Results 1 to 10 of about 1,097,866 (354)

Review: ‘Gimme five’: future challenges in multiple sclerosis. ECTRIMS Lecture 2009 [PDF]

open access: yes, 2010
This article is based on the ECTRIMS lecture given at the 25th ECTRIMS meeting which was held in Düsseldorf, Germany, from 9 to 12 September 2009. Five challenges have been identified: (1) safeguarding the principles of medical ethics; (2) optimizing the
Bartholomaus I.   +44 more
core   +1 more source

Eye Tracking Impact on Quality-of-Life of ALS Patients [PDF]

open access: yes, 2008
Chronic neurological disorders in their advanced phase are characterized by a progressive loss of mobility (use of upper and lower limbs), speech and social life.
And Vignola, A.   +7 more
core   +1 more source

Nintedanib for systemic sclerosis–associated interstitial lung disease [PDF]

open access: yes, 2019
BackgroundInterstitial lung disease (ILD) is a common manifestation of systemic sclerosis and a leading cause of systemic sclerosis-related death. Nintedanib, a tyrosine kinase inhibitor, has been shown to have antifibrotic and antiinflammatory effects ...
Alves, Margarida   +16 more
core   +3 more sources

A rare case of tumoral scleromyxedema

open access: yesIndian Journal of Dermatology, 2020
Scleromyxedema is an uncommon disease, affecting the skin mainly and other internal organs sometimes, characterized by fibroblasts proliferation, fibrosis, and mucous deposition in the absence of thyroid disorder.
Ali Sadeghinia   +5 more
doaj   +1 more source

Identification of a novel TSC2 c.3610G > A, p.G1204R mutation contribute to aberrant splicing in a patient with classical tuberous sclerosis complex: a case report [PDF]

open access: yes, 2018
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by hamartomas in any organ systems. Mutations in the TSC1 or TSC2 gene lead to the dysfunction of hamartin or tuberin proteins, which cause tuberous sclerosis ...
Bottillo, I   +7 more
core   +2 more sources

Melorheostosis in a 12-year-old child

open access: yesSouth African Journal of Radiology, 2001
Melorheostosis (of Leriand Joanny) is a rare, non-genetic sclerotic dysplatic bone disorder presenting at any age, usually from late childhood to adulthood. Its aetiology is unknown. It affects mainly the long bones of the upper and lower limbs, but also
S. Andronikou, B. Smith
doaj   +1 more source

Mesial temporal sclerosis in children Esclerose mesial temporal em crianças

open access: yesArquivos de Neuro-Psiquiatria, 2007
Mesial temporal sclerosis is the most frequent cause of drug-resistant temporal lobe epilepsy but has a satisfactory response to surgery, and is considered infrequent in children.
Eliana Maria Domingues Brandão   +1 more
doaj   +1 more source

Acutely damaged axons are remyelinated in multiple sclerosis and experimental models of demyelination [PDF]

open access: yes, 2017
Remyelination is in the center of new therapies for the treatment of multiple sclerosis to resolve and improve disease symptoms and protect axons from further damage.
Bramlett   +38 more
core   +1 more source

A Case Report of Systemic Sclerosis Complicated by Biventricular Heart Failure, Pulmonary Hypertension and Review of Literature [PDF]

open access: yes, 2017
Background: Systemic sclerosis (SSc) is an autoimmune connective tissue disorder whose aetiology is not fully understood. Skin fibrosis and visceral organs involvement are the hallmarks, and the heart could be disproportionately or subtly involved ...
Akinboro AO   +3 more
core   +1 more source

Anger, Quality of Life and Mood in Multiple Sclerosis [PDF]

open access: yes, 2015
This research was funded by The Multiple Sclerosis Society (UK).Peer reviewedPublisher ...
Cooper, Clare L   +4 more
core   +1 more source

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