-
1
-
-
1842331509
-
Plasma homocysteine as a risk factor for vascular disease
-
The European Concerted Action Project
-
Graham IM, Daly LE, Refsum HM (1997) Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project. JAMA 277:1775-1781
-
(1997)
JAMA
, vol.277
, pp. 1775-1781
-
-
Graham, I.M.1
Daly, L.E.2
Refsum, H.M.3
-
3
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
Kang SS, Wong PW, Susmano A, Sora J, Norusis M, Ruggie N (1991) Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 48:536-545
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.2
Susmano, A.3
Sora, J.4
Norusis, M.5
Ruggie, N.6
-
4
-
-
0023032002
-
Methionine metabolism in mammals. Adaptation to methionine excess
-
Finkelstein JD, Martin JJ (1986) Methionine metabolism in mammals. Adaptation to methionine excess. J Biol Chem 261:1582-1587
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 1582-1587
-
-
Finkelstein, J.D.1
Martin, J.J.2
-
5
-
-
0030897112
-
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease
-
Morita H, Taguchi J, Kurihara H, Kitaoka M, Kaneda H, Kurihara Y, Maemura K, Shindo T, Minamino T, Ohno M, Yamaoki K, Ogasawara K, Aizawa T, Suzuki S, Yazaki Y (1997) Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease. Circulation 95:2032-2036
-
(1997)
Circulation
, vol.95
, pp. 2032-2036
-
-
Morita, H.1
Taguchi, J.2
Kurihara, H.3
Kitaoka, M.4
Kaneda, H.5
Kurihara, Y.6
Maemura, K.7
Shindo, T.8
Minamino, T.9
Ohno, M.10
Yamaoki, K.11
Ogasawara, K.12
Aizawa, T.13
Suzuki, S.14
Yazaki, Y.15
-
6
-
-
0030775334
-
Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease
-
Brattstrom L (1997) Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease. Circulation 96:3805-3807
-
(1997)
Circulation
, vol.96
, pp. 3805-3807
-
-
Brattstrom, L.1
-
7
-
-
0029885203
-
Folate status is the major determinant of fasting total plasma homocysteine levels in maintenance dialysis patients
-
Bostom AG, Shemin D, Lapane KL, Nadeau MR, Sutherland P, Chan J, Rozen R, Yoburn D, Jacques PF, Selhub J, Rosenberg IH (1996) Folate status is the major determinant of fasting total plasma homocysteine levels in maintenance dialysis patients. Atherosclerosis 123:193-202
-
(1996)
Atherosclerosis
, vol.123
, pp. 193-202
-
-
Bostom, A.G.1
Shemin, D.2
Lapane, K.L.3
Nadeau, M.R.4
Sutherland, P.5
Chan, J.6
Rozen, R.7
Yoburn, D.8
Jacques, P.F.9
Selhub, J.10
Rosenberg, I.H.11
-
8
-
-
0032984676
-
Hyperhomocysteinemia in chronic renal disease
-
Bostom AG, Culleton BF (1999) Hyperhomocysteinemia in chronic renal disease. J Am Soc Nephrol 10:891-900
-
(1999)
J. Am. Soc. Nephrol.
, vol.10
, pp. 891-900
-
-
Bostom, A.G.1
Culleton, B.F.2
-
9
-
-
0032759967
-
Reversal of hyperhomocyst(e)inaemia in chronic renal failure - Is folic or folinic acid the answer?
-
Massy ZA (1999) Reversal of hyperhomocyst(e)inaemia in chronic renal failure - is folic or folinic acid the answer? Nephrol Dial Transplant 14:2810-2812
-
(1999)
Nephrol. Dial Transplant.
, vol.14
, pp. 2810-2812
-
-
Massy, Z.A.1
-
10
-
-
0030851289
-
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients
-
Fodinger M, Mannhalter C, Wolfl G, Pabinger I, Muller E, Schmid R, Horl WH, Sunder-Plassmann G (1997) Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients. Kidney Int 52:517-523
-
(1997)
Kidney Int.
, vol.52
, pp. 517-523
-
-
Fodinger, M.1
Mannhalter, C.2
Wolfl, G.3
Pabinger, I.4
Muller, E.5
Schmid, R.6
Horl, W.H.7
Sunder-Plassmann, G.8
-
11
-
-
0032919128
-
Hyperhomocyst(e)inaemia in children with chronic renal failure
-
Lilien M, Duran M, Van Hoeck K, Poll-The BT, Schroder C (1999) Hyperhomocyst(e)inaemia in children with chronic renal failure. Nephrol Dial Transplant 14:366-368
-
(1999)
Nephrol. Dial Transplant.
