Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt–Jakob Disease MV1 Subtype
Neuropathology and Applied Neurobiology, Volume 52, Issue 3, June 2026.We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Satish K. Nemani +6 more
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A Case Report of Abdominal Myoclonus Following Anterior Cerebral Artery Stroke. [PDF]
Tremor Other Hyperkinet Mov (N Y)Nokhrina K +3 more
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Myoclonus associated with tranexamic acid administration in a patient on veno-arterial extracorporeal membrane oxygenation support: A case report. [PDF]
World J Crit Care MedDimitriadis F +12 more
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Case Report: Progressive myoclonus epilepsy as an early manifestation of neuronopathic Gaucher disease. [PDF]
Front NeurosciFang Z +5 more
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Sialidosis type I: How to alleviate disabling myoclonic seizures?-A multicenter analysis of eight cases and review of the literature. [PDF]
Epilepsia OpenGburek-Augustat J +15 more
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The "Hallett Sign" of Functional Jerky Movement Disorder. [PDF]
Mov DisordStone J +6 more
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Serotonin syndrome associated with concomitant tramadol and linezolid therapy: a case report and literature review. [PDF]
Front PharmacolZhao H, Liu K, Zheng Y, Ni L.
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Prenatal-Onset Lethal Adenylosuccinate Lyase Deficiency Diagnosed by Rapid Whole Genome Sequencing: A Case Report. [PDF]
CureusDusek J +5 more
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Gastrointestinal Pseudo‐Obstruction Is Not an Uncommon Phenotypic Manifestation of POLG1 Variants
European Journal of Neurology, Volume 33, Issue 6, June 2026.
Josef Finsterer
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