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Oxalosis
LE WE PMID CA
Oxalosis2078Oxalose

Adenine phosphoribosyl transferase

Alanine glyoxylate aminotransferase

Autophagy

Cystinosis

Cystinuria

Endosymbiosis

Evolution

Fanconi s syndrome

Fructose intolerance

Glyoxal

GlyoxylaseI

Inflammation (BASKET)

Ion channel (Anion)

Lesch Nyhan syndrome

Metabolomics

Methylglyoxal

Mitochondria (Mitochondriopathy)

Nephrocalcinosis

Nephrolithiasis

Oxalosis

Peptide

Peroxisomes

Pexophagy

Phosphoribosylpyrophosphate synthetase

Protein (ptm Glycation)

Protein (Transport)

Tyrosinemia

Wilson s disease

Xanthine

2004  
1
Persistent cutaneous manifestations of hyperoxaluria after combined hepatorenal transplantation.
[15347492] Dermatol Online J 10(1): 10 (2004)
2000  
2
Current approaches to the management of primary hyperoxaluria.
[10833178] Arch Dis Child 82(6): 470-3 (2000)
2001  
3
1977  
4
Histopathological occurrence and characterisation of calcium oxalate: a review.
[72077] J Clin Pathol 30(9): 800-11 (1977)
2008  
5
Recurrence of primary hyperoxaluria: an avoidable catastrophe following kidney transplant.
[18626169] J Postgrad Med 54(3): 206-8 (2008)
1999  
6
Primary hyperoxaluria type 1.
[10354306] Kidney Int 55(6): 2533-47 (1999)
2005  
7
Primary hyperoxaluria: from gene defects to designer drugs?
[15956068] Nephrol Dial Transplant 20(8): 1525-9 (2005)
2003  
8
Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome.
[12543880] Nephrol Dial Transplant 18(2): 273-9 (2003)
2005  
9
Development of a physiologically based pharmacokinetic model for ethylene glycol and its metabolite, glycolic Acid, in rats and humans.
[15716482] Toxicol Sci 85(1): 476-90 (2005)
1996  
10
Initial manifestation of primary hyperoxaluria type I in adults-- recognition, diagnosis, and management.
[8779202] West J Med 164(1): 42-53 (1996)
1991  
11
Primary hyperoxaluria: therapeutic strategies for the 90's.
[1787639] Kidney Int 40(3): 389-99 (1991)
1978  
12
Oxalic acid and the hyperoxaluric syndromes.
[351269] Kidney Int 13(5): 410-7 (1978)
2004  
13
Type 1 primary hyperoxaluria in pediatric patients: renal sonographic patterns.
[15547226] AJR Am J Roentgenol 183(6): 1767-70 (2004)
2005  
14
Molecular etiology of primary hyperoxaluria type 1: new directions for treatment.
[15961951] Am J Nephrol 25(3): 303-10 (2005)
2004  
15
Diagnostic and therapeutic strategies in hyperoxaluria: a plea for early intervention.
[14671036] Nephrol Dial Transplant 19(1): 39-42 (2004)
2010  
16
Diagnostic examination of the child with urolithiasis or nephrocalcinosis.
[19104842] Pediatr Nephrol 25(3): 403-13 (2010)
2010  
17
Nephrolithiasis related to inborn metabolic diseases.
[19156444] Pediatr Nephrol 25(3): 415-24 (2010)
2010  
18
Cardiac abnormalities in primary hyperoxaluria.
[20921818] Circ J 74(11): 2403-9 (2010)
2010  
19
Evolutionary origins of metabolic compartmentalization in eukaryotes.
[20124349] Philos Trans R Soc Lond B Biol Sci 365(1541): 847-55 (2010)
2010  
20
Molecular mechanism and physiological role of pexophagy.
[20083110] FEBS Lett 584(7): 1367-73 (2010)
2011  
21
Studies on a unique organelle localization of a liver enzyme, serine:pyruvate (or alanine:glyoxylate) aminotransferase.
[21558762] Proc Jpn Acad Ser B Phys Biol Sci 87(5): 274-86 (2011)
2011  
22
Primary hyperoxaluria type 1 in Tunisian children.
[21308625] Tunis Med 89(2): 163-7 (2011)
2007  
23
Synthetic, biologically active amphiphilic peptides.
[17589872] Chem Biodivers 4(6): 1395-412 (2007)
2008  
24
Protein and nucleotide damage by glyoxal and methylglyoxal in physiological systems--role in ageing and disease.
[18533367] Drug Metabol Drug Interact 23(1-2): 125-50 (2008)
2009  
25
Peroxisomal dysfunction in inflammatory childhood white matter disorders: an unexpected contributor to neuropathology.
[19605772] J Child Neurol 24(9): 1147-57 (2009)
2006  
26
Autophagy in organelle homeostasis: peroxisome turnover.
[16973210] Mol Aspects Med 27(5-6): 483-94 (2006)
2010  
27
Nephrocalcinosis in animal models with and without stones.
[20658131] Urol Res 38(6): 429-38 (2010)

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