Literature DB >> 31783740

Exercise and Progressive Supranuclear Palsy: the need for explicit exercise reporting.

Susan C Slade1, Martin Underwood2, Jennifer L McGinley3, Meg E Morris4,5.   

Abstract

BACKGROUND: Progressive Supranuclear Palsy (PSP) is the most frequent form of atypical Parkinsonism. Although there is preliminary evidence for the benefits of gait rehabilitation, balance training and oculomotor exercises in PSP, the quality of reporting of exercise therapies appears mixed. The current investigation aims to evaluate the comprehensiveness of reporting of exercise and physical activity interventions in the PSP literature.
METHODS: Two independent reviewers used the Consensus on Exercise Reporting Template (CERT) to extract all exercise intervention data from 11 studies included in a systematic review. CERT items covered: 'what' (materials), 'who' (instructor qualifications), 'how' (delivery), 'where' (location), 'when', 'how much' (dosage), 'tailoring' (what, how), and 'how well' (fidelity) exercise delivery complied with the protocol. Each exercise item was scored '1' (adequately reported) or '0' (not adequately reported or unclear). The CERT score was calculated, as well as the percentage of studies that reported each CERT item.
RESULTS: The CERT scores ranged from 3 to 12 out of 19. No PSP studies adequately described exercise elements that would allow exact replication of the interventions. Well-described items included exercise equipment, exercise settings, exercise therapy scheduling, frequency and duration. Poorly described items included decision rules for exercise progression, instructor qualifications, exercise adherence, motivation strategies, safety and adverse events associated with exercise therapies. DISCUSSION: The results revealed variability in the reporting of physical therapies for people living with PSP. Future exercise trials need to more comprehensively describe equipment, instructor qualifications, exercise and physical activity type, dosage, setting, individual tailoring of exercises, supervision, adherence, motivation strategies, progression decisions, safety and adverse events.
CONCLUSION: Although beneficial for people living with PSP, exercise and physical therapy interventions have been inadequately reported. It is recommended that evidence-based reporting templates be utilised to comprehensively document therapeutic exercise design, delivery and evaluation.

Entities:  

Keywords:  Atypical parkinsonism; Exercise; Progressive Supranuclear palsy; Rehabilitation

Mesh:

Year:  2019        PMID: 31783740      PMCID: PMC6884751          DOI: 10.1186/s12883-019-1539-4

Source DB:  PubMed          Journal:  BMC Neurol        ISSN: 1471-2377            Impact factor:   2.474


Background

Progressive Supranuclear Palsy (PSP) is comparatively rare. Nevertheless, it is the most frequent form of atypical Parkinsonism [1-3]. The prevalence estimates range from 5 to 6 per 100,000 [4] to 18 per 100,000 [5]. Although difficult to diagnose the International Parkinson and Movement Disorders Society (MDS-PSP) clinical criteria have provided expert guidance [6]. Given the rapid decline in movement control, balance, and oculo-motor control in people with PSP, exercise and physical activities may be important to health and wellbeing [7, 8]. People with PSP also have an increased risk of falls [7, 8]. Strength training, gait rehabilitation, falls education and other forms of exercise and physical activity [7, 8], alongside optimal medical management, are argued to improve quality of life for people with this debilitating condition [7, 8]. Exercise therapy can be helpful for people with idiopathic Parkinsonism [9, 10]. Physiotherapy that includes treadmill gait training, cueing, dance and martial arts has benefits for gait, balance and quality of life in some individuals [11]. In addition, progressive resistance strength training is beneficial for gait, falls prevention and community ambulation [12-14]. High-intensity interval treadmill training is safe, feasible and beneficial for motor symptoms such as gait and balance in the early stages of idiopathic Parkinson’s disease (PD) [15]. Falls prevention interventions for PD, including progressive resistive strength training, movement strategies and education, have shown reduced falls rates when delivered in outpatient settings [9]. In clinical settings people living with PSP often receive an idiopathic PD exercise and movement rehabilitation program because initial symptoms or difficulty with function and activity limitations can appear similar [16, 17]. Whether or not this is appropriate is open to question. Exercises and structured physical therapies are also thought to be beneficial for individuals living with PSP [16-19], yet the evidence is based on a small number of underpowered and heterogeneous studies [20]. In addition, these studies have not used a consistent core set of outcome measures for disability, falls, movement disorders, wellbeing and quality of life [20]. Some balance, gaze and gait variables have been measured although they have not been reported in a consistent manner [20]. There is preliminary evidence in small observational studies for the benefits of oculomotor exercises for balance and walking speed in PSP [21, 22]. Gait training and cueing have demonstrated benefits for balance, reduced falls and quality of life [23-26]. For findings to be understood, and to inform components for future PSP trials, it is important to report how exercises are designed, delivered and evaluated. Best practice for exercise, rehabilitation and physical activity programs is to use an evidence-based reporting template to detail the exercise type, content, setting, instructor qualifications and skills, exercise equipment, dosage, progression decision rules, and motivation and adherence strategies to be used by patients and therapists [27-30]. For exercise programs to be safely and effectively translated into clinical practice, several important intervention elements need to be described [28, 29]. The Consensus on Exercise Reporting Template (CERT) provides a framework for reporting these elements [28-30]. The template affords a standardised method for exercise data extraction across a range of study designs. It assists readers, peer-reviewers and editors with the appraisal of exercise reporting quality and reporting of the content of exercise programs [28]. The template can also guide exercise protocol development and the structuring of recommendations for clinical implementation [28]. The aim of the current investigation is to evaluate the comprehensiveness of reporting of exercise and physical activity interventions reported in the PSP literature.

