I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Elpeleg, O. N.
81
results:
Search for persons
X
Format
Online (81)
Mediatypes
Articles (Online) (68)
OpenAccess-fulltext (13)
Sorted by: Relevance
Sorted by: Year
?
1
Protracted Clinical Course for Patientsd with Canavan Disea..:
Zelnik, N.
;
Luder, A. S.
;
Elpeleg, O. N.
...
Developmental Medicine & Child Neurology. 35 (2008) 4 - p. 355-358 , 2008
Link:
https://doi.org/10.1111/..
?
2
Sustained oral lysine supplementation in ornithine δ‐aminot..:
Elpeleg, O. N.
;
Korman, S. H.
Journal of Inherited Metabolic Disease. 24 (2001) 3 - p. 423-424 , 2001
Link:
https://doi.org/10.1023/..
?
3
The spectrum of mutations of the aspartoacylase gene in Can..:
Elpeleg, O. N.
;
Shaag, A.
Journal of Inherited Metabolic Disease. 22 (1999) 4 - p. 531-534 , 1999
Link:
https://doi.org/10.1023/..
?
4
Prenatal diagnosis of Canavan disease — Problems and dilemm..:
Besley, G. T. N.
;
Elpeleg, O. N.
;
Shaag, A.
...
Journal of Inherited Metabolic Disease. 22 (1999) 3 - p. 263-266 , 1999
Link:
https://doi.org/10.1023/..
?
5
Lipoamide dehydrogenase deficiency: A new cause for recurre..:
Elpeleg, O.N.
;
Saada, A.B.
;
Shaag, A.
...
Muscle & Nerve. 20 (1997) 2 - p. 238-240 , 1997
Link:
https://doi.org/10.1002/..
?
6
β‐Ketothiolase (2‐methylacetoacetyl‐coenzyme a thiolase) de..:
Gibson, K. M.
;
Elpeleg, O. N.
;
Bennett, M. J.
Journal of Inherited Metabolic Disease. 19 (1996) 5 - p. 698-699 , 1996
Link:
https://doi.org/10.1007/..
?
7
Congenital lacticacidemia caused by lipoamide dehydrogenase..:
Elpeleg, O.N.
;
Ruitenbeek, W.
;
Jakobs, C.
...
The Journal of Pediatrics. 126 (1995) 1 - p. 72-74 , 1995
Link:
https://doi.org/10.1016/..
?
8
Prenatal detection of Canavan disease (aspartoacylase defic..:
Elpeleg, O. N.
;
Shaag, A.
;
Anikster, Y.
.
Journal of Inherited Metabolic Disease. 17 (1994) 6 - p. 664-666 , 1994
Link:
https://doi.org/10.1007/..
?
9
Complications following oat head aspiration:
Maayan, C. H.
;
Avital, A.
;
Elpeleg, O. N.
...
Pediatric Pulmonology. 15 (1993) 1 - p. 52-54 , 1993
Link:
https://doi.org/10.1002/..
?
10
Reliable prenatal diagnosis of Canavan disease (aspartoacyl..:
Bennett, M. J.
;
Gibson, K. M.
;
Sherwood, W. G.
...
Journal of Inherited Metabolic Disease. 16 (1993) 5 - p. 831-836 , 1993
Link:
https://doi.org/10.1007/..
?
11
Behr's Syndrome and 3-Methylglutaconic Aciduria:
Sheffer, R.N.
;
Zlotogora, J.
;
Elpeleg, O.N.
..
American Journal of Ophthalmology. 114 (1992) 4 - p. 494-497 , 1992
Link:
https://doi.org/10.1016/..
?
12
3‐Methylglutaconic aciduria with persistent metabolic acido..:
Elpeleg, O. N.
;
Meiron, D.
;
Barash, V.
...
Journal of Inherited Metabolic Disease. 13 (1990) 2 - p. 235-236 , 1990
Link:
https://doi.org/10.1007/..
?
13
Late-onset form of partial N-acetylglutamate synthetase def..:
Elpeleg, O. N.
;
Colombo, J. P.
;
Amir, N.
..
European Journal of Pediatrics. 149 (1990) 9 - p. 634-636 , 1990
Link:
https://doi.org/10.1007/..
?
14
Recurrent, familial Reye-like syndrome with a new complex a..:
Elpeleg, O. N.
;
Christensen, E.
;
Hurvitz, H.
.
European Journal of Pediatrics. 149 (1990) 10 - p. 709-712 , 1990
Link:
https://doi.org/10.1007/..
?
15
Glycogen storage disease, Fanconi nephropathy, abnormal gal..:
Hurvitz, H.
;
Elpeleg, O. N.
;
Barash, V.
...
European Journal of Pediatrics. 149 (1989) 1 - p. 48-51 , 1989
Link:
https://doi.org/10.1007/..
1-15