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Acta Oto-Laryngologica Volume 100, 1985 - Issue 1-2
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Original Article

Electrocochleographic Changes in the Hearing Loss Associated with X-Linked Hypophosphataemic Osteomalacia

S. O'malley Department of Otolaryngology, Manchester Royal Infirmary, Manchester, England
,
R. T. Ramsden Department of Otolaryngology, Manchester Royal Infirmary, Manchester, England
,
A. Latif Department of Otolaryngology, Manchester Royal Infirmary, Manchester, England
,
R. Kane Department of Otolaryngology, Manchester Royal Infirmary, Manchester, England
&
M. Davies Department of Medicine, Manchester Royal Infirmary, Manchester, England
Pages 13-18 | Published online: 08 Jul 2009

Citations (16)

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Read on this site (2)

Robert H. Margolis, Samuel C. Levine, Eric M. Foamier, Lisa L. Hunter, Sharon L. Smith & David J. Lilly. (1992) Tympanic Electrocochleography: Normal and Abnormal Patterns of Response. Audiology 31:1, pages 8-24.
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. (1989) British Society of Audiology Short Papers Meeting on Experimental Studies of Hearing and Deafness University of Cambridge, 22nd and 23rd September 1988. British Journal of Audiology 23:2, pages 143-174.
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Articles from other publishers (14)

Yanmei Wang, Jihan Lyu, Xiaoqing Qian, Binjun Chen, Haojie Sun, Wenwei Luo, Fanglu Chi, Hongzhe Li & Dongdong Ren. (2023) Involvement of Dmp1 in the Precise Regulation of Hair Bundle Formation in the Developing Cochlea. Biology 12:4, pages 625.
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Giampiero Igli Baroncelli & Stefano Mora. (2021) X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management. Frontiers in Endocrinology 12.
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Signe Sparre Beck-Nielsen, Zulf Mughal, Dieter Haffner, Ola Nilsson, Elena Levtchenko, Gema Ariceta, Carmen de Lucas Collantes, Dirk Schnabel, Ravi Jandhyala & Outi Mäkitie. (2019) FGF23 and its role in X-linked hypophosphatemia-related morbidity. Orphanet Journal of Rare Diseases 14:1.
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Douglas Chesher, Michael Oddy, Ulpee Darbar, Parag Sayal, Adrian Casey, Aidan Ryan, Annalisa Sechi, Charlotte Simister, Aoife Waters, Yehani Wedatilake, Robin H. Lachmann & Elaine Murphy. (2018) Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations. Journal of Inherited Metabolic Disease 41:5, pages 865-876.
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Cameron C. Wick, Sharon J. Lin, Heping Yu, Cliff A. Megerian & Qing Yin Zheng. (2017) Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation. American Journal of Otolaryngology 38:1, pages 44-51.
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Cameron C. Wick, Maroun T. Semaan, Qing Yin Zheng & Cliff A. Megerian. (2014) A Genetic Murine Model of Endolymphatic Hydrops: The Phex Mouse. Current Otorhinolaryngology Reports 2:3, pages 144-151.
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Ingrid A. Holm, Michael J. Econs & Thomas O. Carpenter. 2012. Pediatric Bone. Pediatric Bone 699 726 .
Hassane Izzedine, Frederic Tankere, Vincent Launay-Vacher & Gilbert Deray. (2004) Ear and kidney syndromes: Molecular versus clinical approach. Kidney International 65:2, pages 369-385.
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INGRID A. HOLM, MICHAEL J. ECONS.THOMAS O. CARPENTER. 2003. Pediatric Bone. Pediatric Bone 603 XVI .
Roger M. Francis & Peter L. Selby. (1997) Osteomalacia. Baillière's Clinical Endocrinology and Metabolism 11:1, pages 145-163.
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J. Edward Spence, Gad Kainer & James C. M. Chan. 1989. Inheritance of Kidney and Urinary Tract Diseases. Inheritance of Kidney and Urinary Tract Diseases 167 176 .
S.P. O'Malley, J.E. Adams, M. Davies & R.T. Ramsden. (1988) The petrous temporal bone and deafness in X-linked hypophosphataemic osteomalacia. Clinical Radiology 39:5, pages 528-530.
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R.V. Thakker & J.L.H. O'Riordan. (1988) 7 Inherited forms of rickets and osteomalacia. Baillière's Clinical Endocrinology and Metabolism 2:1, pages 157-191.
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Avihu Boneh, Theresa M. Reade, Charles R. Scriver, Ellen Rishikof, John M. Opitz & James F. Reynolds. (2005) Audiometric evidence for two forms of X‐linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse . American Journal of Medical Genetics 27:4, pages 997-1003.
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