Materials and methods

Systematic review

As a first step in this analysis we conducted a systematic review of exercise and physical activity interventions for people with PSP. This has been reported in detail elsewhere [20] and is summarised as follows. The protocol was pre-registered on PROSPERO (CRD42018103845) (https://www.crd.york.ac.uk/prospero), methods followed Cochrane guidelines [31] and reporting followed Preferred Reporting Items for Systematic review and Meta-Analysis (PRISMA) guidance [32, 33]. Two reviewers independently conducted all of the review stages and agreement was reached by discussion and research team consensus. English language, peer-reviewed published studies of any design, and conducted in any setting, were eligible for inclusion. Nine electronic databases were searched until August 18, 2019 using terms such as exercise, physical activity, rehabilitation, and synonyms for PSP. Reference lists were searched and content experts were consulted.

CERT data extraction and analysis of exercise interventions

Two reviewers (SCS and MEM) independently extracted all exercise intervention component data from the included studies by using the 16-item CERT checklist [27]. CERT items span the following domains: ‘what’ (materials), ‘who’ (instructor qualifications), ‘how’ (delivery), ‘where’ (location), ‘when’, ‘how much’ (dosage), ‘tailoring’ (what, how), and ‘how well’ (fidelity). The CERT Explanation and Elaboration statement [29] provided further guidance. If information was missing, one reviewer (SCS) searched for, and retrieved, any published protocols, online appendices and supplementary data for additional data extraction. Each item was scored ‘1’ (adequately reported) or ‘0’ (not adequately reported or unclear), and a score out of a total of 19 was calculated. The independently extracted data were examined for consistency and any discrepancies were resolved through discussion between the reviewers. Intervention content was summarised in table format under headings such as study design and sample size, setting, type of exercise and mode of delivery, program duration and dosage. The quality and comprehensiveness of reporting were analysed and presented using the example of McGregor et al. [34]. The CERT score (with a possible total of 19) and the number (and percentage) of studies that reported each CERT item were calculated, summarised in narrative form and reported graphically.

Results

The results of the systematic review have been reported in detail elsewhere [20] and are summarised as follows. There were 11 included studies, with an overall total of 99 participants [21–26, 35–39]. All studies were assessed as having a moderate to high risk of bias. Study designs included randomised/quasi-randomised controlled trials, quasi-experimental studies, cohort and case studies. The intervention characteristics are described in Table 1. Intervention effects were typically small to moderate or not statistically significant. There was preliminary evidence that treadmill training with harness support, auditory-cued motor training and robot-assisted gait rehabilitation might be helpful for some people in the early stages of PSP [20]. The systematic review found insufficient evidence of benefits of movement rehabilitation in the advanced stages of PSP [20]. It also remains unclear whether therapeutic exercises shown to be effective for people living with idiopathic Parkinson’s disease benefits those with PSP [20].
Table 1

