|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
9030
|
|
pubmed:dateCreated |
1996-10-31
|
|
pubmed:abstractText |
The creatine/creatine-phosphate system is essential for the storage and transmission of phosphate-bound energy in muscle and brain. In infants, inefficiency or failure of this metabolic pathway can impair the development of motor control and mentation.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
0140-6736
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
21
|
|
pubmed:volume |
348
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
789-90
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:8813986-Basal Ganglia Diseases,
pubmed-meshheading:8813986-Brain,
pubmed-meshheading:8813986-Creatine,
pubmed-meshheading:8813986-Developmental Disabilities,
pubmed-meshheading:8813986-Guanidinoacetate N-Methyltransferase,
pubmed-meshheading:8813986-Humans,
pubmed-meshheading:8813986-Infant,
pubmed-meshheading:8813986-Male,
pubmed-meshheading:8813986-Metabolism, Inborn Errors,
pubmed-meshheading:8813986-Methyltransferases,
pubmed-meshheading:8813986-Time Factors
|
|
pubmed:year |
1996
|
|
pubmed:articleTitle |
Creatine replacement therapy in guanidinoacetate methyltransferase deficiency, a novel inborn error of metabolism.
|
|
pubmed:affiliation |
Department of Paediatric Neurology, University Children's Hospital, Göttingen, Germany.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
