Skip to main navigation
Skip to search
Skip to main content
Sort by
INIS
diseases
100%
data
100%
surveys
100%
homozygotes
100%
heterozygotes
100%
methionine
100%
patients
66%
mutations
50%
concentration
33%
plasma
33%
screening
16%
liver
16%
nmr imaging
16%
damage
16%
genotype
16%
pregnancy
16%
management
16%
newborns
16%
elevation
16%
atp
16%
conversion
16%
catalysis
16%
homocysteine
16%
isoenzymes
16%
Keyphrases
Homozygote
100%
Compound Heterozygous mutation
100%
MAT1A
100%
Methionine
66%
S-adenosylmethionine
50%
Hypermethioninemia
50%
Pathophysiological Mechanisms
16%
Genotype
16%
Treatment Regimen
16%
Liver Function
16%
Screening Program
16%
Optimal Management
16%
Heterozygote
16%
Demyelination
16%
MRI Findings
16%
Total Homocysteine
16%
Isoenzymes
16%
Methionine Restriction
16%
CNS Damage
16%
Cystathionine beta-synthase
16%
S-adenosylmethionine Decarboxylase
16%
Patient's Will
16%
Medicine and Dentistry
Methionine
100%
Homozygote
100%
Diseases
100%
S-Adenosyl Methionine
60%
Hypermethioninemia
60%
Magnetic Resonance Imaging
20%
Supplementation
20%
Adenosine Triphosphate
20%
Neonatal Infant
20%
Homocysteine
20%
Liver Function
20%
Methionine Adenosyltransferase
20%
Cystathionine Beta Synthase
20%
Demyelination
20%
Isoenzyme
20%
Biochemistry, Genetics and Molecular Biology
Homozygote
100%
Methionine
100%
S-Adenosyl Methionine
50%
Blood Plasma
33%
Adenosine Triphosphate
16%
Homocysteine
16%
Liver Function
16%
Isoenzyme
16%
Cystathionine Beta Synthase
16%
Magnetic Resonance Imaging
16%
Pharmacology, Toxicology and Pharmaceutical Science
Methionine
100%
Diseases
100%
S-Adenosyl Methionine
60%
Adenosine Triphosphate
20%
Homocysteine
20%
Demyelination
20%
Methionine Adenosyltransferase
20%
Cystathionine Beta Synthase
20%
Isoenzyme
20%
Neuroscience
Methionine
100%
S Adenosylmethionine
60%
Blood Plasma
40%
Magnetic Resonance Imaging
20%
Adenosine Triphosphate
20%
Homocysteine
20%
Cystathionine Beta Synthase
20%
Methionine Adenosyltransferase
20%
Isoenzyme
20%