M Indelman
Overview
Explore the profile of M Indelman including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
88
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Recent Articles
1.
Khamaysi Z, Bochner R, Indelman M, Magal L, Avitan-Hersh E, Sarig O, et al.
Br J Dermatol
. 2016 Jan;
175(1):178-81.
PMID: 26822128
Aberrant sonic hedgehog signalling, mostly due to PTCH1 mutations, has been shown to play a central role in the pathogenesis of basal cell carcinoma (BCC), as well as in basal...
2.
Israeli S, Goldberg I, Fuchs-Telem D, Bergman R, Indelman M, Bitterman-Deutsch O, et al.
Clin Exp Dermatol
. 2013 Apr;
38(8):911-6.
PMID: 23621129
Background: Autosomal recessive congenital ichthyosis (ARCI) is the term given to a complex and heterogeneous group of cornification disorders associated with mutations in at least eight distinct genes. Mutation distribution...
3.
Bergman R, Mercer A, Indelman M, Sprecher E, Haim N, Zoller L, et al.
Br J Dermatol
. 2011 Aug;
166(2):455-7.
PMID: 21848689
No abstract available.
4.
Hershkovitz D, Lugassy J, Indelman M, Bergman R, Sprecher E
Clin Exp Dermatol
. 2008 Nov;
34(2):224-8.
PMID: 19018793
Background: Striate palmoplantar keratoderma (SPPK) has been shown to be caused by mutations in at least three genes: DSG1, DSP and KRT1. Methods: Three families with nine affected members were...
5.
Khamaysi Z, Indelman M, Bergman R, Sprecher E
J Eur Acad Dermatol Venereol
. 2007 Oct;
21(10):1437-8.
PMID: 17958870
No abstract available.
6.
Indelman M, Eason J, Hummel M, Loza O, Suri M, Leys M, et al.
Clin Exp Dermatol
. 2007 Mar;
32(2):191-6.
PMID: 17342797
Background: Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive disorder characterized by sparse and short hair, heralding progressive degeneration of the retinal pigment epithelium, which leads to...
7.
Sprecher E, Indelman M, Khamaysi Z, Lugassy J, Petronius D, Bergman R
Br J Dermatol
. 2007 Feb;
156(3):572-4.
PMID: 17300252
No abstract available.
8.
Hershkovitz T, Hassoun G, Indelman M, Shlush L, Bergman R, Pollack S, et al.
Clin Exp Dermatol
. 2006 May;
31(3):435-40.
PMID: 16681595
Background: Prolidase deficiency is a complex disease characterized by various skin manifestations accompanied by mental retardation, facial dysmorphism and susceptibility to pyogenic infections. Methods: We assessed a patient presenting a...
9.
Indelman M, Leibu R, Jammal A, Bergman R, Sprecher E
Br J Dermatol
. 2005 Aug;
153(3):635-8.
PMID: 16120155
Background: Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive disorder characterized by sparse and short scalp hair from birth, followed within a few years by progressive macular...
10.
Tal O, Bergman R, Alcalay J, Indelman M, Sprecher E
Clin Exp Dermatol
. 2005 Jan;
30(1):64-7.
PMID: 15663507
Mutations in the keratin 1 (KRT1) gene underlie epidermolytic hyperkeratosis (EHK). This autosomal dominant disorder is characterized by phenotypic heterogeneity. In the present study, we assessed a 33-year-old individual presenting...