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Leshinsky-Silver, Esther
74
results:
Search for persons
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Online (74)
Mediatypes
Articles (Online) (62)
OpenAccess-fulltext (12)
Sorted by: Relevance
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?
1
Severe growth deficiency, microcephaly, intellectual disabi..:
Leshinsky-Silver, Esther
;
Ling, Jiqiang
;
Wu, Jiang
...
neurogenetics. 18 (2017) 3 - p. 141-146 , 2017
Link:
https://doi.org/10.1007/..
?
2
A diagnostic approach to pediatric early onset chorea:
Blumkin, Lubov
;
Zerem, Ayelet
;
Ben-Pazi, Hilla
...
European Journal of Paediatric Neurology. 21 (2017) - p. e215-e216 , 2017
Link:
https://doi.org/10.1016/..
?
3
Does a normal dystrophin staining in muscle biopsy rule out..:
Ginzberg, Mira
;
Lerman-Sagie, Tally
;
Sadeh, Menachem
...
European Journal of Paediatric Neurology. 21 (2017) - p. e235 , 2017
Link:
https://doi.org/10.1016/..
?
4
RARS2 mutations cause early onset epileptic encephalopathy ..:
Nishri, Daniella
;
Goldberg-Stern, Hadassa
;
Noyman, Iris
...
European Journal of Paediatric Neurology. 20 (2016) 3 - p. 412-417 , 2016
Link:
https://doi.org/10.1016/..
?
5
Painful small fiber neuropathy with gastroparesis: A new ph..:
Dabby, Ron
;
Sadeh, Menachem
;
Broitman, Yelena
...
Journal of Clinical Neuroscience. 26 (2016) - p. 84-88 , 2016
Link:
https://doi.org/10.1016/..
?
6
Utility of Whole Exome Sequencing for Genetic Diagnosis of ..:
Kuperberg, Maya
;
Lev, Dorit
;
Blumkin, Lubov
...
Journal of Child Neurology. 31 (2016) 14 - p. 1534-1539 , 2016
Link:
https://doi.org/10.1177/..
?
7
Paroxysmal tonic upward gaze as a presentation of de-novo m..:
Blumkin, Lubov
;
Leshinsky-Silver, Esther
;
Michelson, Marina
...
European Journal of Paediatric Neurology. 19 (2015) 3 - p. 292-297 , 2015
Link:
https://doi.org/10.1016/..
?
8
Atypical presentation of Costeff syndrome-severe psychomoto..:
Carmi, Nirit
;
Lev, Dorit
;
Leshinsky-Silver, Esther
...
European Journal of Paediatric Neurology. 19 (2015) 6 - p. 733-736 , 2015
Link:
https://doi.org/10.1016/..
?
9
Molecular and functional studies of retinal degeneration as..:
Blumkin, Lubov
;
Bradshaw, Teisha
;
Michelson, Marina
...
European Journal of Paediatric Neurology. 19 (2015) 4 - p. 472-476 , 2015
Link:
https://doi.org/10.1016/..
?
10
Adult onset limb-girdle muscular dystrophy — A recessive ti..:
Dabby, Ron
;
Sadeh, Menachem
;
Hilton-Jones, David
...
Journal of the Neurological Sciences. 351 (2015) 1-2 - p. 120-123 , 2015
Link:
https://doi.org/10.1016/..
?
11
Crowdfunding Effort Identifies the Causative Mutation in a ..:
Isakov, Ofer
;
Lev, Dorit
;
Blumkin, Lubov
...
Journal of Genetics and Genomics. 42 (2015) 2 - p. 79-81 , 2015
Link:
https://doi.org/10.1016/..
?
12
Paternal germline mosaicism of a SCN2A mutation results in ..:
Zerem, Ayelet
;
Lev, Dorit
;
Blumkin, Lubov
...
European Journal of Paediatric Neurology. 18 (2014) 5 - p. 567-571 , 2014
Link:
https://doi.org/10.1016/..
?
13
A newly recognized syndrome of severe growth deficiency, mi..:
Vinkler, Chana
;
Leshinsky-Silver, Esther
;
Michelson, Marina
...
European Journal of Medical Genetics. 57 (2014) 6 - p. 288-292 , 2014
Link:
https://doi.org/10.1016/..
?
14
Expansion of the spectrum of TUBB4A-related disorders: a ne..:
Blumkin, Lubov
;
Halevy, Ayelet
;
Ben-Ami-Raichman, Dominique
...
neurogenetics. , 2014
Link:
https://doi.org/10.1007/..
?
15
Reply to: The many faces of TUBB4A mutations:
Blumkin, Lubov
;
Halevy, Ayelet
;
Ben-Ami-Raichman, Dominique
...
neurogenetics. , 2014
Link:
https://doi.org/10.1007/..
1-15