(FTLD) has been refined by robust computational imaging studies in recent years. This has
led to the characterisation of phenotype-1-16 and genotypeassociated 17-23 patterns of …

Figure 1: Representative axial lumbar spine MR T2‑weighted images of the patient with SMA
type 1 and unaffected age‑matched control. Significant bilateral atrophy of the ventral roots …

Die Spinale Muskelatrophie (SMA) ist eine autosomal-rezessiv vererbte neurodegenerative
Erkrankung, die meist durch biallele Deletionen im Survival of Motor Neuron 1 (SMN1) Gen …

In recent years, spinal muscular atrophy (SMA) has made progress in multidisciplinary
treatment and disease-modifying therapeutic drugs, so that the progress has significantly …

Friedreich's ataxia (FRDA) is a devastating, inherited neurodegenerative disorder that can
manifest from early childhood through to old age. There have been many therapeutic trials of …

Quantitative spinal cord (SC) magnetic resonance imaging (MRI) is fraught with challenges,
among which is the lack of standardized imaging protocols. Here we present a prospectively …

Abstract (EN) Background: Spinal Muscular Atrophy (SMA) is a motor neuron disease
caused by depletion of the survival motor neuron protein (SMN) leading to progressive …

CEREBRAL CHANGES IN POLIOMYELITIS SURVIVORS:A COMPUTATIONAL
NEUROIMAGING STUDY Page 1 i CEREBRAL CHANGES IN POLIOMYELITIS …

Muscular Dystrophy is a term used to describe a series of genetic illnesses that affect the
development of skeletal muscles, which also causes a series of brain anomalies such as …

Quantitative MRI (qMRI) aims to provide objective continuous metrics that specifically reflect
the morphology, microstructure and/or chemical composition of tissues 1, 2, thereby …