Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Saleem Rahima"'
Autor:
Sarita Sasidharanpillai, Saleem Rahima, Manikoth Payyanadan Binitha, Ettapurath N Abdul Latheef, Aparna Govindan, Dhanya Prashant, Rajwa Rahman
Publikováno v:
Indian Journal of Dermatology, Vol 64, Iss 1, Pp 77-80 (2019)
Externí odkaz:
https://doaj.org/article/f5565f5d1f834491827fd3974e8a628e
Autor:
Sarita Sasidharanpillai, Amal Shyam, Shiny P Manakkad, Ettapurath N Abdul Latheef, Saleem Rahima, Nina Paul
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 172-173 (2019)
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis where the affected manifests mottled pigmentation with intermingled hyper- and hypo-pigmented macules. On most occasions, the lesions begin on limbs and then extend to trunk. Most
Externí odkaz:
https://doaj.org/article/e6ec20fb83e949e58fcf4ac9ba8fa9f5
Publikováno v:
Indian Journal of Dermatology, Vol 60, Iss 4, Pp 424-424 (2015)
Externí odkaz:
https://doaj.org/article/25b88c71067045c9b225b48aaf71db7b
Autor:
Saleem Rahima, Aparna S Vidya, P. Jishna, Sarita Sasidharanpillai, Valiyaveettil Bindu, Ahmed Nadeem
Publikováno v:
Journal of Skin and Sexually Transmitted Diseases. 2:137-139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d07b597a692d7dd38457aeab62e56373
https://doi.org/10.25259/jsstd_39_2019
https://doi.org/10.25259/jsstd_39_2019
Autor:
Rajwa Rahman, Ettapurath N Abdul Latheef, Manikoth Payyanadan Binitha, Dhanya Prashant, Saleem Rahima, Aparna Govindan, Sarita Sasidharanpillai
Publikováno v:
Indian Journal of Dermatology, Vol 64, Iss 1, Pp 77-80 (2019)
Indian Journal of Dermatology
Indian Journal of Dermatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd1067ceefe441f3bbd9e98d6b1bd51
http://www.e-ijd.org/article.asp?issn=0019-5154
http://www.e-ijd.org/article.asp?issn=0019-5154
Autor:
Saleem Rahima, Nina Paul, Sarita Sasidharanpillai, Ettapurath N Abdul Latheef, Amal Shyam, Shiny P Manakkad
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 20, Iss 2, Pp 172-173 (2019)
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis where the affected manifests mottled pigmentation with intermingled hyper- and hypo-pigmented macules. On most occasions, the lesions begin on limbs and then extend to trunk. Most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3429798e239e7c1937ddaf295d53b4
http://www.ijpd.in/article.asp?issn=2319-7250
http://www.ijpd.in/article.asp?issn=2319-7250
Autor:
Najeeba Riyaz, Valiaveetil Bindu, Ahmedali Nermin, Saleem Rahima, Ettappurath N Abdul Latheef, Sarita Sasidharanpillai
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology, Vol 80, Iss 4, Pp 358-361 (2014)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03f172e30bda2e90b38ec80246b17846
http://www.ijdvl.com/article.asp?issn=0378-6323
http://www.ijdvl.com/article.asp?issn=0378-6323
Publikováno v:
Indian Journal of Sexually Transmitted Diseases
Gumma is a characteristic lesion of tertiary syphilis that is rare nowadays, but still rarer is squamous cell carcinoma (SCC) arising from it. A 74-year-old male presented with throat pain and nasal twang with a past history of genital ulcer. Examina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c4e946f3aad7fcbb19c773e9a92d2c9
http://europepmc.org/articles/PMC4555910
http://europepmc.org/articles/PMC4555910
Publikováno v:
International Journal of Research in Dermatology. 3:207
Background: Foot dermatoses are a common malady in children. It has a varied presentation ranging from patchy fissured scaly lesions to disabling highly inflammatory vesicular eruption. A role for foot wear exacerbating these dermatoses is a possibil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbb2ec371f02a79b5b8275d96639f9e1
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20171027
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20171027
Publikováno v:
International Journal of Research in Dermatology. 3:134
Background: Stevens Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are considered as the severest end of spectrum of erythema multiforme. Various etiologies like infections, drugs and malignancies have been proposed. The aim of the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59a0811a3c339aef971983553f2f0bfd
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20170802
https://doi.org/10.18203/issn.2455-4529.intjresdermatol20170802