Khamaysi Z - Search Results

1

A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.

Israeli S, Khamaysi Z, Fuchs-Telem D, Nousbeck J, Bergman R, Sarig O, Sprecher E. Israeli S, et al. Among authors: khamaysi z. Am J Hum Genet. 2011 Apr 8;88(4):482-7. doi: 10.1016/j.ajhg.2011.02.011. Am J Hum Genet. 2011. PMID: 21439540 Free PMC article.

2

To ASLO or Not to ASLO: Utility of the ASLO Test in Dermatology.

Tibi A, Khamaysi Z, Avitan-Hersh E. Tibi A, et al. Among authors: khamaysi z. Isr Med Assoc J. 2024 Apr;26(4):222-225. Isr Med Assoc J. 2024. PMID: 38616666 Free article.

3

Insect bite-like reaction associated with mantle cell lymphoma: clinicopathological, immunopathological, and molecular studies.

Khamaysi Z, Dodiuk-Gad RP, Weltfriend S, Ben-Arieh Y, Dann EJ, Sahar D, Bergman R. Khamaysi Z, et al. Am J Dermatopathol. 2005 Aug;27(4):290-5. doi: 10.1097/01.dad.0000164607.41402.40. Am J Dermatopathol. 2005. PMID: 16121047

4

Pleomorphic CD8+ small/medium size cutaneous T-cell lymphoma.

Khamaysi Z, Ben-Arieh Y, Epelbaum R, Bergman R. Khamaysi Z, et al. Am J Dermatopathol. 2006 Oct;28(5):434-7. doi: 10.1097/01.dad.0000210389.36724.dd. Am J Dermatopathol. 2006. PMID: 17012921

5

Galli-Galli disease is an acantholytic variant of Dowling-Degos disease.

Sprecher E, Indelman M, Khamaysi Z, Lugassy J, Petronius D, Bergman R. Sprecher E, et al. Among authors: khamaysi z. Br J Dermatol. 2007 Mar;156(3):572-4. doi: 10.1111/j.1365-2133.2006.07703.x. Br J Dermatol. 2007. PMID: 17300252 No abstract available.

6

Familial palmoplantar keratoderma: not always hereditary.

Khamaysi Z, Indelman M, Bergman R, Sprecher E. Khamaysi Z, et al. J Eur Acad Dermatol Venereol. 2007 Nov;21(10):1437-8. doi: 10.1111/j.1468-3083.2007.02251.x. J Eur Acad Dermatol Venereol. 2007. PMID: 17958870 No abstract available.

7

Nail dystrophy in focal acral hyperkeratosis: a distinctive feature?

Khamaysi Z, Bergman R, Sprecher E. Khamaysi Z, et al. J Eur Acad Dermatol Venereol. 2008 Jul;22(7):891-3. doi: 10.1111/j.1468-3083.2007.02494.x. Epub 2008 May 6. J Eur Acad Dermatol Venereol. 2008. PMID: 18462306 No abstract available.

8

A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.

Nahum S, Pasternack SM, Pforr J, Indelman M, Wollnik B, Bergman R, Nöthen MM, König A, Khamaysi Z, Betz RC, Sprecher E. Nahum S, et al. Among authors: khamaysi z. Arch Dermatol Res. 2009 Jun;301(5):391-3. doi: 10.1007/s00403-008-0903-9. Epub 2008 Sep 27. Arch Dermatol Res. 2009. PMID: 18820939

9

A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy.

Avitan-Hersh E, Indelman M, Khamaysi Z, Leibu R, Bergman R. Avitan-Hersh E, et al. Among authors: khamaysi z. Int J Dermatol. 2012 Mar;51(3):325-7. doi: 10.1111/j.1365-4632.2011.04973.x. Int J Dermatol. 2012. PMID: 22348569 No abstract available.

10

Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.

Khamaysi Z, Bochner R, Indelman M, Magal L, Avitan-Hersh E, Sarig O, Sprecher E, Bergman R. Khamaysi Z, et al. Br J Dermatol. 2016 Jul;175(1):178-81. doi: 10.1111/bjd.14425. Epub 2016 Jun 20. Br J Dermatol. 2016. PMID: 26822128

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