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Therapie
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June 12, 2016
Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?
Imen Chatti, Isabelle Creveaux, Jean-Baptiste Woillard, et al.
Heart Views : the Official Journal of the Gulf Heart Association
|
August 25, 2025
A Milestone in Cardiac Care in Iraq: One-year Follow-up after the Nation's First Continuous-flow Left Ventricular Assist Device Implantation, Paving the Way for Heart Transplantation
Ali Saad Merzah, Jasmin Hanke, Günes Dogan, et al.
Archives of Oral Biology
|
August 5, 2016
Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis
Marwa Haddaji Mastouri, Peter De Coster, Aicha Zaghabani, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
March 28, 2015
Cerebral aneurysm in a 12-year-old boy with a STAT3 mutation (hyper-IgE syndrome)
Yoon Kim, Jillian A Nard, Ali Saad, et al.
La Tunisie Medicale
|
January 3, 2025
RS35705950 polymorphism of MUC5B Gene: Association with Rheumatoid Arthritis and Interstitial lung disease in Tunisian Population
Azza Saad, Khadija Baccouche, Hajer Fodha, et al.
The American Journal of Medicine
|
October 9, 2024
Rethinking Our Roots: The Ground-Up Approach to Heart Health & Planetary Sustainability
Ali Saad, Eric J Brandt, Kamil F Faridi, et al.
Genetic Testing
|
December 17, 2008
Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role
Olfa Siala, Fatma Kammoun Feki, Nacim Louhichi, et al.
Journal of Assisted Reproduction and Genetics
|
April 18, 2016
A new mutation identified in SPATA16 in two globozoospermic patients
Elias ElInati, Camille Fossard, Ozlem Okutman, et al.
Journal of Pediatric Genetics
|
September 13, 2016
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits
Hela Ben Khelifa, Molka Kammoun, Hanene Hannachi, et al.
International Journal of Fertility & Sterility
|
June 24, 2018
Subtelomeric Rearrangements in Patients with Recurrent Miscarriage
Amani Hajlaoui, Wafa Slimani, Molka Kammoun, et al.
Page
of 36
Search research articles
Search
Showing results (161-170 of 359) with videos related to
Sort By:
Page
of 36
Therapie
|
June 12, 2016
Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?
Imen Chatti, Isabelle Creveaux, Jean-Baptiste Woillard, et al.
Heart Views : the Official Journal of the Gulf Heart Association
|
August 25, 2025
A Milestone in Cardiac Care in Iraq: One-year Follow-up after the Nation's First Continuous-flow Left Ventricular Assist Device Implantation, Paving the Way for Heart Transplantation
Ali Saad Merzah, Jasmin Hanke, Günes Dogan, et al.
Archives of Oral Biology
|
August 5, 2016
Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis
Marwa Haddaji Mastouri, Peter De Coster, Aicha Zaghabani, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology
|
March 28, 2015
Cerebral aneurysm in a 12-year-old boy with a STAT3 mutation (hyper-IgE syndrome)
Yoon Kim, Jillian A Nard, Ali Saad, et al.
La Tunisie Medicale
|
January 3, 2025
RS35705950 polymorphism of MUC5B Gene: Association with Rheumatoid Arthritis and Interstitial lung disease in Tunisian Population
Azza Saad, Khadija Baccouche, Hajer Fodha, et al.
The American Journal of Medicine
|
October 9, 2024
Rethinking Our Roots: The Ground-Up Approach to Heart Health & Planetary Sustainability
Ali Saad, Eric J Brandt, Kamil F Faridi, et al.
Genetic Testing
|
December 17, 2008
Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role
Olfa Siala, Fatma Kammoun Feki, Nacim Louhichi, et al.
Journal of Assisted Reproduction and Genetics
|
April 18, 2016
A new mutation identified in SPATA16 in two globozoospermic patients
Elias ElInati, Camille Fossard, Ozlem Okutman, et al.
Journal of Pediatric Genetics
|
September 13, 2016
Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits
Hela Ben Khelifa, Molka Kammoun, Hanene Hannachi, et al.
International Journal of Fertility & Sterility
|
June 24, 2018
Subtelomeric Rearrangements in Patients with Recurrent Miscarriage
Amani Hajlaoui, Wafa Slimani, Molka Kammoun, et al.
Page
of 36