Mahajnah M - Search Results

1

Clinical Features at the Time of Diagnosis of Benign Epilepsy With Centrotemporal Spikes Do Not Predict Subsequent Seizures.

Watemberg N, Afunevitz S, Ganelin-Cohen E, Mahajnah M. Watemberg N, et al. Among authors: mahajnah m. Pediatr Neurol. 2018 Nov;88:36-39. doi: 10.1016/j.pediatrneurol.2018.08.024. Epub 2018 Sep 5. Pediatr Neurol. 2018. PMID: 30337131

2

Pediatric-onset gelastic seizures: clinical data and outcome.

Shahar E, Kramer U, Mahajnah M, Lerman-Sagie T, Goez R, Gross V, Kutai M, Genizi J. Shahar E, et al. Among authors: mahajnah m. Pediatr Neurol. 2007 Jul;37(1):29-34. doi: 10.1016/j.pediatrneurol.2007.03.003. Pediatr Neurol. 2007. PMID: 17628219

3

Phenotypic heterogeneity in consanguineous patients with a common CLN8 mutation.

Mahajnah M, Zelnik N. Mahajnah M, et al. Pediatr Neurol. 2012 Oct;47(4):303-5. doi: 10.1016/j.pediatrneurol.2012.05.016. Pediatr Neurol. 2012. PMID: 22964447

4

The influence of excessive chewing gum use on headache frequency and severity among adolescents.

Watemberg N, Matar M, Har-Gil M, Mahajnah M. Watemberg N, et al. Among authors: mahajnah m. Pediatr Neurol. 2014 Jan;50(1):69-72. doi: 10.1016/j.pediatrneurol.2013.08.015. Epub 2013 Nov 1. Pediatr Neurol. 2014. PMID: 24188910

5

Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.

Afawi Z, Oliver KL, Kivity S, Mazarib A, Blatt I, Neufeld MY, Helbig KL, Goldberg-Stern H, Misk AJ, Straussberg R, Walid S, Mahajnah M, Lerman-Sagie T, Ben-Zeev B, Kahana E, Masalha R, Kramer U, Ekstein D, Shorer Z, Wallace RH, Mangelsdorf M, MacPherson JN, Carvill GL, Mefford HC, Jackson GD, Scheffer IE, Bahlo M, Gecz J, Heron SE, Corbett M, Mulley JC, Dibbens LM, Korczyn AD, Berkovic SF. Afawi Z, et al. Among authors: mahajnah m. Neurology. 2016 Feb 23;86(8):713-22. doi: 10.1212/WNL.0000000000002404. Epub 2016 Jan 22. Neurology. 2016. PMID: 26802095 Free PMC article.

6

A Prospective Case Study of the Safety and Efficacy of Lysine-Restricted Diet and Arginine Supplementation Therapy in a Patient With Pyridoxine-Dependent Epilepsy Caused by Mutations in ALDH7A1.

Mahajnah M, Corderio D, Austin V, Herd S, Mutch C, Carter M, Struys E, Mercimek-Mahmutoglu S. Mahajnah M, et al. Pediatr Neurol. 2016 Jul;60:60-5. doi: 10.1016/j.pediatrneurol.2016.03.008. Epub 2016 Apr 13. Pediatr Neurol. 2016. PMID: 27212567

7

Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy.

Sharkia R, Shalev SA, Zalan A, Marom-David M, Watemberg N, Urquhart JE, Daly SB, Bhaskar SS, Williams SG, Newman WG, Spiegel R, Azem A, Elpeleg O, Mahajnah M. Sharkia R, et al. Among authors: mahajnah m. Am J Med Genet A. 2017 Apr;173(4):1051-1055. doi: 10.1002/ajmg.a.38140. Am J Med Genet A. 2017. PMID: 28328138

8

Pseudotumor Cerebri Syndrome: From Childhood to Adulthood Risk Factors and Clinical Presentation.

Mahajnah M, Genizi J, Zahalka H, Andreus R, Zelnik N. Mahajnah M, et al. J Child Neurol. 2020 Apr;35(5):311-316. doi: 10.1177/0883073819895179. Epub 2020 Jan 13. J Child Neurol. 2020. PMID: 31928127

9

Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect the diagnostic yield?

Rozenblat T, Kraus D, Mahajnah M, Goldberg-Stern H, Watemberg N. Rozenblat T, et al. Among authors: mahajnah m. Seizure. 2020 Jul;79:86-89. doi: 10.1016/j.seizure.2020.03.013. Epub 2020 May 8. Seizure. 2020. PMID: 32446208 Free article. Clinical Trial.

10

Corrigendum to "Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?" [Seizure 79 (2020) 86-89].

Rozenblat T, Kraus D, Mahajnah M, Goldberg-Stern H, Watemberg N. Rozenblat T, et al. Among authors: mahajnah m. Seizure. 2021 Jan;84:132. doi: 10.1016/j.seizure.2020.11.001. Epub 2020 Nov 23. Seizure. 2021. PMID: 33243601 Free article. No abstract available.

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