-
1
-
-
0018746314
-
Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa
-
Arden GB, Fox B (1976) Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa. Nature 279: 534-536
-
(1976)
Nature
, vol.279
, pp. 534-536
-
-
Arden, G.B.1
Fox, B.2
-
2
-
-
0002836205
-
Eine graphische Oberfläche zur generierung von datenbankanfragen basierend auf einem objektorientierten datenmodell
-
Banhart F, Klaeren H, Zrenner E (1995) Eine graphische Oberfläche zur Generierung von Datenbankanfragen basierend auf einem objektorientierten Datenmodell. GI-Datenbank Rundbrief 13: 64-66
-
(1995)
GI-datenbank Rundbrief
, vol.13
, pp. 64-66
-
-
Banhart, F.1
Klaeren, H.2
Zrenner, E.3
-
3
-
-
0026777641
-
Ultrastructure of connecting cilia in different forms of retinitis pigmentosa
-
Barrong SD, Chaitin MH, Fliesler SJ, Possin DE, Jacobson SG, Milam AH (1992) Ultrastructure of connecting cilia in different forms of retinitis pigmentosa. Arch Ophthalmol 110: 706-710
-
(1992)
Arch Ophthalmol
, vol.110
, pp. 706-710
-
-
Barrong, S.D.1
Chaitin, M.H.2
Fliesler, S.J.3
Possin, D.E.4
Jacobson, S.G.5
Milam, A.H.6
-
4
-
-
0015591918
-
New tables for the determination of percentile loss of speech hearing
-
Boenninghaus HG, Roser D (1973) New tables for the determination of percentile loss of speech hearing. Z Laryngol Rhinol Otol 52: 153-161
-
(1973)
Z Laryngol Rhinol Otol
, vol.52
, pp. 153-161
-
-
Boenninghaus, H.G.1
Roser, D.2
-
5
-
-
0031032971
-
A newly identified locus for Usher syndrome type I, USH 1 E, maps to chromosome 21q21
-
Chaib H, Kaplan J, Gerber S, Vincent C, Ayadi H, Slim R, Munnich A, Weissenbach J, Petit C (1997) A newly identified locus for Usher syndrome type I, USH 1 E, maps to chromosome 21q21. Hum Mol Genet 6: 27-31
-
(1997)
Hum Mol Genet
, vol.6
, pp. 27-31
-
-
Chaib, H.1
Kaplan, J.2
Gerber, S.3
Vincent, C.4
Ayadi, H.5
Slim, R.6
Munnich, A.7
Weissenbach, J.8
Petit, C.9
-
6
-
-
0344694546
-
-
Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J (1997) Isolation of a novel human homologue of the gene coding for echinoderm microtubule associated protein (EMAP) from the Usher syndrome type IA locus at 14q32.
-
(1997)
Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule Associated Protein (EMAP) from the Usher Syndrome Type IA Locus at 14q32
-
-
Eudy, J.D.1
Ma-Edmonds, M.2
Yao, S.F.3
Talmadge, C.B.4
Kelley, P.M.5
Weston, M.D.6
Kimberling, W.J.7
Sumegi, J.8
-
7
-
-
0023772923
-
Quantitative evaluation of hearing disorders in expert assessment. A recent recommendation for calculating the percentage of hearing loss
-
Feldmann H (1988) Quantitative evaluation of hearing disorders in expert assessment. A recent recommendation for calculating the percentage of hearing loss. Laryngol Rhinol Otol [Stuttg] 67: 319-325
-
(1988)
Laryngol Rhinol Otol [stuttg]
, vol.67
, pp. 319-325
-
-
Feldmann, H.1
-
8
-
-
0020599803
-
Usher's syndrome
-
Fishman GA, Kumar A, Joseph ME, Torok N, Anderson RJ (1983) Usher's syndrome. Arch Ophthalmol 101: 1367-1374
-
(1983)
Arch Ophthalmol
, vol.101
, pp. 1367-1374
-
-
Fishman, G.A.1
Kumar, A.2
Joseph, M.E.3
Torok, N.4
Anderson, R.J.5
-
9
-
-
0021955368
-
Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa
-
Fishman GA, Anderson RJ, Lourenco P (1985) Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa. Br J Ophthalmol 69: 263-266
-
(1985)
Br J Ophthalmol
, vol.69
, pp. 263-266
-
-
Fishman, G.A.1
Anderson, R.J.2
Lourenco, P.3
-
10
-
-
0030057559
-
Evidence for a fourth locus in Usher syndrome type I
-
Gerber S, Larget-Piet D, Rozet JM, Bonneau D, Mathieu M, Der Kaloustian V, Munnich A, Kaplan J (1996) Evidence for a fourth locus in Usher syndrome type I. J Med Genet 33: 77-79
