Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Alex, Zvulunov"'
Publikováno v:
JMIR Dermatology, Vol 6, p e49278 (2023)
BackgroundInadequate control of atopic dermatitis (AD) increases the frequency of exacerbations and reduces the quality of life. Mobile health apps provide information and communication technology and may increase treatment adherence and facilitate d
Externí odkaz:
https://doaj.org/article/e653ae09fcb54b3f820c129b7dfed894
Publikováno v:
Pediatric endocrinology reviews : PER [Pediatr Endocrinol Rev] 2015 Sep; Vol. 13 (1), pp. 477-8.
Publikováno v:
Pediatric endocrinology reviews : PER. 13(1)
Akademický článek
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Autor:
Ayelet Ollech, Michal Solomon, Amir Horev, Shiran Reiss-Huss, Dan Ben-Amitai, Alex Zvulunov, Rivka Friedland, Vered Atar-Snir, Vered Pessach-Molcho, Aviv Barzilai, Shoshana Greenberger
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 18, p adv00322 (2020)
Cutaneous leishmaniasis poses a therapeutic challenge in the paediatric population. The aim of this study was to assess the efficacy and safety of miltefosine treatment for Old World cutaneous leishmaniasis in paediatric patients. A multicentre retro
Externí odkaz:
https://doaj.org/article/7d1f196d6fb642099ee9404c3ab4e317
Akademický článek
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Publikováno v:
Pediatric dermatologyREFERENCES. 37(5)
Background/objectives Lichen sclerosus is a rare, pruritic, mucocutaneous disease affecting mostly the anogenital area. Reports have occasionally associated lichen sclerosus with overlapping vascular lesions. This study explores this association in c
Publikováno v:
Dermatology Research and Practice, Vol 2012 (2012)
Externí odkaz:
https://doaj.org/article/f90508389a604e4fad135275cd4bf3a6
Autor:
Ibrahim, Alatawneh, Alex, Zvulunov
Publikováno v:
Harefuah. 159(1)
Neutrophilic dermatosis of the hands (NDH) is a rare localized variant of Sweet's syndrome occurring predominantly over dorsa of hands. Both Sweet's syndrome and its dorsal hand variant have been reported in association with malignancies, inflammator
Autor:
Raed Khoury, Yael Barhum, Rachel Straussberg, Yuval Yogev, Ohad S. Birk, Ruijuan Xu, Alex Zvulunov, Izolda Mileva, Cungui Mao, Vadim Dolgin, Osnat Konen
Publikováno v:
Eur J Hum Genet
Sphingolipidoses are monogenic lipid storage diseases caused by variants in enzymes of lipid synthesis and metabolism. We describe an autosomal recessive complex neurological disorder affecting consanguineous kindred. All four affected individuals, b