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Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease.
Gratacòs M, Escaramís G, Bustamante M, Saus E, Agüera Z, Bayés M, Cellini E, de Cid R, Fernández-Aranda F, Forcano L, González JR, Gorwood P, Hebebrand J, Hinney A, Mercader JM, Nacmias B, Ramoz N, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Estivill X. Gratacòs M, et al. Among authors: nacmias b. J Psychiatr Res. 2010 Oct;44(13):834-40. doi: 10.1016/j.jpsychires.2010.01.009. Epub 2010 Mar 9. J Psychiatr Res. 2010. PMID: 20219210
HLA A2 allele is associated with age at onset of Alzheimer's disease.
Ballerini C, Nacmias B, Rombolà G, Marcon G, Massacesi L, Sorbi S. Ballerini C, et al. Among authors: nacmias b. Ann Neurol. 1999 Mar;45(3):397-400. doi: 10.1002/1531-8249(199903)45:3<397::aid-ana18>3.0.co;2-4. Ann Neurol. 1999. PMID: 10072057
Genetic risk factors in familial Alzheimer's disease.
Sorbi S, Forleo P, Tedde A, Cellini E, Ciantelli M, Bagnoli S, Nacmias B. Sorbi S, et al. Among authors: nacmias b. Mech Ageing Dev. 2001 Nov;122(16):1951-60. doi: 10.1016/s0047-6374(01)00308-6. Mech Ageing Dev. 2001. PMID: 11589913 Review.
The 5-HT(2A) -1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres.
Gorwood P, Adès J, Bellodi L, Cellini E, Collier DA, Di Bella D, Di Bernardo M, Estivill X, Fernandez-Aranda F, Gratacos M, Hebebrand J, Hinney A, Hu X, Karwautz A, Kipman A, Mouren-Siméoni MC, Nacmias B, Ribasés M, Remschmidt H, Ricca V, Rotella CM, Sorbi S, Treasure J; EC Framework V 'Factors in Healthy Eating' consortium. Gorwood P, et al. Among authors: nacmias b. Mol Psychiatry. 2002;7(1):90-4. doi: 10.1038/sj.mp.4000938. Mol Psychiatry. 2002. PMID: 11803452
5-HT2A receptor gene polymorphism and eating disorders.
Ricca V, Nacmias B, Cellini E, Di Bernardo M, Rotella CM, Sorbi S. Ricca V, et al. Among authors: nacmias b. Neurosci Lett. 2002 Apr 26;323(2):105-8. doi: 10.1016/s0304-3940(02)00088-5. Neurosci Lett. 2002. PMID: 11950504
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa.
Gabrovsek M, Brecelj-Anderluh M, Bellodi L, Cellini E, Di Bella D, Estivill X, Fernandez-Aranda F, Freeman B, Geller F, Gratacos M, Haigh R, Hebebrand J, Hinney A, Holliday J, Hu X, Karwautz A, Nacmias B, Ribases M, Remschmidt H, Komel R, Sorbi S, Tomori M, Treasure J, Wagner G, Zhao J, Collier DA. Gabrovsek M, et al. Among authors: nacmias b. Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):68-72. doi: 10.1002/ajmg.b.20085. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14681918
373 results