G. Takada

发表

Assessment of a New Piezoelectric Transducer Sensor for Noninvasive Cardiorespiratory Monitoring of Newborn Infants in the NICU

Kyoichi Ono, Nobuya Inagaki, Akira Ishida, 2010, Neonatology.

A hippocampal lesion detected by high-field 3 tesla magnetic resonance imaging in a patient with temporal lobe epilepsy.

M. Sasaki, G. Takada, Y. Sawaishi, 2005, The Tohoku journal of experimental medicine.

Prolonged hypothermia protects neonatal rat brain against hypoxic-ischemia by reducing both apoptosis and necrosis

A. Ishida, Masanari Kawamura, Shinobu Miura, 2005, Brain and Development.

A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

K. Hayasaka, G. Takada, W. Sato, 1994, Biochemistry and molecular biology international.

Growth of School Children in Akita Prefecture

Toshiaki Tanaka, G. Takada, T. Okamura, 1994 .

Increased numbers of macrophages in tracheal aspirates in premature infants with funisitis

G. Takada, H. Arai, T. Matsuda, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Short-term fasting alters neonatal rat striatal dopamine levels and serotonin metabolism: an in vivo microdialysis study.

A. Ishida, G. Takada, W. Nakajima, 1997, Brain research. Developmental brain research.

Calpain inhibitor MDL 28170 protects hypoxic–ischemic brain injury in neonatal rats by inhibition of both apoptosis and necrosis

A. Ishida, Masanari Kawamura, Shinobu Miura, 2005, Brain Research.

Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family

K. Higashi, G. Takada, A. Koizumi, 1998, Human Genetics.

Aseptic Meningitis Associated With Cephalosporins in an Infant With Trisomy 21

A. Ishida, G. Takada, W. Nakajima, 2007, Journal of child neurology.

Elevated Sphingomyelinase and Hypercytokinemia in Hemophagocytic Lymphohistiocytosis

Tsutomu Takahashi, M. Yano, G. Takada, 2002, Journal of pediatric hematology/oncology.

Familial mediterranean fever medicated with an herbal medicine in Japan

N. Uemura, Tsutomu Takahashi, G. Takada, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

Niemann-Pick disease type C: cataplexy and hypocretin in cerebrospinal fluid.

A. Noguchi, Tsutomu Takahashi, T. Kanbayashi, 2006, The Tohoku journal of experimental medicine.

Positron emission tomography in juvenile Alexander disease

J. Hatazawa, T. Okudera, G. Takada, 1999, Journal of the Neurological Sciences.

Serum alanine aminotransferase activity in obese children

G. Takada, Y. Tazawa, F. Nishinomiya, 1997, Acta paediatrica.

Serum uric acid as an obesity-related indicator in early adolescence.

Tsutomu Takahashi, G. Takada, T. Ohno, 2006, The Tohoku journal of experimental medicine.

Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients.

T. Saheki, Keiko Kobayashi, S. Kanzaki, 2004, Molecular genetics and metabolism.

Excessive playing of home computer games by children presenting unexplained symptoms.

G. Takada, Y. Tazawa, A. V. Soukalo, 1997, The Journal of pediatrics.

Johanson-Blizzard Syndrome: Loss of Glucagon Secretion Response to Insulin-induced Hypoglycemia

Tsutomu Takahashi, G. Takada, S. Tsuchida, 2004 .

Niemann-Pick type C disease: novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency.

H. Ninomiya, Tsutomu Takahashi, G. Takada, 2006, Molecular genetics and metabolism.

Five novel SLC7A7 variants and y+L gene‐expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance

K. Ihara, T. Hara, A. Nakai, 2002, Human Mutation.

Elastogenesis in cultured dermal fibroblasts from patients with lysosomal beta-galactosidase, protective protein/cathepsin A and neuraminidase-1 deficiencies.

