Distribution of acetylcholinesterase molecular forms in neural and non-neural sections of human muscle

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.

Revue neurologique·2016

[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience].

Revue neurologique·2013

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization.

Neuropathology and applied neurobiology·2010

Muscular differentiation of chicken myotubes in a simple defined synthetic culture medium and in serum supplemented media: Expression of the molecular forms of acetylcholinesterase.

Neurochemistry international·2010

The polymorphism of cholinesterase in vertebrates.

Neurochemistry international·2010

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7.

Journal of neurology·2009

Aromatic amino acid decarboxylase - exploring the structural and functional role of its N-terminal domain using deficiency-associated variants.

FEBS letters·2026

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FEBS letters·2026

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FEBS letters·2026

DNA ligase LigE increases bacterial transformation with damaged extracellular DNA.

FEBS letters·2026

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FEBS letters·2026

Inhibition of dipeptidyl peptidase 7 impairs lysophagy in LLOMe-treated HepG2 cells.

FEBS letters·2026

Corticomuscular coupling alterations during task-dependent bimanual coordination after stroke: A multimodal functional near-infrared spectroscopy-surface electromyography analysis.

Neural regeneration research·2026

Peripheral nerve regeneration: Sensory and motor neurons and tissue engineering repair strategies.

Neural regeneration research·2026

Metformin Use Is Associated With Reduced Rates of Primary Nerve Decompression Surgery and Revision in Type 2 Diabetes: A Retrospective Cohort Study.

Journal of hand surgery global online·2026

Extradural C1-C2 Dumbbell Schwannoma Mimicking an Intradural Lesion on MRI: A Case Report.

Cureus·2026

Cross-Tissue Inflammatory Convergence Supports a Putative Muscle-Brain Axis in Alzheimer's Disease.

bioRxiv : the preprint server for biology·2026

A CNS-targeted atovaquone nanotherapy mitigates complement activation and neuromuscular degeneration in ALS.

Materials today. Bio·2026

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Distribution of acetylcholinesterase molecular forms in neural and non-neural sections of human muscle

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Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.

[Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy--The French National Congenital Myasthenic Syndrome Network experience].

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization.

Muscular differentiation of chicken myotubes in a simple defined synthetic culture medium and in serum supplemented media: Expression of the molecular forms of acetylcholinesterase.

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Distribution of acetylcholinesterase molecular forms in neural and non-neural sections of human muscle

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