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Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause? Cover

Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause?

Open Access
|Jun 2016

References

  1. 1
    StrickPLDumRPFiezJACerebellum and nonmotor functionAnnu Rev Neurosci200932413434doi: 10.1146/annurev.neuro.31.060407.12560619555291
  2. 2
    SchmahmannJDThe role of the cerebellum in cognition and emotion: personal reflections since 1982 on the Dysmetria of thought hypothesis, and its historical evolution from theory to therapyNeuropsychol Rev201020236260doi: 10.1007/s11065-010-9142-x20821056
  3. 3
    BostanACDumRPStrickPLThe basal ganglia communicate with the cerebellumProc Natl Acad Sci201010784528456doi: 10.1073/pnas.100049610720404184
  4. 4
    MiddletonFAStrickPLCerebellar projections to the prefrontal cortex of the primateJ Neurosci20012170071211160449
  5. 5
    WuTHallettMThe cerebellum in Parkinson’s diseaseBrain2013136696709doi: 10.1093/brain/aws36023404337
  6. 6
    FilipPLunguOVBarešMDystonia and the cerebellum: a new field of interest in movement disordersClin Neurophysiol201312412691276doi: 10.1016/j.clinph.2013.01.00323422326
  7. 7
    MothersillOKnee-ZaskaCDonohoeGEmotion and theory of mind in schizophrenia-investigating the role of the cerebellumCerebellum201615357368doi: 10.1007/s12311-015-0696-226155761
  8. 8
    FilipPLunguOVMantoMUBarešMLinking essential tremor to the cerebellum: physiological evidenceCerebellum2015113[Epub ahead of print]doi: 10.1007/s12311-015-0740-2
  9. 9
    WongJCEscaygAIlluminating the cerebellum as a potential target for treating epilepsyEpilepsy Curr201515277278doi: 10.5698/1535-7511-15.5.27726448735
  10. 10
    DowRSFernandez-GuardiolaAManniEThe influence of the cerebellum on experimental epilepsyElectroencephalogr Clin Neurophysiol196214383398doi: 10.1016/0013-4694(62)90115-313887605
  11. 11
    HuttonJTFrostJDJrFosterJThe influence of the cerebellum in cat penicillin epilepsyEpilepsia197213401408doi: 10.1111/j.1528-1157.1972.tb04580.x4626569
  12. 12
    MesiwalaAHKurataniJDAvellinoAMRobertsTSSoteroMAEllenbogenRGFocal motor seizures with secondary generalization arising in the cerebellum. Case report and review of the literatureJ Neurosurg200297190196doi: 10.3171/jns.2002.97.1.019012134911
  13. 13
    YoungGBOppenheimerSRGordonBAet alAtaxia in institutionalized patients with epilepsyCan J Neurol Sci199421252258doi: 10.1017/S03171671000412388000981
  14. 14
    MatsumotoMNakagawaTInoueTet alAtaxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptorNature1996379168171doi: 10.1038/379168a08538767
  15. 15
    PenaSDCoimbraRLAtaxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathyClin Genet201587e13doi: 10.1111/cge.12542">10.1111/cge.12542">10.1111/cge.1254225477152
  16. 16
    CrossJHAroraRHeckemannRAet alNeurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndromeDev Med Child Neurol201355846856doi: 10.1111/dmcn.1217123924083
  17. 17
    FarhanSMMurphyLMRobinsonJFet alLinkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxiaEpilepsia201455e106111doi: 10.1111/epi.1273025060828
  18. 18
    BerkovicSFGenetics of epilepsy in clinical practiceEpilepsy Curr201515192196doi: 10.5698/1535-7511-15.4.19226316866
  19. 19
    LiaoYAnttonenAKLiukkonenEet alSCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and painNeurology20107514541458doi: 10.1212/WNL.0b013e3181f8812e20956790
  20. 20
    ImbriciPJaffeSLEunsonLHet alDysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxiaBrain200412726822692doi: 10.1093/brain/awh30115483044
