I agree that this site is using cookies. You can find further informations here.
X
Shaag, A.
178  results:
Search for persons X
?
1

OC20.07: Fetal exome sequencing: yield and limitations obse..:

Daum, H. ; Meiner, V. ; Eilat, A....
Ultrasound in Obstetrics & Gynecology.  52 (2018)  S1 - p. 49-49 , 2018
Link: https://doi.org/10.1002/..
 
?
2

EP11.03: The impact of late amniocentesis in the chromosoma..:

Daum, H. ; Ben‐David, A. ; Nadjari, M....
Ultrasound in Obstetrics & Gynecology.  52 (2018)  S1 - p. 243-244 , 2018
Link: https://doi.org/10.1002/..
 
?
3

Mitochondrial epileptic encephalopathy, 3‐methylglutaconic ..:

Shahrour, M.A. ; Staretz‐Chacham, O. ; Dayan, D....
Clinical Genetics.  91 (2016)  5 - p. 690-696 , 2016
Link: https://doi.org/10.1111/..
 
?
4

Severe infantile male encephalopathy is a result of early p..:

Spiegel, R. ; Shalev, S. ; Bercovich, D....
Clinical Genetics.  90 (2016)  6 - p. 560-562 , 2016
Link: https://doi.org/10.1111/..
 
?
5

The use of whole exome sequencing for the diagnosis of auto..:

Shamriz, O. ; Shaag, A. ; Yaacov, B....
Clinical Genetics.  92 (2016)  1 - p. 80-85 , 2016
Link: https://doi.org/10.1111/..
 
?
6

O23 – 1732 Childhood relapsing immune-mediated polyneuropat..:

Nevo, Y ; Ben Zeev, B ; Tabib, A...
European Journal of Paediatric Neurology.  17 (2013)  - p. S8 , 2013
Link: https://doi.org/10.1016/..
 
?
7

P.6.9 Childhood relapsing immune-mediated polyneuropathy an..:

Nevo, Y. ; Ben-Zeev, B. ; Tabib, A....
Neuromuscular Disorders.  23 (2013)  9-10 - p. 772-773 , 2013
Link: https://doi.org/10.1016/..
 
?
8

A deleterious mutation in the LOXHD1 gene causes autosomal ..:

Edvardson, S. ; Jalas, C. ; Shaag, A....
American Journal of Medical Genetics Part A.  155 (2011)  5 - p. 1170-1172 , 2011
Link: https://doi.org/10.1002/..
 
?
9

2FC1.5 Exome sequencing and disease prediction implicate a ..:

Edvardson, S. ; Erlich, Y. ; Elpeleg, O....
European Journal of Paediatric Neurology.  15 (2011)  - p. S19 , 2011
Link: https://doi.org/10.1016/..
 
?
10

Severe infantile type of carnitine palmitoyltransferase II ..:

Spiegel, R. ; Shaag, A. ; Gutman, A....
Journal of Inherited Metabolic Disease.  30 (2007)  2 - p. 266-266 , 2007
Link: https://doi.org/10.1007/..
 
?
11

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/..
 
?
12

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/..
 
?
13

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/..
 
?
14

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/..
 
?
15

Sodium dodecyl sulphate dependent NADPH oxidation: An alter..:

Sha'ag, D.
Journal of Biochemical and Biophysical Methods.  19 (1989)  1 - p. 121-128 , 1989
Link: https://doi.org/10.1016/..
 
1-15