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

323 related items for PubMed ID: 12811783

  • 1. Adult Hallervorden-Spatz syndrome simulating amyotrophic lateral sclerosis.
    Vasconcelos OM, Harter DH, Duffy C, McDonough B, Seidman JG, Seidman CE, Campbell WW.
    Muscle Nerve; 2003 Jul; 28(1):118-22. PubMed ID: 12811783
    [Abstract] [Full Text] [Related]

  • 2. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration.
    Thomas M, Hayflick SJ, Jankovic J.
    Mov Disord; 2004 Jan; 19(1):36-42. PubMed ID: 14743358
    [Abstract] [Full Text] [Related]

  • 3. Pure akinesia: an unusual phenotype of Hallervorden-Spatz syndrome.
    Molinuevo JL, Martí MJ, Blesa R, Tolosa E.
    Mov Disord; 2003 Nov; 18(11):1351-3. PubMed ID: 14639680
    [Abstract] [Full Text] [Related]

  • 4. Pantothenate kinase associated neurodegeneration (Hallervorden-Spatz syndrome).
    Kapoor S, Hortnagel K, Gogia S, Paul R, Malhotra V, Prakash A.
    Indian J Pediatr; 2005 Mar; 72(3):261-3. PubMed ID: 15812126
    [Abstract] [Full Text] [Related]

  • 5. [Tourettism, hemiballism and juvenile Parkinsonism: expanding the clinical spectrum of the neurodegeneration associated to pantothenate kinase deficiency (Hallervorden Spatz syndrome)].
    Carod-Artal FJ, Vargas AP, Marinho PB, Fernandes-Silva TV, Portugal D.
    Rev Neurol; 2005 Mar; 38(4):327-31. PubMed ID: 14997456
    [Abstract] [Full Text] [Related]

  • 6. First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene.
    Zumrová A, Krepelová A, Kyncl M, Maríková T, Prosková M, Cíbochová R, Sebronová V, Komárek V.
    Neuro Endocrinol Lett; 2005 Jun; 26(3):213-8. PubMed ID: 15990724
    [Abstract] [Full Text] [Related]

  • 7. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
    Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J.
    N Engl J Med; 2003 Jan 02; 348(1):33-40. PubMed ID: 12510040
    [Abstract] [Full Text] [Related]

  • 8. Hallervorden-Spatz syndrome in two siblings diagnosed by clinical features and magnetic resonance imaging.
    Tiamkao S, Nitinavakarn B, Jitpimolmard S.
    J Med Assoc Thai; 2000 Dec 02; 83(12):1535-40. PubMed ID: 11253896
    [Abstract] [Full Text] [Related]

  • 9. Hallervorden-Spatz syndrome resembling a typical Tourette syndrome.
    Scarano V, Pellecchia MT, Filla A, Barone P.
    Mov Disord; 2002 May 02; 17(3):618-20. PubMed ID: 12112223
    [Abstract] [Full Text] [Related]

  • 10. The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome.
    Baumeister FA, Auer DP, Hörtnagel K, Freisinger P, Meitinger T.
    Neuropediatrics; 2005 Jun 02; 36(3):221-2. PubMed ID: 15944911
    [Abstract] [Full Text] [Related]

  • 11. Frontotemporal dementia-amyotrophic lateral sclerosis complex is simulated by neurodegeneration with brain iron accumulation.
    Santillo AF, Skoglund L, Lindau M, Eeg-Olofsson KE, Tovi M, Engler H, Brundin RM, Ingvast S, Lannfelt L, Glaser A, Kilander L.
    Alzheimer Dis Assoc Disord; 2009 Jun 02; 23(3):298-300. PubMed ID: 19568152
    [Abstract] [Full Text] [Related]

  • 12. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.
    Zhou B, Westaway SK, Levinson B, Johnson MA, Gitschier J, Hayflick SJ.
    Nat Genet; 2001 Aug 02; 28(4):345-9. PubMed ID: 11479594
    [Abstract] [Full Text] [Related]

  • 13. Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation.
    Hartig MB, Hörtnagel K, Garavaglia B, Zorzi G, Kmiec T, Klopstock T, Rostasy K, Svetel M, Kostic VS, Schuelke M, Botz E, Weindl A, Novakovic I, Nardocci N, Prokisch H, Meitinger T.
    Ann Neurol; 2006 Feb 02; 59(2):248-56. PubMed ID: 16437574
    [Abstract] [Full Text] [Related]

  • 14. Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations.
    Sethi KD, Adams RJ, Loring DW, el Gammal T.
    Ann Neurol; 1988 Nov 02; 24(5):692-4. PubMed ID: 3202617
    [Abstract] [Full Text] [Related]

  • 15. [Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].
    Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 02; 22(2):189-91. PubMed ID: 15793782
    [Abstract] [Full Text] [Related]

  • 16. Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
    Valentino P, Annesi G, Cirò Candiano IC, Annesi F, Civitelli D, Tarantino P, Naso F, Spadafora P, Carrideo S, De Marco EV, Consoli D, Zappia M, Gambardella A, Quattrone A.
    Mov Disord; 2006 Feb 02; 21(2):252-4. PubMed ID: 16149094
    [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. Neurodegeneration with brain iron accumulation: clinical, radiographic and genetic heterogeneity and corresponding therapeutic options.
    Clement F, Devos D, Moreau C, Coubes P, Destee A, Defebvre L.
    Acta Neurol Belg; 2007 Mar 02; 107(1):26-31. PubMed ID: 17569231
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.