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Research Papers authored with others published in International Journals in the Qaseem University
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  • Research Publications in Scientific Journals

    • Research Papers authored with others published in International Journals

      • Zedan M, Gamil N, El-Assmy M, Fayez E, Nasef N, Fouda A, Settin A..

        Montelukast as an episodic modifier for acute viral bronchiolitis: a randomized trial.

        Allergy Asthma Proc. 2010 Mar;31(2):147-53..
        March 2010
      • ettin AA, Algasham A, Dowaidar M, Ismail H..

        Methylene tetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms related to overweight/obesity among Saudi subjects from Qassim Region.

        Dis Markers. 2009;27(2):97-102..
        July 2009
      • Algasham A, Ismail H, Dewaidar M, Settin AA..

        Methylenetetrahydrofolate reductase and angiotensin-converting enzyme gene polymorphisms among Saudi population from Qassim region.

        Genet Test Mol Biomarkers. 2009 Dec;13(6):817-20..
        2009
      • Settin A, Hassan H, El-Baz R, Hassan T..

        Association of cytokine gene polymorphisms with psoriasis in cases from the Nile Delta of Egypt.

        Acta Dermatovenerol Alp Panonica Adriat. 2009 Sep;18(3):105-12..
        2009
      • Settin A, Elbaz R, Abbas A, Abd-Al-Samad A, Noaman A..

        Angiotensin-converting enzyme gene insertion/deletion polymorphism in Egyptian patients with myocardial infarction.

        J Renin Angiotensin Aldosterone Syst. 2009 Jun;10(2):96-100..
        2009
      • Settin A, Ismail A, El-Magd MA, El-Baz R, Kazamel A..

        Gene polymorphisms of TNF-alpha-308 (G/A), IL-10(-1082) (G/A), IL-6(-174) (G/C) and IL-1Ra (VNTR) in Egyptian cases with type 1 diabetes mellitus.

        Autoimmunity. 2009 Jan;42(1):50-5..
        2009
      • Essam H. Jiffri, Neda Bogari, Khaled H. Zidan,Salwa Teama and Nasser A. Elhawary.

        molecular updating of β-thalassemia mutations in the upper Egyptian population

        Hemoglobin.
        34(6):538-47 2010
      • Settin A, Elshazli R, Salama A, ElBaz R..

        Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian women with unexplained recurrent pregnancy loss.

        Genet Test Mol Biomarkers..
        Dec;15(12):887-92. 2011
      • Aljarallah B, Ali A, Dowaidar M, Settin A..

        Prevalence of α-1-antitrypsin gene mutations in Saudi Arabia.

        Saudi J Gastroenterol..
        Jul-Aug;17(4):256-60. 2011
      • Settin A, Alkasem R, Ali E, ElBaz R, Mashaley AM..

        Factor V Leiden and prothrombin gene mutations in Egyptian cases with unexplained recurrent pregnancy loss.

        Hematology..
        Jan;16(1):59-63. 2011
      • Saadia Z, Alzolibani AA, Al Robaee A, Al Shobaili HA, Settin AA..

        Cutaneous Manifestations of Hypothyroidism amongst Gynecological consultations.

        Int J Health Sci (Qassim)..
        Nov;4(2):168-77. 2010
      • Trakadis YJ, Alfares A, Bodamer OA, Buyukavci M, Christodoulou J, Connor P, Glamuzina E, Gonzalez-Fernandez F, Bibi H, Echenne B, Manoli I, Mitchell J, Nordwall M, Prasad C, Scaglia F, Schiff M, Schrewe B, Touati G, Tchan MC, Varet B, Venditti CP, Zafeiriou D, Rupar CA, Rosenblatt DS, Watkins D, Braverman N..

        Update on transcobalamin deficiency: clinical presentation, treatment and outcome.

        J Inherit Metab Dis..
        Dec 2013
      • Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly M, Pugh T, Funke B, Rehm H, Lebo M..

        A systematic approach to assessing the clinical significance of genetic variants.

        Clin Genet..
        Nov 2013
      • Miller D, Alfares A..

        Whole Genome Sequencing: Ready for Prime Time?

        Clin Chem,.
        Dec 2012
      • Alfares A, Nunez LD, Al-Thihli K, Mitchell J, Melançon S, Anastasio N, Ha KC, Majewski J, Rosenblatt DS, Braverman N..

        Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype.

