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

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.

3

Outcome of pregnancies in women receiving velaglucerase alfa for Gaucher disease.

Elstein D, Hughes D, Goker-Alpan O, Stivel M, Baris HN, Cohen IJ, Granovsky-Grisaru S, Samueloff A, Mehta A, Zimran A. Elstein D, et al. Among authors: stivel m. J Obstet Gynaecol Res. 2014 Apr;40(4):968-75. doi: 10.1111/jog.12254. Epub 2014 Feb 26. J Obstet Gynaecol Res. 2014. PMID: 24612151

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

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

6

Massive plasmocytosis due to methimazole-induced bone marrow toxicity.

Breier DV, Rendo P, Gonzalez J, Shilton G, Stivel M, Goldztein S. Breier DV, et al. Among authors: stivel m. Am J Hematol. 2001 Aug;67(4):259-61. doi: 10.1002/ajh.1127. Am J Hematol. 2001. PMID: 11443640 Free article.

7

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.

8

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

9

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

10

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

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