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D Damiani, MA Mascolli, MJ Almeida, F Jaubert, M Fellous, V Dichtchekenian, P R Tobo, C A Moreira-Filho, N Setian. Persistence of Müllerian Remnants in Complete Androgen Insensitivity Syndrome
J Pediatr Endocrinol Metab
15:1553-6, 2002
Damiani, D.; Dichtchekenian, V. & Setian, N. O enigma da determinação gonadal : o que existe além do cromossomo Y
Arq Bras Endocrinol Metab
44(3):248-56, 2000
E de Baere, B Lemercier, S Christin-Maitre, D Durval, L Messiaen, M Fellous, R Veitia. FOXL2 mutation screening in a large panel of POF patients and XX males
J Med Genet
39:e43-45, 2002
Nuvarte Setian; Caroline M. Tanaka; Durval Damiani; Vaê Dichtchekenian; Jorge D. A. Carneiro; Elbio A. D\'Amico. Hypopituitarism, Deficiency of Factors V and VIII, and von Willebrand Factor: Na Uncommon Association
J Peditar Endocrinol Metabol
15:331-3, 2002
Della Manna, T.; Damiani, D.; Haber, J.S.; Steinmetz, L.; Silva, A C.; Lima, S.C.; Setian, N. Treatment of Diabetic Ketoacidosis: Subcutaneous Lispro versus Continuous Intravenous Regular Insulin
J Ped Endocrinol Metab
14:1064, 2001
Nuvarte Setian, Regina S.F. Andrade, Hilton Kuperman, Thaís Della Manna, Vaê Dichtchekenian, Durval Damiani. Precocious Puberty: An Endocrine Manifestation in Congenital Toxoplasmosis
J Pediatr Endocrinol Metab
15:1487-90, 2002
Witchel, S.F.; Smith, R.L ;Crivellaro, C. E.; Della Manna, T.; Dichtchekenian, V.; Setian, N.; Damiani, D. Cyp21 Mutations in brazilian patients with 21-hydroxylase deficiency
Hum Genet
106(4):414-9, 2000
Damiani, D.; Guedes, D.R.; Fellous, M.; Barbaux, S.; Mcelreavey, K.; Kalil, J.; Goldberg, A.C.K.; Moreira-Filho, C.A.; Barbosa, A.; Della-Manna, T.; Dichtchekenian, V. & Setian, N. Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments
J Pediatr Endocrinol Metab
12:827-31, 1999
Damiani, D.; Guedes, D.R.; Fellous, M.; Barbaux, S.; Mcelreavey, K.; Kalil, J.; Goldberg, A.C.K.; Moreira-Filho, C.A.; Barbosa, A.; Della-Manna, T.; Dichtchekenian, V. & Setian, N. Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments
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Damiani, D.; Guedes, D.R.; Fellous, M.; Barbaux, S.; Mcelreavey, K.; Kalil, J.; Goldberg, A.C.K.; Moreira-Filho, C.A.; Barbosa, A.; Della-Manna, T.; Dichtchekenian, V. & Setian, N. Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments
J Pediatric Endocrinol Metab
11:665-9, 1998
Dr. Durval Damiani
Dirección profesional:
Instituto da Criança Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo. Av. Dr. Enéas de Carvalho Aguiar 647, São Paulo, Brasil
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