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Yıl 2023, Cilt: 40 Sayı: 3, 522 - 529, 30.09.2023

Öz

Kaynakça

  • 1. Hartley SE, Goodwin PC, Goldbart J. Experiences of attendance at a neuromuscular centre: perceptions of adults with neuromuscular disorders. Disabil Rehabil. 2011;33(12):1022-32.
  • 2. Morrison BM. Neuromuscular Diseases. Semin Neurol. 2016;36(5):409-18.
  • 3. Mary P, Servais L, Vialle R. Neuromuscular diseases: Diagnosis and management. Orthop Traumatol Surg Res. 2018;104(1S):S89-S95.
  • 4. Neuromuscular Disorders in Clinical Practice, Bashar Katirji HJK, Robert L. Ruff, editor. Second Edition: Springer Science+Business Media; 2014.
  • 5. Bekiroğlu S, Gökçearslan Çiftçi E. Nöromüsküler Hasta Ailelerinin Yaşadıkları Güçlükler. Türkiye Sosyal Araştırmalar Dergisi. 2017;21(3):704-22.
  • 6. Roy AJ, Van den Bergh P, Van Damme P, Doggen K, Van Casteren V, Committee BS. Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR). Acta Neurol Belg. 2015;115(2):97-104.
  • 7. Younger DS, Gordon PH. Diagnosis in neuromuscular diseases. Neurol Clin. 1996;14(1):135-68.
  • 8. Rowland LP. Cramps, spasms and muscle stiffness. Rev Neurol. 1985;141(4):261-73.
  • 9. Gascon-Navarro JA, De La Torre-Aguilar MJ, Fernandez-Ramos JA, Torres-Borrego J, Perez-Navero JL. Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital. Ital J Pediatr. 2021;47(1):228.
  • 10. Hiller LB, Wade CK. Upper extremity functional assessment scales in children with Duchenne muscular dystrophy: a comparison. Arch Phys Med Rehabil. 1992;73(6):527-34.
  • 11. McDonald CM, Henrickson EK, Abresch RT, Florence J, Eagle M, Gappmaier E, et al. The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve. 2013;48(3):357-68.
  • 12. Mentiplay BF, Clark RA, Bower KJ, Williams G, Pua YH. Five times sit-to-stand following stroke: Relationship with strength and balance. Gait Posture. 2020;78:35-9.
  • 13. Kobayashi T, Morimoto T, Shimanoe C, Ono R, Otani K, Mawatari M. A Simplified Screening Tool for the One-Leg Standing Test to Determine the Severity of Locomotive Syndrome. Life (Basel). 2023;13(5):1190.
  • 14. Bennell K, Dobson F, Hinman R. Measures of physical performance assessments: Self-Paced Walk Test (SPWT), Stair Climb Test (SCT), Six-Minute Walk Test (6MWT), Chair Stand Test (CST), Timed Up & Go (TUG), Sock Test, Lift and Carry Test (LCT), and Car Task. Arthritis Care Res 2011;63(11):350-70.
  • 15. Brooke MH, Griggs RC, Mendell JR, Fenichel GM, Shumate JB, Pellegrino RJ. Clinical trial in Duchenne dystrophy. I. The design of the protocol. Muscle Nerve. 1981;4(3):186-97.
  • 16. Keith RA, Granger CV, Hamilton BB, Sherwin FS. The functional independence measure: a new tool for rehabilitation. Adv Clin Rehabil. 1987(1):6-18.
  • 17. Yetişgin A. Clinical characteristics affecting motor recovery and ambulation in stroke patients. J Phys Ther Sci. 2017;29(2):216-20.
  • 18. Dykiert D, Der G, Starr JM, Deary IJ. Why is Mini-Mental state examination performance correlated with estimated premorbid cognitive ability? Psychol Med. 2016;46(12):2647-54.
  • 19. de Visser M . Late-onset myopathies: clinical features and diagnosis. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology. 2020 Dec;39(4):235-44.
