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    1. Wong, A; Naik, M; Chan, C; Chua, YL; Chua, T
      Giant coronary aneurysms with multiple vascular aneurysms: A rare manifestation of hyperhomocysteinemia

      CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
    2. Sigit, JI; Hages, M; Brensing, KA; Frotscher, U; Pietrzik, K; von Bergmann, K; Lutjohann, D
      Total plasma homocysteine and related amino acids in end-stage renal disease (ESRD) patients measured by gas chromatography-mass spectrometry - Comparison with the Abbott IMx homocysteine assay and the HPLC method

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    3. Bagi, Z; Ungvari, Z; Szollar, L; Koller, A
      Flow-induced constriction in arterioles of hyperhomocysteinemic rats is due to impaired nitric oxide and enhanced thromboxane A(2) mediation

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    4. Shan, XY; Dunbrack, RL; Christopher, SA; Kruger, WD
      Mutations in the regulatory domain of cystathionine beta-synthase can functionally suppress patient-derived mutations in cis

      HUMAN MOLECULAR GENETICS
    5. Marr, JE; Halliwell-Ewen, J; Fisher, B; Soler, L; Ainsworth, JR
      Associations of high myopia in childhood

      EYE
    6. Janosik, M; Meier, M; Kery, V; Oliveriusova, J; Burkhard, P; Kraus, JP
      Crystallization and preliminary X-ray diffraction analysis of the active core of human recombinant cystathionine beta-synthase: an enzyme involved invascular disease

      ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY
    7. Hong, SH; Song, J; Kim, JQ
      Genetic variation of the methylenetetrahydrofolate reductase and cystathionine beta-synthase genes in Korean patients with coronary artery disease and a new polymorphism in intron 7

      MOLECULAR AND CELLULAR PROBES
    8. Cahill, M; Gallagher, P; Whitehead, A; Acheson, R
      Autosomal dominant peripheral cystic retinal patches and non-cystic retinal tufts associated with peripapillary crescents, retinal breaks and uveitis

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    9. Powers, JM; Rosenblatt, DS; Schmidt, RE; Cross, AH; Black, JT; Moser, AB; Moser, HW; Morgan, DJ
      Neurological and neuropathologic heterogeneity in two brothers with cobalamin C deficiency

      ANNALS OF NEUROLOGY
    10. Linnebank, M; Homberger, A; Junker, R; Nowak-Goettl, U; Harms, E; Koch, HG
      High prevalence of the 1278T mutation of the human cystathionine beta-synthase detected by a novel screening application

      THROMBOSIS AND HAEMOSTASIS
    11. Meier, M; Janosik, M; Kery, V; Kraus, JP; Burkhard, P
      Structure of human cystathionine beta-synthase: a unique pyridoxal 5 '-phosphate-dependent heme protein

      EMBO JOURNAL
    12. Spence, JD; Howard, VJ; Chambless, LE; Malinow, MR; Pettigrew, LC; Stampfer, M; Toole, JF
      Vitamin intervention for stroke prevention (VISP) trial: Rationale and design

      NEUROEPIDEMIOLOGY
    13. Biancheri, R; Cerone, R; Schiaffino, MC; Caruso, U; Veneselli, E; Perrone, MV; Rossi, A; Gatti, R
      Cobalamin (Cbl) C/D deficiency: Clinical, neurophysiological and neuroradiologic findings in 14 cases

      NEUROPEDIATRICS
    14. Roth, J; Goebeler, M; Ludwig, S; Wagner, L; Kilian, K; Sorg, C; Harms, E; Schulze-Osthoff, K; Koch, HG
      Homocysteine inhibits tumor necrosis factor-induced activation of endothelium via modulation of nuclear factor-kappa b activity

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
    15. Hanratty, CG; McAuley, DF; McGrath, LT; Young, IS; Johnston, GD
      Hyperhomocysteinaemia in young adults is not associated with impaired endothelial function

      CLINICAL SCIENCE
    16. Moat, SJ; Bonham, JR; Powers, HJ
      Role of aminothiols as a component of the plasma antioxidant system and relevance to homocysteine-mediated vascular disease