, vol.14
, pp. 366-368
-
-
Lilien, M.1
Duran, M.2
Van Hoeck, K.3
Poll-The, B.T.4
Schroder, C.5
-
12
-
-
0344563614
-
Treatment of hyperhomocysteinemia in children on dialysis by folic acid
-
Schroder CH, Wan de Boer A, Giesen AM, Monnens LAH, Blom H (1999) Treatment of hyperhomocysteinemia in children on dialysis by folic acid. Pediatr Nephrol 13:583-585
-
(1999)
Pediatr. Nephrol.
, vol.13
, pp. 583-585
-
-
Schroder, C.H.1
Wan de Boer, A.2
Giesen, A.M.3
Monnens, L.A.H.4
Blom, H.5
-
13
-
-
0034746482
-
Folate, vitamin B12, and sulfur amino acid levels in patients with renal failure
-
Litwin M, Abuauba M, Wawer ZT, Grenda R, Kuryt T, Pietraszek E (2001) Folate, vitamin B12, and sulfur amino acid levels in patients with renal failure. Pediatr Nephrol 16:127-132
-
(2001)
Pediatr. Nephrol.
, vol.16
, pp. 127-132
-
-
Litwin, M.1
Abuauba, M.2
Wawer, Z.T.3
Grenda, R.4
Kuryt, T.5
Pietraszek, E.6
-
14
-
-
0034820784
-
Plasma homocysteine concentration in children with chronic renal failure
-
Merouani A, Lambert M, Delvin EE, Genest J Jr, Robitaille P, Rozen R (2001) Plasma homocysteine concentration in children with chronic renal failure. Pediatr Nephrol 16:805-811
-
(2001)
Pediatr. Nephrol.
, vol.16
, pp. 805-811
-
-
Merouani, A.1
Lambert, M.2
Delvin, E.E.3
Genest J., Jr.4
Robitaille, P.5
Rozen, R.6
-
15
-
-
0021998161
-
A method for estimating nitrogen intake of patients with chronic renal failure
-
Maroni BJ, Steinman TI, Mitch WE (1985) A method for estimating nitrogen intake of patients with chronic renal failure. Kidney Int 27:58-65
-
(1985)
Kidney Int.
, vol.27
, pp. 58-65
-
-
Maroni, B.J.1
Steinman, T.I.2
Mitch, W.E.3
-
16
-
-
0032545257
-
Determination of plasma and serum homocysteine by high-performance liquid chromatography with fluorescence detection
-
Minniti G, Piana A, Armani U, Cerone R (1998) Determination of plasma and serum homocysteine by high-performance liquid chromatography with fluorescence detection. J Chromatogr A 828:401-405
-
(1998)
J. Chromatogr. A
, vol.828
, pp. 401-405
-
-
Minniti, G.1
Piana, A.2
Armani, U.3
Cerone, R.4
-
17
-
-
0031806315
-
No net renal extraction of homocysteine in fasting humans
-
Guldener C van, Donker AJ, Jakobs C, Teerlink T, Meer K de, Stehouwer CD (1998) No net renal extraction of homocysteine in fasting humans. Kidney Int 54:166-169
-
(1998)
Kidney Int.
, vol.54
, pp. 166-169
-
-
Guldener, C.1
van Donker, A.J.2
Jakobs, C.3
Teerlink, T.4
Meer, K.5
de Stehouwer, C.D.6
-
18
-
-
0034820739
-
Hyperhomocysteinemia in chronic renal failure patients: Relation to nutritional status and cardiovascular disease
-
Suliman ME, Lindholm B, Barany P, Bergstrom J (2001) Hyperhomocysteinemia in chronic renal failure patients: relation to nutritional status and cardiovascular disease. Clin Chem Lab Med 39:734-738
-
(2001)
Clin. Chem. Lab. Med.
, vol.39
, pp. 734-738
-
-
Suliman, M.E.1
Lindholm, B.2
Barany, P.3
Bergstrom, J.4
-
19
-
-
0035662178
-
Deficiencies of folate and vitamin B(6) exert distinct effects on homocysteine, serine, and methionine kinetics
-
Cuskelly GJ, Stacpoole PW, Williamson J, Baumgartner TG, Gregory JF 3rd (2001) Deficiencies of folate and vitamin B(6) exert distinct effects on homocysteine, serine, and methionine kinetics. Am J Physiol Endocrinol Metab 281:E1182-E1190
-
(2001)
Am. J. Physiol. Endocrinol. Metab.
, vol.281
-
-
Cuskelly, G.J.1
Stacpoole, P.W.2
Williamson, J.3
Baumgartner, T.G.4
Gregory J.F. III5
-
20
-
-
0034058544
-
The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients
-
Kimura H, Gejyo F, Suzuki S, Miyazaki R (2000) The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients. J Am Soc Nephrol 11:885-893.
-
(2000)
J. Am. Soc. Nephrol.
, vol.11
, pp. 885-893
-
-
Kimura, H.1
Gejyo, F.2
Suzuki, S.3
Miyazaki, R.4
|