-
(1996)
J Med Genet
, vol.33
, pp. 77-79
-
-
Gerber, S.1
Larget-Piet, D.2
Rozet, J.M.3
Bonneau, D.4
Mathieu, M.5
Der Kaloustian, V.6
Munnich, A.7
Kaplan, J.8
-
11
-
-
0028972472
-
Mouse model for Usher syndrome: Linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
-
Heckenlively JR, Chang B, Erway LC, Peng C, Hawes NL, Hageman GS, Roderick TH (1995) Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. Proc Natl Acad Sci 92: 11100-11104n
-
(1995)
Proc Natl Acad Sci
, vol.92
-
-
Heckenlively, J.R.1
Chang, B.2
Erway, L.C.3
Peng, C.4
Hawes, N.L.5
Hageman, G.S.6
Roderick, T.H.7
-
13
-
-
0027058632
-
A gene for usher syndrome type I (USH 1 A) maps to chromosome 14q
-
Kaplan J, Gerber S, Bonneau D, Rozet JM, Delrieu O, Briard ML, Dollfus H, Ghazi I, Dufier JL, Frezal J, et al (1992) A gene for Usher syndrome type I (USH 1 A) maps to chromosome 14q. Genomics 14: 979-987
-
(1992)
Genomics
, vol.14
, pp. 979-987
-
-
Kaplan, J.1
Gerber, S.2
Bonneau, D.3
Rozet, J.M.4
Delrieu, O.5
Briard, M.L.6
Dollfus, H.7
Ghazi, I.8
Dufier, J.L.9
Frezal, J.10
-
14
-
-
0344262860
-
-
Reference deleted
-
Reference deleted
-
-
-
-
15
-
-
0025308736
-
Localization of Usher syndrome type II to chromosome 1q
-
Kimberling WJ, Weston MD, Moller C, Davenport SL, Shugart YY, Priluck IA, Martini A, Milani M, Smith RJ (1990) Localization of Usher syndrome type II to chromosome 1q. Genomics 7: 245-249
-
(1990)
Genomics
, vol.7
, pp. 245-249
-
-
Kimberling, W.J.1
Weston, M.D.2
Moller, C.3
Davenport, S.L.4
Shugart, Y.Y.5
Priluck, I.A.6
Martini, A.7
Milani, M.8
Smith, R.J.9
-
16
-
-
0027058412
-
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
-
Kimberling WJ, Moller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, et al (1992) Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11. Genomics 14: 988-994
-
(1992)
Genomics
, vol.14
, pp. 988-994
-
-
Kimberling, W.J.1
Moller, C.G.2
Davenport, S.3
Priluck, I.A.4
Beighton, P.H.5
Greenberg, J.6
Reardon, W.7
Weston, M.D.8
Kenyon, J.B.9
Grunkemeyer, J.A.10
-
17
-
-
0031962544
-
Lateralized and bilateral olfactory function in patients with chronic sinusitis compared with healthy control subjects
-
Klimek L, Hummel T, Moll B, Kobal G, Mann WJ (1998) Lateralized and bilateral olfactory function in patients with chronic sinusitis compared with healthy control subjects. Laryngoscope 108: 111-114
-
(1998)
Laryngoscope
, vol.108
, pp. 111-114
-
-
Klimek, L.1
Hummel, T.2
Moll, B.3
Kobal, G.4
Mann, W.J.5
-
18
-
-
0029618243
-
Diagnostische methoden zur erfassung von Riechstörungen bei neurologischen Erkrankungen
-
Kobal G, Stefan H (1995) Diagnostische Methoden zur Erfassung von Riechstörungen bei neurologischen Erkrankungen. Nervenarzt 66: 869-884
-
(1995)
Nervenarzt
, vol.66
, pp. 869-884
-
-
Kobal, G.1
Stefan, H.2
-
19
-
-
0029018990
-
Standard for clinical electroretinography
-
Marmor M, Zrenner E (1995) Standard for clinical electroretinography. Doc Ophthalmol 89: 199-210
-
(1995)
Doc Ophthalmol
, vol.89
, pp. 199-210
-
-
Marmor, M.1
Zrenner, E.2
-
20
-
-
0019846001
-
Two forms of autosomal dominant primary retinitis pigmentosa
-
Massof RW, Finkelstein D (1981) Two forms of autosomal dominant primary retinitis pigmentosa. Doc Ophthalmol 51: 289-346
-
(1981)
Doc Ophthalmol
, vol.51
, pp. 289-346
-
-
Massof, R.W.1
Finkelstein, D.2
-
21
-
-
0024590795
-
Usher syndrome: An otoneurologic study
-
Moller CG, Kimberling WJ, Davenport SL, Priluck I, White V, Biscone-Halterman K, Odkvist LM, Brookhouser PE, Lund G, Grissom TJ (1989) Usher syndrome: an otoneurologic study. Laryngoscope 99: 73-79
-
(1989)
