Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

Chronic inflammatory demyelinating polyradiculoneuropathy: a prevalence study in south east England.

Journal of neurology, neurosurgery, and psychiatry·1999

Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy.

Journal of neurology·1999

Diabetic peripheral neuropathies: their cost to patient and society and the value of knowledge of risk factors for development of interventions.

European neurology·1999

Clinical and laboratory findings in referrals for mitochondrial DNA analysis.

Archives of disease in childhood·1998

Neural architecture in transected rabbit sciatic nerve after prolonged nonreinnervation.

Journal of anatomy·1998

The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease.

Brain : a journal of neurology·1998

Evaluating consistency and variation in mainstream germline cancer genetic and genomic testing.

Journal of medical genetics·2026

Prophylactic total gastrectomy in germline CDH1 carriers: results across 25 years from a systematic review and meta-analysis.

Journal of medical genetics·2026

Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

Journal of medical genetics·2026

Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

Journal of medical genetics·2026

Solid tumours in RASopathies: insights from a large monocentric cohort and systematic review of the literature.

Journal of medical genetics·2026

Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.

Journal of medical genetics·2026

Monoamine receptors of intrinsic spinal neurons and their role in mammalian locomotor control: from physiology to pathology.

Reviews in the neurosciences·2026

Nanotechnology meets neurodegeneration: restoring lysosomal function with nanovectors.

Expert opinion on drug delivery·2026

Neurofibromatosis Type 1: An Imaging Review of Multisystem Manifestations in Children.

Journal of neuroimaging : official journal of the American Society of Neuroimaging·2026

Altered oligodendroglial cell development and increased myelination in SCN2A gain-of-function-linked epilepsy.

Acta neuropathologica communications·2026

Elevated atherogenic index of plasma in multiple sclerosis: association with metabolic profile in a cross-sectional study.

BMC neurology·2026

Combined pharmacological targeting of NAD+ metabolism preserves central and peripheral axons in an ex vivo model of Wallerian degeneration.

Experimental neurology·2026

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Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

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Chronic inflammatory demyelinating polyradiculoneuropathy: a prevalence study in south east England.

Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy.

Diabetic peripheral neuropathies: their cost to patient and society and the value of knowledge of risk factors for development of interventions.

Clinical and laboratory findings in referrals for mitochondrial DNA analysis.

Neural architecture in transected rabbit sciatic nerve after prolonged nonreinnervation.

The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease.

Evaluating consistency and variation in mainstream germline cancer genetic and genomic testing.

Prophylactic total gastrectomy in germline CDH1 carriers: results across 25 years from a systematic review and meta-analysis.

Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

Solid tumours in RASopathies: insights from a large monocentric cohort and systematic review of the literature.

Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.

Monoamine receptors of intrinsic spinal neurons and their role in mammalian locomotor control: from physiology to pathology.

Nanotechnology meets neurodegeneration: restoring lysosomal function with nanovectors.

Neurofibromatosis Type 1: An Imaging Review of Multisystem Manifestations in Children.

Altered oligodendroglial cell development and increased myelination in SCN2A gain-of-function-linked epilepsy.

Elevated atherogenic index of plasma in multiple sclerosis: association with metabolic profile in a cross-sectional study.

Combined pharmacological targeting of NAD+ metabolism preserves central and peripheral axons in an ex vivo model of Wallerian degeneration.

Related Experiment Videos

Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

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