  21. 21
    Leshinsky-SilverEShuvalovRInbarSCohenSLevDLerman-SagieTJuvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescenceJ Child Neurol201126476481doi: 10.1177/088307381038461521196529
  22. 22
    JoensuuTTegelbergSReinmaaEet alGene expression alterations in the cerebellum and granule neurons of Cstb(-/-) mouse are associated with early synaptic changes and inflammationPLoS One20149e89321doi: 10.1371/journal.pone.008932124586687
  23. 23
    OrtolanoSVieitezIAgis-BalboaRCSpuchCLoss of GABAergic cortical neurons underlies the neuropathology of Lafora diseaseMol Brain201477doi: 10.1186/1756-6606-7-724472629
  24. 24
    MoleSEWilliamsRENeuronal ceroid-lipofuscinosesPagonRAAdamMPArdingerHHet alGeneReviews(®) [Internet]Seattle, WAUniversity of Washington1993[cited 2015 Aug 23]Available from: http://www.ncbi.nlm.nih.gov/books/NBK1428/
  25. 25
    YadidGSotnik-BarkaiITornatoreCet alNeurochemical alterations in the cerebellum of a murine model of Niemann–Pick type C diseaseBrain Res1998799(2)250256doi: 10.1016/S0006-8993(98)00449-19675302
  26. 26
    BadhwarABerkovicSFDowlingJPet alAction myoclonus-renal failure syndrome: characterization of a unique cerebro-renal disorderBrain200412721732182doi: 10.1093/brain/awh26315364701
  27. 27
    FinstererJZarrouk MahjoubSEpilepsy in mitochondrial disordersSeizure201221316321doi: 10.1016/j.seizure.2012.03.00322459315
  28. 28
    Pérez-DueñasBTomaCOrmazábalAet alProgressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 geneJ Inherit Metab Dis201033795802doi: 10.1007/s10545-010-9196-120857335
  29. 29
    MüllerKIBekkelundSIEpilepsy in a patient with ataxia caused by vitamin E deficiencyBMJ Case Rep20112011piibcr0120113728doi: 10.1136/bcr.01.2011.3728
  30. 30
    SenSKeoughKGibsonJClinical reasoning: novel GLUT1-DS mutation: refractory seizures and ataxiaNeurology201584e111e114doi: 10.1212/WNL.000000000000146725870456
  31. 31
    JavedSSafdarAForsterAet alRefractory coeliac disease associated with late onset epilepsy, ataxia, tremor and progressive myoclonus with giant cortical evoked potentials-a case report and review of literatureSeizure201221482485doi: 10.1016/j.seizure.2012.04.00322565067
  32. 32
    BhatiaKPBrownPGregoryRet alProgressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellumBrain199511810871093doi: 10.1093/brain/118.5.10877496772
  33. 33
    NanriKShibuyaMTaguchiTHasegawaATanakaNSelective loss of Purkinje cells in a patient with anti-gliadin-antibody-positive autoimmune cerebellar ataxiaDiagn Pathol2011614doi: 10.1186/1746-1596-6-1421294863
  34. 34
    McFarlandKNLiuJLandrianIet alRepeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizuresNeurogenetics2014155964doi: 10.1007/s10048-013-0385-624318420
  35. 35
    TeiveHAMunhozRPRaskinSet alSpinocerebellar ataxia type 10: frequency of epilepsy in a large sample of Brazilian patientsMov Disord20102528752878doi: 10.1002/mds.2332420818609
  36. 36
    LinXAshizawaTRecent progress in spinocerebellar ataxia type-10 (SCA10)Cerebellum200543742doi: 10.1080/1473422051000789715895557
  37. 37
    GeorgievaZPartonMCerebellar ataxia and epilepsy with anti-GAD antibodies: treatment with IVIG and plasmapheresisBMJ Case Rep20142014piibcr2013202314doi: 10.1136/bcr-2013-202314
  38. 38
    FonnumFStorm-MathisenJWalbergFGlutamate decarboxylase in inhibitory neurons. A study of the enzyme in Purkinje cell axons and boutons in the catBrain Res197020259275doi: 10.1016/0006-8993(70)90293-35511234
