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Ben‐Zeev, B.
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1

"Virtual patch clamp analysis" for predicting the functiona..:

Bielopolski, N. ; Heyman, E. ; Bassan, H....
Epilepsy Research.  186 (2022)  - p. 107002 , 2022
Link: https://doi.org/10.1016/..
 
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Microcephaly, intractable seizures and developmental delay ..:

Pode‐Shakked, B. ; Barash, H. ; Ziv, L....
Clinical Genetics.  91 (2016)  5 - p. 725-738 , 2016
Link: https://doi.org/10.1111/..
 
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3

The Neuropsychological profile of patients with 3‐Methylglu..:

Sofer, S. ; Schweiger, A. ; Blumkin, L....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  168 (2015)  3 - p. 197-203 , 2015
Link: https://doi.org/10.1002/..
 
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4

Multicenter long‐term follow‐up of children with idiopathic..:

Cohen‐Sadan, S. ; Kramer, U. ; Ben‐Zeev, B....
European Journal of Neurology.  16 (2009)  5 - p. 555-555 , 2009
Link: https://doi.org/10.1111/..
 
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5

Multicenter long‐term follow‐up of children with idiopathic..:

Cohen‐Sadan, S. ; Kramer, U. ; Ben‐Zeev, B....
European Journal of Neurology.  16 (2009)  4 - p. 482-487 , 2009
Link: https://doi.org/10.1111/..
 
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6

P0954 CACHEXIA AS THE ONLY PRESENTING SYMPTOM OF MITOCHONDR..:

Weiss, B. ; Ben‐Zeev, B. ; Hirano, M....
Journal of Pediatric Gastroenterology and Nutrition.  39 (2004)  S1 - p. , 2004
Link: https://doi.org/10.1002/..
 
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7

Behçet's disease in a child:

Barash, J. ; Sthoeger, D. ; Ben‐Zeev, B.
Arthritis & Rheumatism.  34 (1991)  6 - p. 791-791 , 1991
Link: https://doi.org/10.1002/..
 
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8

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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9

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/..
 
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10

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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11

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/..
 
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12

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/..
 
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13

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/..
 
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14

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/..
 
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15

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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