Results 81 to 90 of about 4,338 (139)
Two patients are described, a mother and son, who were initially clinically diagnosed with hereditary spastic paraparesis. This was rectified after very long chain fatty acid testing confirmed adrenomyeloneuropathy (AMN).
Patel, Salil B, Gutowski, Nicholas J.
core +1 more source
Extending B AMN with concurrency
This paper outlines an approach to concurrent specification in B Abstract Machine Notation (AMN), using a combination of linear temporal logic and Ada style task ...
Lano, K +5 more
core +1 more source
Reducing compliance uncertainty with AMN measurements
In IEC CISPR 16-4-2 [1, 2] tight impedance requirements are given for artificial mains networks (AMN). Unfortunately, these tight requirements will support measurement uncertainty but still not guarantee low compliance uncertainty if the whole test set ...
Coenen, Mart +3 more
core +1 more source
Evaluating the Use of the Ottobock C-Brace® for Restoration of Gait in Adrenomyeloneuropathy
Adrenomyeloneuropathy (AMN) is an X-linked neurodegenerative disorder that results in progressive axonal demyelination and disturbances to gait and mobility.
Guldan, Samantha J
core
Functional speech disorder in a patient with X-linked adrenomyeloneuropathy: a diagnostic challenge. [PDF]
León JSS +5 more
europepmc +1 more source
Adrenoleukodystrophy in adults: phenotypic characterisation and natural history in a large cohort. [PDF]
Benzoni C +12 more
europepmc +1 more source
X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report. [PDF]
Chang MC, Yang S.
europepmc +1 more source
Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy. [PDF]
Meier K +8 more
europepmc +1 more source

