Treffer 1 - 8 von 8 für Suche 'Algahtani, Raghad H', Suchdauer: 0,39s Treffer weiter einschränken
  1. 1
    Hashimoto`s Encephalopathy Presenting with Progressive Cerebellar Ataxia

    Hashimoto`s Encephalopathy Presenting with Progressive Cerebellar Ataxia von Algahtani, Hussein A, Fatani, Anmar N, Shirah, Bader H, Algahtani, Raghad H


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  2. 2
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran


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  3. 3
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Naseer, Muhammad Imran, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman


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  4. 4
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran


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  5. 5
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran


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  6. 6
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran


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  7. 7
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran


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  8. 8
    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 von Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Naseer, Muhammad Imran, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman


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