-
1
-
-
0024342063
-
Plasma homocysteine, a risk factor for vascular disease: Plasma levels in health, disease, and drug therapy
-
Ueland PM, Refsum H. Plasma homocysteine, a risk factor for vascular disease: plasma levels in health, disease, and drug therapy. J Lab Clin Med. 1989;114:473-501.
-
(1989)
J Lab Clin Med
, vol.114
, pp. 473-501
-
-
Ueland, P.M.1
Refsum, H.2
-
2
-
-
0029939676
-
Homocysteine and vascular disease
-
McCully KS. Homocysteine and vascular disease. Nat Med. 1996;2:386-389.
-
(1996)
Nat Med
, vol.2
, pp. 386-389
-
-
McCully, K.S.1
-
3
-
-
0029921114
-
Hyperhomocysteinemia as a risk factor for deep-vein thrombosis
-
den Heijer M, Koster T, Blom HJ, et al. Hyperhomocysteinemia as a risk factor for deep-vein thrombosis. N Engl J Med. 1996;334:759-762.
-
(1996)
N Engl J Med
, vol.334
, pp. 759-762
-
-
Den Heijer, M.1
Koster, T.2
Blom, H.J.3
-
4
-
-
0032569645
-
Meta-analysis of hyperhomocysteinemia as a risk factor for venous thromboembolic disease
-
Ray JG. Meta-analysis of hyperhomocysteinemia as a risk factor for venous thromboembolic disease. Arch Intern Med. 1998;158:2101-2106.
-
(1998)
Arch Intern Med
, vol.158
, pp. 2101-2106
-
-
Ray, J.G.1
-
5
-
-
0031733260
-
Hyperhomocysteinemia and venous thrombosis: A meta-analysis
-
den Heijer M, Rosendaal FR, Blom HJ, et al. Hyperhomocysteinemia and venous thrombosis: a meta-analysis. Thromb Haemost. 1998;80:874-877.
-
(1998)
Thromb Haemost
, vol.80
, pp. 874-877
-
-
Den Heijer, M.1
Rosendaal, F.R.2
Blom, H.J.3
-
6
-
-
18344398980
-
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the co-existence of the FV Leiden and the prothombin A2O210 mutation
-
Margaglione M, D'Andrea G, d'Addedda M, et al. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the co-existence of the FV Leiden and the prothombin A2O210 mutation. Thomb Haemost. 1998;79:907-911.
-
(1998)
Thomb Haemost
, vol.79
, pp. 907-911
-
-
Margaglione, M.1
D'Andrea, G.2
D'Addedda, M.3
-
7
-
-
0032836991
-
Deep venous thrombosis as the presenting feature in a patient with celiac disease and homocysteinaema
-
Grigg AP. Deep venous thrombosis as the presenting feature in a patient with celiac disease and homocysteinaema. Aust NZ J Med. 1999;29:566-567.
-
(1999)
Aust NZ J Med
, vol.29
, pp. 566-567
-
-
Grigg, A.P.1
-
8
-
-
0348193849
-
Deep venous thrombosis of the leg in acquired thrombophilia- hyperhomocysteinemia as a consequence of undetected celiac disease
-
Kremer Hovinga JA, Baerlocher G, Wuillemin WA, et al. Deep venous thrombosis of the leg in acquired thrombophilia-hyperhomocysteinemia as a consequence of undetected celiac disease. Ther Umsch. 1999;56:519-522.
-
(1999)
Ther Umsch
, vol.56
, pp. 519-522
-
-
Kremer Hovinga, J.A.1
Baerlocher, G.2
Wuillemin, W.A.3
-
9
-
-
0034684405
-
Splenic vein thrombosis and celiac disease: A fortuitous association?
-
Andres E, Pflumio F, Knab MC, et al. Splenic vein thrombosis and celiac disease: a fortuitous association? Presse Med. 2000;29:1933-1934.