  • 20. Kooi-van Es M, Erasmus CE, de Swart BJM, Voet NBM, van der Wees PJ, de Groot IJM, et al; studygroup Dutch pediatric rehabilitation centers. Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study. J Neuromuscul Dis. 2020;7(3):287-95.
  • 21. Kaya P, Alemdaroğlu İ, Yılmaz Ö, Karaduman A, Topaloğlu H. Effect of muscle weakness distribution on balance in neuromuscular disease. Pediatr Int. 2015;57(1):92-7.
  • 22. Swash M, Schwartz MS. Neuromuscular diseases: a practical approach to diagnosis and management. 2013: Springer Science & Business Media
  • 23. Féasson L, Camdessanché JP, El Mandhi L, Calmels P, Millet GY. Fatigue and neuromuscular diseases. Ann Readapt Med Phys. 2006;49(6):289-300, 75-84.
  • 24. Merkies IS, Schmitz PI, Samijn JP, van der Meche FG, van Doorn PA. Fatigue in immune-mediated polyneuropathies.European Inflammatory Neuropathy Cause and Treatment (INCAT) Group. Neurology 1999;53(8):1648-54.
  • 25. Paul RH, Cohen RA, Goldstein JM, Gilchrist JM. Fatigue and its impact on patients with myasthenia gravis. Muscle Nerve. 2000;23(9):1402-6.
  • 26. Keesey JC. Clinical evaluation and management of myasthenia gravis. Muscle Nerve. 2004;29(4):484-505.
  • 27. Kent-Braun JA, Miller RG. Central fatigue during isometric exercise in amyotrophic lateral sclerosis. Muscle Nerve 2000;23(6):909-14.
  • 28. Horemans HL, Nollet F, Beelen A, Lankhorst GJ. A comparison of 4 questionnaires to measure fatigue in postpoliomyelitis syndrome. Arch Phys Med Rehabil 2004;85(3):392-8.
  • 29. Garssen MP, Bussman JB, Schmitz PI, Zandbergen A, Welter TG, Merkies IS, et al. Physical training and fatigue, fitness, and quality of life in Guillain-Barré syndrome and CIDP. Neurology. 2004;63(12):2393-5.
  • 30. Bellofatto M, Bertini A, Tramacere I, Manganelli F, Fabrizi GM, Schenone A, et al; Italian CMT Network. Frequency, entity and determinants of fatigue in Charcot-Marie-Tooth disease. Eur J Neurol. 2023;30(3):710-18.
  • 31. Elliot DL, Buist NR, Goldberg L, Kennaway NG, Powell BR, Kuehl KS. Metabolic myopathies: evaluation by graded exercise testing. Medicine (Baltimore). 1989 May;68(3):163-72.
  • 32. Audag N, Liistro G, Goubau C, Vandervelde L, Poncin W, Toussaint M, Van den Bergh P, Reychler G. Screening for oropharyngeal dysphagia in adult patients with neuromuscular diseases using the Sydney Swallow Questionnaire. Muscle Nerve. 2021 Sep;64(3):277-84.
  • 33. Knuijt S, Kalf JG, de Swart BJ, Drost G, Hendricks HT, Geurts AC, et al. Dysarthria and dysphagia are highly prevalent among various types of neuromuscular diseases. Disabil Rehabil. 2014;36(15):1285-9.
  • 34. Es MK, Erasmus CE, Houwen S, de Groot IJM, Voet NBM, van den Engel-Hoek L. Early detection of dysphagia and dysarthria in children with neuromuscular disorders: Diagnostic accuracy of a Screening list for Physicians. J Pediatr Rehabil Med. 2020;13(1):17-23.
  • 35. Macht M, King JC, Wimbish T, Clark BJ, Benson AB, Burnham EL, et al. Post-extubation dysphagia is associated with longer hospitalization in survivors of critical illness with neurologic impairment. Crit Care. 2013;17(3):R119.
