Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Vijetha Rai"'
Autor:
Varadraj Vasant Pai, Tukaram Sori, Kikkeri Narayanshetty Naveen, Sharatchandra Bhimrao Athanikar, Vijetha Rai, Dinesh Udupi Shastry
Publikováno v:
Indian Dermatology Online Journal, Vol 5, Iss 1, Pp 44-47 (2014)
Epidermolysis bullosa (EB) pruriginosa is a very rare pattern of dystrophic EB caused by type VII collagen gene mutation, with distinctive clinico-pathological features. It is characterized by nodular prurigo-like lichenified lesions, nail dystrophy,
Externí odkaz:
https://doaj.org/article/adc4f903827f4d4689a9b35ee430e11d
Autor:
Varadraj V Pai, Kikkeri Narayanshetty Naveen, Sharatchandra Bhimrao Athanikar, Dinesh Udupi Shastri, Vijetha Rai
Publikováno v:
Indian Journal of Dermatology, Vol 59, Iss 3, Pp 287-289 (2014)
Reactive perforating collagenosis (RPC) is a rare form of transepithelial elimination, in which genetically altered collagen is extruded through the epidermis. Of the acquired and inherited form, inherited form is extremely rare. Here, we present two
Externí odkaz:
https://doaj.org/article/74142ca78bfb4b02862557546ae5ccdc
Publikováno v:
Indian Journal of Dermatology, Vol 58, Iss 3, Pp 248-248 (2013)
Externí odkaz:
https://doaj.org/article/8ae7b091204540019facdd205fa4f434
Publikováno v:
International Journal of Health Sciences and Pharmacy. :13-17
Hailey-Hailey disease (HHD), also called as familial benign chronic pemphigus, is a rare autosomal dominant blistering skin disease with waxing and waning in its clinical course. It is characterized by the presence of flaccid vesiculo-pustules, crust
Autor:
Vijetha Rai, Edwin Dias
Publikováno v:
International Journal of Health Sciences and Pharmacy. :68-71
A 3 years old child with a history of ingestion of Paracetamol tablet due to fever Presented with rashes all over the body, nikolsky sign positive diagnosed as toxic epidermal necrosis, was treated With supportive management antibiotics and dexametha
Hailey-Hailey disease (HHD), also called as familial benign chronic pemphigus, is a rare autosomal dominant blistering skin disease with waxing and waning in its clinical course. It is characterized by the presence of flaccid vesiculo-pustules, crust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e988b94e53d9ac96674f39be8804ae5f
Autor:
Dinesh Udupi Shastry, Tukaram Sori, Varadraj V Pai, Kikkeri Narayanshetty Naveen, Sharatchandra B Athanikar, Vijetha Rai
Publikováno v:
Indian Dermatology Online Journal, Vol 5, Iss 1, Pp 44-47 (2014)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
Epidermolysis bullosa (EB) pruriginosa is a very rare pattern of dystrophic EB caused by type VII collagen gene mutation, with distinctive clinico-pathological features. It is characterized by nodular prurigo-like lichenified lesions, nail dystrophy,
Autor:
Vijetha Rai, Sharatchandra B Athanikar, Naveen Narayanshetty Kikkeri, Varadraj V Pai, Anil Myageri
Publikováno v:
Indian Journal of Sexually Transmitted Diseases
Pyoderma gangrenosum (PG) is a rare inflammatory disorder of unknown etiology characterized by neutrophilic infiltration of the dermis and destruction of tissue. PG is diagnosed after excluding more commonly occurring condition presenting with simila
Autor:
Sharatchandra B Athanikar, Dinesh Udupi Shastri, Vijetha Rai, Varadraj V Pai, Kikkeri Narayanshetty Naveen
Publikováno v:
Indian Journal of Dermatology
Indian Journal of Dermatology, Vol 59, Iss 3, Pp 287-289 (2014)
Indian Journal of Dermatology, Vol 59, Iss 3, Pp 287-289 (2014)
Reactive perforating collagenosis (RPC) is a rare form of transepithelial elimination, in which genetically altered collagen is extruded through the epidermis. Of the acquired and inherited form, inherited form is extremely rare. Here, we present two
Autor:
Kikkeri Narayanasetty, Naveen, Varadraj V, Pai, Sharatchandra B, Athanikar, Vidhisha S, Athanikar, Vijetha, Rai
Publikováno v:
Cutis. 95(3)