Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Shah Parvaiz"'
Publikováno v:
Indian Journal of Dermatology, Vol 55, Iss 4, Pp 355-358 (2010)
Background: Systemic sclerosis is a multisystemic autoimmune disorder. Intravenous dexamethasone pulse therapy has been used since 1998. Aim: The aim was to report the beneficial effects of dexamethasone pulse in patients of systemic sclerosis vis-á
Externí odkaz:
https://doaj.org/article/a9deb14bd04a47f0928ce1afa4cae77c
Autor:
Hassan Iffat, Mashkoor Ahmed, Hayat Bhat Mohammad, Manaan Qazi, Shah Parvaiz Ahmad, Masood Qazi
Publikováno v:
Nasza Dermatologia Online, Vol 1, Iss 2, Pp 19-21 (2010)
Chronic mucocutaneous candidiasis(CMC) is a rare group of overlapping syndromes that have in common a clinical pattern of persistent and diffuse cutaneous or mucosal candidal infections. It is usually associated with multiple endocrine dysfunctions a
Externí odkaz:
https://doaj.org/article/b19d354673e64d29a54974e20d60228d
Publikováno v:
Indian Journal of Dermatology, Vol 47, Iss 3, Pp 156-158 (2002)
Serum lipid profile was evaluated in twenty leprosy patients (paucibacillary and multibacillary cases) and twenty age and sex matched healthy controls. The serum lipid profile of the two groups showed no statistically significant difference.
Externí odkaz:
https://doaj.org/article/930f958196c4437b84a2f8de38ee9ffb
Publikováno v:
Indian Journal of Dermatology, Vol 47, Iss 3, Pp 171-172 (2002)
Monilethrix is a rare heritable disorder characterized by a structural defect of the hair with increased fragility. We here by report a case of monilethrix in a nine year old male child in view of the rarity of this condition.
Externí odkaz:
https://doaj.org/article/850c92e263894b0ea0618aa34957e3e7
Autor:
Hassan Iffat, Shah Parvaiz
Publikováno v:
Indian Journal of Dermatology, Vol 45, Iss 3, Pp 143-144 (2000)
A 40 year old male developed pigmented patches on both legs for last 4 months. These non blaching lesions with telangiectses at the periphery were mostly annular in shape but a few were arciform. Some lesions showed central atrophy. History and syste
Externí odkaz:
https://doaj.org/article/5a90bb04323048529873d88f3ed1d751
Publikováno v:
Indian Journal of Dermatology, Vol 43, Iss 2, Pp 86-87 (1998)
Papillion Lefevre syndrome is a disorder of keratinization transmitted in an autosomal recessive fashion. Here we are reporting a case of similar disorder because of its rarity.
Externí odkaz:
https://doaj.org/article/ed83558733a34ed599ba5ecb2795b986
Publikováno v:
In Gene Reports December 2021 25
Autor:
Farooq, Rabia, Majid, Sabhiya, Ahmad Bhat, Showkat, Amin, Shajrul, Hayat Bhat, Mohammad, Ahmad Wani, Hilal, Ahmad Shah, Parvaiz
Publikováno v:
In Translational Metabolic Syndrome Research December 2018 1:39-47
Autor:
Malik, Rawoof, Farooq, Rabia, Mehta, Promela, Ishaq, Sheikh, Din, Insha, Shah, Parvaiz, Majid, Sabhiya *
Publikováno v:
In Canadian Journal of Diabetes June 2018 42(3):251-256
Publikováno v:
Journal of Cardiovascular Disease Research (Journal of Cardiovascular Disease Research); 2022, Vol. 13` Issue 8, p716-723, 8p