  • 36. McIntyre M, Doeltgen S, Dalton N, Koppa M, Chimunda T. Post-extubation dysphagia incidence in critically ill patients: A systematic review and meta-analysis. Aust Crit Care. 2021;34(1):67-75.
  • 37. Schröder JB, Marian T, Muhle P, Claus I, Thomas C, Ruck T, et al. Intubation, tracheostomy, and decannulation in patients with Guillain-Barré-syndrome-does dysphagia matter? Muscle Nerve. 2019;59(2):194-200.
  • 38. Chio A, Mora G, Lauria G. Pain in amyotrophic lateral sclerosis. Lancet Neurol. 2017;16(2):144-57.
  • 39. Åkerblom Y, Zetterberg L, Larsson BJ, Nyholm D, Nygren I, Åsenlöf P. Pain, disease severity and associations with individual quality of life in patients with motor neuron diseases. BMC Palliat Care. 2021;20(1):154.
  • 40. Miró J, Gertz KJ, Carter GT, Jensen MP. Chronic pain in neuromuscular disease: pain site and intensity differentially impacts function. Phys Med Rehabil Clin N Am. 2012;23(4):895-902.
  • 41. Jensen TS, Karlsson P, Gylfadottir SS, Andersen ST, Bennett DL, Tankisi H, et al. Painful and non-painful diabetic neuropathy, diagnostic challenges and implications for future management. Brain. 2021;144(6):1632-45.
  • 42. Jensen MP, Hoffman AJ, Stoelb BL, Abresch RT, Carter GT, McDonald CM. Chronic pain in persons with myotonic and facioscapulohumeral muscular dystrophy. Arch Phys Med Rehabil. 2008;89(2):320-8.
  • 43. Pousada García T, Loureiro JP, González BG, Nieto-Rivero L. Assistive technology based on client-centered for occupational performance in neuromuscular conditions. Medicine (Baltimore). 2019 Jun;98(25):e15983.
  • 44. Casey KS. Creating an assistive technology clinic: The experience of the Johns Hopkins AT Clinic for patients with ALS. Neurorehabilitation. 2011;28:281-93.
  • 45. Frank AO. Duchenne muscular dystrophy: assistive technology and preparing for employment. BMJ. 2020;368:m758.
  • 46. Connors K, Mahony L, Morgan P. Variation in assistive technology use in Motor Neuron Disease according to clinical phenotypes and ALS Functional Rating Scale - Revised Score: A prospective observational study. NeuroRehabilitation. 2019;44(2):303-13.
  • 47. Pieterse AJ, Luttikhold TB, de Laat K, Bloem BR, van Engelen BG, Munneke M. Falls in patients with neuromuscular disorders. J Neurol Sci. 2006 Dec;251(1-2):87-90.
  • 48. Ofran Y, Schwartz I, Shabat S, Seyres M, Karniel N, Portnoy S. Falls in Post-Polio Patients: Prevalence and Risk Factors. Biology. 2021;10(11):1110.
  • 49. Francis GJ, Cook AE, Morrish DW, Chan KM, Acharya HJ. What is the Fracture Risk in Patients at a Multidisciplinary Neuromuscular Clinic? J Neuromuscul Dis. 2018;5(1):93-8.
  • 50. Orsini M, Carolina A, Ferreira AF, de Assis ACD, Magalhães T, Teixeira S, et al. Cognitive impairment in neuromuscular diseases: A systematic review. Neurol Int. 2018 Jul 4;10(2):7473.
  • 51. Phukan J, Elamin M, Bede P, Jordan N, Gallagher L, Byrne S, Lynch C, Pender N, Hardiman O. The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):102-8.
  • 52. Consonni M, Dalla Bella E, Bersano E, Lauria G. Cognitive and behavioural impairment in amyotrophic lateral sclerosis: A landmark of the disease? A mini review of longitudinal studies. Neurosci Lett. 2021;754:135898.

