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 *

96 related articles for article (PubMed ID: 1880538)

  • 1. Hereditary spastic dystonia: a new mitochondrial encephalopathy? Putaminal necrosis as a diagnostic sign.
    Bruyn GW; Vielvoye GJ; Went LN
    J Neurol Sci; 1991 Jun; 103(2):195-202. PubMed ID: 1880538
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings.
    Bruyn GW; Bots GT; Went LN; Klinkhamer PJ
    J Neurol Sci; 1992 Nov; 113(1):55-61. PubMed ID: 1469456
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutations.
    Meire FM; Van Coster R; Cochaux P; Obermaier-Kusser B; Candaele C; Martin JJ
    Ophthalmic Genet; 1995 Sep; 16(3):119-26. PubMed ID: 8556281
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.
    Leuzzi V; Bertini E; De Negri AM; Gallucci M; Garavaglia B
    J Neurol Neurosurg Psychiatry; 1992 Jan; 55(1):16-9. PubMed ID: 1548491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation.
    Shoffner JM; Brown MD; Stugard C; Jun AS; Pollock S; Haas RH; Kaufman A; Koontz D; Kim Y; Graham JR
    Ann Neurol; 1995 Aug; 38(2):163-9. PubMed ID: 7654063
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical variability in maternally inherited leber hereditary optic neuropathy with the G14459A mutation.
    Tarnopolsky MA; Baker SK; Myint T; Maxner CE; Robitaille J; Robinson BH
    Am J Med Genet A; 2004 Feb; 124A(4):372-6. PubMed ID: 14735584
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L; Smeets HJ; Hendrickx A; Bettink-Remeijer MW; Maat-Kievit A; Schoonderwoerd KC; Sluiter W; de Coo IF; Hintzen RQ
    Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Progressive dystonia with optic atrophy in a Jewish-Iraqi family.
    Korn-Lubetzki I; Blumenfeld A; Gomori JM; Soffer D; Steiner I
    J Neurol Sci; 1997 Oct; 151(1):57-63. PubMed ID: 9335011
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leber's hereditary optic neuropathy and complex I deficiency in muscle.
    Larsson NG; Andersen O; Holme E; Oldfors A; Wahlström J
    Ann Neurol; 1991 Nov; 30(5):701-8. PubMed ID: 1763894
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Four siblings with Hallervorden-Spatz disease.
    Vaher U; Napa A; Nurmiste A; Piirsoo A; Sibul H; Talvik T
    Brain Dev; 2001 Jul; 23(4):236-9. PubMed ID: 11377002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lesions of the putamen and dystonia: CT and magnetic resonance imaging.
    Burton K; Farrell K; Li D; Calne DB
    Neurology; 1984 Jul; 34(7):962-5. PubMed ID: 6539874
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Leber's disease and dystonia: a mitochondrial disease.
    Novotny EJ; Singh G; Wallace DC; Dorfman LJ; Louis A; Sogg RL; Steinman L
    Neurology; 1986 Aug; 36(8):1053-60. PubMed ID: 3736869
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation.
    Murakami T; Mita S; Tokunaga M; Maeda H; Ueyama H; Kumamoto T; Uchino M; Ando M
    J Neurol Sci; 1996 Oct; 142(1-2):111-3. PubMed ID: 8902729
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Putaminal necrosis presenting with hemidystonia.
    Kawano H; Takeuchi Y; Misawa A; Sawada T; Imahori Y
    Pediatr Neurol; 2000 Mar; 22(3):222-4. PubMed ID: 10734254
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss.
    Jacobson DM; Stone EM
    J Clin Neuroophthalmol; 1991 Sep; 11(3):152-7. PubMed ID: 1836796
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
    Newman NJ; Lott MT; Wallace DC
    Am J Ophthalmol; 1991 Jun; 111(6):750-62. PubMed ID: 2039048
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Idiopathic putamino-caudal atrophy: a rare cause of hemidystonia].
    Korn-Lubetzki I; Reches A
    Rev Neurol (Paris); 1994; 150(5):359-62. PubMed ID: 7878322
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial dystonia and visual failure with striatal CT lucencies.
    Marsden CD; Lang AE; Quinn NP; McDonald WI; Abdallat A; Nimri S
    J Neurol Neurosurg Psychiatry; 1986 May; 49(5):500-9. PubMed ID: 3711913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary optic neuropathies: from clinical signs to diagnosis].
    Meunier I; Lenaers G; Hamel C; Defoort-Dhellemmes S
    J Fr Ophtalmol; 2013 Dec; 36(10):886-900. PubMed ID: 24161764
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.
    Stone EM; Coppinger JM; Kardon RH; Donelson J
    Arch Ophthalmol; 1990 Oct; 108(10):1417-20. PubMed ID: 1977373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.