X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (9) 9
humans (8) 8
male (8) 8
female (7) 7
middle aged (5) 5
risk factors (5) 5
chronic kidney failure (4) 4
genetic aspects (4) 4
health aspects (4) 4
aged (3) 3
dementia (3) 3
dialysis (3) 3
kidney diseases (3) 3
pediatrics (3) 3
pedigree (3) 3
adult (2) 2
aged, 80 and over (2) 2
alport syndrome (2) 2
biomarker (2) 2
biomarkers - blood (2) 2
care and treatment (2) 2
chronic kidney disease (2) 2
cognitive ability (2) 2
cognitive dysfunction - epidemiology (2) 2
cognitive dysfunction - etiology (2) 2
cognitive dysfunction - physiopathology (2) 2
diagnosis (2) 2
female genital diseases and pregnancy complications (2) 2
genes (2) 2
genetics (2) 2
genetics & heredity (2) 2
hearing impairment (2) 2
hemodialysis (2) 2
impairment (2) 2
medical laboratory technology (2) 2
mortality (2) 2
mutation (2) 2
nephropathy (2) 2
patients (2) 2
renal dialysis - adverse effects (2) 2
renal insufficiency, chronic - blood (2) 2
renal insufficiency, chronic - physiopathology (2) 2
research article (2) 2
screening (2) 2
urologic and male genital diseases (2) 2
5200 (1) 1
abridged index medicus (1) 1
adolescent (1) 1
adtkd-umod (1) 1
adults (1) 1
agrin - blood (1) 1
all-cause mortality (1) 1
alleles (1) 1
allelomorphism (1) 1
alport-syndrome (1) 1
american-college (1) 1
analysis (1) 1
antimicrobial cationic peptides - chemistry (1) 1
antimicrobial cationic peptides - genetics (1) 1
antimicrobial cationic peptides - metabolism (1) 1
aortic pressure (1) 1
arrhythmias, cardiac - diagnosis (1) 1
arrhythmias, cardiac - genetics (1) 1
arterial stiffness (1) 1
basement-membrane nephropathy (1) 1
batteries (1) 1
beta-defensins (1) 1
biological markers (1) 1
biology and life sciences (1) 1
biopsy (1) 1
blood pressure monitoring, ambulatory - methods (1) 1
blood urea nitrogen (1) 1
blotting, western (1) 1
c-terminal-agrin-fragment (1) 1
caf (1) 1
cardiomyopathies - diagnosis (1) 1
cardiomyopathies - genetics (1) 1
cardiomyopathy (1) 1
cardiomyopathy, hypertrophic - genetics (1) 1
cardiomyopathy, hypertrophic - pathology (1) 1
case-control studies (1) 1
child (1) 1
child, preschool (1) 1
children (1) 1
cognition (1) 1
cognition - physiology (1) 1
cognitive dysfunction (1) 1
cognitive dysfunction - diagnosis (1) 1
cognitive dysfunction - diagnostic imaging (1) 1
cognitive impairment (1) 1
cognitive neurology (1) 1
cognitive neuroscience (1) 1
cognitive science (1) 1
cohort (1) 1
col4a3 (1) 1
col4a3/col4a4 mutations (1) 1
col4a5 (1) 1
collagen gene (1) 1
combined modality therapy (1) 1
comparative analysis (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Journal Article
MMW - Fortschritte der Medizin, ISSN 1438-3276, 7/2015, Volume 157, Issue 13, pp. 54 - 61
Obwohl schwerwiegende Elektrolytentgleisungen relativ selten im ambulanten Bereich auftreten, sollten Hausärzte wissen, wie es zu Schwankungen der Natrium-... 
hypokalemia | Medicine & Public Health | hypernatremia | hyponatremia | hyperkalemia | General Practice / Family Medicine | Internal Medicine | Electrolytes | Hypokalemia | Hyper-natremia | Hyperkalemia | Hyponatremia
Journal Article
FRONTIERS IN PEDIATRICS, ISSN 2296-2360, 11/2019, Volume 7, p. 485
Background: Alport syndrome (AS) is a progressive kidney disorder leading to end stage renal disease (ESRD). Extrarenal symptoms like hearing loss and ocular... 
ESRD | GUIDELINES | hearing impairment | AMERICAN-COLLEGE | STANDARDS | MEDICAL GENETICS | NATURAL-HISTORY | IDENTIFICATION | Gly624Asp | IMPACT | COLLAGEN GENE | Alport syndrome | DIGENIC INHERITANCE | PEDIATRICS | MUTATIONS | Chronic kidney failure | Genetic aspects | COL4A5 | p.Gly624Asp
Journal Article
Journal Article
Journal Article
Eplasty, 2012, Volume 12, p. e9
The radial forearm free flap (RFFF) is the most commonly used free flap in head and neck reconstructive surgery. However, despite excellent results with... 
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 02/2016, Volume 98, Issue 2, p. 358
  Molecular diagnosis of mitochondrial disorders is challenging because of extreme clinical and genetic heterogeneity. By exome sequencing, we identified three... 
Pediatrics | Mitochondria | Genetics | Mutation | Metabolic disorders
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.