-
1
-
-
0001046663
-
Hereditary motor and sensory neuropathies
-
Dyck PJ (ed). Philadelphia, WB Saunders
-
Dyck PJ, Chance P, Lebo R, et al: Hereditary motor and sensory neuropathies, in Dyck PJ (ed): Peripheral Neuropathy, ed 3. Philadelphia, WB Saunders, 1993, pp 1094-136
-
(1993)
Peripheral Neuropathy, Ed 3
, pp. 1094-1136
-
-
Dyck, P.J.1
Chance, P.2
Lebo, R.3
-
2
-
-
0018942439
-
The clinical feature of hereditary motor and sensory neuropathy type I and II
-
Harding AE, Thomas PK: The clinical feature of hereditary motor and sensory neuropathy type I and II. Brain 1980;103: 259-80
-
(1980)
Brain
, vol.103
, pp. 259-280
-
-
Harding, A.E.1
Thomas, P.K.2
-
3
-
-
0023733976
-
Respiratory muscle dysfunction in hereditary neuropathy
-
Hogan RG: Respiratory muscle dysfunction in hereditary neuropathy. Arch Intern Med 1988;148:1707-8
-
(1988)
Arch Intern Med
, vol.148
, pp. 1707-1708
-
-
Hogan, R.G.1
-
4
-
-
0030985749
-
The phenotypic manifestations of chromosome 17p11.2 duplication
-
Thomas PK, Marqus W, Davis MB, et al: The phenotypic manifestations of chromosome 17p11.2 duplication. Brain 1997;120:465-78
-
(1997)
Brain
, vol.120
, pp. 465-478
-
-
Thomas, P.K.1
Marqus, W.2
Davis, M.B.3
-
5
-
-
0023133395
-
Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease)
-
Chan CK, Moshenin V, Loke J, et al: Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Chest 1987;91:567-70
-
(1987)
Chest
, vol.91
, pp. 567-570
-
-
Chan, C.K.1
Moshenin, V.2
Loke, J.3
-
6
-
-
0024450545
-
Phrenic involvement in Charcot-Marie-Tooth disease
-
Gilchrist D, Chan CK, Deck JHN: Phrenic involvement in Charcot-Marie-Tooth disease. Chest 1989;96:1197-9
-
(1989)
Chest
, vol.96
, pp. 1197-1199
-
-
Gilchrist, D.1
Chan, C.K.2
Deck, J.H.N.3
-
7
-
-
0023934516
-
Diaphragm weakness in Charcot-Marie-Tooth disease
-
Laroche CM, Carroll N, Moxham J, et al: Diaphragm weakness in Charcot-Marie-Tooth disease. Thorax 1988;43: 478-9
-
(1988)
Thorax
, vol.43
, pp. 478-479
-
-
Laroche, C.M.1
Carroll, N.2
Moxham, J.3
-
8
-
-
0024339752
-
Respiratory muscle weakness in Charcot-Marie-Tooth disease: A field study
-
Nathanson BN, Yu DG, Chan CK: Respiratory muscle weakness in Charcot-Marie-Tooth disease: A field study. Arch Intern Med 1989;149:1389-91
-
(1989)
Arch Intern Med
, vol.149
, pp. 1389-1391
-
-
Nathanson, B.N.1
Yu, D.G.2
Chan, C.K.3
-
9
-
-
0025363925
-
Diaphragmatic weakness in hereditary motor and sensory neuropathy
-
Hardie R, Harding AE, Hirsch N, et al: Diaphragmatic weakness in hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 1990;53:348-50
-
(1990)
J Neurol Neurosurg Psychiatry
, vol.53
, pp. 348-350
-
-
Hardie, R.1
Harding, A.E.2
Hirsch, N.3
-
10
-
-
0026576563
-
Evaluation of phrenic nerve and pulmonary function in hereditary motor and sensory neuropathy, type I
-
Carter GT, Kilmer DD, Bonekat HW, et al: Evaluation of phrenic nerve and pulmonary function in hereditary motor and sensory neuropathy, type I. Muscle Nerve 1992;15:459-62
-
(1992)
Muscle Nerve
, vol.15
, pp. 459-462
-
-
Carter, G.T.1
Kilmer, D.D.2
Bonekat, H.W.3
-
11
-
-
0028824947
-
Profiles of neuromuscular diseases: Hereditary motor and sensory neuropathy, types I and II
-
Carter GT, Abresch RT, Fowler WM Jr, et al: Profiles of neuromuscular diseases: Hereditary motor and sensory neuropathy, types I and II. Am J Phys Med Rehabil 1995;74:S140-9
-
(1995)
Am J Phys Med Rehabil
, vol.74
-
-
Carter, G.T.1
Abresch, R.T.2
Fowler W.M., Jr.3
-
12
-
-
0021356638
-
Electrophysiological evaluation of diaphragm by transcutaneous phrenic nerve stimulation
-
Markand ON, Kinkaid JC, Pourmand RA, et al: Electrophysiological evaluation of diaphragm by transcutaneous phrenic nerve stimulation. Neurology 1984;34: 604-14
-
(1984)
Neurology
, vol.34
, pp. 604-614
-
-
Markand, O.N.1
Kinkaid, J.C.2
Pourmand, R.A.3
-
13
-
-
0034193168
-
Phrenic nerve conduction study in demyelinating neuropathies and open-heart surgery
-
Cruz-Martinez A, Armijo A, Fermoso A, et al: Phrenic nerve conduction study in demyelinating neuropathies and open-heart surgery. Clin Neurophysiol 2000; 111:821-25
-
(2000)
Clin Neurophysiol
, vol.111
, pp. 821-825
-
-
Cruz-Martinez, A.1
Armijo, A.2
Fermoso, A.3
-
14
-
-
1842326763
-
Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletions
-