-
(2000)
Presse Med
, vol.29
, pp. 1933-1934
-
-
Andres, E.1
Pflumio, F.2
Knab, M.C.3
-
10
-
-
0036089455
-
Reversible hypertension following coeliac disease treatment: The role of moderate hyperhomocysteinemia and vascular endothelial dysfunction
-
Lim PO, Tzemos N, Farquharson CAJ, et al. Reversible hypertension following coeliac disease treatment: the role of moderate hyperhomocysteinemia and vascular endothelial dysfunction. J Hum Hypertens. 2002;16:411-415.
-
(2002)
J Hum Hypertens
, vol.16
, pp. 411-415
-
-
Lim, P.O.1
Tzemos, N.2
Farquharson, C.A.J.3
-
11
-
-
0036044889
-
Hyperhomocysteinemia in a celiac disease heterozyote for the two common mutations (C677T and A1298C) of the methylenetetrahydrofolate reductase gene. Case report
-
Hozyasz K, Milanowski A. Hyperhomocysteinemia in a celiac disease heterozyote for the two common mutations (C677T and A1298C) of the methylenetetrahydrofolate reductase gene. Case report. Med Wieku Rozwoj. 2002;6:57-61.
-
(2002)
Med Wieku Rozwoj
, vol.6
, pp. 57-61
-
-
Hozyasz, K.1
Milanowski, A.2
-
12
-
-
0036278513
-
Recurrent stroke in a young patient with celiac disease and hyperhomocysteinemia
-
Gefel D, Doncheva M, Ben-Valid E, et al. Recurrent stroke in a young patient with celiac disease and hyperhomocysteinemia. IMAJ. 2002;4:222-223.
-
(2002)
IMAJ
, vol.4
, pp. 222-223
-
-
Gefel, D.1
Doncheva, M.2
Ben-Valid, E.3
-
13
-
-
12244269685
-
Latent coeliac disease, hyperhomocysteinemia and pulmonary thromboembolism: A close link?
-
Gabrielli M, Santoliquido A, Gasbarrini G, et al. Latent coeliac disease, hyperhomocysteinemia and pulmonary thromboembolism: a close link? Thromb Haemost. 2003;89:203-204.
-
(2003)
Thromb Haemost
, vol.89
, pp. 203-204
-
-
Gabrielli, M.1
Santoliquido, A.2
Gasbarrini, G.3
-
14
-
-
0033364256
-
The histopathology of celiac disease: Time for a standardized report scheme for pathologists
-
Oberhuber G, Granditsch G, Vogelsang H. The histopathology of celiac disease: time for a standardized report scheme for pathologists. Eur J Gastroenterol Hepatol. 1999;11:1185-1194.
-
(1999)
Eur J Gastroenterol Hepatol
, vol.11
, pp. 1185-1194
-
-
Oberhuber, G.1
Granditsch, G.2
Vogelsang, H.3
-
15
-
-
0026515461
-
Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiological approach to the spectrum of gluten sensitivity
-
Marsh MN. Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiological approach to the spectrum of gluten sensitivity. Gastroenterology. 1992;102:330-354.
-
(1992)
Gastroenterology
, vol.102
, pp. 330-354
-
-
Marsh, M.N.1
-
16
-
-
0029738540
-
The common "thermolabile" variant of methelenetetrahydrofolate reductase is a major determinant of mild hyperhomocysteinemia
-
Harmon DL, Woodside JV, Yarnell JWG, et al. The common "thermolabile" variant of methelenetetrahydrofolate reductase is a major determinant of mild hyperhomocysteinemia. Q J Med. 1996;89:571-577.
-
(1996)
Q J Med
, vol.89
, pp. 571-577
-
-
Harmon, D.L.1
Woodside, J.V.2
Yarnell, J.W.G.3
-
17
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
-
Jacques PF, Bostom AG, Williams RR, et al. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation. 1996;93:7-9.
-
(1996)
Circulation
, vol.93
, pp. 7-9
-
-
Jacques, P.F.1
Bostom, A.G.2
Williams, R.R.3
-
18
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Gen. 1995;10:111-113.
