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Pacing and Clinical Electrophysiology : PACE
|
July 15, 2015
The Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long QT Syndrome
Kristian L Poulsen, Mostafa Hotait, Kirstine Calloe, et al.
Pediatric Cardiology
|
August 11, 2012
Research in congenital heart disease: a comparative bibliometric analysis between developing and developed countries
Theresa Farhat, Zahi Abdul-Sater, Mounir Obeid, et al.
Frontiers in Immunology
|
February 6, 2025
Deciphering the role of IL17RA in psoriasis and chronic mucocutaneous candidiasis: shared pathways and distinct manifestations
Ayat Kadhi, Edward Eid, Michel J Massaad, et al.
Photodermatology, Photoimmunology & Photomedicine
|
December 1, 2020
Comparative characterization of sun exposed and sun protected skin-derived mesenchymal-like stem cells in variegate porphyria and healthy individuals
Rémi Safi, Elie Malek, Georges Nemer, et al.
Plos One
|
December 11, 2012
Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia
Zahi Abdul-Sater, Amin Yehya, Jean Beresian, et al.
JAMA Dermatology
|
September 13, 2018
Use of Topical Glycolic Acid Plus a Lovastatin-Cholesterol Combination Cream for the Treatment of Autosomal Recessive Congenital Ichthyoses
Samar Khalil, Tara Bardawil, Serena Saade, et al.
Human Genomics
|
August 1, 2024
Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol
Jamil Alenbawi, Yasser A Al-Sarraj, Umm-Kulthum I Umlai, et al.
Chemico-Biological Interactions
|
May 3, 2008
Copper-adenine complex, a compound, with multi-biochemical targets and potential anti-cancer effect
Hassan H Hammud, Georges Nemer, Walid Sawma, et al.
Postgraduate Medical Journal
|
September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseases
Lamiaa Hamie, Georges Daoud, Georges Nemer, et al.
Journal of Dermatological Science
|
December 6, 2018
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis
Hadla Hariri, Mazen Kurban, Christiane Al-Haddad, et al.
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of 12
Search research articles
Search
Showing results (71-80 of 111) with videos related to
Sort By:
Page
of 12
Pacing and Clinical Electrophysiology : PACE
|
July 15, 2015
The Mutation P.T613a in the Pore Helix of the Kv 11.1 Potassium Channel is Associated with Long QT Syndrome
Kristian L Poulsen, Mostafa Hotait, Kirstine Calloe, et al.
Pediatric Cardiology
|
August 11, 2012
Research in congenital heart disease: a comparative bibliometric analysis between developing and developed countries
Theresa Farhat, Zahi Abdul-Sater, Mounir Obeid, et al.
Frontiers in Immunology
|
February 6, 2025
Deciphering the role of IL17RA in psoriasis and chronic mucocutaneous candidiasis: shared pathways and distinct manifestations
Ayat Kadhi, Edward Eid, Michel J Massaad, et al.
Photodermatology, Photoimmunology & Photomedicine
|
December 1, 2020
Comparative characterization of sun exposed and sun protected skin-derived mesenchymal-like stem cells in variegate porphyria and healthy individuals
Rémi Safi, Elie Malek, Georges Nemer, et al.
Plos One
|
December 11, 2012
Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia
Zahi Abdul-Sater, Amin Yehya, Jean Beresian, et al.
JAMA Dermatology
|
September 13, 2018
Use of Topical Glycolic Acid Plus a Lovastatin-Cholesterol Combination Cream for the Treatment of Autosomal Recessive Congenital Ichthyoses
Samar Khalil, Tara Bardawil, Serena Saade, et al.
Human Genomics
|
August 1, 2024
Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol
Jamil Alenbawi, Yasser A Al-Sarraj, Umm-Kulthum I Umlai, et al.
Chemico-Biological Interactions
|
May 3, 2008
Copper-adenine complex, a compound, with multi-biochemical targets and potential anti-cancer effect
Hassan H Hammud, Georges Nemer, Walid Sawma, et al.
Postgraduate Medical Journal
|
September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseases
Lamiaa Hamie, Georges Daoud, Georges Nemer, et al.
Journal of Dermatological Science
|
December 6, 2018
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis
Hadla Hariri, Mazen Kurban, Christiane Al-Haddad, et al.
Page
of 12