Results 51 to 60 of about 238 (143)

Subacute combined degeneration of the spinal cord masking motor neuron disease: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Subacute combined degeneration of the spinal cord is a potentially reversible myelopathy typically associated with vitamin B12 deficiency. There is predominant involvement of spinal cord posterior and lateral tracts, and manifestations include
Paula Loveland   +3 more
doaj   +1 more source

Characterization of Phylogroups, Virulence Factors and Antimicrobial Resistance in Canine Pyometra‐associated Escherichia coli

open access: yesVeterinary Medicine and Science, Volume 12, Issue 5, September 2026.
This study characterized 56 Escherichia coli isolates obtained from canine pyometra, which predominantly belonged to phylogroup B2 and harboured multiple virulence genes, with high multidrug resistance rates indicating potential clinical and zoonotic risks. ABSTRACT The presence of multidrug‐resistant extraintestinal pathogenic Escherichia coli (ExPEC)
İnci Başak Müştak   +4 more
wiley   +1 more source

Subacute Combined Degeneration as the Initial Manifestation of Folate Deficiency

open access: yesActa Médica Portuguesa
n/a.
Joana Sousa Varela   +4 more
doaj   +1 more source

Megaloblastic Anaemia with Ataxia in a Four-Year-Old Child: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Vitamin B12 deficiency is an important yet frequently neglected cause of megaloblastic anaemia in children, most notably among populations with limited access to animal food sources.
M Swetha   +3 more
doaj   +1 more source

The m.14484T>C MT‐ND6 Mutation Presenting with a Hereditary Spastic‐Paraparesis Phenotype

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Gabriel Amorelli   +4 more
wiley   +1 more source

Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy

open access: yesClinical Genetics, Volume 110, Issue 3, Page 336-346, September 2026.
Opticus atrophy—Genetic testing with WES/WGS in 62 patients with optic atrophy provided a genetic diagnosis in 21 patients (33.9%). 42.9% of these involved non‐OPA1 genes, including WFS1, ACO2, NR2F1, UCHL1, CACNA1F, and COQ2, where the genetic diagnosis prompted additional clinical evaluation, surveillance, or therapeutic intervention.
Katrine M. Johannesen   +9 more
wiley   +1 more source

Outbreak of poisoning by sodium hydrogen methylarsonate (MSMA)—an arsenic‐based herbicide—in horses in Brazil

open access: yesEquine Veterinary Journal, Volume 58, Issue 5, Page 1258-1268, September 2026.
Abstract Background Arsenic poisoning in horses is rarely reported in the literature. However, arsenic compounds can be present in rodenticides, pesticides, and herbicides, representing a potential source of accidental exposure for horses. Objective To describe the epidemiological, clinical, and laboratory findings from a herd of 31 horses exposed to ...
Gabriella Faria Pereira   +7 more
wiley   +1 more source

Nitrous oxide-induced subacute combined degeneration of the spinal cord

open access: yesProceedings of Singapore Healthcare
The differential diagnoses of a patient presenting with motor weakness is broad and requires a systematic approach at the Emergency Department when evaluating its underlying cause.
Georgina Kwek   +4 more
doaj   +1 more source

Neurophysiological Characteristics of Nitrous Oxide‐Induced Polyneuropathy: A Case Series

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Background Nitrous oxide (N2O) misuse is a growing health concern, with N2O‐induced neurological disorders increasingly reported across Europe. Among these, N2O‐induced polyneuropathy (PNP) can lead to permanent deficits, yet its neurophysiological characteristics remain inconsistently described.
Tanya Elisabeth Bentley   +3 more
wiley   +1 more source

A 50-year-old female with dysuria, dysporia, numbness and weakness of extremities

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2015
This paper reports one patient, with a history of autoimmune gastritis, who presented dysuria and dysporia for 5 years, weakness of left upper limb for one and a half years, and numbness and weakness of extremities for 2 months.
Lin PENG   +3 more
doaj  

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