  39. 39
    DamMBolwigTHertzMBajorecJLomaxPDamAMDoes seizure activity produce Purkinje cell lossEpilepsia198425747751doi: 10.1111/j.1528-1157.1984.tb03486.x6510383
  40. 40
    DoganVBAn anti-GAD autoantibody-associated cerebellar syndrome case: a curable cause of ataxiaNeurol Sci20153619291931doi: 10.1007/s10072-015-2280-426058956
  41. 41
    BürkKStrzelczykAReifPSet alMesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13)Int J Neurosci2013123278282doi: 10.3109/00207454.2012.75518023215817
  42. 42
    BelluzzoMMusho-IlbehSMontiFPizzolatoGA case of nocturnal frontal lobe epilepsy in a patient with spinocerebellar ataxia type 17Seizure201221805806doi: 10.1016/j.seizure.2012.08.00622999214
  43. 43
    GolombMRIllnerAChristensenCKWalshLEA child with Friedreich’s ataxia and epilepsyJ Child Neurol200520248250doi: 10.1177/0883073805020003120115832621
  44. 44
    BennettHSSelmanJERapinIRoseANonconvulsive epileptiform activity appearing as ataxiaAm J Dis Child19821363032doi: 10.1001/archpedi.1982.039704600180037055106
  45. 45
    SpielmeyerWThe anatomic substratum of the convulsive stateArch Neurol Psychiatry193023869875doi: 10.1001/archneurpsyc.1930.02220110025002
  46. 46
    SelhorstJBKaufmanBHorwitzSJDiphenylhydantoin-induced cerebellar degenerationArch Neurol197227453455doi: 10.1001/archneur.1972.004901700850124342796
  47. 47
    KesslerCHenningsenHReutherRChristianWCerebellar atrophy in epileptic patients: computer tomography studyFortschr Neurol Psychiatr198553437441doi: 10.1055/s-2007-10019894077007
  48. 48
    ParkKMHanYHKimTHet alCerebellar white matter changes in patients with newly diagnosed partial epilepsy of unknown etiologyClin Neurol Neurosurg20151382530doi: 10.1016/j.clineuro.2015.07.01726264723
  49. 49
    LawsonJAVogrinSBleaselAFCookMJByeAMECerebral and cerebellar volume reduction in children with intractable epilepsyEpilepsia20004114561462doi: 10.1111/j.1528-1157.2000.tb00122.x11077460
  50. 50
    HagemannGLemieuxLFreeSLet alCerebellar volumes in newly diagnosed and chronic epilepsyJ Neurol200224916511658doi: 10.1007/s00415-002-0843-912529786
  51. 51
    SalcmanMDefendiniRCorrellJGilmanSNeuropathological changes in cerebellar biopsies of epileptic patientsAnn Neurol197831019doi: 10.1002/ana.410030104655651
  52. 52
    CrooksRMitchellTThomMPatterns of cerebellar atrophy in patients with chronic epilepsy: a quantitative neuropathological studyEpilepsy Res2000416373doi: 10.1016/S0920-1211(00)00133-910924869
  53. 53
    LiYDuHXieBet alCerebellum abnormalities in idiopathic generalized epilepsy with generalized tonic-clonic seizures revealed by diffusion tensor imagingPLoS One20105e15219doi: 10.1371/journal.pone.001521921203575
  54. 54
    BohnenNIO’BrienTJMullanBPSoELCerebellar changes in partial seizures: clinical correlations of quantitative SPECT and MRI analysisEpilepsia199839640650doi: 10.1111/j.1528-1157.1998.tb01433.x9637607
  55. 55
    SavicIAltshulerLPassaroEBaxterLEngelJJrLocalized cerebellar hypometabolism in patients with complex partial seizuresEpilepsia199637781787doi: 10.1111/j.1528-1157.1996.tb00652.x8764819
  56. 56
    WonJHLeeJDChungTSParkCYLeeBIIncreased contralateral cerebellar uptake of technetium-99m-HMPAO on ictal brain SPECTJ Nucl Med1996374264298772637
  57. 57
    ShinWCHongSBTaeWSSeoDWKimSEIctal hyperperfusion of cerebellum and basal ganglia in temporal lobe epilepsy: SPECT subtraction with MRI coregistrationJ Nucl Med20014285385811390547
  58. 58
