-
1
-
-
0021998698
-
Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease
-
Boers GHJ, Smals AG, Trijbels FJ, et al: Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease. N Engl J Med 313:709-715, 1985
-
(1985)
N Engl J Med
, vol.313
, pp. 709-715
-
-
Boers, G.H.J.1
Smals, A.G.2
Trijbels, F.J.3
-
2
-
-
0025756673
-
Hyperhomocysteinemia: An independent risk factor for vascular disease
-
Clarke R, Daly L, Robinson K, et al: Hyperhomocysteinemia: An independent risk factor for vascular disease. N Engl J Med 324:1149-1155, 1991
-
(1991)
N Engl J Med
, vol.324
, pp. 1149-1155
-
-
Clarke, R.1
Daly, L.2
Robinson, K.3
-
3
-
-
0018602014
-
Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance
-
National Diabetes Data Group: Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes 28:1039-1057, 1979
-
(1979)
Diabetes
, vol.28
, pp. 1039-1057
-
-
-
4
-
-
0021072739
-
Unique efficacy of methionine metabolism in premenopausal women may protect against vascular disease in the reproductive years
-
Boers GH, Smals AG, Trijbels, FJM, et al: Unique efficacy of methionine metabolism in premenopausal women may protect against vascular disease in the reproductive years. J Clin Invest 72:1971-1976, 1983
-
(1983)
J Clin Invest
, vol.72
, pp. 1971-1976
-
-
Boers, G.H.1
Smals, A.G.2
Trijbels, F.J.M.3
-
5
-
-
0025848779
-
Rapid high performance liquid Chromatographic assay for total homocysteine levels in human serum
-
Ubbink JB, Hayward Vermaak WJ, Bissport S: Rapid high performance liquid Chromatographic assay for total homocysteine levels in human serum. J Chromatogr 565:441-446, 1991
-
(1991)
J Chromatogr
, vol.565
, pp. 441-446
-
-
Ubbink, J.B.1
Hayward Vermaak, W.J.2
Bissport, S.3
-
6
-
-
0025361139
-
Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: Paradigm of pitfalls in phenotypes
-
McGill JJ, Mettler G, Rosenblatt DS, et al: Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: Paradigm of pitfalls in phenotypes. Am J Med Genet 36:45-52, 1990
-
(1990)
Am J Med Genet
, vol.36
, pp. 45-52
-
-
McGill, J.J.1
Mettler, G.2
Rosenblatt, D.S.3
-
7
-
-
0000363006
-
Disorders of transsulfuration
-
Scriver CR, Beaudet AL, Sly WS, et al (eds): New York, NY, McGraw-Hill
-
Mudd SH, Levy HL, Skovby F: Disorders of transsulfuration, in Scriver CR, Beaudet AL, Sly WS, et al (eds): The Metabolic Basis of Inherited Disease (ed 6). New York, NY, McGraw-Hill, 1989, pp 693-734
-
(1989)
The Metabolic Basis of Inherited Disease (Ed 6)
, pp. 693-734
-
-
Mudd, S.H.1
Levy, H.L.2
Skovby, F.3
-
8
-
-
0026782089
-
Summary and highlights of XIV International Diabetes Federation Satellite Symposium on Macrovascular Complications of Diabetes
-
Gwynne JT, McMillan DE: Summary and highlights of XIV International Diabetes Federation Satellite Symposium on Macrovascular Complications of Diabetes. Diabetes 41:116-119, 1992 (suppl 2)
-
(1992)
Diabetes
, vol.41
, Issue.2 SUPPL.
, pp. 116-119
-
-
Gwynne, J.T.1
McMillan, D.E.2
-
9
-
-
0025911079
-
Increased levels of plasma homocysteine are associated with nephropathy, but not severe retinopathy in type 1 diabetes mellitus
-
Hultberg B, Agardh E, Andersson A, et al: Increased levels of plasma homocysteine are associated with nephropathy, but not severe retinopathy in type 1 diabetes mellitus. Scand J Clin Lab Invest 51:277-282, 1991
-
(1991)
Scand J Clin Lab Invest
, vol.51
, pp. 277-282
-
-
Hultberg, B.1
Agardh, E.2
Andersson, A.3
-
10
-
-
0018651563
-
Sulphur containing amino acids in chronic renal failure with particular reference to homocystine and cysteine-homocysteirie mixed disulfide
-
Wilcken DE, Gupta VJ: Sulphur containing amino acids in chronic renal failure with particular reference to homocystine and cysteine-homocysteirie mixed disulfide. Eur J Clin Invest 9:301-307, 1979
-
(1979)
Eur J Clin Invest
, vol.9
, pp. 301-307
-
-
Wilcken, D.E.1
Gupta, V.J.2
-
11
-
-
0015247121
-
An intrinsic blood platelet abnormality in an homocystinuric boy, corrected by pyridoxine administration
-
Zweifler AJ, Allen RJ: An intrinsic blood platelet abnormality in an homocystinuric boy, corrected by pyridoxine administration. Thromb Diathes Haemorrh 26:15-21, 1971
-
(1971)
Thromb Diathes Haemorrh
, vol.26
, pp. 15-21
-
-
Zweifler, A.J.1
Allen, R.J.2
-
12
-
-
0028670093
-
Combined vitamin B6 plus folic acid therapy in young patients with arteriosclerosis and hyperhomocysteinemia
-
Van den Berg M, Franken DG, Boers GHJ, et al: Combined vitamin B6 plus folic acid therapy in young patients with arteriosclerosis and hyperhomocysteinemia. J Vasc Surg 20:933-940, 1994
-
(1994)
J Vasc Surg
, vol.20
, pp. 933-940
-
-
Van Den Berg, M.1
Franken, D.G.2
Boers, G.H.J.3
|