Intervention characteristics

StudySample sizeStudy designSettingExerciseModalityProgram durationDosage
Clerici 2017, Italy [23]24RCTRehabilitation hospitalGait training - aerobic, intensive, motor-cognitive, goal based exerciseTreadmill versus Lokomat robotic treadmill4 weeks4 daily 1-h sessions, 5/week
Di Pancrazio 2013, Italy [39]10Cohort studyRehabilitation hospitalWeight relieving harness for walking (SPAD) plus vibration sensory stimulation (VISS)Treadmill8 weeks3/week
Irons 2015, USA [36]1Case studyOutpatientWeight relieving harness for walking on a treadmill type elliptical walker/trainerElliptical cross trainer8 weeks3/week for a total of 24 sessions
Nicolai 2010, Germany [24]8Cohort studyOutpatientDynamic exercises from 6 posture & balance categories with increasing difficulty & complexity(1) sitting (2) standing (3) transfers (4) sway (5) reaching or stepping one direction (6) multi direction stepping with added limb movement6 weeks45 min sessions, 3/week
Sale 2014, Italy [25]5Cohort studyOutpatientProgram of robot-assisted walking sessions for 20 - 45 min, 5 times a week for 4 weeks.Walkway force platform4 weeks20-45 min, 5/week
Seamon 2017, USA [37]1Case studyIn-homeVirtual exer-gaming “YourShape” and mini gamesXbox Kinect6 weeks12 1-h sessions
Suteerawattananon 2002, USA [35]1Case studyResearch laboratoryBody weight supported unloaded gaitPacer treadmill8 weeks1.5 h sessions, 3/week
Wallace 2013, USA [38]1Case studyIn-homeWeighted vest, with motion-capture technology, to improve movement and postureWeighted vest on or offNot reportedNot reported
Wittwer 2018, Australia5Case seriesIn-homeGait training program and rhythmic auditory cues (RACs)Cued exercises in sitting, standing, walking4 weeks30–60 min, 2/week
Zampieri 2008, Italy [21]19Quasi RCTResearch laboratoryExercises included tandem stance practice with eyes open and closed, turning 360° while marching in place; sit-to-stand and stand-to-sit practice on a chair. Treatment group received eye movement & visual awareness trainingBalance vs balance + eye movement4 weeks1 h, 3/week
Zampieri 2009, Italy [22]19Quasi RCTResearch laboratoryAs aboveBalance vs balance + eye movement4 weeks1 h, 3/week
Intervention characteristics

CERT data extraction and data analysis

The CERT items reported for each study are summarised in Table 2. The CERT scores ranged from three to 12 out of a possible 19 points (Fig. 1). None of the included studies adequately described the minimum number of elements considered by the CERT panel to enable replication; either, clinically, or in research (Fig. 2). The authors of one study provided additional online data with an intervention description [23]. We did not find any published protocol papers.
Table 2

Study reporting of each CERT item

CERT itemClerici 2017Di Pancrazio 2013Irons 2015Nicolai 2010Sale 2014Seamon 2017Suteerawattanon 2002Wallace 2013Wittwer 2019Zampieri 2008Zampieri 2009
1. EquipmentX
2. QualificationsXXXXXXXX
3. Individual/GroupXXXX
4. SupervisionXXXX
5. AdherenceXXXXXXXX
6. MotivationXXXXXX
7a. Progression ruleXXXXXXXXX
7b. Progression describedXXXX
8. Exercise detailXXXX
9. Home programXXXXXXXX
10. Non-exercise componentsXXXXXXXXX
11. Adverse eventsXXXXXXXXXX
12. SettingXX
13. Intervention describedX
14a. Generic/tailoredXXXXXX
14b.Tailoring methodXXXXXXXX
15. Starting levelXXXXXX
16a. Fidelity measureXXXXXXXXXXX
16b. Fidelity describedXXXXXXXXXX

✓ reported CERT item, X did not report CERT item

Fig. 1

Consensus on Exercise Reporting Template applied to included studies

Fig. 2

Reporting quality of exercise interventions as assessed with the Consensus on Exercise Reporting Template (CERT)

Study reporting of each CERT item ✓ reported CERT item, X did not report CERT item Consensus on Exercise Reporting Template applied to included studies Reporting quality of exercise interventions as assessed with the Consensus on Exercise Reporting Template (CERT) The well-described items included the equipment (such as treadmills, weighted vests and virtual gaming), setting (in home or at movement disorders clinics and hospital outpatient departments). The session durations ranged from 20 to 60 min, the intervention frequency ranged from two to five sessions per week and the intervention duration ranged from four to 8 weeks. A decision rule by which to determine the starting level and exercise progression, occurrence and type of exercise-related adverse events and fidelity of the actual intervention to the planned intervention were rarely described. The comprehensiveness of reporting for each of the CERT items is summarised under abbreviated headings in the following text.

