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M Zein

Showing results (61-70 of 130) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 1, 2020
The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literatureMalena Daich Varela, Priyam Jani, Wadih M Zein, et al.
International Journal of Environmental Research and Public Health|March 10, 2022
Prevalence Estimates and Risk Factors of Anxiety among Healthcare Workers in Jordan over One Year of the COVID-19 Pandemic: A Cross-Sectional StudyAhmed Yassin, Abdel-Hameed Al-Mistarehi, Khalid El-Salem, et al.
American Journal of Ophthalmology|May 21, 2023
Natural History of Visual Dysfunction in ABCA4 Retinopathy and Its Genetic CorrelatesMaximilian Pfau, Laryssa A Huryn, Marisa P Boyle, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 21, 2022
Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosisRaeLynn Forsyth, Melissa A Parisi, Burak Altintas, et al.
International Journal of General Medicine|October 29, 2020
Prevalence and Predictors of Thyroid Dysfunction Among Type 2 Diabetic Patients: A Case-Control StudyAdi H Khassawneh, Abdel-Hameed Al-Mistarehi, Anas M Zein Alaabdin, et al.
International Journal of General Medicine|October 11, 2022
Prevalence and Pattern of Dyslipidemia and Its Associated Factors Among Patients with Type 2 Diabetes Mellitus in Jordan: A Cross-Sectional StudyThekraiat M Al Quran, Ziad A Bataineh, Abdel-Hameed Al-Mistarehi, et al.
Investigative Ophthalmology & Visual Science|September 11, 2014
CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone functionWadih M Zein, Brett G Jeffrey, Henry E Wiley, et al.
Ophthalmic Genetics|July 26, 2017
A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matchingChen Wang, Flavia Brancusi, Zaheer M Valivullah, et al.
Genes|May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal DystrophiesVolha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
BMJ Case Reports|February 5, 2026
ROSAH syndrome lacking splenomegaly and complete anhidrosisLuiza De Gregori Dutra, Gisandra de Fátima Stangherlin, Heloísa Chiarini, et al.
Pageof 13

Showing results (61-70 of 130) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 1, 2020
The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literatureMalena Daich Varela, Priyam Jani, Wadih M Zein, et al.
International Journal of Environmental Research and Public Health|March 10, 2022
Prevalence Estimates and Risk Factors of Anxiety among Healthcare Workers in Jordan over One Year of the COVID-19 Pandemic: A Cross-Sectional StudyAhmed Yassin, Abdel-Hameed Al-Mistarehi, Khalid El-Salem, et al.
American Journal of Ophthalmology|May 21, 2023
Natural History of Visual Dysfunction in ABCA4 Retinopathy and Its Genetic CorrelatesMaximilian Pfau, Laryssa A Huryn, Marisa P Boyle, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 21, 2022
Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosisRaeLynn Forsyth, Melissa A Parisi, Burak Altintas, et al.
International Journal of General Medicine|October 29, 2020
Prevalence and Predictors of Thyroid Dysfunction Among Type 2 Diabetic Patients: A Case-Control StudyAdi H Khassawneh, Abdel-Hameed Al-Mistarehi, Anas M Zein Alaabdin, et al.
International Journal of General Medicine|October 11, 2022
Prevalence and Pattern of Dyslipidemia and Its Associated Factors Among Patients with Type 2 Diabetes Mellitus in Jordan: A Cross-Sectional StudyThekraiat M Al Quran, Ziad A Bataineh, Abdel-Hameed Al-Mistarehi, et al.
Investigative Ophthalmology & Visual Science|September 11, 2014
CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone functionWadih M Zein, Brett G Jeffrey, Henry E Wiley, et al.
Ophthalmic Genetics|July 26, 2017
A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matchingChen Wang, Flavia Brancusi, Zaheer M Valivullah, et al.
Genes|May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal DystrophiesVolha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
BMJ Case Reports|February 5, 2026
ROSAH syndrome lacking splenomegaly and complete anhidrosisLuiza De Gregori Dutra, Gisandra de Fátima Stangherlin, Heloísa Chiarini, et al.
Pageof 13