Results 231 to 240 of about 5,012,650 (270)
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METABOLIC PRECURSORS OF METHYLMALONIC ACID IN VITAMIN-B12 DEFICIENCY
The Lancet, 1967Abstract Valine, isoleucine and sodium propionate have been investigated as precursors of urinary methylmalonic acid in patients with vitamin B12 deficiency. Valine was administered to fifteen patients with vitamin B12 deficiency and provoked an increased excretion of methylmalonic acid in all cases. The same dose of valine had no effect on excretion
J.Hywel Jones, D. Gompertz, J.P. Knowles
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Journal of Inherited Metabolic Disease, 2020
Methylcitric acid (MCA) analysis has been mainly utilized for the diagnosis of propionate disorders or as a second‐tier test in newborn screening, but its utility for patients monitoring still needs to be established.
Evelina Maines+14 more
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Methylcitric acid (MCA) analysis has been mainly utilized for the diagnosis of propionate disorders or as a second‐tier test in newborn screening, but its utility for patients monitoring still needs to be established.
Evelina Maines+14 more
semanticscholar +1 more source
The assay of methylmalonic acid in urine
Clinica Chimica Acta, 1972Abstract The assay of methylmalonic acid in urine by modifications of the method of Giorgio and Plaut 5 , together with the use of a three wavelength correction is described. This revised procedure made possible the detection of small increases in the output of methylmalonic acid in vitamin B 12 deficiency which could not be estimated by the ...
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Kinetics and mechanism for the iodination of methylmalonic acid [PDF]
AbstractThe reaction\documentclass{article}\pagestyle{empty}\begin{document}$ CH\left({CH_3 } \right)\left({COOH} \right)_2 + I_2 \rightleftharpoons CI(CH_3)\left({COOH} \right)_2 + H^ + + I^ - $\end{document} was followed spectrophotometrically at 353 nm and 470 nm at 25°C under various conditions of pH and methylmalonic acid concentration.
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Pediatric Transplantation, 2010
Methylmalonic acidemia with complete mutase deficiency (mut(0) type) is an inborn error of metabolism with high mortality and morbidity. LT has been suggested to be a solution to this disease, but elevation of urinary and blood MMA was still observed after LT.
Yin-Hsiu Chien+6 more
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Methylmalonic acidemia with complete mutase deficiency (mut(0) type) is an inborn error of metabolism with high mortality and morbidity. LT has been suggested to be a solution to this disease, but elevation of urinary and blood MMA was still observed after LT.
Yin-Hsiu Chien+6 more
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Serum Vitamin B12 and Methylmalonic Acid Status in Migraineurs: A Case‐Control Study
Headache, 2019Although the exact pathophysiological mechanistic pathways that result in the initiation of migraine attacks remain unclear, there are some proposed mechanisms including neurogenic inflammation, trigeminovascular system activation, vascular dysfunction ...
M. Togha+4 more
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A rapid method for the analysis of urinary methylmalonic acid
Clinica Chimica Acta, 1972Abstract A method for the determination of urinary methylmalonic acid, applicable on a routine clinical basis, is described. The method is based on the isolation of a mono-tooligo-carboxylic acid fraction from urine by a series of ether extractions and the subsequent gas Chromatographie analysis of these acids as their trimethylsilyl esters and ...
K. Itiaba+4 more
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Serum cobalamin and methylmalonic acid in Alzheimer dementia
Acta Neurologica Scandinavica, 2009The cobalamin status was evaluated in Alzheimer dementia (n = 26), other dementias (n = 24), various gerontopsychiatric disorders (n = 25), and in neuro-psychiatrically healthy controls (n = 20). Supplementing serum cobalamin we measured methylmalonic acid (MMA), a metabolite accumulating early in cobalamin deficiency.
M. Ø. Kristensen+4 more
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N2O and Urine Methylmalonic Acid in Man
Scandinavian Journal of Haematology, 1983The excretion of methylmalonic acid was measured and deoxyuridine suppression test (dU‐test) was performed in 5 patients before and after 24 h of ventilation with nitrous oxide. The mean urinary 2‐methylmalonic acid was increased from 90 to 320 μmol/24 h and the dU‐tests became abnormal. These findings indicate that the 2 vitamin B‐12 dependent enzymes,
Leif Freund+3 more
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Zhonghua yi xue za zhi, 2013
To analyze the levels of methylmalonic acid and methylcitrate in urine, propionylcarnitine (C3) in plasma and C3/acetylcarnitine (C2) of patients with methylmalonic acidemia (MMA) and explore their applications in the diagnosis of MMA.From December 2003 to March 2012, a total of 162 patients with MMA (MMA group) and 200 healthy children (control group)
Wenjuan Qiu+9 more
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To analyze the levels of methylmalonic acid and methylcitrate in urine, propionylcarnitine (C3) in plasma and C3/acetylcarnitine (C2) of patients with methylmalonic acidemia (MMA) and explore their applications in the diagnosis of MMA.From December 2003 to March 2012, a total of 162 patients with MMA (MMA group) and 200 healthy children (control group)
Wenjuan Qiu+9 more
openaire +2 more sources