H. Sakuraba, Tsutomu Takahashi, G. Takada, 2006, The journal of medical investigation : JMI.

Relationship of feeding modality to clinical features in Japanese infants with idiopathic neonatal hepatitis of the non‐familial form

G. Takada, Y. Tazawa, D. Abukawa, 1996, Acta paediatrica Japonica : Overseas edition.

Mass screening for Wilson’s disease: Results and recommendations

F. Endo, T. Kitagawa, G. Takada, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

Congenital hypomyelination neuropathy: decreased expression of the P2 protein in peripheral nerve with normal DNA sequence of the coding region

I. Nonaka, K. Hayasaka, K. Sugai, 1995, Journal of the Neurological Sciences.

Active hypothalamic-pituitary-gonadal axis in an infant with X-linked adrenal hypoplasia congenita.

G. Takada, T. Takahashi, I. Takahashi, 1997, The Journal of pediatrics.

Juvenile Alexander disease with a novel mutation in glial fibrillary acidic protein gene.

G. Takada, Y. Sawaishi, T. Yano, 2002, Neurology.

Acid sphingomyelinase: relation of 93lysine residue on the ratio of intracellular to secreted enzyme activity.

E. Schuchman, Tsutomu Takahashi, G. Takada, 2005, The Tohoku journal of experimental medicine.

A case of fatal infectious mononucleosis presenting with fulminant hepatic failure associated with an extensive CD8-positive lymphocyte infiltration in the liver.

M. Nose, S. Tsuchiya, G. Takada, 1993, Human pathology.

The relationship between serum transaminase activities and fatty liver in children with simple obesity

G. Takada, Y. Tazawa, F. Nishinomiya, 1995, Acta paediatrica Japonica : Overseas edition.

Mutational analyses of AVPR2 gene in three Japanese families with X‐linked nephrogenic diabetes insipidus: Two recurrent mutations, R137H and ΔV278, caused by the hypermutability at CpG dinucleotides

H. Kito, Y. Suzuki, T. Suzuki, 1998, Human mutation.

Renovascular hypertension due to antithrombin deficiency in childhood

Satoshi Takahashi, Tsutomu Takahashi, G. Takada, 2004, Pediatric Nephrology.

Molecular and population genetics of phenylketonuria in Orientals: Correlation between phenotype and genotype

G. Isshiki, G. Takada, Y. Shigematsu, 1994, Journal of Inherited Metabolic Disease.

Evidence for the association of ultraviolet-C and H(2)O(2)-induced apoptosis with acid sphingomyelinase activation.

H. Ida, G. Takada, T. Takahashi, 2001, Biochimica et biophysica acta.

Striatal perfusion of indomethacin attenuates dopamine increase in immature rat brain exposed to anoxia: an in vivo microdialysis study

A. Ishida, G. Takada, W. Nakajima, 1999, Brain Research.

Cytotoxic activity against tumour cells mediated by intermediate TCR cells in the liver and spleen

T. Abo, S. Seki, G. Takada, 1996, Immunology.

Effect of tetrahydrobiopterin and 5-hydroxytryptophan on hereditary progressive dystonia with marked diurnal fluctuation: a suggestion of the serotonergic system involvement.

A. Ishida, G. Takada, I. Toyoshima, 1988, The Tohoku journal of experimental medicine.

Transient neurotoxicity associated with FK506: MR findings.

N. Tomura, S. Takahashi, G. Takada, 1998, Journal of computer assisted tomography.

SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families

A. Noguchi, Tsutomu Takahashi, G. Takada, 2000, Human mutation.

Recurrent URAT1 gene mutations and prevalence of renal hypouricemia in Japanese

Tsutomu Takahashi, G. Takada, S. Tsuchida, 2005, Pediatric Nephrology.

Thyroid dysgenesis caused by PAX8 mutation: the hypermutability with CpG dinucleotides at codon 31.

M. Nakamura, G. Takada, T. Takahashi, 2001, The Journal of pediatrics.

A PTPN11 gene mutation (Y63C) causing Noonan syndrome is not associated with short stature in general population.

