Search Results - Muhammad Imran Naseer
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Editorial: Current Trends in Medicinal Plant Research and Neurodegenerative Disorders by Muhammad Ayaz, Tahir Ali, Tahir Ali, Abdul Sadiq, Farhat Ullah, Muhammad Imran Naseer, Muhammad Imran Naseer
Published 2022Call Number: Loading…Connect to this object online.
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2
Identification of Novel Gene Signatures using Next-Generation Sequencing Data from COVID-19 Infection Models: Focus on Neuro-COVID and Potential Therapeutics by Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Muhammad Imran Naseer, Muhammad Imran Naseer
Published 2021Call Number: Loading…Connect to this object online.
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3
A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report by Osama Y. Muthaffar, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Abrar Ashi, Abrar Ashi, Muhammad Imran Naseer, Muhammad Imran Naseer
Published 2023Call Number: Loading…Connect to this object online.
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4
Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families by Muhammad Imran Naseer, Muhammad Imran Naseer, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar
Published 2022Call Number: Loading…Connect to this object online.
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5
Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease by Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Samah Saharti, Osama Y. Muthaffar
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6
Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy by Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrhman Abdulkareem, Angham Abdulrhman Abdulkareem, Mahmood Rasool, Mahmood Rasool, Hussein Algahtani, Osama Yousef Muthaffar, Peter Natesan Pushparaj, Peter Natesan Pushparaj
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7
Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly by Muhammad Imran Naseer, Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Yousef Muthaffar, Sameera Sogaty, Hiba Alkhatabi, Hiba Alkhatabi, Sarah Almaghrabi, Sarah Almaghrabi, Adeel G. Chaudhary, Adeel G. Chaudhary, Adeel G. Chaudhary
Published 2021Call Number: Loading…Connect to this object online.
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8
Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis by Maryam Iqbal, Sulaiman Shams, Huma Rafiq, Momin Khan, Shahid Khan, Umer Sadique Khattak, Sahib Gul Afridi, Fehmida Bibi, Angham Abdulrhman Abdulkareem, Muhammad Imran Naseer
Published 2023Call Number: Loading…Connect to this object online.
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