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جامعة القصيم
عمادة البحث العلمي
 
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شروط البحث: قسم: طب أمراض الأطفال
  • الأبحاث المنشورة بالمجلات العلمية

    • الأبحاث الفردية المنشورة في المجلات الدولية

      • Jalal Ali Bilal.

        Prevalence and Clinical Characteristics of Primary Epstein–Barr Virus Infection Among Children Presented with Cervical Lymphadenopathy

        journal of clinical and diagnostic research.
        1/7 2015
    • الأبحاث المشتركة المنشورة في المجلات الدولية

      • 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
      • 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
      • 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
      • 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
    • الأبحاث المشتركة المنشورة في المجلات المحلية أو الإقليمية

      • Bilal JA1, Alsammani MA, Ahmed MI.

        Acute Toxoplasma gondii infection in children with reactive hyperplasia of the cervical lymph nodes

        Saudi Medical Journal.
        30/7 2014
      • Jalal Ali Bilal, Eltahir Medani Elshibly.

        Etiology and clinical pattern of cervical lymphadenopathy in Sudanese children

        Sudanese Journal of Paediatrics.
        2012
      • Elsayed K.Abdelkarim, Yasser F. Abdelraheem, Emad M. Hammad, Gamal A. Askar, Ahmad Alrobaee, Hany A. Alshobaili, Abdullateef A. Alzolibani and Ahmad A. O. Alshareef.

        Role of growth hormone in children with neurofibromatosis type 1 with short stature.

        . Alazhar J of Ped..
        . Vol 12, no 2, june 2009
      • Ahmad Alrubei, Abdullatif Alzolibani, Amira Kasamel, Ahmad Settin.

        IL-10 Implications in Psoriasis

        International Journal of Health Sciences, Qassim University, Vol. 2, No. 1, pp. 53-58, (January 2008/Muharram 1429H).
        2008
      • 22. Ahmad Settin, Hala AlMarsafawy, Ahmad AlHussieny, Moataz Dowaidar..

        Dysmorphic features, consanguinity and cytogenetic pattern of congenital heart diseases, (pilot study from Mansoura Locality, Egypt).

        International Journal of Health Sciences, Qassim University, Vol. 2, No. 2, pp. 197-202, (July 2008/Jumada II 1429H).
        2008
      • Emad Hammad1, Yasser F Rezk1, Khaled Saad1, Asmaa Farghaly2.

        Study of some minerals, trace elements and antioxidants in refractory childhood epilepsy

        Alexandria Journal of Pediatrics, ,.
        july 2010
  • الأبحاث المقبولة للنشر بالمجلات العلمية

    • الأبحاث المشتركة المقبولة للنشر في المجلات الدولية

      • Rizk El-Baz1; Ahmad Settin1; Azza Ismaeel2; Abd Allah Khaleel3, Tarek Abbas3, Wafaa Tolba2, Wafaa Abd Allah2, Mohammed Abd El-Kader Sobh3.

        MTHFR C677T, A1298C and ACE I/D polymorphisms as risk factors for diabetic nephropathy among type II diabetic patients

        J Renin Angiotensin Aldosterone Syst. ..
        2012
      • Ahmad A Settina, Abdullah Alghashamb, Ahmad Alia, Moataz Dowaidara and Hisham Ismailc.

        Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared to other populations

        Hematology..
        2012
      • 2. Settin A, El-Bastar S, Gouida M, El Sherif M, Elleithy M, Girgis N..

        Flow cytometry for cell cycle parameters in healthcare workers potentially exposed to ionizing radiation.

        THE JOURNAL OF THE EGYPTIAN PUBLIC HEALTH ASSOCIATION.
        2010
      • 3. Dowaidar M, Settin A..

        Risk of Myocardial Infarction Related to Factor V Leiden Mutation (Meta-Analysis)

        GeneticTesting and Molecular Biomarkers.(in press).
        2010
    • الأبحاث المشتركة المقبولة للنشر في المجلات المحلية أو الإقليمية

      • Omer M. Suliman, Mohammed J. Ahmed, Jalal A. Bilal.

        Clinical characteristics and needle aspiration management of Bacillus Calmette-Guérin lymphadenitis in children

        Saudi Medical Journal.
        19/1 2015
  • المشاركة في المؤتمرات والندوات وورش العمل

    • المشاركات بالأوراق العلمية كمتحدث مدعو Invited speaker في المؤتمرات والندوات وورش العمل الدولية المحكمة

      • Ahmed Alfares.

        What we have learned from sequencing 3000 individuals with Hypertrophy Cardiomyopathy

        The 1st annual Meeting for the Saudi Society of Medical Genetics. April 2015.
        April 2015
      • Ahmed Alfares.

        Newborn screening programs pitfalls

        Workshop in Newborn screening.
        May 2015
      • Ahmad A Settina,Abdullah AlGashamb, Moataz Dowaidara and Hisham Ismailc.

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

        24th meeting of Saudi Biological society ;Biotechnology : reality and application ;.
        7-9/1/2009 2009
      • Hisham A Ismail(1), Abdullah A Alghasham (2), Moataz M Dowaidar(3), Ahmad A Settin(3),.

