The role of hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with retinal artery occlusion

2002 ◽  
Vol 134 (1) ◽  
pp. 57-61 ◽  
Author(s):  
Martin Weger ◽  
Olaf Stanger ◽  
Hannes Deutschmann ◽  
Franz Josef Leitner ◽  
Wilfried Renner ◽  
...  
2021 ◽  
pp. 112067212110006
Author(s):  
Manuel Marques ◽  
Francisco Alves ◽  
Miguel Leitão ◽  
Catarina Rodrigues ◽  
Joana Tavares Ferreira

The role of polymorphisms of methylenetetrahydrofolate reductase (MTHFR) gene in retinal vein occlusion (RVO) is a theme of discussion since the first reports of RVO in patients with MTHFR C677T mutation and without classic acquired risk factors for retinal vascular disease. The association between MTHFR polymorphisms and RVO has been studied over the last 20 years producing conflicting results. This review aims to summarize the literature concerning the role MTHFR polymorphisms as risk factors for RVO.


Stroke ◽  
2005 ◽  
Vol 36 (2) ◽  
pp. 249-252 ◽  
Author(s):  
Martin Weger ◽  
Iris Steinbrugger ◽  
Anton Haas ◽  
Winfried März ◽  
Yosuf El-Shabrawi ◽  
...  

Eye ◽  
2003 ◽  
Vol 17 (6) ◽  
pp. 731-734 ◽  
Author(s):  
M Weger ◽  
W Renner ◽  
O Pinter ◽  
O Stanger ◽  
W Temmel ◽  
...  

2020 ◽  
Vol 43 (9) ◽  
pp. 992-999
Author(s):  
Ryan A. Watson ◽  
Jennifer Wellings ◽  
Rittu Hingorani ◽  
Tingting Zhan ◽  
Daniel R. Frisch ◽  
...  

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