UB Paderborn / Katalog / Suche / in CDI

Weight-for-height charts for Japanese children based on the year 2000 Report of School Health Statistics Research

Clinical Pediatric Endocrinology, 2016, Vol.25(2), pp.77-82

2016

Volltextzugriff (PDF)

The Role of N-Terminal Pro-B-Type Natriuretic Peptide in the Diagnosis of Congestive Heart Failure in Children: Correlation With the Heart Failure Score and Comparison With B-Type Natriuretic Peptide

Circulation Journal, 2010, Vol.74(5), pp.998-1005

2010

Volltextzugriff (PDF)

Etiology of Severe Sensorineural Hearing Loss in Children: Independent Impact of Congenital Cytomegalovirus Infection and GJB2 Mutations

The Journal of infectious diseases, 2007-03, Vol.195 (6), p.782-788

2007

Volltextzugriff (PDF)

Pediatric Endocrinology: Our Present Status and Future Prospects

Endocrine Journal, 2010, Vol.57(1), pp.1-2

FUJIEDA, Kenji

2010

Volltextzugriff (PDF)

Molecular Basis of Neonatal Diabetes in Japanese Patients

The journal of clinical endocrinology and metabolism, 2007-10, Vol.92 (10), p.3979-3985

2007

Volltextzugriff (PDF)

Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients

The journal of clinical endocrinology and metabolism, 2009-05, Vol.94 (5), p.1723-1731

2009

Volltextzugriff (PDF)

New reference values for thyroid volume by ultrasound in iodine-sufficient schoolchildren: a World Health Organization/Nutrition for Health and Development Iodine Deficiency Study Group Report

The American journal of clinical nutrition, 2004-02, Vol.79 (2), p.231-237

2004

Volltextzugriff (PDF)

A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure

Endocrine Journal, 2009, Vol.56(4), pp.619-624

2009

Volltextzugriff (PDF)

Induction Chemotherapy Followed by Low-Dose Involved-Field Radiotherapy for Intracranial Germ Cell Tumors

Journal of clinical oncology, 2002-02, Vol.20 (3), p.857-865

Aoyama, H.

2002

Volltextzugriff (PDF)

Proximal Promoter of the Cytochrome P450 Oxidoreductase Gene: Identification of Microdeletions Involving the Untranslated Exon 1 and Critical Function of the SP1 Binding Sites

The journal of clinical endocrinology and metabolism, 2011-11, Vol.96 (11), p.E1881-E1887

2011

Volltextzugriff (PDF)

Transforming growth factor-β1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways

Biochemical and biophysical research communications, 2009-06, Vol.383 (4), p.475-479

2009

Volltextzugriff (PDF)

Conditional Deletion of Neuronal Cyclin-Dependent Kinase 5 in Developing Forebrain Results in Microglial Activation and Neurodegeneration

The American journal of pathology, 2010, Vol.176 (1), p.320-329

2010

Volltextzugriff (PDF)

Elevated Free Thyroxine Levels Detected by a Neonatal Screening System

Pediatric research, 2009-09, Vol.66 (3), p.312-316

2009

Volltextzugriff (PDF)

Dried Umbilical Cords in the Retrospective Diagnosis of Congenital Cytomegalovirus Infection as a Cause of Developmental Delays

Clinical infectious diseases, 2009-05, Vol.48 (10), p.e93-e95

2009

Volltextzugriff (PDF)

A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica

Endocrine Journal, 2007, Vol.54(4), pp.637-641

2007

Volltextzugriff (PDF)

An observational study of the effectiveness and safety of growth hormone (Humatrope®) treatment in Japanese children with growth hormone deficiency or Turner syndrome

Endocrine Journal, 2013, Vol.60(1), pp.57-64

2013

Volltextzugriff (PDF)

Increased Na reabsorption via the Na–Cl cotransporter in autosomal recessive pseudohypoaldosteronism

Clinical and experimental nephrology, 2010-06, Vol.14 (3), p.228-232

2010

Volltextzugriff (PDF)

Prevalence and risk factors of vitamin D deficiency rickets in Hokkaido, Japan

Pediatrics international, 2009-08, Vol.51 (4), p.559-562

2009

Volltextzugriff (PDF)

