Добірка наукової літератури з теми "Progressive weakness"

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Статті в журналах з теми "Progressive weakness"

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Macknight, J. M. "PROGRESSIVE WEAKNESS- WEIGHTLIFTER." Medicine & Science in Sports & Exercise 30, Supplement (1998): 132. http://dx.doi.org/10.1097/00005768-199805001-00748.

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Carswell, Christopher, Luke C. Northey, Leo Davies, Nobuhiro Yuki, and Matthew C. Kiernan. "Progressive bilateral facial weakness." Practical Neurology 15, no. 1 (2014): 76–79. http://dx.doi.org/10.1136/practneurol-2014-000989.

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Galloway, Gloria, Michael J. Giuliani, and David Lacomis. "October 1996 — Rapidly Progressive Weakness." Brain Pathology 7, no. 2 (1997): 837–38. http://dx.doi.org/10.1111/j.1750-3639.1997.tb01068.x.

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Navalkele, Digvijaya D., Maria-Magdalena Georgescu, Dennis K. Burns, Tasha Greenberg, and Steven Vernino. "Progressive Leg Pain and Weakness." JAMA Neurology 70, no. 4 (2013): 510. http://dx.doi.org/10.1001/jamaneurol.2013.2158.

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Lewis, D. W., and P. H. Berman. "Progressive Weakness in Infancy and Childhood." Pediatrics in Review 8, no. 7 (1987): 200–208. http://dx.doi.org/10.1542/pir.8-7-200.

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Sim, Li Ean, and Kevin Tan. "Progressive Weakness, Cognitive Dysfunction and Seizures." Annals of the Academy of Medicine, Singapore 45, no. 7 (2016): 330–31. http://dx.doi.org/10.47102/annals-acadmedsg.v45n7p330.

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Lewis, Donald W., and Peter H. Berman. "Progressive Weakness in Infancy and Childhood." Pediatrics In Review 8, no. 7 (1987): 200–208. http://dx.doi.org/10.1542/pir.8.7.200.

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The child with progressive weakness may have a disorder at one of many possible levels within the nervous system. By establishing the pace and character of the weakness and by localizing the anatomic site of the pathologic condition to either the upper or the lower motor neuron unit, a scheme for systematic evaluation can be developed.
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Younger, David. "Differential Diagnosis of Progressive Flaccid Weakness." Seminars in Neurology 13, no. 03 (1993): 241–46. http://dx.doi.org/10.1055/s-2008-1041130.

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Asbill, Mark C., and Randolph B. Shey. "Progressive Back Pain and Leg Weakness." Hospital Practice 25, sup5 (1990): 132–35. http://dx.doi.org/10.1080/21548331.1990.11704118.

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Lakhotia, Arpita. "A Child With Progressive Leg Weakness." Pediatric Neurology 74 (September 2017): 104–5. http://dx.doi.org/10.1016/j.pediatrneurol.2017.05.001.

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Дисертації з теми "Progressive weakness"

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Arnould, David. "Reconditionnement musculaire dans un modèle murin de myopathie centronucléaire autosomique dominante par inactivation du gène myostatine." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSES008/document.

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La myopathie centronucléaire autosomique dominante (MCN-AD) est une maladie congénitale rare liée à des mutations principalement retrouvées dans le gène dynamine-2. La majorité des patients atteints de MCN-AD présente une évolution lentement progressive, avec une perte de masse et de force musculaire. A ce jour, aucune thérapie n’est disponible pour la MCN-AD. Des interventions thérapeutiques visant à limiter la progression et la sévérité de l’atteinte musculaire ainsi qu’à améliorer la qualité de vie des patients, sont donc nécessaires. Nous faisons l’hypothèse qu’une hypertrophie induite par
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Книги з теми "Progressive weakness"

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Kussmaul, Adolf. On a previously undescribed peculiar arterial disease (Periarteritis nodosa), accompanied by Bright's disease and rapidly progressive general muscle weakness. Mayo Foundation, 1996.

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Kussmaul, Adolf. On a previous undescribed peculiar arterial disease (Periarteritis nodosa), accompanied by Bright's disease and rapidly progressive general muscle weakness. Mayo Foundation, 1996.

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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 48-Year-Old with Progressive Weakness and Pain. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0005.

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Guillain-Barré syndrome may present in several ways, although predominant proximal weakness is a common feature of the disease to recognize. The differential diagnosis may be extensive and can include infection, vasculitis, toxin exposure, and malignancy. A lumbar puncture must be done with minimal delay to evaluate for cerebrospinal fluid (CSF) albuminocytological dissociation, however results may be normal early in the course of the disease. EMG/NCS are helpful to support the diagnosis, and early treatment with intravenous immunoglobulin (IVIG) is essential. This chapter discusses the clinic
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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 55-Year-Old Female with Slowly Progressive Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0010.

