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EBioMedicine, ISSN 2352-3964, 01/2019, Volume 39, pp. 27 - 28
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 9/2008, Volume 167, Issue 9, pp. 1037 - 1047
Journal Article
Journal Article
Pediatric nephrology (Berlin, Germany), ISSN 0931-041X, 04/2019, pp. 1 - 10
Measurement of neonatal renal function is challenging, and accurate, easy-to-use markers to estimate glomerular filtration rate (eGFR) are lacking. This study... 
Creatinine | Neonates | Cystatin | Renal function | Epidermal growth factor receptors | Infants | Gestational age | Glomerular filtration rate | Renal insufficiency | Prediction models | Cystatin C | Inulin | Age
Journal Article
Vaccine, ISSN 0264-410X, 2016, Volume 34, Issue 41, pp. 4948 - 4954
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 3/2018, Volume 33, Issue 3, pp. 473 - 483
Journal Article
FRONTIERS IN PEDIATRICS, ISSN 2296-2360, 03/2019, Volume 7, p. 88
Background: Autosomal Dominant Polycystic Kidney Disease (ADPKD) is increasingly diagnosed during childhood by the presence of renal cysts in patients with a... 
SIZE | INJURY | uNGAL | CONSORTIUM | ADPKD | children | PEDIATRICS | SPECTRUM | TKV | RENAL VOLUME | PROGRESSION | SEVERITY | renal impairment | Carrier proteins | Neutrophils | Physiological aspects | Development and progression | Children | Biological markers | Health aspects | Polycystic kidney disease | Diseases | Pediatrics | Care and treatment
Journal Article
Revue Medicale Suisse, ISSN 1660-9379, 02/2019, Volume 15, Issue 638, pp. 384 - 389
Journal Article
Revue medicale suisse, ISSN 1660-9379, 02/2019, Volume 15, Issue 638, p. 384
Vitamin D deficiency is increasing in Switzerland. If cases of rickets are scarce, pediatricians are often dealing with patients presenting vitamin D... 
Vitamin D Deficiency - diagnosis | Vitamin D Deficiency - complications | Humans | Rickets - drug therapy | Risk Factors | Vitamin D Deficiency - drug therapy | Research | Rickets - etiology | Vitamin D - therapeutic use | Vitamins - therapeutic use | Switzerland | Rickets - diagnosis
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 12/2013, Volume 28, Issue 12, pp. 2299 - 2306
Minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) are the most common causes of idiopathic nephrotic syndrome (INS). We have evaluated... 
Low-molecular-weight proteins | Pediatrics | Minimal change disease | Medicine & Public Health | Focal segmental glomerulosclerosis | Urinary NGAL | Idiopathic nephrotic syndrome | NGAL | STEROID RESPONSIVENESS | CHILDHOOD | CHILDREN | RENAL TUBULAR UPTAKE | BETA-2-MICROGLOBULIN | COMPETITION | UROLOGY & NEPHROLOGY | PEDIATRICS | Acute-Phase Proteins - urine | Predictive Value of Tests | Recurrence | Biomarkers - urine | Molecular Weight | Prospective Studies | Age Factors | Humans | Proto-Oncogene Proteins - urine | Child, Preschool | Lipocalins - urine | Nephrosis, Lipoid - complications | Glomerulosclerosis, Focal Segmental - complications | Case-Control Studies | Glomerulosclerosis, Focal Segmental - physiopathology | Proteinuria - diagnosis | Acetylglucosaminidase - urine | Child | Nephrotic Syndrome - diagnosis | Kidney - physiopathology | Proteinuria - etiology | Glomerular Filtration Rate | Nephrosis, Lipoid - diagnosis | Cross-Sectional Studies | Creatinine - urine | Nephrosis, Lipoid - physiopathology | Proteinuria - physiopathology | Glomerulosclerosis, Focal Segmental - diagnosis | Lipocalin-2 | Nephrotic Syndrome - physiopathology | Adolescent | ROC Curve | Alpha-Globulins - urine | Nephrotic Syndrome - etiology | Medicine, Experimental | Medical research | Nephrotic syndrome | Research | Children | Diseases
Journal Article
Revue medicale suisse, ISSN 1660-9379, 02/2016, Volume 12, Issue 507, p. 387
Suspected renal inherited disorders are regularly evaluated in nephrology consultations both in adults and children. A positive family history and/or a typical... 
Humans | Kidney Diseases - diagnosis | Genetic Counseling | Genetic Testing - methods | Kidney Diseases - genetics | Pregnancy | Kidney Diseases - epidemiology | Adult | Female | High-Throughput Nucleotide Sequencing | Genetic Testing - trends | Prenatal Diagnosis - methods | Child
Journal Article