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Genes
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January 1, 2020
Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Frontiers in Genetics
|
June 2, 2022
Novel Missense and Splice Site Mutations in <i>USH2A</i>, <i>CDH23</i>, <i>PCDH15</i>, and <i>ADGRV1</i> Are Associated With Usher Syndrome in Lebanon
Lama Jaffal, Hanane Akhdar, Hawraa Joumaa, et al.
Genes
|
February 21, 2019
Novel Missense Mutations in <i>BEST1</i> Are Associated with Bestrophinopathies in Lebanese Patients
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 20, 2018
Retinal detachment in albinism
Ahmad M Mansour, Jay Chhablani, J Fernando Arevalo, et al.
Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie
|
October 24, 2024
Use of opioids and opioid alternatives during general anesthesia: a pan-Canadian survey among anesthesiologists
Michael Verret, Manoj M Lalu, Alexandre Assi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
November 17, 2025
MRI scoring systems in neonatal encephalopathy and neurodevelopmental outcomes: a systematic review
Emma Finnegan, Alexandre Assi, Ella Carroll, et al.
British Journal of Anaesthesia
|
February 8, 2024
Intraoperative pharmacologic opioid minimisation strategies and patient-centred outcomes after surgery: a scoping review
Michael Verret, Nhat H Lam, Manoj Lalu, et al.
The British Journal of Ophthalmology
|
April 30, 2021
Clinical characteristics of full thickness macular holes that closed without surgery
Sami H Uwaydat, Ahmad Mansour, Francisco J Ascaso, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
Genes
|
January 1, 2020
Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Frontiers in Genetics
|
June 2, 2022
Novel Missense and Splice Site Mutations in <i>USH2A</i>, <i>CDH23</i>, <i>PCDH15</i>, and <i>ADGRV1</i> Are Associated With Usher Syndrome in Lebanon
Lama Jaffal, Hanane Akhdar, Hawraa Joumaa, et al.
Genes
|
February 21, 2019
Novel Missense Mutations in <i>BEST1</i> Are Associated with Bestrophinopathies in Lebanese Patients
Lama Jaffal, Wissam H Joumaa, Alexandre Assi, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 20, 2018
Retinal detachment in albinism
Ahmad M Mansour, Jay Chhablani, J Fernando Arevalo, et al.
Canadian Journal of Anaesthesia = Journal Canadien D'Anesthesie
|
October 24, 2024
Use of opioids and opioid alternatives during general anesthesia: a pan-Canadian survey among anesthesiologists
Michael Verret, Manoj M Lalu, Alexandre Assi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
November 17, 2025
MRI scoring systems in neonatal encephalopathy and neurodevelopmental outcomes: a systematic review
Emma Finnegan, Alexandre Assi, Ella Carroll, et al.
British Journal of Anaesthesia
|
February 8, 2024
Intraoperative pharmacologic opioid minimisation strategies and patient-centred outcomes after surgery: a scoping review
Michael Verret, Nhat H Lam, Manoj Lalu, et al.
The British Journal of Ophthalmology
|
April 30, 2021
Clinical characteristics of full thickness macular holes that closed without surgery
Sami H Uwaydat, Ahmad Mansour, Francisco J Ascaso, et al.
Page
of 2