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...

Unravelling leptin variants: advancing precision medicine in obesity

Nature reviews. Endocrinology, 2023-10, Vol.19 (10), p.562-563

2023

Volltextzugriff (PDF)

Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016

Obesity facts, 2016-06, Vol.9 (3), p.158-173

2016

Volltextzugriff (PDF)

Current Treatments for Patients with Genetic Obesity

Journal of clinical research in pediatric endocrinology, 2023-05, Vol.15 (2), p.108-119

2023

Volltextzugriff (PDF)

IMPROVE 2022 International Meeting on Pathway‐Related Obesity: Vision of Excellence

Clinical obesity, 2024-06, Vol.14 (3), p.e12659-n/a

2024

Volltextzugriff (PDF)

Hyperphagia and impulsivity: use of self-administered Dykens' and in-house impulsivity questionnaires to characterize eating behaviors in children with severe and early-onset obesity

Orphanet journal of rare diseases, 2024-02, Vol.19 (1), p.84-84, Article 84

2024

Volltextzugriff (PDF)

Diagnosing undernutrition children and adults: new French criteria. Why, for what and for whom? A joint statement of the French National Authority for Health and French Federation of Nutrition

British journal of nutrition, 2022-03, Vol.127 (5), p.739-751

2022

Volltextzugriff (PDF)

Genome wide association study identifies KCNMA1 contributing to human obesity

BMC medical genomics, 2011-06, Vol.4 (1), p.51-51

2011

Volltextzugriff (PDF)

Evaluation of a melanocortin-4 receptor (MC4R) agonist (Setmelanotide) in MC4R deficiency

Molecular metabolism (Germany), 2017-10, Vol.6 (10), p.1321-1329

2017

Volltextzugriff (PDF)

Molecular Genetics of Human Obesity-Associated MC4R Mutations

Annals of the New York Academy of Sciences, 2003-06, Vol.994 (1), p.49-57

2003

Volltextzugriff (PDF)

Multichamber Dysfunction in Children and Adolescents With Severe Obesity: A Cardiac Magnetic Resonance Imaging Myocardial Strain Study

Journal of magnetic resonance imaging, 2021-11, Vol.54 (5), p.1393-1403

2021

Volltextzugriff (PDF)

Republication de : Surpoids et obésité de l’enfant et l’adolescent : quel parcours de soins en 2023 ?

Journal de pédiatrie et de puériculture, 2024-09, Vol.37 (5), p.303-310

Dubern, Béatrice

2024

Volltextzugriff (PDF)

Bariatric procedures including Roux-en-Y gastric bypass in French adolescents

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2023-08, Vol.30 (6), p.408-414

2023

Volltextzugriff (PDF)

Surpoids et obésité de l’enfant et l’adolescent : quel parcours de soins en 2023 ?

Nutrition clinique et métabolisme, 2023-12, Vol.37 (2), p.2S46-2S51

Dubern, Béatrice

2023

Volltextzugriff (PDF)

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

The Journal of clinical investigation, 2017-01, Vol.127 (1), p.293-305

2017

Volltextzugriff (PDF)

Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study

The Lancet (British edition), 2001-10, Vol.358 (9291), p.1400-1404

2001

Volltextzugriff (PDF)

Association of Arterial Stiffness and Endothelial Dysfunction with Metabolic Syndrome in Obese Children

The Journal of pediatrics, 2008-07, Vol.153 (1), p.65-70.e1

2008

Volltextzugriff (PDF)

Novel pharmacological MC4R agonists can efficiently activate mutated MC4R from obese patient with impaired endogenous agonist response

Journal of endocrinology, 2010-11, Vol.207 (2), p.177-183

2010

Volltextzugriff (PDF)

Homozygous Null Mutation of the Melanocortin-4 Receptor and Severe Early-Onset Obesity

The Journal of pediatrics, 2007-06, Vol.150 (6), p.613-617.e1

2007

Volltextzugriff (PDF)

Rare melanocortin-3 receptor mutations with in vitro functional consequences are associated with human obesity

Human molecular genetics, 2011-01, Vol.20 (2), p.392-399

2011

Volltextzugriff (PDF)

Dénutrition chez l’enfant et l’adolescent obèse

Nutrition clinique et métabolisme, 2017-10, Vol.31 (4), p.290-293

Dubern, Béatrice

2017

Volltextzugriff (PDF)

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Human molecular genetics, 2003-01, Vol.12 (2), p.145-153

2003

Volltextzugriff (PDF)

Activité physique en pédiatrie

Nutrition clinique et métabolisme, 2014-12, Vol.28 (4), p.259-262

Dubern, Béatrice

2014

Volltextzugriff (PDF)

Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

Pediatric research, 2008-02, Vol.63 (2), p.211-216

2008

Volltextzugriff (PDF)

Chirurgie bariatrique : enjeux et limites chez l’adolescent obèse

Nutrition clinique et métabolisme, 2014-05, Vol.28 (2), p.90-94

Dubern, Béatrice

2014

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Aktive Filter

ThemaObesity

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(33)
Mit Volltextzugriff
(34)

Publikationsform

Artikel
(35)
Buchkapitel
(2)

Sprache

Englisch
(30)
Französisch
(7)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Unravelling leptin variants: advancing precision medicine in obesity

Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016

Current Treatments for Patients with Genetic Obesity

IMPROVE 2022 International Meeting on Pathway‐Related Obesity: Vision of Excellence

Hyperphagia and impulsivity: use of self-administered Dykens' and in-house impulsivity questionnaires to characterize eating behaviors in children with severe and early-onset obesity

Diagnosing undernutrition children and adults: new French criteria. Why, for what and for whom? A joint statement of the French National Authority for Health and French Federation of Nutrition

Genome wide association study identifies KCNMA1 contributing to human obesity

Evaluation of a melanocortin-4 receptor (MC4R) agonist (Setmelanotide) in MC4R deficiency

Molecular Genetics of Human Obesity-Associated MC4R Mutations

Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia

Multichamber Dysfunction in Children and Adolescents With Severe Obesity: A Cardiac Magnetic Resonance Imaging Myocardial Strain Study

Republication de : Surpoids et obésité de l’enfant et l’adolescent : quel parcours de soins en 2023 ?

Bariatric procedures including Roux-en-Y gastric bypass in French adolescents

Surpoids et obésité de l’enfant et l’adolescent : quel parcours de soins en 2023 ?

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study

Association of Arterial Stiffness and Endothelial Dysfunction with Metabolic Syndrome in Obese Children

Novel pharmacological MC4R agonists can efficiently activate mutated MC4R from obese patient with impaired endogenous agonist response

Homozygous Null Mutation of the Melanocortin-4 Receptor and Severe Early-Onset Obesity

Rare melanocortin-3 receptor mutations with in vitro functional consequences are associated with human obesity

Dénutrition chez l’enfant et l’adolescent obèse

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Activité physique en pédiatrie

Mutational Analysis of the Pro-opiomelanocortin Gene in French Obese Children Led to the Identification of a Novel Deleterious Heterozygous Mutation Located in the α-Melanocyte Stimulating Hormone Domain

Chirurgie bariatrique : enjeux et limites chez l’adolescent obèse

Aktive Filter

Suchergebnisse filtern