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1 erwent detailed neurological examination and electrodiagnostic and genetic testing for the major know
2 ndrome) has been advanced primarily based on electrodiagnostic and limited pathological data, but rem
3                                   Antemortem electrodiagnostics and radiologic imaging indicated a di
4                   We evaluated the clinical, electrodiagnostic, and histopathological features of 14
5 vated serum creatine kinase level, myopathic electrodiagnostic changes, brain MRI with cobblestone co
6                 Furthermore, the traditional electrodiagnostic classification into axonal and demyeli
7 osis of GBS subtype if the proposed modified electrodiagnostic criteria are used.
8 wer-extremity sensory and motor deficits and electrodiagnostic evidence of a length-dependent mixed d
9  that best distinguish between patients with electrodiagnostic evidence of CTS and patients without i
10                                              Electrodiagnostic examination showed severely low compou
11 s or small series; however, its clinical and electrodiagnostic features have not been well characteri
12                   We report the clinical and electrodiagnostic findings in 49 affected family members
13                                              Electrodiagnostic findings were consistent with a necrot
14                                              Electrodiagnostic findings were consistent with bilatera
15 tion, retinal nerve fiber layer thinning, or electrodiagnostic findings.
16                             The clinical and electrodiagnostic hallmarks suggest selective motor fibe
17 ripheral nerve injury relies on clinical and electrodiagnostic information, supplemented by intraoper
18 tertiary ophthalmology center with access to electrodiagnostic services from February 18, 2009, throu
19                                              Electrodiagnostic studies and a sural nerve biopsy showe
20                                              Electrodiagnostic studies are an important early step in
21                                              Electrodiagnostic studies evaluating for disorders of ne
22                      We emphasize the use of electrodiagnostic studies to investigate patients with b
23 magnetic resonance imaging, ultrasonography, electrodiagnostic studies, and muscle biopsies (n = 3).
24 erve fibre density, which was independent of electrodiagnostic test severity.
25 ailed ophthalmic examination, accompanied by electrodiagnostic testing (EDT) and dysmorphologic asses
26                                              Electrodiagnostic testing and magnetic resonance imaging
27  objective methods for assessment, including electrodiagnostic testing and nerve imaging, provide add
28                                       Serial electrodiagnostic testing demonstrated a rapidly progres
29 hic scans were abnormal in all patients, and electrodiagnostic testing revealed rod and cone dysfunct
30           An approach to laboratory testing, electrodiagnostic testing, and imaging to exclude diseas
31 n maneuvers were independently compared with electrodiagnostic testing.
32 ic assessment, including retinal imaging and electrodiagnostic testing.
33 idence of spinal cord motor neuron injury on electrodiagnostic testing.
34                                              Electrodiagnostic tests and magnetic resonance imaging o
35                       In contrast, expensive electrodiagnostic tests and magnetic resonance imaging r
36                        Moreover, the role of electrodiagnostic tests needs to be further defined, and

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