Clinical profiles of neuromuscular disorders: a tertiary hospital experience

Yıl 2023, Cilt: 40 Sayı: 3, 522 - 529, 30.09.2023

Öz

This study aimed to identify the symptoms and disease-related features of the most common neuromuscular disorders (NMD) to establish an appropriate multidisciplinary approach in a specific field.A total of 46 patients, 26 (56.5%) women and 20 (43.5%) men with a median age of 46.0 (17.0-72.0) years were divided into three groups according to the affected part of the motor unit: Group I (neuronopathy group, n=11), motor neuron diseases; Group II (neuropathy group, n=13), peripheral neuropathies; and Group III (myopathy group, n=22), myopathies. Demographic and clinical features, functional level, muscular strength, balance, dexterity, activities of daily living, functional performance, global cognitive status test scores, respiratory symptoms, and pulmonary test results were recorded from patient files.There was a significant difference between the mean ages of Groups II and III (p =0.046). A significant difference was observed in muscle weakness between Groups II and III (p = 0.044). The prevalence of dysarthria and speech disorders was higher in Group III (33.3%) compared to Groups II (10%) and I (12.2%). The summarized mini-mental test scores were significantly lower in Group I than in Groups II and III (p =0.047 and p = 0.034, respectively). The nine-hole peg test scores were significantly longer in Group I than in the other groups (p = 0.034 and 0.038, respectively). In this study, NMD were divided into three main groups, and the most common symptoms and clinical findings were evaluated. Fatigue and muscle weakness were the most common symptoms shared by all groups. The mean age of the disease was lowest in the myopathy group. Dysarthria was most common in the neuropathy group. Cognitive impairment was most common in the neuronopathy group.

