Carolina Barnett

researcher ORCID ID = 0000-0001-5546-0221

Carolina Barnett is …
instance of (P31):
humanQ5

External links are
P2798Loop ID682356
P496ORCID iD0000-0001-5546-0221
P1153Scopus author ID54794905900

P734family nameBarnettQ21492126
BarnettQ21492126
BarnettQ21492126
P735given nameCarolinaQ5044762
CarolinaQ5044762
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q33638581A conceptual framework for evaluating impairments in myasthenia gravis
Q39446606Association of social support with quality of life in patients with polyneuropathy
Q30909468Canadian administrative health data can identify patients with myasthenia gravis
Q39519599Changes in quality of life scores with intravenous immunoglobulin or plasmapheresis in patients with myasthenia gravis
Q38544804Choosing drugs for the treatment of diabetic neuropathy
Q92593994Chronic stress, depression and personality type in patients with myasthenia gravis
Q64228443Clinical Measures of Bulbar Dysfunction in ALS
Q96348277Comparison of the Single Simple Question and the Patient Acceptable Symptom state in Myasthenia Gravis
Q30278029Construction and validation of the chronic acquired polyneuropathy patient-reported index (CAP-PRI): A disease-specific, health-related quality-of-life instrument
Q40369807Cost-minimization analysis comparing intravenous immunoglobulin with plasma exchange in the management of patients with myasthenia gravis
Q49635783Cramps frequency and severity are correlated with small and large nerve fiber measures in type 1 diabetes
Q41171757Development and validation of the Myasthenia Gravis Impairment Index
Q45832498EPID-21ONE-YEAR INSTITUTIONAL REPORT OF THE FIRST CANADIAN ADULT NF1 MULTIDISCIPLINARY CLINIC, REPORTED IN THE CONTEXT OF SYSTEMATICALLY-IDENTIFIED EXPERIENCES OF PREVIOUSLY ESTABLISHED CENTERS.
Q57468483EQ-5D-5L and SF-6D Health Utility Index Scores in Patients with Myasthenia Gravis
Q48166944Effects of napping on neuromuscular fatigue in myasthenia gravis
Q98391166Efficacy and Safety of High Infusion Rate IVIG in CIDP
Q39061034Electrophysiological testing is correlated with myasthenia gravis severity
Q35834424Elevated Vibration Perception Thresholds in CIDP Patients Indicate More Severe Neuropathy and Lower Treatment Response Rates
Q40316742Epidemiology of myasthenia gravis in Ontario, Canada
Q90625227Evidence of persistent improvements with long-term subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy
Q92980147Evidence of small-fiber neuropathy in neurofibromatosis type 1
Q47653512Fatigue is a relevant outcome in patients with Myasthenia Gravis
Q57419025Fcγ Receptor Polymorphisms Do Not Predict Response to Intravenous Immunoglobulin in Myasthenia Gravis
Q40313742Frequent laboratory abnormalities in CIDP patients
Q57176138Gelsolin Familial Amyloidosis Peripheral Neuropathy in Canada: A Case Report
Q87661729INCAT disability score: a critical analysis of its measurement properties
Q48326036IVIG and PLEX in the treatment of myasthenia gravis.
Q30276744International clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15r
Q38261531Intravenous immunoglobulin as treatment for myasthenia gravis: current evidence and outcomes
Q50057656Laboratory Abnormalities in Polyneuropathy and Electrophysiological Correlations
Q36185699Laser Doppler Flare Imaging and Quantitative Thermal Thresholds Testing Performance in Small and Mixed Fiber Neuropathies
Q87839582Minimal clinically important difference in myasthenia gravis: outcomes from a randomized trial
Q44599026Missed diagnosis of osteoporosis and failure to treat adults with hip fracture in Chile
Q47123513Myasthenia Gravis Impairment Index: Responsiveness, meaningful change, and relative efficiency
Q39207965Neurofibromatosis Clinic: A Report on Patient Demographics and Evaluation of the Clinic
Q98218470Patient-acceptable symptom states in myasthenia gravis
Q104286239Performance of Different Criteria for Refractory Myasthenia Gravis
Q61909339Performance of individual items of the quantitative myasthenia gravis score
Q83878582Predictors of response to immunomodulation in patients with myasthenia gravis
Q86982825Prevalence of muscle cramps in patients with diabetes
Q37589680Psychometric Properties of the Quantitative Myasthenia Gravis Score and the Myasthenia Gravis Composite Scale
Q92888071Qualitative, Patient-Centered Assessment of Muscle Cramp Impact and Severity
Q97543730Quality of life in patients with neurofibromatosis type 1 and 2 in Canada
Q48351231Quantitative sonographic assessment of myotonia
Q47851560Recording Fewer Than 20 Potential Pairs With SFEMG May Suffice for the Diagnosis of Myasthenia Gravis
Q90075812Reliability and validity of speech & pause measures during passage reading in ALS
Q38939549Repetitive facial nerve stimulation in myasthenia gravis 1min after muscle activation is inferior to testing a second muscle at rest
Q38861799Repetitive nerve stimulation cutoff values for the diagnosis of myasthenia gravis
Q38372339Rituximab as treatment for anti-MuSK myasthenia gravis: Multicenter blinded prospective review
Q93045868Serious infections in patients with myasthenia gravis: population-based cohort study
Q57176112Sex differences in neuropathic pain intensity in diabetes
Q83099491Sural-to-radial amplitude ratio in the diagnosis of diabetic sensorimotor polyneuropathy
Q35107092The characteristics of chronic inflammatory demyelinating polyneuropathy in patients with and without diabetes--an observational study
Q47219297The high frequency of monoclonal gammopathy in patients with diabetic sensorimotor polyneuropathy
Q91451807The median to ulnar cross-sectional surface area ratio in carpal tunnel syndrome
Q48438130The quantitative myasthenia gravis score: comparison with clinical, electrophysiological, and laboratory markers
Q39357030The utility of a single simple question in the evaluation of patients with myasthenia gravis
Q34976633Thymectomy for non-thymomatous myasthenia gravis: a propensity score matched study
Q66724826Thymectomy may not be associated with clinical improvement in MuSK myasthenia gravis
Q35804676Treatment Responsiveness in CIDP Patients with Diabetes Is Associated with Higher Degrees of Demyelination
Q92337544Ultrasound in Multifocal Motor Neuropathy: Clinical and Electrophysiological Correlations

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