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...

AB110. Genotype and phenotype of 107 patients with congenital hyperinsulinism

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB110-AB110

2017

Volltextzugriff (PDF)

AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

Clinical, para-clincal and outcomes of diabetes ketoacidosis in Vietnam national hospital pediatrics

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P13-P13, Article P13

2015

Volltextzugriff (PDF)

AB069. Effect of osteogenesis imperfecta on children and their families

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P124-P124, Article P124

2015

Volltextzugriff (PDF)

AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB125. Neonatal diabetes mellitus due to insulin gene mutation

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

Adrenocortical tumor in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P51-P51, Article P51

2015

Volltextzugriff (PDF)

Congenital adrenal hyperplasia with cholestatic jaundice: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P55-P55, Article P55

2015

Volltextzugriff (PDF)

Hypopituitarism due to central nervous system germinoma: a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P118-P118, Article P118

2015

Volltextzugriff (PDF)

Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P25-P25, Article P25

2015

Volltextzugriff (PDF)

Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P119-P119, Article P119

2015

Volltextzugriff (PDF)

AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

AB131. Genotype, phenotype of transient neonatal diabetes mellitus

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

Eye and renal complication in pediatric patients with diabetes mellitus type 1

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P23-P23, Article P23

2015

Volltextzugriff (PDF)

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P52-P52, Article P52

2015

Volltextzugriff (PDF)

AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

Annals of translational medicine, 2015-09, Vol.3 (Suppl 2)

2015

Volltextzugriff (PDF)

Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P50-P50, Article P50

2015

Volltextzugriff (PDF)

Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P49-P49, Article P49

2015

Volltextzugriff (PDF)

The pattern of disorders of sex development in Vietnamese children

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P115-P115, Article P115

2015

Volltextzugriff (PDF)

Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.P12-P12, Article P12

2015

Volltextzugriff (PDF)

1 – 25 von 133

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(83)
Mit Volltextzugriff
(106)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(51)
Technology
(24)
Poster Presentation
(23)
Life Sciences & Biomedicine
(21)
Physical Sciences
(15)
Engineering
(13)
Part 4: Oral/poster
(11)
Computer Science
(10)
Computer Science, Artificial Intelligence
(10)
Chemistry
(9)
Artificial Intelligence
(7)
Environmental Sciences
(7)
Environmental Sciences & Ecology
(7)
Vietnam
(7)
Humans
(6)
Classification
(5)
Infectious Diseases
(5)
Sentiment Analysis
(5)
Social Sciences
(5)
Zinc Oxide
(5)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

AB110. Genotype and phenotype of 107 patients with congenital hyperinsulinism

AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center

Clinical, para-clincal and outcomes of diabetes ketoacidosis in Vietnam national hospital pediatrics

AB069. Effect of osteogenesis imperfecta on children and their families

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome

AB128. Neonatal diabetes mellitus: genotype, phenotype and outcome

AB125. Neonatal diabetes mellitus due to insulin gene mutation

AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years

Adrenocortical tumor in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Congenital adrenal hyperplasia with cholestatic jaundice: a case report

Hypopituitarism due to central nervous system germinoma: a case report

Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case

Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report

AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism

AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

AB131. Genotype, phenotype of transient neonatal diabetes mellitus

Eye and renal complication in pediatric patients with diabetes mellitus type 1

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families

Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam

The pattern of disorders of sex development in Vietnamese children

Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation

Suchergebnisse filtern