Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Raymond L Rosales"'
Publikováno v:
Annals of Movement Disorders, Vol 5, Iss 2, Pp 118-120 (2022)
Hemifacial spasm (HFS) is a movement disorder characterized by involuntary twitching of the facial muscles of one side of the face. Here, we report the case of a 31-year-old woman with relapsingremitting multiple sclerosis who presented with left-sid
Externí odkaz:
https://doaj.org/article/90b6deef8e214f728e78d9d2e6c2c5f1
Autor:
Raymond L Rosales, Jovita Balcaitiene, Hugues Berard, Pascal Maisonobe, Khean Jin Goh, Witsanu Kumthornthip, Mazlina Mazlan, Lydia Abdul Latif, Mary Mildred D. Delos Santos, Chayaporn Chotiyarnwong, Phakamas Tanvijit, Odessa Nuez, Keng He Kong
Publikováno v:
Toxins, Vol 10, Iss 7, p 253 (2018)
The ONTIME study investigated whether early post-stroke abobotulinumtoxinA injection delays appearance or progression of upper limb spasticity (ULS) symptoms. ONTIME (NCT02321436) was a 28-week, exploratory, double-blind, randomized, placebo-controll
Externí odkaz:
https://doaj.org/article/933435a48f264829b2c891b31e964bb7
Autor:
John C Middlebrooks, Harry S Nick, S H Subramony, Joel Advincula, Raymond L Rosales, Lillian V Lee, Tetsuo Ashizawa, Michael F Waters
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76749 (2013)
Normal sound localization requires precise comparisons of sound timing and pressure levels between the two ears. The primary localization cues are interaural time differences, ITD, and interaural level differences, ILD. Voltage-gated potassium channe
Externí odkaz:
https://doaj.org/article/fede54f6a951423aaf26816e7dffb6c6
Autor:
Raymond L. Rosales, Nicholas V. C. Chia, Witsanu Kumthornthip, Khean Jin Goh, Choon Soon Mak, Keng He Kong, Yee Sien Ng, Li Wei Chou, M. Jeanne Flordelis, Thuy Do, Pascal Maisonobe, Leonard S. W. Li, Areerat Suputtitada
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
PurposeDescribe real-life practice and outcomes in the management of post-stroke upper limb spasticity with botulinum toxin A (BoNT-A) in Asian settings.MethodsSubgroup analysis of a prospective, observational study (NCT01020500) of adult patients (
Externí odkaz:
https://doaj.org/article/8bee9e78d51842ff96f338a8be05ea42
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-4 (2022)
Abstract Background Myoclonus-dystonia is a rare movement disorder with an autosomal dominant inheritance pattern characterized by a combination of myoclonic jerks and dystonia that may have psychiatric manifestations. Our aim is to present neurologi
Externí odkaz:
https://doaj.org/article/d936928c38524d429c2de9a0c164cb0f
Autor:
Björn-Hergen Laabs, Christine Klein, Jelena Pozojevic, Aloysius Domingo, Norbert Brüggemann, Karen Grütz, Raymond L. Rosales, Roland Dominic Jamora, Gerard Saranza, Cid Czarina E. Diesta, Michael Wittig, Susen Schaake, Marija Dulovic-Mahlow, Jana Quismundo, Pia Otto, Patrick Acuna, Criscely Go, Nutan Sharma, Trisha Multhaupt-Buell, Ulrich Müller, Henrike Hanssen, Fabian Kilpert, Andre Franke, Arndt Rolfs, Peter Bauer, Valerija Dobričić, Katja Lohmann, Laurie J. Ozelius, Frank J. Kaiser, Inke R. König, Ana Westenberger
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-8 (2021)
Age at onset of X-linked dystonia-parkinsonism is 50% explained by the length of a repeat in an SVA insert. The authors perform a GWAS for genetic modifiers and discover three more loci, accounting for another 13% of variability in age at onset with
Externí odkaz:
https://doaj.org/article/11ebd21e7c7b492c804497da333f8fd9
Autor:
Raymond L. Rosales, Mary Camille E. Rosales, Danica Jane S.J. Robles, Ron Christian Neil T. Rodriguez, Nadia Beatrice S. Romana, Joseph Mariuz B. Rosales, Gerardo B. Salazar, Richelle Ann S. Santiano
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 7, Iss , Pp 100169- (2022)
Introduction: Prevalence of Parkinson’s Disease (PD) in the Philippines has been estimated to be
Externí odkaz:
https://doaj.org/article/c9358a270ccb4ff3990b72df7e25c964
Autor:
Lalaine B Villaflor-Oida, Raymond L Rosales, Ma. Antonia Aurora M Valencia, Michelle G Sy, Yuh-Jyh Jong
Publikováno v:
Journal of Medicine, University of Santo Tomas. 7:1138-1143
Spinal muscular atrophy (SMA) is the most common inherited lethal disease in children. Confirmatory diagnosis is based on molecular genetic testing of survival motor neuron (SMN) genes. We aimed to describe the phenotypic presentation of Filipino inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d520066f1b291534f4565b07b958490
https://doi.org/10.35460/2546-1621.2022-0025
https://doi.org/10.35460/2546-1621.2022-0025
Publikováno v:
Journal of Medicine, University of Santo Tomas. 7:1181-1185
Rationale: Duchenne muscular dystrophy (DMD) is a disease that primarily manifests in the early stages of life and progressively affects muscle strength resulting in quadriparesis and ultimately resulting in premature death secondary to cardiac or re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd0e07ebcf4e5eca094b5c977abb5b0f
https://doi.org/10.35460/2546-1621.2023-0022
https://doi.org/10.35460/2546-1621.2023-0022
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 5, Iss , Pp 100100- (2021)
Introduction: X-linked dystonia-parkinsonism (XDP) is a progressive movement disorder which also encompasses non-motor features and alterations in activities of daily living. The study aims to translate the Parts IIIB (Non-Motor Features) and IV (Act
Externí odkaz:
https://doaj.org/article/c38bc791a76f4f10894e940a81cad3a3