Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M A, El Darouti"'
Publikováno v:
Clinical and Experimental Dermatology. 40:35-38
Summary Kallin syndrome (KS) is a variant of epidermolysis bullosa simplex (EBS), which, in addition to the classic features of EBS, also presents with deafness, alopecia, hypodontia and nail dystrophy. We report the case of a 17-year-old boy who pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64b0066c6d601df4fd6970a3e9ebdce3
https://doi.org/10.1111/ced.12463
https://doi.org/10.1111/ced.12463
Autor:
Rehab A. Hegazy, Dina M. Kadry, H. S. Abdelhaliem, D. I. Shehab, Ola M. Abu Zeid, M. A. El Darouti, Marwah A. Saleh, D.M. Abdel Halim
Publikováno v:
Journal of cosmetic dermatology. 15(2)
SummaryBackground Many studies have suggested a strong relation between diet and acne. Many patients with acne believe that spicy and salty foods exacerbate acne. Aim To assess the relationship between the dietary intake of salty and spicy food and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25590f3e03276c76bbb772f16d773e62
https://pubmed.ncbi.nlm.nih.gov/26648163
https://pubmed.ncbi.nlm.nih.gov/26648163
Autor:
M A, El Darouti, S, Hussein, S R, Al Tahlawy, M, Al Fangary, H M, Mashaly, E, El Nabarawy, A, Al Tawdy, M, Fawzi, R M, Abdel Hay
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 25(3)
Nail changes in leprotic patients are not specific to leprosy, and may be observed in other peripheral neuropathies. Diabetes is one of the diseases that present with nail dystrophy secondary to peripheral neuropathy, vasculopathy, trauma and infecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09e82cf7f43609abf59207e63f427d8d
https://pubmed.ncbi.nlm.nih.gov/20609034
https://pubmed.ncbi.nlm.nih.gov/20609034
Publikováno v:
Journal of Cutaneous Pathology. 27:183-185
Epidermotropic lymphocytes in mycosis fungoides typically reside in clear lacunae. The material forming this space is unknown. Thirty specimens from 30 patients with mycosis fungoides were stained with alcian blue, modified Mowry's colloidal iron and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b070aff8a3e2928af71bd07d15dea1
https://doi.org/10.1034/j.1600-0560.2000.027004183.x
https://doi.org/10.1034/j.1600-0560.2000.027004183.x
Autor:
M. A. El Darouti, S. M. Al Rubaie
Publikováno v:
International Journal of Dermatology. 29:126-128
Seven patients with xeroderma pigmentosum are presented. Abnormal karyotyping, found in one case, could be associated with an increased risk of the development of neoplasia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ff7ab8181f38d87e334dff45ae1045d
https://doi.org/10.1111/j.1365-4362.1990.tb04084.x
https://doi.org/10.1111/j.1365-4362.1990.tb04084.x
Autor:
S. M. Al Rubaie, M. A. El Darouti
Publikováno v:
International journal of dermatology. 29(1)
A combination of both intralesional stibogluconate injection and superficial cryotherapy (not including the base of the lesion nor the 1-2 mm rim of the surrounding normal skin) was performed in an attempt to improve the therapeutic efficacy of eithe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3691036c3a5cfac85232766911d2e986
https://pubmed.ncbi.nlm.nih.gov/2158487
https://pubmed.ncbi.nlm.nih.gov/2158487
Autor:
M A, el Darouti
Publikováno v:
The American Journal of dermatopathology.
Familial melanopathy with giant melanocytes is a unique pigmentary disorder that to the best of the author's knowledge has not been described before. The clinical and pathological features of this disorder, herein described in four patients, are very
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b6ec8a530c5d49b175f429ce0cb03df8
https://pubmed.ncbi.nlm.nih.gov/6528935
https://pubmed.ncbi.nlm.nih.gov/6528935
Publikováno v:
International journal of dermatology. 27(1)
Papillon-Lefevre syndrome is a rare autosomal recessive disorder of palmoplantar keratinization in which there is a unique association of the palmoplantar hyperkeratosis and premature loss of both deciduous and permanent teeth. We report three patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf9c9cce3edd6c95464a2bb4171f7e6a
https://pubmed.ncbi.nlm.nih.gov/2964426
https://pubmed.ncbi.nlm.nih.gov/2964426