|1.||Walter, Michael A: 6 articles (09/2011 - 06/2002)|
|2.||Tanwar, Mukesh: 3 articles (03/2014 - 01/2009)|
|3.||Dada, Tanuj: 3 articles (03/2014 - 01/2009)|
|4.||Dada, Rima: 3 articles (03/2014 - 01/2009)|
|5.||Semina, Elena V: 3 articles (01/2014 - 09/2011)|
|6.||Kwon, Young H: 3 articles (01/2012 - 02/2003)|
|7.||Stone, Edwin M: 3 articles (01/2012 - 02/2002)|
|8.||Berry, Fred B: 3 articles (09/2011 - 02/2005)|
|9.||Lehmann, Ordan J: 3 articles (09/2009 - 06/2002)|
|10.||Martin, Donna M: 2 articles (02/2015 - 10/2011)|
08/15/2015 - "Since loss-of-function mutations in FOXC1 are associated with Axenfeld-Rieger syndrome, the genetic findings in combination with re-evaluation of the patient's clinical data resulted in a corrected diagnosis of Axenfeld-Rieger syndrome with developmental glaucoma. "
08/15/2015 - "Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma."
06/01/2015 - "Indeed, abnormalities in neural crest development cause craniofacial defects and ocular anomalies, such as Axenfeld-Rieger syndrome and primary congenital glaucoma. "
05/01/2014 - "We report an unusual case of Axenfeld-Rieger Syndrome with secondary glaucoma managed with Ologen(®) implant. "
05/01/2014 - "OLOGEN(®) implant in the management of glaucoma in an unusual case of Axenfeld-Rieger syndrome."
06/01/1999 - "Thirty-eight eyes of 29 patients were included in the study; 34 eyes (89.5%) had refractory primary congenital glaucoma with documented failure of primary surgery, 2 eyes (5.3%) had Axenfeld-Rieger syndrome and 2 eyes (5.3%) had aniridia. "
01/01/2015 - "The search software identified 29 congenital aniridia, 6 Axenfeld/Rieger syndrome, 11 BEPS, 3 Nanophthalmos, and 3 Rubinstein-Taybi syndrome. "
01/01/2011 - "Combined aniridia ring implantation and cataract surgery in an Axenfeld-Rieger syndrome: a UBM report."
01/01/2011 - "To describe ultrasound biomicroscopy (UBM) features in a patient with Axenfeld-Rieger syndrome (ARS) and cataract before and after anterior segment surgery using intraocular lens (IOL) and aniridic ring implantation (Morcher Aniridia rings 50 D). "
10/01/2015 - "Other secondary developmental corneal diseases may include Axenfeld-Rieger syndrome, Aniridia, and primary congenital glaucoma, all of which have specific genotypic characterization. "
01/01/1978 - "The results of this study indicate that the Rieger syndrome is an autosomal dominant syndrome whose cardinal features are hypodontia, goniodysgenesis, and failure of the periumbilical skin to involute properly."
07/07/1998 - "If accompanied by hypodontia, midface hypoplasia, and umbilical anomalies, the designation "Rieger syndrome" is appropriate. "
06/01/1998 - "The autosomal dominant Rieger syndrome (RS) manifests hypodontia, adontia, iridogoniodysgenesis and umbilical anomalies. "
01/01/1978 - "Fourteen patients with hypodontia and the ocular features of the Rieger syndrome were examined for the presence of systemic anomalies. "
01/01/2014 - "Patients with Axenfeld-Rieger Syndrome (ARS) present various dental abnormalities, including hypodontia, and enamel hypoplasia. "
|1.||cytochrome P-450 CYP1B1 (CYP1B1)
|2.||Transcription Factors (Transcription Factor)
|4.||dominant type Iridogoniodysgenesis
|7.||Treacher Collins-Franceschetti syndrome
|10.||Omphalocele cleft palate syndrome lethal
|1.||Intraocular Lenses (Intraocular Lens)