Volume 18, supplement 2, September 2016

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Progressive Myoclonus Epilepsies: State-of-the-Art (p.1-164)
Invited Editors: Berge A. Minassian, Pasquale Striano, Giuliano Avanzini
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Preface

Progressive Myoclonus Epilepsy: The Gene-Empowered Era (p.1-2)
Berge A. Minassian, Pasquale Striano, Giuliano Avanzini
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Review articles

The history of progressive myoclonus epilepsies (p.3-10)
Pierre Genton, Pasquale Striano, Berge A. Minassian
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Neurophysiology of myoclonus and progressive myoclonus epilepsies (p.11-27)
Giuliano Avanzini, Hiroshi Shibasaki, Guido Rubboli, Laura Canafoglia, Ferruccio Panzica, Silvana Franceschetti, Mark Hallett
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Unverricht-Lundborg disease (p.28-37)
Arielle Crespel, Edoardo Ferlazzo, Silvana Franceschetti, Pierre Genton, Riadh Gouider, Reetta Kälviäinen, Miikka Korja, Maria K. Lehtinen, Esa Mervaala, Michele Simonato, Annika Vaarmann
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Lafora disease (p.38-62)
Julie Turnbull, Erica Tiberia, Pasquale Striano, Pierre Genton, Stirling Carpenter, Cameron A. Ackerley, Berge A. Minassian
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SCARB2/LIMP2 deficiency in action myoclonus-renal failure syndrome (p.63-72)
Leanne Dibbens, Michael Schwake, Paul Saftig, Guido Rubboli
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Neuronal ceroid lipofuscinoses (p.73-88)
Dragos A. Nita, Sara E. Mole, Berge A. Minassian
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Sialidoses (p.89-93)
Silvana Franceschetti, Laura Canafoglia
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Myoclonus epilepsy in mitochondrial disorders (p.94-102)
Costanza Lamperti, Massimo Zeviani
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Progressive myoclonus epilepsy associated with neuroserpin inclusion bodies (neuroserpinosis) (p.103-10)
Benoit D. Roussel, David A. Lomas, Damian C. Crowther
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GOSR2: a progressive myoclonus epilepsy gene (p.111-4)
Leanne M. Dibbens, Guido Rubboli
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KCTD7-related progressive myoclonus epilepsy (p.115-9)
Patrick Van Bogaert
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Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis (p.120-7)
Edoardo Ferlazzo, Pasquale Striano, Domenico Italiano, Tiziana Calarese, Sara Gasparini, Nicola Vanni, Floriana Fruscione, Pierre Genton, Federico Zara
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Spinal muscular atrophy associated with progressive myoclonus epilepsy (p.128-34)
Haluk Topaloglu, Judith Melki
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Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations (p.135-8)
Fábio A. Nascimento, Danielle M. Andrade
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Autosomal dominant cortical tremor, myoclonus and epilepsy (p.139-44)
Pasquale Striano, Federico Zara
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Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials (p.145-53)
Roberto Michelucci, Elena Pasini, Patrizia Riguzzi, Eva Andermann, Reetta Kälviäinen, Pierre Genton
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Post-modern therapeutic approaches for progressive myoclonus epilepsy (p.154-8)
Berge A. Minassian
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