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1947 1
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1951 12
1952 7
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1954 4
1955 5
1956 6
1957 3
1958 3
1959 5
1960 6
1961 5
1962 7
1963 8
1964 10
1965 13
1966 16
1967 24
1968 13
1969 19
1970 27
1971 20
1972 27
1973 58
1974 52
1975 52
1976 36
1977 32
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1980 43
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1986 48
1987 51
1988 55
1989 66
1990 60
1991 78
1992 81
1993 71
1994 88
1995 87
1996 102
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1998 93
1999 109
2000 91
2001 91
2002 99
2003 114
2004 127
2005 138
2006 156
2007 187
2008 173
2009 163
2010 157
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2013 223
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2015 276
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6,364 results

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Page 1
Axenfeld-Rieger Syndrome.
Zamora EA, Tripathy K, Salini B. Zamora EA, et al. 2024 Feb 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2024 Feb 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 30860739 Free Books & Documents.
Another significant advancement came from the Austrian ophthalmologist Herwigh Rieger, who described a distinct set of ocular abnormalities known as the "Rieger anomaly." ...In current medical terminology, the terms Axenfeld anomaly, Rieger anomaly, and Ri
Another significant advancement came from the Austrian ophthalmologist Herwigh Rieger, who described a distinct set of ocular abnorma …
Ophthalmological Manifestations of Axenfeld-Rieger Syndrome: Current Perspectives.
Michels K, Bohnsack BL. Michels K, et al. Clin Ophthalmol. 2023 Mar 10;17:819-828. doi: 10.2147/OPTH.S379853. eCollection 2023. Clin Ophthalmol. 2023. PMID: 36926528 Free PMC article. Review.
Axenfeld-Rieger syndrome (ARS) is a rare congenital disease that is primarily characterized by ocular anterior segment anomalies but is also associated with craniofacial, dental, cardiac, and neurologic abnormalities. ...Within the eye, ARS is classically defined as the co …
Axenfeld-Rieger syndrome (ARS) is a rare congenital disease that is primarily characterized by ocular anterior segment anomalies but …
Rieger syndrome: a clinical, molecular, and biochemical analysis.
Amendt BA, Semina EV, Alward WL. Amendt BA, et al. Cell Mol Life Sci. 2000 Oct;57(11):1652-66. doi: 10.1007/pl00000647. Cell Mol Life Sci. 2000. PMID: 11092457 Review.
Rieger syndrome (RIEG 1; MIM 180500) is an autosomal dominant disorder of morphogenesis. It is a phenotypically heterogeneous disorder characterized by malformations of the eyes, teeth, and umbilicus. RIEG belongs to the Axenfeld-Rieger group of anomalies, which inc
Rieger syndrome (RIEG 1; MIM 180500) is an autosomal dominant disorder of morphogenesis. It is a phenotypically heterogeneous disorde
Axenfeld-Rieger syndrome: new perspectives.
Chang TC, Summers CG, Schimmenti LA, Grajewski AL. Chang TC, et al. Br J Ophthalmol. 2012 Mar;96(3):318-22. doi: 10.1136/bjophthalmol-2011-300801. Epub 2011 Dec 23. Br J Ophthalmol. 2012. PMID: 22199394 Review.
Axenfeld-Rieger syndrome is a genetic disease affecting multiple organ systems. ...Recent advances in molecular genetics have identified two major genes, PITX2 and FOXC1, demonstrating a wide spectrum of mutations, which aids in the molecular diagnosis of the disease, alth …
Axenfeld-Rieger syndrome is a genetic disease affecting multiple organ systems. ...Recent advances in molecular genetics have identif …
Aniridia and Axenfeld-Rieger Syndrome: Clinical presentations, molecular genetics and current/emerging therapies.
Chrystal PW, Walter MA. Chrystal PW, et al. Exp Eye Res. 2019 Dec;189:107815. doi: 10.1016/j.exer.2019.107815. Epub 2019 Sep 24. Exp Eye Res. 2019. PMID: 31560925 Review.
Aniridia and Axenfeld-Rieger Syndrome are related, human ocular disorders that are typically inherited in an autosomal dominant manner. ...This review will focus on describing the clinical presentations of Aniridia and Axenfeld-Rieger Syndrome as well as the molecul …
Aniridia and Axenfeld-Rieger Syndrome are related, human ocular disorders that are typically inherited in an autosomal dominant manne …
Axenfeld-Rieger syndrome in the age of molecular genetics.
Alward WL. Alward WL. Am J Ophthalmol. 2000 Jul;130(1):107-15. doi: 10.1016/s0002-9394(00)00525-0. Am J Ophthalmol. 2000. PMID: 11004268 Review.
Mutations in these genes can cause a wide variety of phenotypes that share features with Axenfeld-Rieger syndrome. Axenfeld anomaly, Rieger anomaly, Rieger syndrome, iridogoniodysgenesis anomaly, iridogoniodysgenesis syndrome, iris hypoplasia, and familial gl …
Mutations in these genes can cause a wide variety of phenotypes that share features with Axenfeld-Rieger syndrome. Axenfeld anomaly, …
Rieger.
WALTER H. WALTER H. Trans Am Acad Ophthalmol Otolaryngol. 1951 Sep-Oct;55:745-6. Trans Am Acad Ophthalmol Otolaryngol. 1951. PMID: 14893318 No abstract available.
Cardiac anomalies in Axenfeld-Rieger syndrome.
Valikodath N, Johns JA, Godown J. Valikodath N, et al. Cardiol Young. 2023 Jul;33(7):1229-1231. doi: 10.1017/S1047951122003857. Epub 2022 Dec 22. Cardiol Young. 2023. PMID: 36543336
Axenfeld-Rieger syndrome is a rare multi-system disorder associated with cardiac anomalies. All patients with a diagnosis of Axenfeld-Rieger syndrome were identified from our electronic medical record. ...
Axenfeld-Rieger syndrome is a rare multi-system disorder associated with cardiac anomalies. All patients with a diagnosis of Axenfeld …
Axenfeld-Rieger syndrome. A spectrum of developmental disorders.
Shields MB, Buckley E, Klintworth GK, Thresher R. Shields MB, et al. Surv Ophthalmol. 1985 May-Jun;29(6):387-409. doi: 10.1016/0039-6257(85)90205-x. Surv Ophthalmol. 1985. PMID: 3892740 Review.
The clinical and histopathologic features of Axenfeld's anomaly and Rieger's anomaly and syndrome are reviewed, and recent findings regarding the pathogenesis of this spectrum of developmental disorders are discussed. ...Recent observations regarding the mechanism o …
The clinical and histopathologic features of Axenfeld's anomaly and Rieger's anomaly and syndrome are reviewed, and recent fin …
Rieger Syndrome: Rehabilitation With Dental Implants.
Pirih FQ, Casarin M, Perussolo J, Ozaki M, Carnio JG, Camargo PM, Galvan M. Pirih FQ, et al. Clin Adv Periodontics. 2019 Dec;9(4):172-176. doi: 10.1002/cap.10065. Epub 2019 Aug 8. Clin Adv Periodontics. 2019. PMID: 31490031
INTRODUCTION: Axenfeld-Rieger syndrome (ARS), also known as Rieger syndrome, is a rare autosomal dominant condition defined by craniofacial, ocular, dental, periumbilical, and systemic anomalies. ...
INTRODUCTION: Axenfeld-Rieger syndrome (ARS), also known as Rieger syndrome, is a rare autosomal dominant condition defined by …
6,364 results