Sadaka Y - Search Results

1

A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers.

Perez Y, Wormser O, Sadaka Y, Birk R, Narkis G, Birk OS. Perez Y, et al. Among authors: sadaka y. Biomed Res Int. 2017;2017:3470234. doi: 10.1155/2017/3470234. Epub 2017 Oct 8. Biomed Res Int. 2017. PMID: 29119105 Free PMC article.

2

CDC174, a novel component of the exon junction complex whose mutation underlies a syndrome of hypotonia and psychomotor developmental delay.

Volodarsky M, Lichtig H, Leibson T, Sadaka Y, Kadir R, Perez Y, Liani-Leibson K, Gradstein L, Shaco-Levy R, Shorer Z, Frank D, Birk OS. Volodarsky M, et al. Among authors: sadaka y. Hum Mol Genet. 2015 Nov 15;24(22):6485-91. doi: 10.1093/hmg/ddv357. Epub 2015 Sep 10. Hum Mol Genet. 2015. PMID: 26358778

3

Transcript-Based Diagnosis and Expanded Phenotype of an Intronic Mutation in TPM3 Myopathy.

Yogev Y, Bistritzer J, Sadaka Y, Michaelovsky A, Cavari Y, Feinstein Y, Abu-Madegem M, Fellig Y, Wormser O, Drabkin M, Halperin D, Birk OS. Yogev Y, et al. Among authors: sadaka y. Mol Diagn Ther. 2022 Sep;26(5):561-568. doi: 10.1007/s40291-022-00601-6. Epub 2022 Jul 7. Mol Diagn Ther. 2022. PMID: 35796944

4

MYORG is associated with recessive primary familial brain calcification.

Arkadir D, Lossos A, Rahat D, Abu Snineh M, Schueler-Furman O, Nitschke S, Minassian BA, Sadaka Y, Lerer I, Tabach Y, Meiner V. Arkadir D, et al. Among authors: sadaka y. Ann Clin Transl Neurol. 2018 Nov 15;6(1):106-113. doi: 10.1002/acn3.684. eCollection 2019 Jan. Ann Clin Transl Neurol. 2018. PMID: 30656188 Free PMC article.

5

Validation of actigraphy with continuous video-electroencephalography in children with epilepsy.

Sadaka Y, Sadeh A, Bradbury L, Massicotte C, Zak M, Go C, Shorer Z, Weiss SK. Sadaka Y, et al. Sleep Med. 2014 Sep;15(9):1075-81. doi: 10.1016/j.sleep.2014.04.021. Epub 2014 Jun 2. Sleep Med. 2014. PMID: 24974198

6

New DSM-5 criteria for ADHD - Does it matter?

Rigler T, Manor I, Kalansky A, Shorer Z, Noyman I, Sadaka Y. Rigler T, et al. Among authors: sadaka y. Compr Psychiatry. 2016 Jul;68:56-9. doi: 10.1016/j.comppsych.2016.03.008. Epub 2016 Mar 30. Compr Psychiatry. 2016. PMID: 27234183

7

CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene.

Heimer G, Sadaka Y, Israelian L, Feiglin A, Ruggieri A, Marshall CR, Scherer SW, Ganelin-Cohen E, Marek-Yagel D, Tzadok M, Nissenkorn A, Anikster Y, Minassian BA, Zeev BB. Heimer G, et al. Among authors: sadaka y. J Child Neurol. 2015 Nov;30(13):1749-56. doi: 10.1177/0883073815579708. Epub 2015 Apr 20. J Child Neurol. 2015. PMID: 25895915

8

2010 McDonald criteria for diagnosing pediatric multiple sclerosis.

Sadaka Y, Verhey LH, Shroff MM, Branson HM, Arnold DL, Narayanan S, Sled JG, Bar-Or A, Sadovnick AD, McGowan M, Marrie RA, Banwell B; Canadian Pediatric Demyelinating Disease Network. Sadaka Y, et al. Ann Neurol. 2012 Aug;72(2):211-23. doi: 10.1002/ana.23575. Ann Neurol. 2012. PMID: 22926854

9

Short-course antibiotic treatment for community-acquired alveolar pneumonia in ambulatory children: a double-blind, randomized, placebo-controlled trial.

Greenberg D, Givon-Lavi N, Sadaka Y, Ben-Shimol S, Bar-Ziv J, Dagan R. Greenberg D, et al. Among authors: sadaka y. Pediatr Infect Dis J. 2014 Feb;33(2):136-42. doi: 10.1097/INF.0000000000000023. Pediatr Infect Dis J. 2014. PMID: 23989106 Clinical Trial.

10

Memory consolidation in children with epilepsy: does sleep matter?

Sud S, Sadaka Y, Massicotte C, Smith ML, Bradbury L, Go C, Weiss SK. Sud S, et al. Among authors: sadaka y. Epilepsy Behav. 2014 Feb;31:176-80. doi: 10.1016/j.yebeh.2013.12.012. Epub 2014 Jan 14. Epilepsy Behav. 2014. PMID: 24434309

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