Works by Abdulrahim, Maha

Results: 5
    1

    The Status of B Vitamin in Saudi Adults: A Review.

    Published in:
    Current Research in Nutrition & Food Science, 2023, v. 11, n. 3, p. 894, doi. 10.12944/CRNFSJ.11.3.01
    By:
    • ALJAADI, ABEER M.;
    • ALSUNAID, FAHDAH F.;
    • ABDULRAHIM, MAHA;
    • ALMEHMADI, NAJLAA H.;
    • ALZABEN, ABEER SALMAN
    Publication type:
    Article
    2

    Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype.

    Published in:
    2024
    By:
    • Elsayed, Liena Elbaghir Omer;
    • AlHarbi, Norah Ayed;
    • Alqarni, Ashwaq Mohammed;
    • Eltayeb, Huda Hussein Elwasila;
    • Mostafa, Noura Mostafa Mohamed;
    • Abdulrahim, Maha Mohammed;
    • Zaid, Hadeel Ibrahim Bin;
    • Alanzi, Latifah Mansour;
    • Ababtain, Sarah Abdullah;
    • Aldulaijan, Khawlah;
    • Aloyouni, Sheka Yagub;
    • Othman, Moneeb Abdullah Kassem;
    • Alkheilewi, Mohammad Abdullah;
    • Binduraihem, Adel Mohammed;
    • Alrukban, Hadeel Abdollah;
    • Ahmed, Hiba Yousif;
    • AlRadini, Faten Abdullah;
    • Alahdal, Hadil Mohammad;
    • Mushiba, Aziza Mufareh;
    • Alzaher, Omaima Abdulazeem
    Publication type:
    Correction Notice
    3

    SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion.

    Published in:
    Journal of Inherited Metabolic Disease Reports, 2021, v. 60, n. 1, p. 75, doi. 10.1002/jmd2.12218
    By:
    • Aldosary, Mazhor;
    • Baselm, Shahad;
    • Abdulrahim, Maha;
    • Almass, Rawan;
    • Alsagob, Maysoon;
    • AlMasseri, Zainab;
    • Huma, Rozeena;
    • AlQuait, Laila;
    • Al‐Shidi, Tarfa;
    • Al‐Obeid, Eman;
    • AlBakheet, Albandary;
    • Alahideb, Basma;
    • Alahaidib, Lujane;
    • Qari, Alya;
    • Taylor, Robert W.;
    • Colak, Dilek;
    • AlSayed, Moeenaldeen D.;
    • Kaya, Namik
    Publication type:
    Article
    4

    Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies.

    Published in:
    Human Mutation, 2019, v. 40, n. 11, p. 1985, doi. 10.1002/humu.23844
    By:
    • Suleiman, Jehan;
    • Riedhammer, Korbinian M.;
    • Jicinsky, Timothy;
    • Mundt, Melinda;
    • Werner, Laurie;
    • Gusic, Mirjana;
    • Burgemeister, Anna L.;
    • Alsaif, Hessa S.;
    • Abdulrahim, Maha;
    • Moghrabi, Nabil N;
    • Nicolas‐Jilwan, Manal;
    • AlSayed, Moeenaldeen;
    • Bi, Weimin;
    • Sampath, Srirangan;
    • Alkuraya, Fowzan S.;
    • El‐Hattab, Ayman W.
    Publication type:
    Article
    5

    Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis.

    Published in:
    Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2256
    By:
    • Alabdulrazzaq, Fatima;
    • Alanzi, Talal;
    • Al‐Balool, Haya H.;
    • Gardham, Alice;
    • Wakeling, Emma;
    • Leitch, Harry G.;
    • AlSayed, Moeenaldeen;
    • Abdulrahim, Maha;
    • Aladwani, Abdulaziz;
    • Romito, Antonio;
    • Kampe, Kapil;
    • Ferdinandusse, Sacha;
    • Aboelanine, Ashraf H.;
    • Abdullah, Amira;
    • Alwadani, Amal;
    • Bastaki, Laila;
    • Vaz, Frédéric M.;
    • Bertoli‐Avella, Aida M.;
    • Marafi, Dana
    Publication type:
    Article