Haupt A, Schöls L, Przuntek H, et al: Polymorphisms in the PMP-22 gene region (17p11.2-12) are crucial for simplified diagnosis of duplications/deletions. Hum Genet 1997;99:688-91
-
(1997)
Hum Genet
, vol.99
, pp. 688-691
-
-
Haupt, A.1
Schöls, L.2
Przuntek, H.3
-
17
-
-
0019457107
-
Reference spirometric values using techniques and equipment that meet ATS recommendations
-
Crapo RO, Morris AH, Gardner RM: Reference spirometric values using techniques and equipment that meet ATS recommendations. Am Rev Respir Dis 1981; 123:659-64
-
(1981)
Am Rev Respir Dis
, vol.123
, pp. 659-664
-
-
Crapo, R.O.1
Morris, A.H.2
Gardner, R.M.3
-
18
-
-
0022994154
-
Reference values for vital capacity and flow-volume curves from a general population study
-
Paoletti P, Pistelli G, Fazzi P, et al: Reference values for vital capacity and flow-volume curves from a general population study. Bull Eur Physiopathol Respir 1986;22:451-9
-
(1986)
Bull Eur Physiopathol Respir
, vol.22
, pp. 451-459
-
-
Paoletti, P.1
Pistelli, G.2
Fazzi, P.3
-
19
-
-
0014514097
-
Maximal respiratory pressures: Normal values and relationship to age and sex
-
Black LF, Hyatt RE: Maximal respiratory pressures: Normal values and relationship to age and sex. Am Rev Respir Dis 1969;99:696-702
-
(1969)
Am Rev Respir Dis
, vol.99
, pp. 696-702
-
-
Black, L.F.1
Hyatt, R.E.2
-
20
-
-
0025764311
-
AAEM Minimonograph 11: Needle examination in clinical electromyography
-
Daube JR: AAEM Minimonograph 11: Needle examination in clinical electromyography. Muscle Nerve 1991;14:685-700
-
(1991)
Muscle Nerve
, vol.14
, pp. 685-700
-
-
Daube, J.R.1
-
21
-
-
0028356510
-
Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis
-
Dyck PJ, Litchy WJ, Minnerath S, et al: Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis. Ann Neurol 1994;35:608-15
-
(1994)
Ann Neurol
, vol.35
, pp. 608-615
-
-
Dyck, P.J.1
Litchy, W.J.2
Minnerath, S.3
-
22
-
-
0033048959
-
Laryngeal electromyographic findings in Charcot-Marie-Tooth disease type II
-
Dray TG, Robinson LR, Hillel AD: Laryngeal electromyographic findings in Charcot-Marie-Tooth disease type II. Arch Neurol 1999;56:863-5
-
(1999)
Arch Neurol
, vol.56
, pp. 863-865
-
-
Dray, T.G.1
Robinson, L.R.2
Hillel, A.D.3
-
23
-
-
0031407462
-
Central motor pathway evaluation using magnetic coil stimulation in hereditary motor and sensory neuropathy type I (HMSN type I, Charcot-Marie-Tooth disease)
-
Sartucci F, Sagliocco L, Murri L: Central motor pathway evaluation using magnetic coil stimulation in hereditary motor and sensory neuropathy type I (HMSN type I, Charcot-Marie-Tooth disease). Int J Neurosci 1997;92:145-60
-
(1997)
Int J Neurosci
, vol.92
, pp. 145-160
-
-
Sartucci, F.1
Sagliocco, L.2
Murri, L.3
-
24
-
-
0023672945
-
Charcot-Marie-Tooth disease and respiratory failure
-
Dyer EL, Challan AS: Charcot-Marie-Tooth disease and respiratory failure. Chest 1988;93:221
-
(1988)
Chest
, vol.93
, pp. 221
-
-
Dyer, E.L.1
Challan, A.S.2
-
25
-
-
0026952632
-
Charcot-Marie-Tooth disease with diaphragmatic weakness
-
Osanai S, Akiba Y, Nakano H, et al: Charcot-Marie-Tooth disease with diaphragmatic weakness. Intern Med 1992; 31:1267-70
-
(1992)
Intern Med
, vol.31
, pp. 1267-1270
-
-
Osanai, S.1
Akiba, Y.2
Nakano, H.3
-
26
-
-
0141749082
-
Pulmonary rehabilitation, including artificial ventilation in hereditary motor and sensory neuropathy, type I
-
Varlotta GP, Feinberg JH, Yang GW, et al: Pulmonary rehabilitation, including artificial ventilation in hereditary motor and sensory neuropathy, type I. Arch Phys Med Rehabil 1990;71:760
-
(1990)
Arch Phys Med Rehabil
, vol.71
, pp. 760
-
-
Varlotta, G.P.1
Feinberg, J.H.2
Yang, G.W.3
-
27
-
-
0023688950
-
Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type I
-
Eichacker PQ, Spiro A, Sherman M, et al: Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type I. Arch Intern Med 1988;148: 1739-40
-
(1988)
Arch Intern Med
, vol.148
, pp. 1739-1740
-
-
Eichacker, P.Q.1
Spiro, A.2
Sherman, M.3
-
28
-
-
0023263493
-
Determinants of respiratory muscle weakness in stable chronic neuromuscular disorders
-
Vincken W, Elleker MG, Cosio MG: Determinants of respiratory muscle weakness in stable chronic neuromuscular disorders. Am J Med 1987;82:53-8
-
(1987)
Am J Med
, vol.82
, pp. 53-58
-
-
Vincken, W.1
Elleker, M.G.2
Cosio, M.G.3
|