    YuWKrook-MagnusonECognitive collaborations: bidirectional functional connectivity between the cerebellum and the hippocampusFront Syst Neurosci20159177doi: 10.3389/fnsys.2015.0017726732845
  59. 59
    SpechtUMayTSchulzRet alCerebellar atrophy and prognosis after temporal lobe resectionJ Neurol Neurosurg Psychiatry199762501506doi: 10.1136/jnnp.62.5.5019153610
  60. 60
    Van GaalenJKerstensFGMaasRPHärmarkLvan de WarrenburgBPDrug-induced cerebellar ataxia: a systematic reviewCNS Drugs20142811391153doi: 10.1007/s40263-014-0200-425391707
  61. 61
    AwadaAAmenePal JumahMal BeladiK[Residual cerebellar ataxia following acute phenytoin intoxication]Rev Neurol (Paris)1999155306308doi: RNE-04-1999-155-4-0000-0000-101019-ART9510367328
  62. 62
    GuptaMPatidarYKhwajaGAChowdhuryDBatraADasguptaAPersistent cerebellar ataxia with cerebellar cognitive affective syndrome due to acute phenytoin intoxication: a case reportNeurol Asia201318107111
  63. 63
    ShanmugarajahPHoggardNHowellSet alPhenytoin and cerebellar ataxia: not all down to toxicity?J Neurol Neurosurg Psychiatry201384e2e2doi: 10.1136/jnnp-2013-306573.10325346970
  64. 64
    GazullaJErreaJMBenaventeITordesillasCJTreatment of ataxia in cortical cerebellar atrophy with the GABAergic drug gabapentin. A preliminary studyEur Neurol200452711doi: 10.1159/00007925215218338
  65. 65
    VermaRKoriPValproate-induced encephalopathy with predominant pancerebellar syndromeIndian J Pharmacol201244129130doi: 10.4103/0253-7613.9188622345888
  66. 66
    ShillHAFifeTDValproic acid toxicity mimicking multiple system atrophyNeurology20005519361937doi: 10.1212/WNL.55.12.193611134407
  67. 67
    NakamuraKYoshidaKMiyazakiDMoritaHIkedaSSpinocerebellar ataxia type 6 (SCA6): clinical pilot trial with gabapentinJ Neurol Sci2009278107111doi: 10.1016/j.jns.2008.12.01719157422
  68. 68
    HorsleyVDr. Hughlings Jackson’s views of the functions of the cerebellum, as illustrated by recent research: being the Hughlings Jackson Lecture for 1906Br Med J19071803808doi: 10.1136/bmj.1.2414.80320763157
  69. 69
    McCroryPRBladinPFBerkovicSFThe cerebellar seizures of Hughlings JacksonNeurology19995218881890doi: 10.1212/WNL.52.9.188810371539
  70. 70
    BoopSWhelessJVan PoppelKMcGregorABoopFACerebellar seizuresJ Neurosurg Pediatr201312288292doi: 10.3171/2013.5.PEDS139423808728
  71. 71
    BadawyRALaiAVogrinSJCookMJSubcortical epilepsyNeurology20138019011907doi: 10.1212/WNL.0b013e3182929f4f23671345
  72. 72
    MartinsWAPaglioliEHembMPalminiADysplastic cerebellar epilepsy: complete seizure control following resection of a gangliogliomaCerebellum2015725[Epub ahead of print]doi: 10.1007/s12311-015-0705-5
  73. 73
    StrazzerSZuccaCFiocchiIGenitoriLCastelliEEpilepsy and neuropsychologic deficit in a child with cerebellar astrocytomaJ Child Neurol200621817820doi: 10.1177/0883073806021009170116970895
  74. 74
    HarveyASJayakaPDuchownyMet alHemifacial seizures and cerebellar ganglioglioma: an epilepsy syndrome of infancy with seizures of cerebellar originAnn Neurol1996409198doi: 10.1002/ana.4104001158687198
  75. 75
    HanaiSOkazakiKFujikawaYet alHemifacial seizures due to ganglioglioma of cerebellumBrain Dev201032499501doi: 10.1016/j.braindev.2009.06.00519628347
  76. 76
    DagcinarAHilmi KayaAAli TaşdemirHKuruogluESabancilarZSavAA fourth ventricular ganglioneurocytoma representing with cerebellar epilepsy: a case report and review of the literatureEur J Paediatr Neurol200711257260doi: 10.1016/j.ejpn.2007.02.00517418600
  77. 77
