scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1032212282 |
P356 | DOI | 10.1007/S10545-007-0791-8 |
P698 | PubMed publication ID | 18210212 |
P2093 | author name string | W R Wilcox | |
B D Pressman | |||
N Vatanavicharn | |||
P2860 | cites work | Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism | Q34306924 |
Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency | Q34521242 | ||
Acute and chronic pancreatitis in patients with inborn errors of metabolism | Q34525325 | ||
Cerebral edema associated with betaine treatment in classical homocystinuria | Q34546947 | ||
Diffusion-weighted MR imaging in leukodystrophies | Q36195762 | ||
Homocysteine and cysteine - albumin binding in homocystinuria: assessment of cysteine status and implications for glutathione synthesis? | Q44190663 | ||
Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacy | Q44739436 | ||
Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia | Q44796909 | ||
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency | Q48104004 | ||
Effect of hypermethioninemia on some parameters of oxidative stress and on Na(+),K (+)-ATPase activity in hippocampus of rats. | Q48181585 | ||
Demyelination and inborn errors of the single carbon transfer pathway | Q48469745 | ||
Wernicke encephalopathy: MR findings at clinical presentation in twenty-six alcoholic and nonalcoholic patients. | Q51741937 | ||
Increased lipid peroxidation as a mechanism of methionine-induced atherosclerosis in rabbits | Q72028521 | ||
Hyperhomocysteinemia following oral methionine load is associated with increased lipid peroxidation | Q73627437 | ||
5-Oxoprolinuria in patients with and without defects in the gamma-glutamyl cycle | Q74643481 | ||
P921 | main subject | homocystinuria | Q994859 |
case report | Q2782326 | ||
P304 | page(s) | 477-481 | |
P577 | publication date | 2008-01-22 | |
P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
P1476 | title | Reversible leukoencephalopathy with acute neurological deterioration and permanent residua in classical homocystinuria: A case report | |
P478 | volume | 31 Suppl 3 |