Erythema nodosum leprosum post‐COVID‐19 vaccination: endemic while pandemic
Fachler, T., Olshtain‐Pops, K., Horev, L.
Published in Journal of the European Academy of Dermatology and Venereology (01.07.2022)
Published in Journal of the European Academy of Dermatology and Venereology (01.07.2022)
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Journal Article
Pyoderma gangrenosum along superficial vein thrombosis during pregnancy
Renert-Yuval, Y., Ramot, Y., Ophir, I., Ingber, A., Horev, L.
Published in Clinical and experimental dermatology (01.01.2016)
Published in Clinical and experimental dermatology (01.01.2016)
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Journal Article
Squamous cell carcinoma in situ in association with HPV 11 in Netherton's syndrome patient: a case report
Shreberk-Hassidim, R., Hassidim, A., Adler, N., Horev, L., Maly, A., Zlotogorski, A., Ramot, Y.
Published in Journal of the European Academy of Dermatology and Venereology (01.12.2016)
Published in Journal of the European Academy of Dermatology and Venereology (01.12.2016)
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Journal Article
CYLD mutations in familial skin appendage tumours
Saggar, S, Chernoff, K A, Lodha, S, Horev, L, Kohl, S, Honjo, R S, Brandt, H R C, Hartmann, K, Celebi, J T
Published in Journal of medical genetics (01.05.2008)
Published in Journal of medical genetics (01.05.2008)
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Journal Article
Kerion celsi of the vulva: An unusual location
Shreberk-Hassidim, R., Ramot, Y., Maly, A., Horev, L., Zlotogorski, A.
Published in Journal de mycologie médicale (01.12.2014)
Published in Journal de mycologie médicale (01.12.2014)
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Journal Article
Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex
Horev, L., Babay, S., Ramot, Y., Saad-Edin, B., Moorad, S., Ingber, A., Maly, A., Zlotogorski, A.
Published in British journal of dermatology (1951) (01.05.2011)
Published in British journal of dermatology (1951) (01.05.2011)
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Journal Article
A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma
Minder, EI, Schneider-Yin, X, Mamet, R, Horev, L, Neuenschwander, S, Baumer, A, Austerlitz, F, Puy, H, Schoenfeld, N
Published in Journal of the European Academy of Dermatology and Venereology (01.11.2010)
Published in Journal of the European Academy of Dermatology and Venereology (01.11.2010)
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Journal Article
Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24
Martinez-Mir, A, Zlotogorski, A, Londono, D, Gordon, D, Grunn, A, Uribe, E, Horev, L, Ruiz, I M, Davalos, N O, Alayan, O, Liu, J, Gilliam, T C, Salas-Alanis, J C, Christiano, A M
Published in Journal of medical genetics (01.12.2003)
Published in Journal of medical genetics (01.12.2003)
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Journal Article
Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
Horev, L., Glaser, B., Metzker, A., Ben-Amitai, D., Vardy, D., Zlotogorski, A.
Published in Human heredity (01.09.2000)
Published in Human heredity (01.09.2000)
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Journal Article
Exacerbation of Hailey-Hailey Disease Following SARS-CoV-2 Vaccination
Armoni-Weiss, G, Sheffer-Levi, S, Horev, L, Klapholz, L, Avitan-Hersh, E, Zlotogorski, A, Ramot, Y
Published in Acta dermato-venereologica (22.09.2021)
Published in Acta dermato-venereologica (22.09.2021)
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Journal Article
Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency
Horev, L., Waran Lalin, T., Martinez-Mir, A., Bagheri, B. A., Tadin-Strapps, M., Schneiderman, P. I., Grossman, M. E., Bickers, D. R., Christiano, A. M.
Published in Clinical and experimental dermatology (01.01.2003)
Published in Clinical and experimental dermatology (01.01.2003)
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Journal Article
South American cutaneous leishmaniasis: report of ten cases in Israeli travelers
Zlotogorski, A, Gilead, L, Jonas, F, Horev, L, Klaus, S.N
Published in Journal of the European Academy of Dermatology and Venereology (01.07.1998)
Published in Journal of the European Academy of Dermatology and Venereology (01.07.1998)
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Journal Article
A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance: Novel mutation in coil 2A of KRT86 causing monilethrix
De Cruz, R., Horev, L., Green, J., Babay, S., Sladden, M., Zlotogorski, A., Sinclair, R.
Published in British journal of dermatology (1951) (01.06.2012)
Published in British journal of dermatology (1951) (01.06.2012)
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