Results 61 to 70 of about 2,957 (204)
Muscle &Nerve, Volume 72, Issue 2, Page 286-293, August 2025.ABSTRACT Introduction/Aims Hereditary transthyretin amyloidosis (ATTRv) is an autosomal dominant multisystem disorder that occurs worldwide. The most common mutation in the United States, V142I, has previously been described as having a primarily cardiac presentation.
Urvi Desai +3 more
wiley +1 more source
Muscle &Nerve, Volume 71, Issue 6, Page 979-985, June 2025.ABSTRACT Introduction/Aims Cervical spinal cord injury (SCI) significantly impairs upper limb function, affecting patients' quality of life. Nerve transfer surgery can restore arm and hand function, but its success depends on the health of infralesional lower motor neurons (LMNs).
Adenike A. Adewuyi +4 more
wiley +1 more source
Correlation of Michigan neuropathy screening instrument, United Kingdom screening test and electrodiagnosis for early detection of diabetic peripheral neuropathy [PDF]
, 2016 Background: Almost half of Diabetic Peripheral Neuropathies (DPNs) are symptom-free. Methods including questionnaires and electrodiagnosis (EDx) can be fruitful for easy reach to early diagnosis, correct treatments of diabetic neuropathy, and so decline ...
Bagher Larijani +7 more
core +1 more source
مجله علمی دانشگاه علوم پزشکی کردستان, 2021 Background and Aim: Carpal tunnel syndrome (CTS) is the most common peripheral mononeuropathy which is caused by nerve compression, in the wrist area (carpal tunnel). The use of ultrasound for the examination and diagnosis of musculoskeletal diseases has
Zana Ramezani +3 more
doaj
Electrodiagnosis in paediatric ophthalmogenetics [PDF]
International Journal of Psychophysiology, 1994 In the present overview, practical application of the visual evoked potential (VEP) in paediatric neuro-ophthalmology is described across a wide range of ophthalmogenetic disorders, including albinism, Pelizaeus-Merzbacher disease and spastic paraplegia.
openaire +2 more sources
Clinical Genetics, Volume 107, Issue 6, Page 600-611, June 2025.This study provides clinical practice guidelines to streamline genetic testing for inherited retinal dystrophies (IRDs), underscoring the critical role of molecular diagnosis in enhancing patient care. These recommendations aim to elevate diagnostic accuracy, guide therapeutic decisions, and ultimately improve patient outcomes, marking a significant ...
João Pedro Marques +6 more
wiley +1 more source
Stimulus electrodiagnosis and motor and functional evaluations during ulnar nerve recovery
, 2016 BACKGROUND: Distal ulnar nerve injury leads to impairment of hand function due to motor and sensorial changes. Stimulus electrodiagnosis (SE) is a method of assessing and monitoring the development of this type of injury.
Cunha,Agnes F. S. +5 more
core +1 more source
Arquivos de Neuro-Psiquiatria, 2010 The temporal branch of the facial nerve is particularly vulnerable to traumatic injuries during surgical procedures. It may also be affected in clinical conditions.
Paula Fabiana Sobral da Silva +3 more
doaj +1 more source
Diagnosis and Management of Multifocal Motor Neuropathy in the United Kingdom: A Multicentre Survey
Journal of the Peripheral Nervous System, Volume 30, Issue 2, June 2025.ABSTRACT Background We conducted a survey to determine the current diagnosis and treatment of multifocal motor neuropathy (MMN) in the United Kingdom. Methods Demographic, diagnostic and treatment data were collected at nine UK neuroscience centres. Results Ninety‐five subjects were included. Mean age at diagnosis was 49.9 years (SD: 11.4).
Yusuf A. Rajabally +18 more
wiley +1 more source