Results 231 to 240 of about 5,705,352 (293)

Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos   +5 more
wiley   +1 more source

Advancing multilevel Bayesian networks with efficient Bayesian inference. [PDF]

open access: yesStat Methods Med Res
Yirdaw BE   +3 more
europepmc   +1 more source

Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran   +13 more
wiley   +1 more source

On quivers, spectral networks and black holes. [PDF]

open access: yesLett Math Phys
Arnaudo P, Grassi A, Hao Q.
europepmc   +1 more source

Identification of linear parameter varying models

Proceedings of the 38th IEEE Conference on Decision and Control (Cat. No.99CH36304), 2002
AbstractWe consider identification of a certain class of discrete‐time nonlinear systems known as linear parameter varying system. We assume that inputs, outputs and the scheduling parameters are directly measured, and a form of the functional dependence of the system coefficients on the parameters is known.
BAMIEH B., GIARRÈ, Laura
openaire   +2 more sources

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