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...

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

European journal of clinical nutrition, 2020-08, Vol.74 (8), p.1173-1180

2020

Volltextzugriff (PDF)

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A376-A377

2012

Volltextzugriff (PDF)

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

Journal of Pediatric Endocrinology and Metabolism, 2010-11, Vol.23 (11), p.1123-1132

2010

Volltextzugriff (PDF)

Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Journal of endocrinological investigation, 2019-04, Vol.42 (4), p.453-470

2019

Volltextzugriff (PDF)

A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

Genetic counseling, 2014-01, Vol.25 (3), p.331

2014

Volltextzugriff (PDF)

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Journal of Pediatric Endocrinology and Metabolism, 2008-08, Vol.21 (8), p.781-788

2008

Volltextzugriff (PDF)

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Experimental and clinical endocrinology & diabetes, 2009-07, Vol.117 (7), p.312-315

2009

Volltextzugriff (PDF)

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Journal of Pediatric Endocrinology and Metabolism, 2006-05, Vol.19 (5), p.741

2006

Volltextzugriff (PDF)

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Journal of bone and mineral research, 2016-08, Vol.31 (8), p.1577-1585

2016

Volltextzugriff (PDF)

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Experimental and clinical endocrinology & diabetes, 2009-06, Vol.117 (6), p.301-304

2009

Volltextzugriff (PDF)

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Journal of Pediatric Endocrinology and Metabolism, 2004-11, Vol.17 (11), p.1565

2004

Volltextzugriff (PDF)

Multiple dose IVIG treatment in neonatal immune hemolytic jaundice

Journal of tropical pediatrics (1980), 2001-02, Vol.47 (1), p.50-53

2001

Volltextzugriff (PDF)

Hajdu-Cheney syndrome with growth hormone deficiency and neuropathy

Journal of Pediatric Endocrinology and Metabolism, 2000-07, Vol.13 (7), p.951

2000

Volltextzugriff (PDF)

An Infantile Cushing Syndrome Due to Misuse of Topical Steroid

Pediatric dermatology, 2004-09, Vol.21 (5), p.561-563

2004

Volltextzugriff (PDF)

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Yearbook of Paediatric Endocrinology, 2018-09

2018

Volltextzugriff (PDF)

Pica and Intoxication in Childhood

Clinical pediatrics, 2000-10, Vol.39 (10), p.624-625

2000

Volltextzugriff (PDF)

Diurnal variation of height in children

Pediatrics international, 2005-12, Vol.47 (6), p.645-648

2005

Volltextzugriff (PDF)

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Journal of Pediatric Endocrinology and Metabolism, 2005-01, Vol.18 (10), p.949

2005

Volltextzugriff (PDF)

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Journal of Pediatric Endocrinology and Metabolism, 2009-10, Vol.22 (10), p.937-946

2009

Volltextzugriff (PDF)

Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

Experimental and clinical endocrinology & diabetes, 2009-02, Vol.117 (2), p.57-59

2009

Volltextzugriff (PDF)

Antioxidant superoxide dismutase activity in obese children

Biological trace element research, 2004-06, Vol.98 (3), p.219-228

2004

Volltextzugriff (PDF)

Zinc Deficiency: a Contributing Factor of Short Stature in Growth Hormone Deficient Children

Journal of tropical pediatrics (1980), 2003-06, Vol.49 (3), p.187-188

2003

Volltextzugriff (PDF)

Is hypertriglyceridaemia a new concept for visceral leishmaniasis?

Annals of tropical paediatrics, 2004-12, Vol.24 (4), p.369-369

2004

Volltextzugriff (PDF)

Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies

Journal of Pediatric Endocrinology and Metabolism, 2006-01, Vol.19 (1), p.39

2006

Volltextzugriff (PDF)

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(23)

Publikationsform

Artikel
(38)

Sprache

Englisch
(38)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Multiple dose IVIG treatment in neonatal immune hemolytic jaundice

Hajdu-Cheney syndrome with growth hormone deficiency and neuropathy

An Infantile Cushing Syndrome Due to Misuse of Topical Steroid

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Pica and Intoxication in Childhood

Diurnal variation of height in children

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: an analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosis

Antioxidant superoxide dismutase activity in obese children

Zinc Deficiency: a Contributing Factor of Short Stature in Growth Hormone Deficient Children

Is hypertriglyceridaemia a new concept for visceral leishmaniasis?

Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies

Suchergebnisse filtern