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Muhammad Arif Nadeem

Showing results (71-80 of 83) with videos related to

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RSC Advances|September 6, 2024
DFT and comparative adsorption study of NiO, MnO, and Mn<sub>2</sub>NiO<sub>4</sub> nanomaterials for the removal of amaranth dye from synthetic waterMadiha Ahmad, Qamar Riaz, Mehwish Tabassum, et al.
European Journal of Human Genetics : EJHG|October 11, 2023
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndromeMadiha Amin Malik, Muhammad Arif Nadeem Saqib, Edwin Mientjes, et al.
Experimental Eye Research|March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defectsEhsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
Frontiers in Genetics|May 16, 2022
Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual DisabilityAhmed Waqas, Anam Nayab, Shabnam Shaheen, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|November 28, 2020
Karachi Cancer Registry (KCR): Age-Standardized Incidence Rate by Age-Group and Gender in a Mega City of PakistanShahid Pervez, Adnan A Jabbar, Ghulam Haider, et al.
Pediatric Neurology|November 6, 2022
Spectrum of Common Pediatric Neurological Disorders: A Cross-Sectional Study From Three Tertiary Care Centres Across PakistanPrem Chand, Tipu Sultan, Shazia Kulsoom, et al.
Trials|August 1, 2019
Tranexamic acid for acute gastrointestinal bleeding (the HALT-IT trial): statistical analysis plan for an international, randomised, double-blind, placebo-controlled trialAmy Brenner, Adefemi Afolabi, Syed Masroor Ahmad, et al.
Journal of the Neurological Sciences|August 10, 2023
Neurological disorders and disability in Pakistan: A cross-sectional multicenter studyMohammad Wasay, Safia Awan, Naila Shahbaz, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Human Genetics|September 1, 2018
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disabilityRegie Lyn P Santos-Cortez, Valeed Khan, Falak Sher Khan, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
RSC Advances|September 6, 2024
DFT and comparative adsorption study of NiO, MnO, and Mn<sub>2</sub>NiO<sub>4</sub> nanomaterials for the removal of amaranth dye from synthetic waterMadiha Ahmad, Qamar Riaz, Mehwish Tabassum, et al.
European Journal of Human Genetics : EJHG|October 11, 2023
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndromeMadiha Amin Malik, Muhammad Arif Nadeem Saqib, Edwin Mientjes, et al.
Experimental Eye Research|March 21, 2016
Genetic analysis of consanguineous families presenting with congenital ocular defectsEhsan Ullah, Muhammad Arif Nadeem Saqib, Sundus Sajid, et al.
Frontiers in Genetics|May 16, 2022
Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual DisabilityAhmed Waqas, Anam Nayab, Shabnam Shaheen, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|November 28, 2020
Karachi Cancer Registry (KCR): Age-Standardized Incidence Rate by Age-Group and Gender in a Mega City of PakistanShahid Pervez, Adnan A Jabbar, Ghulam Haider, et al.
Pediatric Neurology|November 6, 2022
Spectrum of Common Pediatric Neurological Disorders: A Cross-Sectional Study From Three Tertiary Care Centres Across PakistanPrem Chand, Tipu Sultan, Shazia Kulsoom, et al.
Trials|August 1, 2019
Tranexamic acid for acute gastrointestinal bleeding (the HALT-IT trial): statistical analysis plan for an international, randomised, double-blind, placebo-controlled trialAmy Brenner, Adefemi Afolabi, Syed Masroor Ahmad, et al.
Journal of the Neurological Sciences|August 10, 2023
Neurological disorders and disability in Pakistan: A cross-sectional multicenter studyMohammad Wasay, Safia Awan, Naila Shahbaz, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Human Genetics|September 1, 2018
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disabilityRegie Lyn P Santos-Cortez, Valeed Khan, Falak Sher Khan, et al.
Pageof 9