| Year |
Citation |
Score |
| 2020 |
Budde BS, Aly MA, Mohamed MR, Breß A, Altmüller J, Motameny S, Kawalia A, Thiele H, Konrad K, Becker C, Toliat MR, Nürnberg G, Sayed EAF, Mohamed ES, Pfister M, et al. Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. PMID 32279305 DOI: 10.1111/Cge.13754 |
0.392 |
|
| 2017 |
Neuhaus C, Eisenberger T, Decker C, Nagl S, Blank C, Pfister M, Kennerknecht I, Müller-Hofstede C, Charbel Issa P, Heller R, Beck B, Rüther K, Mitter D, Rohrschneider K, Steinhauer U, et al. Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular Genetics & Genomic Medicine. 5: 531-552. PMID 28944237 DOI: 10.1002/Mgg3.312 |
0.363 |
|
| 2015 |
Hassan MA, Shah AA, Szmida E, Smigiel R, Sasiadek MM, Pfister M, Blin N, Bress A. A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment. Journal of Applied Genetics. PMID 25560804 DOI: 10.1007/S13353-014-0263-4 |
0.418 |
|
| 2014 |
Dettling J, Franz C, Zimmermann U, Lee SC, Bress A, Brandt N, Feil R, Pfister M, Engel J, Flamant F, Rüttiger L, Knipper M. Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells. Molecular and Cellular Endocrinology. 382: 26-37. PMID 24012852 DOI: 10.1016/J.Mce.2013.08.025 |
0.355 |
|
| 2011 |
Lubka-Pathak M, Shah AA, Gallozzi M, Müller M, Zimmermann U, Löwenheim H, Pfister M, Knipper M, Blin N, Schimmang T. Altered expression of securin (Pttg1) and serpina3n in the auditory system of hearing-impaired Tff3-deficient mice. Cellular and Molecular Life Sciences : Cmls. 68: 2739-49. PMID 21076990 DOI: 10.1007/S00018-010-0586-1 |
0.355 |
|
| 2010 |
Mohamed MR, Alesutan I, Föller M, Sopjani M, Bress A, Baur M, Salama RH, Bakr MS, Mohamed MA, Blin N, Lang F, Pfister M. Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 26: 959-66. PMID 21220926 DOI: 10.1159/000324004 |
0.409 |
|
| 2010 |
Xia A, Gao SS, Yuan T, Osborn A, Bress A, Pfister M, Maricich SM, Pereira FA, Oghalai JS. Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation. Disease Models & Mechanisms. 3: 209-23. PMID 20142329 DOI: 10.1242/Dmm.004135 |
0.404 |
|
| 2010 |
Mallur PS, Weisstuch A, Pfister M, Mhatre AN, Lalwani AK. Aquaporin-2 and -4: Single nucleotide polymorphisms in Ménire's disease patients Audiological Medicine. 8: 18-23. DOI: 10.3109/16513860903574232 |
0.303 |
|
| 2010 |
Zak M, Bress A, Pfister M, Knipper M, Blin N. ERGIC2, a new member of the OTOF interactome connected with the DFNB9 form of hearing impairment New Biotechnology. 27. DOI: 10.1016/J.Nbt.2010.01.172 |
0.324 |
|
| 2009 |
Baur M, Fransen E, Tropitzsch A, van Laer L, Mauz PS, Van Camp G, Blin N, Pfister M. [Influence of exogenic factors on age-related hearing impairment]. Hno. 57: 1023-8. PMID 19730805 DOI: 10.1007/S00106-009-1900-9 |
0.312 |
|
| 2009 |
Winter H, Rüttiger L, Müller M, Kuhn S, Brandt N, Zimmermann U, Hirt B, Bress A, Sausbier M, Conscience A, Flamant F, Tian Y, Zuo J, Pfister M, Ruth P, et al. Deafness in TRbeta mutants is caused by malformation of the tectorial membrane. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2581-7. PMID 19244534 DOI: 10.1523/Jneurosci.3557-08.2009 |
0.351 |
|
| 2009 |
Friedman RA, Van Laer L, Huentelman MJ, Sheth SS, Van Eyken E, Corneveaux JJ, Tembe WD, Halperin RF, Thorburn AQ, Thys S, Bonneux S, Fransen E, Huyghe J, Pyykkö I, Cremers CW, ... ... Pfister M, et al. GRM7 variants confer susceptibility to age-related hearing impairment. Human Molecular Genetics. 18: 785-96. PMID 19047183 DOI: 10.1093/Hmg/Ddn402 |
