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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 literature
Malena 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 Study
Ahmed 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 Correlates
Maximilian 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 diagnosis
RaeLynn 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 Study
Adi 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 Study
Thekraiat 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 function
Wadih 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 matching
Chen Wang, Flavia Brancusi, Zaheer M Valivullah, et al.
Genes
|
May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal Dystrophies
Volha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
BMJ Case Reports
|
February 5, 2026
ROSAH syndrome lacking splenomegaly and complete anhidrosis
Luiza De Gregori Dutra, Gisandra de Fátima Stangherlin, Heloísa Chiarini, et al.
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Search research articles
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Showing results (61-70 of 130) with videos related to
Sort By:
Page
of 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 literature
Malena 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 Study
Ahmed 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 Correlates
Maximilian 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 diagnosis
RaeLynn 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 Study
Adi 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 Study
Thekraiat 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 function
Wadih 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 matching
Chen Wang, Flavia Brancusi, Zaheer M Valivullah, et al.
Genes
|
May 28, 2022
Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal Dystrophies
Volha V Malechka, Catherine A Cukras, Emily Y Chew, et al.
BMJ Case Reports
|
February 5, 2026
ROSAH syndrome lacking splenomegaly and complete anhidrosis
Luiza De Gregori Dutra, Gisandra de Fátima Stangherlin, Heloísa Chiarini, et al.
Page
of 13