Kiril Malovitski
5PUBLICATIONS
48CO-AUTHORS
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Publications (5)
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|Jan 14, 2026
Defective Function of Inhibitor of κB Kinase Subunit Beta Associated With Multiple Immune-Mediated Disorders.Kiril Malovitski, Noy Keller Rosenthal, Lubna Khair
|Feb 20, 2025
HMCN1 variants aggravate epidermolysis bullosa simplex phenotype.Shir Bergson, Ofer Sarig, Moshe Giladi
|Aug 03, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.Janan Mohamad, Liat Samuelov, Sari Assaf
|Mar 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population.Janan Mohamad, Liat Samuelov, Natalia Malchin
|Jul 04, 2020
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.Janan Mohamad, Arti Nanda, Mor Pavlovsky
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Frequent Collaborators
5 joint publications
Eli Sprecher
4 joint publications
Janan Mohamad
4 joint publications
Ofer Sarig
3 joint publications
Sari Assaf
2 joint publications
Arti Nanda
2 joint publications
Mor Pavlovsky
2 joint publications
Alon Peled
2 joint publications
Natalia Malchin
2 joint publications
Noam Shomron
2 joint publications
Liat Samuelov
