Mona Hnaini
Working Group Member
Pediatric Neuromuscular Fellow, Childrenā€™s Hospital London Health Science Centre
Lebanese Order of Physicians since 2011 | College of Physicians and Surgeons Ontario since 2020
NMD4C Involvement: Knowledge Translation
Biography
Dr. Mona Hnaini completed her General Pediatrics training at Beirut Arab University in 2015. She performed her Pediatric Neurology clinical fellowship at the American University of Beirut between 2016 and 2019. In August 2020, she moved to Canada to sub-specialize in Pediatric Neuromuscular at Childrenā€™s Hospital London Health Science Centre under the supervision of Dr. Craig Campbell. Dr Hnaini is currently a sub investigator in multiple clinical trials for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy diseases.
Recent Publications
Hnaini, M, Downs, M, Miller, MR, Campbell, C, St-Laurent, A. Duchenne muscular dystrophy respiratory profiles from real world registry data. Pediatr Pulmonol. 2023.58 (10)2725-2732 PMID:37539841
Wei, YS, Hnaini, M, ElAloul, B, Zapata, E, Campbell, C. Duchenne Muscular Dystrophy Fatigue Trajectories. Neuropediatrics. 2024.55 (1)42-48 PMID:37236246
Hnaini, M, Cardarelli Leite, L, Carey, T, Campbell, C. A 16-year-old boy with lower extremity muscle wasting and pain. Paediatr Child Health. 2023.28 (2)69-71 PMID:37151931
Schreyer, L, Reilly, J, McConkey, H, Kerkhof, J, Levy, MA, Hu, J et al.. The discovery of the DNA methylation episignature for Duchenne muscular dystrophy. Neuromuscul Disord. 2023.33 (1)5-14 PMID:36572586
Al-Haddad, C, El Moussawi, Z, Hoyeck, S, Mehanna, CJ, El Salloukh, NA, Ismail, K et al.. Amblyopia risk factors among pediatric patients in a hospital-based setting using photoscreening. PLoS One. 2021.16 (7)e0254831 PMID:34324539
Hnaini, M, Darwich, M, Koleilat, N, Jaafar, F, Hanneyan, S, Rahal, S et al.. High-Dose Levetiracetam for Neonatal Seizures: A Retrospective Review. Seizure. 2020.82 7-11 PMID:32950862
Ahmad Hammoud, Rolla Shbarou, Mona Hnaini3 and Chadi Al-Alam4 Electroencephalography Findings in Infants Diagnosed with Brief Resolved Unexplained Event
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