Results 221 to 230 of about 87,063 (285)
Some of the next articles are maybe not open access.

Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges

Nature Reviews Neurology, 2019
Menelaos Pipis   +2 more
exaly   +2 more sources

Delayed Diagnosis of Charcot Foot: A Systematic Review.

Journal of Foot and Ankle Surgery, 2022
This study aims to examine the duration and rate of delayed diagnosis in Charcot foot. We systematically reviewed articles published in Medline, SCOPUS, and Cumulative Index of Nursing and Allied Health Literature to identify articles discussing delayed ...
Genevieve S. Korst   +4 more
semanticscholar   +1 more source

Charcot–Marie–Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective study

European Journal of Neurology, 2021
Charcot–Marie–Tooth (CMT) disease, an untreatable hereditary polyneuropathy, may mimic chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), a treatable neuropathy.
Fabien Hauw   +23 more
semanticscholar   +1 more source

Genotype and phenotype distribution of 435 patients with Charcot–Marie–Tooth disease from central south China

European Journal of Neurology, 2021
The purpose was to provide an overview of genotype and phenotype distribution in a cohort of patients with Charcot–Marie–Tooth disease (CMT) and related disorders from central south China.
Yongzhi Xie   +21 more
semanticscholar   +1 more source

Charcot-Marie-Tooth: From Molecules to Therapy

open access: yesInternational Journal of Molecular Sciences, 2019
Charcot-Marie-Tooth (CMT) is the most prevalent category of inherited neuropathy. The most common inheritance pattern is autosomal dominant, though there also are X-linked and autosomal recessive subtypes. In addition to a variety of inheritance patterns,
J. Morena, Anirudh Gupta, J. Hoyle
exaly   +2 more sources

Charcot Foot

Journal of the American Podiatric Medical Association, 1989
Successful management of the Charcot foot is one of the most challenging undertakings faced by physicians. However, many times such patients undergo prolonged and attentive care only to develop further deformity, and in many cases succumb to amputation.
A S, Banks, E D, McGlamry
openaire   +2 more sources

Charcot spine

Emergency Radiology, 2007
Identification of a destructive spinal process in the acute setting most commonly is related to infection or neoplasm. In the appropriate clinical setting, Charcot spine, also known as neuropathic spinal arthropathy or spinal neuroarthropathy, should be considered.
Michael A, Staloch, Stephen F, Hatem
openaire   +2 more sources

Charcot-Marie-Tooth Disease and Other Hereditary Neuropathies.

Continuum, 2020
PURPOSE OF REVIEW This article provides an overview of Charcot-Marie-Tooth disease (CMT) and other inherited neuropathies. These disorders encompass a broad spectrum with variable motor, sensory, autonomic, and other organ system involvement ...
C. Klein
semanticscholar   +1 more source

Plasma neurofilament light chain as a potential biomarker in Charcot‐Marie‐Tooth disease

European Journal of Neurology, 2020
Charcot‐Marie‐Tooth (CMT) disease is a chronic, slowly progressing disorder. The lack of specific disease progression biomarkers limits the execution of clinical trials. However, neurofilament light chain (NfL) has been suggested as a potential biomarker
E. Millere   +11 more
semanticscholar   +1 more source

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