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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 12921323)

  • 41. Complex tics, stereotypies, and compulsive behavior as clinical presentation of a juvenile progressive dystonia suggestive of Hallervorden-Spatz disease.
    Nardocci N; Rumi V; Combi ML; Angelini L; Mirabile D; Bruzzone MG
    Mov Disord; 1994 May; 9(3):369-71. PubMed ID: 8041384
    [No Abstract]   [Full Text] [Related]  

  • 42. Magnetic resonance imaging in pathologically proven Hallervorden-Spatz disease.
    Schaffert DA; Johnsen SD; Johnson PC; Drayer BP
    Neurology; 1989 Mar; 39(3):440-2. PubMed ID: 2927660
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Adult onset Hallervorden-Spatz disease with psychotic symptoms.
    del Valle-López P; Pérez-García R; Sanguino-Andrés R; González-Pablos E
    Actas Esp Psiquiatr; 2011; 39(4):260-2. PubMed ID: 21769749
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life.
    Angelini L; Nardocci N; Rumi V; Zorzi C; Strada L; Savoiardo M
    J Neurol; 1992 Oct; 239(8):417-25. PubMed ID: 1447570
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Hallerborden Spatz disease.
    Raji V; Dhanasegaran SE; Usha ; Subramanian K; Suresh ; Kumar S
    J Assoc Physicians India; 2006 Apr; 54():320-2. PubMed ID: 16944616
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Hallervorden Spatz syndrome (pantothenate kinase associated neurodegeneration) in two Sardinian brother with homozygous mutation in PANK 2 gene.
    Cossu G; Melis M; Floris G; Hayflick SJ; Spissu A
    J Neurol; 2002 Nov; 249(11):1599-600. PubMed ID: 12532925
    [No Abstract]   [Full Text] [Related]  

  • 47. Unraveling the Hallervorden-Spatz syndrome: pantothenate kinase-associated neurodegeneration is the name.
    Hayflick SJ
    Curr Opin Pediatr; 2003 Dec; 15(6):572-7. PubMed ID: 14631201
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [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; 2004 Feb 16-29; 38(4):327-31. PubMed ID: 14997456
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome.
    Casteels I; Spileers W; Swinnen T; Demaerel P; Silberstein J; Casaer P; Missotten L
    Neuropediatrics; 1994 Oct; 25(5):265-7. PubMed ID: 7885538
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Hallervorden-Spatz syndrome: report of a case].
    Adamo Júnior J
    Arq Neuropsiquiatr; 1993 Mar; 51(1):130-3. PubMed ID: 8215921
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies.
    Neumann M; Adler S; Schlüter O; Kremmer E; Benecke R; Kretzschmar HA
    Acta Neuropathol; 2000 Nov; 100(5):568-74. PubMed ID: 11045680
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Pallidal deep brain stimulation for longstanding severe generalized dystonia in Hallervorden-Spatz syndrome. Case report.
    Umemura A; Jaggi JL; Dolinskas CA; Stern MB; Baltuch GH
    J Neurosurg; 2004 Apr; 100(4):706-9. PubMed ID: 15070127
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Hallervorden-Spatz syndrome in 2 Venezuelan patients].
    Peña JA; Prieto-Carrasquero M; González-Ferrer S
    Invest Clin; 1994 Jun; 35(2):105-14. PubMed ID: 7918758
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism.
    Jankovic J; Kirkpatrick JB; Blomquist KA; Langlais PJ; Bird ED
    Neurology; 1985 Feb; 35(2):227-34. PubMed ID: 3969211
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Sporadic late-onset Hallervorden-Spatz disease presenting as parkinsonism in a Chinese patient.
    Wang LN; Huang KW; Liu ZY
    Chin Med J (Engl); 1990 Aug; 103(8):686-8. PubMed ID: 2122948
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A Novel Mutation in Neurodegeneration with Brain Iron Accumulation - A Case Report.
    Nagarjunakonda S; Daggumati R; Uppala V; Gajula R; Amalakanti S
    Neurol India; 2019; 67(5):1341-1343. PubMed ID: 31744972
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical and MRI study of the Hallervorden-Spatz syndrome: long-term follow-up of one case.
    Ou SF; Chi CS; Shian WJ; Mak SC
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1994; 35(5):439-43. PubMed ID: 7942031
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Diagnosis of Hallervorden-Spatz disease using MRI, (123)I-beta-CIT-SPECT and (123)I-IBZM-SPECT.
    Hermann W; Reuter M; Barthel H; Dietrich J; Georgi P; Wagner A
    Eur Neurol; 2000; 43(3):187-8. PubMed ID: 10765064
    [No Abstract]   [Full Text] [Related]  

  • 59. Follow-up MR studies in Hallervorden-Spatz disease.
    Gallucci M; Cardona F; Arachi M; Splendiani A; Bozzao A; Passariello R
    J Comput Assist Tomogr; 1990; 14(1):118-20. PubMed ID: 2298974
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.