l. Mert-uri F., Bertini E, Messina S, et al. Pilot trial of phenylbtıtyıate in spinal muscular atrophy. Neuromusctıl Disord. 2004; 14: I 30— 135.
Merlini l., Bcrtini E, Minetti C, et al. Motor function- muscle strength relationship in spinal muscular atrophy. Muscle Nevre. 20tl4ı291548—552.
Kroksınark A, Beckımg F., Tulinius M. Muscle strength and motor function in children and adolescents with spinal muscular atrophy 2 and 3. Eur J Pacdiaır Neurol. 200l:5:l9I-I98.
Karaduman A, Erbalıçeci F, 'l'opaloğlu H. Nöromusküler sistem hastalıklarında rehabilitasyon. Fizyoter Rehalıil. 199l 1538—46. Merlini L, Fstournct B, Iannaccone S. et al. 59th FIN-MC International workshop: European SMA randomised trial. Neuromuseul Disorcl. 2002;12:201-210.
_ Main M, Kairon H, Mercuı'i E, et al. The Hammersmith functional motor scale for children with spinal muscular atrophy: a scale to test ability and monitor progress in children with limited aınhulation. Eur ] Paediatr Neurol. 20033355459.
îr'. Dubowitz V. Chaos in the classification of SMA: a possible resolution. Ncuromuscul Disord, |995:5:3—5.
Viguos PJ. Management of ıntıseuloskeletal complications in ııeuroınuscular disease: liınh contracrures and the role of streching. Phys Med Rel—ıalıil. l988;2:509—536_
, Willig TN, Bach JR. Roufl'eı MJ, et al. Cortelation of llcxioıı contractures with upper extremity Function and pain l'or spinal muscular atrophy and related congenital ıııyopathy patients. Anı J Phys Med Rehabil. 1995:74133-38.
Eng GD, Binder ll, Koch B. Spinal muscular atrophy: experience in diagnosis and rehabilitation management ol' (ıt) patients. Arch Phys Med Rehabil. 1984;65:549- 553.
lt. Üranata C, Corneliu F, Matrutini P. et al. Promotion of ambularion of patients with spinal muscular atrophy by early fitting ol' knee-ankle—t'oot orthoses. Dev Med Child Neurol. 1987:29:22l—224.
Karaduman A. Progresif müsküler distrot'ıli çocuklarda fizyoterapi ve rehabilitasyon. Hacettepe Üniversitesi, Yayınlanmamış Doktora Tezi. Ankara; 1989.
I3. Stcficıısen B, Lyager S, Werge B, et al. Physical capacity in non- ambulatory pcoplc with Duchenne muscular dystrophy or spinal muscular atrophy: a longitudinal study. Dev Med Child Neurol. 2002;44: 623-632.
Tomassoni T. Role of exercise in the assessment and
management of neuromusaular disease in children. Med
Sci Sports Exerc. l996128:42|-42?.
Aitkens SG. McC'rory MA. Kilmer DD. et al. Moderate
exercise program: its ct‘t'cct in slowly progressive
tlcuromusculsr disease. Arch Phys Med Rehabil. 1993;74:711—715.
?le-tres K, Rudnik S. Forest E, et al. A collaborative study
on the natural history of childhood and juvenile onset
proximal spinal muscular atrophy [type 2 and type 3
sına): 569 patients. JNcurol Sci. 1997;146:67-72.
Fowler WM. Rehabilitation management of muscular
dystrophy and related disorders: comprehensive care.
Arch Phys Med Rehabil. 1932;63:322-328.
Wright NC, Kilmcr DD, McCrot‘y MA, ct al. Aerobic
walking in slowly progressive ueuromuseular disease:
effect of a l2 week program. Arch Phys Med Rehabil. l996;77:64-69.
Kilmer DD. McCrory MA. Wright NC, et al. The effect
of high resistance exercise program in slowly
McCartney N, Morita D, Garner SI 1, ct al. The elTec-t's of
Berg K. Effect of' physical training of school children
Burton A. Davis W. Optimizing the involvement and perfonntmec of children with physical impairments in movement activities. Pediatr Exam Sci. 1990;2z46-56. Evangelism LS. Draeup K, Erickson V. et al. Validity of pedoinctet's for measuring exercise adherence in heart failure patients] Card Fail. 2005;11:366-371.
