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Molecular Genetics & Genomic Medicine
|
April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
Kameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Plos One
|
February 7, 2015
Identification of several mutations in ATP2C1 in Lebanese families: insight into the pathogenesis of Hailey-Hailey disease
Waed Btadini, Ossama K Abou Hassan, Dana Saadeh, et al.
Molecular Genetics and Metabolism
|
December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation
Akl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Journal of Infection in Developing Countries
|
May 14, 2014
Passaging impact of H9N2 avian influenza virus in hamsters on its pathogenicity and genetic variability
Houssam A Shaib, Nelly Cochet, Thierry Ribeiro, et al.
Journal of Gastrointestinal Oncology
|
October 12, 2019
Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19
Rémi Safi, Tala Mohsen-Kanson, Georges Nemer, et al.
Journal of Fungi (Basel, Switzerland)
|
November 27, 2021
Bioexploration and Phylogenetic Placement of Entomopathogenic Fungi of the Genus <i>Beauveria</i> in Soils of Lebanon Cedar Forests
Charbel Al Khoury, Georges Nemer, Richard Humber, et al.
Plos One
|
November 25, 2020
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population
Fadi S Saadeh, Rami Z Morsi, Abdallah El-Kurdi, et al.
Cardiac Electrophysiology Clinics
|
February 28, 2016
The Muscle-Bound Heart
Marwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Child Psychiatry and Human Development
|
February 26, 2026
Sex-Based Differences in Clinical and Social Outcomes in Qatari Youth with ADHD
Sheema Hashem, Saba F Elhag, Zainab Awada, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy
Akl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 111) with videos related to
Sort By:
Page
of 12
Molecular Genetics & Genomic Medicine
|
April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
Kameel Kassab, Hadla Hariri, Lara Gharibeh, et al.
Plos One
|
February 7, 2015
Identification of several mutations in ATP2C1 in Lebanese families: insight into the pathogenesis of Hailey-Hailey disease
Waed Btadini, Ossama K Abou Hassan, Dana Saadeh, et al.
Molecular Genetics and Metabolism
|
December 15, 2010
Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation
Akl C Fahed, Raya M Safa, Fadi F Haddad, et al.
Journal of Infection in Developing Countries
|
May 14, 2014
Passaging impact of H9N2 avian influenza virus in hamsters on its pathogenicity and genetic variability
Houssam A Shaib, Nelly Cochet, Thierry Ribeiro, et al.
Journal of Gastrointestinal Oncology
|
October 12, 2019
Loss of ferrochelatase is protective against colon cancer cells: ferrochelatase a possible regulator of the long noncoding RNA H19
Rémi Safi, Tala Mohsen-Kanson, Georges Nemer, et al.
Journal of Fungi (Basel, Switzerland)
|
November 27, 2021
Bioexploration and Phylogenetic Placement of Entomopathogenic Fungi of the Genus <i>Beauveria</i> in Soils of Lebanon Cedar Forests
Charbel Al Khoury, Georges Nemer, Richard Humber, et al.
Plos One
|
November 25, 2020
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population
Fadi S Saadeh, Rami Z Morsi, Abdallah El-Kurdi, et al.
Cardiac Electrophysiology Clinics
|
February 28, 2016
The Muscle-Bound Heart
Marwan M Refaat, Akl C Fahed, Sylvana Hassanieh, et al.
Child Psychiatry and Human Development
|
February 26, 2026
Sex-Based Differences in Clinical and Social Outcomes in Qatari Youth with ADHD
Sheema Hashem, Saba F Elhag, Zainab Awada, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2016
Variable expressivity and co-occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy
Akl C Fahed, Ruby Khalaf, Rony Salloum, et al.
Page
of 12