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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

525 related items for PubMed ID: 26786361

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  • 22. Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotype.
    Nixon TRW, Alexander P, Richards A, McNinch A, Bearcroft PWP, Cobben J, Snead MP.
    Am J Med Genet A; 2019 Aug; 179(8):1498-1506. PubMed ID: 31090205
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  • 27. Cephalometrics in Stickler syndrome: Objectification of the typical facial appearance.
    Acke FR, Dhooge IJ, Malfait F, De Leenheer EM, De Pauw GA.
    J Craniomaxillofac Surg; 2016 Jul; 44(7):848-53. PubMed ID: 27193475
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  • 28. Importance of early diagnosis of Stickler syndrome in newborns.
    Antunes RB, Alonso N, Paula RG.
    J Plast Reconstr Aesthet Surg; 2012 Aug; 65(8):1029-34. PubMed ID: 22424767
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  • 30. Hearing Outcomes in Stickler Syndrome: Variation Due to COL2A1 and COL11A1.
    Bath F, Swanson D, Zavala H, Chinnadurai S, Roby BB.
    Cleft Palate Craniofac J; 2022 Aug; 59(8):970-975. PubMed ID: 34238052
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  • 32. Slight-mild sensorineural hearing loss in children: audiometric, clinical, and risk factor profiles.
    Cone BK, Wake M, Tobin S, Poulakis Z, Rickards FW.
    Ear Hear; 2010 Apr; 31(2):202-12. PubMed ID: 20054279
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  • 33. Audiological findings in Williams syndrome: a study of 69 patients.
    Barozzi S, Soi D, Comiotto E, Borghi A, Gavioli C, Spreafico E, Gagliardi C, Selicorni A, Forti S, Ambrosetti U, Cesarani A, Brambilla D.
    Am J Med Genet A; 2012 Apr; 158A(4):759-71. PubMed ID: 22411878
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  • 34. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies.
    Zwirner P, Wilichowski E.
    Laryngoscope; 2001 Mar; 111(3):515-21. PubMed ID: 11224785
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  • 35. Case report of the first molecular diagnosis of Stickler syndrome with a pathogenic COL2A1 variant in a Mongolia family.
    Wu H, Che S, Li S, Cheng Y, Xiao J, Liu Z.
    Mol Genet Genomic Med; 2021 Oct; 9(10):e1781. PubMed ID: 34405586
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  • 36. Otoacoustic emissions in patients with hypotension.
    Balatsouras DG, Korres S, Simaskos N, Kandiloros D, Ferekidis E, Economou C.
    J Laryngol Otol; 2003 Apr; 117(4):265-9. PubMed ID: 12816214
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  • 37. Audiologic evidence for further genetic heterogeneity at DFNA2.
    Stern RE, Lalwani AK.
    Acta Otolaryngol; 2002 Oct; 122(7):730-5. PubMed ID: 12484650
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