Kaynakça

  • 1. Hartley SE, Goodwin PC, Goldbart J. Experiences of attendance at a neuromuscular centre: perceptions of adults with neuromuscular disorders. Disabil Rehabil. 2011;33(12):1022-32.
  • 2. Morrison BM. Neuromuscular Diseases. Semin Neurol. 2016;36(5):409-18.
  • 3. Mary P, Servais L, Vialle R. Neuromuscular diseases: Diagnosis and management. Orthop Traumatol Surg Res. 2018;104(1S):S89-S95.
  • 4. Neuromuscular Disorders in Clinical Practice, Bashar Katirji HJK, Robert L. Ruff, editor. Second Edition: Springer Science+Business Media; 2014.
  • 5. Bekiroğlu S, Gökçearslan Çiftçi E. Nöromüsküler Hasta Ailelerinin Yaşadıkları Güçlükler. Türkiye Sosyal Araştırmalar Dergisi. 2017;21(3):704-22.
  • 6. Roy AJ, Van den Bergh P, Van Damme P, Doggen K, Van Casteren V, Committee BS. Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR). Acta Neurol Belg. 2015;115(2):97-104.
  • 7. Younger DS, Gordon PH. Diagnosis in neuromuscular diseases. Neurol Clin. 1996;14(1):135-68.
  • 8. Rowland LP. Cramps, spasms and muscle stiffness. Rev Neurol. 1985;141(4):261-73.
  • 9. Gascon-Navarro JA, De La Torre-Aguilar MJ, Fernandez-Ramos JA, Torres-Borrego J, Perez-Navero JL. Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital. Ital J Pediatr. 2021;47(1):228.
  • 10. Hiller LB, Wade CK. Upper extremity functional assessment scales in children with Duchenne muscular dystrophy: a comparison. Arch Phys Med Rehabil. 1992;73(6):527-34.
  • 11. McDonald CM, Henrickson EK, Abresch RT, Florence J, Eagle M, Gappmaier E, et al. The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve. 2013;48(3):357-68.
  • 12. Mentiplay BF, Clark RA, Bower KJ, Williams G, Pua YH. Five times sit-to-stand following stroke: Relationship with strength and balance. Gait Posture. 2020;78:35-9.
  • 13. Kobayashi T, Morimoto T, Shimanoe C, Ono R, Otani K, Mawatari M. A Simplified Screening Tool for the One-Leg Standing Test to Determine the Severity of Locomotive Syndrome. Life (Basel). 2023;13(5):1190.
  • 14. Bennell K, Dobson F, Hinman R. Measures of physical performance assessments: Self-Paced Walk Test (SPWT), Stair Climb Test (SCT), Six-Minute Walk Test (6MWT), Chair Stand Test (CST), Timed Up & Go (TUG), Sock Test, Lift and Carry Test (LCT), and Car Task. Arthritis Care Res 2011;63(11):350-70.
  • 15. Brooke MH, Griggs RC, Mendell JR, Fenichel GM, Shumate JB, Pellegrino RJ. Clinical trial in Duchenne dystrophy. I. The design of the protocol. Muscle Nerve. 1981;4(3):186-97.
  • 16. Keith RA, Granger CV, Hamilton BB, Sherwin FS. The functional independence measure: a new tool for rehabilitation. Adv Clin Rehabil. 1987(1):6-18.
  • 17. Yetişgin A. Clinical characteristics affecting motor recovery and ambulation in stroke patients. J Phys Ther Sci. 2017;29(2):216-20.
  • 18. Dykiert D, Der G, Starr JM, Deary IJ. Why is Mini-Mental state examination performance correlated with estimated premorbid cognitive ability? Psychol Med. 2016;46(12):2647-54.
  • 19. de Visser M . Late-onset myopathies: clinical features and diagnosis. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology. 2020 Dec;39(4):235-44.
  • 20. Kooi-van Es M, Erasmus CE, de Swart BJM, Voet NBM, van der Wees PJ, de Groot IJM, et al; studygroup Dutch pediatric rehabilitation centers. Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study. J Neuromuscul Dis. 2020;7(3):287-95.
  • 21. Kaya P, Alemdaroğlu İ, Yılmaz Ö, Karaduman A, Topaloğlu H. Effect of muscle weakness distribution on balance in neuromuscular disease. Pediatr Int. 2015;57(1):92-7.
  • 22. Swash M, Schwartz MS. Neuromuscular diseases: a practical approach to diagnosis and management. 2013: Springer Science & Business Media
  • 23. Féasson L, Camdessanché JP, El Mandhi L, Calmels P, Millet GY. Fatigue and neuromuscular diseases. Ann Readapt Med Phys. 2006;49(6):289-300, 75-84.
  • 24. Merkies IS, Schmitz PI, Samijn JP, van der Meche FG, van Doorn PA. Fatigue in immune-mediated polyneuropathies.European Inflammatory Neuropathy Cause and Treatment (INCAT) Group. Neurology 1999;53(8):1648-54.
  • 25. Paul RH, Cohen RA, Goldstein JM, Gilchrist JM. Fatigue and its impact on patients with myasthenia gravis. Muscle Nerve. 2000;23(9):1402-6.
  • 26. Keesey JC. Clinical evaluation and management of myasthenia gravis. Muscle Nerve. 2004;29(4):484-505.
  • 27. Kent-Braun JA, Miller RG. Central fatigue during isometric exercise in amyotrophic lateral sclerosis. Muscle Nerve 2000;23(6):909-14.
  • 28. Horemans HL, Nollet F, Beelen A, Lankhorst GJ. A comparison of 4 questionnaires to measure fatigue in postpoliomyelitis syndrome. Arch Phys Med Rehabil 2004;85(3):392-8.
  • 29. Garssen MP, Bussman JB, Schmitz PI, Zandbergen A, Welter TG, Merkies IS, et al. Physical training and fatigue, fitness, and quality of life in Guillain-Barré syndrome and CIDP. Neurology. 2004;63(12):2393-5.