0.317 |
|
| 2008 |
Heidrych P, Zimmermann U, Bress A, Pusch CM, Ruth P, Pfister M, Knipper M, Blin N. Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form. Human Molecular Genetics. 17: 3814-21. PMID 18772196 DOI: 10.1093/Hmg/Ddn279 |
0.312 |
|
| 2008 |
Huyghe JR, Van Laer L, Hendrickx JJ, Fransen E, Demeester K, Topsakal V, Kunst S, Manninen M, Jensen M, Bonaconsa A, Mazzoli M, Baur M, Hannula S, Mäki-Torkko E, Espeso A, ... ... Pfister M, et al. Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. American Journal of Human Genetics. 83: 401-7. PMID 18760390 DOI: 10.1016/J.Ajhg.2008.08.002 |
0.302 |
|
| 2008 |
Fransen E, Topsakal V, Hendrickx JJ, Van Laer L, Huyghe JR, Van Eyken E, Lemkens N, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Tropitzsch A, Bonaconsa A, Mazzoli M, Espeso A, ... ... Pfister M, et al. Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study. Journal of the Association For Research in Otolaryngology : Jaro. 9: 264-76; discussion 2. PMID 18543032 DOI: 10.1007/S10162-008-0123-1 |
0.341 |
|
| 2008 |
Lubka M, Müller M, Baus-Loncar M, Hinz M, Blaschke K, Hoffmann W, Pfister M, Löwenheim H, Pusch CM, Knipper M, Blin N. Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 21: 437-44. PMID 18453751 DOI: 10.1159/000129636 |
0.378 |
|
| 2008 |
Van Laer L, Van Eyken E, Fransen E, Huyghe JR, Topsakal V, Hendrickx JJ, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Baur M, Bonaconsa A, Mazzoli M, Espeso A, Verbruggen K, ... ... Pfister M, et al. The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. Human Molecular Genetics. 17: 159-69. PMID 17921507 DOI: 10.1093/Hmg/Ddm292 |
0.334 |
|
| 2008 |
Brosch S, Rauffeisen A, Baur M, Michels L, Trefz FK, Pfister M. [Propionic acidemia and sensorineural hearing loss: is there a connection at the molecular genetics level?]. Hno. 56: 37-42. PMID 17415538 DOI: 10.1007/S00106-007-1560-6 |
0.323 |
|
| 2007 |
Tóth T, Kupka S, Haack B, Fazakas F, Muszbek L, Blin N, Pfister M, Sziklai I. Coincidence of mutations in different connexin genes in Hungarian patients. International Journal of Molecular Medicine. 20: 315-21. PMID 17671735 DOI: 10.3892/Ijmm.20.3.315 |
0.382 |
|
| 2007 |
Brosch S, Baur M, Blin N, Reinert S, Pfister M. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome. International Journal of Molecular Medicine. 20: 85-9. PMID 17549393 DOI: 10.3892/Ijmm.20.1.85 |
0.36 |
|
| 2007 |
Van Eyken E, Van Camp G, Fransen E, Topsakal V, Hendrickx JJ, Demeester K, Van De Heyning P, Mäki-Torkko E, Hannula S, Sorri M, Jensen M, Parving A, Bille M, Baur M, Pfister M, et al. Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment Journal of Medical Genetics. 44: 570-578. PMID 17513527 DOI: 10.1136/Jmg.2007.049205 |
0.317 |
|
| 2007 |
Chen W, Meyer NC, Mckenna MJ, Pfister M, McBride DJ, Fukushima K, Thys M, Camp GV, Smith RJH. Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis Clinical Genetics. 71: 406-414. PMID 17489845 DOI: 10.1111/J.1399-0004.2007.00794.X |
0.372 |
|
| 2006 |
Schug N, Braig C, Zimmermann U, Engel J, Winter H, Ruth P, Blin N, Pfister M, Kalbacher H, Knipper M. Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat. The European Journal of Neuroscience. 24: 3372-80. PMID 17229086 DOI: 10.1111/J.1460-9568.2006.05225.X |
0.317 |
|
| 2006 |
