Results 41 to 50 of about 308,984 (157)

Diabetic Foot Syndrome: A Paradigm of Complexity and a Call for Comprehensive Ownership by the Diabetologists

open access: yes
Diabetes/Metabolism Research and Reviews, Volume 42, Issue 6, September 2026.
Vittorio Oteri, Luca Dalla Paola
wiley   +1 more source

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long‐Read Sequencing and RNA Analysis

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 9, September 2026.
Long‐read sequencing phased multiple VPS41 variants and established the biallelic configuration in a patient with autosomal recessive spinocerebellar ataxia 29. Transcript analysis revealed distinct allele‐specific splicing abnormalities, while the patient also showed clinical features beyond the typical phenotype.
Natsuki Nakamura   +17 more
wiley   +1 more source

Charcot foot

open access: yesLa Revue du praticien, 2021
Noura, Naji   +3 more
  +5 more sources

Risk factors for Charcot foot

open access: yes, 2015
Objective Diabetes mellitus is the main cause of Charcot neuroarthropathy and is clinically classified as follows: Charcot foot, acute Charcot foot (ACF) when there is inflammation, and inactive Charcot foot when inflammatory signs are absent. The aim of
Marcos André Lima Nunes (6154964)   +8 more
core   +1 more source

Exploring Awareness of and Self‐Reported Adherence to Neuromuscular Clinical Practice Guidelines Among Australian and New Zealand Health Professionals: A Cross‐Sectional Survey Study

open access: yesJournal of Evaluation in Clinical Practice, Volume 32, Issue 6, September 2026.
ABSTRACT Background and Purpose There is limited evidence describing awareness and adherence to clinical practice guidelines for neuromuscular disorders. This study aimed to assess awareness of and self‐reported adherence to clinical practice guidelines for neuromuscular disorders among Australian and New Zealand health professionals.
Rachel A. Kennedy   +6 more
wiley   +1 more source

Charcot’s foot

open access: yesJournal of Experimental and Clinical Medicine, 2014
Charcot’s arthropathy which occurs due to loss of pain and proprioceptive sensation is a chronic, destructive joint disease affecting bone, joint and soft tissues. Although it may be seen as a part of many diseases which cause peripheral neuropathy, most common cause is diabetic neuropathy.
TİTİZ, Hafize   +5 more
openaire   +3 more sources

Clinical Development of Therapies for Charcot–Marie–Tooth Disease: Recommendations for Trial Design, Endpoints, and Regulatory Pathways

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Charcot–Marie–Tooth disease (CMT) encompasses a heterogeneous group of inherited peripheral neuropathies. Despite being the most common genetic neurological condition, individual CMT subtypes are rare, presenting unique challenges for therapeutic development.
Charles K. Abrams   +24 more
wiley   +1 more source

Initiative for Quality Improvement and Epidemiology in Multidisciplinary Diabetic Foot Clinics (IQED-Foot) - Results of the 4th data collection (audit years 2013-2014)

open access: yes, 2017
<p>This report describes the results of the fourth audit among the recognized diabetic foot clinics in Belgium (hereafter referred to as “centres”). The results are compared to those from previous audits.
P. Lauwers   +12 more
core  

The diabetic foot: Charcot joint and osteomyelitis

open access: yes, 2006
Foot problems are common causes of disability in diabetic patients with as many as 25% expected to develop severe foot or leg problems during their lifetimes.
Giurato L., UCCIOLI, LUIGI
core   +1 more source

Biallelic SCO2 Variants Presenting as Motor‐Predominant Axonal Neuropathy With Complex IV Deficiency

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Background and Aims SCO2 encodes a mitochondrial copper chaperone required for cytochrome c oxidase (COX) assembly and is classically associated with severe multisystem mitochondrial disease. We characterize a motor‐predominant axonal neuropathy presentation associated with biallelic SCO2 variants.
Adriana P. Rebelo   +5 more
wiley   +1 more source

Home - About - Disclaimer - Privacy