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Serum alanine aminotransferase activity in obese children

Acta Paediatrica, 1997-03, Vol.86 (3), p.238-241

1997

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Genetic Epidemiology of the Carnitine Transporter OCTN2 Gene in a Japanese Population and Phenotypic Characterization in Japanese Pedigrees with Primary Systemic Carnitine Deficiency

Human molecular genetics, 1999-11, Vol.8 (12), p.2247-2254

1999

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

Clinical genetics, 2001-12, Vol.60 (6), p.447-451

2001

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Effects of acute preload reduction on myocardial velocity during isovolumic contraction and myocardial acceleration in pediatric patients

Pediatric cardiology, 2006-02, Vol.27 (1), p.32-36

2006

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Niemann–Pick type C disease: Novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency

Molecular genetics and metabolism, 2006-02, Vol.87 (2), p.113-121

2006

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

Molecular genetics and metabolism, 2004-11, Vol.83 (3), p.213-219

2004

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Development of an efficient production method for β-mannosidase by the creation of an overexpression system in Aspergillus aculeatus

Letters in applied microbiology, 2007-08, Vol.45 (2), p.142-147

2007

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

Clinical genetics, 2002-03, Vol.61 (3), p.222-225

2002

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Molecular beam epitaxial growth of wide bandgap ZnMgO alloy films on (1 1 1)-oriented Si substrate toward UV-detector applications

Journal of crystal growth, 2005-05, Vol.278 (1), p.288-292

2005

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Acid sphingomyelinase deficiency: Cardiac dysfunction and characteristic findings of the coronary arteries

Journal of inherited metabolic disease, 2006-02, Vol.29 (1), p.232-234

2006

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Body mass index can predict left ventricular diastolic filling in asymptomatic obese children

Pediatric cardiology, 2001-07, Vol.22 (4), p.273-278

2001

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Crystal Structures of d-Tagatose 3-Epimerase from Pseudomonas cichorii and Its Complexes with d-Tagatose and d-Fructose

Journal of molecular biology, 2007-11, Vol.374 (2), p.443-453

2007

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Development of an efficient production method for ?-mannosidase by the creation of an overexpression system in Aspergillus aculeatus

Letters in applied microbiology, 2007-08, Vol.45 (2), p.142-147

2007

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

The Journal of pediatrics, 1997-03, Vol.130 (3), p.485-488

1997

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P-89 An infant with radio-ulnarsynostosis and myelodysplastic syndrome (RCMD) had trisomy 8 and responded to immunosuppressive therapy

Leukemia research, 2005, Vol.29, p.S58-S58

2005

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Expression of Aspergillus aculeatus No. F-50 cellobiohydrolase I (cbhI) and beta-glucosidase 1 (bgl1) genes by Saccharomyces cerevisiae

Bioscience, biotechnology, and biochemistry, 1998-08, Vol.62 (8), p.1615-1618

1998

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Johanson-blizzard syndrome: loss of glucagon secretion response to insulin-induced hypoglycemia

Journal of Pediatric Endocrinology and Metabolism, 2004-08, Vol.17 (8), p.1141

2004

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Changes in pulmonary venous flow patterns in patients with ventricular septal defect

Pediatric cardiology, 2002-09, Vol.23 (5), p.491-495

2002

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Posterior descending coronary artery flow reserve assessment by Doppler echocardiography in children with and without congenital heart defect: comparison with invasive technique

Pediatric cardiology, 2004-11, Vol.25 (6), p.647-653

2004

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

Nature genetics, 1999-01, Vol.21 (1), p.91-94

1999

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Practice of Free Jejunal Transfer for Esophageal Reconstruction

Nippon Kikan Shokudoka Gakkai kaiho, 2020-04, Vol.71 (2), p.122-123

2020

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Mutation of the Myelin Po Gene in Charcot-Marie-Tooth Neuropathy Type 1

Biochemical and biophysical research communications, 1993-08, Vol.194 (3), p.1317-1322

1993

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

Brain research, 2005-03, Vol.1037 (1), p.59-69

2005

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Acute cerebellitis

Cerebellum (London, England), 2002-07, Vol.1 (3), p.223-228

2002

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

Brain & development (Tokyo. 1979), 2005-10, Vol.27 (7), p.517-526

2005

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Serum alanine aminotransferase activity in obese children

Genetic Epidemiology of the Carnitine Transporter OCTN2 Gene in a Japanese Population and Phenotypic Characterization in Japanese Pedigrees with Primary Systemic Carnitine Deficiency

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

Effects of acute preload reduction on myocardial velocity during isovolumic contraction and myocardial acceleration in pediatric patients

Niemann–Pick type C disease: Novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency

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

Development of an efficient production method for β-mannosidase by the creation of an overexpression system in Aspergillus aculeatus

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

Molecular beam epitaxial growth of wide bandgap ZnMgO alloy films on (1 1 1)-oriented Si substrate toward UV-detector applications

Acid sphingomyelinase deficiency: Cardiac dysfunction and characteristic findings of the coronary arteries

Body mass index can predict left ventricular diastolic filling in asymptomatic obese children

Crystal Structures of d-Tagatose 3-Epimerase from Pseudomonas cichorii and Its Complexes with d-Tagatose and d-Fructose

Development of an efficient production method for ?-mannosidase by the creation of an overexpression system in Aspergillus aculeatus

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

P-89 An infant with radio-ulnarsynostosis and myelodysplastic syndrome (RCMD) had trisomy 8 and responded to immunosuppressive therapy

Expression of Aspergillus aculeatus No. F-50 cellobiohydrolase I (cbhI) and beta-glucosidase 1 (bgl1) genes by Saccharomyces cerevisiae

Johanson-blizzard syndrome: loss of glucagon secretion response to insulin-induced hypoglycemia

Changes in pulmonary venous flow patterns in patients with ventricular septal defect

Posterior descending coronary artery flow reserve assessment by Doppler echocardiography in children with and without congenital heart defect: comparison with invasive technique

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

Practice of Free Jejunal Transfer for Esophageal Reconstruction

Mutation of the Myelin Po Gene in Charcot-Marie-Tooth Neuropathy Type 1

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

Acute cerebellitis

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

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