-
(1995)
Nat Gen
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
19
-
-
0029895024
-
Elevated total plasma homocysteine and C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease
-
de Franchis R, Mancini FP, D'Angelo A, et al. Elevated total plasma homocysteine and C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease. Am J Hum Genet. 1996;59:262-264.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 262-264
-
-
De Franchis, R.1
Mancini, F.P.2
D'Angelo, A.3
-
20
-
-
0029827313
-
Homocysteine and risk of premature coronary heart disease: Evidence for a common gene mutation
-
Gallagher PM, Meleady R, Shields DC, et al. Homocysteine and risk of premature coronary heart disease: evidence for a common gene mutation. Circulation. 1996;94:2154-2158.
-
(1996)
Circulation
, vol.94
, pp. 2154-2158
-
-
Gallagher, P.M.1
Meleady, R.2
Shields, D.C.3
-
21
-
-
0029855024
-
A methylenetetrahydrofolate reducatase polymorphism and the risk of colorectal cancer
-
Chen J, Giovannucci E, Kelsey K, et al. A methylenetetrahydrofolate reducatase polymorphism and the risk of colorectal cancer. Cancer Res. 1996;56:4862-4864.
-
(1996)
Cancer Res
, vol.56
, pp. 4862-4864
-
-
Chen, J.1
Giovannucci, E.2
Kelsey, K.3
-
22
-
-
0005775025
-
The incidence of the gene for thermolabile methylenetetrahydrofolate reductase in African Americans
-
McAndrew PE, Brandt JT, Pearl DK, et al. The incidence of the gene for thermolabile methylenetetrahydrofolate reductase in African Americans. Thromb Res. 1996;83:195-198.
-
(1996)
Thromb Res
, vol.83
, pp. 195-198
-
-
McAndrew, P.E.1
Brandt, J.T.2
Pearl, D.K.3
-
23
-
-
0030897112
-
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease
-
Morita H, Taguchi J, Kurihara H, et al. Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease. Circulation. 1997;95:2032-2036.
-
(1997)
Circulation
, vol.95
, pp. 2032-2036
-
-
Morita, H.1
Taguchi, J.2
Kurihara, H.3
-
24
-
-
0030760946
-
A common mutation in the methylenetetrahydrofolate reducatase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (Factor V: Q506)
-
Cattaneo M, Tsai MY, Bucciarelli P, et al. A common mutation in the methylenetetrahydrofolate reducatase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (Factor V: Q506). Arterioscler Thromb Vasc Biol. 1997;17:1662-1666.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1662-1666
-
-
Cattaneo, M.1
Tsai, M.Y.2
Bucciarelli, P.3
-
25
-
-
0032343873
-
The C677T mutuation in the methylenetetrahydrofolate reductase gene in Koreans
-
Park KS, Podskarbi T, Yoo EA, et al. The C677T mutuation in the methylenetetrahydrofolate reductase gene in Koreans. Korean J Genet. 1998;20:23-28.
-
(1998)
Korean J Genet
, vol.20
, pp. 23-28
-
-
Park, K.S.1
Podskarbi, T.2
Yoo, E.A.3
-
26
-
-
2642701740
-
Analysis of the C677T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups
-
Franco RF, Araujo AG, Guerreiro JF, et al. Analysis of the C677T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups. Thromb Haemost. 1998;79:119-121.
-
(1998)
Thromb Haemost
, vol.79
, pp. 119-121
-
-
Franco, R.F.1
Araujo, A.G.2
Guerreiro, J.F.3
-
27
-
-
0032125774
-
Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida
-
Shaw GM, Rozen R, Finnell RH, et al. Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida. Am J Epidemiol. 1998;148:30-37.
-
(1998)
Am J Epidemiol
, vol.148
, pp. 30-37
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
-
28
-
-
0032042477
-
Frequency of Factor V (FV) Leiden and C677T methylenetetrahydrofolate reductase (MTHFR) mutations in Colombians
-
Vanegas OC, Giusti B, Fernandez CMR, et al. Frequency of Factor V (FV) Leiden and C677T methylenetetrahydrofolate reductase (MTHFR) mutations in Colombians. Thromb Haemost. 1998;79:883-884.