      CLINICAL SCIENCE
    17. Dilley, A; Hooper, WC; El-Jamil, M; Renshaw, M; Wenger, NK; Evatt, BL
      Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR C -> T677) and cystathione beta-synthase (CBS G -> A919, CBS T -> c833)are not associated with myocardial infarction in African Americans

      THROMBOSIS RESEARCH
    18. Flemming, KD; Nguyen, TT; Abu-Lebdeh, HS; Parisi, JE; Wiebers, DO; Sicks, JRD; O'Fallon, WM; Petty, GW
      Hyperhomocysteinemia in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

      MAYO CLINIC PROCEEDINGS
    19. Anadiotis, G; Ierardi-Curto, L; Kaplan, PB; Berry, GT
      Ornithine transcarbamylase deficiency and pancreatitis

      JOURNAL OF PEDIATRICS
    20. Dicker-Brown, A; Fonseca, VA; Fink, LA; Kern, PA
      The effect of glucose and insulin on the activity of methylene tetrahydrofolate reductase and cystathionine-beta-synthase: studies in hepatocytes

      ATHEROSCLEROSIS
    21. Batra, S; Lowenheim, M
      Chronic relapsing pancreatitis

      CLINICAL PEDIATRICS
    22. Cavalca, V; Cighetti, G; Bamonti, F; Loaldi, A; Bortone, L; Novembrino, C; De Franceschi, M; Belardinelli, R; Guazzi, MD
      Oxidative stress and homocysteine in coronary artery disease

      CLINICAL CHEMISTRY
    23. Tsai, MY; McGovern, P; Kennedy, EL; Hanson, NQ
      Short-term variability in the measurement of plasma homocysteine, fasting and post-methionine loading

      CLINICAL BIOCHEMISTRY
    24. Davi, G; Di Minno, G; Coppola, A; Andria, G; Cerbone, AM; Madonna, P; Tufano, A; Falco, A; Marchesani, P; Ciabattoni, G; Patrono, C
      Oxidative stress and platelet activation in homozygous homocystinuria

      CIRCULATION
    25. Janosik, M; Kery, V; Gaustadnes, M; Maclean, KN; Kraus, JP
      Regulation of human cystathionine beta-synthase by S-adenosyl-L-methionine: Evidence for two catalytically active conformations involving an autoinhibitory domain in the C-terminal region

      BIOCHEMISTRY
    26. Abdelmalek, MF; Angulo, P; Jorgensen, RA; Sylvestre, PB; Lindor, KD
      Betaine, a promising new agent for patients with nonalcoholic steatohepatitis: Results of a pilot study

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    27. Kuhara, T; Ohse, M; Ohdoi, C; Ishida, S
      Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography-mass spectrometry

      JOURNAL OF CHROMATOGRAPHY B
    28. Kuhara, T; Ohse, M; Ohdoi, C; Ishida, S
      Differential diagnosis of homocystinuria by urease treatment, isotope dilution and gas chromatography-mass spectrometry

      JOURNAL OF CHROMATOGRAPHY B
    29. Joober, R; Benkelfat, C; Lal, S; Bloom, D; Labelle, A; Lalonde, P; Turecki, G; Rozen, R; Rouleau, GA
      Association between the methylenetetrahydrofolate reductase 677C -> T missense mutation and schizophrenia

      MOLECULAR PSYCHIATRY
    30. Majors, AK; Pyeritz, RE
      A deficiency of cysteine impairs fibrillin-1 deposition: Implications for the pathogenesis of cystathionine beta-synthase deficiency

      MOLECULAR GENETICS AND METABOLISM
    31. Ungvari, Z; Sarkadi-Nagy, E; Bagi, Z; Szollar, L; Koller, A
      Simultaneously increased TxA(2) activity in isolated arterioles and platelets of rats with hyperhomocysteinemia

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    32. Gaustadnes, M; Rudiger, N; Rasmussen, K; Ingerslev, J
      Familial thrombophilia associated with homozygosity for the cystathionine beta-synthase 833T -> C mutation

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    33. Goyette, P; Rozen, R
      The thermolabile variant 677C -> T can further reduce activity when expressed in CIS with severe mutations for human methylenetetrahydrofolate reductase

