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Dissociation between Clinical Evaluation and Peld Score in the Setting of Pediatric Living-Related Liver Transplantation in Japan: A Eighteen Year Single Center Experience

Journal of hepatology, 2016, Vol.64 (2), p.S544-S545

2016

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Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings

Clinical genetics, 2008-06, Vol.73 (6), p.535-544

2008

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Reg gene expression is increased in rat gastric enterochromaffin-like cells following water immersion stress

Gastroenterology (New York, N.Y. 1943), 1996-07, Vol.111 (1), p.45-55

1996

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Frequent Detection of the Human Herpesvirus 6-Specific Genomes in the Livers of Children with Various Liver Diseases

Journal of Clinical Microbiology, 2001-06, Vol.39 (6), p.2173-2177

2001

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Indication for redo hepatic portoenterostomy for insufficient bile drainage in biliary atresia: re-evaluation in the era of liver transplantation

Pediatric surgery international, 2003-06, Vol.19 (4), p.256-259

2003

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Does pancreatico-biliary maljunction play a role in spontaneous perforation of the bile duct in children?

Pediatric surgery international, 2000-11, Vol.16 (8), p.550-553

2000

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FRI-468 - Dissociation between Clinical Evaluation and Peld Score in the Setting of Pediatric Living-Related Liver Transplantation in Japan: A Eighteen Year Single Center Experience

Journal of hepatology, 2016, Vol.64 (2), p.S544-S545

2016

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Chronic hepatitis in an infant, in association with human herpesvirus-6 infection

The Journal of pediatrics, 1997-09, Vol.131 (3), p.473-475

1997

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Loss of EDB+ fibronectin isoform is associated with differentiation of alveolar epithelial cells in human fetal lung

The American journal of pathology, 1997-08, Vol.151 (2), p.403-412

1997

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Rhabdomyoma of the Orbit in a Child

American journal of ophthalmology, 1997-01, Vol.123 (1), p.142-144

1997

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Placental features in preterm infants with periventricular leukomalacia

Pediatrics (Evanston), 2002-04, Vol.109 (4), p.650

2002

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A novel mutation of the down-regulated in adenoma gene in a Japanese case with congential chloride diarrhea. Mutations in brief no. 198. Online

Human mutation, 1998, Vol.12 (5), p.362-362

1998

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Functional Ileus in Neonates: Hirschsprung's Disease-Allied Disorders versus Meconium-Related Ileus

European journal of pediatric surgery, 1999-12, Vol.9 (6), p.392-395

1999

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A Large Outbreak of Foodborne Infection Attributed to Providencia alcalifaciens

The Journal of infectious diseases, 2001-10, Vol.184 (8), p.1050-1055

2001

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Successful stenting for renal artery stenosis in a patient with Alagille syndrome

Pediatric nephrology (Berlin, West), 2005-06, Vol.20 (6), p.831-833

2005

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P0778 LONG TERM GROWTH CATCH‐UP AFTER SMALL BOWEL TRANSPLANTATION FOR CONGENITAL MICROVILLUS INCLUSION DISEASE

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (S1), p.S352-S352

2004

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P0778 LONG TERM GROWTH CATCH-UP AFTER SMALL BOWEL TRANSPLANTATION FOR CONGENITAL MICROVILLUS INCLUSION DISEASE

Journal of pediatric gastroenterology and nutrition, 2004-06, Vol.39 (Supplement 1), p.S352

2004

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Feasibility of duct-to-duct biliary reconstruction in pediatric living related liver transplantation: Report of three cases

Pediatric transplantation, 2006-03, Vol.10 (2), p.248-251

2006

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Rapid progression of intrapulmonary arteriovenous shunting in polysplenia syndrome associated with biliary atresia

Pediatric pulmonology, 2003-06, Vol.35 (6), p.494-498

2003

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Development of intrapulmonary arteriovenous shunting in postoperative biliary atresia: Evaluation by contrast-enhanced echocardiography

Journal of pediatric surgery, 2000-11, Vol.35 (11), p.1647-1650

2000

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Inhibition of thalamic ventrobasal complex neurons by glutamate infusion into the thalamic reticular nucleus in rats

Journal of neuroscience research, 1984, Vol.12 (1), p.93-100

1984

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Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease

Brain & development (Tokyo. 1979), 2006, Vol.28 (1), p.60-62

2006

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Hypomelanosis of Ito associated with hemimegalencephaly

No to hattatsu, 1994-11, Vol.26 (6), p.518

1994

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207 AN INFANTILE CASE OF DIENCEPHALIC SYNDROME WITH LOW LEVEL OF OREXIN IN CSF AND HIGH LEVELS OF SERUM GH

Clinical Pediatric Endocrinology, 2003, Vol.12 (2), p.161-161

2003

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189 Thyroid function abnormalities associated with Amiodarone treatment

Clinical Pediatric Endocrinology, 2003, Vol.12 (2), p.157-157

2003

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Dissociation between Clinical Evaluation and Peld Score in the Setting of Pediatric Living-Related Liver Transplantation in Japan: A Eighteen Year Single Center Experience

Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings

Reg gene expression is increased in rat gastric enterochromaffin-like cells following water immersion stress

Frequent Detection of the Human Herpesvirus 6-Specific Genomes in the Livers of Children with Various Liver Diseases

Indication for redo hepatic portoenterostomy for insufficient bile drainage in biliary atresia: re-evaluation in the era of liver transplantation

Does pancreatico-biliary maljunction play a role in spontaneous perforation of the bile duct in children?

FRI-468 - Dissociation between Clinical Evaluation and Peld Score in the Setting of Pediatric Living-Related Liver Transplantation in Japan: A Eighteen Year Single Center Experience

Chronic hepatitis in an infant, in association with human herpesvirus-6 infection

Loss of EDB+ fibronectin isoform is associated with differentiation of alveolar epithelial cells in human fetal lung

Rhabdomyoma of the Orbit in a Child

Placental features in preterm infants with periventricular leukomalacia

A novel mutation of the down-regulated in adenoma gene in a Japanese case with congential chloride diarrhea. Mutations in brief no. 198. Online

Functional Ileus in Neonates: Hirschsprung's Disease-Allied Disorders versus Meconium-Related Ileus

A Large Outbreak of Foodborne Infection Attributed to Providencia alcalifaciens

Successful stenting for renal artery stenosis in a patient with Alagille syndrome

P0778 LONG TERM GROWTH CATCH‐UP AFTER SMALL BOWEL TRANSPLANTATION FOR CONGENITAL MICROVILLUS INCLUSION DISEASE

P0778 LONG TERM GROWTH CATCH-UP AFTER SMALL BOWEL TRANSPLANTATION FOR CONGENITAL MICROVILLUS INCLUSION DISEASE

Feasibility of duct-to-duct biliary reconstruction in pediatric living related liver transplantation: Report of three cases

Rapid progression of intrapulmonary arteriovenous shunting in polysplenia syndrome associated with biliary atresia

Development of intrapulmonary arteriovenous shunting in postoperative biliary atresia: Evaluation by contrast-enhanced echocardiography

Inhibition of thalamic ventrobasal complex neurons by glutamate infusion into the thalamic reticular nucleus in rats

Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease

Hypomelanosis of Ito associated with hemimegalencephaly

207 AN INFANTILE CASE OF DIENCEPHALIC SYNDROME WITH LOW LEVEL OF OREXIN IN CSF AND HIGH LEVELS OF SERUM GH

189 Thyroid function abnormalities associated with Amiodarone treatment

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