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Chronic inflammatory demyelinating polyneuropathy (CIPD) typically presents with both proximal and distal weakness, areflexia, and distal sensory findings. Two-thirds of patients have a progressive course over many months to years, however one-third of patients have a relapsing course with partial or complete recovery. It is important to be aware of several systemic disorders which may be associated with CIDP. Immunoglobulin M antibody–producing neuropathies have a monoclonal protein that is usually detected with serum protein electrophoresis, which may mimic CIDP. This chapter emphasizes the
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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. An 18-Year-Old Male with Slowly Progressive Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0028.

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Slow progression of proximal weakness in an adult may suggest Becker muscular dystrophy, but limb-girdle muscular dystrophy needs to be considered. This chapter discusses a diagnostic approach that includes the utility of ever-evolving genetic tests. Electromyography is helpful in cases of suspected muscular dystrophy without a family history, if creatine kinase levels are low, or in evaluation of possible female carriers for BMD who are symptomatic. Management considerations are also outlined. A muscular dystrophy clinic with a multidisciplinary approach is helpful for coordination of care. A
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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 35-Year-Old Man with Progressive Left-Hand Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0001.

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Multifocal motor neuropathy (MMN) may be mistaken for common entrapment neuropathies, although absence of significant sensory findings is a helpful clue to the diagnosis. Multifocal motor neuropathy may also mimic motor neuron disease. Electrophysiological evidence of conduction block at a nerve site not typically prone to compression is consistent with MMN. A positive anti-GM1 antibody also supports the diagnosis. First-line treatment of MMN is intravenous immunoglobulin (IVIG), and the majority of patients have rapid improvement of their weakness. The clinical features, differential diagnosi
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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 30-Year-Old Male Requiring Management of Progressive Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0006.

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Management of Guillain-Barré syndrome involves several factors. Pulmonary function tests are important to monitor. Telemetry and blood pressure must be monitored because of the significant risk of autonomic dysfunction. Intravenous immunoglobulin is the immunotherapy of choice for this disease, as it is less complicated to administer than plasma exchange. Supportive management issues to address include deep vein thrombosis prophylaxis, bowel/bladder care as ileus and urinary retention may be develop secondary to dysautonomia, physical/occupational/speech therapy consults, nutrition, and pain c
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Cohen, Jeffrey A., Justin J. Mowchun, Victoria H. Lawson, and Nathaniel M. Robbins. A 68-Year-Old Female with Progressive Pain and Weakness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190491901.003.0027.

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Statin myopathy can occur at anytime during use. This chapter discusses an approach to diagnosis, and emphasizes management considerations, including awareness of statin metabolism by the cytochrome P-450 system. A statin must be discontinued in any patient with evidence of myopathy or myalgias. A muscle biopsy should be done in cases that do not improve clinically or by creatine kinase level. It is important to note that there are cases of apparent statin myopathy which transform into a chronic autoimmune inflammatory myopathy. Antibodies to hydroxymethylglutaryl coenzyme A (HMG-CoA) reductas
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Shaibani, Aziz. Distal Leg Weakness. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199898152.003.0016.

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Plantar flexion and/or extension weakness is usually neuromuscular in nature. Rarely, focal foot dystonia, ankle arthritis, and spasticity lead to diagnostic confusion. Painful sequential foot drop is a common feature of vasculitis. Preserved EDB bulk in the face of foot drop is a feature of myopathy. Progressive painless weakness of the foot flexion and extension with normal sensation and brisk deep tendon reflexes are typically seen in ALS. In patients with chronic bilateral foot drop, examination of the scapulae is essential to rule out scapuloperoneal syndrome and FSHD. In inflammatory neu
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Shaibani, Aziz. Distal Leg Weakness. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190661304.003.0016.

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Plantar flexion and extension weakness are usually neuromuscular in nature. Rarely, focal foot dystonia, ankle arthritis, and spasticity lead to diagnostic confusion. Painful, sequential foot drop is a common feature of vasculitis. Preserved extensor digitorum brevis (EDB) bulk in the face of foot drop is a feature of myopathy. Progressive, painless weakness of the foot flexion and extension with normal sensation and brisk deep tendon reflexes (DTRs) are typically seen in amyotrophic lateral sclerosis (ALS). In patients with chronic, bilateral foot drop, examination of the scapulae is essentia
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Частини книг з теми "Progressive weakness"

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Dolezal, Ondrej. "Progressive Weakness." In Clinical Cases in Neurology. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-58297-4_17.

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Tarulli, Andrew. "Rapidly Progressive Weakness." In Neurology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-55598-6_12.

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Tarulli, Andrew. "Rapidly Progressive Weakness." In Neurology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29632-6_12.