        J Med Genet.
        Jul 2011
      • Gribouval O, Morinière V, Pawtowski A, Arrondel C, Sallinen SL, Saloranta C, Clericuzio C, Viot G, Tantau J, Blesson S, Cloarec S, Machet MC, Chitayat D, Thauvin C, Laurent N, Sampson JR, Bernstein JA, Clemenson A, Prieur F, Daniel L, Levy-Mozziconacci A, Lachlan K, Alessandri JL, Cartault F, Rivière JP, Picard N, Baumann C, Delezoide AL, Belar Ortega M, Chassaing N, Labrune P, Yu S, Firth H, Wellesley D, Bitzan M, Alfares A, Braverman N, Krogh L, Tolmie J, Gaspar H, Doray B, Majore S, Bonneau D, Triau S, Loirat C, David A, Bartholdi D, Peleg A, Brackman D, Stone R, DeBerardinis R, Corvol P, Michaud A, Antignac C, Gubler MC..

        Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.

        Hum Mutat..
        Feb 2012
      • Laura Pilozzi-Edmonds, Thomas A. Maher, Raveen K. Basran, Aubrey Milunsky, Khalid Al-Thihli1, Nancy E. Braverman, Ahmed Alfares..

        Fraternal twins with Aarskog–Scott syndrome due to maternal germline mosaicism

        Am J Med Genet A..
        Aug 2011
      • Al Fares A, Millington GWM, Tischkowitz M..

        Dermatological features of inherited cancer syndromes in adults

        Clin Exp Dermatol.
        Feb 2010
      • A. Alfares, K. Al-Thihli, J. Mitchell, S. Melançon, D. S. Rosenblatt, N. Braverman..

        Combined malonic and methylmalonic aciduria (CMAMMA): an apparently benign organic aciduria detected through the Quebec Newborn Screening Program (QNSP)

        Society for Inherited Metabolic Disorders.
        Nov 2009
      • Jalal A Bilal, Gasim I Gasim, Mohamed T Abdien, Khalid A Elmardi, Elfatih M Malik, and Ishag Adam.

        Poor adherence to the malaria management protocol among health workers attending under-five year old febrile children at Omdurman Hospital, Sudan

        Malalria Journal.
        28/1 2015
      • Karim Eldin M Salih, Jalal A Bilal, Mona A Alfadeel, Yassin Hamid, Widad Eldouch, Elfatih Elsammani, Salah A Ibrahim, and Ishag Adam.

        Poor adherence to the World Health Organization guidelines of treatment of severe pneumonia in children at Khartoum, Sudan

        BMC Research Notes.
        14/8 2014
      • Shahad M Hussein,1 Yasir Salih,1 Duria A Rayis,1 Jalal A Bilal,2 and Ishag Adam.

        Low neonatal blood glucose levels in cesarean-delivered term newborns at Khartoum Hospital, Sudan

        Diagnostic Pathology.
        9/6 2014
      • Jalal Ali Bilal,1 Mohammad Issa Ahmad,2 Ahmad A. Al Robaee,3 Abdullateef A. Alzolibani,4 Hani A. Al Shobaili,5 and Mohammed Saleh Al-Khowailed.

        Pattern of Bacterial Colonization of Atopic Dermatitis in Saudi Children

        Journal of Clinical and Diagnostic Research.
        10/9 2013
      • Magzoub Abbas Magzoub,1,& Naser Eldin Bilal,2 Jalal Ali Bilal,3 and Omran Fadl Osman.

        Rotavirus infection among Sudanese children younger than 5 years of age: a cross sectional hospital-based study

        Pan African Medical Journal.
        10/11 2013
      • Abdullateef A. Alzolibani1 ✉, Ahmad A. Al Robaee1 , Hani A. Al Shobaili1 , Jalal A. Bilal2 , Mohammad Issa Ahmad3 , Ghada Bin Saif.

        Documentation of vancomycin-resistant Staphylococcus aureus (VRSA) among children with atopic dermatitis in the Qassim region, Saudi Arabia

        Acta Dermatovenerologica Alpina, Pannonica et Adriatica.
        25/10 2012
      • Ashour BA, Gassier A, Shami Y, Bilal JA, Adam I.

        Neonatal outcome in Misurata Central Hospital, Libya

        Journal of Science.
        4/2 2014
      • M.I. Ahmed, A.H. Aldoma, M.A. Alzohyrey, J.A. Bilal and N.S. Saeed.