    GanYCConnollyMBSteinbokPEpilepsy associated with a cerebellar arachnoid cyst: seizure control following fenestration of the cystChilds Nerv Syst200824125134doi: 10.1007/s00381-007-0439-x17680249
  78. 78
    KohKNLimBCHwangHet alCerebellum can be a possible generator of progressive myoclonusJ Child Neurol201025728731doi: 10.1177/088307380934227319773463
  79. 79
    HambergerABockENordborgCet alBiochemical correlates to cortical dysplasia, gliosis, and astrocytoma infiltration in human epileptogenic cortexNeurochem Res199318(4)511518doi: 10.1007/BF009672558474570
  80. 80
    FountasKNKapsalakiEHadjigeorgiouGCerebellar stimulation in the management of medically intractable epilepsy: a systematic and critical reviewNeurosurg Focus201029E8doi: 10.3171/2010.5.FOCUS1011120672925
  81. 81
    KrosLEelkman RoodaOHDe ZeeuwCIHoebeekFEControlling cerebellar output to treat refractory epilepsyTrends Neurosci201538787799doi: 10.1016/j.tins.2015.10.00226602765
  82. 82
    RijkersKMoers-HornikxVMHemmesRJet alSustained reduction of cerebellar activity in experimental epilepsyBioMed Res Int20152015718591doi: 10.1155/2015/71859126417599
  83. 83
    BuijinkAWGBroersmaMvan der StouweAMMet alCerebellar atrophy in cortical myoclonic tremor and not in hereditary essential tremor – a voxel-based morphometry studyCerebellum20153019doi: 10.1007/s12311-015-0734-0
  84. 84
    Krook-MagnusonESzaboGGArmstrongCOijalaMSolteszICerebellar directed optogenetic intervention inhibits spontaneous hippocampal seizures in a mouse model of temporal lobe epilepsyeNeuro20141piie.2014doi: 10.1523/eneuro.0005-14.2014
  85. 85
    BrighinaFDanieleOPiazzaAGigliaGFierroBHemispheric cerebellar rTMS to treat drug-resistant epilepsy: case reportsNeurosci Lett2006397229233doi: 10.1016/j.neulet.2005.12.05016426754
  86. 86
    LarsenJCarvillGLGardellaEet alThe phenotypic spectrum of SCN8A encephalopathyNeurology201584480489doi: 10.1212/WNL.000000000000121125568300
  87. 87
    GilfillanGDSelmerKKRoxrudIet alSLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeAm J Hum Genet20088210031010doi: 10.1016/j.ajhg.2008.01.01318342287
  88. 88
    DamajLLupien-MeilleurALortieAet alCACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptomsEur J Hum Genet20152315051512doi: 10.1038/ejhg.2015.2125735478
  89. 89
    FreezeHEklundEANgBPattersonMCNeurology of inherited glycosylation disordersLancet Neurol201211453466doi: 10.1016/S1474-4422(12)70040-622516080
  90. 90
    NachbauerWEigentlerABoeschSAcquired ataxias: the clinical spectrum, diagnosis and managementJ Neurol201526213851393doi: 10.1007/s00415-015-7685-825808499
  91. 91
    TsaoCYCerebellar ataxia, vertical supranuclear gaze palsy, sensorineural deafness, epilepsy, dementia, and hallucinations in an adolescent maleSemin Pediatr Neurol201421106108doi: 10.1016/j.spen.2014.04.01225149939
  92. 92
    HarirchianMHShandizEETurnbullJMinassianBAShahsiahRLafora disease: a case report, pathologic and genetic studyIndian J Pathol Microbiol201154374375doi: 10.4103/0377-4929.8164521623095
  93. 93
    Delgado-EscuetaAVAdvances in lafora progressive myoclonus epilepsyCurr Neurol Neurosci Rep20077(5)428433doi: 10.1007/s11910-007-0066-717764634
  94. 94
    MoleSECotmanSLGenetics of the neuronal ceroid lipofuscinoses (Batten disease). Biochimica et Biophysica Acta (BBA)Mol Basis Dis20151852(10, Part B)22372241doi: 10.1016/j.bbadis.2015.05.011
  95. 95
    Vieira de Rezende PintoWBSgobbi de SouzaPVPedrosoJLBarsottiniOGVariable phenotype and severity of sialidosis expressed in two siblings presenting with ataxia and macular cherry-red spotsJ Clin Neurosci20132013271328doi: 10.1016/j.jocn.2012.12.01423870618