      HUMAN MUTATION
    34. Sibani, S; Christensen, B; O'Ferrall, E; Saadi, I; Hiou-Tim, F; Rosenblatt, DS; Rozen, R
      Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria

      HUMAN MUTATION
    35. Rubba, P
      Anti-inflammatory action of statins and reduction of homocysteinemia by vitamin supplementation: Interactions among strategies for cardiovascular prevention

      NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES
    36. Buscher, HCJL; Barendregt, WB; Boers, GHJ; van der Vliet, JA
      Hyperhomocysteinemia as a cause of superior vena cava syndrome

      ANNALS OF VASCULAR SURGERY
    37. Fattal-Valevski, A; Bassan, H; Korman, SH; Lerman-Sagie, T; Gutman, A; Harel, S
      Methylenetetrahydrofolate reductase deficiency: Importance of early diagnosis

      JOURNAL OF CHILD NEUROLOGY
    38. Gaustadnes, M; Rudiger, N; Rasmussen, K; Ingerslev, J
      Intermediate and severe hyperhomocysteinemia with thrombosis: A study of genetic determinants

      THROMBOSIS AND HAEMOSTASIS
    39. Blom, HJ
      Genetic determinants of hyperhomocysteinaemia: the roles of cystathionine beta-synthase and 5,10-methylenetetrahydrofolate reductase

      EUROPEAN JOURNAL OF PEDIATRICS
    40. Katzenschlager, R; Burgmann, H; Ehringer, H; Minar, E
      Vasospasmus: a rare manifestation of homocystinuria

      VASA-JOURNAL OF VASCULAR DISEASES
    41. Baethmann, M; Wendel, U; Hoffmann, GF; Gohlich-Ratmann, G; Kleinlein, B; Seiffert, P; Blom, H; Voit, T
      Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolatereductase deficiency

      NEUROPEDIATRICS
    42. Miyao, M; Morita, H; Hosoi, T; Kurihara, H; Inoue, S; Hoshino, S; Shiraki, M; Yazaki, Y; Ouchi, Y
      Association of methylenetetrahydrofolate reductase (MTHFR) polymorphism with bone mineral density in postmenopausal Japanese women

      CALCIFIED TISSUE INTERNATIONAL
    43. Yang, F; Hanson, NQ; Schwichtenberg, K; Tsai, MY
      Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: A single nucleotide substitution in the second repeat prevents multiple alternate splicing

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Makris, M
      Hyperhomocysteinemia and thrombosis

      CLINICAL AND LABORATORY HAEMATOLOGY
    45. Walter, JH
      Inborn errors of metabolism and pregnancy

      JOURNAL OF INHERITED METABOLIC DISEASE
    46. Estrov, Y; Scaglia, F; Bodamer, OAF
      Psychiatric symptoms of inherited metabolic disease

      JOURNAL OF INHERITED METABOLIC DISEASE
    47. Coppola, A; Davi, G; De Stefano, V; Mancini, FP; Cerbone, AM; Di Minno, G
      Homocysteine, coagulation, platelet function, and thrombosis

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    48. Yap, S; Naughten, ER; Wilcken, B; Wilcken, DEL; Boers, GHJ
      Vascular complications of severe hyperhomocysteinemia in patients with homocystinuria due to cystathionine beta-synthase deficiency: Effects of homocysteine-lowering therapy

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    49. Ciani, F; Donati, MA; Tulli, G; Poggi, GM; Pasquini, E; Rosenblatt, DS; Zammarchi, E
      Lethal late onset cblB methylmalonic aciduria

      CRITICAL CARE MEDICINE
    50. Cella, G; Burlina, A; Sbarai, A; Motta, G; Girolami, A; Berrettini, M; Strauss, W
      Tissue factor pathway inhibitor levels in patients with homocystinuria

      THROMBOSIS RESEARCH
    51. Mayerhofer, K; Hefler, L; Zeisler, H; Tempfer, C; Bodner, K; Stockler-Ipsiroglu, S; Muhl, A; Kaider, A; Schatten, C; Leodolter, S; Husslein, P; Kainz, C
      Serum homocyst(e)ine levels in women with preeclampsia

