These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

1187 related items for PubMed ID: 16996580

  • 1. Familial arthropathy in Saudi Arabian children: demographic, clinical, and biochemical features.
    Al-Mayouf SM.
    Semin Arthritis Rheum; 2007 Feb; 36(4):256-61. PubMed ID: 16996580
    [Abstract] [Full Text] [Related]

  • 2. Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: clinical and molecular genetic findings in 22 patients.
    Albuhairan I, Al-Mayouf SM.
    Semin Arthritis Rheum; 2013 Oct; 43(2):292-6. PubMed ID: 23290693
    [Abstract] [Full Text] [Related]

  • 3. Joint hypermobility syndrome in childhood. A not so benign multisystem disorder?
    Adib N, Davies K, Grahame R, Woo P, Murray KJ.
    Rheumatology (Oxford); 2005 Jun; 44(6):744-50. PubMed ID: 15728418
    [Abstract] [Full Text] [Related]

  • 4. The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.
    Bahabri SA, Suwairi WM, Laxer RM, Polinkovsky A, Dalaan AA, Warman ML.
    Arthritis Rheum; 1998 Apr; 41(4):730-5. PubMed ID: 9550484
    [Abstract] [Full Text] [Related]

  • 5. Stroke in Saudi children. Epidemiology, clinical features and risk factors.
    Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Al-Nasser MN, Nasir AA, Khoja WA, Kabiraj MM.
    Saudi Med J; 2006 Mar; 27 Suppl 1():S12-20. PubMed ID: 16532126
    [Abstract] [Full Text] [Related]

  • 6. Pattern of clinical features of Kawasaki disease.
    Muzaffer MA, Al-Mayouf SM.
    Saudi Med J; 2002 Apr; 23(4):409-12. PubMed ID: 11953766
    [Abstract] [Full Text] [Related]

  • 7. Sydenham's chorea in western Pennsylvania.
    Zomorrodi A, Wald ER.
    Pediatrics; 2006 Apr; 117(4):e675-9. PubMed ID: 16533893
    [Abstract] [Full Text] [Related]

  • 8. Benign familial and non-familial infantile seizures (Fukuyama-Watanabe-Vigevano syndrome): a study of 14 cases from Saudi Arabia.
    Saadeldin IY, Housawi Y, Al Nemri A, Al Hifzi I.
    Brain Dev; 2010 May; 32(5):378-84. PubMed ID: 19464832
    [Abstract] [Full Text] [Related]

  • 9. Comparison of clinical and laboratory variables in familial versus sporadic systemic onset juvenile idiopathic arthritis.
    Al-Mayouf SM, Madi SM, AlMane K, Al Jummah S.
    J Rheumatol; 2006 Mar; 33(3):597-600. PubMed ID: 16511928
    [Abstract] [Full Text] [Related]

  • 10. Uveitis survey in children.
    Hamade IH, Al Shamsi HN, Al Dhibi H, Chacra CB, Abu El-Asrar AM, Tabbara KF.
    Br J Ophthalmol; 2009 May; 93(5):569-72. PubMed ID: 19074918
    [Abstract] [Full Text] [Related]

  • 11. New form of idiopathic osteolysis: nodulosis, arthropathy and osteolysis (NAO) syndrome.
    Al-Mayouf SM, Majeed M, Hugosson C, Bahabri S.
    Am J Med Genet; 2000 Jul 03; 93(1):5-10. PubMed ID: 10861675
    [Abstract] [Full Text] [Related]

  • 12. Al-Aqeel Sewairi syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy. The first genetic defect of matrix metalloproteinase 2 gene.
    Al-Aqeel AI.
    Saudi Med J; 2005 Jan 03; 26(1):24-30. PubMed ID: 15756348
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 60.