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Literature DB >> 15290264

Hearing impairment in familial X-linked hypophosphatemic rickets.

Gadi Fishman¹, Denise Miller-Hansen, Cynthia Jacobsen, Virender K Singhal, Uri S Alon.

Abstract

Entities: Disease

Mesh：

Year: 2004 PMID： 15290264 DOI： 10.1007/s00431-004-1504-z

Source DB: PubMed Journal: Eur J Pediatr ISSN： 0340-6199 Impact factor: 3.183

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5 in total

1. Sensorineural deafness associated with recessive hypophosphataemic rickets.

Authors: N Weir
Journal: J Laryngol Otol Date: 1977-08 Impact factor: 1.469

2. Congenital malformations of the inner ear: a classification based on embryogenesis.

Authors: R K Jackler; W M Luxford; W F House
Journal: Laryngoscope Date: 1987-03 Impact factor: 3.325

3. Audiologic findings in young patients with hypophosphatemic bone disease.

Authors: M Meister; A Johnson; G R Popelka; G S Kim; M P Whyte
Journal: Ann Otol Rhinol Laryngol Date: 1986 Jul-Aug Impact factor: 1.547

4. Impaired hearing in X-linked hypophosphataemic (vitamin-D-resistant) osteomalacia.

Authors: M Davies; R Kane; J Valentine
Journal: Ann Intern Med Date: 1984-02 Impact factor: 25.391

5. Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse.

Authors: A Boneh; T M Reade; C R Scriver; E Rishikof
Journal: Am J Med Genet Date: 1987-08

5 in total

14 in total

1. Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation.

Authors: Cameron C Wick; Sharon J Lin; Heping Yu; Cliff A Megerian; Qing Yin Zheng
Journal: Am J Otolaryngol Date: 2016-09-28 Impact factor: 1.808

Review 2. FGF23 and Associated Disorders of Phosphate Wasting.

Authors: Anisha Gohil; Erik A Imel
Journal: Pediatr Endocrinol Rev Date: 2019-09

3. A novel auditory ossicles membrane and the development of conductive hearing loss in Dmp1-null mice.

Authors: Kun Lv; Haiyang Huang; Xing Yi; Mark E Chertoff; Chaoyuan Li; Baozhi Yuan; Robert J Hinton; Jian Q Feng
Journal: Bone Date: 2017-06-08 Impact factor: 4.398

4. Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease.

Authors: Simone Rask Nielsen; Stinus Gadegaard Hansen; Claus Bistrup; Klaus Brusgaard; Anja Lisbeth Frederiksen
Journal: Calcif Tissue Int Date: 2022-08-02 Impact factor: 4.000

10. Kbus/Idr, a mutant mouse strain with skeletal abnormalities and hypophosphatemia: identification as an allele of 'Hyp'.

Authors: Kenji Moriyama; Atsuko Hanai; Kazuyuki Mekada; Atsushi Yoshiki; Katsueki Ogiwara; Atsushi Kimura; Takayuki Takahashi
Journal: J Biomed Sci Date: 2011-08-20 Impact factor: 8.410

Hearing impairment in familial X-linked hypophosphatemic rickets.

1. Sensorineural deafness associated with recessive hypophosphataemic rickets.

2. Congenital malformations of the inner ear: a classification based on embryogenesis.

3. Audiologic findings in young patients with hypophosphatemic bone disease.

4. Impaired hearing in X-linked hypophosphataemic (vitamin-D-resistant) osteomalacia.

5. Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse.

1. Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation.

Review 2. FGF23 and Associated Disorders of Phosphate Wasting.

3. A novel auditory ossicles membrane and the development of conductive hearing loss in Dmp1-null mice.

4. Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease.

5. A mouse model with postnatal endolymphatic hydrops and hearing loss.

Review 6. Hypophosphatemic rickets due to perturbations in renal tubular function.

7. A Genetic Murine Model of Endolymphatic Hydrops: The Phex Mouse.

Review 8. Congenital Conditions of Hypophosphatemia in Children.

Review 9. New Therapies for Hypophosphatemia-Related to FGF23 Excess.

10. Kbus/Idr, a mutant mouse strain with skeletal abnormalities and hypophosphatemia: identification as an allele of 'Hyp'.