      WIENER KLINISCHE WOCHENSCHRIFT
    52. Finkelstein, JD
      Homocysteine: A history in progress

      NUTRITION REVIEWS
    53. Stern, LL; Bagley, PJ; Rosenberg, IH; Selhub, J
      Conversion of 5-formyltetrahydrofolic acid to 5-methyltetrahydrofolic acidis unimpaired in folate-adequate persons homozygous for the C677T mutationin the methylenetetrahydrofolate reductase gene

      JOURNAL OF NUTRITION
    54. Krumdieck, CL; Prince, CW
      Mechanisms of homocysteine toxicity on connective tissues: Implications for the morbidity of aging

      JOURNAL OF NUTRITION
    55. Bode, MK; Laitinen, P; Risteli, J; Uusimaa, P; Juvonen, T
      Atherosclerosis, type I collagen cross-linking and homocysteine

      ATHEROSCLEROSIS
    56. Tribouilloy, CM; Peltier, M; Peltier, MCI; Trojette, F; Andrejak, M; Lesbre, JPM
      Plasma homocysteine and severity of thoracic aortic atherosclerosis

      CHEST
    57. Aras, O; Hanson, NQ; Yang, F; Tsai, MY
      Influence of 699C -> T and 1080C -> T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels

      CLINICAL GENETICS
    58. Cahill, M; Karabatzaki, M; Meleady, R; Refsum, H; Ueland, P; Shields, D; Mooney, D; Graham, I
      Raised plasma homocysteine as a risk factor for retinal vascular occlusivedisease

      BRITISH JOURNAL OF OPHTHALMOLOGY
    59. Bellieni, CV; Ferrari, F; De Felice, C; Bagnoli, F; Cioni, M; Farnetani, M; Gatti, MG; Buonocore, G
      EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria

      BIOLOGY OF THE NEONATE
    60. Togawa, T; Sengupta, S; Chen, H; Robinson, K; Nonevski, I; Majors, AK; Jacobsen, DW
      Mechanisms for the formation of protein-bound homocysteine in human plasma

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    61. Grubben, MJ; Boers, GH; Blom, HJ; Broekhuizen, R; de Jong, R; van Rijt, L; de Ruijter, E; Swinkels, DW; Nagengast, FM; Katan, MB
      Unfiltered coffee increases plasma homocysteine concentrations in healthy volunteers: a randomized trial

      AMERICAN JOURNAL OF CLINICAL NUTRITION
    62. Muller, T; Woitalla, D; Hunsdiek, A; Kuhn, W
      Elevated plasma levels of homocysteine in dystonia

      ACTA NEUROLOGICA SCANDINAVICA
    63. Accinni, R; Bartesaghi, S; De Leo, G; Cursano, CF; Achilli, G; Loaldi, A; Cellerino, C; Parodi, O
      Screening of homocysteine from newborn blood spots by high-performance liquid chromatography with coulometric array detection

      JOURNAL OF CHROMATOGRAPHY A
    64. Andersson, HC; Marble, M; Shapira, E
      Long-term outcome in treated combined methylmalonic acidemia and homocystinemia

      GENETICS IN MEDICINE
    65. Tsai, MY; Yang, F; Bignell, M; Aras, O; Hanson, NQ
      Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5 '-phosphate concentration

      MOLECULAR GENETICS AND METABOLISM
    66. Chace, DH; Naylor, EW
      Expansion of newborn screening programs using automated tandem mass spectrometry

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    67. Chambers, JC; Obeid, OA; Kooner, JS
      Physiological increments in plasma homocysteine induce vascular endothelial dysfunction in normal human subjects

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    68. de Franchis, R; Kraus, E; Kozich, V; Sebastio, G; Kraus, JP
      Four novel mutations in the cystathionine beta-synthase gene: Effect of a second linked mutation on the severity of the homocystinuric phenotype

      HUMAN MUTATION
    69. Kraus, JP; Janosik, M; Kozich, V; Mandell, R; Shih, V; Sperandeo, MP; Sebastio, G; de Franchis, R; Andria, G; Kluijtmans, LAJ; Blom, H; Boers, GHJ; Gordon, RB; Kamoun, P; Tsai, MY; Kruger, WD; Koch, HG; Ohura, T; Gaustadnes, M
      Cystathionine beta-synthase mutations in homocystinuria

