Morel Y - Search Results

1

[Non alcoholic steatohepatitis: a multifactorial, frequent, paucysymptomatic liver disease with a fibrotic outcome].

Laroussi N, Mosnier JF, Morel Y, Deugnier Y, Dumas O, Audigier JC. Laroussi N, et al. Among authors: morel y. Gastroenterol Clin Biol. 2002 May;26(5):475-9. Gastroenterol Clin Biol. 2002. PMID: 12122357 Free article. French.

2

[Role of the hemochromatosis gene in prophyria cutanea tarda. Prospective study of 56 cases].

Skowron F, Bérard F, Grézard P, Wolf F, Morel Y, Perrot H. Skowron F, et al. Among authors: morel y. Ann Dermatol Venereol. 2001 May;128(5):600-4. Ann Dermatol Venereol. 2001. PMID: 11427792 Free article. French.

3

Clinical report of three patients with hereditary hemochromatosis and movement disorders.

Demarquay G, Setiey A, Morel Y, Trepo C, Chazot G, Broussolle E. Demarquay G, et al. Among authors: morel y. Mov Disord. 2000 Nov;15(6):1204-9. doi: 10.1002/1531-8257(200011)15:6<1204::aid-mds1021>3.0.co;2-t. Mov Disord. 2000. PMID: 11104206 Review.

4

[Hirsutism. Two familial cases of 21-hydroxylase deficiency].

Roux S, Morel Y, Gorin I, Escande JP. Roux S, et al. Among authors: morel y. Ann Dermatol Venereol. 1995;122(10):697-700. Ann Dermatol Venereol. 1995. PMID: 8687058 French.

5

[Late diagnoses of 21-hydroxylase deficiencies in children (after the age of 3 years].

Carel JC, Marrakchi Z, Roger M, Morel Y, Chaussain JL. Carel JC, et al. Among authors: morel y. Ann Pediatr (Paris). 1993 Sep;40(7):410-20. Ann Pediatr (Paris). 1993. PMID: 8239392 French.

6

[Adrenal hypoplasia congenita: four new cases in children].

Pélissier P, Merlin E, Prieur F, David M, Malpuech G, Forest MG, Morel Y, Nicolino M, Richard O, Stéphan JL. Pélissier P, et al. Among authors: morel y. Arch Pediatr. 2005 Apr;12(4):380-4. doi: 10.1016/j.arcped.2005.01.007. Arch Pediatr. 2005. PMID: 15808425 French.

7

[Association of mixed gonadal dysgenesis and non-classic 21-hydroxylase deficiency].

Del Pino O, Carel JC, Barbet JP, Morel Y, Chaussain JL. Del Pino O, et al. Among authors: morel y. Arch Pediatr. 1996 Dec;3(12):1258-61. doi: 10.1016/s0929-693x(97)85938-6. Arch Pediatr. 1996. PMID: 9033792 French.

8

[Haemochromatosis screening in 120 patients complaining with persistant fatigue].

Vital Durand D, François S, Nové-Josserand R, Durupt S, Durieu I, Morel Y, Rousset H. Vital Durand D, et al. Among authors: morel y. Rev Med Interne. 2004 Sep;25(9):623-8. doi: 10.1016/j.revmed.2004.04.016. Rev Med Interne. 2004. PMID: 15363617 French.

9

21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease.

Forest MG, Tardy V, Nicolino M, David M, Morel Y. Forest MG, et al. Among authors: morel y. Ann Endocrinol (Paris). 2005 Jun;66(3):225-32. doi: 10.1016/s0003-4266(05)81754-8. Ann Endocrinol (Paris). 2005. PMID: 15988383 Review.

10

[21 hydroxylase deficiency: new strategies emerging from molecular studies].

Morel Y, Tardy V, Costa JM, Forest MG, David M. Morel Y, et al. Ann Endocrinol (Paris). 2003 Dec;64(6):456-70. Ann Endocrinol (Paris). 2003. PMID: 15067252 French. No abstract available.

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