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

267 related items for PubMed ID: 23337011

  • 21. Williams-Beuren syndrome diagnosis using fluorescence in situ hybridization.
    Osborne LR, Joseph-George AM, Scherer SW.
    Methods Mol Med; 2006; 126():113-28. PubMed ID: 16930009
    [Abstract] [Full Text] [Related]

  • 22. Coexisting seizures in patients with infantile spasms confirmed by long-term video-electroencephalography monitoring.
    Kim H, Lee JH, Ryu HW, Lim BC, Chae JH, Choi J, Kim KJ, Hwang YS, Hwang H.
    Epilepsy Res; 2012 Aug; 101(1-2):70-5. PubMed ID: 22459640
    [Abstract] [Full Text] [Related]

  • 23. Williams-Beuren Syndrome and Burkitt Leukemia.
    Zhukova N, Naqvi A.
    J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
    [Abstract] [Full Text] [Related]

  • 24. An infant with Williams-Beuren syndrome and Ebstein anomaly.
    Williams DA, Cook AL.
    Cardiol Young; 2010 Aug; 20(4):445-7. PubMed ID: 20465859
    [Abstract] [Full Text] [Related]

  • 25. Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.
    Yau EK, Lo IF, Lam ST.
    Hong Kong Med J; 2004 Feb; 10(1):22-7. PubMed ID: 14967851
    [Abstract] [Full Text] [Related]

  • 26. Clinical and neuropsychiatric status in children with Williams-Beuren Syndrome in Upper Egypt.
    Saad K, Abdelrahman AA, Abdallah AM, Othman HA, Badry R.
    Asian J Psychiatr; 2013 Dec; 6(6):560-5. PubMed ID: 24309873
    [Abstract] [Full Text] [Related]

  • 27. Williams Syndrome with Infantile Spasms.
    Polat İ, Karaoglu P, Ayanoglu M, Yis U, Hiz S.
    Indian J Pediatr; 2015 Aug; 82(8):757-8. PubMed ID: 25772942
    [No Abstract] [Full Text] [Related]

  • 28. MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions.
    Kirchhoff M, Bisgaard AM, Bryndorf T, Gerdes T.
    Eur J Med Genet; 2007 Aug; 50(1):33-42. PubMed ID: 17090394
    [Abstract] [Full Text] [Related]

  • 29. Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.
    Ferrero GB, Biamino E, Sorasio L, Banaudi E, Peruzzi L, Forzano S, di Cantogno LV, Silengo MC.
    Eur J Med Genet; 2007 Aug; 50(5):327-37. PubMed ID: 17625998
    [Abstract] [Full Text] [Related]

  • 30. Ictal electroencephalographic findings of neonatal seizures in preterm infants.
    Okumura A, Hayakawa F, Kato T, Itomi K, Maruyama K, Kubota T, Suzuki M, Kidokoro H, Watanabe K.
    Brain Dev; 2008 Apr; 30(4):261-8. PubMed ID: 17920220
    [Abstract] [Full Text] [Related]

  • 31. Death following tonsillectomy in a child with Williams syndrome.
    Monfared A, Messner A.
    Int J Pediatr Otorhinolaryngol; 2006 Jun; 70(6):1133-5. PubMed ID: 16406078
    [Abstract] [Full Text] [Related]

  • 32. Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.
    Lugo M, Wong ZC, Billington CJ, Parrish PCR, Muldoon G, Liu D, Pober BR, Kozel BA.
    Am J Med Genet A; 2020 May; 182(5):1008-1020. PubMed ID: 32077592
    [Abstract] [Full Text] [Related]

  • 33. Diagnosis and management of medical problems in adults with Williams-Beuren syndrome.
    Pober BR, Morris CA.
    Am J Med Genet C Semin Med Genet; 2007 Aug 15; 145C(3):280-90. PubMed ID: 17639596
    [Abstract] [Full Text] [Related]

  • 34. Clinical and electrographic features of epileptic spasms persisting beyond the second year of life.
    de Menezes MA, Rho JM.
    Epilepsia; 2002 Jun 15; 43(6):623-30. PubMed ID: 12060022
    [Abstract] [Full Text] [Related]

  • 35. [Williams-Beuren syndrome: diagnosis and ocular manifestations].
    Offret H, Laplace O.
    J Fr Ophtalmol; 1995 Jun 15; 18(11):699-702. PubMed ID: 8745768
    [Abstract] [Full Text] [Related]

  • 36. Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder.
    Kaplan P, Wang PP, Francke U.
    J Child Neurol; 2001 Mar 15; 16(3):177-90. PubMed ID: 11305686
    [No Abstract] [Full Text] [Related]

  • 37. The contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.
    Vandeweyer G, Van der Aa N, Reyniers E, Kooy RF.
    Am J Hum Genet; 2012 Jun 08; 90(6):1071-8. PubMed ID: 22608712
    [Abstract] [Full Text] [Related]

  • 38. Ictal apnea of epileptic origin.
    Tezer FI, Rémi J, Noachtar S.
    Neurology; 2009 Mar 03; 72(9):855-7. PubMed ID: 19255415
    [No Abstract] [Full Text] [Related]

  • 39. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
    Mizugishi K, Yamanaka K, Kuwajima K, Kondo I.
    J Hum Genet; 1998 Mar 03; 43(3):178-81. PubMed ID: 9747030
    [Abstract] [Full Text] [Related]

  • 40. Neonatal apneic seizure of occipital lobe origin: continuous video-EEG recording.
    Castro Conde JR, González-Hernández T, González Barrios D, González Campo C.
    Pediatrics; 2012 Jun 03; 129(6):e1616-20. PubMed ID: 22641764
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 14.