Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,213,210 papers from all fields of science
Search
Sign In
Create Free Account
beta-methylcrotonylglycine
Known as:
3-Methylcrotonylglycine
, Glycine, N-(3-methyl-1-oxo-2-butenyl)-
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
3-Methylcrotonylglycine:PrThr:Pt:Urine:Ord
analogs & derivatives
Broader (1)
Glycine
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Metabolic profiling of infant urine using comprehensive two-dimensional gas chromatography: Application to the diagnosis of organic acidurias and biomarker discovery.
K. Kouremenos
,
J. Pitt
,
P. Marriott
Journal of Chromatography A
2010
Corpus ID: 13496547
2009
2009
3-Methylcrotonyl-CoA Carboxylase Deficiency: Phenotypic Variability in a Family
F. Tuba Eminoğlu
,
Aysima Ozcelik
,
+5 authors
M. Baumgartner
Journal of Child Neurology
2009
Corpus ID: 5718225
A family with 3-methylcrotonyl-CoA carboxylase deficiency with different clinical features is described. A 15-month-old boy, who…
Expand
1999
1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency
C. Steen
,
E. Baumgartner
,
+5 authors
A. Kohlschütter
European Journal of Pediatrics
1999
Corpus ID: 21949568
Abstract A mildly retarded infant with failure to thrive developed hypoglycaemia, focal seizures, respiratory failure and…
Expand
1992
1992
Familial hypotonia of childhood caused by isolated 3-methylcrotonyl-coenzyme A carboxylase deficiency.
O. Elpeleg
,
S. Havkin
,
V. Barash
,
C. Jakobs
,
B. Glick
,
R. Shalev
Jornal de Pediatria
1992
Corpus ID: 21125965
1991
1991
Screening Newborns for Multiple Organic Acidurias in Dried Filter Paper Urine Samples: Method Development
M. Tuchman
,
M. McCann
,
P. E. Johnson
,
B. Lemieux
Pediatric Research
1991
Corpus ID: 2734738
Screening urine for inherited and acquired organic acidurias in newborns has the potential of preventing severe disease, mental…
Expand
1989
1989
[Biotinidase deficiency: a congenital metabolic disease which can be successfully treatment with vitamin H].
J. Nothjunge
,
I. Krägeloh-Mann
,
T. Suormala
,
E. Baumgartner
Monatsschrift Kinderheilkunde : Organ der…
1989
Corpus ID: 21623529
At the age of 13 months a patient developed muscular hypotonia, deafness of the inner ear and cutaneous symptoms (alopecia; skin…
Expand
1988
1988
Abnormal organic aciduria in biotin deficiency: the rat is similar to the human.
D. Mock
,
N. Mock
,
S. Weintraub
Journal of Laboratory and Clinical Medicine
1988
Corpus ID: 22446893
We sought to determine whether the biotin-deficient rat excretes the same constellation of abnormal organic acids in urine that…
Expand
1981
1981
Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutrition.
C. L. Kien
,
E. Kohler
,
+4 authors
H. Baker
Jornal de Pediatria
1981
Corpus ID: 21319361
1978
1978
3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria.
S. Wysocki
,
R. Hähnel
Clinica chimica acta; international journal of…
1978
Corpus ID: 41179278
1976
1976
Application of glass capillary-column gas chromatography-mass spectrometry to the studies of human diseases.
Egil Jellum
,
P. Storseth
,
J. Alexander
,
P. Helland
,
O. Stokke
,
E. Teig
Journal of Chromatography A
1976
Corpus ID: 45114958
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE