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1
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0027943907
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A cure for benign positional vertigo
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McClure JA, Parnes LS: A cure for benign positional vertigo. Baillière's Clinical Neurology 1994, 3:537-545. McClure and Parnes reviewed the pathophysiology of benign positional vertigo and discuss the theoretical basis for the positional maneuvers. They describe three patients who developed horizontal canal benign positional vertigo after being treated with the particle repositioning maneuver for posterior canal benign positional vertigo.
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(1994)
Baillière's Clinical Neurology
, vol.3
, pp. 537-545
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McClure, J.A.1
Parnes, L.S.2
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2
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0028890963
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Positional vertigo related to semicircular canalithiasis
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Epley JM: Positional vertigo related to semicircular canalithiasis. Otolaryngol Head Neck Surg 1995, 112:154-161. Epley reviews his extensive experience in treating benign positional vertigo with the particle repositioning maneuver. He emphasizes the importance of vibration applied to the mastoid bone during the maneuver.
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(1995)
Otolaryngol Head Neck Surg
, vol.112
, pp. 154-161
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Epley, J.M.1
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3
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0028307559
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Therapy for benign paroxysmal positioning vertigo, revisited
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Brandt T, Steddin S, Eng D. Daroff RB: Therapy for benign paroxysmal positioning vertigo, revisited. Neurology 1994, 44: 796-800. This review article summarizes the latest information regarding the pathophysiology of benign positional vertigo and the different positional maneuvers that have been used to treat it.
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(1994)
Neurology
, vol.44
, pp. 796-800
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Brandt, T.1
Steddin, S.2
Eng, D.3
Daroff, R.B.4
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4
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0027937076
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Modified liberatory maneuver effective treatment for benign paroxysmal positional vertigo
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Harvey SA, Hain TC, Adamiec LC: Modified liberatory maneuver effective treatment for benign paroxysmal positional vertigo. Laryngoscope 1994, 104:1206-1212.
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(1994)
Laryngoscope
, vol.104
, pp. 1206-1212
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Harvey, S.A.1
Hain, T.C.2
Adamiec, L.C.3
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5
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0028059663
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Particle repositioning maneuver for benign paroxysmal positional vertigo
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Welling DB, Barnes DE: Particle repositioning maneuver for benign paroxysmal positional vertigo. Laryngoscope 1994, 104:946-949.
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(1994)
Laryngoscope
, vol.104
, pp. 946-949
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Welling, D.B.1
Barnes, D.E.2
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6
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9244259968
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Bedside cure for benign positional vertigo
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Fife TD: Bedside cure for benign positional vertigo. BNI Quarterly 1994, 10:2-8. This review contains excellent illustrations explaining the characteristics of the positional nystagmus and demonstrating how to perform the particle repositioning maneuver.
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(1994)
BNI Quarterly
, vol.10
, pp. 2-8
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Fife, T.D.1
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7
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0029050743
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Mastoid oscillation: A critical factor for success in the canalith repositioning procedure
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Li JC: Mastoid oscillation: a critical factor for success in the canalith repositioning procedure. Otolaryngol Head Neck Surg 1995, 112: 670-675.
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(1995)
Otolaryngol Head Neck Surg
, vol.112
, pp. 670-675
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Li, J.C.1
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8
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0028988233
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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
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de Kok YJM, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FP: Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 1995, 267:685-688. This is a first report of a mutation in one of the POU domain genes which are critical in the development of the inner ear. The mutation results in deafness with fixation of the stapes, the most common X-linked form of hearing.
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(1995)
Science
, vol.267
, pp. 685-688
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De Kok, Y.J.M.1
Van Der Maarel, S.M.2
Bitner-Glindzicz, M.3
Huber, I.4
Monaco, A.P.5
Malcolm, S.6
Pembrey, M.E.7
Ropers, H.H.8
Cremers, F.P.9
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9
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0028306509
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A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
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Guilford P, Ayadia H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C: A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Molec Genet 1994, 3:989-993.
