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Gomez, Christopher M.
One or more keywords matched the following items that are connected to Gomez, Christopher M.
Item TypeName
Concept Caspases
Concept Caspase 3
Concept Caspase 7
Concept Caspase 9
Academic Article Focal caspase activation underlies the endplate myopathy in slow-channel syndrome.
Academic Article Skeletal muscle IP3R1 receptors amplify physiological and pathological synaptic calcium signals.
Academic Article Selective inhibition of caspases in skeletal muscle reverses the apoptotic synaptic degeneration in slow-channel myasthenic syndrome.
Academic Article Health related quality of life in Friedreich Ataxia in a large heterogeneous cohort.
Academic Article Emergent life events in the delivery of a caregiver-mediated evidence-based intervention for children with autism spectrum disorder in publicly funded mental health services.
Academic Article Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean.
Academic Article The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3.
Academic Article Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia.
Academic Article Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization.
Academic Article Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6.
Academic Article Prevalence of RFC1-mediated spinocerebellar ataxia in a North American ataxia cohort.
Academic Article Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits.
Academic Article Inertial Sensor Algorithms to Characterize Turning in Neurological Patients With Turn Hesitations.
Academic Article Commentary to: "The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6" by Rentiya et al., Cerebellum 2020;19(3):459-464).
Academic Article De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus.
Academic Article Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort.
Academic Article Gait Variability in Spinocerebellar Ataxia Assessed Using Wearable Inertial Sensors.
Academic Article CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity.
Academic Article Genotypic Differences in Networks Supporting Regional Predictors of Speech Rate in Spinocerebellar Ataxia: Preliminary Observations.
Academic Article The Transcription Factor, a1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development.
Academic Article Natural History of Friedreich Ataxia: Heterogeneity of Neurologic Progression and Consequences for Clinical Trial Design.
Academic Article HER2 c-Terminal Fragments Are Expressed via Internal Translation of the HER2 mRNA.
Academic Article Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome.
Academic Article Correction: The Transcription Factor, a1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development.
Academic Article Intermuscular Coherence in Spinocerebellar Ataxias 3 and 6: a Preliminary Study.
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