Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 226,160,443 papers from all fields of science
Search
Sign In
Create Free Account
Ethanolaminosis
Known as:
Ethanolamine Kinase Deficiency
, Ethanolaminuria
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
Broader (2)
Brain Diseases, Metabolic
Inborn Errors of Metabolism
congenital deficiency
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1992
1992
Beta-mannosidosis and ethanolaminuria in a female patient
H. Wijburg
,
J. Jong
,
R. Wevers
,
J. Bakkeren
,
F. Trijbels
,
R. Sengers
European Journal of Pediatrics
1992
Corpus ID: 40899959
Sir: [3-mannosidosis is a lysosomal storage disorder caused by deficiency of the enzyme ~-mannosidase. We would like to report a…
Expand
1992
1992
Dignity of the perinatal optimality score of Prechtl
H. Manzke
European Journal of Pediatrics
1992
Corpus ID: 2654915
Sir: [3-mannosidosis is a lysosomal storage disorder caused by deficiency of the enzyme ~-mannosidase. We would like to report a…
Expand
1988
1988
Ethanolaminuria: a non-specific laboratory finding in the seriously ill infant.
D. Cole
,
S. Farag
,
K. Dooley
Clinical Biochemistry
1988
Corpus ID: 19451695
1977
1977
[Ethanolaminosis, a generalized storage disease with cardiomegaly, cerebral dysfunction and early death].
K. Vietor
,
B. Havsteen
,
D. Harms
,
H. Busse
,
F. Freitag
Monatsschrift fur Kinderheilkunde
1977
Corpus ID: 30848195
1951
1951
Ethanolaminuria; an obscure metabolic defect associated with a case of primary hepatoma.
Dent Ce
,
Fowler Di
,
Walshe Jm
Biochemical Journal
1951
Corpus ID: 88648695
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