-
1
-
-
0025785479
-
Absence of both auditory evoked potentials and auditory percepts dependent on timing cues
-
Starr A, McPherson D, Patterson J, et al. Absence of both auditory evoked potentials and auditory percepts dependent on timing cues. Brain 1991;114:1157-1180
-
(1991)
Brain
, vol.114
, pp. 1157-1180
-
-
Starr, A.1
McPherson, D.2
Patterson, J.3
-
3
-
-
0027497478
-
Does type I afferent dysfunction reveal itself through lack of efferent suppression?
-
Berlin CI, Hood LJ, Cecola RP, et al. Does type I afferent dysfunction reveal itself through lack of efferent suppression? Hear Res 1993;65:40-50
-
(1993)
Hear Res
, vol.65
, pp. 40-50
-
-
Berlin, C.I.1
Hood, L.J.2
Cecola, R.P.3
-
4
-
-
0015250514
-
Cochlear potentials: A status report
-
Dallos P. Cochlear potentials: a status report. Audiology 1972; 11:29-41
-
(1972)
Audiology
, vol.11
, pp. 29-41
-
-
Dallos, P.1
-
5
-
-
0002976655
-
Clinical value of cochlear microphonic recordings
-
Ruben RJ, Elberling C, Salomon G, ed. Baltimore: University Park Press
-
Aran JM, Charlet de Sauvage R. Clinical value of cochlear microphonic recordings. In: Ruben RJ, Elberling C, Salomon G, ed. Electrocochleography. Baltimore: University Park Press, 1976:55-65
-
(1976)
Electrocochleography
, pp. 55-65
-
-
Aran, J.M.1
Charlet De Sauvage, R.2
-
6
-
-
0018649517
-
Evidence of mechanical nonlinearity and frequency selective wave amplification in the cochlea
-
Kemp DT. Evidence of mechanical nonlinearity and frequency selective wave amplification in the cochlea. Arch Otorhinolaryngol 1979;224:37-45
-
(1979)
Arch Otorhinolaryngol
, vol.224
, pp. 37-45
-
-
Kemp, D.T.1
-
7
-
-
0025339857
-
A guide to the effective use of otoacoustic emissions
-
Kemp DT, Ryen S, Bray P. A guide to the effective use of otoacoustic emissions. Ear Hear 1990;11:93-105
-
(1990)
Ear Hear
, vol.11
, pp. 93-105
-
-
Kemp, D.T.1
Ryen, S.2
Bray, P.3
-
8
-
-
0025762475
-
Otoacoustic emissions in an adult with severe hearing loss
-
Prieve BA, Gorga MP, Neely ST. Otoacoustic emissions in an adult with severe hearing loss. J Speech Hear Res 1991;34:379-385
-
(1991)
J Speech Hear Res
, vol.34
, pp. 379-385
-
-
Prieve, B.A.1
Gorga, M.P.2
Neely, S.T.3
-
9
-
-
16044365767
-
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24
-
Kalaydjieva L, Hallmayer J, Chandler D, et al. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat Genet 1996;14:214-217
-
(1996)
Nat Genet
, vol.14
, pp. 214-217
-
-
Kalaydjieva, L.1
Hallmayer, J.2
Chandler, D.3
-
10
-
-
0031882018
-
Hereditary motor and sensory neuropathy-lorn, a novel demyelinating neuropathy associated with deafness in gypsies: Clinical, electrophysiological and nerve biopsy findings
-
Kalaydjieva L, Nikolova A, Turnev I, et al. Hereditary motor and sensory neuropathy-Lorn, a novel demyelinating neuropathy associated with deafness in gypsies: clinical, electrophysiological and nerve biopsy findings. Brain 1998;121:399-408
-
(1998)
Brain
, vol.121
, pp. 399-408
-
-
Kalaydjieva, L.1
Nikolova, A.2
Turnev, I.3
-
11
-
-
0032078756
-
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family
-
Merlini L, Villanova M, Sabatelli P, et al. Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family. Neuromuscul Disord 1998;8:182-185
-
(1998)
Neuromuscul Disord
, vol.8
, pp. 182-185
-
-
Merlini, L.1
Villanova, M.2
Sabatelli, P.3
-
13
-
-
0003796765
-
-
Cleveland: Department of Epidemiology and Biostatistics, Case Western Reserve University
-
SAGE. Statistical Analysis for Genetic Epidemiology, Release 2.2. Cleveland: Department of Epidemiology and Biostatistics, Case Western Reserve University, 1994
-
(1994)
Statistical Analysis for Genetic Epidemiology, Release 2.2
-
-
-
14
-
-
26544460193
-
Mapping a BAC contig and physical map covering chromosome 8q24, looking for a HMSN-Lom gene
