UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review

Molecular genetics & genomic medicine, 2024-04, Vol.12 (4), p.e2439-n/a

2024

Volltextzugriff (PDF)

tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly

BMJ open diabetes research & care, 2020-10, Vol.8 (1), p.e001601

2020

Volltextzugriff (PDF)

FTO gene polymorphisms and obesity risk in Chinese population: a meta-analysis

World journal of pediatrics : WJP, 2019-08, Vol.15 (4), p.382-389

2019

Volltextzugriff (PDF)

Iron overload is related to elevated blood glucose levels in obese children and aggravates high glucose-induced endothelial cell dysfunction in vitro

BMJ open diabetes research & care, 2020-07, Vol.8 (1), p.e001426

2020

Volltextzugriff (PDF)

A novel HNF4A mutation identified in a child with maturity onset diabetes of the young

World journal of pediatrics : WJP, 2022-11, Vol.18 (11), p.778-780

2022

Volltextzugriff (PDF)

β‐Cell function in obese children and adolescents with metabolic syndrome compared to isolated obesity

Pediatric diabetes, 2019-11, Vol.20 (7), p.861-870

2019

Volltextzugriff (PDF)

Impact of BMI on gonadorelin‐stimulated LH peak in premenarcheal girls with idiopathic central precocious puberty

Obesity (Silver Spring, Md.), 2015-03, Vol.23 (3), p.637-643

2015

Volltextzugriff (PDF)

Clinical Incidence and Characteristics of Newly Diagnosed Type 1 Diabetes in Chinese Children and Adolescents: A Nationwide Registry Study of 34 Medical Centers

Frontiers in pediatrics, 2022-06, Vol.10, p.888370-888370

2022

Volltextzugriff (PDF)

Surrogate markers and predictors of endogenous insulin secretion in children and adolescents with type 1 diabetes

World journal of pediatrics : WJP, 2021-02, Vol.17 (1), p.99-105

2021

Volltextzugriff (PDF)

A rabbit model of pediatric nonalcoholic steatohepatitis： The role of adiponectin

World journal of gastroenterology : WJG, 2009-02, Vol.15 (8), p.912-918

2009

Volltextzugriff (PDF)

Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes

Journal of Pediatric Endocrinology and Metabolism, 2019-07, Vol.32 (7), p.759-765

2019

Volltextzugriff (PDF)

Gitelman syndrome combined with growth hormone deficiency: Three cases report

Medicine (Baltimore), 2019-10, Vol.98 (40), p.e17244-e17244

2019

Volltextzugriff (PDF)

Development and validation of a novel non-invasive test for diagnosing nonalcoholic fatty liver disease in Chinese children

World journal of pediatrics : WJP, 2024-04, Vol.20 (4), p.413-421

2024

Volltextzugriff (PDF)

Continuous age- and sex-specific reference ranges of liver enzymes in Chinese children and application in pediatric non-alcoholic fatty liver disease

World journal of pediatrics : WJP, 2024-02

2024

Volltextzugriff (PDF)

Chinese Siblings with Prader-Willi Syndrome Inherited from Their Paternal Grandmother

Indian pediatrics, 2019-09, Vol.56 (9), p.789-791

2019

Volltextzugriff (PDF)

Kikuchi-Fujimoto disease manifesting as recurrent thrombocytopenia and Mobitz type II atrioventricular block in a 7-year-old girl: a case report and analysis of 138 Chinese childhood Kikuchi-Fujimoto cases with 10 years of follow-up in 97 patients

Acta Paediatrica, 2007-12, Vol.96 (12), p.1844-1847

2007

Volltextzugriff (PDF)

Diagnostic performance of convolutional neural network-based Tanner-Whitehouse 3 bone age assessment system

Quantitative imaging in medicine and surgery, 2020-03, Vol.10 (3), p.657-667

2020

Volltextzugriff (PDF)

Early activation of the inhibin B/FSH axis in obese Tanner stage G1PH1 boys

Clinical endocrinology (Oxford), 2006-09, Vol.65 (3), p.327-332

2006

Volltextzugriff (PDF)

X-linked recessive combined pituitary hormone deficiency is mapped to Xp22.3–Xp11 in a Chinese family

Genomics (San Diego, Calif.), 2011-12, Vol.98 (6), p.440-444

2011

Volltextzugriff (PDF)

Effects of obesity on peak level of luteinizing hormone in gonadotropin-releasing hormone agonist test and obesity-related hormones in girls with central precocious puberty