      HUMAN MUTATION
    70. Gemery, J; Reid, S; Pagan-Marin, H; Yucel, EK
      Hyperhomocysteinemia presenting as chronic inferior vena caval thrombosis in an adolescent

      JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY
    71. Wilson, A; Leclerc, D; Rosenblatt, DS; Gravel, RA
      Molecular basis for methionine synthase reductase deficiency in patients belonging to the cbIE complementation group of disorders in folate/cobalaminmetabolism

      HUMAN MOLECULAR GENETICS
    72. De Jong, SC; Stehouwer, CDA; Van den Berg, M; Geurts, TW; Bouter, LM; Rauwerda, JA
      Normohomocysteinaemia and vitamin-treated hyperhomocysteinaemia are associated with similar risks of cardiovascular events in patients with prematureperipheral arterial occlusive disease. A prospective cohort study

      JOURNAL OF INTERNAL MEDICINE
    73. Sharabi, Y; Doolman, R; Rosenthal, T; Grossman, E; Rachima-Maoz, C; Nussinovitch, N; Sela, B
      Homocysteine levels in hypertensive patients with a history of cardiac or cerebral atherothrombotic events

      AMERICAN JOURNAL OF HYPERTENSION
    74. Leclerc, D; Odievre, MH; Wu, Q; Wilson, A; Huizenga, JJ; Rozen, R; Scherer, SW; Gravel, RA
      Molecular cloning, expression and physical mapping of the human methioninesynthase reductase gene

      GENE
    75. Pepe, G; Vanegas, OC; Rickards, O; Giusti, B; Comeglio, P; Brunelli, T; Marcucci, R; Prisco, D; Gensini, GF; Abbate, R
      World distribution of the TS33C/844INS68 CBS in cis double mutation: a reliable anthropological marker

      HUMAN GENETICS
    76. Yap, S; O'Donnell, KA; O'Neill, C; Mayne, PD; Thornton, P; Naughten, E
      Factor V Leiden (Arg506Gln), a confounding genetic risk factor but not mandatory for the occurrence of venous thromboembolism in homozygotes and obligate heterozygotes for cystathionine beta-synthase deficiency

      THROMBOSIS AND HAEMOSTASIS
    77. Labrune, P; Zittoun, J; Duvaltier, I; Trioche, P; Niaudet, P; Odievre, M
      Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency

      EUROPEAN JOURNAL OF PEDIATRICS
    78. Guthikonda, S; Haynes, WG
      Homocysteine as a novel risk factor for atherosclerosis

      CURRENT OPINION IN CARDIOLOGY
    79. Cretel, E; Cacoub, P; Amoura, Z; Hausfater, P; Elalamy, I; Richemond, J; Piette, JC
      Resistance to activated protein C and portal vein thrombosis: two cases and review of literature

      REVUE DE MEDECINE INTERNE
    80. Usui, M; Matsuoka, H; Miyazaki, H; Ueda, S; Okuda, S; Imaizumi, T
      Endothelial dysfunction by acute hyperhomocyst(e)inaemia: restoration by folic acid

      CLINICAL SCIENCE
    81. Bibi, H; Gelman-Kohan, Z; Baumgartner, ER; Rosenblatt, DS
      Transcobalamin II deficiency with methylmalonic aciduria in three sisters

      JOURNAL OF INHERITED METABOLIC DISEASE
    82. Augoustides-Savvopoulou, P; Mylonas, I; Sewell, AC; Rosenblatt, DS
      Reversible dementia in an adolescent with cblC disease: Clinical heterogeneity within the same family

      JOURNAL OF INHERITED METABOLIC DISEASE
    83. Enns, GM; Barkovich, AJ; Rosenblatt, DS; Fredrick, DR; Weisiger, K; Ohnstad, C; Packman, S
      Progressive neurological deterioration and MRI changes in cblC methylmalonic acidaemia treated with hydroxocobalamin

