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Pediatric Nephrology, ISSN 0931-041X, 7/2018, Volume 33, Issue 7, pp. 1275 - 1276
The unit of the HOG-creatinine ratio presented in this article is calculated in μmol/mg creatinine instead of the demonstrated unit of μmol/μmol. This applies... 
Pediatrics | Nephrology | Medicine & Public Health | Urology | Creatinine | Primary hyperoxaluria | Hyperoxaluria
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, pp. 438 - 447
Die Inzidenz und Prävalenz von Steinerkrankungen haben in den letzten Jahren deutlich zugenommen. Es ist von entscheidender Bedeutung, möglichst frühzeitig... 
Human Genetics | Nephrocalcinosis | Hyperkalziurie | Gene Therapy | Gynecology | Nephrocalcinose | Oncology | Nephrolithiasis | Hypocitraturia | Medicine/Public Health, general | Hypercalciuria | Medicine & Public Health | Hyperoxalurie | Hypocitraturie | Hyperoxaluria | Reproductive Medicine
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, p. 438
Die Inzidenz und Pravalenz von Steinerkrankungen haben in den letzten Jahren deutlich zugenommen. Es ist von entscheidender Bedeutung, moglichst fruhzeitig... 
Journal Article
Medizinische Genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, pp. 438 - 447
Journal Article
Nephrology Dialysis Transplantation, ISSN 0931-0509, 05/2015, Volume 30, Issue suppl_3, pp. iii391 - iii392
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, pp. 410 - 421
Das steroid-resistente nephrotische Syndrom (SRNS) mit dem histomorphologischen Korrelat der fokal-segmentalen Glomerulosklerose (FSGS) stellt eine bedeutende... 
Human Genetics | SRNS | SSNS | Gene Therapy | Gynecology | Oncology | Steroid-resistant nephrotic syndrome | Medicine/Public Health, general | Mutationsanalyse | Medicine & Public Health | Steroid-resistentes nephrotisches Syndrom | FSGS | Mutational analysis | Reproductive Medicine
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 12/2016, Volume 68, Issue 6, pp. A18 - A21
Journal Article
Medizinische Genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, pp. 410 - 421
Journal Article
medizinische genetik, ISSN 0936-5931, 12/2018, Volume 30, Issue 4, p. 410
Das steroid-resistente nephrotische Syndrom (SRNS) mit dem histomorphologischen Korrelat der fokal-segmentalen Glomerulosklerose (FSGS) stellt eine bedeutende... 
Journal Article
Stem Cell Research, ISSN 1873-5061, 12/2019, Volume 41, p. 101626
Primary Hyperoxaluria Type I (PH1) is a rare autosomal recessive metabolic disorder characterized by defects in enzymes involved in glyoxylate metabolism. PH1... 
Journal Article
Journal of Pediatric Biochemistry, ISSN 1879-5390, 2014, Volume 4, Issue 2, pp. 101 - 110
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 08/2013, Volume 123, Issue 8, pp. 3243 - 3253
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 4170 - 12
Recently, the Mucin-1 (MUC1) gene has been identified as a causal gene of autosomal dominant tubulointerstitial kidney disease (ADTKD). Most causative... 
TUBULOINTERSTITIAL KIDNEY-DISEASE | DIAGNOSIS | CELLS | MUC1 GENE | MANAGEMENT | MULTIDISCIPLINARY SCIENCES | CHROMOSOME-1 | DOMINANT | TYPE-1 | NEPHROPATHY | EXPRESSION | SMRT protein | Phenotypes | Kidneys | Mucin | Mutation | Kidney diseases
Journal Article
Journal of Pediatric Biochemistry, ISSN 1879-5390, 2014, Volume 4, Issue 2, pp. 101 - 110
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 12/2019, Volume 96, Issue 6, pp. 1389 - 1399
Primary hyperoxaluria type 2 is a rare inherited disorder of glyoxylate metabolism causing nephrocalcinosis, renal stone formation and ultimately kidney... 
PH2 | oxalate | clinical outcome | CKD | primary hyperoxaluria type 2
Journal Article
Kidney International, ISSN 0085-2538, 06/2018, Volume 93, Issue 6, pp. 1308 - 1319
In diseases of many parenchymatous organs, heterogeneous deterioration of individual functional units determines the clinical prognosis. However, the molecular... 
glomerulus proteomic analysis | albuminuria | focal segmental glomerulosclerosis | proximal tubule | podocyte | ANALYSIS REVEALS | QUANTIFICATION | VALIDATION | CLASSIFICATION | IDENTIFICATION | ENDOCYTOSIS | PODOCYTES | PHOSPHOPROTEOMIC ANALYSIS | COMPUTATIONAL PLATFORM | UROLOGY & NEPHROLOGY | CATHEPSIN-B | Proteostasis | Humans | Nephrotic Syndrome - metabolism | Male | Nephrotic Syndrome - genetics | Proteinuria - pathology | Glomerulonephritis - metabolism | Nephrons - pathology | Tandem Mass Spectrometry | Nephrons - physiopathology | Proteomics - methods | Glomerulonephritis - physiopathology | Extracellular Matrix Proteins - metabolism | Repressor Proteins - metabolism | Disease Models, Animal | Biomarkers - metabolism | Reproducibility of Results | Lysosome-Associated Membrane Glycoproteins - metabolism | Podocytes - metabolism | Glomerulonephritis - genetics | Nephrotic Syndrome - pathology | Proteinuria - metabolism | Repressor Proteins - genetics | Proteome | Podocytes - pathology | Proteinuria - genetics | Biological Variation, Individual | Mice, Knockout | Proteinuria - physiopathology | Animals | Nephrotic Syndrome - physiopathology | Glomerulonephritis - pathology | Lysosome-Associated Membrane Glycoproteins - genetics | Mice | Nephrons - metabolism | Serum Albumin - metabolism | Animal models | Transcription factors | Peptides | Homeostasis | Sclerosis | Datasets | Proteins | Lasers | Rodents | Extracellular matrix | Matrix protein | Chronic illnesses | Urine | Kidneys | Tubules | Mass spectroscopy | Histology | Patients | Biopsy | Morphology | Proteomics | Protein expression | Mutation | Kidney diseases | Lysosomal protein | Proteinuria
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