Paroxysmal word deafness secondary to focal epilepsy

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A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family.

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Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.

European journal of neurology·2015

Overexpression of miR-210 is associated with SDH-related pheochromocytomas, paragangliomas, and gastrointestinal stromal tumours.

Endocrine-related cancer·2014

SPAST mutations in Australian patients with hereditary spastic paraplegia.

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Paternal Valproate Exposure and Offspring Neurodevelopmental Outcomes.

Neurology·2026

Application of the 2024 McDonald Criteria: Earlier Diagnosis and Avoiding Misdiagnosis of Multiple Sclerosis in a Global Setting.

Neurology·2026

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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP·2026

From Pathogenicity to Mechanism: A Variant Interpretation Framework for Monogenic Epilepsy.

Clinical genetics·2026

A case report of crossed aphasia, grasping, and intermanual conflict with the left hand.

Neurocase·2026

Discovery of the Novel HLA-C*08:01:44 Allele in a Taiwanese Individual.

HLA·2026

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HLA·2026

Related Experiment Videos

Paroxysmal word deafness secondary to focal epilepsy

Related Concept Videos

Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene.

Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donation.

A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family.

Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.

Overexpression of miR-210 is associated with SDH-related pheochromocytomas, paragangliomas, and gastrointestinal stromal tumours.

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Paroxysmal word deafness secondary to focal epilepsy

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