Zobrazeno 1 - 6
of 6
pro vyhledávání: '"W. Afthab Jameela"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 4, Pp WC01-WC06 (2017)
Introduction: Pemphigus, an autoimmune disease, was fatal before the era of corticosteroids. With the advent of steroids, mortality decreased but morbidity was present due to the side effects of high dose steroids. Newer drugs targeted at the mol
Externí odkaz:
https://doaj.org/article/37ff5470125d43de959e49fce6020824
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 10, Pp WC06-WC09 (2016)
Introduction: Trophic ulcers secondary to leprosy pose a great stigma to the patients and remain a challenge to the treating dermatologists. The discovery of Platelet Rich Plasma (PRP) with its favourable role in wound healing is a boon for the p
Externí odkaz:
https://doaj.org/article/c82bea1bf7ab4c45b2ada83621cff00a
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 3, Pp WD01-WD02 (2016)
Dyschromatosis Universalis Hereditaria (DUH) belongs to a group of congenital diffuse reticulate pigmentary disorders characterised by both hypo and hyper pigmented macules. It is both hereditary and sporadic. A number of associated cutaneous and sy
Externí odkaz:
https://doaj.org/article/a8500033ecbd4146907ae08a77218fcd
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 4, Pp WC01-WC06 (2017)
Introduction Pemphigus, an autoimmune disease, was fatal before the era of corticosteroids. With the advent of steroids, mortality decreased but morbidity was present due to the side effects of high dose steroids. Newer drugs targeted at the molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdb83fdff435d672293b486f5b3b49fb
https://doi.org/10.7860/jcdr/2017/21868.9717
https://doi.org/10.7860/jcdr/2017/21868.9717
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 3, Pp WD01-WD02 (2016)
Dyschromatosis Universalis Hereditaria (DUH) belongs to a group of congenital diffuse reticulate pigmentary disorders characterised by both hypo and hyper pigmented macules. It is both hereditary and sporadic. A number of associated cutaneous and sys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb28dae05474ea2bcb25e152aac069c1
https://europepmc.org/articles/PMC4843368/
https://europepmc.org/articles/PMC4843368/
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