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 *

113 related articles for article (PubMed ID: 2392218)

  • 21. Advanced neuroimaging methods in the study of movement disorders: dystonia and blepharospasm.
    Mazziotta JC; Hutchinson M; Fife TD; Woods R
    Adv Neurol; 1998; 78():153-60. PubMed ID: 9750912
    [No Abstract]   [Full Text] [Related]  

  • 22. [Nuclear magnetic resonance in the Hallervorden-Spatz syndrome].
    Vogl T; Bauer M; Seiderer M; Rath M
    Digitale Bilddiagn; 1984 Jun; 4(2):66-8. PubMed ID: 6467815
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hemi-dystonia due to focal basal ganglia lesion after head injury and improved by stereotaxic thalamotomy.
    Andrew J; Fowler C; Harrison MJ
    J Neurol Neurosurg Psychiatry; 1982 Mar; 45(3):276. PubMed ID: 7045291
    [No Abstract]   [Full Text] [Related]  

  • 24. Siblings with a progressive neurodegenerative condition associated with basal ganglia calcifications, retinitis pigmentosa and decreased levels of fucosidase--a new presentation?
    Portoian-Shuhaiber S; Gumaa K; Hamalawi H; Malla OK; Teebi AS; Al-Rashied A
    J Inherit Metab Dis; 1987; 10(4):397-8. PubMed ID: 3126360
    [No Abstract]   [Full Text] [Related]  

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

  • 26. Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome.
    Tennison MB; Bouldin TW; Whaley RA
    Neurology; 1988 Jan; 38(1):154-5. PubMed ID: 3336450
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Computed tomography in Hallervorden-Spatz disease.
    Boltshauser E; Lang W; Janzer R; Briner J; Spiess H; Kleihues P; Isler W
    Neuropediatrics; 1987 May; 18(2):81-3. PubMed ID: 3601001
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Meige syndrome (blepharospasm-oromandibular dystonia) after long-term neuroleptic therapy.
    Weiner WJ; Nausieda PA; Glantz RH
    Neurology; 1981 Dec; 31(12):1555-6. PubMed ID: 6118844
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Computed tomography in oculocraniosomatic disease (Kearns-Sayre syndrome).
    Seigel RS; Seeger JF; Gabrielsen TO; Allen RJ
    Radiology; 1979 Jan; 130(1):159-64. PubMed ID: 758643
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Blepharospasm associated with olivopontocerebellar atrophy.
    Janati A; Metzer WS; Archer RL; Nickols J; Raval J
    J Clin Neuroophthalmol; 1989 Dec; 9(4):281-4. PubMed ID: 2531169
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Blepharospasm and orofacial-cervical dystonia: clinical and pharmacological findings in 100 patients.
    Jankovic J; Ford J
    Ann Neurol; 1983 Apr; 13(4):402-11. PubMed ID: 6838174
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.
    Zhu M; Zhu X; Wan H; Hong D
    Parkinsonism Relat Disord; 2014 Mar; 20(3):353-4. PubMed ID: 24411498
    [No Abstract]   [Full Text] [Related]  

  • 34. Dystonic tremor and blepharospasm in a patient with deletion of 18q.
    Tereshko Y; Belgrado E; Lettieri C; Passon N; Damante G; Gigli GL; Valente M
    Clin Neurol Neurosurg; 2023 Jan; 224():107549. PubMed ID: 36502650
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor tics.
    Blackburn PR; Zimmermann MT; Gass JM; Harris KG; Cousin MA; Boczek NJ; Ross OA; Klee EW; Brazis PW; Van Gerpen JA; Atwal PS
    BMC Med Genet; 2016 Dec; 17(1):93. PubMed ID: 27919237
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
    Defazio G; Brancati F; Valente EM; Caputo V; Pizzuti A; Martino D; Abbruzzese G; Livrea P; Berardelli A; Dallapiccola B
    Mov Disord; 2003 Feb; 18(2):207-12. PubMed ID: 12539217
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Blepharospasm--oromandibular dystonia (Meige's syndrome) misdiagnosed as secondary hemifacial spasm.
    Gottlieb JS; May M
    Am J Otol; 1984 Jan; 5(3):206-10. PubMed ID: 6720874
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Blepharospasm: a review of 264 patients.
    Grandas F; Elston J; Quinn N; Marsden CD
    J Neurol Neurosurg Psychiatry; 1988 Jun; 51(6):767-72. PubMed ID: 3404184
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Computed tomography in Hallervorden-Spatz disease.
    Dooling EC; Richardson EP; Davis KR
    Neurology; 1980 Oct; 30(10):1128-30. PubMed ID: 7191506
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.