45 results on '"Cohen‐Barak, Eran"'
Search Results
2. Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene
3. Trends of Diagnosis, Disease Course, and Treatment of Atopic Dermatitis 2012–2021: Real-World Data from a Large Healthcare Provider
4. Homozygote loss-of-function variants in the human COCH gene underlie hearing loss
5. The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome
6. Switching from baricitinib to dupilumab as an advanced‐line treatment in pediatric patients with atopic dermatitis: a retrospective cohort study.
7. Treatment with Methotrexate in Infants and Toddlers with Atopic Dermatitis: A Retrospective Multi-Center Study
8. Translational implications of Th17-skewed inflammation due to genetic deficiency of a cadherin stress sensor
9. Epidermal stratification requires retromer-mediated desmoglein-1 recycling
10. Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy
11. ESDR292 - Heterozygous pathogenic variants affecting the the highly conserved VWFA domain of integrin-β4 cause isolated nail dystrophy
12. Potential di‐genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex
13. A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia
14. Characteristics of Atopic Dermatitis Patients Treated with Crisaborole: Real-World Data from a Large Healthcare Provider Database in Israel
15. A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia.
16. Concomitant variants in NF1 , LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitor
17. Parental mosaic cutaneous‐gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis‐deafness syndrome
18. ESDR175 - Concomitant LZTR1 and NF1 mutations contribute to the diversity of the Neurofibromatosis 1 phenotypic spectrum
19. Acral peeling in Nagashima type palmo‐plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion
20. A homozygous variant in CHMP3is associated with complex hereditary spastic paraplegia
21. Combination therapy of cyclosporine and anti-tumor necrosis factor α in psoriasis: a case series of 10 patients
22. Supplementary Material 1 - Supplemental material for An Update on the Cutaneous Manifestations of Darier Disease
23. Supplementary Material 2 - Supplemental material for An Update on the Cutaneous Manifestations of Darier Disease
24. LEPOARD syndrome: A report of a case with a novel PTPN11 mutation
25. Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population
26. An unusual co-occurrence of Langerhans cell histiocytosis and Rosai–Dorfman disease: report of a case and review of the literature
27. Concomitant variants in NF1, LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitor.
28. An Update on the Cutaneous Manifestations of Darier Disease
29. Th17-skewed inflammation due to genetic deficiency of a cadherin stress sensor
30. Proximity Ligation Assay for Detecting Protein‐Protein Interactions and Protein Modifications in Cells and Tissues in Situ
31. Infantile haemangiomas and quality of life
32. Parental mosaic cutaneous‐gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis‐deafness syndrome.
33. Acral peeling in Nagashima type palmo‐plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion.
34. Homozygote loss-of-function variants in the human COCH gene underlie hearing loss
35. A Nonjunctional, Nonsyndromic Case of Junctional Epidermolysis Bullosa With Renal and Respiratory Involvement
36. Toxic epidermal necrolysis–like dermatomyositis associated with antimelanoma differentiation antigen 5
37. Homozygote loss-of-function variants in the human COCHgene underlie hearing loss
38. Biologic drug survival in Israeli psoriasis patients
39. Kaposi's sarcoma in a patient with pemphigus vulgaris
40. An unusual co-occurrence of Langerhans cell histiocytosis and Rosai-Dorfman disease: report of a case and review of the literature
41. Kaposi's sarcoma in a patient with pemphigus vulgaris.
42. Wells’ Syndrome Induced by Ustekinumab.
43. Desmoglein 4 Mutation Underlies Autosomal Recessive Keratosis Pilaris Atrophicans.
44. Diagnosis, treatment, and long‐term outcomes of pediatric pemphigus: a retrospective study at tertiary medical centers.
45. Toxic epidermal necrolysis-like dermatomyositis associated with antimelanoma differentiation antigen 5.
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