Results 261 to 270 of about 273,790 (308)
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Inherited Peripheral Neuropathy

Seminars in Neurology, 1999
Hereditary disorders of the peripheral nerves constitute a group of frequently encountered neurological diseases. Charcot-Marie-Tooth neuropathy type 1 (CMT1) is genetically heterogeneous and characterized by demyelination with moderately to severely reduced nerve conduction velocities, absent muscle stretch reflexes and onion bulb formation.
M P, Keller, P F, Chance
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Painful peripheral neuropathy

Current Treatment Options in Neurology, 2002
Treatment of neuropathic pain is the primary focus of management for many patients with painful peripheral neuropathies. Neuropathic pain is a common feature of many peripheral neuropathies including those associated with diabetes, uremia, HIV infection, and alcohol abuse.
Gil I., Wolfe, Richard J., Barohn
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Autoimmune peripheral neuropathies

Clinica Chimica Acta, 2015
Peripheral nervous system axons and myelin have unique potential protein, proteolipid, and ganglioside antigenic determinants. Despite the existence of a blood-nerve barrier, both humoral and cellular immunity can be directed against peripheral axons and myelin.
Pierre R, Bourque   +2 more
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Autonomic Peripheral Neuropathy

Neurologic Clinics, 2005
This article provides a summary of the autonomic neuropathies, including neuropathies associated with diabetes mellitus, neuropathies due to amyloid deposition, immune-mediated autonomic neuropathies (including those associated with a paraneoplastic syndrome), inherited autonomic neuropathies, and toxic autonomic neuropathies.
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Diabetic Peripheral Neuropathy

2022
Diabetic painless and painful peripheral neuropathy remains the most frequent complication of diabetes mellitus, but the pathophysiology remains undescribed, there are no robust clinical endpoints and no efficient treatment exists. This hampers good clinical practice, fruitful clinical research and successful pharmacological trials, necessary for the ...
Røikjer, Johan; id_orcid 0000-0002-4578-1328   +1 more
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Paraneoplastic peripheral neuropathies

2020
The PNS Euronet group criteria have classified paraneoplastic peripheral neuropathies as definite or possible according as to whether the neuropathy is a classical paraneoplastic disorder, the presence of onconeural antibodies, the delay between tumor and neuropathy, and improvement of the neuropathy with tumor treatment. Denny Brown's subacute sensory
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Ischemic Peripheral Neuropathy

Physical Medicine and Rehabilitation Clinics of North America, 2001
Ischemic neuropathy from sources other than diabetes is less common, but can be encountered in clinical practice. Diagnosis can be challenging, and many patients may be referred to the electrodiagnostic laboratory. Overlapping mononeuritis multiplex is a common presentation, but distal symmetric polyneuropathy and monomelic neuropathy patterns can be ...
V, Ugalde, B S, Rosen
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ACQUIRED PERIPHERAL NEUROPATHY

Neurologic Clinics, 1997
This article reviews the acquired causes of polyneuropathy other than diabetic and acute-onset neuropathies. The author gives a general method to simplify the diagnosis of chronic polyneuropathy. The acquired polyneuropathies are discussed under four main headings: metabolic disorders, toxic or deficiency states, infections, and immune-mediated. Recent
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PAINFUL PERIPHERAL NEUROPATHIES

Medical Clinics of North America, 1999
This article reviews the current pathophysiology of painful peripheral neuropathies, their differential diagnosis, and management.
P D, Vaillancourt, H M, Langevin
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ATYPICAL PERIPHERAL NEUROPATHIES

Hand Clinics, 1992
Systemic disease and metabolic imbalance may be associated with peripheral nerve focal compressive neuropathies. The nerve may be primarily involved, or symptoms may result from chronic tenosynovitis or synovitis. We review the more commonly occurring compressive neuropathies associated with underlying systemic disorders.
P C, Dell, R M, Guzewicz
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