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(1994)
Hum Molec Genet
, vol.3
, pp. 989-993
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Guilford, P.1
Ayadia, H.2
Blanchard, S.3
Chaib, H.4
Le Paslier, D.5
Weissenbach, J.6
Drira, M.7
Petit, C.8
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10
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0028555358
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A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
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Chaib H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgan A, Petit C: A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum Molec Gene 1994, 3:2219-2222.
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(1994)
Hum Molec Gene
, vol.3
, pp. 2219-2222
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Chaib, H.1
Lina-Granade, G.2
Guilford, P.3
Plauchu, H.4
Levilliers, J.5
Morgan, A.6
Petit, C.7
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11
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85035166088
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A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q
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Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C: A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genet 1994, 624-28.
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(1994)
Nature Genet
, pp. 624-628
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Guilford, P.1
Ben Arab, S.2
Blanchard, S.3
Levilliers, J.4
Weissenbach, J.5
Belkahia, A.6
Petit, C.7
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12
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0028101878
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Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families
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Coucke P, Van Camp G, Djoyodiharjo B, Smith SD, Frants RR, Padberg GW, Darby JK, Huizing EH, Cremers CW, Kimberling WJ et al.: Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med 1994, 331:425-431.
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(1994)
N Engl J Med
, vol.331
, pp. 425-431
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Coucke, P.1
Van Camp, G.2
Djoyodiharjo, B.3
Smith, S.D.4
Frants, R.R.5
Padberg, G.W.6
Darby, J.K.7
Huizing, E.H.8
Cremers, C.W.9
Kimberling, W.J.10
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13
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0028168648
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Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen gennes in autosomal recessive Alport syndrome
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Mochizuki T, Lemmink HH, Mariyama M, Antignac C, Gubler MC, Pivson Y, Verellen-Dumoulin C, Chan B, Schroder CH, Smeets HJ et al.: Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen gennes in autosomal recessive Alport syndrome. Nature Genet 1994, 8:77-81. This report identifies mutations in two different genes for collagen IV in the autosomal recessive form of Alport syndrome. Both the X-linked and recessive form of this disorder have now been shown to be caused by genetic defects in type IV collagen. As type IV collagen is a key component of basement membranes in the inner ear and kidney, this genetic abnormality explains the combined kidney and inner ear disorder.
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(1994)
Nature Genet
, vol.8
, pp. 77-81
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Mochizuki, T.1
Lemmink, H.H.2
Mariyama, M.3
Antignac, C.4
Gubler, M.C.5
Pivson, Y.6
Verellen-Dumoulin, C.7
Chan, B.8
Schroder, C.H.9
Smeets, H.J.10
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14
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0028815440
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Defective myosin VIIA gene responsible for usher syndrome type 1b
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Weil D, Blanchard S, Kaplan J, Guilford R, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD et al.: Defective myosin VIIA gene responsible for usher syndrome type 1b. Nature 1995, 374:60-61. One type of Usher syndrome was found to be caused by a genetic defect in myosin VIIa. As myosin is important for stereocilliary function, defects in this protein can explain the loss of auditory and vestibular function associated with this syndrome.
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(1995)
Nature
, vol.374
, pp. 60-61
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Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, R.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
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15
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0028919918
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Episodic ataxias as channelopathies
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Griggs RC, Nutt JG: Episodic ataxias as channelopathies. Ann Neurol 1995, 37:285-287.
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(1995)
Ann Neurol
, vol.37
, pp. 285-287
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Griggs, R.C.1
Nutt, J.G.2
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16
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0028136739
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A gene for episodic ataxia/ myokymia maps to chromosome 12p13
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Litt M, Kramer P, Browne D, Gancher S, Brunt ER, Root D, Phromchotikul T, Dubay CJ, Nutt J: A gene for episodic ataxia/ myokymia maps to chromosome 12p13. Am J Hum Genet 1994, 55:702-709.
