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Items: 1 to 20 of 95

1.

Genetic aspects of severe childhood obesity.

Farooqi IS.

Pediatr Endocrinol Rev. 2006 Dec;3 Suppl 4:528-36. Review.

PMID:
17237739
2.

Insights from the genetics of severe childhood obesity.

Farooqi S.

Horm Res. 2007;68 Suppl 5:5-7. doi: 10.1159/000110462. Epub 2007 Dec 10. Review.

PMID:
18174694
3.

Genetic and hereditary aspects of childhood obesity.

Farooqi IS.

Best Pract Res Clin Endocrinol Metab. 2005 Sep;19(3):359-74. Review.

PMID:
16150380
4.

[Management of children and adolescents with severe obesity].

Valerio G, Licenziati MR, Tanas R, Morino G, Ambruzzi AM, Balsamo A, Brambilla P, Bruzzi P, Calcaterra V, Crinò A, De Falco R, Franzese A, Giordano U, Grugni G, Iaccarino Idelson P, Iughetti L, Maffeis C, Manco M, Miraglia Del Giudice E, Mozzillo E, Zito E, Bernasconi S; Gruppo di Studio Obesità Infantile della Società Italiana di Endocrinologia e Diabetologia Pediatrica.

Minerva Pediatr. 2012 Aug;64(4):413-31. Review. Italian.

PMID:
22728613
5.

[Nutritional and psychosomatic aspects of morbid obesity].

Hauner H, Herzog W.

Chirurg. 2008 Sep;79(9):819-25. doi: 10.1007/s00104-008-1535-5. German.

PMID:
18649065
6.

[Monogenic and syndromic symptoms of morbid obesity. Rare but important].

Wiegand S, Krude H.

Internist (Berl). 2015 Feb;56(2):111-2, 114-20. doi: 10.1007/s00108-014-3532-8. German.

PMID:
25630806
7.

[Genetic causes of obesity].

Wangensteen T, Undlien D, Tonstad S, Retterstøl L.

Tidsskr Nor Laegeforen. 2005 Nov 17;125(22):3090-3. Review. Norwegian.

8.

Monogenic obesity in humans.

Farooqi IS, O'Rahilly S.

Annu Rev Med. 2005;56:443-58. Review.

PMID:
15660521
9.

Severe obstructive sleep apnea in a child with melanocortin-4 receptor deficiency.

Pillai S, Nandalike K, Kogelman Y, Muzumdar R, Balk SJ, Arens R.

J Clin Sleep Med. 2014 Jan 15;10(1):99-101. doi: 10.5664/jcsm.3374.

10.

[Association of FTO gene polymorphisms and morbid obesity in the population of Extremadura (Spain)].

Rodríguez-López R, González-Carpio M, Serrano MV, Torres G, García de Cáceres MT, Herrera T, Román A, Rubio M, Méndez P, Hernández-Sáez R, Núñez M, Luengo LM.

Endocrinol Nutr. 2010 May;57(5):203-9. doi: 10.1016/j.endonu.2010.03.002. Epub 2010 Apr 24. Spanish.

PMID:
20418190
11.

Familial aggregation of morbid obesity.

Adams TD, Hunt SC, Mason LA, Ramirez ME, Fisher AG, Williams RR.

Obes Res. 1993 Jul;1(4):261-70.

12.

[Obesity].

León Sanz M.

Nutr Hosp. 1999 May;14 Suppl 2:92S-104S. Spanish.

PMID:
10548031
13.

State intervention in life-threatening childhood obesity.

Murtagh L, Ludwig DS.

JAMA. 2011 Jul 13;306(2):206-7. doi: 10.1001/jama.2011.903. No abstract available.

PMID:
21750301
14.

Pediatric obesity. An overview of etiology and treatment.

Schonfeld-Warden N, Warden CH.

Pediatr Clin North Am. 1997 Apr;44(2):339-61. Review.

PMID:
9130924
15.

ENU mutagenesis identifies mice with morbid obesity and severe hyperinsulinemia caused by a novel mutation in leptin.

Hong CJ, Tsai PJ, Cheng CY, Chou CK, Jheng HF, Chuang YC, Yang CN, Lin YT, Hsu CW, Cheng IH, Chen SY, Tsai SJ, Liou YJ, Tsai YS.

PLoS One. 2010 Dec 9;5(12):e15333. doi: 10.1371/journal.pone.0015333.

16.

Leptin receptor gene polymorphisms and morbid obesity in Mexican patients.

Rojano-Rodriguez ME, Beristain-Hernandez JL, Zavaleta-Villa B, Maravilla P, Romero-Valdovinos M, Olivo-Diaz A.

Hereditas. 2016 Feb 22;153:2. doi: 10.1186/s41065-016-0006-0. eCollection 2016.

17.

Is severe obesity a form of addiction? Rationale, clinical approach, and controlled clinical trial.

Riva G, Bacchetta M, Cesa G, Conti S, Castelnuovo G, Mantovani F, Molinari E.

Cyberpsychol Behav. 2006 Aug;9(4):457-79.

PMID:
16901250
18.

Clinical aspects of obesity in childhood and adolescence.

Kiess W, Galler A, Reich A, Müller G, Kapellen T, Deutscher J, Raile K, Kratzsch J.

Obes Rev. 2001 Feb;2(1):29-36. Review.

PMID:
12119634
19.

Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity.

Oksanen L, Mustajoki P, Kaprio J, Kainulainen K, Jänne O, Peltonen L, Kontula K.

Int J Obes Relat Metab Disord. 1996 Dec;20(12):1055-61.

PMID:
8968849
20.

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. doi: 10.1016/j.ymgme.2009.04.002. Epub 2009 Apr 9.

PMID:
19427251

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