A. Koizumi, Tsutomu Takahashi, G. Takada, 2006, The Tohoku journal of experimental medicine.

Acute cerebellitis caused by Coxiella burnetii

K. Hirai, G. Takada, Y. Sawaishi, 1999, Annals of neurology.

Pulse methylprednisolone therapy in type 3 adenovirus pneumonia with hypercytokinemia.

H. Saito, Tsutomu Takahashi, G. Takada, 2006, Tohoku journal of experimental medicine.

Split notochord syndrome: ileal duplication causing intermittent episodes of vomiting.

H. Nanjo, A. Noguchi, Tsutomu Takahashi, 2006, The Tohoku journal of experimental medicine.

Relationships between clinical and histological profiles of non‐familial idiopathic neonatal hepatitis

G. Takada, Y. Tazawa, D. Abukawa, 1996, Acta paediatrica Japonica : Overseas edition.

Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency.

T. Matsuishi, S. Kibira, J. Nezu, 1999, Human molecular genetics.

A case of tubulo-interstitial nephritis with exfoliative dermatitis and hepatitis due to phenobarbital hypersensitivity

K. Hayasaka, G. Takada, Y. Sawaishi, 2005, European Journal of Pediatrics.

Case of congenital infection with Candida glabrata in one infant in a set of twins

G. Takada, A. Sato, H. Arai, 2002, Pediatrics international : official journal of the Japan Pediatric Society.

Effect of anoxia on striatal monoamine metabolism in immature rat brain compared with that of hypoxia: an in vivo microdialysis study

A. Ishida, G. Takada, W. Nakajima, 1996, Brain Research.

Enzyme therapy in Gaucher disease type 2: an autopsy case.

H. Ida, Y. Yoshida, G. Takada, 1998, The Tohoku journal of experimental medicine.

Prolonged activation of the hypothalamus– pituitary–gonadal axis in a child with X‐linked adrenal hypoplasia congenita

Tsutomu Takahashi, G. Takada, I. Takahashi, 2000, Clinical endocrinology.

A new locus for a dominant form of multinodular goiter on 3q26.1-q26.3.

G. Takada, A. Koizumi, Y. Wada, 2001, Biochemical and biophysical research communications.

Dexamethasone-Induced Prenatal Alveolar Wall Thinning Is Associated with a Decrease in EIIIA+ Fibronectin Isoform in the Fetal Rat Lung

A. Ishida, G. Takada, H. Arai, 2005, Neonatology.

DISTAL PULMONARY CELL PROLIFERATION IS ASSOCIATED WITH THE EXPRESSION OF EIIIA+ FIBRONECTIN IN THEDEVELOPING RAT LUNG

A. Ishida, G. Takada, Yasushi Takahashi, 2003, Experimental lung research.

An exonic mutation of the GH‐1 gene causing familial isolated growth hormone deficiency type II

T. Sato, G. Takada, T. Takahashi, 2002, Clinical genetics.

An SEDL gene mutation in a Japanese kindred of X‐linked spondyloepiphyseal dysplasia tarda

G. Takada, S. Tsuchida, T. Takahashi, 2002, Clinical genetics.

A Case of Neonatal Choriocarcinoma

A. Ishida, G. Takada, Y. Takahashi, 1997, American journal of perinatology.

Loss of EDB+ Fibronectin Isoform is associated with Differentiation of Alveolar Epithelial Cells in Human Fetal Lung. † 1458

K. Sekiguchi, M. Nakayama, S. Mushiake, 1997, Pediatric Research.

Long-acting gonadotropin-releasing hormone analogue treatment for central precocious puberty in maternal uniparental disomy chromosome 14.