        . Laboratory containment of wild polioviruses survey and inventory in Sudan

        Research Journal of Microbiology.
        2008
      • Alfares AA, Kelly MA, McDermott G, Funke BH, Lebo MS, Baxter SB, Shen J, McLaughlin HM, Clark EH, Babb LJ, Cox SW, DePalma SR, Ho CY, Seidman JG, Seidman CE, Rehm HL.

        Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity

        genetic in medicine.
        Jan 2015
      • Ashwaq AlE’ed · Abdullah AlSonbul · Sulaiman M. Al‑Mayouf.

        Safety and efficacy of combined cyclophosphamide and rituximab treatment in recalcitrant childhood lupus

        Rheumatol Int.
        12 November 2013
      • Ashwaq AlE’ed , Hadeel AlManea , Sulaiman M. Al-Mayouf.

        Childhood systemic sarcoid-like necrotizing granulomatous disease: Another piece of the puzzle

        International Journal of Pediatrics and Adolescent Medicine.
        7 October 2014
      • Alhanouf AlSaleem , Ashwaq AlE’ed , Afaf AlSaghier , Sulaiman M. Al-Mayouf.

        Vitamin D status in children with systemic lupus erythematosus and its association with clinical and laboratory parameters

        Clincal Rheumatology.
        4 November 2014
      • Ashwaq A. AlE’ed, Sulaiman M. Al-Mayouf.

        Systemic lupus erythematosus in Arab children Differences and similarities with different ethnicities

        Saudi Medical Journal.
        29 April 2014
      • Ashwaq AlE’ed, Patricia Vega-Fernandez, Eyal Muscal, Claas Hinze, Lori B. Tucker, Simone Appenzeller, Brigitte Bader-Meunier, Johannes Roth, Vicenç Torrente-Segarra, Marisa S Klein-Gitelman, Deborah M Levy, Tresa Roebuck-Spencer and Hermine Brunner.

        The Challenges of Diagnosing Cognitive Dysfunction with Neuropsychiatric Systemic Lupus Erythematosus in Childhood.

        Arthritis Care & Research.
        29 November 2016
      • Ahmed Alfares e,i,⁎, Majid Alfadhel b,c, TariqWani a, Saud Alsahli c, Iram Alluhaydan b, Fuad Al Mutairi b,c, Ali Alothaimc,e, Mohammed Albalwi c,e, Lamia Al subaie b, Saeed Alturki e,c,Waleed Al-Twaijri c,d, Muhammad Alrifai c,d, Ahmed Al-Rumayya c,d, Seham Alameer f, Eissa Faqeeh a, Ali Alasmari a, Abdulaziz Alsamman a, Soha Tashkandia a, Abdulaziz Alghamdi g, Amal Alhashemg, Brahim Tabarki g, Saad AlShahwan g, Khalid Hundallah g, SamiWali g, Homoud Al-Hebbi g, Amir Babiker h, Sarar Mohamed h, Wafaa Eyaid b,c, Abdul Ali Peer Zada a.

        A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield

        Molecular Genetics and Metabolism.
        April 2017
      • Hannadi Alamri1, Fuad Al Mutairi2,3, Johara Alothman4, Ali Alothaim1,3, Majid Alfadhel2,3 & Ahmed Alfares.

        Diabetic ketoacidosis in vanishing white matter

        Clinical Case Reports.
        March 2016
      • Majid Alfadhel1,2,3,6* , Mohammed Benmeakel2, Mohammad Arif Hossain1,7, Fuad Al Mutairi1,2,3, Ali Al Othaim2,3,4, Ahmed A. Alfares3,4,5, Mohammed Al Balwi2,3,4, Abdullah Alzaben1,2,3 and Wafaa Eyaid1,2,3.

        Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia

        Orphanet Journal of Rare Diseases.
        April 2016
      • Majid Alfadhel1 · Marwan Nashabat1 · Hanan Al Qahtani2 · Ahmed Alfares3 · Fuad Al Mutairi1 · Hesham Al Shaalan2 · Ganka V. Douglas4 · Klaas Wierenga5 · Jane Juusola4 · Muhammad Talal Alrifai6 · Stefan T. Arold7 · Fowzan Alkuraya8,9 · Qais Abu Ali4.

        Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non‑ketotic hyperglycinemia in humans

        Hum Genet.
        April 2016
      • Alfares A1, Al-Khenaizan S2,3, Al Mutairi F2,4..

        Peeling skin syndrome associated with novel variant in FLG2 gene

        Am J Med Genet A.
        Sep 2017
 
 
  عدد زيارات هذا الموقع 5756901
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