X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (126) 126
index medicus (103) 103
propionic acidemia (99) 99
male (68) 68
female (60) 60
genetics & heredity (54) 54
pediatrics (53) 53
child, preschool (50) 50
child (48) 48
infant (47) 47
metabolism (46) 46
management (41) 41
methylmalonic acidemia (41) 41
infant, newborn (37) 37
medicine, research & experimental (37) 37
endocrinology & metabolism (31) 31
methylmalonic aciduria (27) 27
children (26) 26
adolescent (24) 24
adult (24) 24
animals (23) 23
diagnosis (22) 22
transplantation (22) 22
liver (21) 21
liver transplantation (21) 21
physiological aspects (21) 21
enzymes (20) 20
metabolites (20) 20
mutation (20) 20
treatment outcome (20) 20
amino acid metabolism, inborn errors - diagnosis (19) 19
care and treatment (19) 19
medicine & public health (19) 19
propionic acid (19) 19
biochemistry, general (18) 18
propionates - blood (18) 18
internal medicine (17) 17
research (17) 17
amino acid metabolism, inborn errors - therapy (16) 16
article (16) 16
biochemistry & molecular biology (16) 16
metabolic diseases (16) 16
propionates - metabolism (16) 16
propionic acidemia - genetics (15) 15
propionic aciduria (15) 15
cardiomyopathy (14) 14
health aspects (14) 14
human genetics (14) 14
inborn-errors (14) 14
metabolic disorders (14) 14
mitochondria (14) 14
oxidative stress (14) 14
propionic acidemia - diagnosis (14) 14
young adult (14) 14
amino acid metabolism, inborn errors - diet therapy (13) 13
medicine (13) 13
propionic acidemia - therapy (13) 13
retrospective studies (13) 13
amino acid metabolism, inborn errors - genetics (12) 12
amino acid metabolism, inborn errors - metabolism (12) 12
diet (12) 12
genetic aspects (12) 12
hyperammonemia (12) 12
propionic acidemia - complications (12) 12
aciduria (11) 11
amino acid metabolism, inborn errors - blood (11) 11
amino acid metabolism, inborn errors - complications (11) 11
deficiency (11) 11
disease (11) 11
fatty acids (11) 11
propionic acidemia - physiopathology (11) 11
time factors (11) 11
amino acids (10) 10
ammonia (10) 10
analysis (10) 10
autism (10) 10
carnitine (10) 10
coa carboxylase (10) 10
dietary supplements (10) 10
liver-transplantation (10) 10
methylmalonyl-coa decarboxylase - genetics (10) 10
prognosis (10) 10
rats (10) 10
syrup-urine-disease (10) 10
tandem mass-spectrometry (10) 10
brain (9) 9
clinical neurology (9) 9
coa dehydrogenase-deficiency (9) 9
disorders (9) 9
identification (9) 9
methylmalonyl-coa decarboxylase - metabolism (9) 9
mutations (9) 9
organic acidurias (9) 9
propionic acidemia - surgery (9) 9
surgery (9) 9
urine (9) 9
acids (8) 8
chain fatty-acids (8) 8
infants (8) 8
inhibition (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Genetics and Metabolism, ISSN 1096-7192, 09/2017, Volume 122, Issue 1-2, pp. 51 - 59
Journal Article
Journal Article
Journal Article
Brain & Development, ISSN 0387-7604, 2010, Volume 33, Issue 5, pp. 428 - 431
Journal Article
Journal Article
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 09/2014, Volume 9, Issue 1, p. 130
Journal Article