Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nelly Rubeiz"'
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:
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
Autor:
Serena Saade, Samar Khalil, Divina Justina Hasbani, Carla Stephan, Tara Bardawil, Adele Chedraoui, Ossama Abbas, Nelly Rubeiz, Mazen Kurban
Publikováno v:
Drug Combination Therapy. 5:7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6955c55396f7b6c73d53e3424330829
https://doi.org/10.53388/dct20230007
https://doi.org/10.53388/dct20230007
Publikováno v:
Pediatric Dermatology. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ec9445f6661da7cbcdc1ea6aa6d316
https://doi.org/10.1111/pde.14396
https://doi.org/10.1111/pde.14396
Autor:
Ossama Abbas, Abdul Ghani Kibbi, Divina-Justina Hasbani, Bilal Abdallah, Nelly Rubeiz, Lamiaa Hamie, Mazen Kurban, Christina Bergqvist
Publikováno v:
American Journal of Medical Genetics Part A. 176:733-738
Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects (CHILD syndrome) is a rare X-linked dominant genodermatosis caused by mutations in the NAD(P) dependent steroid dehydrogenase-like protein gene. Its defect leads to accumulation of to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e38cb75e4ed41fbb138cb3ee9838e5
https://doi.org/10.1002/ajmg.a.38619
https://doi.org/10.1002/ajmg.a.38619
Autor:
Benjamin Haibe-Kains, Edward Eid, Mazen Kurban, Ghassan M. Matar, Salah Zeineldine, Ghassan Dbaibo, Jean-Pierre Bikorimana, Riam Shammaa, Nehme El Hachem, Ossama Abbas, Georges Nemer, Nelly Rubeiz, Moutih Rafei
Publikováno v:
iScience, Vol 23, Iss 11, Pp 101697-(2020)
iScience
iScience
The beginning of the twenty-first 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 coronavirus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aae49a3b6119d0d12d8367f065b61f6
https://doi.org/10.1016/j.isci.2020.101697
https://doi.org/10.1016/j.isci.2020.101697
Publikováno v:
Journal of the American Academy of Dermatology. 63:1036-1041
Background Pachydermoperiostosis (PDP) is a rare hereditary disorder characterized by digital clubbing, periostosis, and pachydermia. Pachydermia results in leonine facies, a major cause of cosmetic and functional morbidity in these patients. Its tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::022a79149b511a91ea712d43bed8ec2b
https://doi.org/10.1016/j.jaad.2009.08.067
https://doi.org/10.1016/j.jaad.2009.08.067
Autor:
Mazen Kurban, Divina Justina Hasbani, Samar Khalil, Tara Bardawil, Serena Saade, Nehmat Ramadan, Georges Nemer, Adele Chedraoui, Nelly Rubeiz, Ossama Abbas
Publikováno v:
JAMA Dermatology. 154:1320
Importance Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of disorders caused by defects in signaling pathways involved in epidermal proliferation and differentiation, leading to a wide range of skin manifestations. Therape
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73d31333ae642074a7adead2ecc14de1
https://doi.org/10.1001/jamadermatol.2018.2904
https://doi.org/10.1001/jamadermatol.2018.2904
Publikováno v:
International Journal of Dermatology. 49:1244-1249
Buck T, 2008, INT J DERMATOL, V47, P775, DOI 10.1111-j.1365-4632.2008.03859.x; Cohen PR, 2002, ARCH DERMATOL, V138, P400, DOI 10.1001-archderm.138.3.400; Cohen PR, 2007, ORPHANET J RARE DIS, V2, DOI 10.1186-1750-1172-2-34; COHEN PR, 1993, CLIN DERMAT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea877e073231e4a0456ac9cb5aa00e9c
https://doi.org/10.1111/j.1365-4632.2009.04233.x
https://doi.org/10.1111/j.1365-4632.2009.04233.x
Autor:
Nelly Rubeiz, Ghada El-Hajj Fuleihan
Publikováno v:
Clinics in Dermatology. 24:281-288
Dermatologic manifestations of parathyroid-related disorders, although rare in sporadic cases, are not uncommon in familial syndromes. Patients with familial hyperparathyroidism have several types of skin lesions. In multiple endocrine neoplasia 1, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0935f5a721eaf19b5dd9fa9d156f72d4
https://doi.org/10.1016/j.clindermatol.2006.04.003
https://doi.org/10.1016/j.clindermatol.2006.04.003