Kasinetz L - Search Results

1

Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis.

Jayoussi-Assalia R, Etzioni A, Notarangelo LD, Brill-Zamir R, Kasinetz L, Kadouri E, Gershoni-Baruch R. Jayoussi-Assalia R, et al. Among authors: kasinetz l. Prenat Diagn. 2000 Oct;20(10):822-3. doi: 10.1002/1097-0223(200010)20:10<822::aid-pd935>3.0.co;2-k. Prenat Diagn. 2000. PMID: 11038461

2

Detection of transplanted liver cells to the spleen by semiquantitative analysis using PCR for the Sry region on the Y chromosome.

Veitzman E, Shenkar L, Shoshany G, Kasinetz L, Gershoni-Baruch R, Brill Zamir R, Baruch Y. Veitzman E, et al. Among authors: kasinetz l. Transplant Proc. 2000 Jun;32(4):721-3. doi: 10.1016/s0041-1345(00)00957-x. Transplant Proc. 2000. PMID: 10856559 No abstract available.

3

Association of the C677T polymorphism in the MTHFR gene with breast and/or ovarian cancer risk in Jewish women.

Gershoni-Baruch R, Dagan E, Israeli D, Kasinetz L, Kadouri E, Friedman E. Gershoni-Baruch R, et al. Among authors: kasinetz l. Eur J Cancer. 2000 Dec;36(18):2313-6. doi: 10.1016/s0959-8049(00)00306-3. Eur J Cancer. 2000. PMID: 11094304

4

The musculoskeletal manifestations of familial Mediterranean fever in children genetically diagnosed with the disease.

Brik R, Shinawi M, Kasinetz L, Gershoni-Baruch R. Brik R, et al. Among authors: kasinetz l. Arthritis Rheum. 2001 Jun;44(6):1416-9. doi: 10.1002/1529-0131(200106)44:6<1416::AID-ART236>3.0.CO;2-6. Arthritis Rheum. 2001. PMID: 11407703 Free article.

5

Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers.

Gershoni-Baruch R, Patael Y, Dagan, Figer A, Kasinetz L, Kadouri E, Bruchim Bar Sade R, Friedman E. Gershoni-Baruch R, et al. Among authors: kasinetz l. Br J Cancer. 2000 Jul;83(2):153-5. doi: 10.1054/bjoc.2000.1248. Br J Cancer. 2000. PMID: 10901363 Free PMC article.

6

Familial Mediterranean fever: high gene frequency and heterogeneous disease among an Israeli-Arab population.

Shinawi M, Brik R, Berant M, Kasinetz L, Gershoni-Baruch R. Shinawi M, et al. Among authors: kasinetz l. J Rheumatol. 2000 Jun;27(6):1492-5. J Rheumatol. 2000. PMID: 10852276

7

Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan Jews.

Paperna T, Gershoni-Baruch R, Badarneh K, Kasinetz L, Hochberg Z. Paperna T, et al. Among authors: kasinetz l. J Clin Endocrinol Metab. 2005 Sep;90(9):5463-5. doi: 10.1210/jc.2005-1145. Epub 2005 Jul 19. J Clin Endocrinol Metab. 2005. PMID: 16030166

8

A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers.

Levy-Lahad E, Lahad A, Eisenberg S, Dagan E, Paperna T, Kasinetz L, Catane R, Kaufman B, Beller U, Renbaum P, Gershoni-Baruch R. Levy-Lahad E, et al. Among authors: kasinetz l. Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3232-6. doi: 10.1073/pnas.051624098. Proc Natl Acad Sci U S A. 2001. PMID: 11248061 Free PMC article.

9

Web-based question-answering service of a family physician -- the characteristics of queries in a non-commercial open forum.

Vinker S, Weinfass M, Kasinetz LM, Kitai E, Kaiserman I. Vinker S, et al. Among authors: kasinetz lm. Med Inform Internet Med. 2007 Jun;32(2):123-9. doi: 10.1080/14639230601178653. Med Inform Internet Med. 2007. PMID: 17541862

10

Urgent referrals to a specialist by family physicians--is the "urgency" real: a prospective study.

Vinker S, Kaiserman I, Karni A, Kitai E, Kasinetz LM, Elhayany A, Nakar S. Vinker S, et al. Among authors: kasinetz lm. Eur J Gen Pract. 2007;13(1):37-9. doi: 10.1080/13814780600881003. Eur J Gen Pract. 2007. PMID: 17366293 Free article. No abstract available.

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