Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Neveen S Seifeldin"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 189-193 (2015)
We report a 2.5 year old male, first in order of birth of first cousin consanguineous parents with the typical features of Berardinelli–Seip congenital lipodystrophy 2 (BSCL2) since birth with moderate mental retardation. He had generalized lipodys
Externí odkaz:
https://doaj.org/article/12f33885b6274e13a0852b1d0f1dff19
Publikováno v:
Advances in Dermatology and Allergology/Postȩpy Dermatologii i Alergologii
Introduction Inherited ichthyoses are caused by mutations in various genes important for keratinocyte differentiation and epidermal barrier function. Although ichthyoses are rare disorders, they require costly long-term medical management, and thus t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd33519abcc93208ef82bfc34313a019
https://doi.org/10.5114/ada.2018.75238
https://doi.org/10.5114/ada.2018.75238
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 189-193 (2015)
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 189-193
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 189-193
We report a 2.5 year old male, first in order of birth of first cousin consanguineous parents with the typical features of Berardinelli–Seip congenital lipodystrophy 2 (BSCL2) since birth with moderate mental retardation. He had generalized lipodys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec5f5d354f614a46e0b4717e9e76966
https://doi.org/10.1016/j.ejmhg.2014.08.004
https://doi.org/10.1016/j.ejmhg.2014.08.004
Publikováno v:
Egyptian Journal of Medical Human Genetics. 13(2):227-231
A female, 26 months old with features supporting the diagnosis of neonatal progeroid syndrome was presented. She had prenatal and postnatal growth failure, generalized lipoatrophy except for fat pads in the suprabuttock areas, triangular face, pseudo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec5b092b94f743e150b65b21d846dd8f
Publikováno v:
Egyptian Journal of Medical Human Genetics. 13(2):233-237
Rubinstein-Taybi Syndrome (RTS) is a multiple congenital anomaly syndrome characterized by mental retardation, broad thumbs and toes, short stature, growth retardation and distinctive facial features. We report an Egyptian patient, 5 months old with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c60e0e3850ffd030675914c851ce840e
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 13, No 1 (2012); 45-62
As clinical geneticists, we recently reviewed our 43years experience in an attempt to represent the frequency of genetic disorders in the Division of Genetics at Pediatric Hospital, Faculty of Medicine, Ain-Shams University, Cairo, Egypt, during the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5ca19bca4354e4b741488c913c8d0c
Autor:
Neveen S. Seifeldin, Heba M. Diab, Marwa Zaki, Salwa Teama, Saleh A. K. Saleh, Nasser A. Elhawary
Publikováno v:
The Open Andrology Journal. 2:11-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fab72c52bd177aaf4e36aa8fafd0505a
https://doi.org/10.2174/1876827x01002010011
https://doi.org/10.2174/1876827x01002010011
Autor:
Neveen S. Seifeldin, Rabah M. Shawky
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 16, No 4 (2015); 287-290
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 4, Pp 287-290 (2015)
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 4, Pp 287-290 (2015)
Antihistamines are a group of medications which can inhibit various histaminic actions at one of two histamine receptors (H1 or H2). H1 receptor antagonists are used for the relief of allergic dermatological and nondermatological conditions. We will
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e8dbb77f96a5c8d52204f234d8b792e
https://www.ajol.info/index.php/ejhg/article/view/124765
https://www.ajol.info/index.php/ejhg/article/view/124765
Publikováno v:
International journal of dermatology. 55(11)
Background Increasing evidence has shown that serum microRNA (miR) levels are useful biomarkers for the diagnosis, prognosis, and therapeutic value in various diseases. Psoriasis is characterized by a specific miR expression profile, with a character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95cfd919fd399347e659c581edb23bd5
https://pubmed.ncbi.nlm.nih.gov/27371164
https://pubmed.ncbi.nlm.nih.gov/27371164
Publikováno v:
International journal of dermatology. 54(10)
Background LIGHT (the name of which is derived from “homologous to lymphotoxins, exhibits inducible expression, competes with herpes simplex virus glycoprotein D for herpes simplex virus entry mediator, and expressed by T lymphocytes”), is a memb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3006d89075a60ee813d64a08e27e27
https://pubmed.ncbi.nlm.nih.gov/26043794
https://pubmed.ncbi.nlm.nih.gov/26043794