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 *

109 related articles for article (PubMed ID: 3436724)

  • 1. Otolaryngological manifestations of the Stickler syndrome.
    Lucarini JW; Liberfarb RM; Eavey RD
    Int J Pediatr Otorhinolaryngol; 1987 Dec; 14(2-3):215-22. PubMed ID: 3436724
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Auditory dysfunction in Stickler syndrome.
    Szymko-Bennett YM; Mastroianni MA; Shotland LI; Davis J; Ondrey FG; Balog JZ; Rudy SF; McCullagh L; Levy HP; Liberfarb RM; Francomano CA; Griffith AJ
    Arch Otolaryngol Head Neck Surg; 2001 Sep; 127(9):1061-8. PubMed ID: 11556853
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and Molecular genetics of Stickler syndrome.
    Snead MP; Yates JR
    J Med Genet; 1999 May; 36(5):353-9. PubMed ID: 10353778
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Auditory phenotype in Stickler syndrome: results of audiometric analysis in 20 patients.
    Acke FR; Swinnen FK; Malfait F; Dhooge IJ; De Leenheer EM
    Eur Arch Otorhinolaryngol; 2016 Oct; 273(10):3025-34. PubMed ID: 26786361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature.
    Higuchi Y; Hasegawa K; Yamashita M; Tanaka H; Tsukahara H
    J Med Case Rep; 2017 Aug; 11(1):237. PubMed ID: 28841907
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Lens coloboma and lens dislocation in Stickler (Marshall) syndrome].
    Schlote T; Völker M; Knorr M; Thiel HJ
    Klin Monbl Augenheilkd; 1997 Apr; 210(4):227-8. PubMed ID: 9235398
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical diagnosis of Larsen syndrome, Stickler syndrome and Loeys-Dietz syndrome in a 19-year old male: a case report.
    Riise N; Lindberg BR; Kulseth MA; Fredwall SO; Lundby R; Estensen ME; Drolsum L; Merckoll E; Krohg-Sørensen K; Paus B
    BMC Med Genet; 2018 Aug; 19(1):155. PubMed ID: 30170566
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Otolaryngological manifestations of cleidocranial dysplasia, concentrating on audiological findings.
    Visosky AM; Johnson J; Bingea B; Gurney T; Lalwani AK
    Laryngoscope; 2003 Sep; 113(9):1508-14. PubMed ID: 12972925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stickler syndrome: an underdiagnosed disease. Report of a family.
    De Keyzer TH; De Veuster I; Smets RM
    Bull Soc Belge Ophtalmol; 2011; (318):45-9. PubMed ID: 22003765
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Orofacial features of Treacher Collins syndrome.
    Martelli-Junior H; Coletta RD; Miranda RT; Barros LM; Swerts MS; Bonan PR
    Med Oral Patol Oral Cir Bucal; 2009 Jul; 14(7):E344-8. PubMed ID: 19300363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial syndrome of unusual triangular facies associated with cleft palate, malocclusion, midfacial hypoplasia and sensorineural hearing loss in two siblings. Is it a new autosomal recessive syndrome?
    Balcı S; Akcan B; Vargel İ; Tümer C; Enacar A
    Clin Dysmorphol; 2004 Apr; 13(2):71-74. PubMed ID: 15057120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.
    Admiraal RJ; Brunner HG; Dijkstra TL; Huygen PL; Cremers CW
    Laryngoscope; 2000 Mar; 110(3 Pt 1):457-61. PubMed ID: 10718438
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Facio-oculo-acoustico-renal (FOAR) syndrome: case report and review.
    Schowalter DB; Pagon RA; Kalina RE; McDonald R
    Am J Med Genet; 1997 Mar; 69(1):45-9; discussion 44. PubMed ID: 9066882
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics and hearing loss: a review of Stickler syndrome.
    Nowak CB
    J Commun Disord; 1998; 31(5):437-53; 453-4. PubMed ID: 9777489
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey.
    Stickler GB; Hughes W; Houchin P
    Genet Med; 2001; 3(3):192-6. PubMed ID: 11388760
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Difficulties in anesthetic management of patients with micrognathia: report of a patient with Stickler syndrome.
    Küçükyavuz Z; Ozkaynak O; Tüzüner AM; Kişnişçi R
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Dec; 102(6):e33-6. PubMed ID: 17138163
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Foveal Hypoplasia in Patients with Stickler Syndrome.
    Matsushita I; Nagata T; Hayashi T; Kimoto K; Kubota T; Ohji M; Kusaka S; Kondo H
    Ophthalmology; 2017 Jun; 124(6):896-902. PubMed ID: 28283280
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stickler syndrome: exploring prophylaxis for retinal detachment.
    Coussa RG; Sears J; Traboulsi EI
    Curr Opin Ophthalmol; 2019 Sep; 30(5):306-313. PubMed ID: 31313752
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.