These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 8898273)

  • 1. Hearing loss in oto-spondylo-megaepiphyseal dysplasia (OSMED): case studies.
    Katbamna B; Westbrook MK
    J Am Acad Audiol; 1996 Oct; 7(5):365-9. PubMed ID: 8898273
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oto-spondylo-megaepiphyseal dysplasia (OSMED): clinical and radiological findings in sibs homozygous for premature stop codon mutation in the COL11A2 gene.
    Temtamy SA; Männikkö M; Abdel-Salam GM; Hassan NA; Ala-Kokko L; Afifi HH
    Am J Med Genet A; 2006 Jun; 140(11):1189-95. PubMed ID: 16637051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A type II collagen mutation also results in oto-spondylo-megaepiphyseal dysplasia.
    Miyamoto Y; Nakashima E; Hiraoka H; Ohashi H; Ikegawa S
    Hum Genet; 2005 Nov; 118(2):175-8. PubMed ID: 16189708
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [2 cases of oto-spondylo-megaephyseal dysplasia].
    Bigozzi M; Cerboni F; Pellegrini A
    Acta Otorhinolaryngol Ital; 2001 Jun; 21(3):179-86. PubMed ID: 11677845
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oto-spondylo-megaepiphyseal dysplasia (OSMED).
    Giedion A; Brandner M; Lecannellier J; Muhar U; Prader A; Sulzer J; Zweymüller E
    Helv Paediatr Acta; 1982 Sep; 37(4):361-80. PubMed ID: 7153059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene.
    van Steensel MA; Buma P; de Waal Malefijt MC; van den Hoogen FH; Brunner HG
    Am J Med Genet; 1997 Jun; 70(3):315-23. PubMed ID: 9188673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bone dysplasia, midface hypoplasia, and deafness: three new patients and review of the literature.
    Kääriäinen H; Barrow M; Hennekam R
    Am J Med Genet; 1993 Apr; 46(2):223-7. PubMed ID: 8484414
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New Insights on the Genetic Basis Underlying SHILCA Syndrome: Characterization of the
    Abad-Morales V; Wert A; Ruiz Gómez MÁ; Navarro R; Pomares E
    Int J Mol Sci; 2021 Feb; 22(5):. PubMed ID: 33668384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis.
    Karaer K; Rosti RO; Torun D; Sanal HT; Bahçe M; Güran S
    Turk J Pediatr; 2011; 53(3):346-51. PubMed ID: 21980822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spondylo-megaepiphyseal-metaphyseal dysplasia: an unusual bone dysplasia.
    Agarwal PP; Srinivasan A; Sharma R; Kabra M; Gupta AK
    Pediatr Radiol; 2003 Dec; 33(12):893-6. PubMed ID: 13680008
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hearing assessment in pre-school children with speech delay.
    Psillas G; Psifidis A; Antoniadou-Hitoglou M; Kouloulas A
    Auris Nasus Larynx; 2006 Sep; 33(3):259-63. PubMed ID: 16420975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The type XI collagenopathies.
    Spranger J
    Pediatr Radiol; 1998 Oct; 28(10):745-50. PubMed ID: 9799295
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Noncongenital hereditary hearing loss in children. Prospective documentation.
    Madell JR; Sculerati N
    Arch Otolaryngol Head Neck Surg; 1991 Mar; 117(3):332-5. PubMed ID: 1998574
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Audiologic Manifestations of Marshall Syndrome.
    Bacciu A; Di Lella F; Iaccarino I; Pasanisi E; Fava G; Vincenti V; Falcioni M
    Otol Neurotol; 2018 Sep; 39(8):e691-e698. PubMed ID: 30020262
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spondylo-megaepiphyseal-metaphyseal dysplasia: a new bone dysplasia resembling cleidocranial dysplasia.
    Silverman FN; Reiley MA
    Radiology; 1985 Aug; 156(2):365-71. PubMed ID: 3925497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Facioscapulohumeral muscular dystrophy and accompanying hearing loss.
    Meyerson MD; Lewis E; Ill K
    Arch Otolaryngol; 1984 Apr; 110(4):261-6. PubMed ID: 6704043
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Otologic and audiologic characteristics of children with skeletal dysplasia in central China.
    Chen G; Fu S; Dong J; Zhang L
    Acta Otolaryngol; 2013 Jul; 133(7):728-32. PubMed ID: 23768058
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Progressive sensorineural hearing loss in association with distal renal tubular acidosis.
    Brown MT; Cunningham MJ; Ingelfinger JR; Becker AN
    Arch Otolaryngol Head Neck Surg; 1993 Apr; 119(4):458-60. PubMed ID: 8457310
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial sensorineural hearing loss: a correlative study of audiologic, radiographic, and vestibular findings.
    Chan KH; Eelkema EA; Furman JM; Kamerer DB
    Ann Otol Rhinol Laryngol; 1991 Aug; 100(8):620-5. PubMed ID: 1872511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate.
    Simsek-Kiper PO; Kosukcu C; Akgun-Dogan O; Gocmen R; Utine GE; Soyer T; Korkmaz-Toygar A; Nishimura G; Alikasifoglu M; Boduroglu K
    Eur J Med Genet; 2019 Jan; 62(1):21-26. PubMed ID: 29704686
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.