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Muhammad I Khan

Showing results (31-40 of 43) with videos related to

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Materials (Basel, Switzerland)|April 2, 2025
RETRACTED: Hussain et al. The Effect of 600 keV Ag Ion Irradiation on the Structural, Optical, and Photovoltaic Properties of MAPbBr<sub>3</sub> Films for Perovksite Solar Cell Applications. <i>Materials</i> 2022, <i>15</i>, 5299Saddam Hussain, Norah Alwadai, Muhammad I Khan, et al.
Materials (Basel, Switzerland)|August 12, 2022
RETRACTED: The Effect of 600 keV Ag Ion Irradiation on the Structural, Optical, and Photovoltaic Properties of MAPbBr3 Films for Perovksite Solar Cell ApplicationsSaddam Hussain, Norah Alwadai, Muhammad I Khan, et al.
Molecular Genetics & Genomic Medicine|May 14, 2020
Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndromeValeria Lo Faro, Sorath N Siddiqui, Muhammad I Khan, et al.
Clinical & Experimental Ophthalmology|August 6, 2014
Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucomaShazia Micheal, Humaira Ayub, Saemah N Zafar, et al.
Talanta|April 13, 2011
A new HPLC method for the simultaneous determination of ascorbic acid and aminothiols in human plasma and erythrocytes using electrochemical detectionAbad Khan, Muhammad I Khan, Zafar Iqbal, et al.
Journal of Infection and Public Health|April 13, 2021
Early prediction keys for COVID-19 cases progression: A meta-analysisMostafa M Khodeir, Hassan A Shabana, Abdullah S Alkhamiss, et al.
BMJ Open Gastroenterology|January 7, 2022
Effect of COVID-19 on presentations of decompensated liver disease in ScotlandThomas Manship, Paul N Brennan, Iona Campbell, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosaMaleeha Azam, Rob W J Collin, Ayesha Malik, et al.
Investigative Ophthalmology & Visual Science|May 31, 2014
IMPG2-associated retinitis pigmentosa displays relatively early macular involvementRamon A C van Huet, Rob W J Collin, Anna M Siemiatkowska, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Materials (Basel, Switzerland)|April 2, 2025
RETRACTED: Hussain et al. The Effect of 600 keV Ag Ion Irradiation on the Structural, Optical, and Photovoltaic Properties of MAPbBr<sub>3</sub> Films for Perovksite Solar Cell Applications. <i>Materials</i> 2022, <i>15</i>, 5299Saddam Hussain, Norah Alwadai, Muhammad I Khan, et al.
Materials (Basel, Switzerland)|August 12, 2022
RETRACTED: The Effect of 600 keV Ag Ion Irradiation on the Structural, Optical, and Photovoltaic Properties of MAPbBr3 Films for Perovksite Solar Cell ApplicationsSaddam Hussain, Norah Alwadai, Muhammad I Khan, et al.
Molecular Genetics & Genomic Medicine|May 14, 2020
Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndromeValeria Lo Faro, Sorath N Siddiqui, Muhammad I Khan, et al.
Clinical & Experimental Ophthalmology|August 6, 2014
Identification of novel CYP1B1 gene mutations in patients with primary congenital and primary open-angle glaucomaShazia Micheal, Humaira Ayub, Saemah N Zafar, et al.
Talanta|April 13, 2011
A new HPLC method for the simultaneous determination of ascorbic acid and aminothiols in human plasma and erythrocytes using electrochemical detectionAbad Khan, Muhammad I Khan, Zafar Iqbal, et al.
Journal of Infection and Public Health|April 13, 2021
Early prediction keys for COVID-19 cases progression: A meta-analysisMostafa M Khodeir, Hassan A Shabana, Abdullah S Alkhamiss, et al.
BMJ Open Gastroenterology|January 7, 2022
Effect of COVID-19 on presentations of decompensated liver disease in ScotlandThomas Manship, Paul N Brennan, Iona Campbell, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 12, 2011
Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosaMaleeha Azam, Rob W J Collin, Ayesha Malik, et al.
Investigative Ophthalmology & Visual Science|May 31, 2014
IMPG2-associated retinitis pigmentosa displays relatively early macular involvementRamon A C van Huet, Rob W J Collin, Anna M Siemiatkowska, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
Pageof 5