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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

321 related items for PubMed ID: 25752200

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  • 23. Unverricht-Lundborg disease.
    Crespel A, Ferlazzo E, Franceschetti S, Genton P, Gouider R, Kälviäinen R, Korja M, Lehtinen MK, Mervaala E, Simonato M, Vaarmann A.
    Epileptic Disord; 2016 Sep 01; 18(S2):28-37. PubMed ID: 27582036
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  • 26. Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
    Lafrenière RG, Rochefort DL, Chrétien N, Rommens JM, Cochius JI, Kälviäinen R, Nousiainen U, Patry G, Farrell K, Söderfeldt B, Federico A, Hale BR, Cossio OH, Sørensen T, Pouliot MA, Kmiec T, Uldall P, Janszky J, Pranzatelli MR, Andermann F, Andermann E, Rouleau GA.
    Nat Genet; 1997 Mar 01; 15(3):298-302. PubMed ID: 9054946
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  • 28. Abnormal response to photic stimulation in juvenile myoclonic epilepsy: an EEG-fMRI study.
    Bartolini E, Pesaresi I, Fabbri S, Cecchi P, Giorgi FS, Sartucci F, Bonuccelli U, Cosottini M.
    Epilepsia; 2014 Jul 01; 55(7):1038-47. PubMed ID: 24861441
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  • 29. A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.
    Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK.
    Epilepsy Res; 2005 Jul 01; 66(1-3):91-8. PubMed ID: 16112844
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  • 35. The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.
    Rozycka A, Steinborn B, Trzeciak WH.
    Seizure; 2009 Oct 01; 18(8):601-3. PubMed ID: 19577488
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  • 40. The molecular genetic bases of the progressive myoclonus epilepsies.
    Serratosa JM, Gardiner RM, Lehesjoki AE, Pennacchio LA, Myers RM.
    Adv Neurol; 1999 Oct 01; 79():383-98. PubMed ID: 10514828
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