Aharoni S - Search Results

1

Atypical Clinical Presentations of Pediatric Acute Immune-Mediated Polyneuropathy.

Yosha-Orpaz N, Aharoni S, Rabie M, Nevo Y. Yosha-Orpaz N, et al. Among authors: aharoni s. J Child Neurol. 2019 Apr;34(5):268-276. doi: 10.1177/0883073818825213. Epub 2019 Jan 23. J Child Neurol. 2019. PMID: 30674221

2

CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy.

Nevo Y, Ben-Zeev B, Tabib A, Straussberg R, Anikster Y, Shorer Z, Fattal-Valevski A, Ta-Shma A, Aharoni S, Rabie M, Zenvirt S, Goldshmidt H, Fellig Y, Shaag A, Mevorach D, Elpeleg O. Nevo Y, et al. Among authors: aharoni s. Blood. 2013 Jan 3;121(1):129-35. doi: 10.1182/blood-2012-07-441857. Epub 2012 Nov 13. Blood. 2013. PMID: 23149847 Free article.

3

Variable myopathic presentation in a single family with novel skeletal RYR1 mutation.

Attali R, Aharoni S, Treves S, Rokach O, Becker Cohen M, Fellig Y, Straussberg R, Dor T, Daana M, Mitrani-Rosenbaum S, Nevo Y. Attali R, et al. Among authors: aharoni s. PLoS One. 2013 Jul 24;8(7):e69296. doi: 10.1371/journal.pone.0069296. Print 2013. PLoS One. 2013. PMID: 23894444 Free PMC article.

4

Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus.

Goldberg-Stern H, Aharoni S, Afawi Z, Bennett O, Appenzeller S, Pendziwiat M, Kuhlenbäumer G, Basel-Vanagaite L, Shuper A, Korczyn AD, Helbig I. Goldberg-Stern H, et al. Among authors: aharoni s. J Child Neurol. 2014 Feb;29(2):221-6. doi: 10.1177/0883073813509016. Epub 2013 Nov 20. J Child Neurol. 2014. PMID: 24257433

5

Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel.

Aharoni S, Barwick KE, Straussberg R, Harlalka GV, Nevo Y, Chioza BA, McEntagart MM, Mimouni-Bloch A, Weedon M, Crosby AH. Aharoni S, et al. BMC Med Genet. 2016 Nov 16;17(1):82. doi: 10.1186/s12881-016-0343-x. BMC Med Genet. 2016. PMID: 27852232 Free PMC article.

6

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization.

Aharoni S, Sadeh M, Shapira Y, Edvardson S, Daana M, Dor-Wollman T, Mimouni-Bloch A, Halevy A, Cohen R, Sagie L, Argov Z, Rabie M, Spiegel R, Chervinsky I, Orenstein N, Engel AG, Nevo Y. Aharoni S, et al. Neuromuscul Disord. 2017 Feb;27(2):136-140. doi: 10.1016/j.nmd.2016.11.014. Epub 2016 Nov 24. Neuromuscul Disord. 2017. PMID: 28024842 Free PMC article.

7

Small-fiber neuropathy associated with autoinflammatory syndromes in children and adolescents.

Shinkarevsky Fleitman I, Nevo Y, Harel L, Amarilyo G, Dori A, Agmon-Levin N, Kachko L, Zaks Hoffer G, Dabby R, Rabie M, Aharoni S. Shinkarevsky Fleitman I, et al. Among authors: aharoni s. Muscle Nerve. 2020 Jun;61(6):791-796. doi: 10.1002/mus.26857. Epub 2020 Mar 17. Muscle Nerve. 2020. PMID: 32133669

8

Prognostic Parameters of Acute Transverse Myelitis in Children.

Ganelin-Cohen E, Konen O, Nevo Y, Cohen R, Halevy A, Shuper A, Aharoni S. Ganelin-Cohen E, et al. Among authors: aharoni s. J Child Neurol. 2020 Dec;35(14):999-1003. doi: 10.1177/0883073820947512. Epub 2020 Aug 18. J Child Neurol. 2020. PMID: 32808576

9

Impact of a national population-based carrier-screening program on spinal muscular atrophy births.

Aharoni S, Nevo Y, Orenstein N, Basel-Salmon L, Ben-Shachar S, Mussaffi H, Sagi-Dain L, Cohen R, Singer A. Aharoni S, et al. Neuromuscul Disord. 2020 Dec;30(12):970-974. doi: 10.1016/j.nmd.2020.10.005. Epub 2020 Oct 20. Neuromuscul Disord. 2020. PMID: 33218846

10

COVID-19 in advanced Duchenne/Becker muscular dystrophy patients.

Levine H, Prais D, Aharoni S, Nevo Y, Katz J, Rahmani E, Goldberg L, Scheuerman O. Levine H, et al. Among authors: aharoni s. Neuromuscul Disord. 2021 Jul;31(7):607-611. doi: 10.1016/j.nmd.2021.03.011. Epub 2021 Apr 6. Neuromuscul Disord. 2021. PMID: 34053847 Free PMC article.

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