Zhongguo dang dai er ke za zhi, 2015-08, Vol.17 (8), p.763

2015

Volltextzugriff (PDF)

Effects of short- and long-acting recombinant human growth hormone (PEG-rhGH) on left ventricular function in children with growth hormone deficiency

Acta Paediatrica, 2011-01, Vol.100 (1), p.140-142

2011

Volltextzugriff (PDF)

A clinical follow-up study of premature thelarche in infants under two years of age

Zhongguo dang dai er ke za zhi, 2013-04, Vol.15 (4), p.285

2013

Volltextzugriff (PDF)

Detection of thyroid antibodies in children with type 1 diabetes mellitus

Zhongguo dang dai er ke za zhi, 2012-01, Vol.14 (1), p.38

2012

Volltextzugriff (PDF)

A 10-year review of childhood type 1 diabetes mellitus and the clinical value of interleukin-10 in diabetic ketoacidosis

Zhongguo dang dai er ke za zhi, 2010-11, Vol.12 (11), p.849

2010

Volltextzugriff (PDF)

A case of beta-ketothiolase deficiency

Zhonghua er ke za zhi, 2006-09, Vol.44 (9), p.703

2006

Volltextzugriff (PDF)

1 – 25 von 155

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(108)
Mit Volltextzugriff
(130)

Publikationsform

Artikel
(147)
Tagungsberichte
(8)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(97)
Life Sciences & Biomedicine
(54)
Humans
(44)
Male
(31)
Female
(29)
Physical Sciences
(28)
Technology
(24)
Child
(22)
Pediatrics
(16)
Chemistry
(15)
Adolescent
(13)
Engineering
(13)
Materials Science
(13)
Adult
(9)
Child, Preschool
(9)
Materials Science, Multidisciplinary
(9)
Pharmacology & Pharmacy
(9)
Medicine
(8)
Medicine & Public Health
(8)
Animals
(7)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review

tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly

FTO gene polymorphisms and obesity risk in Chinese population: a meta-analysis

Iron overload is related to elevated blood glucose levels in obese children and aggravates high glucose-induced endothelial cell dysfunction in vitro

A novel HNF4A mutation identified in a child with maturity onset diabetes of the young

β‐Cell function in obese children and adolescents with metabolic syndrome compared to isolated obesity

Impact of BMI on gonadorelin‐stimulated LH peak in premenarcheal girls with idiopathic central precocious puberty

Clinical Incidence and Characteristics of Newly Diagnosed Type 1 Diabetes in Chinese Children and Adolescents: A Nationwide Registry Study of 34 Medical Centers

Surrogate markers and predictors of endogenous insulin secretion in children and adolescents with type 1 diabetes

A rabbit model of pediatric nonalcoholic steatohepatitis： The role of adiponectin

Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes

Gitelman syndrome combined with growth hormone deficiency: Three cases report

Development and validation of a novel non-invasive test for diagnosing nonalcoholic fatty liver disease in Chinese children

Continuous age- and sex-specific reference ranges of liver enzymes in Chinese children and application in pediatric non-alcoholic fatty liver disease

Chinese Siblings with Prader-Willi Syndrome Inherited from Their Paternal Grandmother

Kikuchi-Fujimoto disease manifesting as recurrent thrombocytopenia and Mobitz type II atrioventricular block in a 7-year-old girl: a case report and analysis of 138 Chinese childhood Kikuchi-Fujimoto cases with 10 years of follow-up in 97 patients

Diagnostic performance of convolutional neural network-based Tanner-Whitehouse 3 bone age assessment system

Early activation of the inhibin B/FSH axis in obese Tanner stage G1PH1 boys

X-linked recessive combined pituitary hormone deficiency is mapped to Xp22.3–Xp11 in a Chinese family

Effects of obesity on peak level of luteinizing hormone in gonadotropin-releasing hormone agonist test and obesity-related hormones in girls with central precocious puberty

Effects of short- and long-acting recombinant human growth hormone (PEG-rhGH) on left ventricular function in children with growth hormone deficiency

A clinical follow-up study of premature thelarche in infants under two years of age

Detection of thyroid antibodies in children with type 1 diabetes mellitus

A 10-year review of childhood type 1 diabetes mellitus and the clinical value of interleukin-10 in diabetic ketoacidosis

A case of beta-ketothiolase deficiency

Suchergebnisse filtern