-
De Jonge RR, Dye D, Yanakiev P, et al. Mapping a BAC contig and physical map covering chromosome 8q24, looking for a HMSN-Lom gene. Am J Hum Genet 1998;63:A248
-
(1998)
Am J Hum Genet
, vol.63
-
-
De Jonge, R.R.1
Dye, D.2
Yanakiev, P.3
-
15
-
-
0002744896
-
Neural generators of auditory evoked potentials
-
Jacobson JT, ed. Boston: Allyn & Bacon
-
Moller AR. Neural generators of auditory evoked potentials. In: Jacobson JT, ed. Principles and applications in auditory evoked potentials. Boston: Allyn & Bacon, 1994:23-46
-
(1994)
Principles and Applications in Auditory Evoked Potentials
, pp. 23-46
-
-
Moller, A.R.1
-
16
-
-
0030452124
-
Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: De novo dominant point mutation of the PMP22 gene
-
Ionasescu VV, Searby C, Greenberg SA. Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 gene. J Med Genet 1996;33:1048-1049
-
(1996)
J Med Genet
, vol.33
, pp. 1048-1049
-
-
Ionasescu, V.V.1
Searby, C.2
Greenberg, S.A.3
-
17
-
-
0024457455
-
Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1
-
Dyck PJ, Karnes JL, Lambert EH. Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1. Neurology 1989; 39:1302-1308
-
(1989)
Neurology
, vol.39
, pp. 1302-1308
-
-
Dyck, P.J.1
Karnes, J.L.2
Lambert, E.H.3
-
18
-
-
0024493702
-
Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1
-
Roy EP, Gutmann L, Riggs JE. Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1. Muscle Nerve 1989;12:52-55
-
(1989)
Muscle Nerve
, vol.12
, pp. 52-55
-
-
Roy, E.P.1
Gutmann, L.2
Riggs, J.E.3
-
19
-
-
0001046663
-
Hereditary motor and sensory neuropathies
-
Dyck PJ, Thomas PK, eds. Philadelphia: WB Saunders
-
Dyck PJ, Chance P, Lebo R, Carney JA. Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PK, eds. Peripheral neuropathy. Philadelphia: WB Saunders, 1993:1096-1114
-
(1993)
Peripheral Neuropathy
, pp. 1096-1114
-
-
Dyck, P.J.1
Chance, P.2
Lebo, R.3
Carney, J.A.4
-
20
-
-
0020215057
-
Die hereditaren motorisch-sensiblen neuropathien
-
Meier C, Tackmann W. Die hereditaren motorisch-sensiblen Neuropathien. Fortschr Neurol Psychiatr 1982;50:349-365
-
(1982)
Fortschr Neurol Psychiatr
, vol.50
, pp. 349-365
-
-
Meier, C.1
Tackmann, W.2
-
21
-
-
0020554379
-
Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type
-
Gutmann L, Fakadej A, Riggs JE. Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type. Muscle Nerve 1983; 6:515-519
-
(1983)
Muscle Nerve
, vol.6
, pp. 515-519
-
-
Gutmann, L.1
Fakadej, A.2
Riggs, J.E.3
-
22
-
-
0030034214
-
Longitudinal studies of the duplication from Charcot-Marie-Tooth polyneuropathy
-
Killian JM, Tiwari PS, Jacobson S, et al. Longitudinal studies of the duplication from Charcot-Marie-Tooth polyneuropathy. Muscle Nerve 1996;19:74-78
-
(1996)
Muscle Nerve
, vol.19
, pp. 74-78
-
-
Killian, J.M.1
Tiwari, P.S.2
Jacobson, S.3
-
23
-
-
0030985749
-
The phenotypic manifestation of chromosome 17p11.2 duplication
-
Thomas PK, Marques W Jr, Davis MB, et al. The phenotypic manifestation of chromosome 17p11.2 duplication. Brain 1997; 120:465-478
-
(1997)
Brain
, vol.120
, pp. 465-478
-
-
Thomas, P.K.1
Marques W., Jr.2
Davis, M.B.3
-
24
-
-
0021139112
-
Decreased axon caliber and neurofilaments in hereditary motor and sensory neuropathy type I
-
Nukada H, Dyck PJ. Decreased axon caliber and neurofilaments in hereditary motor and sensory neuropathy type I. Ann Neurol 1984;16:238-241
-
(1984)
Ann Neurol
, vol.16
, pp. 238-241
-
-
Nukada, H.1
Dyck, P.J.2
-
25
-
-
0026514249
-
Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)
-
Gabreels-Festen AA, Joosten EM, Gabreels FJ, et al. Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I). J Neurol Sci 1992; 107:145-154
-
(1992)
J Neurol Sci
, vol.107
