Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Hind M Almohanna"'
Autor:
Maysa T. Eshmawi, Hajer Yousef Al-Mudaiheem, Mohammed Fatani, Yousef Binamer, Mohammed Alajlan, Ru’aa Alharithy, Hend Alotaibi, Hind M. Almohanna, Adel Alsantali, Abdulaziz Madani, Nadya Al-Faraidy, Falk G. Bechara, Ahmed H. Al-Jedai
Publikováno v:
Journal of Dermatological Treatment, Vol 35, Iss 1 (2024)
Purpose: There is limited information about the diagnosis and treatment of hidradenitis suppurativa (HS) in the Kingdom of Saudi Arabia (KSA). This Delphi consensus study was conducted to develop recommendations for the management of HS in the KSA.Me
Externí odkaz:
https://doaj.org/article/23debf434ce442bdb277f3795ecc0de8
Publikováno v:
JAAD Case Reports, Vol 43, Iss , Pp 76-79 (2024)
Externí odkaz:
https://doaj.org/article/98cee595d0e54b6d91bf07dc424fc320
Publikováno v:
Case Reports in Dermatology, Vol 14, Iss 2, Pp 164-168 (2022)
Disseminated zoster affects immunocompromised individuals and has a nondermatomal distribution. We report a 28-year-old male who initially presented to the dermatology clinic with pinprick sensation over the right side of his face that was followed b
Externí odkaz:
https://doaj.org/article/e23d7b5d3b4a4776964d4804244ccf51
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous pap
Externí odkaz:
https://doaj.org/article/8d61a89e86a54ef089996f3135fa1334
Publikováno v:
Dermatology and Therapy, Vol 9, Iss 1, Pp 51-70 (2018)
Abstract People commonly inquire about vitamin and mineral supplementation and diet as a means to prevent or manage dermatological diseases and, in particular, hair loss. Answering these queries is frequently challenging, given the enormous and confl
Externí odkaz:
https://doaj.org/article/67f5a572fd064e0394d8ade929fb2070
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous papule over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0561a2b79d67334136dee861a178dbc5
http://europepmc.org/articles/PMC8418680
http://europepmc.org/articles/PMC8418680
Publikováno v:
Dermatology and Therapy, Vol 9, Iss 3, Pp 421-448 (2019)
Dermatology and Therapy
Dermatology and Therapy
Hair loss in early childhood represents a broad differential diagnosis which can be a diagnostic and therapeutic challenge for a physician. It is important to consider the diagnosis of a genetic hair disorder. Genetic hair disorders are a large group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b2d5f0243721c506175de7431127a5e
http://link.springer.com/article/10.1007/s13555-019-0313-2
http://link.springer.com/article/10.1007/s13555-019-0313-2
Graham-Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of Lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non-fibrosing alopecia of the axilla and groin, and a follicular spinous papule over the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::278236c5dd87ab895c5a69422864e89a
https://doi.org/10.22541/au.162609269.94365100/v1
https://doi.org/10.22541/au.162609269.94365100/v1
Publikováno v:
The journal of investigative dermatology. Symposium proceedings. 20(1)
Platelet-rich plasma (PRP) is an autologous preparation of plasma with concentrated platelets containing various growth factors and cytokines that enhance the body's inherent capacity to repair and regenerate hair follicles. A few studies and case re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13702f801cdf7b252497e0be1bb92130
https://pubmed.ncbi.nlm.nih.gov/33099384
https://pubmed.ncbi.nlm.nih.gov/33099384
Publikováno v:
Skin Appendage Disord
Primary cutaneous follicle center lymphoma (PCFCL) is a rare type of indolent, low-grade cutaneous B-cell lymphoma with an excellent prognosis. It usually presents with erythematous nodules and plaques on the head, neck, or back. The diagnosis is pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e26888a7a29e95cda0f10aaf95a983a
https://doi.org/10.1159/000501174
https://doi.org/10.1159/000501174