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

155 related items for PubMed ID: 487310

  • 21. Pneumoencephalographic radio-anatomical variants in the posterior cranial fossa.
    Hammer B, Scherrer H.
    Neuroradiology; 1973 Apr; 5(2):107-10. PubMed ID: 4788968
    [No Abstract] [Full Text] [Related]

  • 22. Erythrocyte protoporphyrin levels in patients with Friedreich's and other ataxias.
    Morgan RO, Naglie G, Horrobin DF, Barbeau A.
    Can J Neurol Sci; 1979 May; 6(2):227-32. PubMed ID: 487315
    [Abstract] [Full Text] [Related]

  • 23. Movement disorders in mitochondrial diseases.
    Tranchant C, Anheim M.
    Rev Neurol (Paris); 2016 May; 172(8-9):524-529. PubMed ID: 27476418
    [Abstract] [Full Text] [Related]

  • 24. Retinal and pontine striations: neurodiagnostic signs of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Leavitt JA, Singer W, Brown WL, Pulido JS, Brodsky MC.
    J Neuroophthalmol; 2014 Dec; 34(4):369-71. PubMed ID: 25237835
    [Abstract] [Full Text] [Related]

  • 25. Visual involvement in Friedreich's ataxia and hereditary spastic ataxia. A clinical and visual evoked response study.
    Livingstone IR, Mastaglia FL, Edis R, Howe JW.
    Arch Neurol; 1981 Feb; 38(2):75-9. PubMed ID: 7469840
    [Abstract] [Full Text] [Related]

  • 26. Radiology of a large cisterna magna cyst. A case report.
    Alker GJ, Glasauer FE, Leslie EV.
    Arch Neurol; 1979 Jun; 36(6):376-9. PubMed ID: 454237
    [Abstract] [Full Text] [Related]

  • 27. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
    Sridharan R, Radhakrishnan K, Ashok PP, Mousa ME.
    Brain; 1985 Dec; 108 ( Pt 4)():831-43. PubMed ID: 4075075
    [Abstract] [Full Text] [Related]

  • 28. Cerebellum and neuropsychiatric disorders: insights from ARSACS.
    Mignarri A, Tessa A, Carluccio MA, Rufa A, Storti E, Bonelli G, Marcotulli C, Santorelli FM, Leonardi L, Casali C, Federico A, Dotti MT.
    Neurol Sci; 2014 Jan; 35(1):95-7. PubMed ID: 24318559
    [Abstract] [Full Text] [Related]

  • 29. Reviewing the genetic causes of spastic-ataxias.
    de Bot ST, Willemsen MA, Vermeer S, Kremer HP, van de Warrenburg BP.
    Neurology; 2012 Oct 02; 79(14):1507-14. PubMed ID: 23033504
    [Abstract] [Full Text] [Related]

  • 30. Visual, auditory and somatosensory pathway involvement in hereditary cerebellar ataxia, Friedreich's ataxia and familial spastic paraplegia.
    Pedersen L, Trojaborg W.
    Electroencephalogr Clin Neurophysiol; 1981 Oct 02; 52(4):283-97. PubMed ID: 6169505
    [Abstract] [Full Text] [Related]

  • 31. Cisternal changes produced by experimental balloon tumours in the posterior cranial fossa. A post-mortem investigation.
    Lindqvist M.
    Acta Radiol Diagn (Stockh); 1978 Oct 02; 19(4):561-77. PubMed ID: 362832
    [Abstract] [Full Text] [Related]

  • 32. [Pneumotomography of posterior cranial fossa].
    Betz H.
    Fortschr Geb Rontgenstr Nuklearmed; 1968 Sep 02; 109(3):319-24. PubMed ID: 4991611
    [No Abstract] [Full Text] [Related]

  • 33. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): typical clinical and neuroimaging features in a Brazilian family.
    Pedroso JL, Braga-Neto P, Abrahão A, Rivero RL, Abdalla C, Abdala N, Barsottini OG.
    Arq Neuropsiquiatr; 2011 Sep 02; 69(2B):288-91. PubMed ID: 21625752
    [Abstract] [Full Text] [Related]

  • 34. Oculomotor and vestibular findings in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Dionne J, Wright G, Barber H, Bouchard R, Bouchard JP.
    Can J Neurol Sci; 1979 May 02; 6(2):177-84. PubMed ID: 487307
    [Abstract] [Full Text] [Related]

  • 35. Pyruvate dehydrogenase, lipoamide dehydrogenase and citrate synthase activity in fibroblasts from patients with Friedreich's and Charlevoix-Saguenay ataxia.
    Melancon SB, Potier M, Dallaire L, Rollin P, Fontaine G, Grenier B.
    Can J Neurol Sci; 1979 May 02; 6(2):241-2. PubMed ID: 487317
    [Abstract] [Full Text] [Related]

  • 36. Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
    Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM.
    Neurology; 2004 Jan 13; 62(1):103-6. PubMed ID: 14718707
    [Abstract] [Full Text] [Related]

  • 37. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a family report from South Brazil.
    Burguêz D, Oliveira CM, Rockenbach MABC, Fussiger H, Vedolin LM, Winckler PB, Maestri MK, Finkelsztejn A, Santorelli FM, Jardim LB, Saute JAM.
    Arq Neuropsiquiatr; 2017 Jun 13; 75(6):339-344. PubMed ID: 28658401
    [Abstract] [Full Text] [Related]

  • 38. Leucocyte glutamate dehydrogenase in various hereditary ataxias.
    Barbeau A, Charbonneau M, Cloutier T.
    Can J Neurol Sci; 1980 Nov 13; 7(4):421-4. PubMed ID: 7214257
    [Abstract] [Full Text] [Related]

  • 39. Pattern-reversal visual evoked potentials in the hereditary ataxias and spinal degenerations.
    Bird TD, Crill WE.
    Ann Neurol; 1981 Mar 13; 9(3):243-50. PubMed ID: 7224589
    [Abstract] [Full Text] [Related]

  • 40. Urodynamic evaluation of patients with hereditary ataxias.
    Vezina JG, Bouchard JP, Bouchard R.
    Can J Neurol Sci; 1982 May 13; 9(2):127-9. PubMed ID: 7104878
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.