Whitney R - Search Results

1

The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions.

Man A, Di Scipio M, Grewal S, Suk Y, Trinari E, Ejaz R, Whitney R. Man A, et al. Among authors: whitney r. Genes (Basel). 2024 Mar 4;15(3):332. doi: 10.3390/genes15030332. Genes (Basel). 2024. PMID: 38540392 Free PMC article. Review.

2

Epilepsy Management in Tuberous Sclerosis Complex: Existing and Evolving Therapies and Future Considerations.

Nabavi Nouri M, Zak M, Jain P, Whitney R. Nabavi Nouri M, et al. Among authors: whitney r. Pediatr Neurol. 2022 Jan;126:11-19. doi: 10.1016/j.pediatrneurol.2021.09.017. Epub 2021 Sep 30. Pediatr Neurol. 2022. PMID: 34740132 Review.

3

The state of pediatric tuberous sclerosis complex epilepsy care: Results from a national survey.

Whitney R, Zak M, Haile D, Nabavi Nouri M. Whitney R, et al. Epilepsia Open. 2022 Dec;7(4):718-728. doi: 10.1002/epi4.12652. Epub 2022 Oct 5. Epilepsia Open. 2022. PMID: 36161285 Free PMC article.

4

The effect of mTOR inhibition on obstructive hydrocephalus in patients with tuberous sclerosis complex (TSC) related subependymal giant cell astrocytoma (SEGA).

Weidman DR, Palasamudram S, Zak M, Whitney R, McCoy B, Bouffet E, Taylor M, Shroff M, Bartels U. Weidman DR, et al. Among authors: whitney r. J Neurooncol. 2020 May;147(3):731-736. doi: 10.1007/s11060-020-03487-8. Epub 2020 Apr 13. J Neurooncol. 2020. PMID: 32285309

5

The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort.

Alsowat D, Whitney R, Hewson S, Jain P, Chan V, Kabir N, Amburgey K, Noone D, Lemaire M, McCoy B, Zak M. Alsowat D, et al. Among authors: whitney r. Child Neurol Open. 2021 May 4;8:2329048X211012817. doi: 10.1177/2329048X211012817. eCollection 2021 Jan-Dec. Child Neurol Open. 2021. PMID: 34017900 Free PMC article.

6

Genetics and SUDEP: Challenges and Future Directions.

Whitney R, Sharma S, Jones KC, RamachandranNair R. Whitney R, et al. Seizure. 2023 Aug;110:188-193. doi: 10.1016/j.seizure.2023.07.002. Epub 2023 Jul 2. Seizure. 2023. PMID: 37413779 Review.

7

A Review of Investigations for Patients With Tuberous Sclerosis Complex Who Were Referred to the Tuberous Sclerosis Clinic at The Hospital for Sick Children: Identifying Gaps in Surveillance.

Alsowat D, Zak M, McCoy B, Kabir N, Al-Mehmadi S, Chan V, Whitney R. Alsowat D, et al. Among authors: whitney r. Pediatr Neurol. 2020 Jan;102:44-48. doi: 10.1016/j.pediatrneurol.2019.06.018. Epub 2019 Jul 4. Pediatr Neurol. 2020. PMID: 31362847

8

The Utility of Surveillance Electroencephalography to Guide Early Antiepileptic Drug Therapy in Infants With Tuberous Sclerosis Complex.

Whitney R, Jan S, Zak M, McCoy B. Whitney R, et al. Pediatr Neurol. 2017 Jul;72:76-80. doi: 10.1016/j.pediatrneurol.2017.04.009. Epub 2017 Apr 18. Pediatr Neurol. 2017. PMID: 28506505

9

Early-Onset Developmental and Epileptic Encephalopathies of Infancy: An Overview of the Genetic Basis and Clinical Features.

Morrison-Levy N, Borlot F, Jain P, Whitney R. Morrison-Levy N, et al. Among authors: whitney r. Pediatr Neurol. 2021 Mar;116:85-94. doi: 10.1016/j.pediatrneurol.2020.12.001. Epub 2020 Dec 13. Pediatr Neurol. 2021. PMID: 33515866 Review.

10

The genetic landscape of developmental and epileptic encephalopathy with spike-and-wave activation in sleep.

Freibauer AE, RamachandranNair R, Jain P, Jones KC, Whitney R. Freibauer AE, et al. Among authors: whitney r. Seizure. 2023 Aug;110:119-125. doi: 10.1016/j.seizure.2023.06.017. Epub 2023 Jun 20. Seizure. 2023. PMID: 37352690

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