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(1994)
Am J Hum Genet
, vol.55
, pp. 702-709
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Litt, M.1
Kramer, P.2
Browne, D.3
Gancher, S.4
Brunt, E.R.5
Root, D.6
Phromchotikul, T.7
Dubay, C.J.8
Nutt, J.9
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17
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0028963974
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A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p
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Vahedi K, Joutel A, Van Bogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E: A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p. Ann Neurol 1995, 37:289-293. This is a first report of a chromosomal locus for the gene associated with the variant of familial periodic ataxia associated with interictal nystagmus. Of particular interest, the same genetic locus has been linked to familial hemiplegic migraine and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
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(1995)
Ann Neurol
, vol.37
, pp. 289-293
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Vahedi, K.1
Joutel, A.2
Van Bogaert, P.3
Ducros, A.4
Maciazeck, J.5
Bach, J.F.6
Bousser, M.G.7
Tournier-Lasserve, E.8
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18
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0028920029
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Mapping the gene for acetazolamide responsive hereditary paroxysmal cerebellar ataxia to chromosome 19p
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von Brederlow B, Hahn AF, Koopman WJ, Ebers GC, Bulman DE: Mapping the gene for acetazolamide responsive hereditary paroxysmal cerebellar ataxia to chromosome 19p. Hum Molec Genet 1995, 4:279-284.
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(1995)
Hum Molec Genet
, vol.4
, pp. 279-284
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Von Brederlow, B.1
Hahn, A.F.2
Koopman, W.J.3
Ebers, G.C.4
Bulman, D.E.5
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19
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0029048004
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A locus for the nystagmus-associated form of episodic ataxia maps to an 11 cM region on chromosome 19p
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Kramer P, Yue Q, Gancher ST, Nutt JG, Baloh R, Smith E, Browne D, Bussey K, Lorrien E, Nelson S et al.. A locus for the nystagmus-associated form of episodic ataxia maps to an 11 cM region on chromosome 19p. Amer J Hum Genet 1995, 57:182-185.
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(1995)
Amer J Hum Genet
, vol.57
, pp. 182-185
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Kramer, P.1
Yue, Q.2
Gancher, S.T.3
Nutt, J.G.4
Baloh, R.5
Smith, E.6
Browne, D.7
Bussey, K.8
Lorrien, E.9
Nelson, S.10
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20
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0028124225
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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
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Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M: Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genet 1994, 8:136-140. This is the first report of a neurologic syndrome resulting from a mutation in a brain potassium channel gene. It is likely that other neurologic disorders including the other form of familial periodic ataxia also result from defects in brain ion channels. A feature shared by all of the known ion channel disorders is responsiveness to acetazolamide.
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(1994)
Nature Genet
, vol.8
, pp. 136-140
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Browne, D.L.1
Gancher, S.T.2
Nutt, J.G.3
Brunt, E.R.4
Smith, E.A.5
Kramer, P.6
Litt, M.7
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21
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0028345911
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A randomized, controlled assessment of the canalith repositioning maneuver
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Blakley BW: A randomized, controlled assessment of the canalith repositioning maneuver. Otolaryngol Head Neck Surg 1994, 110:391-396.
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(1994)
Otolaryngol Head Neck Surg
, vol.110
, pp. 391-396
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Blakley, B.W.1
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22
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0027762760
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Horizontal semicircular canal variant of benign positional vertigo
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Baloh RW, Jacobson K, Honrubia V: Horizontal semicircular canal variant of benign positional vertigo. Neurology 1993, 43:2542-2549.
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(1993)
Neurology
, vol.43
, pp. 2542-2549
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Baloh, R.W.1
Jacobson, K.2
Honrubia, V.3
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23
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0029144635
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Persistent direction-changing positional nystagmus: Another variant of benign positional nystagmus?
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Baloh RW, Yue Q, Jacobson KM, Honrubia V: Persistent direction-changing positional nystagmus: Another variant of benign positional nystagmus? Neurology 1995, 45:1297-1301. A form of positional nystagmus commonly attributed to central lesions was shown to be a variant of benign positional nystagmus. Both geotropic and ageotropic positional nystagmus can result from abnormal debris within the horizontal semicircular canal.
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(1995)
Neurology
, vol.45
, pp. 1297-1301
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Baloh, R.W.1
Yue, Q.2
Jacobson, K.M.3
Honrubia, V.4
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24
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0028037429
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Horizontal benign positional vertigo
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Lempert T: Horizontal benign positional vertigo [Letter]. Neurology 1994, 44:2213-2214.
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(1994)
Neurology
, vol.44
, pp. 2213-2214
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Lempert, T.1
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