A. Koizumi, Tsutomu Takahashi, G. Takada, 2005, The Tohoku journal of experimental medicine.

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

G. Tsujimoto, T. Matsuishi, J. Nezu, 1999, Nature Genetics.

Methaemoglobinaemia after inhalation of nitric oxide in infant with pulmonary hypertension

A. Ishida, G. Takada, W. Nakajima, 1997, The Lancet.

Immunohistochemical study on transforming growth factor-beta1 expression in liver fibrosis of Down's syndrome with transient abnormal myelopoiesis.

A. Ishida, G. Takada, F. Nishinomiya, 1999, Human pathology.

Osteopontin expression in the liver with severe perisinusoidal fibrosis: Autopsy case of Down syndrome with transient myeloproliferative disorder

A. Ishida, T. Yoshioka, Y. Doi, 2007, Pathology international.

Intraventricular ascorbic acid administration decreases hypoxic–ischemic brain injury in newborn rats

A. Ishida, Masanari Kawamura, Shinobu Miura, 2006, Brain Research.

SSPE following neonatal measles infection.

G. Takada, Y. Sawaishi, T. Yano, 1999, Pediatric neurology.

Idiopathic Neonatal Hepatitis Presenting as Neonatal Hepatic Siderosis and Steatosis

T. Konno, G. Takada, Y. Tazawa, 1998, Digestive Diseases and Sciences.

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

K. Hayasaka, G. Takada, W. Sato, 1993, Journal of Inherited Metabolic Disease.

Tropoelastin regulates chemokine expression in fibroblasts in Costello syndrome.

D. Tsuji, Reiko Fujinawa, Y. Kozutsumi, 2008, Biochemical and biophysical research communications.

Hypersomnia due to acute disseminated encephalomyelitis in a 5-year-old girl.

Y. Hishikawa, T. Shimizu, T. Kanbayashi, 2001, Sleep medicine.

Acute cerebellitis

G. Takada, Y. Sawaishi, 2008, The Cerebellum.

Choroid Plexus Carcinoma Presented with Spinal Dysfunction Caused by a Drop Metastasis: A Case Report

Y. Yoshida, G. Takada, K. Mizoi, 2003, Journal of Neuro-Oncology.

Leukoencephalopathy around a tumor cyst following intracystic methotrexate injection.

G. Takada, Y. Sawaishi, T. Yano, 2005, Pediatric neurology.

Significant decrease in tropoelastin gene expression in fibroblasts from a Japanese Costello syndrome patient with impaired elastogenesis and enhanced proliferation.

D. Tsuji, H. Sakuraba, Tsutomu Takahashi, 2006, Journal of biochemistry.

Neuroprotection of edaravone on hypoxic-ischemic brain injury in neonatal rats.

A. Ishida, G. Takada, W. Nakajima, 2004, Brain research. Developmental brain research.

Distribution of acid sphingomyelinase in human various body fluids.

G. Takada, T. Takahashi, I. Takahashi, 2000, The Tohoku journal of experimental medicine.

Signaling pathway for radiation-induced apoptosis in the lymphoblasts from neuronopathic (type A) and non-neuronopathic (type B) forms of Niemann–Pick disease

Y. Minamiya, A. Ishida, Tsutomu Takahashi, 2002, Journal of the Neurological Sciences.

Heterogeneity of liver disorder in type B Niemann-Pick disease.

T. Tokudome, G. Takada, K. Akiyama, 1997, Human pathology.

Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic forms.

R. Desnick, E. Schuchman, Tsutomu Takahashi, 1992, The Journal of biological chemistry.

Identification of a missense mutation (S436R) in the acid sphingomyelinase gene from a Japanese patient with type B Niemann–Pick disease

R. Desnick, E. Schuchman, Tsutomu Takahashi, 1992, Human mutation.

Mutational analyses in four Japanese families with X-linked liver phosphorylase kinase deficiency type 1

Y. Kuroda, K. Inui, T. Nishigaki, 1998, Journal of Inherited Metabolic Disease.

Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome

G. Nishimura, K. Higashi, G. Takada, 2001, Clinical genetics.

Psychosocial Dwarfism: A Case Report

A. Noguchi, Tsutomu Takahashi, G. Takada, 2005 .

No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment

K. Tachibana, Hiroyuki Tanaka, K. Fujieda, 2006, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

X‐linked adrenal hypoplasia congenita: Testicular histology before puberty

Tetsuo Kato, H. Nanjo, Tsutomu Takahashi, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Cranial computed tomography scans of premature babies predict their eventual learning disabilities.