-
(1998)
Thromb Haemost
, vol.79
, pp. 883-884
-
-
Vanegas, O.C.1
Giusti, B.2
Fernandez, C.M.R.3
-
29
-
-
0035057410
-
C677T and A1298C Polymorphisms of the methylenetetrahydrofolate reductase gene: Incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
-
Hanson NQ, Aras O, Yang F, et al. C677T and A1298C Polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease. Clin Chem. 2001;47:661-666.
-
(2001)
Clin Chem.
, vol.47
, pp. 661-666
-
-
Hanson, N.Q.1
Aras, O.2
Yang, F.3
-
30
-
-
0344898475
-
Prevalence of the C677T substitution of the methylenetetrahydrofolate reductase (MTHFR) gene in Wisconsin
-
Qi Z, Hoffman G, Kurtycz D, et al. Prevalence of the C677T substitution of the methylenetetrahydrofolate reductase (MTHFR) gene in Wisconsin. Genet Med. 2003;5:458-459.
-
(2003)
Genet Med
, vol.5
, pp. 458-459
-
-
Qi, Z.1
Hoffman, G.2
Kurtycz, D.3
-
31
-
-
0033812945
-
Genetic modulation of homocysteinemia
-
Rozen R. Genetic modulation of homocysteinemia. Semin Thromb Hemostas. 2000;26:255-261.
-
(2000)
Semin Thromb Hemostas
, vol.26
, pp. 255-261
-
-
Rozen, R.1
-
32
-
-
0023614510
-
Acute mesenteric ischemia: A presenting feature of celiac disease?
-
Upadhyay R, Park RH, Russell RI, et al. Acute mesenteric ischemia: a presenting feature of celiac disease? Br Med J (Clin Res Ed). 1987;295:958-959.
-
(1987)
Br Med J (Clin Res Ed)
, vol.295
, pp. 958-959
-
-
Upadhyay, R.1
Park, R.H.2
Russell, R.I.3
-
33
-
-
0025140314
-
Budd-Chiari syndrome and total villous atrophy in children: Apropos of 3 case reports
-
Boudhina T, Ghram N, Ben Becher S, et al. Budd-Chiari syndrome and total villous atrophy in children: apropos of 3 case reports. Tunis Med. 1990;68:59-62.
-
(1990)
Tunis Med
, vol.68
, pp. 59-62
-
-
Boudhina, T.1
Ghram, N.2
Ben Becher, S.3
-
34
-
-
0025348541
-
Hemiplegia revealing Budd-Chiari syndrome associated with celiac disease in an infant
-
Hamdi A, Ayachi R, Saad H, et al. Hemiplegia revealing Budd-Chiari syndrome associated with celiac disease in an infant. Presse Med. 1900;19:1011-1012.
-
(1900)
Presse Med
, vol.19
, pp. 1011-1012
-
-
Hamdi, A.1
Ayachi, R.2
Saad, H.3
-
35
-
-
0028300196
-
Association of hepatic vein obstruction and celiac disease in North African subjects
-
Marteau P, Cadranel JF, Messing B, et al. Association of hepatic vein obstruction and celiac disease in North African subjects. J Hepatol. 1994;20:650-653.
-
(1994)
J Hepatol
, vol.20
, pp. 650-653
-
-
Marteau, P.1
Cadranel, J.F.2
Messing, B.3
-
37
-
-
0036518731
-
Celiac disease and Budd-Chiarai syndrome: An uncommon association
-
Manzano ML, Garfia C, Manzanares J, et al. Celiac disease and Budd-Chiarai syndrome: an uncommon association. Gastroenterol Hepatol. 2002;25:159-161.
-
(2002)
Gastroenterol Hepatol
, vol.25
, pp. 159-161
-
-
Manzano, M.L.1
Garfia, C.2
Manzanares, J.3
-
38
-
-
17644447726
-
Assocation of Budd-Chiari syndrome and celiac disease
-
El Younsi S, Nassif T, Kuoch V, et al. Assocation of Budd-Chiari syndrome and celiac disease. Gastroenterol Clin Biol. 2003;27:236-237.