Laryngoscope
, vol.99
, pp. 73-79
-
-
Moller, C.G.1
Kimberling, W.J.2
Davenport, S.L.3
Priluck, I.4
White, V.5
Biscone-Halterman, K.6
Odkvist, L.M.7
Brookhouser, P.E.8
Lund, G.9
Grissom, T.J.10
-
22
-
-
0028836898
-
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q
-
Sankila EM, Pakarinen L, Kaariainen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A (1995) Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q. Hum Mol Genet 4: 93-98
-
(1995)
Hum Mol Genet
, vol.4
, pp. 93-98
-
-
Sankila, E.M.1
Pakarinen, L.2
Kaariainen, H.3
Aittomäki, K.4
Karjalainen, S.5
Sistonen, P.6
De La Chapelle, A.7
-
23
-
-
0344694543
-
A comparison of inherited retinal dystrophies - results of a data base analysis
-
Seeliger M, Rüther K, Apfelstedt-Sylla E, Banhart F, Zrenner E (1995) A comparison of inherited retinal dystrophies - results of a data base analysis. German J Ophthalmol [Suppl] 4: 126
-
(1995)
German J Ophthalmol [Suppl]
, vol.4
, pp. 126
-
-
Seeliger, M.1
Rüther, K.2
Apfelstedt-Sylla, E.3
Banhart, F.4
Zrenner, E.5
-
24
-
-
0032006956
-
Multifocal electroretinography in retinitis pigmentosa
-
Seeliger MW, Kretschmann UH, Rüther KW, Apfelstedt-Sylla E, Zrenner E (1998) Multifocal electroretinography in retinitis pigmentosa. Am J Ophthalmol 125: 214-226
-
(1998)
Am J Ophthalmol
, vol.125
, pp. 214-226
-
-
Seeliger, M.W.1
Kretschmann, U.H.2
Rüther, K.W.3
Apfelstedt-Sylla, E.4
Zrenner, E.5
-
25
-
-
0027058291
-
Localization of two genes for Usher syndrome type I to chromosome 11
-
Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ (1992) Localization of two genes for Usher syndrome type I to chromosome 11. Genomics 14: 995-1002
-
(1992)
Genomics
, vol.14
, pp. 995-1002
-
-
Smith, R.J.1
Berlin, C.I.2
Hejtmancik, J.F.3
Keats, B.J.4
Kimberling, W.J.5
-
26
-
-
0028295151
-
Clinical diagnosis of the Usher syndromes
-
Smith RJ, Berlin Cl, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, Moller CG, Pelias MZ, Tranebjaerg L (1994) Clinical diagnosis of the Usher syndromes. Am J Med Genet 50: 32-38
-
(1994)
Am J Med Genet
, vol.50
, pp. 32-38
-
-
Smith, R.J.1
Berlin, C.I.2
Hejtmancik, J.F.3
Keats, B.J.4
Kimberling, W.J.5
Lewis, R.A.6
Moller, C.G.7
Pelias, M.Z.8
Tranebjaerg, L.9
-
27
-
-
0345125244
-
-
Reference deleted
-
Reference deleted
-
-
-
-
28
-
-
0028815440
-
Defective myosin VIIa gene responsible for usher syndrome type IB
-
Weil D, Blanchard S, Kaplan J, Gullford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD (1995) Defective myosin VIIa gene responsible for Usher syndrome type IB. Nature 374: 60-61
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Gullford, P.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
-
29
-
-
19244362118
-
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
-
Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ (1996) Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. Am J Hum Genet 59: 1074-1083
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1074-1083
-
-
Weston, M.D.1
Kelley, P.M.2
Overbeck, L.D.3
Wagenaar, M.4
Orten, D.J.5
Hasson, T.6
Chen, Z.Y.7
Corey, D.8
Mooseker, M.9
Sumegi, J.10
Cremers, C.11
Moller, C.12
Jacobson, S.G.13
Gorin, M.B.14
Kimberling, W.J.15
-
31
-
-
0026604415
-
Retinitis Pigmentosa. Klinische befunde, molekulargenctische ergebnisse und forschungsperspektiven
-
Zrenner E, Rüther K, Apfelstedt-Sylla E (1992) Retinitis Pigmentosa. Klinische Befunde, molekulargenctische Ergebnisse und Forschungsperspektiven. Ophthalmologe 89: 5-21
-
(1992)
Ophthalmologe
, vol.89
, pp. 5-21
-
-
Zrenner, E.1
Rüther, K.2
Apfelstedt-Sylla, E.3
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