hepatocyte growth factor is constitutively produced by human bone marrow stromal cells and indirectly promotes hematopoiesis.

K. Matsumoto, T. Nakamura, Toshikazu Nakamura, 1997, Blood.

Long-term response to zonisamide in patients with West syndrome.

Y. Toribe, J. Ono, K. Imai, 2002, Neurology.

SSCP analysis by RT‐PCR for the prenatal diagnosis of Niemann‐Pick disease type C

E. Nanba, Toshiyuki Yamamoto, K. Inui, 2001, Prenatal diagnosis.

Immunohistochemical Demonstration of GM2-Ganglioside in the Central Nervous System of a 19-week-old Fetus of Tay-Sachs Disease

M. Taniike, Y. Hirabayashi, K. Inui, 1989, Journal of Inherited Metabolic Disease.

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy.

M. Taniike, M. Taniike, H. Fujimura, 1992, Biochemical and biophysical research communications.

Glycogen storage disease type Ia: molecular diagnosis of 51 Japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells.

Kazutoshi Takahashi, Y. Matsubara, K. Narisawa, 2000, American journal of medical genetics.

Impaired degradation of chondroitin sulfate in GM2‐gangliosidosis

S. Okada, Tomochika Kato, Tohru Yutaka, 1982, Clinical genetics.

Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A.

J. O'brien, S. Okada, S. Okada, 1970, The Journal of pediatrics.