Landau M - Search Results

1

Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor.

Lotem M, Raben M, Zeltser R, Landau M, Sela M, Wygoda M, Tochner ZA. Lotem M, et al. Among authors: landau m. Br J Dermatol. 2001 Jun;144(6):1284-6. doi: 10.1046/j.1365-2133.2001.04262.x. Br J Dermatol. 2001. PMID: 11422071 No abstract available.

2

Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families.

Yakobson E, Shemesh P, Azizi E, Winkler E, Lassam N, Hogg D, Brookes S, Peters G, Lotem M, Zlotogorski A, Landau M, Safro M, Shafir R, Friedman E, Peretz H. Yakobson E, et al. Among authors: landau m. Eur J Hum Genet. 2000 Aug;8(8):590-6. doi: 10.1038/sj.ejhg.5200505. Eur J Hum Genet. 2000. PMID: 10951521

3

Squamous cell carcinoma--70 years after irradiation.

Ophir J, Wolf R, Tamir A, Landau M. Ophir J, et al. Among authors: landau m. Dermatology. 1992;184(3):213-5. doi: 10.1159/000247545. Dermatology. 1992. PMID: 1392116

4

Adolescent-onset ichthyosiform-like erythroderma with lichenoid tissue reaction: a new entity?

Mevorah B, Landau M, Gat A, De Viragh P, Brenner S. Mevorah B, et al. Among authors: landau m. Br J Dermatol. 2001 May;144(5):1063-6. doi: 10.1046/j.1365-2133.2001.04200.x. Br J Dermatol. 2001. PMID: 11359399

5

Screening for tumour suppressor p16(CDKN2A) germline mutations in Israeli melanoma families.

Yakobson EA, Zlotogorski A, Shafir R, Cohen M, Icekson M, Landau M, Brenner S, Usher S, Peretz H. Yakobson EA, et al. Among authors: landau m. Clin Chem Lab Med. 1998 Aug;36(8):645-8. doi: 10.1515/CCLM.1998.114. Clin Chem Lab Med. 1998. PMID: 9806478

6

A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.

Rosenberg N, Hauschner H, Peretz H, Mor-Cohen R, Landau M, Shenkman B, Kenet G, Coller BS, Awidi AA, Seligsohn U. Rosenberg N, et al. Among authors: landau m. J Thromb Haemost. 2005 Dec;3(12):2764-72. doi: 10.1111/j.1538-7836.2005.01618.x. J Thromb Haemost. 2005. PMID: 16359514 Free PMC article.

7

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients.

Fromovich-Amit Y, Zivelin A, Rosenberg N, Tamary H, Landau M, Seligsohn U. Fromovich-Amit Y, et al. Among authors: landau m. J Thromb Haemost. 2004 Oct;2(10):1774-81. doi: 10.1111/j.1538-7836.2004.00921.x. J Thromb Haemost. 2004. PMID: 15456489 Free article.

8

Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families.

Vysokovsky A, Saxena R, Landau M, Zivelin A, Eskaraev R, Rosenberg N, Seligsohn U, Inbal A. Vysokovsky A, et al. Among authors: landau m. J Thromb Haemost. 2004 Oct;2(10):1790-7. doi: 10.1111/j.1538-7836.2004.00908.x. J Thromb Haemost. 2004. PMID: 15456491 Free article.

9

Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata.

Chuang GS, Martinez-Mir A, Geyer A, Engler DE, Glaser B, Cserhalmi-Friedman PB, Gordon D, Horev L, Lukash B, Herman E, Cid MP, Brenner S, Landau M, Sprecher E, Garcia Muret MP, Christiano AM, Zlotogorski A. Chuang GS, et al. Among authors: landau m. J Am Acad Dermatol. 2005 Mar;52(3 Pt 1):410-6. doi: 10.1016/j.jaad.2004.08.051. J Am Acad Dermatol. 2005. PMID: 15761418 Free article.

10

Scabid: an unusual id reaction to scabies.

Brenner S, Wolf R, Landau M. Brenner S, et al. Among authors: landau m. Int J Dermatol. 1993 Feb;32(2):128-9. doi: 10.1111/j.1365-4362.1993.tb01454.x. Int J Dermatol. 1993. PMID: 8440556 No abstract available.

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