  96. 96
    GrabowskiGAZimranAIdaHGaucher disease types 1 and 3: phenotypic characterization of large populations from the ICGG Gaucher RegistryAm J Hematol201590Suppl 1S12S18doi: 10.1002/ajh.2406326096741
  97. 97
    DiMauroSHiranoMMERRFPagonRAAdamMPArdingerHHet alGeneReviews(®) [Internet]Seattle, WAUniversity of Washington1993[cited 2015 Nov 23]Available from: http://www.ncbi.nlm.nih.gov/books/NBK1520/
  98. 98
    LehesjokiAEGardinerMProgressive myoclonus epilepsy: Unverricht-Lundborg disease and neuronal ceroid lipofuscinosesNoebelsJLAvoliMRogawskiMAOlsenRWDelgado-EscuetaAVJasper’s basic mechanisms of the epilepsies [Internet]4th edBethesda, MDNational Center for Biotechnology Information (US)2012[cited 2015 Aug 23]Available from: http://www.ncbi.nlm.nih.gov/books/NBK98154/.doi: 10.1093/med/9780199746545.001.0001
  99. 99
    AmromDAndermannFAndermannEAction myoclonus – renal failure syndromeGeneReviews[Internet]Seattle, WAUniversity of Washington1993[cited 2016 Mar 30, 1993Available from: http://www.ncbi.nlm.nih.gov/books/NBK333437/
  100. 100
    VaamondeJMuruzabalJTuñónTet alAbnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome)J Neurol Neurosurg Psychiatry199255128132doi: 10.1136/jnnp.55.2.1281538218
  101. 101
    MocellinRWalterfangMVelakoulisDHashimoto’s encephalopathy: epidemiology, pathogenesis and managementCNS Drugs200721799811doi: 10.2165/00023210-200721100-0000217850170
  102. 102
    WhaleyNRFujiokaSWszolekZKAutosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristicsOrphanet J Rare Dis2011633doi: 10.1186/1750-1172-6-3321619691
  103. 103
    SerratosaJMMinassianBAGaneshSGene defects in progressive myoclonus epilepsyEpilepsia20105175doi: 10.1111/j.1528-1167.2010.02861.x
  104. 104
    RossiMPerez-LloretSDoldanLet alAutosomal dominant cerebellar ataxias: a systematic review of clinical featuresEur J Neurol201421607615doi: 10.1111/ene.1235024765663
  105. 105
    TanNCKZhouYTanASCChongSSLeeWLSpinocerebellar ataxia type 2 with focal epilepsy – an unusual associationAnn Acad Med Singap20043310310615008574
  106. 106
    ChoubtumLWitoonpanichPHanchaiphiboolkulSet alAnalysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre studyBMC Neurol201515166doi: 10.1186/s12883-015-0425-y26374734
  107. 107
    MantoM-UThe wide spectrum of spinocerebellar ataxias (SCAs)Cerebellum2005426doi: 10.1080/1473422051000791415895552
  108. 108
    PulstSMSpinocerebellar ataxia type 13. GeneReviews(®) [Internet]1993[cited 2016 Mar 30]Available from: http://www.ncbi.nlm.nih.gov/books/NBK1225/
  109. 109
    ParkHKimH-JJeonBSParkinsonism in Spinocerebellar ataxiaBioMed Res Int20152015111doi: 10.1155/2015/125273
  110. 110
    Friedreich ataxia [Internet]Genetics Home Reference2016[cited 2016 Mar 30]doi: https://ghr.nlm.nih.gov/condition/friedreich-ataxia
  111. 111
    GattiRAtaxia-telangiectasiaGeneReviews[Internet]1993[cited 2016 Mar 30]Available from: http://www.ncbi.nlm.nih.gov/books/NBK26468/
DOI: https://doi.org/10.5334/tohm.331 | Journal eISSN: 2160-8288
Language: English
Submitted on: Mar 6, 2016
Accepted on: May 5, 2016
Published on: Jun 23, 2016
Published by: Columbia University Libraries/Information Services
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2016 Václav Marcián, Pavel Filip, Martin Bareš, Milan Brázdil, published by Columbia University Libraries/Information Services
This work is licensed under the Creative Commons License.