User profiles for Alex Zvulunov
Alex Zvulunov, MD, MHAVerified email at DrZvulunov.com Cited by 3120 |
Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia: world statistical analysis
A Zvulunov, Y Barak, A Metzker - Archives of dermatology, 1995 - jamanetwork.com
Background and Design: The concurrent finding of neurofibromatosis type 1 (NF), juvenile
chronic myelogenous leukemia (JCML), and juvenile xanthogranuloma (JXG) has been …
chronic myelogenous leukemia (JCML), and juvenile xanthogranuloma (JXG) has been …
[HTML][HTML] Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase
…, M Pasmanik-Chor, M Indelman, A Zvulunov… - The American Journal of …, 2007 - cell.com
In this article, we describe a novel autosomal recessive ichthyosis with hypotrichosis
syndrome, characterized by congenital ichthyosis associated with abnormal hair. Using …
syndrome, characterized by congenital ichthyosis associated with abnormal hair. Using …
Bullous pemphigoid in infancy: clinical and epidemiologic characteristics
…, D Mimouni, A Adir-Shani, M Zlotkin, A Zvulunov - Journal of the American …, 2008 - Elsevier
BACKGROUND: Recent cases of infants with bullous pemphigoid (BP) prompted us to explore
the clinical and laboratory features of childhood BP. OBJECTIVES: We sought to explore …
the clinical and laboratory features of childhood BP. OBJECTIVES: We sought to explore …
Oral propranolol therapy for infantile hemangiomas beyond the proliferation phase: a multicenter retrospective study
A Zvulunov, C McCuaig, IJ Frieden… - Pediatric …, 2011 - Wiley Online Library
Pharmacological therapies for infantile hemangiomas were considered effective only during
the proliferative phases. Recently reported beneficial effects of propranolol may extend …
the proliferative phases. Recently reported beneficial effects of propranolol may extend …
[PDF][PDF] Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease
…, I Conte, I Maystadt, S Demuth, A Zvulunov… - The American Journal of …, 2012 - cell.com
Microphthalmia with linear skin lesions (MLS) is an X-linked dominant male-lethal disorder
associated with mutations in holocytochrome c-type synthase (HCCS), which encodes a …
associated with mutations in holocytochrome c-type synthase (HCCS), which encodes a …
[PDF][PDF] Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion
…, S Rajpopat, J Fischer, V Oji, A Zvulunov… - The American Journal of …, 2011 - cell.com
Autosomal-recessive exfoliative ichthyosis presents shortly after birth as dry, scaly skin over
most of the body with coarse peeling of nonerythematous skin on the palms and soles, …
most of the body with coarse peeling of nonerythematous skin on the palms and soles, …
Juvenile mycosis fungoides: cutaneous T-cell lymphoma with frequent follicular involvement
…, B Davidovici, M David, A Zvulunov… - Journal of the American …, 2014 - Elsevier
Background The literature on mycosis fungoides (MF) in children/adolescents is sparse.
Objective We sought to evaluate the characteristics of juvenile MF in a large cohort. Methods …
Objective We sought to evaluate the characteristics of juvenile MF in a large cohort. Methods …
Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein
RY Birnbaum, A Zvulunov, D Hallel-Halevy… - Nature …, 2006 - nature.com
We describe an Israeli Jewish Moroccan family presenting with autosomal dominant seborrhea-like
dermatosis with psoriasiform elements, including enhanced keratinocyte proliferation…
dermatosis with psoriasiform elements, including enhanced keratinocyte proliferation…
Thiamine deficiency in infancy: long-term follow-up
…, A Brezner, E Heyman, D Inbar, S Kivity, A Zvulunov… - Pediatric …, 2014 - Elsevier
Background In 2003, several hundred Israeli infants risked thiamine deficiency after being
fed a soy-based formula deficient in thiamine. Approximately 20 patients were seriously …
fed a soy-based formula deficient in thiamine. Approximately 20 patients were seriously …
Childhood lichen planus pemphigoides: a case report and review of the literature
…, D Ben‐Amitai, M Feinmesser, A Zvulunov - Pediatric …, 2009 - Wiley Online Library
Lichen planus pemphigoides is a rare autoimmune blistering disease that is characterized
by evolution of vesico‐bullous skin lesions in patients with active lichen planus. We describe …
by evolution of vesico‐bullous skin lesions in patients with active lichen planus. We describe …