Results 121 to 130 of about 66,871 (301)

Gulllain-Barre Syndrome After Trivalent Influenza Vaccination in Adults

open access: yesFrontiers in Neurology, 2019
Lines of evidence suggest trivalent influenza vaccination may be associated with Guillain–Barre syndrome (GBS), an immune-mediated acute inflammatory neuropathy.
Kuo-Hsuan Chang   +10 more
doaj   +1 more source

Sensorimotor polyneuropathy and foot-drop as result of a prostate cancer paraneoplastic syndrome

open access: yes, 2013
John J Bodkin,1 Michael Duff,1,2 Phillip J Seereiter Jr,3 K Kent Chevli1,31State University of New York School of Medicine and Biomedical Sciences Department of Urology, Buffalo; 2Cancer Care of Western New York, Cheektowaga; 3Western New York Urology ...
Bodkin JJ   +3 more
core  

Proteomic profile of CSF obtained at the time of diagnosis determines amyotrophic lateral sclerosis progression and survival: CXCL7 levels in disease prognosis and survival

open access: yesBrain Pathology, EarlyView.
Untargeted multiomic profiling of cerebrospinal fluid reveals that proteomic, but not lipidomic, signatures robustly distinguish ALS patients from controls and stratify individuals by survival, highlighting marked molecular differences between short survival and long survival disease.
Sergio Roca‐Pereira   +19 more
wiley   +1 more source

Rethinking Mitochondrial Parkinson's Disease in the α‐Synuclein Seed Amplification Assays Era

open access: yes
Movement Disorders, EarlyView.
Marco Percetti   +3 more
wiley   +1 more source

Expanding Spectrum of FIG4‐Related Neurological Disorders of Lysosomal Homeostasis: Case Report and Overview of the Potential Genotype–Phenotype Correlations

open access: yesClinical Genetics, EarlyView.
FIG4 is essential for lysosomal homeostasis. FIG4‐related disorders present as a continuous spectrum from the juvenile lethality in Yunis‐Varon syndrome to an increased risk of amyotrophic lateral sclerosis (ALS) in adult life. FIG4‐related disorders comprise a novel group of disorders of lysosomal homeostasis and can be classified into severe ...
Pankaj Prasun, Matthew Rasberry
wiley   +1 more source

A Quantitative Assessment of Upper Limb Motor Function Across Disease Stages in Hereditary Transthyretin Amyloidosis. [PDF]

open access: yesJ Peripher Nerv Syst
ABSTRACT Background and Aims Hereditary transthyretin amyloidosis (ATTRv) is a multisystemic disease where early neuropathy signs are challenging to detect conventionally. This study aimed to evaluate hand motor performance in ATTRv using the Hand Test System (HTS) across disease stages and examine correlations with standard measures.
Hamedani M   +25 more
europepmc   +2 more sources

Polyneuropathy - Diagnostic [PDF]

open access: yesDMW - Deutsche Medizinische Wochenschrift, 2002
B, Schlotter-Weigel, D E, Pongratz
openaire   +2 more sources

Do We Need to Monitor B‐Vitamins and Homocysteine During Initiation of Foslevodopa/Foscarbidopa Therapy?

open access: yes
Movement Disorders, EarlyView.
Aida Shaghaghi‐Zadeh   +8 more
wiley   +1 more source

Childhood subacute inflammatory demyelinating polyneuropathy

open access: yes, 2011
Subacute inflammatory demyelinating polyneuropathy (SIDP) is an acquired immune-mediated peripheral polyneuropathy with clinical course between 4 weeks and 8 weeks. Rare childhood cases with SIDP had been described in the current literature.
Kuan-Wen Chen   +7 more
core   +1 more source

Children's and young people's perspectives on extended reality in paediatric rehabilitation: A qualitative study

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Aim To explore children's and young people's experiences with extended reality (XR) in rehabilitation, their perceptions of its benefits and challenges, and their visions for its future integration. Method A qualitative, interpretive, descriptive study was conducted using semi‐structured interviews and focus groups with children and young people who ...
Jéromine Hervo   +8 more
wiley   +1 more source

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