Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Chandraprakash, Chouhan"'
Publikováno v:
International Journal of Mycobacteriology, Vol 9, Iss 4, Pp 429-434 (2020)
Background: Cutaneous tuberculosis (TB) forms a small subset of extrapulmonary TB and continues to be a significant diagnostic dilemma in routine practice. The present study is an attempt to find the incidence, clinical spectrum, and histopathologica
Externí odkaz:
https://doaj.org/article/da2c42cb2e6943c9866ccc0ca96370d1
Publikováno v:
Clinical Dermatology Review, Vol 4, Iss 2, Pp 173-175 (2020)
Maffucci syndrome, a congenital mesodermal dysplasia, characterized by multiple enchondromas and hemangiomas was first described in 1881, and 200 cases have been reported in the literature since then. Here, we report the case of a 30-year-old male wh
Externí odkaz:
https://doaj.org/article/04166c1dff654ba6bb507fd8210a9710
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology. 88:251-257
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04384b7ff4cc43e69d4fd22085df300b
https://doi.org/10.25259/ijdvl_131_2021
https://doi.org/10.25259/ijdvl_131_2021
Publikováno v:
International Journal of Current Microbiology and Applied Sciences. 9:2733-2742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4301e04bab10e93f1bb96b5b2ad33dec
https://doi.org/10.20546/ijcmas.2020.906.332
https://doi.org/10.20546/ijcmas.2020.906.332
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 5, Pp 352-353 (2015)
Atrichia congenita is a rare genodermatoses is characterized by a mutation of the human hairless (HR) gene on chromosome 8p22. There is loss of scalp hair between one to six months of age, after which no growth occurs. Eyebrow, eyelash, and body hair
Externí odkaz:
https://doaj.org/article/fcf0ba50e93e4853ac5035eda7d322f4
Publikováno v:
Journal of Cutaneous and Aesthetic Surgery. 15:33
Surgical treatment of vitiligo is reserved for stable recalcitrant vitiligo patches. Split-thickness skin grafting (STSG) is an important established modality for the surgical treatment of vitiligo, whereas autologous, non-cultured, non-trypsinized e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3c59062add628102dae7b409d6292c5
https://doi.org/10.4103/jcas.jcas_205_20
https://doi.org/10.4103/jcas.jcas_205_20
Autor:
Sandeep, Pachar, Chandraprakash, Chouhan, Pankaj, Rao, Dilip, Kachhawa, Harshvardhan, Singh, Chimai, Yadav
Publikováno v:
Journal of Cutaneous and Aesthetic Surgery. 15:71
Androgenetic alopecia (AGA) is characterized by androgen-related progressive thinning of the scalp hair in a defined pattern. It has an effect on social and psychological well-being of the patient. It is often recalcitrant to medical treatment alone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ffd5e8821fb9a58ae0e13cc1ef40104
https://doi.org/10.4103/jcas.jcas_232_20
https://doi.org/10.4103/jcas.jcas_232_20
Publikováno v:
International Journal of Medical and Biomedical Studies. 3
Background: In aging, a decline in the regular functions of skin is observed, including cell replacement capacity, barrier function, chemical clearance capacity, sensory perception, mechanical protection, wound healing, immune responsiveness, thermor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580012668a43bc1b8385cf89414c6cfe
https://doi.org/10.32553/ijmbs.v3i4.205
https://doi.org/10.32553/ijmbs.v3i4.205
Publikováno v:
Libyan Journal of Medical Sciences. 5:100
Severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) infection has a wide range of consequences of human body. In the literature, only a few cases with uncertain hair fall related to COVID-19 infection. In the case report, we enumerated a cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1abb720fc7c419369848d1718789c0c
https://doi.org/10.4103/ljms.ljms_109_20
https://doi.org/10.4103/ljms.ljms_109_20
Publikováno v:
Clinical Dermatology Review, Vol 4, Iss 2, Pp 173-175 (2020)
Maffucci syndrome, a congenital mesodermal dysplasia, characterized by multiple enchondromas and hemangiomas was first described in 1881, and 200 cases have been reported in the literature since then. Here, we report the case of a 30-year-old male wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::900d8921bb92dc9968d24e316b838ac9
https://doi.org/10.4103/cdr.cdr_25_19
https://doi.org/10.4103/cdr.cdr_25_19