-
(2003)
Gastroenterol Clin Biol
, vol.27
, pp. 236-237
-
-
El Younsi, S.1
Nassif, T.2
Kuoch, V.3
-
40
-
-
0033974703
-
Associated celiac disease and venous thrombosis
-
Hida M, Erreimi N, Ettair S, et al. Associated celiac disease and venous thrombosis. Arch Pediatr. 2000;7:215-216.
-
(2000)
Arch Pediatr
, vol.7
, pp. 215-216
-
-
Hida, M.1
Erreimi, N.2
Ettair, S.3
-
42
-
-
0142212223
-
Methylenetetrahydrofolate reductase, alcohol dehydrogenase, diet and risk of colorectal adenomas
-
Giovannucci E, Chen J, Smith-Warner SA, et al. Methylenetetrahydrofolate reductase, alcohol dehydrogenase, diet and risk of colorectal adenomas. Cancer Epidemiol Biomarkers Prev. 2003;12:970-979.
-
(2003)
Cancer Epidemiol Biomarkers Prev
, vol.12
, pp. 970-979
-
-
Giovannucci, E.1
Chen, J.2
Smith-Warner, S.A.3
-
43
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med. 1992;327:1832-1835.
-
(1992)
N Engl J Med
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
44
-
-
0028803474
-
A genetic defect in 5,10-methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, et al. A genetic defect in 5,10-methylenetetrahydrofolate reductase in neural tube defects. Q J Med. 1995;88:763-766.
-
(1995)
Q J Med
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
-
45
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NM, Steegers-Theunissen RP, Frosst P, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet. 1995;346:1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.1
Steegers-Theunissen, R.P.2
Frosst, P.3
-
46
-
-
0029849703
-
Decreased methylene tetrahydrofolate reductase activity due to the C677T mutation in families with spina bifida offspring
-
van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, et al. Decreased methylene tetrahydrofolate reductase activity due to the C677T mutation in families with spina bifida offspring. J Mol Med. 1996;74:691-694.
-
(1996)
J Mol Med
, vol.74
, pp. 691-694
-
-
Van Der Put, N.M.1
Van Den Heuvel, L.P.2
Steegers-Theunissen, R.P.3
-
48
-
-
2342464257
-
Homocysteine as a predictive factory for hip fracture in older persons
-
Mclean RR, Jacques PF, Selhub J, et al. Homocysteine as a predictive factory for hip fracture in older persons. N Engl J Med. 2004;350:2042-2049.
-
(2004)
N Engl J Med
, vol.350
, pp. 2042-2049
-
-
Mclean, R.R.1
Jacques, P.F.2
Selhub, J.3
-
49
-
-
15044344341
-
Systematic review: The liver in celiac disease
-
Duggan JM, Duggan AE. Systematic review: the liver in celiac disease. Aliment Pharmacol Ther. 2005;21:515-518.
-
(2005)
Aliment Pharmacol Ther
, vol.21
, pp. 515-518
-
-
Duggan, J.M.1
Duggan, A.E.2
-
51
-
-
17844385292
-
Hyperhomocysteinemia and MTHFR C677T polymorphism promote steatosis and fibrosis in chronic Hepatitis C
-
Adinolfi LE, Ingrosso D, Cesaro G, et al. Hyperhomocysteinemia and MTHFR C677T polymorphism promote steatosis and fibrosis in chronic Hepatitis C. Hepatology. 2005;41:995-1003.
-
(2005)
Hepatology
, vol.41
, pp. 995-1003
-
-
Adinolfi, L.E.1
Ingrosso, D.2
Cesaro, G.3
-
52
-
-
20444481953
-
Prevalence of hyperhomocysteinemia in adult gluten-sensitive enteropathy at diagnosis: Role of B12, folate, and genetics
-
Saibeni S, Lecchi A, Meucci G, et al. Prevalence of hyperhomocysteinemia in adult gluten-sensitive enteropathy at diagnosis: role of B12, folate, and genetics. Clin Gast Hepatol. 2005;3:574-580.
-
(2005)
Clin Gast Hepatol
, vol.3
, pp. 574-580
-
-
Saibeni, S.1
Lecchi, A.2
Meucci, G.3
|