BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 15106290)

  • 1. Rieger syndrome: case report.
    Megighian D; Savastano M; Poli P
    Int Tinnitus J; 2003; 9(2):134-7. PubMed ID: 15106290
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?
    Grosso S; Farnetani MA; Berardi R; Vivarelli R; Vanni M; Morgese G; Balestri P
    Am J Med Genet; 2002 Aug; 111(2):182-6. PubMed ID: 12210347
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome.
    Cunningham ET; Eliott D; Miller NR; Maumenee IH; Green WR
    Arch Ophthalmol; 1998 Jan; 116(1):78-82. PubMed ID: 9445211
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation.
    Yamazaki H; Nakamura T; Hosono K; Yamaguchi T; Hiratsuka Y; Hotta Y; Takahashi M
    Auris Nasus Larynx; 2021 Dec; 48(6):1204-1208. PubMed ID: 32741584
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A; Sokołowska-Oracz A; Pawluczyk-Dyjecińska M; Szaflik JP
    Klin Oczna; 2007; 109(7-9):321-6. PubMed ID: 18260289
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital sensorineural hearing loss.
    Mafee MF; Selis JE; Yannias DA; Valvassori GE; Pruzansky S; Applebaum EL; Capek V
    Radiology; 1984 Feb; 150(2):427-34. PubMed ID: 6691097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inner ear dysplasia in sporadic lacrimo-auriculo-dento-digital syndrome. A case report and review of the literature.
    Meuschel-Wehner S; Klingebiel R; Werbs M
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(5):352-4. PubMed ID: 12417779
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distinctive findings in a patient with Axenfeld-Rieger syndrome using high-resolution AS-OCT.
    Wang D; Wang M; Console JW; He M; Seider MI; Lin SC
    Ophthalmic Surg Lasers Imaging; 2009; 40(6):589-92. PubMed ID: 19928726
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Apert syndrome and hearing loss with ear anomalies: a case report and literature review.
    Huang F; Sweet R; Tewfik TL
    Int J Pediatr Otorhinolaryngol; 2004 Apr; 68(4):495-501. PubMed ID: 15013619
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinics in diagnostic imaging (111): X-linked congenital mixed deafness syndrome.
    Chee NW; Suhailee S; Goh J
    Singapore Med J; 2006 Sep; 47(9):822-4; quiz 825. PubMed ID: 16924369
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inner ear anomalies in cochlear implantees: importance of radiologic measurements in the classification.
    Shim HJ; Shin JE; Chung JW; Lee KS
    Otol Neurotol; 2006 Sep; 27(6):831-7. PubMed ID: 16936569
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Posterior embryotoxon may not be a forme fruste of Axenfeld-Rieger's Syndrome.
    Sim KT; Karri B; Kaye SB
    J AAPOS; 2004 Oct; 8(5):504-6. PubMed ID: 15492748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [HRCT imaging characterized of congenital abnormalities of the inner ear in 45 cases].
    Wang J; Meng M; Huan Y; Zhang J
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2003 Oct; 17(10):583-5. PubMed ID: 14727423
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bilateral prominent schwalbe ring in the anterior chamber in a patient with axenfeld-rieger syndrome and megalocornea.
    Espana EM; Mora R; Liebmann J; Ritch R
    Cornea; 2007 Apr; 26(3):379-81. PubMed ID: 17413972
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
    Strungaru MH; Dinu I; Walter MA
    Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):228-37. PubMed ID: 17197537
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Audiometric characterization of a family with digenic autosomal, dominant, progressive sensorineural hearing loss.
    Borg E; Samuelsson E; Dahl N
    Acta Otolaryngol; 2000 Jan; 120(1):51-7. PubMed ID: 10779186
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.
    Panicker SG; Sampath S; Mandal AK; Reddy AB; Ahmed N; Hasnain SE
    Invest Ophthalmol Vis Sci; 2002 Dec; 43(12):3613-6. PubMed ID: 12454026
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New patterns in genetic and congenital otonephropathies.
    Bergstrom L; Thompson P; Wood RP
    Laryngoscope; 1979 Feb; 89(2 Pt 1):177-94. PubMed ID: 423658
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sensorineural hearing loss in children.
    Lowe LH; Vézina LG
    Radiographics; 1997; 17(5):1079-93. PubMed ID: 9308102
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Contraindication for cochlear implantation in Wildervanck's syndrome].
    Wojnowski W; Obrebowski A; Szyfter W; Walczak M; Karlik M; Kurywczak-Grykiel K
    Otolaryngol Pol; 2004; 58(4):803-6. PubMed ID: 15603393
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.