Results 91 to 100 of about 43,338 (304)

A narrative literature review about alpha‐lipoic acid role in dry eye and ocular surface disease

open access: yesActa Ophthalmologica, EarlyView.
Abstract Ocular surface diseases (OSD) include various conditions that affect the eye's surface, causing discomfort and pain. One such condition, dry eye disease (DED), is a multifactorial disorder that significantly impacts patients' quality of life, with prevalence rates ranging from 5% to 50% and higher incidence in women.
Antonio J. Mateo Orobia   +4 more
wiley   +1 more source

THE MOST FREQUENT TYPES OF DEMYELINATIVE CHARCOT-MARIE-TOOTH DISEASE IN SLOVENIA: A POPULATION-BASED STUDY

open access: yesZdravniški Vestnik, 2003
Background. The most common genetic defect in demyelinative type of Charcot-Marie-Tooth disease (CMT1) is dominantly inherited duplication of 17p11.2 (CMT1A).
Lea Leonardis   +2 more
doaj  

The Electrophysiological Evaluation of Small Fiber Neuropathy in Symptomatic Patients with Vitamin B12 Deficiency before and after Treatment

open access: yesNeurological Sciences and Neurophysiology
Background: Small fiber neuropathy (SFN) leads to sensory and autonomic dysfunction by affecting small-diameter myelinated A-delta and unmyelinated C fibers, with vitamin B12 deficiency identified as one of its causes.
Dilek Agircan   +4 more
doaj   +1 more source

Comparison of the effect of topiramate versus gabapentin on neuropathic pain in patients with polyneuropathy: A randomized clinical trial

open access: yesElectronic Physician, 2017
Background: Neuropathic pain is one of the most common complaints of neurologic clinics. Neuropathic pain is common and important and has inappropriate complications, and despite their importance, there is no effective treatment for them.
Surena Nazarbaghi   +3 more
doaj   +1 more source

Never Late: Cerebrotendinous Xanthomatosis and Improvements in Neurocognitive Functions in an Adult Patient on Chenodeoxycholic Acid Treatment

open access: yesClinical Genetics, EarlyView.
Cerebrotendinous xanthomatosis is due to biallelic pathogenic variants in CYP27A1. We report a new patient and his good neurocognitive outcome on the chenodeoxycholic acid treatment despite therapy starting at the age of 34 years. This highlights the importance of recognizing treatable inherited metabolic diseases at any age.
Randa Sultan   +6 more
wiley   +1 more source

Sensory conduction of the sural nerve in polyneuropathy [PDF]

open access: bronze, 1974
David Burke   +2 more
openalex   +1 more source

Excess Alcohol‐Induced Hospitalisations and Deaths During the First Year of the COVID‐19 Pandemic in Australia

open access: yesDrug and Alcohol Review, EarlyView.
ABSTRACT Introduction Since the onset of COVID‐19, alcohol‐related harm has increased in regions such as the United States and the United Kingdom. We examined whether alcohol‐related harm increased with the pandemic in Australia, and whether the impact varied across sex, age and type of alcohol diagnosis.
Wing See Yuen   +7 more
wiley   +1 more source

Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy

open access: yesArquivos de Neuro-Psiquiatria
Transthyretin familial amyloid polyneuropathy is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy, which if untreated, leads to death in approximately 10 years.
Marcus Vinicius Pinto   +11 more
doaj   +1 more source

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