Works by Mahmood, Saeed

Results: 42
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    Tramadol in traumatic brain injury: Should we continue to use it?

    Published in:
    Journal of Anaesthesiology Clinical Pharmacology, 2015, v. 31, n. 3, p. 344, doi. 10.4103/0970-9185.161670
    By:
    • Mahmood, Saeed;
    • Al-Thani, Hassan;
    • El-Menyar, Ayman;
    • Alani, Mushrek;
    • Al-Hassani, Ammar;
    • Mathrdikkal, Saji;
    • Peralta, Ruben;
    • Latifi, Rifat
    Publication type:
    Article
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    Cholesterol Detection by Electrochemical Sensors: A Review.

    Published in:
    Analytical & Bioanalytical Electrochemistry, 2023, v. 15, n. 9, p. 778, doi. 10.22034/abec.2023.708107
    By:
    • Aldulaimi, Ahmed Kareem Obaid;
    • Majhool, Alhussein Arkan;
    • Saeed, Shakir Mahmood;
    • Adil, Mohaned;
    • Adhab, Ayat Hussein
    Publication type:
    Article
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    Determinants of the Quality of Life of Patients with Sickle Cell Disease in Bahrain: Implications for a Patient-Centered Management Approach at the Primary Health Care.

    Published in:
    Bahrain Medical Bulletin, 2021, v. 43, n. 2, p. 431
    By:
    • AlSaleh, Aseel;
    • Elbarbary, Abdulla;
    • Qashar, Ahmed Al;
    • Alserdieh, Faisal;
    • Alahmed, Fatema;
    • Alhaddar, Hasan;
    • Alsada, Lulwa;
    • Yosri, Mohamed;
    • Saeed, Mahmood;
    • Khudhair, Mina;
    • Salih, Motasem;
    • Fuad, Noora;
    • Alghmadi, Manal;
    • Qarqoor, Fathiya Al;
    • Almarabheh, Amer;
    • Chlif, Sadok;
    • Salah, Afif Ben
    Publication type:
    Article
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    Inflammatory bowel disease in Bahrain: single-center experience.

    Published in:
    Clinical & Experimental Gastroenterology, 2017, v. 10, p. 133, doi. 10.2147/CEG.S127909
    By:
    • Abdulla, Maheeba;
    • Al Saeed, Mahmood;
    • Fardan, Rawdha Hameed;
    • Alalwan, Hawra Faisal;
    • Almosawi, Zahra S. Ali;
    • Almahroos, Amal Fuad;
    • Al Qamish, Jehad
    Publication type:
    Article
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    Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/s13023-014-0119-3
    By:
    • Haghighi, Alireza;
    • Haack, Tobias B.;
    • Atiq, Mehnaz;
    • Mottaghi, Hassan;
    • Haghighi-Kakhki, Hamidreza;
    • Bashir, Rani A.;
    • Ahting, Uwe;
    • Feichtinger, René G.;
    • Mayr, Johannes A.;
    • Rötig, Agnès;
    • Lebre, Anne-Sophie;
    • Klopstock, Thomas;
    • Dworschak, Andrea;
    • Pulido, Nathan;
    • Saeed, Mahmood A.;
    • Saleh-Gohari, Nasrollah;
    • Holzerova, Eliska;
    • Chinnery, Patrick F.;
    • Taylor, Robert W.;
    • Prokisch, Holger
    Publication type:
    Article
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    Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.

    Published in:
    2014
    By:
    • Haghighi, Alireza;
    • Haack, Tobias B;
    • Atiq, Mehnaz;
    • Mottaghi, Hassan;
    • Haghighi-Kakhki, Hamidreza;
    • Bashir, Rani A;
    • Ahting, Uwe;
    • Feichtinger, René G;
    • Mayr, Johannes A;
    • Rötig, Agnès;
    • Lebre, Anne-Sophie;
    • Klopstock, Thomas;
    • Dworschak, Andrea;
    • Pulido, Nathan;
    • Saeed, Mahmood A;
    • Saleh-Gohari, Nasrollah;
    • Holzerova, Eliska;
    • Chinnery, Patrick F;
    • Taylor, Robert W;
    • Prokisch, Holger
    Publication type:
    journal article