(Q47949193)

7 February 2018

title

Genetic and Syndromic Causes of Obesity and its Management (English)

1 reference

7 February 2018

author name string

Ildiko H Koves

series ordinal

1

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7 February 2018

Christian Roth

series ordinal

2

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7 February 2018

publication date

27 November 2017

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7 February 2018

Indian Journal of Pediatrics

published in

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7 February 2018

Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor

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Biologically inactive leptin and early-onset extreme obesity

21 January 2018

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Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene

21 January 2018

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Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis

21 January 2018

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Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene

21 January 2018

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Hypothalamic proopiomelanocortin processing and the regulation of energy balance

21 January 2018

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Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

21 January 2018

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An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity

21 January 2018

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Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity

21 January 2018

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Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist

21 January 2018

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Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism

21 January 2018

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Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

21 January 2018

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Mechanisms of obesity in Prader-Willi syndrome

21 January 2018

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Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood

21 January 2018

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Anesthetic considerations for rapid-onset obesity, hypoventilation, hypothalamic dysfunction, and autonomic dysfunction (ROHHAD) syndrome in children

21 January 2018

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Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours

21 January 2018

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Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.

21 January 2018

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A large multiexonic genomic deletion within the ALMS1 gene causes Alström syndrome in a consanguineous Pakistani family.

21 January 2018

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Whole exome sequencing identifies a homozygous nonsense variation in ALMS1 gene in a patient with syndromic obesity.

21 January 2018

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21 January 2018

Bardet-Biedl syndrome.

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Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling

21 January 2018

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Early-Onset Obesity: Unrecognized First Evidence for GNAS Mutations and Methylation Changes.

21 January 2018

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Screening for hormonal, monogenic, and syndromic disorders in obese infants and children

21 January 2018

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Methylation of SOCS3 is inversely associated with metabolic syndrome in an epigenome-wide association study of obesity

21 January 2018

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Effects of recombinant leptin therapy in a child with congenital leptin deficiency.

21 January 2018

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Response to Letter: "Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline".

21 January 2018

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Effects of metformin on body weight and body composition in obese insulin-resistant children: a randomized clinical trial

21 January 2018

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Metformin in obese children and adolescents: the MOCA trial.

21 January 2018

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Randomized, double-blind, placebo-controlled trial of orlistat for weight loss in adolescents

21 January 2018

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Effect of orlistat on weight and body composition in obese adolescents: a randomized controlled trial

21 January 2018

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Prevalence and phenotypic characterization of MC4R variants in a large pediatric cohort

21 January 2018

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Prader-Willi syndrome: consensus diagnostic criteria.

21 January 2018

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12 December 2020

Melanocortin 4 Receptor Sequence Variations Are Seldom a Cause of Human Obesity: The Swedish Obese Subjects, the HERITAGE Family Study, and a Memphis Cohort

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12 December 2020

Rapid onset obesity, hypoventilation, hypothalamic, autonomic and thermal dysregulation, and neural tumour (ROHHADNET) syndrome presenting with Cushing syndrome

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12 December 2020

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD): a case with additional features and review of the literature

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12 December 2020

A case of rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation, and neural crest tumor: ROHHADNET syndrome

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12 December 2020

Treatment options for children with monogenic forms of obesity

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12 December 2020

Alström syndrome: current perspectives

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12 December 2020

Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity.

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12 December 2020

Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline.

1 reference

12 December 2020

10.1007/S12098-017-2502-2

Identifiers

DOI

1 reference

7 February 2018

1 reference

7 February 2018