Works matching AU Rehman, Aziz ur


Results: 411
    1

    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
    2
    3
    4
    5
    6
    7
    8
    9

    Topological Study of Polycyclic Silicon Carbide Structure.

    Published in:
    Polycyclic Aromatic Compounds, 2023, v. 43, n. 2, p. 1056, doi. 10.1080/10406638.2021.2024861
    By:
    • Pan, Ying-Hao;
    • Khalid, Asma;
    • Ali, Parvez;
    • Rehman, Aziz Ur;
    • Siddiqui, Muhammad Kamran;
    • Ishtiaq, Muhammad;
    • Liu, Jia-Bao
    Publication type:
    Article
    10

    Synthesis, Spectral Evaluation and in Silico Studies of S-Aralkylated 5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiols: As suitable Alzheimer's disease drug candidates.

    Published in:
    Journal of the Chemical Society of Pakistan, 2021, v. 43, n. 6, p. 694, doi. 10.52568/000974/jcsp/43.06.2021
    By:
    • Arfan, Muhammad;
    • Siddiqui, Sabahat Zahra;
    • Abbasi, Muhammad Athar;
    • Aziz-ur-Rehman;
    • Shah, Syed Adnan Ali;
    • Ashraf, Muhammad;
    • Khan, Khalid Mohammed;
    • Saleem, Rahman Shah Zaib;
    • Zaib, Amna Shah
    Publication type:
    Article
    11

    Synthesis, Spectral Evaluation and in Silico Studies of S-Aralkylated 5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiols: As suitable Alzheimer's disease drug candidates.

    Published in:
    Journal of the Chemical Society of Pakistan, 2021, v. 43, n. 6, p. 694, doi. 10.52568/000974/JCSP/43.06.2021
    By:
    • Arfan, Muhammad;
    • Siddiqui, Sabahat Zahra;
    • Abbasi, Muhammad Athar;
    • Aziz-ur-Rehman;
    • Shah, Syed Adnan Ali;
    • Ashraf, Muhammad;
    • Khan, Khalid Mohammed;
    • Saleem, Rahman Shah Zaib;
    • Zaib, Amna Shah
    Publication type:
    Article
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49
    50

    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