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. Author manuscript; available in PMC: 2014 Feb 1.
Published in final edited form as: Physiol Meas. 2013 Jan 28;34(2):203–221. doi: 10.1088/0967-3334/34/2/203

Table 2.

Group averaged diseased-to-normal parameter ratios: mean ± SD and (skewness).

Disease group r1 r2 r3 1/c1 1/c2
ALS (21,148)* 1.0±0.2 (−0.01) 1.8±1.2 (1.9) 1.3±0.7 (2.9) 1.8±1.3 (2.7) 1.4±0.9 (2.7)
Radiculopathy(10, 62) 1.0±0.2 (1.6) 1.2±0.5 (1.7) 1.1±0.3 (0.8) 1.2±0.5 (1.5) 1.2±0.5 (2.6)
Poly/dermatoa (13,37) 1.0±0.3 (0.5) 1.6±1.1 (2.3) 1.2±0.7 (2.4) 1.8±1.5 (1.7) 1.5±1.2 (2.7)
CMTb (4,30) 1.3±0.4 (2) 4.9±4.8 (2) 1.9±0.9 (0.6) 4.9±4.1 (1.7) 2.9±2.2 (1.2)
IBMc (4,39) 0.96±0.2 (0.89) 1.9±1.2 (2.3) 1.1±0.6 (0.7) 2.4±1.7 (1.6) 1.6±1.1 (2.2)
Myotonic Dystrd (3,10) 0.94±0.2 (0.55) 3.4±1.8 (0.7) 2.0±0.84 (0.6) 3.8±2.2 (0.5) 2.8±1.7 (0.3)
FSHDe (3,17) 1.3±0.3 (0.07) 2.0±1.1 (1.1) 1.5±0.86 (1.9) 1.8±1.0 (1.0) 1.8±1.1 (1.9)
Othermyopathyf (5,15) 0.99±0.2 (0.9) 2.6±2.3 (1.2) 1.6±1.2 (1.6) 2.1±1.9 (1.5) 2.3±2.6 (1.7)
“ neuropathyf (5,31) 1.1±0.3 (.01) 1.9±2.3 (2.6) 1.4±0.9 (1.4) 1.6±1.5 (2.7) 1.9±2.1 (2.6)
p-values (and sides) g 0.2 (2 sided) 0.0035 (1) 0.0016 (1) 0.0043 (1) 0.0008 (1)
*

(the number of patients, and the number of muscles examined, including lefts, rights, and repeat measurements)

a

Polymyositis and dermatomyositis combined

b

Charcot-Marie-Tooth disease

c

Inclusion body myositis

d

Myotonic Dystrophy

e

Facioscapulohumeral muscular dystrophy

f

see section 4.7

g

Nominal t-test values for null hypothesis ratio = 1; cf section 5.1