Ronen GM - Search Results

1

Males With MECP2 C-terminal-Related Atypical Rett Syndromes and Their Carrier Mothers.

Ronen GM, Brady LI, Tarnopolsky MA. Ronen GM, et al. Pediatr Neurol. 2017 Feb;67:98-101. doi: 10.1016/j.pediatrneurol.2016.10.012. Epub 2016 Oct 25. Pediatr Neurol. 2017. PMID: 28089766

2

Long-term prognosis in children with neonatal seizures: a population-based study.

Ronen GM, Buckley D, Penney S, Streiner DL. Ronen GM, et al. Neurology. 2007 Nov 6;69(19):1816-22. doi: 10.1212/01.wnl.0000279335.85797.2c. Neurology. 2007. PMID: 17984448

3

Feasibility of pedometer use to assess physical activity and its relationship with quality of life in children with epilepsy: a pilot study.

Whitney R, Bhan H, Persadie N, Streiner D, Bray S, Timmons B, Ronen GM. Whitney R, et al. Among authors: ronen gm. Pediatr Neurol. 2013 Nov;49(5):370-3. doi: 10.1016/j.pediatrneurol.2013.06.002. Epub 2013 Aug 2. Pediatr Neurol. 2013. PMID: 23916862

4

Outcomes trajectories in children with epilepsy: hypotheses and methodology of a Canadian longitudinal observational study.

Ronen GM, Streiner DL, Boyle MH, Cunningham CE, Lach L, Verhey LH, Fayed N, Chen K, Rosenbaum PL; QUALITÉ Group; Connolly M, Bello-Espinosa LE, Rafay MF, Appendino JP, Shevell M, Carmant L. Ronen GM, et al. Pediatr Neurol. 2014 Jan;50(1):38-48. doi: 10.1016/j.pediatrneurol.2013.08.024. Pediatr Neurol. 2014. PMID: 24370172

5

Glucose Transporter Type I Deficiency (G1D) at 25 (1990-2015): Presumptions, Facts, and the Lives of Persons With This Rare Disease.

Pascual JM, Ronen GM. Pascual JM, et al. Among authors: ronen gm. Pediatr Neurol. 2015 Nov;53(5):379-93. doi: 10.1016/j.pediatrneurol.2015.08.001. Epub 2015 Aug 10. Pediatr Neurol. 2015. PMID: 26341673 Free PMC article. Review.

6

Rett Syndrome Turns 50: Themes From a Chronicle: Medical Perspectives and the Human Face of Rett Syndrome.

Ronen GM, Rosenbaum PL. Ronen GM, et al. Pediatr Neurol. 2016 Aug;61:3-10. doi: 10.1016/j.pediatrneurol.2016.04.012. Epub 2016 Apr 29. Pediatr Neurol. 2016. PMID: 27515454

7

Clinical Manifestations Associated With the N-Terminal-Acetyltransferase NAA10 Gene Mutation in a Girl: Ogden Syndrome.

Sidhu M, Brady L, Tarnopolsky M, Ronen GM. Sidhu M, et al. Among authors: ronen gm. Pediatr Neurol. 2017 Nov;76:82-85. doi: 10.1016/j.pediatrneurol.2017.07.010. Epub 2017 Jul 19. Pediatr Neurol. 2017. PMID: 28967461

8

Capturing Meaningful Outcomes in -Pediatric Neurology: Further Reflections on Principles, Challenges, and Opportunities.

Ronen GM. Ronen GM. Pediatr Neurol. 2022 Oct;135:38-43. doi: 10.1016/j.pediatrneurol.2022.07.012. Epub 2022 Aug 5. Pediatr Neurol. 2022. PMID: 35985086 Review.

9

Arthrogryposis multiplex congenita due to congenital myasthenic syndrome.

Vajsar J, Sloane A, MacGregor DL, Ronen GM, Becker LE, Jay V. Vajsar J, et al. Among authors: ronen gm. Pediatr Neurol. 1995 Apr;12(3):237-41. doi: 10.1016/0887-8994(95)00004-y. Pediatr Neurol. 1995. PMID: 7619191

10

From eugenic euthanasia to habilitation of "disabled'' children: Andreas Rett's contribution.

Ronen GM, Meaney B, Dan B, Zimprich F, Stögmann W, Neugebauer W. Ronen GM, et al. J Child Neurol. 2009 Jan;24(1):115-27. doi: 10.1177/0883073808321763. J Child Neurol. 2009. PMID: 19168827

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