Radiofrequency-thermocoagulation in pediatric epilepsy surgery: A systematic review and pooled analysis of cases

Authors: Bottan, Juan S. ^{a, b, ⁎}, Almalki, Fuad ^{d, e}, Nabavi Nouri, Maryam ^{c, e}, Lau, Jonathan C. ^c, Iansavichene, Alla ^f, Gilmore, Greydon ^c, Miller, Michael ^e, de Ribaupierre, Sandrine ^{c, e}, Andrade, Andrea V. ^{c, e}

Source: In Seizure: European Journal of Epilepsy March 2025 126:6-13

Families' Knowledge Change in Paediatric Drug Resistant Epilepsy: A Novel Clinic Model

Authors: Kregel, Michelle, Coulson, Sherry, Nabavi Nouri, Maryam, Sorzano, Rochelle, Andrade, Andrea

Source: Seizure. 108:116-126

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100191337910.0x000001&indx=1&recIds=ETOCvdc_100191337910.0x000001

Impact of number of anti-seizure medications on long-term health-related quality of life in children with epilepsy: A prospective cohort study

Authors: Nabavi Nouri, Maryam, Puka, Klajdi, Palmer, Katie, Speechley, Kathy N.

Source: Seizure. 99:120-126

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100195227689.0x000001&indx=1&recIds=ETOCvdc_100195227689.0x000001

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

Authors: Whitney, Robyn, Zak, Maria, Haile, Denait, Nabavi Nouri, Maryam

Source: Epilepsia open. 7(4):718-728

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100176229043.0x000001&indx=1&recIds=ETOCvdc_100176229043.0x000001

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

Authors: Nabavi Nouri, Maryam, Zak, Maria, Jain, Puneet, Whitney, Robyn

Source: Pediatric neurology. 126:11-19

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100152306019.0x000001&indx=1&recIds=ETOCvdc_100152306019.0x000001

From Alpha-Thalassemia Trait to NPRL3 -Related Epilepsy: A Genomic Diagnostic Odyssey.

Authors: Nabavi Nouri, Maryam^1,2 (AUTHOR) lama.alandijani@lhsc.on.ca, Alandijani, Lama¹ (AUTHOR), van Engelen, Kalene³ (AUTHOR), Tole, Soumitra⁴ (AUTHOR), Lalonde, Emilie⁵ (AUTHOR), Balci, Tugce B.^2,3 (AUTHOR) tugce.balci@lhsc.on.ca

Source: Genes. Jul2024, Vol. 15 Issue 7, p836. 11p.

Subject Terms: *FOCAL cortical dysplasia, *HIPPOCAMPAL sclerosis, *CHILDREN with epilepsy, *PARTIAL epilepsy, *GENETIC disorders, *GLOBIN genes

A Story That Begins Too Soon: A Girl with Untreated Anti-N-Methyl-D-Aspartate Receptor Encephalitis for 14 Years

Authors: Leonard, Sean, Budhram, Adrian, Shevell, Michael, Nabavi Nouri, Maryam

Source: The Canadian Journal of Neurological Sciences; November 2022, Vol. 49 Issue: 6 p826-827, 2p

Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intolerance.

Authors: Nabavi Nouri, Maryam¹, Lamhonwah, Anne‐marie^1,2, Tein, Ingrid^1,2,3 Ingrid.tein@sickkids.ca

Source: Clinical Case Reports. Mar2018, Vol. 6 Issue 3, p499-501. 3p.

Subject Terms: *MUSCLE cramps, *EXERCISE intensity, *PHOSPHORYLASES, *GENETIC mutation, *HOMOZYGOSITY, *MYOGLOBINURIA