Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Amy Robichaux-Viehoever"'
Autor:
Fayza Jaleel, Alyssa Rust, Shirley Cheung, Toni S. Pearson, Keisuke Ueda, Amy Robichaux‐Viehoever, Katie Leger, Keerthana Chintalapati, Danielle Guez‐Barber, Michele Shusterman, Bhooma Aravamuthan
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 2, Pp 242-250 (2024)
Abstract Objective To determine how caregivers describe dystonia in people with cerebral palsy (CP). Methods In this prospective cohort study, paper surveys were administered to caregivers between September 7, 2021 and October 28, 2021 during CP Cent
Externí odkaz:
https://doaj.org/article/ad778660bad24c218d768afc87f82716
Diagnostic and clinical experience of patients with pantothenate kinase-associated neurodegeneration
Autor:
Randall D. Marshall, Abigail Collins, Maria L. Escolar, H. A. Jinnah, Thomas Klopstock, Michael C. Kruer, Aleksandar Videnovic, Amy Robichaux-Viehoever, Colleen Burns, Laura L. Swett, Dennis A. Revicki, Randall H. Bender, William R. Lenderking
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive neurodegenerative disorder with brain iron accumulation (NBIA). Objectives To assess PKAN diagnostic pathway, history, and burden across the spectru
Externí odkaz:
https://doaj.org/article/6908f3b545944cc4a900233e729fcb94
Autor:
Deanna J. Greene, Jonathan M. Koller, Amy Robichaux-Viehoever, Emily C. Bihun, Bradley L. Schlaggar, Kevin J. Black
Publikováno v:
Developmental Cognitive Neuroscience, Vol 11, Iss C, Pp 65-74 (2015)
Tic disorders are childhood onset neuropsychiatric disorders characterized by motor and/or vocal tics. Research has demonstrated that children with chronic tics (including Tourette syndrome and Chronic Tic Disorder: TS/CTD) can suppress tics, particu
Externí odkaz:
https://doaj.org/article/24ffb11150f442feb232bb6523df6f4d
Autor:
Emily Bell, John M. Schreiber, Christos Sidiropoulos, Howard P. Goodkin, Amy Robichaux Viehoever, Erika Axeen
Publikováno v:
Pediatric Neurology. 121:28-32
Background We sought to expand our knowledge of the clinical spectrum of GNAO1-related neurodevelopmental disorders through a caregiver survey reviewing medical and developmental history and development of epilepsy and movement disorders. Methods An
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4972abf59edb1d186a1d61dcdc44c7a
https://doi.org/10.1016/j.pediatrneurol.2021.05.005
https://doi.org/10.1016/j.pediatrneurol.2021.05.005
Autor:
Irene A. Malaty, Seonaid Anderson, Shannon M. Bennett, Cathy L. Budman, Barbara J. Coffey, Keith A. Coffman, Erica Greenberg, Joseph F. McGuire, Kirsten R. Müller-Vahl, Michael S. Okun, Julio Quezada, Amy Robichaux-Viehoever, Kevin J. Black
Publikováno v:
Journal of Clinical Medicine. 11:6470
Over the past 3 years, a global phenomenon has emerged characterized by the sudden onset and frequently rapid escalation of tics and tic-like movements and phonations. These symptoms have occurred not only in youth known to have tics or Tourette synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32289b1af3298778cb60558724841984
https://doi.org/10.3390/jcm11216470
https://doi.org/10.3390/jcm11216470
Diagnostic and clinical experience of patients with pantothenate kinase-associated neurodegeneration
Autor:
Aleksandar Videnovic, Colleen Burns, Hyder A. Jinnah, Abigail Collins, Randall H. Bender, Thomas Klopstock, Randall D Marshall, Michael C. Kruer, Dennis A. Revicki, Maria L. Escolar, William R. Lenderking, Amy Robichaux-Viehoever, Laura L. Swett
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases 14(1), 174 (2019). doi:10.1186/s13023-019-1142-1
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases 14(1), 174 (2019). doi:10.1186/s13023-019-1142-1
Background Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive neurodegenerative disorder with brain iron accumulation (NBIA). Objectives To assess PKAN diagnostic pathway, history, and burden across the spectrum of PKAN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfaf9facb7d089c64763d0d6e77678d7
http://link.springer.com/article/10.1186/s13023-019-1142-1
http://link.springer.com/article/10.1186/s13023-019-1142-1
Autor:
William R. Lenderking, Maria L. Escolar, Laura L. Swett, Aleksandar Videnovic, Amy Robichaux-Viehoever, Abigail Collins, Hyder A. Jinnah, Randall D Marshall, Randall H. Bender, Dennis A. Revicki, Michael C. Kruer, Thomas Klopstock
Publikováno v:
Movement Disorders Clinical Practice
Movement disorders clinical practice 6(2), 139-149 (2019). doi:10.1002/mdc3.12716
Movement disorders clinical practice 6(2), 139-149 (2019). doi:10.1002/mdc3.12716
Objective Pantothenate kinase‐associated neurodegeneration (PKAN) is an autosomal‐recessive, neurodegenerative disorder with a mixed‐motor phenotype caused by a defective PanK2 enzyme, for which there are few adequate treatment options. Clinime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4377d9a45b5e5980be18586a0957ecae
http://europepmc.org/articles/PMC6384181
http://europepmc.org/articles/PMC6384181
Autor:
Melissa L Gittings, Sarah S. Wang, Philip A. Starr, Amy Robichaux-Viehoever, Jill L. Ostrem, Marta San Luciano, Caroline A. Racine, Christa Watson Pereira, Aaron C Viser, Ian O. Bledsoe, Kristen A. Dodenhoff
Publikováno v:
Journal of neurosurgery. Pediatrics, vol 27, iss 2
OBJECTIVEThe aim of this study was to evaluate the feasibility and preliminary efficacy and safety of combined bilateral ventralis oralis posterior/ventralis intermedius (Vop/Vim) deep brain stimulation (DBS) for the treatment of acquired dystonia in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6869a2a55a9c86031128fa51657efdc2
https://pubmed.ncbi.nlm.nih.gov/33254134
https://pubmed.ncbi.nlm.nih.gov/33254134
Autor:
Joseph P. Culver, Arefeh Sherafati, Adam T. Eggebrecht, Christopher D. Smyser, Tracy M. Burns-Yocum, Silvina L. Ferradal, Abraham Z. Snyder, Karla M. Bergonzi, Ben J.A. Palanca, Amy Robichaux-Viehoever, Tamara Hershey, Heather M. Lugar
Publikováno v:
Human Brain Mapping
Motion‐induced artifacts can significantly corrupt optical neuroimaging, as in most neuroimaging modalities. For high‐density diffuse optical tomography (HD‐DOT) with hundreds to thousands of source‐detector pair measurements, motion detectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774bbc037980fe299da088bda2a5c9b1
https://pubmed.ncbi.nlm.nih.gov/32648643
https://pubmed.ncbi.nlm.nih.gov/32648643
Publikováno v:
Seminars in Pediatric Neurology. 25:136-151
Management of movement disorders in children is an evolving field. This article outlines the major categories of treatment options for pediatric movement disorders and general guidelines for their use. We review the evidence for existing therapies, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b186ca1efb27deb110f7f767f25881
https://doi.org/10.1016/j.spen.2018.02.004
https://doi.org/10.1016/j.spen.2018.02.004