Clinical characteristics of Japanese adults with growth hormone deficiency: a HypoCCS database study

Endocrine Journal, 2011, Vol.58(5), pp.325-333

2011

Volltextzugriff (PDF)

Analysis of expression and structure of the rat GH-secretagogue/ghrelin receptor (Ghsr) gene: Roles of epigenetic modifications in transcriptional regulation

Molecular and cellular endocrinology, 2011-10, Vol.345 (1-2), p.1-15

2011

Volltextzugriff (PDF)

Computerized version of the Wisconsin card sorting test in children with high-functioning autistic disorder or attention-deficit/hyperactivity disorder

Brain & development (Tokyo. 1979), 2005-04, Vol.27 (3), p.233-236

2005

Volltextzugriff (PDF)

Actigraphic assessment of sleep disorders in children with chronic fatigue syndrome

Brain & development (Tokyo. 1979), 2008-05, Vol.30 (5), p.329-333

2008

Volltextzugriff (PDF)

Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect

Journal of Thyroid Research, 2010-01, Vol.2010, p.619013-3

2010

Volltextzugriff (PDF)

Long-Term Efficacy and Safety of Two Doses of Growth Hormone in Short Japanese Children Born Small for Gestational Age

Hormone research in paediatrics, 2011-01, Vol.76 (6), p.411-418

2011

Volltextzugriff (PDF)

Silent exonic mutation in the acid-α-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing

Journal of human genetics, 2009-08, Vol.54 (8), p.493-496

2009

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Weight-for-height charts for Japanese children based on the year 2000 Report of School Health Statistics Research

The Role of N-Terminal Pro-B-Type Natriuretic Peptide in the Diagnosis of Congestive Heart Failure in Children: Correlation With the Heart Failure Score and Comparison With B-Type Natriuretic Peptide

Etiology of Severe Sensorineural Hearing Loss in Children: Independent Impact of Congenital Cytomegalovirus Infection and GJB2 Mutations

Pediatric Endocrinology: Our Present Status and Future Prospects

Molecular Basis of Neonatal Diabetes in Japanese Patients

Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients

New reference values for thyroid volume by ultrasound in iodine-sufficient schoolchildren: a World Health Organization/Nutrition for Health and Development Iodine Deficiency Study Group Report

A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure

Induction Chemotherapy Followed by Low-Dose Involved-Field Radiotherapy for Intracranial Germ Cell Tumors

Proximal Promoter of the Cytochrome P450 Oxidoreductase Gene: Identification of Microdeletions Involving the Untranslated Exon 1 and Critical Function of the SP1 Binding Sites

Transforming growth factor-β1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways

Conditional Deletion of Neuronal Cyclin-Dependent Kinase 5 in Developing Forebrain Results in Microglial Activation and Neurodegeneration

Elevated Free Thyroxine Levels Detected by a Neonatal Screening System

Dried Umbilical Cords in the Retrospective Diagnosis of Congenital Cytomegalovirus Infection as a Cause of Developmental Delays

A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica

An observational study of the effectiveness and safety of growth hormone (Humatrope®) treatment in Japanese children with growth hormone deficiency or Turner syndrome

Increased Na reabsorption via the Na–Cl cotransporter in autosomal recessive pseudohypoaldosteronism

Prevalence and risk factors of vitamin D deficiency rickets in Hokkaido, Japan

Clinical characteristics of Japanese adults with growth hormone deficiency: a HypoCCS database study

Analysis of expression and structure of the rat GH-secretagogue/ghrelin receptor (Ghsr) gene: Roles of epigenetic modifications in transcriptional regulation

Computerized version of the Wisconsin card sorting test in children with high-functioning autistic disorder or attention-deficit/hyperactivity disorder

Actigraphic assessment of sleep disorders in children with chronic fatigue syndrome

Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect

Long-Term Efficacy and Safety of Two Doses of Growth Hormone in Short Japanese Children Born Small for Gestational Age

Silent exonic mutation in the acid-α-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing

Suchergebnisse filtern