Vrijens K, Thys S, De Jeu MT, Postnov AA, Pfister M, Cox L, Zwijsen A, Van Hoof V, Mueller M, De Clerck NM, De Zeeuw CI, Van Camp G, Van Laer L. Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome. Neurobiology of Disease. 24: 28-40. PMID 16875832 DOI: 10.1016/J.Nbd.2006.04.016 |
0.372 |
|
| 2006 |
Frey A, Lampert A, Waldegger S, Jeck N, Waldegger P, Artunc F, Seebohm G, Lang UE, Kupka S, Pfister M, Hoppe J, Gerloff C, Schaeffeler E, Schwab M, Lang F. Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds. Hearing Research. 214: 68-75. PMID 16549283 DOI: 10.1016/J.Heares.2006.02.001 |
0.391 |
|
| 2006 |
Palmada M, Schmalisch K, Böhmer C, Schug N, Pfister M, Lang F, Blin N. Loss of function mutations of the GJB2 gene detected in patients with DFNB1-associated hearing impairment Neurobiology of Disease. 22: 112-118. PMID 16300957 DOI: 10.1016/J.Nbd.2005.10.005 |
0.392 |
|
| 2006 |
Tóth T, Pfister M, Zenner HP, Sziklai I. Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment. International Journal of Pediatric Otorhinolaryngology. 70: 201-6. PMID 16043233 DOI: 10.1016/J.Ijporl.2005.06.011 |
0.397 |
|
| 2005 |
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, ... ... Pfister M, et al. GJB2 mutations and degree of hearing loss: a multicenter study. American Journal of Human Genetics. 77: 945-57. PMID 16380907 DOI: 10.1086/497996 |
0.411 |
|
| 2005 |
Yang T, Pfister M, Blin N, Zenner HP, Pusch CM, Smith RJ. Genetic heterogeneity of deafness phenotypes linked to DFNA4. American Journal of Medical Genetics. Part A. 139: 9-12. PMID 16222661 DOI: 10.1002/Ajmg.A.30989 |
0.375 |
|
| 2005 |
Van Laer L, Pfister M, Thys S, Vrijens K, Mueller M, Umans L, Serneels L, Van Nassauw L, Kooy F, Smith RJ, Timmermans JP, Van Leuven F, Van Camp G. Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells. Neurobiology of Disease. 19: 386-99. PMID 16023581 DOI: 10.1016/J.Nbd.2005.01.019 |
0.371 |
|
| 2005 |
Schulte C, Geisthoff U, Lux A, Kupka S, Zenner HP, Blin N, Pfister M. High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients. Human Mutation. 25: 595. PMID 15880681 DOI: 10.1002/Humu.9345 |
0.372 |
|
| 2005 |
Kupka S, Bodden-Kamps B, Baur M, Zenner HP, Pfister M. [Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment]. Hno. 52: 968-72. PMID 15309320 DOI: 10.1007/S00106-003-0994-8 |
0.366 |
|
| 2004 |
Rüttiger L, Sausbier M, Zimmermann U, Winter H, Braig C, Engel J, Knirsch M, Arntz C, Langer P, Hirt B, Müller M, Köpschall I, Pfister M, Münkner S, Rohbock K, et al. Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss. Proceedings of the National Academy of Sciences of the United States of America. 101: 12922-7. PMID 15328414 DOI: 10.1073/Pnas.0402660101 |
0.368 |
|
| 2004 |
Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S. A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 14: 369-76. PMID 15319541 DOI: 10.1159/000080347 |
0.389 |
|
| 2004 |
Riemann K, Pfister M, Blin N, Kupka S. Mitochondrial hearing impairment. Background, genetic predisposition and diagnostic possibilities | Mitochondrial bedingte schwerhörigkeiten. Hintergründe, genetische prädisposition und möglichkeiten der diagnostik Hno. 52: 503-509. PMID 15241512 DOI: 10.1007/S00106-003-0993-9 |
0.339 |
|
| 2004 |
Tóth T, Kupka S, Haack B, Riemann K, Braun S, Fazakas F, Zenner HP, Muszbek L, Blin N, Pfister M, Sziklai I. GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Human Mutation. 23: 631-2. PMID 15146474 DOI: 10.1002/Humu.9250 |