        Polymorohisms in MTHF and ACE genes and the association with hypertension among Saudi population from Qassim region

        The 4th International Conference of Biomarkers in Chronic Diseases المؤتمرالدولى الرابع للمؤشرات الحيوية فى الامراض المزمنة.
        2010
    • المشاركات بالأوراق العلمية كمتحدث مدعو Invited speaker في المؤتمرات والندوات وورش العمل المحلية أو الإقليمية المحكمة

      • Ahmed Alfares.

        Prevention Genetics

        المؤتمر الدولي لخبراء الإعاقة والتأهيل الثاني.
        Mar 2014
      • Ahmed Alfares.

        Newborn Screening and the Role of Molecular Genetics in the Era of Next-Generation Sequencing

        NEW BORN SCREENING FROM SPOT TO DIAGNOSIS AND MANAGEMENT WORKSHOP.
        December 2015
      • Ahmed Alfares.

        Molecular testing in Newborn screening

        Newborn screening workshop in Dammam.
        Feb 2016
      • Ahmed A Alfares.

        Genetics Counseling and Molecular Genetics Laboratory

        Annual Genetics Counseling Carrier Day.
        Feb 2016
    • الأبحاث المنشورة في المؤتمرات والندوات وورش العمل المحلية أو الإقليمية المحكمة

      • Fardous Abdelaal, Naglaa Mostafa, Yasser F. Abdelraheem.

        Helicobacter pylori infection in children with refractory iron deficiency anemia

        the annual scientific conference of Assuit university pediatric department, Egypt.
        September, 2008
      • Khaled H. Zidan, Amal A.Abd elsalam, Nagwa A. Mohammad, , Nasser A. El hawary, Diaa A. Alnashaar.

        molecular genetic study and prenatal diagnosis of beta-thalassemia major in upper Egypt governorates

        The annual scientific conference of Assiut University Pediatric Department and Children Hospital, Egypt.
        september 2009
    • المشاركات بالبحوث كملصقاتPosters في المؤتمرات والندوات وورش العمل الدولية المحكمة

      • Khaled H. Zidan.

        An updated review of beta-thalassemia mutations in the mediterranean area

        the 8th international conference and 1st thalassemia day, Marriot hotel, Cairo, Egypt.
        may 2004
      • Khaled H. Zidan.

        An updated review of beta-thalassemia mutations in the mediterranean area

        the 8th international conference and 1st thalassemia day, Marriot hotel, Cairo, Egypt.
        may 2004
      • A. Alfares, S. Melançon, C. Hawkins, N. Braverman..

        A case of Congenital Hypomyelinating Neuropathy, a rare disorder and expanding the natural history

        ASHG 60th Annual Meeting in Washington, DC.
        Nov 2010
      • A. Alfares, Melissa A. Kelly, Greg McDermott, Jun Shen, Samantha Baxter, Matthew Lebo, Birgit Funke, Heidi L Rehm..

        Genetic Testing for Hypertrophic Cardiomyopathy: Improving Diagnosis and Saving Healthcare Costs

        ACMG Annual Clinical Genetics Meeting in Phoenix.
        Mar 2013
      • Hannadi Alamri, Fuad Al Mutairi, Ali Alothaim, Majid Alfadhel, Ahmed Alfares.

        Diabetic Ketoacidosis in Vanishing White Matter

        The American Society of Human Genetics.
        October 2015
      • Ahmaed Settin, Abdullateef Al Zolibani, Yasser Farouq, Jalal Ali Bilal, Khalid Zedan.

        Measuring internal consistency of items used for assessment of clinical phase medical students in their pediatric course

        Conference: Saudi International Medical Education Conference (SIMEC) 2014.
        23/11 2014
    • المشاركات بالبحوث كملخصات Abstracts

      • Amal Abd-elsalam, Khaled H. Zidan, Naglaa H. El-melegy, Nagwa A. Mohammad.

        Role of antioxidants in nephrotic syndrome in children

        The annual scientific conference of Assiut University Pediatric Department and Children Hospital, Egypt.
        February 2004
  • تنظيم المؤتمرات والندوات وورش العمل

    • اللجان العلمية في المؤتمرات والندوات وورش العمل المحلية الإقليمية

      • Khaled H. Zidan.

        genetic language to physicians

        genetic research center, Ain-Shams university.
        December 2003
      • Ahmed A Alfares.

        اللجنة العلمية

        The 1st annual Meeting for the Saudi Society of Medical Genetics.
        April 2015
  • أي معلومات إضافية لم تذكر في الاستمارة حسب الترتيب السابق

    • أعمال أخري يريد الباحث إضافتها

      • Khaled H. Zidan.

        Senior Residence in Assiut University Hospital, Pediatric Department

        Master Degree of pediatric Diseases, very good in 2003.
        2000-2003 2003
      • Khaled H. Zidan.

        Intesive course for 6 months in Ain-Shams University ,Cairo, Egypt

        Center for genetic diseases, cytogenetic and molecular genetic studies.
        2003-2004 2004
 
 
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