Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Karishma Hemmady"'
Autor:
Satish Udare, Karishma Hemmady
Publikováno v:
Indian Dermatology Online Journal, Vol 7, Iss 4, Pp 290-292 (2016)
A dermatoscope is an important tool in a dermatologist's armamentarium as it can eliminate the need for a biopsy in a wide array of conditions. Porokeratosis was described by Mibelli and Respighi in 1893, as a disorder of keratinization which on the
Externí odkaz:
https://doaj.org/article/47ff6cf5c30e41d9be59f3c2c7abe622
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 7, Pp 65-66 (2015)
Externí odkaz:
https://doaj.org/article/3d21fcbf0e8c4671b032732a17f93bdf
Autor:
Karishma Hemmady, Satish Udare
Publikováno v:
Indian Dermatology Online Journal, Vol 7, Iss 4, Pp 290-292 (2016)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
A dermatoscope is an important tool in a dermatologist's armamentarium as it can eliminate the need for a biopsy in a wide array of conditions. Porokeratosis was described by Mibelli and Respighi in 1893, as a disorder of keratinization which on the
Publikováno v:
Drug delivery and translational research. 8(2)
The epidermal skin barrier plays an important role in protecting underlying structures. It allows the passage of low molecular weight lipophilic molecules, but restricts the passage of hydrophilic molecules and macromolecules. The objective of this s
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 7, Pp 65-66 (2015)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
Sir, Pseudoxanthoma elasticum (PXE) is a rare genetic disorder characterized by fragmentation and mineralization of elastic fibers. It can present with classical cutaneous features with extracutaneous involvement of eyes, medium-sized vessels, and ga
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 1, Pp 121-121 (2016)
Indian Journal of Dermatology
Indian Journal of Dermatology
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized in its full form by severe destructive arthritis, cutaneous nodules, and systemic manifestations. Cutaneous lesions may precede, accompany, or more commonly