0.371 |
|
| 2004 |
Riemann K, Sotlar K, Kupka S, Braun S, Zenner HP, Preyer S, Pfister M, Pusch CM, Blin N. Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genetics and Cytogenetics. 150: 128-35. PMID 15066320 DOI: 10.1016/J.Cancergencyto.2003.10.013 |
0.323 |
|
| 2004 |
Pusch CM, Meyer B, Kupka S, Smith RJ, Lalwani AK, Zenner HP, Blin N, Nürnberg P, Pfister M. Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33. Journal of Molecular Medicine (Berlin, Germany). 82: 398-402. PMID 15042303 DOI: 10.1007/S00109-004-0538-Z |
0.356 |
|
| 2004 |
Donaudy F, Snoeckx R, Pfister M, Zenner HP, Blin N, Di Stazio M, Ferrara A, Lanzara C, Ficarella R, Declau F, Pusch CM, Nürnberg P, Melchionda S, Zelante L, Ballana E, et al. Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). American Journal of Human Genetics. 74: 770-6. PMID 15015131 DOI: 10.1086/383285 |
0.43 |
|
| 2004 |
Tóth T, Kupka S, Nürnberg P, Thiele H, Zenner HP, Sziklai I, Pfister M. Phenotypic characterization of a DFNA6 family showing low-frequency sensorineural hearing impairment | Phänotypische charakterisierung einer DFNA6-familie mit tieftonschwerhörigkeit Hno. 52: 132-136. PMID 14968315 DOI: 10.1007/S00106-003-0912-0 |
0.439 |
|
| 2004 |
Braun S, Riemann K, Pusch CM, Sotlar K, Pfister M, Kupka S. Paragangliomas of the head and neck region. Review of past and future molecular genetic research | Paragangliome der kopf-hals-region. Ein überblick über die molekulargenetische forschung Hno. 52: 11-17. PMID 14740109 DOI: 10.1007/S00106-003-0959-Y |
0.307 |
|
| 2003 |
Oh N, Kupka S, Mirghomizadeh F, Arold R, Zimmermann R, Blin N, Zenner HP, Pfister M. Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3) | Klinische und molekulargenetische analyse monozygoter zwillinge mit stapes-gusher-syndrom (DFN3) Hno. 51: 629-633. PMID 12942177 DOI: 10.1007/S00106-002-0777-7 |
0.331 |
|
| 2003 |
Tóth T, Kupka S, Sziklai I, Blin N, Zenner HP, Pfister M. Phenotype of patients showing hearing impairment based on the 35delG mutation in the connexin 26 gene | Phänotypische charakterisierung schwerhöriger patienten mit homozygoter 35delG-mutation im connexin-26-gen Hno. 51: 400-404. PMID 12835856 DOI: 10.1007/S00106-002-0737-2 |
0.401 |
|
| 2003 |
Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJ, Timmermans JP, Van Camp G. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochemistry and Cell Biology. 119: 247-56. PMID 12649740 DOI: 10.1007/S00418-003-0495-6 |
0.411 |
|
| 2003 |
Mirghomizadeh F, Pfister M, Blin N, Pusch CM. Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin gene. International Journal of Molecular Medicine. 11: 63-4. PMID 12469219 DOI: 10.3892/Ijmm.11.1.63 |
0.374 |
|
| 2002 |
Pfister M, Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S. A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10. Molecular Medicine (Cambridge, Mass.). 8: 607-11. PMID 12477971 DOI: 10.1007/Bf03402171 |
0.379 |
|
| 2002 |
Maassen MM, Pfister M, Plontke S, Koitschev A, Vögler A, Löwenheim H. Recovery of hearing: Results of delayed medical treatment in patients with idiopathic sudden hearing loss | Erholung der hörschwelle bei verzögert einsetzender therapie des hörsturzes Hno. 50: 1062-1067. PMID 12474128 DOI: 10.1007/S00106-002-0653-5 |
0.34 |
|
| 2002 |
