Works by Malovitski, Kiril

Results: 12

Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis.

Published in:

Experimental Dermatology, 2022, v. 31, n. 4, p. 567, doi. 10.1111/exd.14502

By:

Samuelov, Liat;
Bochner, Ron;
Magal, Lee;
Malovitski, Kiril;
Sagiv, Nadav;
Nousbeck, Janna;
Keren, Aviad;
Fuchs‐Telem, Dana;
Sarig, Ofer;
Gilhar, Amos;
Sprecher, Eli

Publication type:

Article

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population.

Published in:

Experimental Dermatology, 2021, v. 30, n. 9, p. 1290, doi. 10.1111/exd.14345

By:

Mohamad, Janan;
Samuelov, Liat;
Malchin, Natalia;
Rabinowitz, Tom;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Israeli, Shirli;
Grafi‐Cohen, Meital;
Bitterman‐Deutsch, Ora;
Molho‐Pessach, Vered;
Cohen‐Barak, Eran;
Bach, Gideon;
Garty, Ben Zion;
Bergman, Reuven;
Harel, Avikam;
Nanda, Arti;
Lestringant, Giles G.;
McGrath, John;
Shalev, Stavit

Publication type:

Article

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.

Published in:

Experimental Dermatology, 2020, v. 29, n. 8, p. 742, doi. 10.1111/exd.14140

By:

Mohamad, Janan;
Nanda, Arti;
Pavlovsky, Mor;
Peled, Alon;
Malchin, Natalia;
Malovitski, Kiril;
Pramanik, Rashida;
Weissglas‐Volkov, Daphna;
Shomron, Noam;
McGrath, John;
Sprecher, Eli;
Sarig, Ofer

Publication type:

Article

Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma.

Published in:

British Journal of Dermatology, 2023, v. 189, n. 3, p. 302, doi. 10.1093/bjd/ljad167

By:

Malovitski, Kiril;
Sarig, Ofer;
Feller, Yarden;
Bergson, Shir;
Assaf, Sari;
Mohamad, Janan;
Pavlovsky, Mor;
Giladi, Moshe;
Sprecher, Eli

Publication type:

Article

Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy.

Published in:

British Journal of Dermatology, 2022, v. 187, n. 5, p. 826, doi. 10.1111/bjd.21774

By:

Malovitski, Kiril;
Meijers, Odile;
Cohen‐Barak, Eran;
Bergman, James;
Adir, Noam;
Giladi, Moshe;
Shalev, Stavit;
Sarig, Ofer;
Schwartz, Janice;
Evans, Holly;
Sprecher, Eli;
Samuelov, Liat

Publication type:

Article

A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes.

Published in:

British Journal of Dermatology, 2022, v. 187, n. 5, p. 773, doi. 10.1111/bjd.21766

By:

Mohamad, Janan;
Sarig, Ofer;
Beattie, Paula;
Malovitski, Kiril;
Assaf, Sari;
O'Toole, Edel;
Schwartz, Janice;
Evans, Holly;
Samuelov, Liat;
Sprecher, Eli

Publication type:

Article

Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence*.

Published in:

British Journal of Dermatology, 2022, v. 187, n. 3, p. 392, doi. 10.1111/bjd.21674

By:

Pavlovsky, Mor;
Peled, Alon;
Sarig, Ofer;
Astman, Nadav;
Malki, Liron;
Meijers, Odile;
Assaf, Sari;
Schwartz, Janice;
Malovitski, Kiril;
Hansen, David;
Sprecher, Eli;
Samuelov, Liat

Publication type:

Article

Neonatal inflammatory skin and bowel disease type 1 caused by a complex genetic defect and responsive to combined anti‐tumour necrosis factor‐α and interleukin‐12/23 blockade.

Published in:

British Journal of Dermatology, 2022, v. 186, n. 6, p. 1026, doi. 10.1111/bjd.20978

By:

Samuelov, Liat;
Sarig, Ofer;
Malovitski, Kiril;
Bergson, Shir;
Meijers, Odile;
Shouval, Dror S.;
Sprecher, Eli

Publication type:

Article

Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.

Published in:

Pediatric Dermatology, 2023, v. 40, n. 6, p. 1021, doi. 10.1111/pde.15440

By:

Bergson, Shir;
Daniely, Daniel;
Bomze, David;
Mohamad, Janan;
Malovitski, Kiril;
Meijers, Odile;
Briskin, Valeria;
Bihari, Ofer;
Malchin, Natalia;
Israeli, Shirli;
Mashiah, Jacob;
Falik‐Zaccai, Tzipora;
Avitan‐Hersh, Emily;
Eskin‐Schwartz, Marina;
Allon‐Shalev, Stavit;
Sarig, Ofer;
Sprecher, Eli;
Samuelov, Liat

Publication type:

Article

Epidermolysis bullosa simplex due to bi‐allelic DST mutations: Case series and review of the literature.

Published in:

Pediatric Dermatology, 2021, v. 38, n. 2, p. 436, doi. 10.1111/pde.14477

By:

Ganani, Dalit;
Malovitski, Kiril;
Sarig, Ofer;
Gat, Andrea;
Sprecher, Eli;
Samuelov, Liat

Publication type:

Article

Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2879, doi. 10.1002/ajmg.a.62924

By:

Mohamad, Janan;
Samuelov, Liat;
Assaf, Sari;
Malki, Liron;
Malovitski, Kiril;
Meijers, Odile;
Adir, Noam;
Granot, Ester;
Pavlovsky, Mor;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article

Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09951-x

By:

Assaf, Sari;
Vodo, Dan;
Malovitski, Kiril;
Mohamad, Janan;
Bergson, Shir;
Feller, Yarden;
Malki, Liron;
Sarig, Ofer;
Sprecher, Eli

Publication type:

Article