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...

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2

Clinical endocrinology (Oxford), 2024-02

2024

Volltextzugriff (PDF)

The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected

Hormone research in paediatrics, 2017-01, Vol.87 (1), p.7-14

2017

Volltextzugriff (PDF)

Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic

Journal of clinical research in pediatric endocrinology, 2024-09, Vol.16 (3), p.256-263

2024

Volltextzugriff (PDF)

Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2023-06, Vol.15 (2), p.172-181

2023

Volltextzugriff (PDF)

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

Journal of clinical research in pediatric endocrinology, 2018-09, Vol.10 (3), p.247-255

2018

Volltextzugriff (PDF)

Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth

Turkish Archives of Pediatrics, 2023-09, Vol.58 (5), p.539-545

2023

Volltextzugriff (PDF)

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.163-167

2017

Volltextzugriff (PDF)

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries

Cardiovascular Journal of Africa, 2019-03, Vol.30 (2), p.e7-e8

2019

Volltextzugriff (PDF)

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

Hormone research in paediatrics, 2016-01, Vol.85 (6), p.421-425

2016

Volltextzugriff (PDF)

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

Journal of clinical research in pediatric endocrinology, 2014-12, Vol.6 (4), p.254-257

2014

Volltextzugriff (PDF)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.211-217

2016

Volltextzugriff (PDF)

Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents

Ultrasound in medicine & biology, 2014-05, Vol.40 (5), p.871-876

2014

Volltextzugriff (PDF)

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.168-171

2017

Volltextzugriff (PDF)

Three cases of Wolfram syndrome with different clinical aspects

Journal of Pediatric Endocrinology and Metabolism, 2015-03, Vol.28 (3-4), p.433

2015

Volltextzugriff (PDF)

Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Journal of pediatric & adolescent gynecology, 2015-02, Vol.28 (1), p.6-11

2015

Volltextzugriff (PDF)

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

Journal of clinical research in pediatric endocrinology, 2015-06, Vol.7 (2), p.144-147

2015

Volltextzugriff (PDF)

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?

European journal of pediatrics, 2012-10, Vol.171 (10), p.1497-1502

2012

Volltextzugriff (PDF)

Is There a Predictive Factor for an Association with Autoimmune Glandular Disease in Children Diagnosed with Celiac Disease?

Journal of clinical research in pediatric endocrinology, 2022-12, Vol.14 (4), p.409-414

2022

Volltextzugriff (PDF)

Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success

Journal of clinical research in pediatric endocrinology, 2023-06, Vol.15 (2), p.225-229

2023

Volltextzugriff (PDF)

Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism

Journal of clinical research in pediatric endocrinology, 2023-06, Vol.15 (2), p.160-171

2023

Volltextzugriff (PDF)

A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment

Journal of clinical research in pediatric endocrinology, 2019-09, Vol.11 (3), p.301-305

2019

Volltextzugriff (PDF)

TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review

Journal of clinical research in pediatric endocrinology, 2022-03, Vol.14 (1), p.114-118

2022

Volltextzugriff (PDF)

Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease

Journal of clinical research in pediatric endocrinology, 2023-03, Vol.15 (1), p.62-68

2023

Volltextzugriff (PDF)

Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience

Journal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.88-99

2021

Volltextzugriff (PDF)

1 – 25 von 50

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(46)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(50)

Sprache

Englisch
(49)
Türkisch
(3)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected

Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic

Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

Three cases of Wolfram syndrome with different clinical aspects

Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?

Is There a Predictive Factor for an Association with Autoimmune Glandular Disease in Children Diagnosed with Celiac Disease?

Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success

Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism

A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment

TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review

Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease

Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience

Suchergebnisse filtern