Liat Samuelov

19PUBLICATIONS
30CO-AUTHORS
Neurology and neuromuscular diseasesGenetic immunologyEpidemiological modellingNeonatologyAllergy
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Publications (19)

|Nov 24, 2022
Ustekinumab therapy for Netherton syndrome.

Liat Samuelov, Waseem Shehadeh, Ofer Sarig

|Aug 03, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1.

Janan Mohamad, Liat Samuelov, Sari Assaf

|Jul 13, 2022
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy.

Kiril Malovitski, Odile Meijers, Eran Cohen-Barak

|Jun 09, 2022
Real-life experience of upadacitinib for the treatment of adult patients with moderate-to-severe atopic dermatitis - a case series.

G Feraru, M J Nevet, L Samuelov

|Jan 07, 2022
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.

Liat Samuelov, Ofer Sarig, Kiril Malovitski

|Nov 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasis.

Liat Samuelov, Ron Bochner, Lee Magal

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Frequent Collaborators

10 joint publications

Eli Sprecher

9 joint publications

Ofer Sarig

3 joint publications

Janan Mohamad

3 joint publications

Sari Assaf