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Author/Creator Srour, M.

3. Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy. Issue 2 (21st December 2017)

Authors:
Perrier, S.; Gauquelin, L.; Tétreault, M.; Tran, L.T.; Webb, N.; Srour, M.; Mitchell, J.J.; Brunel‐Guitton, C.; Majewski, J.; Long, V.; Keller, S.; Gambello, M.J.; Simons, C.; Vanderver, A.; Bernard, G.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 2(2018)
Page Start:
396
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study. (November 2020)

Authors:
Dermer, E.; Spahr, A.; Tran, L. T.; Mirchi, A.; Pelletier, F.; Guerrero, K.; Ahmed, S.; Brais, B.; Braverman, N.; Buhas, D.; Chandratre, S.; Chenier, S.; Chrestian, N.; Desmeules, M.; Dilenge, M. E.; Laflamme, J.; Larbrisseau, A.; Legault, G.; Lim, K. Y.; Maftei, C.
Journal:
Journal of child neurology
Issue:
Volume 35:Number 13(2020:Dec.)
Page Start:
901
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations. (September 2020)

Authors:
Villa, R.; Fergnani, V.G.C.; Silipigni, R.; Guerneri, S.; Cinnante, C.; Guala, A.; Danesino, C.; Scola, E.; Conte, G.; Fumagalli, M.; Gangi, S.; Colombo, L.; Picciolini, O.; Ajmone, P.F.; Accogli, A.; Madia, F.; Tassano, E.; Scala, M.; Capra, V.; Srour, M.
Journal:
European journal of paediatric neurology
Issue:
Volume 28(2020)
Page Start:
110
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