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Веред Мольхо-Песах

 Доктор Веред Мольхо-Песах - специалист в области детской дерматологии

Отделение: Педиатрия, Дерматология
Должность: Дерматолог, педиатр
Языки: Английский, Иврит
Принимает: детей и взрослых
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 Доктор Веред Мольхо-Песах - специалист в области детской дерматологии

Образование

Выпускница медицинского факультета Еврейского факультета в Иерусалиме (2000 г.)

Специализация

Дерматолог, специалист в области детской дерматологии.

Профессиональная деятельность

Врач отделения дерматологии, клиника “Хадасса Эйн-Керем”.

Научные публикации

Real-world efficacy and safety of dupilumab for paediatric atopic dermatitis: a multicentre retrospective study
IL-7-dependent and -independent lineages of IL-7R-dependent human T cells
A case of congenital pili multigemini
Phototherapy for the treatment of cutaneous graft-versus-host disease: A systematic review
Characterization of Paediatric Prurigo Nodularis: A Multicentre Retrospective, Observational Study
Management of Atopy with Dupilumab and Omalizumab in CADINS Disease
Sclerotic-Type Cutaneous Chronic Graft-Versus-Host Disease Exhibits Activation of T Helper 1 and OX40 Cytokines
Topical phage therapy in a mouse model of Cutibacterium acnes-induced acne-like lesions
Retraction Notice to "Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation"
Infantile anogenital digitate keratoses: A case series of a novel entity
Acrofacial necrotic ulcers in an infant: An undiagnosed presentation
Dominant-negative signal transducer and activator of transcription (STAT)3 variants in adult patients: A single center experience
Giant congenital melanocytic naevus with a novel CUX1-BRAF fusion mutation treated with trametinib
Tumor necrosis factor-α inhibitor-induced follicular psoriasiform eruption
LGR5 expressing skin fibroblasts define a major cellular hub perturbed in scleroderma
RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1
Acral peeling skin syndrome resulting from a novel homozygous mutation in the CSTA gene-A report of two cases
Dupilumab-induced ocular surface disease: A systematic review
Cutaneous Adverse Events to Targeted Therapies and Immuno-therapies in Children: A Retrospective Study of 103 Patients from Two Tertiary Haemato-Oncology Referral Centres
Chronic demodicosis in patients with immune dysregulation: An unexpected infectious manifestation of Signal transducer and activator of transcription (STAT)1 gain-of-function
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population
Multiple Nasal Papules in a 12-year-old Boy: A Quiz
Dupilumab for pediatric prurigo nodularis: A case report
Cutaneous Leishmaniasis Treated with Miltefosine: A Case Series of 10 Paediatric Patients
Antibiotic Susceptibility of Cutibacterium acnes Strains Isolated from Israeli Acne Patients
Poststreptococcal Pustulosis
Introductory histopathological findings may shed light on COVID-19 paediatric hyperinflammatory shock syndrome
Subcutaneous granuloma annulare mimicking dermatomyositis
Exogenous interleukin-2 can rescue in-vitro T cell activation and proliferation in patients with a novel capping protein regulator and myosin 1 linker 2 mutation
The molluscum contagiosum BOTE sign-Infected or inflamed?
EFFECTIVE TREATMENT FOR BULLOUS PEMPHIGOID WITH OMALIZUMAB
Skin toxicity following treosulfan-thiotepa-fludarabine-based conditioning regimen in non-malignant pediatric patients undergoing hematopoietic stem cell transplantation
STAT1 gain-of-function and chronic demodicosis
Oral and Topical Sirolimus for Vascular Anomalies: A Multicentre Study and Review
Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
Ulcers and Scars on the Trunk of a 20-month-old Boy: A Quiz
Intralesional sodium stibogluconate under inhaled anesthesia for the treatment of cutaneous leishmaniasis in children: A retrospective cohort
Man With Persistent Rash
T+ NK+ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency
Cutaneous Chronic Graft Versus Host Disease Following Allogeneic Haematopoietic Stem Cell Transplantation in Children: A Retrospective Study
Coexistence of Two Rare Autosomal Recessive Disorders: Activation-Induced Cytidine Deaminase Deficiency and Sjogren-Larsson Syndrome
RETRACTED: Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation
Atopic Dermatitis in Israeli Adolescents from 1998 to 2013: Trends in Time and Association with Migraine
Secukinumab for the Treatment of Deficiency of Interleukin 36 Receptor Antagonist in an Adolescent
Tocilizumab Promotes Regulatory T-cell Alleviation in STAT3 Gain-of-function-associated Multi-organ Autoimmune Syndrome
Paediatric Erythema Multiforme: Epidemiological, Clinical and Laboratory Characteristics
Cytokine secretion and NK cell activity in human ADAM17 deficiency
Coxsackievirus A6 Polymorphic Exanthem in Israeli Children
Lymphatic Dissemination in Cutaneous Leishmaniasis Following Local Treatment
H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis
Generalized verrucosis and HPV-3 susceptibility associated with CD4 T-cell lymphopenia caused by inherited human interleukin-7 deficiency
Two Novel Homozygous Desmoplakin Mutations in Carvajal Syndrome
Abortive haemangioma in PHACE(S) syndrome
H syndrome--four new patients from India
IL36RN mutation causing generalized pustular psoriasis in a Palestinian patient
Alopecia areata and down syndrome: a true association or a coincidence
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair
Ophthalmologic Findings in H Syndrome: A Unique Diagnostic Clue
H syndrome: the first 79 patients
The spectrum of radiological findings in H syndrome
Agenesis of the inferior vena cava in H syndrome due to a novel SLC29A3 mutation
Palisaded neutrophilic and granulomatous dermatitis in an adolescent girl with perinuclear antineutrophil cytoplasmic antibody-positive pauci-immune glomerulonephritis and arthritis
Accelerated coronary atherosclerosis and H syndrome
Emperipolesis: an additional common histopathologic finding in H syndrome and Rosai-Dorfman disease
Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology
Blaschko lines and other patterns of cutaneous mosaicism
Conradi-Hünermann-Happle syndrome
H syndrome: novel and recurrent mutations in SLC29A3
Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases
Diabetes mellitus may be the earliest and sole manifestation of the H syndrome
The H syndrome: two novel mutations affecting the same amino acid residue of hENT3
H syndrome and Muckle-Wells syndrome
The H syndrome is caused by mutations in the nucleoside transporter hENT3
The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations
Evidence for clinical and genetic heterogeneity in hereditary benign telangiectasia
Viral carcinogenesis in skin cancer
Ultraviolet radiation and cutaneous carcinogenesis
Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new case and a novel mutation
A novel splice-site mutation in ECM-1 gene in a consanguineous family with lipoid proteinosis
An atypical presentation of lymphomatoid papulosis
Homozygous splice site mutations in PKP1 result in loss of epidermal plakophilin 1 expression and underlie ectodermal dysplasia/skin fragility syndrome in two consanguineous families
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