  • 30. Bellofatto M, Bertini A, Tramacere I, Manganelli F, Fabrizi GM, Schenone A, et al; Italian CMT Network. Frequency, entity and determinants of fatigue in Charcot-Marie-Tooth disease. Eur J Neurol. 2023;30(3):710-18.
  • 31. Elliot DL, Buist NR, Goldberg L, Kennaway NG, Powell BR, Kuehl KS. Metabolic myopathies: evaluation by graded exercise testing. Medicine (Baltimore). 1989 May;68(3):163-72.
  • 32. Audag N, Liistro G, Goubau C, Vandervelde L, Poncin W, Toussaint M, Van den Bergh P, Reychler G. Screening for oropharyngeal dysphagia in adult patients with neuromuscular diseases using the Sydney Swallow Questionnaire. Muscle Nerve. 2021 Sep;64(3):277-84.
  • 33. Knuijt S, Kalf JG, de Swart BJ, Drost G, Hendricks HT, Geurts AC, et al. Dysarthria and dysphagia are highly prevalent among various types of neuromuscular diseases. Disabil Rehabil. 2014;36(15):1285-9.
  • 34. Es MK, Erasmus CE, Houwen S, de Groot IJM, Voet NBM, van den Engel-Hoek L. Early detection of dysphagia and dysarthria in children with neuromuscular disorders: Diagnostic accuracy of a Screening list for Physicians. J Pediatr Rehabil Med. 2020;13(1):17-23.
  • 35. Macht M, King JC, Wimbish T, Clark BJ, Benson AB, Burnham EL, et al. Post-extubation dysphagia is associated with longer hospitalization in survivors of critical illness with neurologic impairment. Crit Care. 2013;17(3):R119.
  • 36. McIntyre M, Doeltgen S, Dalton N, Koppa M, Chimunda T. Post-extubation dysphagia incidence in critically ill patients: A systematic review and meta-analysis. Aust Crit Care. 2021;34(1):67-75.
  • 37. Schröder JB, Marian T, Muhle P, Claus I, Thomas C, Ruck T, et al. Intubation, tracheostomy, and decannulation in patients with Guillain-Barré-syndrome-does dysphagia matter? Muscle Nerve. 2019;59(2):194-200.
  • 38. Chio A, Mora G, Lauria G. Pain in amyotrophic lateral sclerosis. Lancet Neurol. 2017;16(2):144-57.
  • 39. Åkerblom Y, Zetterberg L, Larsson BJ, Nyholm D, Nygren I, Åsenlöf P. Pain, disease severity and associations with individual quality of life in patients with motor neuron diseases. BMC Palliat Care. 2021;20(1):154.
  • 40. Miró J, Gertz KJ, Carter GT, Jensen MP. Chronic pain in neuromuscular disease: pain site and intensity differentially impacts function. Phys Med Rehabil Clin N Am. 2012;23(4):895-902.
  • 41. Jensen TS, Karlsson P, Gylfadottir SS, Andersen ST, Bennett DL, Tankisi H, et al. Painful and non-painful diabetic neuropathy, diagnostic challenges and implications for future management. Brain. 2021;144(6):1632-45.
  • 42. Jensen MP, Hoffman AJ, Stoelb BL, Abresch RT, Carter GT, McDonald CM. Chronic pain in persons with myotonic and facioscapulohumeral muscular dystrophy. Arch Phys Med Rehabil. 2008;89(2):320-8.
  • 43. Pousada García T, Loureiro JP, González BG, Nieto-Rivero L. Assistive technology based on client-centered for occupational performance in neuromuscular conditions. Medicine (Baltimore). 2019 Jun;98(25):e15983.
  • 44. Casey KS. Creating an assistive technology clinic: The experience of the Johns Hopkins AT Clinic for patients with ALS. Neurorehabilitation. 2011;28:281-93.
  • 45. Frank AO. Duchenne muscular dystrophy: assistive technology and preparing for employment. BMJ. 2020;368:m758.
  • 46. Connors K, Mahony L, Morgan P. Variation in assistive technology use in Motor Neuron Disease according to clinical phenotypes and ALS Functional Rating Scale - Revised Score: A prospective observational study. NeuroRehabilitation. 2019;44(2):303-13.
  • 47. Pieterse AJ, Luttikhold TB, de Laat K, Bloem BR, van Engelen BG, Munneke M. Falls in patients with neuromuscular disorders. J Neurol Sci. 2006 Dec;251(1-2):87-90.
  • 48. Ofran Y, Schwartz I, Shabat S, Seyres M, Karniel N, Portnoy S. Falls in Post-Polio Patients: Prevalence and Risk Factors. Biology. 2021;10(11):1110.
  • 49. Francis GJ, Cook AE, Morrish DW, Chan KM, Acharya HJ. What is the Fracture Risk in Patients at a Multidisciplinary Neuromuscular Clinic? J Neuromuscul Dis. 2018;5(1):93-8.
  • 50. Orsini M, Carolina A, Ferreira AF, de Assis ACD, Magalhães T, Teixeira S, et al. Cognitive impairment in neuromuscular diseases: A systematic review. Neurol Int. 2018 Jul 4;10(2):7473.
  • 51. Phukan J, Elamin M, Bede P, Jordan N, Gallagher L, Byrne S, Lynch C, Pender N, Hardiman O. The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):102-8.
  • 52. Consonni M, Dalla Bella E, Bersano E, Lauria G. Cognitive and behavioural impairment in amyotrophic lateral sclerosis: A landmark of the disease? A mini review of longitudinal studies. Neurosci Lett. 2021;754:135898.
Toplam 52 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Research Article
Yazarlar