Item 1: description of exercise equipment

The equipment was described in detail in 10/11 (91%) of studies and included brands and models. For example, photographs of bodyweight-supported treadmills [35], elliptical trainers [36] and audio biofeedback [24] provided clarity.

Item 2: investigator qualifications

The specific medical or allied health discipline was reported in 3/11 (27%) of studies [21, 23, 26]. The level of post-graduate education, years of experience in movement disorders rehabilitation and the use of intervention training programs and manuals were not described in any report.

Item 3: individual or group exercise

While often not specifically described, it was evident from the single case study design [24, 35–38] and case series investigations [26] that some exercise interventions were performed individually (7/11 (64%)). The RCTs were inconsistent with reported individual or group administration [21, 22] and unreported mode of delivery [23].

Item 4: supervision

The type of supervision was reported in 7/11 (64%) studies however this was of limited detail. Nicolai 2010 reported 1:1 supervision and Wittwer et al. reported individual home visits by a physiotherapist [24, 26]. Complex equipment [23, 25, 35, 36, 39] was assumed by the reviewers to require supervision at a clinic. The home-based programs did not report the levels of supervision required by a therapist or care-giver [26, 37, 38].

Item 5: exercise adherence

Measurement of adherence to the exercise or physical therapy program was reported in only 3/11 (27%) studies [26, 35, 38]. The way in which adherence was measured, such as exercise diaries, was not reported either a priori in the methods or by confirmation in the results.

Item 6: motivation strategies

Motivation strategies, such as goal setting, positive reinforcement, attendance at support groups or tele-coaching were not explicitly reported in any publications. However, visual and auditory cues were reported in 5/11 (45%) studies [21, 23, 26, 35, 37]. A virtual reality gaming environment was selected as a specific motivational tool [37]. Auditory and visual cueing could be considered as a motivational strategy or a motor control technique. Nevertheless, a more comprehensive description of the cues would assist with replication.

Item 7a: exercise progression

A priori decision rules for program progression were not well reported (2/11, 18% of studies) [36, 37]. That the interventions were progressed was reported in 7/11 (64%) studies [14, 23–25, 35–37]. Progression was generally informed by subjective assessment rather than by a validated measurement scale.

Item 8: detailed exercise description

The exercises or activities were reported in detail in 7/11 (64%) of the studies [21, 22, 24–26, 35, 37]. In the existing literature, several trials included treadmill walking and needed little extra detail. However, when exercises included gait, motor performance, balance training or functional activities there was generally a lack of detailed description.

Item 9: additional home program

Additional home-based or community-based activities or therapies were reported in 3/11 (27%) of the studies [26, 37, 38]. However explicit detail, that could explain any confounding effects, were not provided.

Item 10: non-exercise components

Non-exercise components such as environmental modifications, education about the condition and self-management such as speech and swallowing strategies were reported in only 2/11 (18%) of the studies [23, 26].

Item 11: risks and adverse events

The presence of exercise-related adverse events was reported in only 1/11 (9%) study [25]. The absence of adverse events reporting is of concern because people living with a diagnosis of PSP can have falls risks, comorbidities, pain, immobility and cognitive impairment.

Item 12: environment and setting

The exercise setting was well described in 9/11 (82%) of the studies. These included home-based interventions [26, 37, 38], movement disorders clinics and hospital outpatient departments [23–25, 36, 39] and research laboratories [21, 22, 35].

Item 13: intervention details

The frequency and duration of the interventions was well described in 10/11 (91%) studies. Most were of 4 to 8 weeks duration and delivered two to three times per week. One study was of unreported duration [38].

Item 14: generic exercises or personalised to individual needs

It was unclear, even with the small sample sizes such as single case studies, that there was tailoring to meet individual needs and capabilities in all of the studies. This was explicitly stated in 5/11 (45%) studies [21, 22, 24, 35, 37]. The method for tailoring to the individual was reported in 3/11 (27%) studies [22, 24, 36].

Item 15: intervention starting level

Testing of pre-study participant physical capability, such as gait speed and quality, was reported in 5/11 (45%) studies [23, 25, 26, 35, 36]. The stage of disease progression and weight-bearing and balance capacity were not always documented.

Item 16: intervention delivered as planned

Deviations from the planned intervention can occur in practice and may influence the observed effect. None of the studies reported how investigator adherence to the research protocol was measured 0/11 (0%). One study (9%) provided an online a priori protocol and reported that the intervention was delivered as planned [23].