      JOURNAL OF INHERITED METABOLIC DISEASE
    84. Abeling, NGGM; van Gennip, AH; Blom, H; Wevers, RA; Vreken, P; van Tinteren, HLG; Bakker, HD
      Rapid diagnosis and methionine administration: Basis for a favourable outcome in a patient with methylene tetrahydrofolate reductase deficiency

      JOURNAL OF INHERITED METABOLIC DISEASE
    85. Undas, A; Domagala, TB; Jankowski, M; Szczeklik, A
      Treatment of hyperhomocysteinemia with folic acid and vitamins B-12 and B-6 attenuates thrombin generation

      THROMBOSIS RESEARCH
    86. Mas, JL; Vignes, S; Weschler, B; Laforet, P
      Headaches, vomiting and left homonymous lateral hemianopia in a 25 year-old man.

      REVUE NEUROLOGIQUE
    87. Li, SCH; Stewart, PM
      Homocystinuria and psychiatric disorder: A case report

      PATHOLOGY
    88. Wang, XL; Duarte, N; Cai, H; Adachi, T; Sim, AS; Cranney, G; Wilcken, DEL
      Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease inthe Australian hospital-based population

      ATHEROSCLEROSIS
    89. Tsai, MY; Welge, BG; Hanson, NQ; Bignell, MK; Vessey, J; Schwichtenberg, K; Yang, F; Bullemer, FE; Rasmussen, R; Graham, KJ
      Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases

      ATHEROSCLEROSIS
    90. Harksen, A; Ueland, PM; Refsum, H; Meyer, K
      Four common mutations of the cystathionine beta-synthase gene detected by multiplex PCR and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

      CLINICAL CHEMISTRY
    91. Dudman, NPB; Temple, SE; Guo, XW; Fu, WY; Perry, MA
      Homocysteine enhances neutrophil-endothelial interactions in both culturedhuman cells and rats in vivo

      CIRCULATION RESEARCH
    92. Doshi, SN; Goodfellow, J; Lewis, MJ; McDowell, IFW
      Homocysteine and endothelial function

      CARDIOVASCULAR RESEARCH
    93. Williams, RH; Maggiore, JA
      Hyperhomocysteinemia - Pathogenesis, clinical significance, laboratory assessment, and treatment

      LABORATORY MEDICINE
    94. Quere, I; Paul, V; Rouillac, C; Janbon, C; London, J; Demaille, J; Kamoun, P; Dufier, JL; Abitbol, M; Chasse, JF
      Spatial and temporal expression of the cystathionine beta-synthase gene during early human development

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    95. Moat, SJ; Bonham, JR; Tanner, MS; Allen, JC; Powers, HJ
      Recommended approaches for the laboratory measurement of homocysteine in the diagnosis and monitoring of patients with hyperhomocysteinaemia

      ANNALS OF CLINICAL BIOCHEMISTRY
    96. Bostom, AG; Silbershatz, H; Rosenberg, IH; Selhub, J; D'Agostino, RB; Wolf, PA; Jacques, PF; Wilson, PWF
      Nonfasting plasma total homocysteine levels and all-cause and cardiovascular disease mortality in elderly Framingham men and women

      ARCHIVES OF INTERNAL MEDICINE
    97. Bostom, AG; Rosenberg, IH; Silbershatz, H; Jacques, PF; Selhub, J; D'Agostino, RB; Wilson, PWF; Wolf, PA
      Nonfasting plasma total homocysteine levels and stroke incidence in elderly persons: The Framingham Study

      ANNALS OF INTERNAL MEDICINE
    98. de Bruijne, ELE; Keulen-de Vos, GHJC; Ouwendijk, RJT
      Ocular venous occlusion and hyperhomocysteinemia

      ANNALS OF INTERNAL MEDICINE
    99. FUCHS J; ROSENBERG T
      CONGENITAL ECTOPIA LENTIS - A DANISH NATIONAL SURVEY

      Acta ophthalmologica Scandinavica
    100. Gallagher, PM; Naughten, E; Hanson, NQ; Schwichtenberg, K; Bignell, M; Yuan, M; Ward, P; Yap, S; Whitehead, AS; Tsai, MY
      Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria

      MOLECULAR GENETICS AND METABOLISM


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Documento generato il 19/10/20 alle ore 23:35:17