Zeynep Tuba Bahtiyarca 0000-0002-3630-2524

Özgür Zeliha Karaahmet 0000-0002-1338-8935

Damla Cankurtaran 0000-0002-6208-3345

Ebru Umay 0000-0002-4137-7731

Yasemin Tombak 0000-0003-0065-5376

Mehlika Panpallı Ateş 0000-0002-9744-9255

Erken Görünüm Tarihi 6 Ekim 2023
Yayımlanma Tarihi 30 Eylül 2023
Gönderilme Tarihi 18 Mart 2023
Kabul Tarihi 21 Ağustos 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 40 Sayı: 3

Kaynak Göster

APA Bahtiyarca, Z. T., Karaahmet, Ö. Z., Cankurtaran, D., Umay, E., vd. (2023). Clinical profiles of neuromuscular disorders: a tertiary hospital experience. Journal of Experimental and Clinical Medicine, 40(3), 522-529.
AMA Bahtiyarca ZT, Karaahmet ÖZ, Cankurtaran D, Umay E, Tombak Y, Panpallı Ateş M. Clinical profiles of neuromuscular disorders: a tertiary hospital experience. J. Exp. Clin. Med. Eylül 2023;40(3):522-529.
Chicago Bahtiyarca, Zeynep Tuba, Özgür Zeliha Karaahmet, Damla Cankurtaran, Ebru Umay, Yasemin Tombak, ve Mehlika Panpallı Ateş. “Clinical Profiles of Neuromuscular Disorders: A Tertiary Hospital Experience”. Journal of Experimental and Clinical Medicine 40, sy. 3 (Eylül 2023): 522-29.
EndNote Bahtiyarca ZT, Karaahmet ÖZ, Cankurtaran D, Umay E, Tombak Y, Panpallı Ateş M (01 Eylül 2023) Clinical profiles of neuromuscular disorders: a tertiary hospital experience. Journal of Experimental and Clinical Medicine 40 3 522–529.
IEEE Z. T. Bahtiyarca, Ö. Z. Karaahmet, D. Cankurtaran, E. Umay, Y. Tombak, ve M. Panpallı Ateş, “Clinical profiles of neuromuscular disorders: a tertiary hospital experience”, J. Exp. Clin. Med., c. 40, sy. 3, ss. 522–529, 2023.
ISNAD Bahtiyarca, Zeynep Tuba vd. “Clinical Profiles of Neuromuscular Disorders: A Tertiary Hospital Experience”. Journal of Experimental and Clinical Medicine 40/3 (Eylül 2023), 522-529.
JAMA Bahtiyarca ZT, Karaahmet ÖZ, Cankurtaran D, Umay E, Tombak Y, Panpallı Ateş M. Clinical profiles of neuromuscular disorders: a tertiary hospital experience. J. Exp. Clin. Med. 2023;40:522–529.
MLA Bahtiyarca, Zeynep Tuba vd. “Clinical Profiles of Neuromuscular Disorders: A Tertiary Hospital Experience”. Journal of Experimental and Clinical Medicine, c. 40, sy. 3, 2023, ss. 522-9.
Vancouver Bahtiyarca ZT, Karaahmet ÖZ, Cankurtaran D, Umay E, Tombak Y, Panpallı Ateş M. Clinical profiles of neuromuscular disorders: a tertiary hospital experience. J. Exp. Clin. Med. 2023;40(3):522-9.