Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Nordau Kanigsberg"'
Autor:
Elena Pastukhova, Nordau Kanigsberg
Publikováno v:
SAGE Open Medical Case Reports, Vol 11 (2023)
Milia are common in children. They are small, keratinizing cysts that arise either as primary epidermoid cysts or secondary to other dermatoses, trauma or certain medications. In the paediatric population, milia are most frequently congenital and res
Externí odkaz:
https://doaj.org/article/b75bff6a2a764a1a84ba9d2e25151737
Autor:
Amanda J Shelley, Nordau Kanigsberg
Publikováno v:
SAGE Open Medical Case Reports, Vol 6 (2018)
Rosai-Dorfman disease (RDD) is a rare histiocytic condition of unknown etiology. Patients with RDD classically present with massive painless cervical lymphadenopathy. However, extra-nodal disease occurs in approximately 40% of cases, with the skin be
Externí odkaz:
https://doaj.org/article/2ff7e74e80ca4c7a965efacc64b5389f
Publikováno v:
SAGE Open Medical Case Reports, Vol 6 (2018)
Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca 2+ -ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found
Externí odkaz:
https://doaj.org/article/07d00e4e33d94f939ffa79a96e0a2698
Autor:
Alison M. R. Castle, Michele L. Ramien, Nordau Kanigsberg, Dina El Demellawy, Jean McGowan‐Jordan, Melanie Beaulieu Bergeron, Christine M. Armour
Publikováno v:
Pediatric Dermatology. 39:107-111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44411486c43d92697eac054e1e345840
https://doi.org/10.1111/pde.14850
https://doi.org/10.1111/pde.14850
Publikováno v:
Dermatologic therapyREFERENCES. 34(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b79893a2b2af833bf9ee1c7e613a5ffb
https://pubmed.ncbi.nlm.nih.gov/34053172
https://pubmed.ncbi.nlm.nih.gov/34053172
Autor:
Beth A. Drolet, Nordau Kanigsberg, Cathryn Sibbald, Carmen Liy-Wong, Irene Lara-Corrales, Jin Ma, Elena Pope
Publikováno v:
JAMA Pediatrics. 176:34
Importance Propranolol for infantile hemangiomas (IH) has been shown to be effective and relatively safe. However, other less lipophilic β-blockers, such as nadolol, may be preferable in individuals who experience propranolol unresponsiveness or adv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d884eede05907334fbeb1b4b66cff66
https://doi.org/10.1001/jamapediatrics.2021.4565
https://doi.org/10.1001/jamapediatrics.2021.4565
Publikováno v:
Pediatric Dermatology. 35:e286-e290
The mTOR inhibitor rapamycin is used systemically for the treatment of vascular lesions. We report the first use of topical rapamycin for the successful treatment of two cases of tufted angioma. The evidence for the use of topical rapamycin in other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db330834a160eaf1636900b41ea912ac
https://doi.org/10.1111/pde.13596
https://doi.org/10.1111/pde.13596
Publikováno v:
Journal of Cutaneous Medicine and Surgery. 21:553-555
Fingolimod is an immune-modulating drug used in the treatment of multiple sclerosis. Histoplasma capsulatum is a dimorphic fungus that can infect humans. Infection with the pathogen typically affects the lungs, but it is usually asymptomatic and self
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de5a10caa36520057d6be579c91b2e0f
https://doi.org/10.1177/1203475417719043
https://doi.org/10.1177/1203475417719043
Publikováno v:
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports, Vol 6 (2018)
SAGE Open Medical Case Reports, Vol 6 (2018)
Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca2+-ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a41282ca0dad77a1264c926f58d4ec32
http://europepmc.org/articles/PMC6134490
http://europepmc.org/articles/PMC6134490
Autor:
Nordau Kanigsberg, Amanda J. Shelley
Publikováno v:
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports, Vol 6 (2018)
SAGE Open Medical Case Reports, Vol 6 (2018)
Rosai-Dorfman disease (RDD) is a rare histiocytic condition of unknown etiology. Patients with RDD classically present with massive painless cervical lymphadenopathy. However, extra-nodal disease occurs in approximately 40% of cases, with the skin be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdb73fbbb3a615708297fed43159cf95
http://europepmc.org/articles/PMC5968663
http://europepmc.org/articles/PMC5968663