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  • 1
    ISSN: 1432-198X
    Keywords: Key words: Oxalate ; Calcium ; Preterm infants ; Term infants ; Gestational age ; Nutritional factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract.   Few data for normal urinary oxalate (Ox) and calcium (Ca) excretion related both to gestational age and nutritional factors have been reported in preterm or term infants. We therefore determined the molar Ox and Ca to creatinine (Cr) ratios in spot urines from 64 preterm and 37 term infants aged 1–60 days, either fed formula or human milk (HM). Only vitamin D was supplemented; renal or metabolic diseases were excluded. Urinary Ox/Cr ratio was higher in preterm than in term infants, both when formula fed (1st month 253 vs. 180 mmol/mol and 2nd month 306 vs. 212 mmol/mol; P〈0.05) or HM fed (206 vs. 169 mmol/mol and 283* vs. 232 mmol/mol; * P〈0.05). Ox/Cr was also higher in formula- than HM-fed preterm infants. The ratio increased during the first 2 months of life irrespective of nutrition. Urinary Ca/Cr ratio was comparable in all groups during the 1st month of life, except for a lower (P〈0.05) value in term infants fed HM (0.10 mol/mol). It increased in all groups during the 2nd month of life, being highest in HM-fed preterm infants (1.86 mol/mol). In conclusion, urinary Ox and Ca excretion is influenced by both gestational age and nutrient intake in preterm and term infants.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-198X
    Keywords: Key words: Cystic fibrosis ; Urolithiasis ; Calcium ; Oxalate ; Uric acid ; Citrate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Patients with cystic fibrosis (CF) have an increased risk of urolithiasis/nephrocalcinosis. To determine potential mechanisms responsible, we studied the urinary excretion of lithogenic and stone-inhibitory substances and calculated the urinary saturation for calcium-oxalate (CaOx), brushite (CaHPO4), and uric acid (UA). We examined 24-h urines in 63 patients with CF (34 female, 29 male) aged 5 months to 36 years. Renal ultrasonography was performed at the time of urine collection. Hyperoxaluria was found in 25 patients (range 0.51 – 1.71 mmol/1.73 m2 per 24 h). Urinary Ca was increased in 13 patients (4.1 – 8.22 mg/kg per 24 h). Hyperuricosuria was found in 16 patients (5.2 – 18.0 mmol/1.73 m2 per 24 h) and hypocitraturia in 14 patients (0.07 – 1.14 mmol/1.73 m2 per 24 h). CaOx saturation was elevated in 26 patients, related to hyperoxaluria in 19 patients. CaHPO4 saturation was increased in 19 patients and UA saturation in 11 patients. Urolithiasis in situ was diagnosed in 1 patient; 3 patients previously had renal stones; 4 patients had present nephrocalcinosis. Elevated excretion of lithogenic substances and urinary supersaturation might lead to the higher risk of urolithiasis/nephrocalcinosis in patients with CF.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 27 (1999), S. 135-140 
    ISSN: 1434-0879
    Keywords: Key words Calcium oxalate ; Nucleation ; Crystallization model ; Particle size distribution ; Laser probe ; Inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To understand the genesis of urinary stones different crystallization models have been developed to simulate the crystallization processes that occur at the beginning of the stone formation. In this study a laser probe working on the principle of the measurement of back-scattered light was mounted on a batch crystallization model, in which calcium oxalate nucleation was induced by titration of an artificial urine with ammonium oxalate. With the laser probe the particle numbers and particle size distributions in the range from 1–250 μm can be measured in a single experiment. Measurement is performed directly at the place of crystal development and, therefore, falsification of the results (by dilution, mechanical transport or isolation, temperature gap, multiple measurements, mathematical calculations after indirect measurements, etc.) is prevented. In a basic urine, containing 7.5 mmol/l calcium (4.13 mmol/l free calcium), nucleation of calcium oxalate appears at a concentration of 0.58 mmol/l oxalate. At the start of nucleation the particle size rises to 7 μm. After addition of citrate and magnesium in concentrations up to 12 mmol/l the metastable limit is clearly shifted up to 1.50 mmol/l oxalate. Both findings are in good agreement with the literature. The laser crystallization model has proved to be useful for the testing of inhibitors and promoters of urinary stone formation.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1433-8726
