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...

Growth hormone, the insulin-like growth factor axis, insulin and cancer risk

Nature reviews. Endocrinology, 2011-01, Vol.7 (1), p.11-24

2011

Volltextzugriff (PDF)

Endocrine Control of Growth

American journal of medical genetics. Part C, Seminars in medical genetics, 2013-05, Vol.163C (2), p.76-85

2013

Volltextzugriff (PDF)

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia

Brain (London, England : 1878), 2019-11, Vol.142 (11), p.3382-3397

2019

Volltextzugriff (PDF)

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

American journal of human genetics, 2013-01, Vol.92 (1), p.131-136

2013

Volltextzugriff (PDF)

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

American journal of human genetics, 2013-04, Vol.92 (4), p.605-613

2013

Volltextzugriff (PDF)

Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

American journal of human genetics, 2011-07, Vol.89 (1), p.148-153

2011

Volltextzugriff (PDF)

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

American journal of human genetics, 2016-02, Vol.98 (2), p.363-372

2016

Volltextzugriff (PDF)

The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

American journal of human genetics, 2009-06, Vol.84 (6), p.801-806

2009

Volltextzugriff (PDF)

Geographical Distribution of Optic Nerve Hypoplasia and Septo-optic Dysplasia in Northwest England

The Journal of pediatrics, 2006, Vol.148 (1), p.85-88

2006

Volltextzugriff (PDF)

Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients

European journal of endocrinology, 2014-05, Vol.170 (5), p.741-747

2014

Volltextzugriff (PDF)

Glucose uptake as an alternative to oxygen uptake for assessing metabolic rate in Danio rerio larvae

Current research in physiology, 2022-01, Vol.5, p.216-223

2022

Volltextzugriff (PDF)

A genetic approach to evaluation of short stature of undetermined cause

The lancet. Diabetes & endocrinology, 2018-07, Vol.6 (7), p.564-574

2018

Volltextzugriff (PDF)

Increased Plasma Incretin Concentrations Identifies a Subset of Patients with Persistent Congenital Hyperinsulinism without KATP Channel Gene Defects

The Journal of pediatrics, 2015, Vol.166 (1), p.191-194

2015

Volltextzugriff (PDF)

The challenge of delivering endocrine care and successful transition to adult services in adolescents with congenital adrenal hyperplasia: experience in a single centre over 18 years

Clinical endocrinology (Oxford), 2013-01, Vol.78 (1), p.23-28

2013

Volltextzugriff (PDF)

Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

The journal of clinical endocrinology and metabolism, 2022-11, Vol.107 (12), p.3287-3301

2022

Volltextzugriff (PDF)

Endocrine control of growth

American journal of medical genetics. Part C, Seminars in medical genetics, 2013-05, Vol.163C (2), p.76

2013

Volltextzugriff (PDF)

Effects of early growth on blood pressure of infants of British European and South Asian origin at one year of age: the Manchester childrenʼs growth and vascular health study

Journal of hypertension, 2008-03, Vol.26 (3), p.412-418

2008

Volltextzugriff (PDF)

Maternal malaria status and metabolic profiles in pregnancy and in cord blood: relationships with birth size in Nigerian infants

Malaria journal, 2012-03, Vol.11 (1), p.75-75, Article 75

2012

Volltextzugriff (PDF)

Rare variants in single-minded 1 (SIM1) are associated with severe obesity

The Journal of clinical investigation, 2013-07, Vol.123 (7), p.3042-3050

2013

Volltextzugriff (PDF)

Combined effects of weight change trajectories and eating behaviors on childhood adiposity status: A birth cohort study

Appetite, 2021-07, Vol.162, p.105174, Article 105174

2021

Volltextzugriff (PDF)

The neuroendocrine sequelae of paediatric craniopharyngioma: a 40-year meta-data analysis of 185 cases from three UK centres

European journal of endocrinology, 2017-03, Vol.176 (3), p.359-369

2017

Volltextzugriff (PDF)

Response to Letter to the Editor From Virú-Loza and Chávez-Nomberto: “Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort”

The journal of clinical endocrinology and metabolism, 2023-06, Vol.108 (6), p.e356-e357

2023

Volltextzugriff (PDF)

Growth Hormone Treatment and Cancer Risk

Endocrinology and metabolism clinics of North America, 2007-03, Vol.36 (1), p.247-263

2007

Volltextzugriff (PDF)

Hypothalamic-pituitary-adrenal function and glucocorticoid sensitivity in atopic dermatitis

Pediatrics (Evanston), 2000-04, Vol.105 (4 Pt 1), p.794-799

2000

Volltextzugriff (PDF)

A dominant-negative mutation of the growth hormone receptor causes familial short stature

Nature genetics, 1997-05, Vol.16 (1), p.13-14

1997

Volltextzugriff (PDF)

1 – 25 von 673

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(574)
Mit Volltextzugriff
(569)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(421)
Life Sciences & Biomedicine
(339)
Humans
(298)
Female
(182)
Male
(178)
Biological And Medical Sciences
(129)
Medical Sciences
(108)
Child
(102)
Endocrinology & Metabolism
(95)
Adolescent
(80)
Animals
(76)
Adult
(73)
Child, Preschool
(60)
Middle Aged
(60)
Genetics & Heredity
(58)
Mutation
(57)
Fundamental And Applied Biological Sciences. Psychology
(56)
Infant
(48)
Physical Sciences
(45)
Pediatrics
(40)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Growth hormone, the insulin-like growth factor axis, insulin and cancer risk

Endocrine Control of Growth

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

Geographical Distribution of Optic Nerve Hypoplasia and Septo-optic Dysplasia in Northwest England

Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients

Glucose uptake as an alternative to oxygen uptake for assessing metabolic rate in Danio rerio larvae

A genetic approach to evaluation of short stature of undetermined cause

Increased Plasma Incretin Concentrations Identifies a Subset of Patients with Persistent Congenital Hyperinsulinism without KATP Channel Gene Defects

The challenge of delivering endocrine care and successful transition to adult services in adolescents with congenital adrenal hyperplasia: experience in a single centre over 18 years

Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

Endocrine control of growth

Effects of early growth on blood pressure of infants of British European and South Asian origin at one year of age: the Manchester childrenʼs growth and vascular health study

Maternal malaria status and metabolic profiles in pregnancy and in cord blood: relationships with birth size in Nigerian infants

Rare variants in single-minded 1 (SIM1) are associated with severe obesity

Combined effects of weight change trajectories and eating behaviors on childhood adiposity status: A birth cohort study

The neuroendocrine sequelae of paediatric craniopharyngioma: a 40-year meta-data analysis of 185 cases from three UK centres

Response to Letter to the Editor From Virú-Loza and Chávez-Nomberto: “Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort”

Growth Hormone Treatment and Cancer Risk

Hypothalamic-pituitary-adrenal function and glucocorticoid sensitivity in atopic dermatitis

A dominant-negative mutation of the growth hormone receptor causes familial short stature

Suchergebnisse filtern