Works matching AU UR-REHMAN, Aziz


Results: 304
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    Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18).

    Published in:
    Human Mutation, 2025, v. 2025, p. 1, doi. 10.1155/humu/3531508
    By:
    • Zanobio, Mariateresa;
    • Nardecchia, Francesca;
    • Cappuccio, Gerarda;
    • Onore, Maria Elena;
    • Di Letto, Pasquale;
    • Rahman, Sarah Iffat;
    • Terrone, Gaetano;
    • Ugga, Lorenzo;
    • De Giorgi, Agnese;
    • Cas, Michele Dei;
    • Trinchera, Marco;
    • Leuzzi, Vincenzo;
    • Piluso, Giulio;
    • Nigro, Vincenzo;
    • Brunetti-Pierri, Nicola;
    • Torella, Annalaura;
    • Aziz, Aziz ur Rehman
    Publication type:
    Article
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    High Occurrence of a Missense Variant (c.471C>A) in the FGF23 Gene Related to Hyperostosis–Hyperphosphatemia Syndrome With a Possible Founder Effect.

    Published in:
    Human Mutation, 2025, v. 2025, p. 1, doi. 10.1155/humu/6382674
    By:
    • Sedghi, Maryam;
    • Gharehdaghi, Elika Esmaeilzadeh;
    • Ziaee, Vahid;
    • Abbasi, Farzaneh;
    • Meybodi, Hamid Reza Aghaei;
    • Smiley, Elina;
    • Mehdizadeh, Mehrzad;
    • Raeeskarami, Seyyed Reza;
    • Aslani, Nahid;
    • Shiran, Sahar Naderi;
    • Vafadar, Mehdi;
    • Amoli, Mahsa M.;
    • Aziz, Aziz ur Rehman
    Publication type:
    Article
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    MANAGING THE RISK OF VTE IN COVID-19 PATIENTS.

    Published in:
    Multi-Knowledge Electronic Comprehensive Journal For Education & Science Publications (MECSJ), 2021, n. 39, p. 1
    By:
    • ABDULLA, JALEEL M.;
    • KHAN, BABUR QAYYUM;
    • UR REHMAN, AZIZ
    Publication type:
    Article
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