BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 32801529)

  • 41. Oral manifestations of the Rieger syndrome: report of case.
    Drum MA; Kaiser-Kupfer MI; Guckes AD; Roberts MW
    J Am Dent Assoc; 1985 Mar; 110(3):343-6. PubMed ID: 3858346
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.
    Walter MA; Mirzayans F; Mears AJ; Hickey K; Pearce WG
    Ophthalmology; 1996 Nov; 103(11):1907-15. PubMed ID: 8942889
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Laser corepraxy in mesodermal iris dysgenesis (Axenfeld-Rieger syndrome) (case report)].
    Arestova NN; Kalinichenko RV; Egiyan NS; Kruglova TB
    Vestn Oftalmol; 2021; 137(2):96-100. PubMed ID: 33881269
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?
    Moog U; Bleeker-Wagemakers EM; Crobach P; Vles JS; Schrander-Stumpel CT
    Am J Med Genet; 1998 Jul; 78(3):263-6. PubMed ID: 9677063
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Atrial septal defect with interatrial aneurysm and Axenfeld-Rieger syndrome.
    Bekir NA; Güngör K
    Acta Ophthalmol Scand; 2000 Feb; 78(1):101-3. PubMed ID: 10726801
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Axenfeld-Rieger syndrome in the age of molecular genetics.
    Alward WL
    Am J Ophthalmol; 2000 Jul; 130(1):107-15. PubMed ID: 11004268
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The Rieger syndrome.
    Jorgenson RJ; Levin LS; Cross HE; Yoder F; Kelly TE
    Am J Med Genet; 1978; 2(3):307-18. PubMed ID: 263445
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Axenfeld-Rieger syndrome associated with severe maxillofacial and skeletal anomalies.
    Gokce G; Oren NC; Ozgonul C
    J Oral Maxillofac Pathol; 2015; 19(1):109. PubMed ID: 26097324
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Current molecular understanding of Axenfeld-Rieger syndrome.
    Hjalt TA; Semina EV
    Expert Rev Mol Med; 2005 Nov; 7(25):1-17. PubMed ID: 16274491
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Idiopathic mitral valve disease in a patient presenting with Axenfeld-Rieger syndrome.
    Antevil J; Umakanthan R; Leacche M; Brewer Z; Solenkova N; Byrne JG; Greelish JP
    J Heart Valve Dis; 2009 May; 18(3):349-51. PubMed ID: 19557997
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A Novel Mutation in
    Hassed SJ; Li S; Xu W; Taylor AC
    Mol Syndromol; 2017 Mar; 8(2):107-109. PubMed ID: 28611552
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Clinical presentation of a variant of Axenfeld-Rieger syndrome associated with subtelomeric 6p deletion.
    Martinez-Glez V; Lorda-Sanchez I; Ramirez JM; Ruiz-Barnes P; Rodriguez de Alba M; Diego-Alvarez D; Ramos C; Searby CC; Nishimura DY; Ayuso C
    Eur J Med Genet; 2007; 50(2):120-7. PubMed ID: 17157569
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
    Idrees F; Bloch-Zupan A; Free SL; Vaideanu D; Thompson PJ; Ashley P; Brice G; Rutland P; Bitner-Glindzicz M; Khaw PT; Fraser S; Sisodiya SM; Sowden JC
    Am J Med Genet B Neuropsychiatr Genet; 2006 Mar; 141B(2):184-91. PubMed ID: 16389592
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.
    de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M; Dufier JL; Menasche M; Abitbol M
    BMC Med Genet; 2006 Nov; 7():82. PubMed ID: 17134502
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Mutations in zebrafish pitx2 model congenital malformations in Axenfeld-Rieger syndrome but do not disrupt left-right placement of visceral organs.
    Ji Y; Buel SM; Amack JD
    Dev Biol; 2016 Aug; 416(1):69-81. PubMed ID: 27297886
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Surgical outcomes of Glaucoma associated with Axenfeld-Rieger syndrome.
    Zepeda EM; Branham K; Moroi SE; Bohnsack BL
    BMC Ophthalmol; 2020 May; 20(1):172. PubMed ID: 32357855
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Axenfeld-Rieger syndrome: further clinical and array delineation of four unrelated patients with a 4q25 microdeletion.
    Titheradge H; Togneri F; McMullan D; Brueton L; Lim D; Williams D
    Am J Med Genet A; 2014 Jul; 164A(7):1695-701. PubMed ID: 24715413
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.