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Publications by Antonio Falace

TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy

American Journal of Human Genetics
Genetics
2010English

Emerging Role of the Autophagy/Lysosomal Degradative Pathway in Neurodevelopmental Disorders With Epilepsy

Frontiers in Cellular Neuroscience
Molecular NeuroscienceCellular
2020English

Related publications

Benign Familial Infantile Epilepsy

2020English

Infantile Epilepsy With Multifocal Myoclonus Caused by TBC1D24 Mutations

Seizure : the journal of the British Epilepsy Association
MedicineNeurology
2019English

UBR5Gene Mutation Is Associated With Familial Adult Myoclonic Epilepsy in a Japanese Family

ISRN Neurology
2012English

Familial Adult Onset Myoclonic Epilepsy Associated With Migraine

Seizure : the journal of the British Epilepsy Association
MedicineNeurology
2000English

A Defect in the Retromer Accessory Protein, SNX27, Manifests by Infantile Myoclonic Epilepsy and Neurodegeneration

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2015English

Familial Adult Myoclonic Epilepsy: A New Expansion Repeats Disorder

Seizure : the journal of the British Epilepsy Association
MedicineNeurology
2019English

Juvenile Myoclonic Epilepsy: An Update

2014English

Juvenile Myoclonic Epilepsy

BMJ
2012English

Juvenile Myoclonic Epilepsy

English

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