Results 171 to 180 of about 1,689,203 (295)
ABSTRACT Objective To determine whether myelin‐sensitive quantitative MRI reveals microstructural abnormalities in normal‐appearing cortex (NACtx) in myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), indicating that conventional MRI underestimates remission residual cortical injury.
Valentina Camera +20 more
wiley +1 more source
Mr J.G. Griffiths as Iago [picture].
Plate on p.59 of: Australian picture pleasure book /Walter G.
Mason, Walter G.
core
Sociolinguistic Context Constrains Bilingual Advantages in Metacognition. [PDF]
Polyanskaya L, Ordin M.
europepmc +1 more source
Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias +3 more
wiley +1 more source
A double canoe, Isle of Pines [picture].
Plate on p. 47 of: Australian picture pleasure book /Walter G.
Mason, Walter G.
core
Global Rather Than Vertical‐Selective Saccadic Abnormalities in Progressive Supranuclear Palsy
ABSTRACT Objective To test whether vertical saccades are preferentially affected in Progressive Supranuclear Palsy (PSP). Methods PSP patients (n = 24) were compared to age‐matched controls (n = 94) and two degenerative groups (Alzheimer's disease, n = 20; Lewy body disease, n = 50).
Duy Duan Nguyen +6 more
wiley +1 more source
Fitz Roy Bridge, near Goulburn, N.S.W. [picture].
Plate on p. 32 of: Australian picture pleasure book /Walter G.
Mason, Walter G.
core
The influence of bilingualism on the assessment and treatment of an Italian-English speaker with the logopenic variant of PPA. [PDF]
Tomasoni R +10 more
europepmc +1 more source
Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder
ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi +6 more
wiley +1 more source
View of Port Jackson from Balmain [picture] /
Plate on p. 1 of: Australian picture pleasure book /Walter G.
Mason, Walter G.
core