Tóth T, Kupka S, Blin N, Pfister M, Sziklai I. [Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary]. Orvosi Hetilap. 143: 2285-9. PMID 12420583 |
0.315 |
|
| 2002 |
Mirghomizadeh F, Pfister M, Apaydin F, Petit C, Kupka S, Pusch CM, Zenner HP, Blin N. Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness. Neurobiology of Disease. 10: 157-64. PMID 12127154 DOI: 10.1006/Nbdi.2002.0488 |
0.368 |
|
| 2002 |
Kupka S, Braun S, Aberle S, Haack B, Ebauer M, Zeissler U, Zenner HP, Blin N, Pfister M. Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment. Human Mutation. 20: 77-8. PMID 12112666 DOI: 10.1002/Humu.9044 |
0.405 |
|
| 2002 |
Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, et al. Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110: 389-94. PMID 12073007 DOI: 10.1007/S00439-002-0719-1 |
0.426 |
|
| 2002 |
Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N. Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation. European Journal of Human Genetics : Ejhg. 10: 95-9. PMID 11938438 DOI: 10.1038/Sj.Ejhg.5200769 |
0.343 |
|
| 2002 |
Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients. Human Mutation. 19: 308-9. PMID 11857751 DOI: 10.1002/Humu.9017 |
0.41 |
|
| 2001 |
Tóth T, Kupka S, Esmer H, Zeissler U, Sziklai I, Zenner HP, Blin N, Pfister M. Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment International Journal of Molecular Medicine. 8: 189-192. PMID 11445873 DOI: 10.3892/Ijmm.8.2.189 |
0.438 |
|
| 2001 |
Lin D, Goldstein JA, Mhatre AN, Lustig LR, Pfister M, Lalwani AK. Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2). Human Mutation. 18: 42-51. PMID 11438992 DOI: 10.1002/Humu.1148 |
0.339 |
|
| 2000 |
Pfister M, Lalwani AK. DFN4: non-syndromic autosomal dominant X-linked sensorineural hearing impairment. Advances in Oto-Rhino-Laryngology. 56: 196-9. PMID 10868235 DOI: 10.1159/000059102 |
0.327 |
|
| 1999 |
Seeliger M, Pfister M, Gendo K, Paasch S, Apfelstedt-Sylla E, Plinkert P, Zenner HP, Zrenner E. Comparative study of visual, auditory, and olfactory function in Usher syndrome. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 237: 301-7. PMID 10208263 DOI: 10.1007/S004170050237 |
0.326 |
|
| 1998 |
Apaydin F, Pfister M, Iber M, Kandogan T, Leal SM, Brändle U, Cura O, Zenner HP. Initial experience with the identification of families with hereditary hearing loss in Turkey | Hereditare schwerhorigkeit in der Turkei erste ergebnisse Hno. 46: 809-814. PMID 9816535 DOI: 10.1007/S001060050317 |
0.383 |
|
| 1998 |
Leal SM, Apaydin F, Barnwell C, Iber M, Kandogan T, Pfister M, Braendle U, Cura O, Schwalb M, Zenner HP, Vitale E. A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9 European Journal of Human Genetics. 6: 341-344. PMID 9781041 DOI: 10.1038/Sj.Ejhg.5200201 |
0.345 |
|
| 1997 |
Pfister M, Maier H, Gummer AW, Preyer S. [In vivo cochleoscopy through the round window]. Hno. 45: 216-21. PMID 9221261 DOI: 10.1007/S001060050107 |
0.576 |
|
| 1994 |
Preyer S, Hemmert W, Pfister M, Zenner HP, Gummer AW. Frequency response of mature guinea-pig outer hair cells to stereociliary displacement. Hearing Research. 77: 116-24. PMID 7928723 DOI: 10.1016/0378-5955(94)90259-3 |
0.664 |
|
| 1993 |
Preyer S, Pfister M, Hemmert W. [Mechanical stimulation of isolated outer hair cells as a test system. Inhibition of transduction by streptomycin treatment]. Hno. 41: 471-4. PMID 7693630 |
0.573 |
|
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