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Hereditary Neuropathy sentence examples within copper zinc superoxide



Carbonic Anhydrase I modifies SOD1-induced motor neuron toxicity in Drosophila via ER stress pathway


Hereditary Neuropathy sentence examples within Common Hereditary Neuropathy



Charcot-Marie-Tooth neuropathy score and ambulation index are both predictors of orthotic need for patients with CMT



Novel mutation in the periaxin gene causal to Charcot–Marie–Tooth disease type 4F



Hereditary neuropathy with liability to pressure palsies



Disorders of mitochondrial dynamics in peripheral neuropathy: Clues from hereditary neuropathy and diabetes.



Rodent models with expression of PMP22: Relevance to dysmyelinating CMT and HNPP



Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion.



Novel mutations in HINT1 gene cause the autosomal recessive axonal neuropathy with neuromyotonia.



Length‐dependent MRI of hereditary neuropathy with liability to pressure palsies



Schizophrenia and Hereditary Polyneuropathy: PMP22 Deletion as a Common Pathophysiological Link?



A charcot‐marie‐tooth type 1B kindred associated with hemifacial spasm and trigeminal neuralgia



A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.



Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsy


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10.3760/CMA.J.ISSN.1671-8925.2019.10.009

Diagnostic value of sensory sparing patterns in childhood immune-mediated acute or chronic inflammatory polyneuropathy



Tracking Pain in Resting State Networks in Patients with Hereditary and Diabetic Neuropathy.


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10.1136/rapm-2019-ESRAABS2019.57

ESRA19-0709 Peripheral nerve block in the patient with pre-existing neuropathy



Genetic epidemiology, demographic, and clinical characteristics of Charcot‐Marie‐tooth disease in the island of Gran Canaria (Spain)



HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients


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10.1126/SCIENCE.365.6453.555-B

Making and breaking contacts


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10.1016/j.clinph.2019.04.350

O-34 Hereditary or inflammatory childhood neuropathy – Electrophysiological abnormalities helpful in the differentiation



Effective and safe tumor inhibition using vinblastine in medulloblastoma


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10.3760/CMA.J.ISSN.1008-6315.2019.04.020

Progress in Gene Therapy of Hereditary Neurological Ion Channel Disease



Acute neurotoxicity following vincristine due to Charcot-Marie-Tooth disease in a young child with medulloblastoma.



PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability


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