Stivel M - Search Results

1

Genetic characterization of a large cohort of Argentine 21-hydroxylase Deficiency.

Fernández CS, Taboas M, Bruque CD, Benavides-Mori B, Belli S, Stivel M, Oneto A, Pasqualini T, Delea M, Espeche LD, Kolomenski JE, Alba L, Buzzalino N, Dain L. Fernández CS, et al. Among authors: stivel m. Clin Endocrinol (Oxf). 2020 Jul;93(1):19-27. doi: 10.1111/cen.14190. Epub 2020 May 3. Clin Endocrinol (Oxf). 2020. PMID: 32289882

2

Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.

Dain LB, Buzzalino ND, Oneto A, Belli S, Stivel M, Pasqualini T, Minutolo C, Charreau EH, Alba LG. Dain LB, et al. Among authors: stivel m. Clin Endocrinol (Oxf). 2002 Feb;56(2):239-45. doi: 10.1046/j.0300-0664.2001.01419.x. Clin Endocrinol (Oxf). 2002. PMID: 11874416

3

Functional studies of p.R132C, p.R149C, p.M283V, p.E431K, and a novel c.652-2A>G mutations of the CYP21A2 gene.

Taboas M, Gómez Acuña L, Scaia MF, Bruque CD, Buzzalino N, Stivel M, Ceballos NR, Dain L. Taboas M, et al. Among authors: stivel m. PLoS One. 2014 Mar 25;9(3):e92181. doi: 10.1371/journal.pone.0092181. eCollection 2014. PLoS One. 2014. PMID: 24667412 Free PMC article.

4

[Pediatric emergency: adrenal insufficiency and adrenal crisis].

Martínez A, Pasqualini T, Stivel M, Heinrich JJ. Martínez A, et al. Among authors: stivel m. Arch Argent Pediatr. 2010 Apr;108(2):167-70. doi: 10.1590/S0325-00752010000200018. Arch Argent Pediatr. 2010. PMID: 20467714 Free article. Spanish.

5

Tetrasomy 21pter-q22.11: molecular, cytogenetic, and clinical findings.

Cerretini R, Luccerini V, Stivel M, Bañares V, Aranda I, Alba L, Pivetta O, Slavutsky I. Cerretini R, et al. Among authors: stivel m. Clin Genet. 1999 Apr;55(4):283-6. doi: 10.1034/j.1399-0004.1999.550414.x. Clin Genet. 1999. PMID: 10361993 No abstract available.

6

Late-onset type of 21-hydroxylase deficiency in childhood.

Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z. Roitman A, et al. Among authors: stivel m. Isr J Med Sci. 1982 Jul;18(7):763-8. Isr J Med Sci. 1982. PMID: 6980865

7

Recurrent hypothermia, hypersomnolence, central sleep apnea, hypodipsia, hypernatremia, hypothyroidism, hyperprolactinemia and growth hormone deficiency in a boy--treatment with clomipramine.

Gurewitz R, Blum I, Lavie P, Pertzelan A, Stivel M, Weinstein R, Galatzer A, Laron Z. Gurewitz R, et al. Among authors: stivel m. Acta Endocrinol Suppl (Copenh). 1986;279:468-72. doi: 10.1530/acta.0.112s468. Acta Endocrinol Suppl (Copenh). 1986. PMID: 3465179

8

Testicular function in prepubertal male pseudohermaphroditism.

Campo S, Moteagudo C, Nicolau G, Pellizzari E, Belgorosky A, Stivel M, Rivarola M. Campo S, et al. Among authors: stivel m. Clin Endocrinol (Oxf). 1981 Jan;14(1):11-22. doi: 10.1111/j.1365-2265.1981.tb00360.x. Clin Endocrinol (Oxf). 1981. PMID: 6261996

9

Adrenocortical function in children with precocious sexual development during treatment with cyproterone acetate.

Stivel MS, Kauli R, Kaufman H, Laron Z. Stivel MS, et al. Clin Endocrinol (Oxf). 1982 Feb;16(2):163-9. doi: 10.1111/j.1365-2265.1982.tb03160.x. Clin Endocrinol (Oxf). 1982. PMID: 6279337

10

Testicular function in post pubertal male pseudohermaphroditism.

Campo S, Stivel M, Nicolau G, Monteagudo C, Rivarola M. Campo S, et al. Among authors: stivel m. Clin Endocrinol (Oxf). 1979 Nov;11(5):481-90. doi: 10.1111/j.1365-2265.1979.tb03100.x. Clin Endocrinol (Oxf). 1979. PMID: 160294

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