Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Hyperhomocysteinemie"'
Autor:
Clóvis Paniz, Denise Grotto, Gabriela Cristina Schmitt, Juliana Valentini, Karen Lílian Schott, Valdeci Juarez Pomblum, Solange Cristina Garcia
Publikováno v:
Jornal Brasileiro de Patologia e Medicina Laboratorial, Vol 41, Iss 5, Pp 323-334 (2005)
INTRODUÇÃO: A vitamina B12 é hidrossolúvel, não-sintetizada pelo organismo humano, presente em alimentos de origem animal. Sua deficiência é muito freqüente entre idosos, vegetarianos e indivíduos que adotam baixa dieta protéica ou apresent
Externí odkaz:
https://doaj.org/article/d50ecf9f20f140b5b1d9c85490d23d8a
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Karin J A Lievers, Henk J. Blom, Godfried H.J. Boers, Martin den Heijer, Petra Verhoef, Frans J.M. Trijbels, Sandra G. Heil
Publikováno v:
Molecular Genetics and Metabolism 71 (2000)
Molecular Genetics and Metabolism, 71, 511-519
Molecular Genetics and Metabolism, 71, pp. 511-519
Molecular Genetics and Metabolism, 71, 511-519
Molecular Genetics and Metabolism, 71, pp. 511-519
Elevated homocysteine levels have been associated with arteriosclerosis and thrombosis. Hyperhomocysteinemia is caused by altered functioning of enzymes of its metabolism due to either inherited or acquired factors. Betaine-homocysteine methyltransfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a5931ba5ae0defb3c1f6ac2f900f723
https://doi.org/10.1006/mgme.2000.3078
https://doi.org/10.1006/mgme.2000.3078
Autor:
Godfried H.J. Boers
Publikováno v:
Seminars in Thrombosis and Hemostasis, 26, 291-5
Seminars in Thrombosis and Hemostasis, 26, 3, pp. 291-5
Seminars in Thrombosis and Hemostasis, 26, 3, pp. 291-5
Evidence of a positive association between mild hyperhomocysteinemia and arterial vascular disease has been accumulating in the last decade. Mild hyperhomocysteinemia acts as an independent vascular risk factor with equal strength as hypercholesterol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cd597db99928906581a271b55ab310c
https://doi.org/10.1055/s-2000-8096
https://doi.org/10.1055/s-2000-8096
Publikováno v:
Seminars in Thrombosis and Hemostasis, 26, 335-40
Seminars in Thrombosis and Hemostasis, 26, 3, pp. 335-40
Seminars in Thrombosis and Hemostasis, 26, 3, pp. 335-40
Homocystinuria (HCU) due to cystathionine beta-synthase (CBS) deficiency leads to severe hyperhomocysteinemia (HHcy). Vascular events (VE) remain the major cause of morbidity and mortality in the untreated patients with HCU. The study on the natural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68a32cb9eebf2bcaade43bac0ab5aad2
https://doi.org/10.1055/s-2000-8100
https://doi.org/10.1055/s-2000-8100
Autor:
M. van Dusseldorp, J.G.A.J. Hautvast, Tom K.A.B. Eskes, Henk J. Blom, Régine P.M. Steegers-Theunissen, I.A.L.M. van Rooij, Chris M.G. Thomas, Ingeborg A. Brouwer
Publikováno v:
Annals of Nutrition & Metabolism, 44, 194-197
Annals of Nutrition & Metabolism, 44, pp. 194-197
Annals of Nutrition & Metabolism 44 (2000)
Annals of Nutrition & Metabolism, 44, pp. 194-197
Annals of Nutrition & Metabolism 44 (2000)
Background/Aims: Elevated plasma total homocysteine (tHcy) concentrations are a risk factor for neural tube defects and vascular diseases. Supplementation with folic acid decreases tHcy. We investigated whether supplementation with 500 µg folic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ef8c4ec39ac17e93b094a6fdad0a7a
https://doi.org/10.1159/000046683
https://doi.org/10.1159/000046683
Autor:
Berg, M. van den, Jong, S.C. de, Deville, W., Rauwerda, J.A., Jakobs, C., Pals, G., Boers, G.H.J., Stehouwer, C.D.A.
Publikováno v:
Netherlands Journal of Medicine, 55, pp. 29-38
Netherlands Journal of Medicine, 55, 29-38
Netherlands Journal of Medicine, 55, 29-38
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ac635c542f3ee7e28fe1caa49bddd631
https://hdl.handle.net/2066/184906
https://hdl.handle.net/2066/184906
Autor:
Kraus, J.P., Janosik, M., Kozich, V., Mandell, R., Shih, V., Sperando, M.P., Sebastio, G., Franchis, R. de, Andria, G., Kluijtmans, L.A.J., Blom, H.J., Boers, G.H.J., Gordon, R.B., Kamoun, P., Tsai, M.Y., Kruger, W.D., Koch, H.G., Ohura, T., Gaustadnes, M.
Publikováno v:
Human Mutation, 13, 362-375
Human Mutation, 13, pp. 362-375
Human Mutation, 13, pp. 362-375
Item does not contain fulltext 14 p.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4b2d118b83d6f31fb635d8858eba9ef9
https://hdl.handle.net/2066/184739
https://hdl.handle.net/2066/184739
Autor:
Hamel, B.C.J., Engels, C.H.A.M., Akker, E. van den, Boers, G.H.J., Dongen, P.W.J. van, Steijlen, P.M.
Publikováno v:
Clinical Genetics, 53, 440-446
Clinical Genetics, 53, pp. 440-446
Clinical Genetics, 53, pp. 440-446
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4eb7315434c8184a1d2acbb4c8700efb
https://hdl.handle.net/2066/166803
https://hdl.handle.net/2066/166803