Results 141 to 150 of about 25,555 (216)

Genetic and molecular mechanisms of the FOXP2-CNTNAP2 pathway in Autism spectrum disorders and speech disorders. [PDF]

J Neural Transm (Vienna)
Song F, Li X, Cheng C, Du J.
europepmc   +1 more source

Diagnosing Apraxia of Speech in Children and Adults When There Is No Gold Standard: A Scoping Review About the Diagnostic Process. [PDF]

Am J Speech Lang Pathol
Haley KL, Jacks A, Mailend ML.
europepmc   +1 more source

Improving Intelligibility in Childhood Apraxia of Speech Through Communication Partner Training. [PDF]

Am J Speech Lang Pathol
Borrie SA, Yoho SE, Barrett TS, Tetzloff KA.   +3 more
europepmc   +1 more source

Frontotemporal dementia: does structural MRI-based clustering match clinical syndromes? [PDF]

Front Neurosci
Singh-Reilly N, Sintini I, Ali F, Duffy JR, Clark HM, Utianski RL, Meade G, Machulda MM, Satoh R, Lowe VJ, Josephs KA, Whitwell JL.   +11 more
europepmc   +1 more source

Asymmetric Upper Limb Dysfunction Demonstrated at the Bedside: A Phenomenology Video. [PDF]

Mov Disord Clin Pract
Lueg G, Fruth M, Neuendorff NR, Wirth R, Hobert MA.   +4 more
europepmc   +1 more source

Qualitative Analysis of Constructional Errors in Neurodegenerative Conditions: A Systematic Review. [PDF]

Brain Sci
Crisci V, Sagliano L, Ferrara A, Salzillo A, Trojano L, Panico F.   +5 more
europepmc   +1 more source

Spectrum of Dystonia in Progressive Supranuclear Palsy: A Prospective Observational Study and Review of Literature. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Gulati K, Pandey S.
europepmc   +1 more source

Prion disease mimicking rapidly progressive Alzheimer disease: case series and systematic review. [PDF]

J Neurol
Elgenidi A, Shir D, Piura YD, Sokol LL, Duara R, Lachner C, Day GS.   +6 more
europepmc   +1 more source

Congenital Ocular Motor Apraxia as the First Sign of Joubert Syndrome: A Case Report. [PDF]

Cureus
Ito M, Koiwa C, Negishi T, Sawada D, Nakao S.   +4 more
europepmc   +1 more source