Pages that link to "Q34540514"
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The following pages link to Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland (Q34540514):
Displaying 50 items.
- Blood lead is a predictor of homocysteine levels in a population-based study of older adults (Q23915647) (← links)
- The effect on endothelial function of vitamin C during methionine induced hyperhomocysteinaemia (Q24800878) (← links)
- Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children (Q25257376) (← links)
- Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management (Q26785500) (← links)
- The Molecular and Cellular Effect of Homocysteine Metabolism Imbalance on Human Health (Q28076483) (← links)
- The history of folic acid (Q28191294) (← links)
- Characterization of human cystathionine β-synthase (Q29039789) (← links)
- Diagnostic classification of the aetiology of mental retardation in children (Q30498876) (← links)
- Hyperhomocysteinemia: an independent risk factor or a simple marker of vascular disease? 2. Epidemiological data (Q30802266) (← links)
- The skin in genetically-controlled metabolic disorders (Q33585598) (← links)
- Tissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuria (Q33585609) (← links)
- Ocular complications in homocystinuria--early and late treated (Q33647202) (← links)
- Lens fringe in homocystinuria (Q33649480) (← links)
- Total homocysteine and cardiovascular disease (Q33785883) (← links)
- Screening tests for glycosaminoglycans in urine: experience from regional interlaboratory surveys (Q33839436) (← links)
- Homocysteine, B vitamins, and coronary artery disease (Q33843655) (← links)
- Anterior dislocation of the lens in homocystinuria (Q33996579) (← links)
- A revisit to the natural history of homocystinuria due to cystathionine beta-synthase deficiency (Q34019705) (← links)
- Homocysteine: an emergent cardiovascular risk factor? (Q34039985) (← links)
- Vitamins and homocysteine metabolism (Q34064189) (← links)
- Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine (Q34079997) (← links)
- Hyperhomocysteinemia and pregnancy--review of our present understanding and therapeutic implications (Q34080418) (← links)
- Hyperhomocysteinemia: a new risk factor for central retinal vein occlusion. (Q34163053) (← links)
- The need for a national policy for the management of inherited metabolic disease (Q34303014) (← links)
- Roles of homocysteine in cell metabolism: old and new functions. (Q34308857) (← links)
- The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to treatment. (Q34390750) (← links)
- Vascular dysfunction in hyperhomocyst(e)inemia. Implications for atherothrombotic disease (Q34395823) (← links)
- Hyperhomocysteinaemia and associated disease (Q34435609) (← links)
- Classical homocystinuria: vascular risk and its prevention (Q34535870) (← links)
- The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America. (Q34564879) (← links)
- Homocyst(e)ine and cardiovascular disease: a systematic review of the evidence with special emphasis on case-control studies and nested case-control studies (Q34577250) (← links)
- The natural history of homocystinuria due to cystathionine beta-synthase deficiency. (Q34693096) (← links)
- Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts (Q34709345) (← links)
- Homocyst(e)ine and coronary heart disease: pharmacoeconomic support for interventions to lower hyperhomocyst(e)inaemia (Q34716812) (← links)
- Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical control (Q34754835) (← links)
- Homocystinuria in New South Wales (Q34986772) (← links)
- Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristics (Q35016769) (← links)
- On the Mechanism of Pyridoxine Responsive Homocystinuria. II. Properties of Normal and Mutant Cystathionine β-Synthase from Cultured Fibroblasts (Q35119811) (← links)
- Homocystinuria: Reduced folate levels during pyridoxine treatment (Q35149086) (← links)
- Mechanisms of Cardiovascular Remodeling in Hyperhomocysteinemia (Q35173832) (← links)
- A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses (Q35232274) (← links)
- Raised plasma homocysteine as a risk factor for retinal vascular occlusive disease (Q35313335) (← links)
- Sulfur containing amino acids and human disease (Q35636141) (← links)
- Hyperhomocysteinemia, endoplasmic reticulum stress, and alcoholic liver injury (Q35799626) (← links)
- Relationship between paraoxonase and homocysteine: crossroads of oxidative diseases (Q35843994) (← links)
- HOMOCYSTINURIA (Q35852957) (← links)
- Ocular correlates of inborn metabolic defects (Q35920065) (← links)
- Treatment of homocystinuria (Q36061592) (← links)
- Treatment of homocystinuria with pyridoxine. A preliminary study (Q36062604) (← links)
- B-vitamins, homocysteine metabolism and CVD. (Q36098211) (← links)