Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathies
暂无分享,去创建一个
[1] I. Blair,et al. A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36 , 2007, Human Genetics.
[2] S. Cuthbert,et al. On the reliability and validity of manual muscle testing: a literature review , 2007, Chiropractic & osteopathy.
[3] O. Combarros,et al. Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles. , 2006, Brain : a journal of neurology.
[4] Richard W. Bohannon. Manual muscle testing: does it meet the standards of an adequate screening test? , 2005, Clinical rehabilitation.
[5] D. Haynor,et al. Characterization of genetically defined types of Charcot-Marie-Tooth neuropathies by using magnetic resonance neurography. , 2005, Journal of neurosurgery.
[6] V. Timmerman,et al. Molecular genetics of distal hereditary motor neuropathies. , 2004, Human molecular genetics.
[7] K. Fischbeck,et al. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. , 2003, American journal of human genetics.
[8] G. Kuhlenbäumer,et al. Clinical features and molecular genetics of hereditary peripheral neuropathies , 2002, Journal of Neurology.
[9] J. Lupski,et al. Charcot‐Marie‐Tooth disease and related neuropathies: Mutation distribution and genotype‐phenotype correlation , 2002, Annals of neurology.
[10] Y. Agid,et al. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases. , 1997, Brain : a journal of neurology.
[11] A. Harding,et al. The phenotypic manifestations of chromosome 17p11.2 duplication. , 1997, Brain : a journal of neurology.
[12] R. Kilcoyne,et al. Patterns of muscle atrophy in the lower limbs in patients with Charcot-Marie-Tooth disease as measured by magnetic resonance imaging. , 1995, The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons.
[13] Nicholas J. Talley,et al. Clinical Examination: A Systematic Guide to Physical Diagnosis , 1993 .
[14] S. Malcolm. Charcot-Marie-Tooth disease type 1. , 1992, Journal of medical genetics.
[15] P. Berck,et al. Relationship of manual muscle testing to objective strength measurements , 1989, Muscle & nerve.
[16] P K Thomas,et al. The clinical features of hereditary motor and sensory neuropathy types I and II. , 1980, Brain : a journal of neurology.
[17] P. Dyck,et al. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. , 1968, Archives of neurology.
[18] A. Harding. Inherited Neuronal Atrophy and Degeneration Predominantly of Lower Motor Neurons , 2005 .
[19] A. Quattrone,et al. MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. , 1998, European neurology.
[20] C. van Broeckhoven,et al. Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease , 2006 .