Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Zahraa Chayed"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is a rare genodermatosis characterized by cutaneous leiomyoma (CLM), uterine leiomyoma (ULM) and renal cell carcinoma (RCC). Five HLRCC patients are presented with a compi
Externí odkaz:
https://doaj.org/article/0298ad6359c747c3a916163b3187f695
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Orphanet Journal of Rare Diseases
Chayed, Z, Kristensen, L K, Ousager, L B, Rønlund, K & Bygum, A 2021, ' Hereditary leiomyomatosis and renal cell carcinoma : a case series and literature review ', Orphanet Journal of Rare Diseases, vol. 16, 34 . https://doi.org/10.1186/s13023-020-01653-9
Orphanet Journal of Rare Diseases
Chayed, Z, Kristensen, L K, Ousager, L B, Rønlund, K & Bygum, A 2021, ' Hereditary leiomyomatosis and renal cell carcinoma : a case series and literature review ', Orphanet Journal of Rare Diseases, vol. 16, 34 . https://doi.org/10.1186/s13023-020-01653-9
Background Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is a rare genodermatosis characterized by cutaneous leiomyoma (CLM), uterine leiomyoma (ULM) and renal cell carcinoma (RCC). Five HLRCC patients are presented with a compiled datab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34ea8efecfa81cf7f7a1138360b26363
https://doaj.org/article/0298ad6359c747c3a916163b3187f695
https://doaj.org/article/0298ad6359c747c3a916163b3187f695
Publikováno v:
Ugeskrift for laeger. 182(21)
In this review, we discuss pigmented purpuric dermatoses (PPD), which are a group of benign, chronic diseases characterised by purpuric eruption. PPD comprise mb. Schamberg, mb. Majocchi, Gougerot-Blum, lichen aureus, and Doucas and Kapetanakis eczem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e1ca0477043ec49167cff6f640e1d8b7
https://pubmed.ncbi.nlm.nih.gov/32515323
https://pubmed.ncbi.nlm.nih.gov/32515323
Autor:
Chayed, Zahraa1 (AUTHOR) zacha15@student.sdu.dk, Kristensen, Lone Krøldrup2 (AUTHOR), Ousager, Lilian Bomme2 (AUTHOR), Rønlund, Karina3 (AUTHOR), Bygum, Anette4 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 1/18/2021, Vol. 16 Issue 1, p1-9. 9p.
Publikováno v:
Medical Devices & Surgical Technology Week; 9/20/2024, p2148-2148, 1p