174 related articles for article (PubMed ID: 29217499)
1. Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India.
Dayal D; Seetharaman K; Panigrahi I; Muthuvel B; Agarwal A
J Clin Res Pediatr Endocrinol; 2018 Jul; 10(3):274-278. PubMed ID: 29217499
[TBL] [Abstract][Full Text] [Related]
2. Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.
Yupanqui-Lozno H; Bastarrachea RA; Yupanqui-Velazco ME; Alvarez-Jaramillo M; Medina-Méndez E; Giraldo-Peña AP; Arias-Serrano A; Torres-Forero C; Garcia-Ordoñez AM; Mastronardi CA; Restrepo CM; Rodriguez-Ayala E; Nava-Gonzalez EJ; Arcos-Burgos M; Kent JW; Cole SA; Licinio J; Celis-Regalado LG
Genes (Basel); 2019 May; 10(5):. PubMed ID: 31067764
[TBL] [Abstract][Full Text] [Related]
3. Novel homozygous leptin receptor mutation in an infant with monogenic obesity.
Boro H; Bundela V; Mannar V; Nagendra L; Jain V; Jain B; Kumar S; Agstam S
Pediatr Endocrinol Diabetes Metab; 2023; 29(2):118-123. PubMed ID: 37728464
[TBL] [Abstract][Full Text] [Related]
4. A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient.
Mazen I; El-Gammal M; Abdel-Hamid M; Amr K
Mol Genet Metab; 2009 Aug; 97(4):305-8. PubMed ID: 19427251
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Early-onset severe obesity due to complete deletion of the leptin gene in a boy.
Ozsu E; Ceylaner S; Onay H
J Pediatr Endocrinol Metab; 2017 Oct; 30(11):1227-1230. PubMed ID: 29040067
[TBL] [Abstract][Full Text] [Related]
8. High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families.
Saeed S; Butt TA; Anwer M; Arslan M; Froguel P
Mol Genet Metab; 2012 May; 106(1):121-6. PubMed ID: 22463805
[TBL] [Abstract][Full Text] [Related]
9. A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness.
Fischer-Posovszky P; von Schnurbein J; Moepps B; Lahr G; Strauss G; Barth TF; Kassubek J; Mühleder H; Möller P; Debatin KM; Gierschik P; Wabitsch M
J Clin Endocrinol Metab; 2010 Jun; 95(6):2836-40. PubMed ID: 20382689
[TBL] [Abstract][Full Text] [Related]
10. Biologically inactive leptin and early-onset extreme obesity.
Wabitsch M; Funcke JB; Lennerz B; Kuhnle-Krahl U; Lahr G; Debatin KM; Vatter P; Gierschik P; Moepps B; Fischer-Posovszky P
N Engl J Med; 2015 Jan; 372(1):48-54. PubMed ID: 25551525
[TBL] [Abstract][Full Text] [Related]
11. Monogenic leptin deficiency in early childhood obesity.
ElSaeed G; Mousa N; El-Mougy F; Hafez M; Khodeera S; Alhelbawy M; Fouda E; Elsheikh S; ElKaffas R; Eldeeb S; Elsharkawy M
Pediatr Obes; 2020 Jan; 15(1):e12574. PubMed ID: 31483094
[TBL] [Abstract][Full Text] [Related]
12. Homozygosity for two missense mutations in the leptin receptor gene (P316:W646C) in a Turkmenian girl with severe early-onset obesity.
Andiran N; Celik N; Andiran F
J Pediatr Endocrinol Metab; 2011; 24(11-12):1043-5. PubMed ID: 22308862
[TBL] [Abstract][Full Text] [Related]
13. The p. N103K mutation of leptin (LEP) gene and severe early onset obesity in Pakistan.
Shabana ; Hasnain S
Biol Res; 2016 Apr; 49():23. PubMed ID: 27075752
[TBL] [Abstract][Full Text] [Related]
14. Fat and energy partitioning: longitudinal observations in leptin-treated adults homozygous for a Lep mutation.
Heymsfield SB; Fong TM; Gantz I; Erondu N
Obesity (Silver Spring); 2006 Feb; 14(2):258-65. PubMed ID: 16571851
[TBL] [Abstract][Full Text] [Related]
15. A Case-Control Study of the Association of Leptin Gene Polymorphisms with Plasma Leptin Levels and Obesity in the Kerala Population.
Manju SK; Anilkumar TR; Vysakh G; Leena BK; Lekshminarayan V; Kumar PG; Shenoy TK
J Obes; 2022; 2022():1040650. PubMed ID: 36619235
[TBL] [Abstract][Full Text] [Related]
16. Leptin deficiency and leptin gene mutations in obese children from Pakistan.
Fatima W; Shahid A; Imran M; Manzoor J; Hasnain S; Rana S; Mahmood S
Int J Pediatr Obes; 2011 Oct; 6(5-6):419-27. PubMed ID: 21854111
[TBL] [Abstract][Full Text] [Related]
17. Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy.
Gibson WT; Farooqi IS; Moreau M; DePaoli AM; Lawrence E; O'Rahilly S; Trussell RA
J Clin Endocrinol Metab; 2004 Oct; 89(10):4821-6. PubMed ID: 15472169
[TBL] [Abstract][Full Text] [Related]
18. When Leptin Is Not There: A Review of What Nonsyndromic Monogenic Obesity Cases Tell Us and the Benefits of Exogenous Leptin.
Salum KCR; Rolando JM; Zembrzuski VM; Carneiro JRI; Mello CB; Maya-Monteiro CM; Bozza PT; Kohlrausch FB; da Fonseca ACP
Front Endocrinol (Lausanne); 2021; 12():722441. PubMed ID: 34504472
[TBL] [Abstract][Full Text] [Related]
19. Early-onset severe obesity due to homozygous p.R105W (c313C> T) mutation in leptin gene in Turkish siblings: Two cases reports.
Fırat SN; Onay H
Obes Res Clin Pract; 2021; 15(6):600-603. PubMed ID: 34802983
[TBL] [Abstract][Full Text] [Related]
20. Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene.
Wabitsch M; Funcke JB; von Schnurbein J; Denzer F; Lahr G; Mazen I; El-Gammal M; Denzer C; Moss A; Debatin KM; Gierschik P; Mistry V; Keogh JM; Farooqi IS; Moepps B; Fischer-Posovszky P
J Clin Endocrinol Metab; 2015 Sep; 100(9):3227-30. PubMed ID: 26186301
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]