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Ben-Zeev, B.
1119
results:
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1
Novel WWOX deleterious variants cause early infantile epile..:
Weisz-Hubshman, M.
;
Meirson, H.
;
Michaelson-Cohen, R.
...
European Journal of Paediatric Neurology. 23 (2019) 3 - p. 418-426 , 2019
Link:
https://doi.org/10.1016/..
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2
Mutations in AIFM1 cause an X-linked childhood cerebellar a..:
Heimer, G.
;
Eyal, E.
;
Zhu, X.
...
European Journal of Paediatric Neurology. 22 (2018) 1 - p. 93-101 , 2018
Link:
https://doi.org/10.1016/..
?
3
A novel inborn error of the Coenzyme Q10 biosynthesis pathw..:
Malicdan, M.
;
Vilboux, T.
;
Ben-Zeev, B.
...
Neuromuscular Disorders. 27 (2017) - p. S176 , 2017
Link:
https://doi.org/10.1016/..
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4
Mutations in AIFM1 cause a potentially treatable X-linked c..:
Nissenkorn, A.
;
Eyal, E.
;
Zhou, X.
...
European Journal of Paediatric Neurology. 21 (2017) - p. e214 , 2017
Link:
https://doi.org/10.1016/..
?
5
Creatine transporter deficiency: Novel mutations and functi..:
Ardon, O.
;
Procter, M.
;
Mao, R.
...
Molecular Genetics and Metabolism Reports. 8 (2016) - p. 20-23 , 2016
Link:
https://doi.org/10.1016/..
?
6
PP05.11 – 3025: A new syndrome with postnatal microcephaly,..:
Fattal-Valevski, A.
;
Ben-Sira, L.
;
Straussberg, R.
...
European Journal of Paediatric Neurology. 19 (2015) - p. S49 , 2015
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
Unilateral Rhythmic Hand Tapping in Rett Syndrome: Is This ..:
Nissenkorn, A.
;
Ben-Zeev, B.
Journal of Child Neurology. 28 (2012) 10 - p. 1210-1214 , 2012
Link:
https://doi.org/10.1177/..
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9
Glatiramer acetate (GA, Copolymer-1) an hypothetical treatm..:
Ben-Zeev, B.
;
Aharoni, R.
;
Nissenkorn, A.
.
Medical Hypotheses. 76 (2011) 2 - p. 190-193 , 2011
Link:
https://doi.org/10.1016/..
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10
P01.3 Abscence status on awakening – a new variant of child..:
Ben-Zeev, B.
;
Nissenkorn, A.
;
Manescu, S.
..
European Journal of Paediatric Neurology. 15 (2011) - p. S32 , 2011
Link:
https://doi.org/10.1016/..
?
11
1FC3.6 Progressive Microcephaly – A Novel Genetic disorder ..:
Fattal-Valevski, A.
;
Ben-Zeev, B.
;
Ben Sira, L.
European Journal of Paediatric Neurology. 15 (2011) - p. S15-S16 , 2011
Link:
https://doi.org/10.1016/..
?
12
Novel mutations in the CDKL5 gene, predicted effects and as..:
Russo, S.
;
Marchi, M.
;
Cogliati, F.
...
neurogenetics. 10 (2009) 3 - p. 241-250 , 2009
Link:
https://doi.org/10.1007/..
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13
Investigating genotype–phenotype relationships in Rett synd..:
Bebbington, A.
;
Anderson, A.
;
Ravine, D.
...
Neurology. 70 (2008) 11 - p. 868-875 , 2008
Link:
https://doi.org/10.1212/..
?
14
ESP012 Normal MRI West syndrome cases: therapy type and dia..:
Goldberg-Stern, H.
;
Cohen-Sadan, S.
;
Ben-Zeev, B.
...
European Journal of Paediatric Neurology. 11 (2007) - p. 63 , 2007
Link:
https://doi.org/10.1016/..
?
15
P0954 CACHEXIA AS THE ONLY PRESENTING SYMPTOM OF MITOCHONDR..:
Weiss, B.
;
Ben-Zeev, B.
;
Hirano, M.
...
Journal of Pediatric Gastroenterology and Nutrition. 39 (2004) Supplement 1 - p. S420 , 2004
Link:
https://doi.org/10.1097/..
1-15