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Epileptic Amnesia as an Alzheimer’s Disease Mimic

Neurogenetics: Congenital Myotonic Dystrophy with asymptomatic mother may be missed by whole exome sequencing; Biopsy, DMPK1 gene testing and EMG may be required to resolve VUS in neonates, A Case report.

Camptocormia, a late complication of statin-associated autoimmune myopathy. (SAM)

At-Home Telespirometry (AHT) in Amyotrophic Lateral Sclerosis (ALS): Digital Health Technology and Quality Control