Discussion

This analysis highlights the need for explicit reporting of therapeutic exercises and structured physical activities in PSP studies. This would enable more rigorous evaluation of the outcomes of exercises and physical activities for people with neurological conditions such as atypical Parkinsonism. People with PSP, as with those who have idiopathic PD, need access to evidence-based therapies that are personalised to their individual needs. This in turn relies upon clinicians having access to clearly reported findings that describe all key dimensions of exercise and physical therapy. The data extraction and analysis identified some well-described exercise program elements in the existing PSP literature. These included the exercise equipment, the setting and the intervention frequencies and durations. The less well described items were the investigator qualifications and training, a priori methods for intervention dosage and progression, tailoring exercises to individual needs, motivation and adherence strategies and non-exercise components, such as cueing, patient education and self-management. The poorly reported items were exercise-related adverse events and the fidelity of implementation of the planned exercise protocols. The less well-described items may be elaborated by the following additional information. A statement of the instructor expertise and any intervention-specific training would indicate whether additional expertise is required. Exercise progression can be guided by measures such as the Borg Rating of Perceived Exertion Scale [40]. Adherence to exercises can be recorded in exercise diaries as attendance or actual performance i.e. number of exercise repetitions. Motivation strategies to encourage persistence with exercises can include interventions such as goal setting with input from the patient and carers, positive feedback about performance by using, for example, quantifiable data from outcome measures such as function, quality of life, gait quality and speed [41, 42], motivational interviewing [43] and ‘patient contracts’ such as written agreements about perceived ability, goals and preferred outcomes [44]. The types of interventions included in our PSP systematic review often used complex equipment at a movement disorders clinic or hospital outpatient department. Very few described home based programs or easily accessible equipment that could be used in the community. The benefits of physical activity and strength training are well established for general health and well-being in older adults [45, 46]. It was surprising that basic forms of exercise such as progressive resistive strength training, gym activities, walking programs, cycling or aquatic therapy and falls prevention education programs have not been reported in the PSP literature. There were some limitations of this analysis. Firstly, it was derived from a recent systematic review in which only 11 studies, with only 99 participants in total, met the eligibility criteria. Whether those studies reflect contemporary clinical practice is unknown. For the current analysis, rigorous methods were used to identify research reports and assess the reporting quality in the included studies. A CERT Explanation and Elaboration Statement that provides guidance specifically for complex neurological rehabilitation could be explored and designed with input from a panel of experts. For future research, it is important to design interventions that have a comprehensive and explicit protocol that can be replicated. Greater use of online supplemental materials now provided by academic and clinically orientated journals is one method of including additional detail. Journal editors and peer reviewers play an integral role in ensuring that exercise, rehabilitation, physical activity and physical therapy research is complete and detailed. Researchers are urged to include qualitative methods in research design for exploration of individual preferences and capabilities that would inform intervention design.

Conclusion

Although exercises may have the potential to benefit people living with PSP [20], currently there are few studies that adequately report all key elements of exercise therapy design, implementation and assessment. Overall, explicit reporting of exercise interventions for PSP was found to be problematic within the existing movement disorders literature, making interventions difficult to replicate. It is recommended that future trials use methods such as the CERT to provide a comprehensive description of exercise and physical activity interventions. Journal and editorial policies are also recommended to encourage adherence to reporting guidelines and standards.
  38 in total

1.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.

Authors:  David Moher; Alessandro Liberati; Jennifer Tetzlaff; Douglas G Altman
Journal:  Ann Intern Med       Date:  2009-07-20       Impact factor: 25.391

2.  Effect of High-Intensity Treadmill Exercise on Motor Symptoms in Patients With De Novo Parkinson Disease: A Phase 2 Randomized Clinical Trial.

Authors:  Margaret Schenkman; Charity G Moore; Wendy M Kohrt; Deborah A Hall; Anthony Delitto; Cynthia L Comella; Deborah A Josbeno; Cory L Christiansen; Brian D Berman; Benzi M Kluger; Edward L Melanson; Samay Jain; Julie A Robichaud; Cynthia Poon; Daniel M Corcos
Journal:  JAMA Neurol       Date:  2018-02-01       Impact factor: 18.302

3.  Supported treadmill training for gait and balance in a patient with progressive supranuclear palsy.

Authors:  Monthaporn Suteerawattananon; Betty MacNeill; Elizabeth J Protas
Journal:  Phys Ther       Date:  2002-05

Review 4.  The diagnosis of progressive supranuclear palsy: current opinions and challenges.

