Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 344

1.

A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients.

Assenza G, Benvenga A, Gennaro E, Tombini M, Campana C, Assenza F, Di Pino G, Di Lazzaro V.

Epilepsia. 2017 Feb;58(2):e31-e35. doi: 10.1111/epi.13626. Epub 2016 Nov 26. Review.

PMID:
27888502
2.

Lafora disease.

Turnbull J, Tiberia E, Striano P, Genton P, Carpenter S, Ackerley CA, Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):38-62. Review.

PMID:
27702709
3.

Neurophysiology of myoclonus and progressive myoclonus epilepsies.

Avanzini G, Shibasaki H, Rubboli G, Canafoglia L, Panzica F, Franceschetti S, Hallett M.

Epileptic Disord. 2016 Sep 1;18(S2):11-27. Review.

PMID:
27702708
4.

Spinal muscular atrophy associated with progressive myoclonus epilepsy.

Topaloglu H, Melki J.

Epileptic Disord. 2016 Sep 1;18(S2):128-134. Review.

PMID:
27647482
5.

Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.

Opri R, Fabrizi GM, Cantalupo G, Ferrarini M, Simonati A, Dalla Bernardina B, Darra F.

Seizure. 2016 Nov;42:1-6. doi: 10.1016/j.seizure.2016.08.008. Epub 2016 Sep 5. Review.

PMID:
27632409
6.

Post-modern therapeutic approaches for progressive myoclonus epilepsy.

Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):154-158. Review.

PMID:
27630083
7.

Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials.

Michelucci R, Pasini E, Riguzzi P, Andermann E, Kälviäinen R, Genton P.

Epileptic Disord. 2016 Sep 1;18(S2):145-153. Review.

PMID:
27629998
8.

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations.

Nascimento FA, Andrade DM.

Epileptic Disord. 2016 Sep 1;18(S2):135-138. Review.

PMID:
27629860
9.

KCTD7-related progressive myoclonus epilepsy.

Van Bogaert P.

Epileptic Disord. 2016 Sep 1;18(S2):115-119. Review.

PMID:
27629772
10.

Neuronal ceroid lipofuscinoses.

Nita DA, Mole SE, Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):73-88. Review.

PMID:
27629553
11.

Sialidoses.

Franceschetti S, Canafoglia L.

Epileptic Disord. 2016 Sep 1;18(S2):89-93. Review.

PMID:
27621198
12.

The history of progressive myoclonus epilepsies.

Genton P, Striano P, Minassian BA.

Epileptic Disord. 2016 Sep 1;18(S2):3-10. Review.

PMID:
27621064
13.

Autosomal dominant cortical tremor, myoclonus and epilepsy.

Striano P, Zara F.

Epileptic Disord. 2016 Sep 1;18(S2):139-144. Review.

PMID:
27618961
14.

GOSR2: a progressive myoclonus epilepsy gene.

Dibbens LM, Rubboli G.

Epileptic Disord. 2016 Sep 1;18(S2):111-114. Review.

PMID:
27618868
15.

Progressive myoclonus epilepsy associated with neuroserpin inclusion bodies (neuroserpinosis).

Roussel BD, Lomas DA, Crowther DC.

Epileptic Disord. 2016 Sep 1;18(S2):103-110. Review.

PMID:
27618835
16.

Myoclonus epilepsy in mitochondrial disorders.

Lamperti C, Zeviani M.

Epileptic Disord. 2016 Sep 1;18(S2):94-102. Review.

PMID:
27618766
17.

SCARB2/LIMP2 deficiency in action myoclonus-renal failure syndrome.

Dibbens L, Schwake M, Saftig P, Rubboli G.

Epileptic Disord. 2016 Sep 1;18(S2):63-72. Review.

PMID:
27582254
18.

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 1;18(S2):28-37. Review.

PMID:
27582036
19.

[Autophagy in Vici syndrome, mucolipidosis type IV and intractable epilepsy].

Hayashi M.

No To Hattatsu. 2016 May;48(3):184-7. Review. Japanese. No abstract available.

PMID:
27349080
20.

Infantile, Childhood, and Adolescent Epilepsies.

Wirrell E.

Continuum (Minneap Minn). 2016 Feb;22(1 Epilepsy):60-93. doi: 10.1212/CON.0000000000000269. Review.

PMID:
26844731

Supplemental Content

Loading ...
Support Center