Nd:YAG 1064-nm laser for residual infantile hemangioma after propranolol treatment von Khamaysi, Z., Pam, N., Zaaroura, H., Avitan-Hersh, E.

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Evaluation of combined treatment with Er:YAG laser and long‐pulsed Nd:YAG laser for the treatment of recalcitrant warts: A prospective randomized controlled trial von Jiryis, B., Avitan‐Hersh, E., Mirmovich, O., Judith Nevet, M., Khamaysi, Z.

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Happle-Tinschert syndrome can be caused by a mosaic SMO mutation and is suggested to be a variant of Curry-Jones syndrome: reply from the authors von Khamaysi, Z., Sprecher, E., Bergman, R.

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Segmental basal cell naevus syndrome caused by an activating mutation in smoothened von Khamaysi, Z., Bochner, R., Indelman, M., Magal, L., Avitan‐Hersh, E., Sarig, O., Sprecher, E., Bergman, R.

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Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype von Vodo, D., Sarig, O., Jeddah, D., Malchin, N., Eskin‐Schwarz, M., Mohamad, J., Rabinowitz, T., Goldberg, I., Shomron, N., Khamaysi, Z., Bergman, R., Sprecher, E.

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Galli-Galli disease is an acantholytic variant of Dowling-Degos disease von Sprecher, E., Indelman, M., Khamaysi, Z., Lugassy, J., Petronius, D., Bergman, R.

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Pleomorphic CD8+ small/medium size cutaneous T-cell lymphoma von KHAMAYSI, Z, BEN-ARIEH, Y, EPELBAUM, R, BERGMAN, R

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Nail dystrophy in focal acral hyperkeratosis: a distinctive feature? von Khamaysi, Z, Bergman, R, Sprecher, E

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Familial palmoplantar keratoderma: not always hereditary von Khamaysi, Z, Indelman, M, Bergman, R, Sprecher, E

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Mutations in GALNT3 , encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis von Sprecher, Eli, Topaz, Orit, Shurman, Daniel L, Bergman, Reuven, Indelman, Margarita, Ratajczak, Paulina, Mizrachi, Mordechai, Khamaysi, Ziad, Behar, Doron, Petronius, Dan, Friedman, Vered, Zelikovic, Israel, Raimer, Sharon, Metzker, Arieh, Richard, Gabriele

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Insect bite-like reaction associated with mantle cell lymphoma : Clinicopathological, immunopathological, and molecular studies von KHAMAYSI, Z, DODIUK-GAD, R. P, WELTFRIEND, S, BEN-ARIEH, Y, DANN, E. J, SAHAR, D, BERGMAN, R

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Reply von Khamaysi, Z., Bergman, R., Weltfriend, S.

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Reply von Khamaysi, Z., Bergman, R., Weltfriend, S.

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Cutaneous Lymphoid Hyperplasia Presenting as a Solitary Facial Nodule: Clinical, Histopathological, Immunophenotypical, and Molecular Studies von Bergman, Reuven, Khamaysi, Ziad, Sahar, Dvora, Ben-Arieh, Yeudith

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Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype von Vodo, D, Sarig, O, Jeddah, D, Malchin, N, Eskin-Schwarz, M, Mohamad, J, Rabinowitz, T, Goldberg, I, Shomron, N, Khamaysi, Z, Bergman, R, Sprecher, E

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Segmental basal cell naevus syndrome caused by an activating mutation in smoothened von Khamaysi, Z, Bochner, R, Indelman, M, Magal, L, Avitan-Hersh, E, Sarig, O, Sprecher, E, Bergman, R

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Segmental basal cell naevus syndrome caused by an activating mutation in smoothened von Khamaysi, Z., Bochner, R., Indelman, M., Magal, L., Avitan-Hersh, E., Sarig, O., Sprecher, E., Bergman, R.

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Nail dystrophy in focal acral hyperkeratosis: a distinctive feature? von Khamaysi, Z, Bergman, R, Sprecher, E

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Familial palmoplantar keratoderma: not always hereditary von Khamaysi, Z, Indelman, M, Bergman, R, Sprecher, E

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The Role of Heparanase in the Pathogenesis of Acute Pancreatitis: A Potential Therapeutic Target von Khamaysi, Iyad, Singh, Preeti, Nasser, Susan, Awad, Hoda, Chowers, Yehuda, Sabo, Edmond, Hammond, Edward, Gralnek, Ian, Minkov, Irena, Noseda, Alessandro, Ilan, Neta, Vlodavsky, Israel, Abassi, Zaid

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