Results 11 to 20 of about 2,089 (162)

Diagnosis of Pure Ulnar Sensory Neuropathy Around the Hypothenar Area Using Orthodromic Inching Sensory Nerve Conduction Study: A Case Report [PDF]

open access: yesAnnals of Rehabilitation Medicine, 2018
Ulnar neuropathy at the wrist is an uncommon disease and pure ulnar sensory neuropathy at the wrist is even rarer. It is difficult to diagnose pure ulnar sensory neuropathy at the wrist by conventional methods.
Min Je Kim   +6 more
doaj   +1 more source

Carpal Tunnel Syndrome and Ulnar Nerve Entrapment at the Elbow Are Not Associated With Plasma Levels of Caspase-3, Caspase-8 or HSP27

open access: yesFrontiers in Neuroscience, 2022
BackgroundNerve compression disorders, such as carpal tunnel syndrome (CTS) and ulnar entrapment at the elbow (UNE), may be associated with apoptosis and neuroprotective mechanisms in the peripheral nerve that may be detected by biomarkers in the blood ...
Elin Bergsten   +8 more
doaj   +1 more source

Anatomical considerations of US-guided carpal tunnel release in daily clinical practice

open access: yesJournal of Ultrasonography, 2023
Carpal tunnel syndrome is the most frequent compression neuropathy with an incidence of one to three subjects per thousand. As specific anatomical variations might lead to unintended damage during surgical interventions, we present a review to elucidate ...
Honis Hanne-Rose   +7 more
doaj   +1 more source

Role of sonography in the diagnosis of the most common peripheral neuropathies

open access: yesPediatria i Medycyna Rodzinna, 2014
In the practice of a general practitioner, the most common peripheral neuropathy reported by patients is carpal tunnel syndrome followed by cubital tunnel syndrome.
Berta Kowalska   +1 more
doaj   +1 more source

A study to analyze the prevalence of nervous anastomosis (Martin–Gruber) in medical students

open access: yesNational Journal of Physiology, Pharmacy and Pharmacology, 2015
Background: In nerve conduction laboratory, various types of cases are encountered. These are generally referred for electrophysiological investigation of the most common syndromes such as carpel tunnel syndrome where there is partial or total sparing of
Nilesh N Kate   +4 more
doaj   +1 more source

Hereditary neuropathy with liability to pressure palsy – epidemiology and diagnosis

open access: yesAktualności Neurologiczne, 2018
The aim of the work is to present current knowledge on epidemiology, causes, symptomatology and diagnosis of hereditary neuropathy with liability to pressure palsy.
Dominik Siutka   +3 more
doaj   +1 more source

Peripheral nerve entrapments—rare causes of a common condition: case series

open access: yesAutopsy and Case Reports, 2021
Compressive syndromes of peripheral nerves both in the upper and lower limbs are part of daily clinical practice; however, the etiological diagnosis can be challenging and impact on the outcome of the patient. We report five cases with rare etiologies of
Laura Mendes de Barros   +4 more
doaj  

Consensus on the Clinical Use of Pregabalin in Peripheral Neuropathic Pain. [PDF]

open access: yesCNS Neurosci Ther
Pregabalin, a second‐generation α2δ calcium‐channel ligand, exerts potent analgesic effects in peripheral neuropathic pain by reducing calcium influx, suppressing excitatory neurotransmitter release, and decreasing neuronal hyperexcitability. Based on a PRISMA‐guided review of 139 studies and multidisciplinary expert consensus, pregabalin demonstrates ...
Lu H   +22 more
europepmc   +2 more sources

Síndrome do canal de Guyon causada por cisto sinovial Guyon's canal syndrome due to a synovial cyst

open access: yesRevista Brasileira de Ortopedia, 2010
Apresentamos um caso de síndrome do canal de Guyon por um cisto sinovial no punho esquerdo de uma paciente do sexo feminino, de 48 anos. A paciente apresentava dor e parestesia na topografia do nervo ulnar, diminuição da força muscular e deformidade na ...
Evandro Silva Ruas   +3 more
doaj   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena   +13 more
wiley   +1 more source

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