Search Results - Mohammad Algahtani

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  1. 141
    A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia

    A novel mutation in ATM gene in a Saudi female with ataxia telangiectasia by Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

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  2. 142
    A novel variant c.3706C>T p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimer's disease 9

    A novel variant c.3706C>T p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimer's disease 9 by Algahtani, Hussein, Shirah, Bader, Alshareef, Alhusain, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

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  3. 143
    A Rare Case of Rhupus Syndrome With Systemic Involvement: A Case Report and Literature Review

    A Rare Case of Rhupus Syndrome With Systemic Involvement: A Case Report and Literature Review by Dairi, Mohammad S, Ashoor, Deema S, Babkier, Ahad S, Algahtani, Rami, Dairi, Khaled S

    Published in Cureus
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  4. 144
    A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging

    A novel mutation in TTN gene in a Saudi patient with bilateral facial weakness and scapular winging by Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

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  5. 145
    A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine

    A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine by Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

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  6. 146
    Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient

    Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient by Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Naseer, Muhammad Imran, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman

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  7. 147
    A Novel Intronic Variant in SLC2A1 Gene in a Saudi Patient with Myoclonic Epilepsy

    A Novel Intronic Variant in SLC2A1 Gene in a Saudi Patient with Myoclonic Epilepsy by Algahtani, Hussein, Shirah, Bader, Albarakaty, Ahmad, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran

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  8. 148
    Low temperature of formation of nickel germanide on crystalline germanium

    Low temperature of formation of nickel germanide on crystalline germanium by Algahtani, Fahid, Blackford, Mark, Alnassar, Mohammad Saleh N., Reeves, Geoffrey K., Leech, Patrick, Pirogova, Elena, Holland, Anthony S.

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