Farah SB - Search Results

1

Isolation and characterization of Y chromosome DNA probes.

Farah SB, Gruenert DC, Lepercq JA, Chueh J, Metzger A, Sartorato EL, Lebo RV, Golbus MS. Farah SB, et al. Biochem Biophys Res Commun. 1992 Nov 30;189(1):581-9. doi: 10.1016/0006-291x(92)91597-j. Biochem Biophys Res Commun. 1992. PMID: 1449506

2

Use of Y-chromosome-specific DNA probes to evaluate an XX male.

Farah SB, Garmes HM, Cavalcanti DP, Mello MP, Porrelli RN, Ramos CF, Sartorato EL. Farah SB, et al. Braz J Med Biol Res. 1991;24(2):149-56. Braz J Med Biol Res. 1991. PMID: 1823227

3

Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.

Farah SB, Ramos CF, de Mello MP, Sartorato EL, Horelli-Kuitunen N, Lopes VL, Cavalcanti DP, Hackel C. Farah SB, et al. Am J Med Genet. 1994 Feb 15;49(4):388-92. doi: 10.1002/ajmg.1320490407. Am J Med Genet. 1994. PMID: 8160730

4

Hematopoietic stem cells for the treatment of genetic disease.

Farah SB, Simpson TJ, Golbus MS. Farah SB, et al. Clin Obstet Gynecol. 1986 Sep;29(3):543-50. Clin Obstet Gynecol. 1986. PMID: 2875820 No abstract available.

5

True agonadism: report of a case analyzed with Y-specific DNA probes.

Maciel-Guerra AT, Farah SB, Garmes HM, Pinto Júnior W, Bustorff da Silva JM, Baptista MT, Marques-de-Faria AP, Guerra Júnior G, de Mello MP. Maciel-Guerra AT, et al. Among authors: farah sb. Am J Med Genet. 1991 Dec 15;41(4):444-5. doi: 10.1002/ajmg.1320410412. Am J Med Genet. 1991. PMID: 1776634

6

Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency.

de-Araujo M, Sanches MR, Suzuki LA, Guerra G Jr, Farah SB, de-Mello MP. de-Araujo M, et al. Among authors: farah sb. Braz J Med Biol Res. 1996 Jan;29(1):1-13. Braz J Med Biol Res. 1996. PMID: 8731325 Review.

7

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11.

Vogt PH, Edelmann A, Kirsch S, Henegariu O, Hirschmann P, Kiesewetter F, Köhn FM, Schill WB, Farah S, Ramos C, Hartmann M, Hartschuh W, Meschede D, Behre HM, Castel A, Nieschlag E, Weidner W, Gröne HJ, Jung A, Engel W, Haidl G. Vogt PH, et al. Hum Mol Genet. 1996 Jul;5(7):933-43. doi: 10.1093/hmg/5.7.933. Hum Mol Genet. 1996. PMID: 8817327

8

High prevalence of alpha-thalassemia in a black population of Brazil.

Sonati MF, Farah SB, Ramalho AS, Costa FF. Sonati MF, et al. Among authors: farah sb. Hemoglobin. 1991;15(4):309-11. doi: 10.3109/03630269109027884. Hemoglobin. 1991. PMID: 1686261 No abstract available.

9

Multimodal thromboprophylaxis in low-risk patients undergoing lower limb arthroplasty: A retrospective observational cohort analysis of 1400 patients with ultrasound screening.

Harrison-Brown M, Scholes C, Douglas SL, Farah SB, Kerr D, Kohan L. Harrison-Brown M, et al. Among authors: farah sb. J Orthop Surg (Hong Kong). 2020 Jan-Apr;28(2):2309499020926790. doi: 10.1177/2309499020926790. J Orthop Surg (Hong Kong). 2020. PMID: 32484038 Free article.

10

Limited penetration of cobalt and chromium ions into the cerebrospinal fluid following metal on metal arthroplasty: a cross-sectional analysis.

Harrison-Brown M, Scholes C, Field C, McQuilty R, Farah SB, Nizam I, Kerr D, Kohan L. Harrison-Brown M, et al. Among authors: farah sb. Clin Toxicol (Phila). 2020 Apr;58(4):233-240. doi: 10.1080/15563650.2019.1636993. Epub 2019 Jul 12. Clin Toxicol (Phila). 2020. PMID: 31298064

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