A. Ishida, G. Takada, Y. Takahashi, 1997, Pediatric neurology.

Acute life-threatening event with rhabdomyolysis after starting on high-dose pyridoxine therapy in an infant with homocystinuria

G. Takada, W. Sato, T. Takahashi, 1998, Journal of Inherited Metabolic Disease.

Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5q.

K. Harada, Tsutomu Takahashi, G. Takada, 1998, American journal of human genetics.

3-Methylglutaconic aciduria type I: Clinical heterogeneity as a neurometabolic disease

A. Ishida, Tsutomu Takahashi, G. Takada, 1999, Journal of Inherited Metabolic Disease.

Progressive facial hemiatrophy after epileptic seizures.

M. Toyono, G. Takada, Y. Sawaishi, 2000, Pediatric neurology.

Migratory basal ganglia lesions in subacute sclerosing panencephalitis (SSPE): Clinical implications of axonal spread

G. Takada, Yasuhiro Watanabe, Y. Sawaishi, 1999, Journal of the Neurological Sciences.

A molecular lesion in a Japanese patient with severe phenotype of 3‐methylglutaconic aciduria type I

Tsutomu Takahashi, G. Takada, M. Matsumori, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Childhood multiple sclerosis treated with plasmapheresis.

G. Takada, Y. Sawaishi, I. Takahashi, 1997, Pediatric neurology.

Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

K. Hayasaka, G. Takada, Y. Sawaishi, 1992, American journal of human genetics.

Lidocaine‐dependent Early Infantile Status Epilepticus with Highly Suppressed EEG

G. Takada, Y. Sawaishi, T. Yano, 2002, Epilepsia.

Effect of weight reduction on serum transaminase activities in children with simple obesity.

G. Takada, Y. Tazawa, F. Nishinomiya, 1996, The Journal of pediatrics.

Ala/Thr60 variant of the Leydig insulin‐like hormone is not associated with cryptorchidism in the Japanese population

Tsutomu Takahashi, G. Takada, I. Takahashi, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

Serum Zn2+-stimulated sphingomyelinase deficiency in type B Niemann-Pick disease

G. Takada, T. Takahashi, I. Takahashi, 1999, European Journal of Pediatrics.

Two siblings with partial trisomy 15 and monosomy 21 associated with central nervous system anomalies.

A. Ishida, G. Takada, Y. Takahashi, 1993, The Tohoku journal of experimental medicine.

Effect of N-Methyl-D-Aspartate and Potassium on Striatal Monoamine Metabolism in Immature Rat: An In Vivo Microdialysis Study

A. Ishida, G. Takada, W. Nakajima, 1998, Neurochemical Research.

Magnesium Attenuates a Striatal Dopamine Increase Induced by Anoxia in the Neonatal Rat Brain: An in Vivo Microdialysis Study

A. Ishida, G. Takada, W. Nakajima, 1997, Pediatric Research.

A case of moyamoya-like vessels combined with brain anomaly.

N. Tomura, S. Takahashi, G. Takada, 1999, Radiation medicine.

Long-acting gonadotropin-releasing hormone analogue treatment for central precocious puberty in maternal uniparental disomy chromosome 14.

A. Koizumi, Tsutomu Takahashi, G. Takada, 2005, The Tohoku journal of experimental medicine.

Anoxic and hypoxic immature rat model for measurement of monoamine using in vivo microdialysis.

A. Ishida, G. Takada, W. Nakajima, 1999, Brain research. Brain research protocols.