, pp. 145-154
-
-
Gabreels-Festen, A.A.1
Joosten, E.M.2
Gabreels, F.J.3
-
26
-
-
0025140994
-
Dinucleotide repeat polymorphism at the D17S250 and D17S261 loci
-
Watson DF, Nachtman FN, Wallace MR, et al. Dinucleotide repeat polymorphism at the D17S250 and D17S261 loci. Nucleic Acids Res 1990;18:4640
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 4640
-
-
Watson, D.F.1
Nachtman, F.N.2
Wallace, M.R.3
-
27
-
-
0027753971
-
Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1
-
Kaku DA, Parry GJ, Malamut R, et al. Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1. Neurology 1993;43:2664-2667
-
(1993)
Neurology
, vol.43
, pp. 2664-2667
-
-
Kaku, D.A.1
Parry, G.J.2
Malamut, R.3
-
28
-
-
0020078781
-
Electrodiagnostic distinction between chronic familial and acquired demyelinative neuropathies
-
Lewis RA, Sumner AJ. Electrodiagnostic distinction between chronic familial and acquired demyelinative neuropathies. Neurology 1982;32:592-596
-
(1982)
Neurology
, vol.32
, pp. 592-596
-
-
Lewis, R.A.1
Sumner, A.J.2
-
29
-
-
0023622633
-
Topography of vestibulocochlear nerve fibers in the posterior cranial fossa
-
Natout MAY, Terr LI, Linthicum FH, House WF. Topography of vestibulocochlear nerve fibers in the posterior cranial fossa. Laryngoscope 1987;97:954-958
-
(1987)
Laryngoscope
, vol.97
, pp. 954-958
-
-
Natout, M.A.Y.1
Terr, L.I.2
Linthicum, F.H.3
House, W.F.4
-
30
-
-
0030969058
-
Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy
-
Chalmers RM, Riordan EP, Wood NW. Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy. J Neurol Neurosurg Psychiatry 1997;62:385-387
-
(1997)
J Neurol Neurosurg Psychiatry
, vol.62
, pp. 385-387
-
-
Chalmers, R.M.1
Riordan, E.P.2
Wood, N.W.3
-
31
-
-
0028356510
-
Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis
-
Dyck JP, Litchy WJ, Minnerath S, et al. Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis. Ann Neurol 1994;35:608-615
-
(1994)
Ann Neurol
, vol.35
, pp. 608-615
-
-
Dyck, J.P.1
Litchy, W.J.2
Minnerath, S.3
-
32
-
-
0017748805
-
Hereditary hypertrophic neuropathy combining features of tic douloureaux, Charcot-Marie-Tooth disease, and deafness
-
Cruse RP, Conomy JP, Wilbourn AJ, Hanson MR. Hereditary hypertrophic neuropathy combining features of tic douloureaux, Charcot-Marie-Tooth disease, and deafness. Cleve Clin Q 1977;44:107-111
-
(1977)
Cleve Clin Q
, vol.44
, pp. 107-111
-
-
Cruse, R.P.1
Conomy, J.P.2
Wilbourn, A.J.3
Hanson, M.R.4
-
33
-
-
0018817642
-
Autosomal recessive forms of hereditary motor and sensory neuropathy
-
Harding AE, Thomas PK. Autosomal recessive forms of hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 1980;43:669-678
-
(1980)
J Neurol Neurosurg Psychiatry
, vol.43
, pp. 669-678
-
-
Harding, A.E.1
Thomas, P.K.2
-
34
-
-
9344241377
-
Autosomal recessive hereditary motor and sensory neuropathy with focal folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
-
Quattrone A, Gambardella A, Bono F, et al. Autosomal recessive hereditary motor and sensory neuropathy with focal folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family. Neurology 1996;46:1318-1324
-
(1996)
Neurology
, vol.46
, pp. 1318-1324
-
-
Quattrone, A.1
Gambardella, A.2
Bono, F.3
-
35
-
-
0029118373
-
A locus of axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26
-
Priest JM, Fischbeck KH, Nouri N, Keats BJ. A locus of axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26. Genomics 1995;29:409-412
-
(1995)
Genomics
, vol.29
, pp. 409-412
-
-
Priest, J.M.1
Fischbeck, K.H.2
Nouri, N.3
Keats, B.J.4
-
36
-
-
0344830618
-
-
Ljubljana, Slovenia: University of Ljubljana
-
Komac-Virant L. Gypsies in Kocevje. Ljubljana, Slovenia: University of Ljubljana, 1994:1-79
-
(1994)
Gypsies in Kocevje
, pp. 1-79
-
-
Komac-Virant, L.1
|