Biyoterapi Rehabfi'itasyon 170“) 2006
Kütüphaneme Ekle
Spinal musküler atrofili olgularda ev programının kas kuvveti ve motor fonksiyon üzerine etkileri
l. Mert-uri F., Bertini E, Messina S, et al. Pilot trial of phenylbtıtyıate in spinal muscular atrophy. Neuromusctıl Disord. 2004; 14: I 30— 135.
Merlini l., Bcrtini E, Minetti C, et al. Motor function- muscle strength relationship in spinal muscular atrophy. Muscle Nevre. 20tl4ı291548—552.
Kroksınark A, Beckımg F., Tulinius M. Muscle strength and motor function in children and adolescents with spinal muscular atrophy 2 and 3. Eur J Pacdiaır Neurol. 200l:5:l9I-I98.
Karaduman A, Erbalıçeci F, 'l'opaloğlu H. Nöromusküler sistem hastalıklarında rehabilitasyon. Fizyoter Rehalıil. 199l 1538—46. Merlini L, Fstournct B, Iannaccone S. et al. 59th FIN-MC International workshop: European SMA randomised trial. Neuromuseul Disorcl. 2002;12:201-210.
_ Main M, Kairon H, Mercuı'i E, et al. The Hammersmith functional motor scale for children with spinal muscular atrophy: a scale to test ability and monitor progress in children with limited aınhulation. Eur ] Paediatr Neurol. 20033355459.
îr'. Dubowitz V. Chaos in the classification of SMA: a possible resolution. Ncuromuscul Disord, |995:5:3—5.
Viguos PJ. Management of ıntıseuloskeletal complications in ııeuroınuscular disease: liınh contracrures and the role of streching. Phys Med Rel—ıalıil. l988;2:509—536_
, Willig TN, Bach JR. Roufl'eı MJ, et al. Cortelation of llcxioıı contractures with upper extremity Function and pain l'or spinal muscular atrophy and related congenital ıııyopathy patients. Anı J Phys Med Rehabil. 1995:74133-38.
Eng GD, Binder ll, Koch B. Spinal muscular atrophy: experience in diagnosis and rehabilitation management ol' (ıt) patients. Arch Phys Med Rehabil. 1984;65:549- 553.
lt. Üranata C, Corneliu F, Matrutini P. et al. Promotion of ambularion of patients with spinal muscular atrophy by early fitting ol' knee-ankle—t'oot orthoses. Dev Med Child Neurol. 1987:29:22l—224.
Karaduman A. Progresif müsküler distrot'ıli çocuklarda fizyoterapi ve rehabilitasyon. Hacettepe Üniversitesi, Yayınlanmamış Doktora Tezi. Ankara; 1989.
I3. Stcficıısen B, Lyager S, Werge B, et al. Physical capacity in non- ambulatory pcoplc with Duchenne muscular dystrophy or spinal muscular atrophy: a longitudinal study. Dev Med Child Neurol. 2002;44: 623-632.
Tomassoni T. Role of exercise in the assessment and
management of neuromusaular disease in children. Med
Sci Sports Exerc. l996128:42|-42?.
Aitkens SG. McC'rory MA. Kilmer DD. et al. Moderate
exercise program: its ct‘t'cct in slowly progressive
tlcuromusculsr disease. Arch Phys Med Rehabil. 1993;74:711—715.
?le-tres K, Rudnik S. Forest E, et al. A collaborative study
on the natural history of childhood and juvenile onset
proximal spinal muscular atrophy [type 2 and type 3
sına): 569 patients. JNcurol Sci. 1997;146:67-72.
Fowler WM. Rehabilitation management of muscular
dystrophy and related disorders: comprehensive care.
Arch Phys Med Rehabil. 1932;63:322-328.
Wright NC, Kilmcr DD, McCrot‘y MA, ct al. Aerobic
walking in slowly progressive ueuromuseular disease:
effect of a l2 week program. Arch Phys Med Rehabil. l996;77:64-69.
Kilmer DD. McCrory MA. Wright NC, et al. The effect
of high resistance exercise program in slowly
McCartney N, Morita D, Garner SI 1, ct al. The elTec-t's of
Berg K. Effect of' physical training of school children
Burton A. Davis W. Optimizing the involvement and perfonntmec of children with physical impairments in movement activities. Pediatr Exam Sci. 1990;2z46-56. Evangelism LS. Draeup K, Erickson V. et al. Validity of pedoinctet's for measuring exercise adherence in heart failure patients] Card Fail. 2005;11:366-371.