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Mehta, Tejas R., Kunal Bhatia, and Niraj Arora. "Rapidly Progressive Muscle Weakness." In Neuromuscular Urgencies and Emergencies. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-53145-4_3.

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Fok, Henry, Kerry Layne, and Adam Nabeebaccus. "Progressive Lower Limb Weakness." In 100 Cases in Acute Medicine, 2nd ed. CRC Press, 2022. http://dx.doi.org/10.1201/9781003241171-30.

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Mahdi-Rogers, Mohamed, Matilde Laurá, and Mary M. Reilly. "Progressive Motor Weakness in a Somalian Man." In Neuromuscular Disease. Springer London, 2016. http://dx.doi.org/10.1007/978-1-4471-2389-7_13.

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Morrow, Jasper M., Janice L. Holton, and Chris Turner. "A Common Cause of Progressive Proximal Weakness…" In Neuromuscular Disease. Springer London, 2016. http://dx.doi.org/10.1007/978-1-4471-2389-7_38.

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Lunn, Michael P. "A Man with Progressive Weakness and Muscle Twitching." In Neuromuscular Disease. Springer London, 2016. http://dx.doi.org/10.1007/978-1-4471-2389-7_9.

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Zhou, Lan, and Dennis K. Burns. "A 42-Year-Old Woman with Progressive Limb Weakness and Breathing Difficulty." In A Case-Based Guide to Neuromuscular Pathology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-25682-1_19.

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Zhou, Lan, and Susan C. Shin. "A 63-Year-Old Man with Progressive Limb Weakness and Slurred Speech." In A Case-Based Guide to Neuromuscular Pathology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-25682-1_22.

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Тези доповідей конференцій з теми "Progressive weakness"

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Nikishkov, Yuri, Guillaume Seon, Andrew Makeev, and Dean Nguyen. "Progressive Fatigue Damage Simulation in Composites based on Explicit Finite Element Formulation." In Vertical Flight Society 73rd Annual Forum & Technology Display. The Vertical Flight Society, 2017. http://dx.doi.org/10.4050/f-0073-2017-12179.

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Advanced polymeric composites are playing a major role in designing high-performance and lightweight vertical lift structures. However, uncertain residual strength and remaining useful life of the composite rotor and airframe structures due to complexity of failure mechanisms and susceptibility to manufacturing irregularities, which may be precursors to structural damage, impose risks that cannot be mitigated exclusively by time-consuming and costly experimental iterations. Validated analysis techniques accelerating design, certification, and qualification of composite structures are needed. O
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Robbins, E., G. Allam, and K. Manzoor. "Progressive Weakness in a Patient with Respiratory Failure: Finding the Uncommon." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a6990.

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Jaber, Samir, Gerald Chanques, Boris Jung, et al. "Rapidly Progressive Diaphragmatic Weakness And Injury During Mechanical Ventilation In Humans." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6613.

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Toloi, Marcella Canato, Thiago Ivan Vilchez Santillan, Kassia Braga Canzian, et al. "Lower limb weakness: a challenge diagnosis." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.713.

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A 46-year-old male patient started a condition of lower back pain radiating to the lower limbs in 2016. He underwent lumbar arthrodesis surgery between L5-S1 due to a herniated disc and reports that after the surgery, his clinical condition improved, remaining asymptomatic over four years. In 2020, he started to experience hypoesthesia in the calf and dorsal region of his right foot, with progressive worsening throughout the year, with a tripping sensation associated with a numbness and decreased distal strength of the right lower limb, with subsequent difficulty in climbing stairs over the ne
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Van Putten, Ashley J., Sridhi M. Patel, Andre Ward, and Hannah L. Winters. "7 Year Old Male With 2 Months Of Progressive Left Sided Weakness." In AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.956.

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Matias, Rafael Braganca Rodrigues, Eduardo Mesquita de Souza, Matheus Alves Silva, et al. "Tubular aggregate myopathy with rhabdomyolysis: an uncommon presentation in elderly male." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.451.

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Introduction: Tubular aggregate myopathy is a rare and an inherited disorder and, differently from metabolic myopathies, is characterized by slowly progressive proximal muscle weakness, cramps and myalgia. The aim to describe an uncommon presentation with rhabdomyolysis overlapping with a tubular aggregate myopathy in elderly men. Case: A 76-year-old male with acute symmetrical inferior limbs weakness and pain. No previous history of muscle weakness. Denied alcohol intake, prior exercise intolerance, fatigue, myoglobinuria, ptosis, or pigmenturia, as well as worsening after periods of fasting.
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Silva, Tarcisio Rubens da, Rayana Elias Maia, and Taísa de Abreu Marques Nogueira. "Progressive thoracolumbar scoliosis culminating in the diagnosis of young pompe disease: case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.044.

