PUBERDADE PRECOCE - AVALIAÇAO LABORATORIAL
Columnista Experto de SIIC Durval Damiani
en colaboración con
Primera edición en siicsalud:
18 de septiembre, 2003
Sección Artículos originales,
subsección
Expertos de Iberoamérica,
página
/des/expertocompleto.php/20052
Especialidad principal:
Pediatría
Especialidades relacionadas:
Diagnóstico por Laboratorio,Endocrinología y Metabolismo,
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(44):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(106):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
Durval Damiani
