Hereditary Hyperekplexia Latest Advances
Find the Latest Research About Hereditary Hyperekplexia
Last Updated: 09/26/2026
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Found 1307 publications
Pearls & Oy-sters: DPPX Antibody-Associated Encephalitis in a Patient With Diarrhea, Tremor, Ocular Flutter, and Cognitive-Psychiatric Changes.
Journal: Neurology
Published: September 01, 2026
An atomic interaction conserved for over 600 million years gates inhibitory neurotransmission.
Journal: bioRxiv : the preprint server for biology
Published: June 05, 2026
Stiff-person syndrome; the diagnostic challenges of a treatable condition
Journal: Nederlands tijdschrift voor geneeskunde
Published: June 02, 2026
DYT-PRKRA Dystonia-Parkinsonism with Pathological Startle: Expanding the Phenotype of PRKRA-Related Disease.
Journal: Movement disorders clinical practice
Published: May 27, 2026
GLRB-Related Hyperekplexia Presenting as Neonatal Seizure-Like Events.
Journal: Journal of paediatrics and child health
Published: May 12, 2026
Individualized repetitive intravenous immunoglobulin therapy for a 79-year-old patient with GlyR antibody-positive PERM: a case report and literature review.
Journal: Frontiers in immunology
Published: April 28, 2026
Case Report: Efgartigimod: a beacon of hope for overlapping stiff-person syndrome and myasthenia gravis following thymoma.
Journal: Frontiers in immunology
Published: March 09, 2026
Sequential efgartigimod and ofatumumab for stiff-person syndrome: a case report illustrating a pathophysiology-informed strategy and literature review.
Journal: Frontiers in immunology
Published: February 15, 2026
Botulinum Toxin Treatment of Stiff Person Syndrome-A Critical Review and Update.
Journal: Toxins
Published: February 01, 2026
Stiff person syndrome: an overview.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 29, 2026
Last Updated: 09/26/2026