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...

Leptin and leptin receptor-related monogenic obesity

Biochimie, 2012-10, Vol.94 (10), p.2111-2115

2012

Volltextzugriff (PDF)

Novel therapeutics in rare genetic obesities: A narrative review

Pharmacological research, 2023-05, Vol.191, p.106763-106763, Article 106763

2023

Volltextzugriff (PDF)

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)

Cart Overexpression Is the Only Identifiable Cause of High Bone Mass in Melanocortin 4 Receptor Deficiency

Endocrinology (Philadelphia), 2006-07, Vol.147 (7), p.3196-3202

2006

Volltextzugriff (PDF)

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

CLINICAL OBESITY, 2024-06, Vol.14 (3), p.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)

Rare genetic causes of obesity: Diagnosis and management in clinical care

Annales d'endocrinologie, 2022-02, Vol.83 (1), p.63-72

2022

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)

Pediatric Home Parenteral Nutrition in France: A six years national survey

Clinical nutrition (Edinburgh, Scotland), 2021-10, Vol.40 (10), p.5278-5287

2021

Volltextzugriff (PDF)

Implication of Heterozygous Variants in Genes of the Leptin-Melanocortin Pathway in Severe Obesity

The journal of clinical endocrinology and metabolism, 2021-10, Vol.106 (10), p.2991-3006

2021

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)

Unexpected Endocrine Features and Normal Pigmentation in a Young Adult Patient Carrying a Novel Homozygous Mutation in the POMC Gene

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4955-4962

2008

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)

Seven Novel Deleterious LEPR Mutations Found in Early-Onset Obesity: a ΔExon6–8 Shared by Subjects From Reunion Island, France, Suggests a Founder Effect

The journal of clinical endocrinology and metabolism, 2015-05, Vol.100 (5), p.E757-E766

2015

Volltextzugriff (PDF)

Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome

Frontiers in immunology, 2018-05, Vol.9, p.1036-1036

2018

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)

Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome

Sleep medicine, 2019-12, Vol.64, p.23-29

2019

Volltextzugriff (PDF)

Metabolic and Adipose Tissue Signatures in Adults With Prader-Willi Syndrome: A Model of Extreme Adiposity

The journal of clinical endocrinology and metabolism, 2015-03, Vol.100 (3), p.850-859

2015

Volltextzugriff (PDF)

Persistent Bloodstream Infection with Kocuria rhizophila Related to a Damaged Central Catheter

Journal of Clinical Microbiology, 2012-04, Vol.50 (4), p.1495-1498

2012

Volltextzugriff (PDF)

Implication of Heterozygous Variants in Genes of the Leptin–Melanocortin Pathway in Severe Obesity

The journal of clinical endocrinology and metabolism, 2021-10, Vol.106 (10), p.2991-3006

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)

Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France[S]

Journal of lipid research, 2016-03, Vol.57 (3), p.482-491

2016

Volltextzugriff (PDF)

1 – 25 von 84

Suche als RSS-Feed

Aktive Filter

KollektioneBooks on EBSCOhost

ThemaPediatrics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(66)

Publikationsform

Sprache

Englisch
(56)
Französisch
(28)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Leptin and leptin receptor-related monogenic obesity

Novel therapeutics in rare genetic obesities: A narrative review

Unravelling leptin variants: advancing precision medicine in obesity

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

Cart Overexpression Is the Only Identifiable Cause of High Bone Mass in Melanocortin 4 Receptor Deficiency

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

Rare genetic causes of obesity: Diagnosis and management in clinical care

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

Pediatric Home Parenteral Nutrition in France: A six years national survey

Implication of Heterozygous Variants in Genes of the Leptin-Melanocortin Pathway in Severe Obesity

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

Unexpected Endocrine Features and Normal Pigmentation in a Young Adult Patient Carrying a Novel Homozygous Mutation in the POMC Gene

Molecular Genetics of Human Obesity-Associated MC4R Mutations

Seven Novel Deleterious LEPR Mutations Found in Early-Onset Obesity: a ΔExon6–8 Shared by Subjects From Reunion Island, France, Suggests a Founder Effect

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

Combined Immunodeficiency in Patients With Trichohepatoenteric Syndrome

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

Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome

Metabolic and Adipose Tissue Signatures in Adults With Prader-Willi Syndrome: A Model of Extreme Adiposity

Persistent Bloodstream Infection with Kocuria rhizophila Related to a Damaged Central Catheter

Implication of Heterozygous Variants in Genes of the Leptin–Melanocortin Pathway in Severe Obesity

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

Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France[S]

Aktive Filter

Suchergebnisse filtern