These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
111 related articles for article (PubMed ID: 26925581)
1. Novel Leptin Receptor Mutations Identified in Two Girls with Severe Obesity Are Associated with Increased Bone Mineral Density. Hannema SE; Wit JM; Houdijk ME; van Haeringen A; Bik EC; Verkerk AJ; Uitterlinden AG; Kant SG; Oostdijk W; Bakker E; Delemarre-van de Waal HA; Losekoot M Horm Res Paediatr; 2016; 85(6):412-20. PubMed ID: 26925581 [TBL] [Abstract][Full Text] [Related]
2. Seven novel deleterious LEPR mutations found in early-onset obesity: a ΔExon6-8 shared by subjects from Reunion Island, France, suggests a founder effect. Huvenne H; Le Beyec J; Pépin D; Alili R; Kherchiche PP; Jeannic E; Frelut ML; Lacorte JM; Nicolino M; Viard A; Laville M; Ledoux S; Tounian P; Poitou C; Dubern B; Clément K J Clin Endocrinol Metab; 2015 May; 100(5):E757-66. PubMed ID: 25751111 [TBL] [Abstract][Full Text] [Related]
3. Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor. Farooqi IS; Wangensteen T; Collins S; Kimber W; Matarese G; Keogh JM; Lank E; Bottomley B; Lopez-Fernandez J; Ferraz-Amaro I; Dattani MT; Ercan O; Myhre AG; Retterstol L; Stanhope R; Edge JA; McKenzie S; Lessan N; Ghodsi M; De Rosa V; Perna F; Fontana S; Barroso I; Undlien DE; O'Rahilly S N Engl J Med; 2007 Jan; 356(3):237-47. PubMed ID: 17229951 [TBL] [Abstract][Full Text] [Related]
4. Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity. Dehghani MR; Mehrjardi MYV; Dilaver N; Tajamolian M; Enayati S; Ebrahimi P; Amoli MM; Farooqi S; Maroofian R Eur J Med Genet; 2018 Aug; 61(8):465-467. PubMed ID: 29545012 [TBL] [Abstract][Full Text] [Related]
5. Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity. Niazi RK; Gjesing AP; Hollensted M; Have CT; Grarup N; Pedersen O; Ullah A; Shahid G; Ahmad W; Gul A; Hansen T BMC Med Genet; 2018 Nov; 19(1):199. PubMed ID: 30442103 [TBL] [Abstract][Full Text] [Related]
6. Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity. Mazen I; El-Gammal M; Abdel-Hamid M; Farooqi IS; Amr K Mol Genet Metab; 2011 Apr; 102(4):461-4. PubMed ID: 21306929 [TBL] [Abstract][Full Text] [Related]
7. Novel LEPR mutations in obese Pakistani children identified by PCR-based enrichment and next generation sequencing. Saeed S; Bonnefond A; Manzoor J; Philippe J; Durand E; Arshad M; Sand O; Butt TA; Falchi M; Arslan M; Froguel P Obesity (Silver Spring); 2014 Apr; 22(4):1112-7. PubMed ID: 24319006 [TBL] [Abstract][Full Text] [Related]
9. Whole exome sequencing reveals novel LEPR frameshift mutation in severely obese children from Western India. Bhatt A; Purani C; Bhargava P; Patel K; Agarbattiwala T; Puvar A; Shah K; Joshi CG; Dhamecha N; Prabhakar M; Joshi M Mol Genet Genomic Med; 2019 Jul; 7(7):e00692. PubMed ID: 31070016 [TBL] [Abstract][Full Text] [Related]
10. Differential effects of leptin receptor mutation on male and female BBDR Gimap5-/Gimap5- spontaneously diabetic rats. Moralejo DH; Hansen CT; Treuting P; Hessner MJ; Fuller JM; Van Yserloo B; Jensen R; Osborne W; Kwitek AE; Lernmark A Physiol Genomics; 2010 Mar; 41(1):9-20. PubMed ID: 19996157 [TBL] [Abstract][Full Text] [Related]
11. Binge eating as a major phenotype of melanocortin 4 receptor gene mutations. Branson R; Potoczna N; Kral JG; Lentes KU; Hoehe MR; Horber FF N Engl J Med; 2003 Mar; 348(12):1096-103. PubMed ID: 12646666 [TBL] [Abstract][Full Text] [Related]
12. Homozygous leptin receptor mutation due to uniparental disomy of chromosome 1: response to bariatric surgery. Le Beyec J; Cugnet-Anceau C; Pépin D; Alili R; Cotillard A; Lacorte JM; Basdevant A; Laville M; Clément K J Clin Endocrinol Metab; 2013 Feb; 98(2):E397-402. PubMed ID: 23275530 [TBL] [Abstract][Full Text] [Related]
13. A novel compound heterozygous leptin receptor mutation causes more severe obesity than in Lepr Berger C; Heyne HO; Heiland T; Dommel S; Höfling C; Guiu-Jurado E; Lorenz J; Roßner S; Dannemann M; Kelso J; Kovacs P; Blüher M; Klöting N J Lipid Res; 2021; 62():100105. PubMed ID: 34390703 [TBL] [Abstract][Full Text] [Related]
14. Effect of obesity on estradiol level, and its relationship to leptin, bone maturation, and bone mineral density in children. Klein KO; Larmore KA; de Lancey E; Brown JM; Considine RV; Hassink SG J Clin Endocrinol Metab; 1998 Oct; 83(10):3469-75. PubMed ID: 9768648 [TBL] [Abstract][Full Text] [Related]
15. LEPR p.Q223R Polymorphism influences plasma leptin levels and body mass index in Tunisian obese patients. Ben Ali S; Kallel A; Sediri Y; Ftouhi B; Feki M; Slimene H; Jemaa R; Kaabachi N Arch Med Res; 2009 Apr; 40(3):186-90. PubMed ID: 19427969 [TBL] [Abstract][Full Text] [Related]
16. A toddler with a novel LEPR mutation. Armağan C; Yılmaz C; Koç A; Abacı A; Ülgenalp A; Böber E; Erçal D; Demir K Hormones (Athens); 2019 Jun; 18(2):237-240. PubMed ID: 30778850 [TBL] [Abstract][Full Text] [Related]
17. Bone structure and composition in a hyperglycemic, obese, and leptin receptor-deficient rat: Microscale characterization of femur and calvarium. Micheletti C; Jolic M; Grandfield K; Shah FA; Palmquist A Bone; 2023 Jul; 172():116747. PubMed ID: 37028238 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel leptin receptor (LEPR) variant and proof of functional relevance directing treatment decisions in patients with morbid obesity. Voigtmann F; Wolf P; Landgraf K; Stein R; Kratzsch J; Schmitz S; Abou Jamra R; Blüher M; Meiler J; Beck-Sickinger AG; Kiess W; Körner A Metabolism; 2021 Mar; 116():154438. PubMed ID: 33221380 [TBL] [Abstract][Full Text] [Related]
20. Bone mass in prepubertal boys is associated with a Gln223Arg amino acid substitution in the leptin receptor. Richert L; Chevalley T; Manen D; Bonjour JP; Rizzoli R; Ferrari S J Clin Endocrinol Metab; 2007 Nov; 92(11):4380-6. PubMed ID: 17785359 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]