Authors:  Farwa Ali; Keith Josephs
Journal:  Expert Rev Neurother       Date:  2018-06-28       Impact factor: 4.618

5.  The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration.

Authors:  Alessandro Liberati; Douglas G Altman; Jennifer Tetzlaff; Cynthia Mulrow; Peter C Gøtzsche; John P A Ioannidis; Mike Clarke; P J Devereaux; Jos Kleijnen; David Moher
Journal:  PLoS Med       Date:  2009-07-21       Impact factor: 11.069

6.  Balance and eye movement training to improve gait in people with progressive supranuclear palsy: quasi-randomized clinical trial.

Authors:  Cris Zampieri; Richard P Di Fabio
Journal:  Phys Ther       Date:  2008-10-23

7.  Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.

Authors:  Günter U Höglinger; Gesine Respondek; Maria Stamelou; Carolin Kurz; Keith A Josephs; Anthony E Lang; Brit Mollenhauer; Ulrich Müller; Christer Nilsson; Jennifer L Whitwell; Thomas Arzberger; Elisabet Englund; Ellen Gelpi; Armin Giese; David J Irwin; Wassilios G Meissner; Alexander Pantelyat; Alex Rajput; John C van Swieten; Claire Troakes; Angelo Antonini; Kailash P Bhatia; Yvette Bordelon; Yaroslau Compta; Jean-Christophe Corvol; Carlo Colosimo; Dennis W Dickson; Richard Dodel; Leslie Ferguson; Murray Grossman; Jan Kassubek; Florian Krismer; Johannes Levin; Stefan Lorenzl; Huw R Morris; Peter Nestor; Wolfgang H Oertel; Werner Poewe; Gil Rabinovici; James B Rowe; Gerard D Schellenberg; Klaus Seppi; Thilo van Eimeren; Gregor K Wenning; Adam L Boxer; Lawrence I Golbe; Irene Litvan
Journal:  Mov Disord       Date:  2017-05-03       Impact factor: 10.338

8.  Effects of robot assisted gait training in progressive supranuclear palsy (PSP): a preliminary report.

Authors:  Patrizio Sale; Fabrizio Stocchi; Daniele Galafate; Maria Francesca De Pandis; Domenica Le Pera; Ivan Sova; Manuela Galli; Calogero Foti; Marco Franceschini
Journal:  Front Hum Neurosci       Date:  2014-04-17       Impact factor: 3.169

Review 9.  Atypical parkinsonism: an update.

Authors:  Maria Stamelou; Guenter U Hoeglinger
Journal:  Curr Opin Neurol       Date:  2013-08       Impact factor: 5.710

Review 10.  Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options.

Authors:  Ruth Lamb; Jonathan D Rohrer; Andrew J Lees; Huw R Morris
Journal:  Curr Treat Options Neurol       Date:  2016-09       Impact factor: 3.598

View more
  2 in total

1.  Enablers to Exercise Participation in Progressive Supranuclear Palsy: Health Professional Perspectives.

Authors:  Meg E Morris; Susan C Slade; Christopher Bruce; Jennifer L McGinley; Bastiaan R Bloem
Journal:  Front Neurol       Date:  2021-02-02       Impact factor: 4.003

Review 2.  Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome: A Consensus Statement of the CurePSP Centers of Care.

Authors:  Brent Bluett; Alexander Y Pantelyat; Irene Litvan; Farwa Ali; Diana Apetauerova; Danny Bega; Lisa Bloom; James Bower; Adam L Boxer; Marian L Dale; Rohit Dhall; Antoine Duquette; Hubert H Fernandez; Jori E Fleisher; Murray Grossman; Michael Howell; Diana R Kerwin; Julie Leegwater-Kim; Christiane Lepage; Peter Alexander Ljubenkov; Martina Mancini; Nikolaus R McFarland; Paolo Moretti; Erica Myrick; Pritika Patel; Laura S Plummer; Federico Rodriguez-Porcel; Julio Rojas; Christos Sidiropoulos; Miriam Sklerov; Leonard L Sokol; Paul J Tuite; Lawren VandeVrede; Jennifer Wilhelm; Anne-Marie A Wills; Tao Xie; Lawrence I Golbe
Journal:  Front Neurol       Date:  2021-07-01       Impact factor: 4.003

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.