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Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin.
Auer-Grumbach M, Weger M, Fink-Puches R, Papić L, Fröhlich E, Auer-Grumbach P, El Shabrawi-Caelen L, Schabhüttl M, Windpassinger C, Senderek J, Budka H, Trajanoski S, Janecke AR, Haas A, Metze D, Pieber TR, Guelly C. Auer-Grumbach M, et al. Brain. 2011 Jun;134(Pt 6):1839-52. doi: 10.1093/brain/awr076. Epub 2011 May 15. Brain. 2011. PMID: 21576112 Free PMC article.
Generalized exfoliative erythroderma since birth. Netherton syndrome.
El Shabrawi-Caelen L, Smolle J, Metze D, Ginter-Hanselmayer G, Raghunath M, Traupe H, Kerl H. El Shabrawi-Caelen L, et al. Arch Dermatol. 2004 Oct;140(10):1275-80. doi: 10.1001/archderm.140.10.1275-a. Arch Dermatol. 2004. PMID: 15492197 No abstract available.
Schmerzhafte hämorrhagische Bullae an den Handrücken.
Deinlein T, Cerroni L, El-Shabrawi-Caelen L, Gruber M, Fink-Puches R. Deinlein T, et al. Among authors: el shabrawi caelen l. J Dtsch Dermatol Ges. 2018 Sep;16(9):1152-1154. doi: 10.1111/ddg.13625_g. J Dtsch Dermatol Ges. 2018. PMID: 30179324 No abstract available.
Alopecia universalis associated with cutaneous T cell lymphoma.
Miteva M, El Shabrawi-Caelen L, Fink-Puches R, Beham-Schmid C, Romanelli P, Kerdel F, Tosti A. Miteva M, et al. Dermatology. 2014;229(2):65-9. doi: 10.1159/000360759. Epub 2014 May 6. Dermatology. 2014. PMID: 24821490
Frontal hair loss and facial skin changes.
Wutte N, El-Shabrawi-Caelen L. Wutte N, et al. J Dtsch Dermatol Ges. 2015 Oct;13(10):1040-3. doi: 10.1111/ddg.12700. J Dtsch Dermatol Ges. 2015. PMID: 26408478 No abstract available.
Basal cell carcinoma with a bonus.
Fried I, Pincus LB, North J, El-Shabrawi-Caelen L. Fried I, et al. J Cutan Pathol. 2011 Mar;38(3):261-3. doi: 10.1111/j.1600-0560.2010.01658_2.x. J Cutan Pathol. 2011. PMID: 21244461 No abstract available.
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.
Basmanav FB, Oprisoreanu AM, Pasternack SM, Thiele H, Fritz G, Wenzel J, Größer L, Wehner M, Wolf S, Fagerberg C, Bygum A, Altmüller J, Rütten A, Parmentier L, El Shabrawi-Caelen L, Hafner C, Nürnberg P, Kruse R, Schoch S, Hanneken S, Betz RC. Basmanav FB, et al. Am J Hum Genet. 2014 Jan 2;94(1):135-43. doi: 10.1016/j.ajhg.2013.12.003. Am J Hum Genet. 2014. PMID: 24387993 Free PMC article.
54 results