Zobrazeno 1 - 10
of 262
pro vyhledávání: '"Ossama, Abbas"'
Publikováno v:
Dermatopathology, Vol 8, Iss 2, Pp 135-146 (2021)
The interface dermatitides encompass a vast array of cutaneous entities which, at times, may present with particular clinical variants with adnexal predilection. Similarly, hair follicle and eccrine gland involvement of some of these entities has bee
Externí odkaz:
https://doaj.org/article/8eca0a53ddaf41fc895c7214a25bc90d
Autor:
Nehme El-Hachem, Edward Eid, Georges Nemer, Ghassan Dbaibo, Ossama Abbas, Nelly Rubeiz, Salah Zeineldine, Ghassan M. Matar, Jean-Pierre Bikorimana, Riam Shammaa, Benjamin Haibe-Kains, Mazen Kurban, Moutih Rafei
Publikováno v:
iScience, Vol 23, Iss 11, Pp 101697- (2020)
Summary: The beginning of the 21st century has been marked by three distinct waves of zoonotic coronavirus outbreaks into the human population. The COVID-19 (coronavirus disease 2019) pandemic is caused by severe acute respiratory syndrome coronaviru
Externí odkaz:
https://doaj.org/article/dd115cc6c1074b86bc6aa8ed197296e1
Autor:
Christina Bergqvist, Rémi Safi, George El Hasbani, Ossama Abbas, Abdulghani Kibbi, Dany Nassar
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 17, p adv00281 (2020)
Formation of neutrophil extracellular traps has been implicated in autoimmunity. However, the presence and clinical relevance of neutrophil extracellular traps in immune-complex-mediated cutaneous small and medium vessel vasculitides has not been inv
Externí odkaz:
https://doaj.org/article/93656517f3a34bc38f9f51798fc221b5
Publikováno v:
Journal of the American Academy of Dermatology. 87:614-622
The genital skin may be affected by a variety of dermatoses, be it inflammatory, infectious, malignant, idiopathic, or others. The red scrotum syndrome is characterized by persistent erythema of the scrotum associated with a burning sensation, hypera
Publikováno v:
International Journal of Dermatology. 61:1359-1363
Eosinophilic ulcer of the oral mucosa is a benign, reactive, self-limited lesion. Its pathogenesis is unclear, and it clinically manifests as a punched-out ulcer with surrounding indurated border, raising suspicion for a possible malignancy. On histo
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 11, Iss 11, p e0005920 (2017)
Scabies is an infestation of the skin by the mite Sarcoptes scabiei. It manifests with pruritic erythematous papules and excoriations, in addition to the pathognomonic burrows. Multiple drugs can be used for treatment, but resistance to conventional
Externí odkaz:
https://doaj.org/article/4cb86d502c2f49d885eb1e8b054ff39f
Publikováno v:
American journal of clinical dermatology. 23(6)
The term 'inherited ichthyosis' refers to a heterogeneous group of mendelian disorders of cornification that involve the integument with varying degrees of scaling. The management of ichthyosis poses a challenge for most physicians. Treatment options
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology. 87:3-13
Differentiating cutaneous diseases that mimic each other clinically and histopathologically can at times be a challenging task for the dermatopathologist. At the same time, differentiation of entities with overlapping features may be crucial for pati
Publikováno v:
International Journal of Dermatology. 60:944-950
Dowling-Degos disease is a rare autosomal dominant genodermatosis. It is characterized by acquired reticulate hyperpigmentation over the flexures, comedone-like follicular papules, and pitted perioral scars that usually develop during adulthood. Muta
Autor:
Samar Khalil, Carla Stephan, Divina J. Hasbani, Serena Saade, Tara Bardawil, Adele Chedraoui, Ossama Abbas, Nelly Rubeiz, Mazen Kurban
Background. Treatment options for Ichthyosis and Ichthyosiform disorders are limited and often unsatisfactory. Topical cholesterol and statin have been previously used with good results. Objective. To assess the change in the disease severity score a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d82b7f00dd12706ae46bafb834207bd9
https://doi.org/10.21203/rs.3.rs-1623248/v1
https://doi.org/10.21203/rs.3.rs-1623248/v1