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Hyperoxaluria was reported to induce renal damage, probably due to toxic effects on renal tubules. Such tubular damage might be expressed by an increase in urinary excretion of marker enzymes such as N-acetyl-β-d-glucosaminidase (NAG). We set out to examine a possible relationship between the excretion of NAG and that of urinary lithogenic and stone-inhibitory substances by analyzing 24-h urine specimens from 56 children with urolithiasis and 25 healthy children with normal renal function and without a history of urolithiasis. The NAG excretion was higher in patients with urolithiasis (3.5 ± 0.51 U/g creatinine) as compared with healthy subjects (1.33 ± 0.14 U/g creatinine, P 〈 0.05). A positive correlation between NAG and oxalate excretion was observed in female patients (r = 0.56; P 〈 0.01). In conclusion, the increase in urinary NAG in children with urolithiasis might express renal tubular damage. It seemed, however, not to be specifically related to the excretion of a single lithogenic substance.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 28 (2000), S. 274-280 
    ISSN: 1434-0879
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This work focuses on the in vitro calcium-oxalate (CaOx) crystallization behaviour of native and synthetic urine samples in order to establish a CaOx crystallization risk index for unprepared native urine. Native 24-h urine samples from healthy persons and from stone-formers were examined. Within a [Ca2+] versus added oxalate (Ox2−) diagram, we observed fields which allow the discrimination of each urine sample in terms of more or less risk. The [Ca2+]/(Ox2−) ratio is calculated and termed the “Bonn-Risk Index” (BRI; per litre). We propose that BRIs 〉1/l denote samples “at risk”, whereas BRIs ≤ 1/l denote those “without risk”. Second, the effects of different concentrations of citrate and Mg2+ on BRI were investigated in artificial urine. The transferability of BRI between native and synthetic urine samples is proved. To evaluate the impact of the proposed BRI, it is compared with the more familiar relative urine saturation index calculated for CaOx and brushite. Urine sampled from stone-formers shows risk indexes between 0.278 and 23.0/l (mean 2.87/l), while urine from healthy persons varied between 0.060 and 4.890/l (mean 1.05/l). Comparing the results of healthy volunteers and patients, the significance of BRI and relative urine supersaturation (RS) with respect to CaOx is P 〈 0.0005 and P=0.013, respectively. Fast and easy to perform, determination of the risk index is a suitable tool for estimating the actual CaOx formation “status”–“at risk” or “without risk”– from the native urine of any person.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 330 (1988), S. 372-373 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 624-628 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1.3-Dioxolan (1a) und 2-Alkyl-1.3-dioxolane (1b-f) sind sehr leicht peroxygenierbar. Als Primärprodukte der Peroxygenierung wurden die Hydroperoxide (2a-f) isoliert. Diese gehen durch Hydrierung quantitativ in Glykolhalbester über. Unter den Bedingungen der Vakuumdestillation bilden sich die dimeren Peroxide (5) und H2O2.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 2491-2493 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der Peroxygenierung von 2.4.6-Trimethyl-(1) und 2.4.6-Triäthyl-1.3.5-trioxan entstehen Monohydroperoxide (z. B. 2). Daraus wurden die dimeren Peroxide (z. B. 3) nach Wasserstoffperoxid-Abspaltung isoliert. 2.4.6-Tri-tert.-butyl-1.3.5-trioxan (4) ergibt bei gleicher Umsetzung neben wenig Monohydroperoxid (5) Trimethylessigsäure und Trimethylacetaldehyd.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 623-629 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unter praktisch gleichen Reaktionsbedingungen können bei der Einwirkung von molekularem Sauerstoff auf verschieden substituierte 2-Halogenmethyl-1.3-dioxolane drei Reaktionsabläufe beobachtet werden: 2-Dichlormethyl- und 2-Trichlormethyl-1.3-dioxolan (4,) bilden primär Hydroperoxide, die zu 1.3-Dioxolon-(2) (6), Chlorwasserstoff und Kohlenmonoxid bzw. Phosgen zerfallen. Aus 2-Chlormethyl- (7a) und 2-Brommethyl-1.3-dioxolan (7b) entstehen die Hydroperoxide (8a, b), unter geeigneten Bedingungen bilden sich die dimeren Peroxide (9a, b). 2-Dibrommethyl- (11) und 2-Tribrommethyl-1.3-dioxolan gehen unter Sauerstoffeinwirkung eine neuartige Umlagerung ein und ergeben die Bromessigsäure-[β-brom-äthylester] (z. B. 12). Die Reaktion ist an die Gegenwart von Sauerstoff gebunden, übliche Radikalbildner bleiben bei Abwesenheit von Sauerstoff unwirksam.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 2069-2073 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Einziges Peroxygenierungsprodukt von 2-Acetonyl-1.3-dioxolan (3) ist 8-Hydroxy-8-methyl-1.4.6.7-tetraoxa-spiro[4.4]nonan (5). Das primär entstehende Hydroperoxid 4 lagert sich augenblicklich in 5 um. Ähnliche spirocyclische Peroxide entstehen aus 2-Hydroperoxy-2-alkenyl-1.3-dioxolanen durch saure Katalyse. Als Stammverbindung dieser Verbindungsklasse wird 1.4.6.7-Tetraoxa-spiro[4.4]nonan (8) beschrieben. Die thermische Behandlung von 2-Hydroperoxy-2-phenyl-1.3-dioxolan führt unter Wasserstoffperoxid-Abspaltung zum dimeren Peroxid.
    Type of Medium: Electronic Resource
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