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Introduction: Pompe’s disease is a neuromuscular condition caused by a metabolic disorder of autosomal recessive inheritance. The deficit of acid alpha-glucosidase causes accumulation of glycogen in the lysosomes of the striated and cardiac muscle. It presents in childhood: hypotonia and cardiorespiratory impairment; but at late-onset: axial and waist muscle weakness. Case report: Patient, female, 20 years old, non-consanguineous parents, with good intra-uterus fetal mobility, was born by cesarean delivery weighing 3.7 kilograms and 51 centimeters. She first walked without support and spoke he
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Hamzah, Mohammed, Nihat Akin, Nasir Memoona, et al. "Facioscapulohumeral muscular dystrophy with inflammatory myopathy presenting with progressive limb and respiratory muscle weakness." In Association of British Neurologists: Annual Meeting Abstracts 2023. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jnnp-2023-abn.59.

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Esechie, Aimalohi, Ahmed Harazeen, Nelitza Rivera Vega, et al. "Cryoglobulinemia and Neuromyelitis optica: a case of progressive weakness and neurocognitive decline (P10-5.026)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000203690.

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Trivellato, Stella de Angelis, Joao Lucas Gomes Salgado, Hendrick Henrique Fernandes Gramasco, et al. "Thoracolumbar progressive myelopathy due to extra-dural arteriovenous fistula." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.223.

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Context: Arteriovenous dural fistulas are the most common spinal vascular malformations and constitute a reversible cause of progressive myelopathy. This disease affects elderly men and are classically found at the thoracolumbar region. Case report: A 69year-old man was admitted to the Neurology outpatient clinic with weakness in his left inferior limb for the past 10 years; 2 years before the evaluation, the weakness progressed also to the right inferior limb, causing inability to walk, and 1 year after the patient noticed urinary incontinence and sexual dysfunction. Physical evaluation showe
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Звіти організацій з теми "Progressive weakness"

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Timm, Eliane, Julia Vieregg, and Ursula Wolf. Movement based mindfulness therapies in patients with multiple sclerosis – a systematic review protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.2.0102.

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Review question / Objective: The aim is to review the clinical benefits of mindful moving techniques for persons with multiple sclerosis. Condition being studied: Multiple sclerosis. Multiple sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system (Gholamzad et al., 2019; Oh, Vidal-Jordana, & Montalban, 2018). It has shown to be increasing since 2013, and as of 2020 the estimated number of people with MS is 2.8 million worldwide (Walton et al., 2020). Due accumulation of relapses or gradual progression, disability from MS is worsening over time (Cameron & Ni
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Corrigan, E. Gerald. Building Effective Banking Systems in Latin America and the Caribbean. Inter-American Development Bank, 1997. http://dx.doi.org/10.18235/0008919.

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This study discusses staple reforms in banking systems in Latin America and the Caribbean to improve their effectiveness. The paper identifies the main problems countries have been experiencing with banking systems, triggered by large credit losses. The direct and indirect costs of banking sector crises have been astonishingly high. The author holds that while the symptoms and costs of banking sector problems are widely recognized, the magnitude of the remedial task is often significantly underestimated. The author then makes a series of observations to keep in mind: First, the acute and costl
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Wang, Zhen, Colin P. West, Brianna E. Vaa Stelling, et al. Measuring Documentation Burden in Healthcare. Agency for Healthcare Research and Quality (AHRQ), 2024. http://dx.doi.org/10.23970/ahrqepctb47.

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Background. The 2009 enactment of the Health Information Technology for Economic and Clinical Health (HITECH) Act and the wide adoption of electronic health record systems (EHR) have ushered an increasing documentation burden, frequently cited as a key factor affecting the work experience of healthcare professionals and a contributor to burnout. Purpose. This Technical Brief aims to identify: (1) measures of documentation burden, including evaluation of validity evidence, strengths, and weaknesses; (2) different perspectives on the appropriateness of different measures of documentation burden;
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Öjendal, Joakim, Monin Nong, Chanmony Sean, Zoe Sidana Bunnath, and Chanrith Ngin. The Political Economy of Land-Water Resource Governance in the Context of Food Security in Cambodia. Cambodia Development Resource Institute, 2023. https://doi.org/10.64202/wp.142.202311.

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Water is central for a variety of livelihoods, development, economic growth, and food production. It is also very important in the large deltas of South and Southeast Asia. Yet, water is turning into a scare resource and global climate change is making its availability more unpredictable. Commercial interests and infrastructure development are also competing for water resources, sometimes at the expense of local smallholders. This report, which is a desk study combined with stakeholder interviews, aims to map out the issues and the previously unknown challenges to efficient water and land mana
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