Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Carolina, Barnett"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Objective To obtain updated estimates of the incidence and prevalence of neurofibromatosis type 1 (NF1) and type 2 (NF2). Study design We conducted a systematic search of NF1 and NF2 incidence or prevalence studies, in OVID Medline, OVID Emb
Externí odkaz:
https://doaj.org/article/ab09340bb3514e8c8e0470a656ab4c6b
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionThe patient acceptable symptom state (PASS) is a reliable way to characterize a patient’s satisfaction with their disease state in a “Yes”/“No” dichotomous manner. There is limited data on the time required to reach an acceptabl
Externí odkaz:
https://doaj.org/article/8326f7095f7f432cb093135a1978b4c8
Autor:
Carolina Barnett, Elisa Candido, Branson Chen, Priscila Pequeno, Patricia C. Parkin, Karen Tu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background There is limited population-based data on Neurofibromatosis type 1 (NF1) in North America. We aimed to develop and validate algorithms using administrative health data and electronic medical records (EMRs) to identify individuals
Externí odkaz:
https://doaj.org/article/3cee17bb5ad24204ba49ef33d5d2b376
Publikováno v:
Digital Biomarkers, Vol 6, Iss 2, Pp 71-82 (2022)
Introduction: Telehealth/remote assessment using readily available 2D mobile cameras and deep learning-based analyses is rapidly becoming a viable option for detecting orofacial and speech impairments associated with neurological and neurodegenerativ
Externí odkaz:
https://doaj.org/article/60d9557d5ab64951bc8cd6c8431b1fca
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-15 (2022)
Abstract Background Noonan syndrome (NS) is a genetic disorder characterized by developmental delays, typical facial gestalt and cardiovascular defects. LZTR1 variants have been recently described in patients with NS and schwannomatosis, but the asso
Externí odkaz:
https://doaj.org/article/62ba543625d740ea856458c99669f680
Autor:
Ellen B. M. Elsman, Nancy J. Butcher, Lidwine B. Mokkink, Caroline B. Terwee, Andrea Tricco, Joel J. Gagnier, Olalekan Lee Aiyegbusi, Carolina Barnett, Maureen Smith, David Moher, Martin Offringa
Publikováno v:
Systematic Reviews, Vol 11, Iss 1, Pp 1-13 (2022)
Abstract Background Systematic reviews of outcome measurement instruments are important tools in the evidence-based selection of these instruments. COSMIN (COnsensus-based Standards for the selection of health Measurement INstruments) has developed a
Externí odkaz:
https://doaj.org/article/182da6fd42504be5a5a2df17adf50873
Autor:
Yana Yunusova, Ashley Waito, Carolina Barnett Tapia, Anna Huynh, Rosemary Martino, Agessandro Abrahao, Gary L. Pattee, James D. Berry, Lorne Zinman, Jordan R. Green
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
PurposeEarly detection and tracking of bulbar dysfunction in amyotrophic lateral sclerosis (ALS) are critical for directing management of the disease. Existing physiological assessments of bulbar dysfunction are often inaccessible and cost-prohibitiv
Externí odkaz:
https://doaj.org/article/ed653f102b6c43b598aec04935874ea6
Autor:
Monica Alcantara, Mylan Ngo, James de la Cruz, Deepak Menon, Carolina Barnett-Tapia, Hans Katzberg, Vera Bril
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveTo investigate the contribution of duration and temporal dispersion (TD) of the distal compound muscle action potential (CMAP) in discriminating chronic inflammatory demyelinating polyneuropathy (CIDP) from diabetic sensorimotor polyneuropat
Externí odkaz:
https://doaj.org/article/355c4c217a9c486fb0db883f6ba08c74
Autor:
James D Berry, Rosemary Martino, Carolina Barnett, Lorne Zinman, Yana Yunusova, Ashley Waito, Anna Huynh, Agessandro Abrahao, Gary L Pattee, Jordan R Green
Publikováno v:
BMJ Open, Vol 12, Iss 3 (2022)
Introduction Early detection and tracking of bulbar dysfunction in amyotrophic lateral sclerosis (ALS) are critical for directing management of the disease. Current clinical bulbar assessment tools are lacking, while existing physiological instrument
Externí odkaz:
https://doaj.org/article/fd8902fd717748edb602629ea58fe5b6
Autor:
Anca Bogdan, Carolina Barnett, Abdulrahman Ali, Mohammed AlQwaifly, Alon Abraham, Shabber Mannan, Eduardo Ng, Vera Bril
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Psychopathology and personality traits may influence the course of autoimmune disorders. With this prospective longitudinal cohort study, we aimed to assess personality, stress and depression in myasthenia patients who relapse and
Externí odkaz:
https://doaj.org/article/770960de52424db98b610d0a14f8ecdb