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Journal Abstract Search

200 related items for PubMed ID: 30145808

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  • 2. The natural history of progressive myoclonus ataxia.
    van der Veen S, Eggink H, Elting JWJ, Sival D, Verschuuren-Bemelmans CC, de Koning TJ, Tijssen MAJ.
    Neurobiol Dis; 2024 Sep; 199():106555. PubMed ID: 38844245
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  • 6. Hereditary branchial myoclonus with spastic paraparesis and cerebellar ataxia: a new autosomal dominant disorder.
    de Yebenes JG, Vazquez A, Rabano J, de Seijas EV, Urra DG, Obregon MC, Barquero MS, Arribas MA, Moreno JL, Alenda JR.
    Neurology; 1988 Apr; 38(4):569-72. PubMed ID: 3352913
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  • 10. Progressive myoclonic ataxia without ragged red fibres: Unverricht-Lundborg disease vs Ramsay Hunt syndrome.
    Shakir RA, Khan RA, al-Zuhair AG.
    Acta Neurol Scand; 1992 Nov; 86(5):470-3. PubMed ID: 1336290
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  • 13. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW.
    Adv Neurol; 1986 Nov; 43():33-55. PubMed ID: 3080851
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  • 14. Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.
    Oliver KL, Franceschetti S, Milligan CJ, Muona M, Mandelstam SA, Canafoglia L, Boguszewska-Chachulska AM, Korczyn AD, Bisulli F, Di Bonaventura C, Ragona F, Michelucci R, Ben-Zeev B, Straussberg R, Panzica F, Massano J, Friedman D, Crespel A, Engelsen BA, Andermann F, Andermann E, Spodar K, Lasek-Bal A, Riguzzi P, Pasini E, Tinuper P, Licchetta L, Gardella E, Lindenau M, Wulf A, Møller RS, Benninger F, Afawi Z, Rubboli G, Reid CA, Maljevic S, Lerche H, Lehesjoki AE, Petrou S, Berkovic SF.
    Ann Neurol; 2017 May; 81(5):677-689. PubMed ID: 28380698
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  • 15. [The basic hereditary myoclonus-epilepsy-dementia syndromes. Progressive myoclonus epilepsies--myoclonic cerebellar dyssynergia--myoclonic variants of the 3 postinfantile types of amaurotic idiocy].
    Diebold K.
    Monogr Gesamtgeb Psychiatr Psychiatry Ser; 1973 May; 8():1-254. PubMed ID: 4269086
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  • 17. Elemental mercury poisoning probably causes cortical myoclonus.
    Ragothaman M, Kulkarni G, Ashraf VV, Pal PK, Chickabasavaiah Y, Shankar SK, Govindappa SS, Satishchandra P, Muthane UB.
    Mov Disord; 2007 Oct 15; 22(13):1964-8. PubMed ID: 17708573
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  • 18. The Ramsay Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalomyopathy with ragged-red fibers and Baltic myoclonus.
    Genton P, Michelucci R, Tassinari CA, Roger J.
    Acta Neurol Scand; 1990 Jan 15; 81(1):8-15. PubMed ID: 2109922
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  • 20. Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum.
    Bhatia KP, Brown P, Gregory R, Lennox GG, Manji H, Thompson PD, Ellison DW, Marsden CD.
    Brain; 1995 Oct 15; 118 ( Pt 5)():1087-93. PubMed ID: 7496772
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