Genetics of the polymicrogyria syndromes

od Jansen, A, Andermann, E
Izdano 2005

Alternating paroxysmal dystonia and hemiplegia in childhood as a symptom of basal ganglia disease.

od Hart, Y M, Tampieri, D, Andermann, E, Andermann, F, Connolly, M, Farrell, K
Izdano 1995

Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

od Pinard, J M, Motte, J, Chiron, C, Brian, R, Andermann, E, Dulac, O
Izdano 1994

A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2

od Lopes-Cendes, I., Scheffer, I. E., Berkovic, S. F., Rousseau, M., Andermann, E., Rouleau, G. A.
Izdano 2000

Folic acid blinded trial in identical twins with fragile X syndrome.

od Rosenblatt, D S, Duschenes, E A, Hellstrom, F V, Golick, M S, Vekemans, M J, Zeesman, S F, Andermann, E
Izdano 1985

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

od Lopes-Cendes, I., Andermann, E., Attig, E., Cendes, F., Bosch, S., Wagner, M., Gerstenbrand, F., Andermann, F., Rouleau, G. A.
Izdano 1994

Recommendations on the use of folic acid supplementation to prevent the recurrence of neural tube defects. Clinical Teratology Committee, Canadian College of Medical Geneticists.

od Van Allen, M I, Fraser, F C, Dallaire, L, Allanson, J, McLeod, D R, Andermann, E, Friedman, J M
Izdano 1993

Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22

od Chan, E, Bulman, D, Paterson, A, Turnbull, J, Andermann, E, Andermann, F, Rouleau, G, Delgado-Escueta, A, Scherer, S, Minassian, B
Izdano 2003

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

od Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Izdano 1991

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

od Casaubon, L. K., Melanson, M., Lopes-Cendes, I., Marineau, C., Andermann, E., Andermann, F., Weissenbach, J., Prévost, C., Bouchard, J. P., Mathieu, J., Rouleau, G. A.
Izdano 1996

Patterns of hippocampal abnormalities in malformations of cortical development

od Montenegro, M A, Kinay, D, Cendes, F, Bernasconi, A, Bernasconi, N, Coan, A C, Li, L M, Guerreiro, M M, Guerreiro, C A M, Lopes‐Cendes, I, Andermann, E, Dubeau, F, Andermann, F
Izdano 2006

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy

od Hannibal, M C., Ruzzo, E K., Miller, L R., Betz, B, Buchan, J G., Knutzen, D M., Barnett, K, Landsverk, M L., Brice, A, LeGuern, E, Bedford, H M., Worrall, B B., Lovitt, S, Appel, S H., Andermann, E, Bird, T D., Chance, P F.
Izdano 2009

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24.

od Phillips, H A, Scheffer, I E, Crossland, K M, Bhatia, K P, Fish, D R, Marsden, C D, Howell, S J, Stephenson, J B, Tolmie, J, Plazzi, G, Eeg-Olofsson, O, Singh, R, Lopes-Cendes, I, Andermann, E, Andermann, F, Berkovic, S F, Mulley, J C
Izdano 1998

Proceed with Care: Direct Predictive Testing for Huntington Disease

od Benjamin, C. M., Adam, S., Wiggins, S., Theilmann, J. L., Copley, T. T., Bloch, M., Squitieri, F., McKellin, W., Cox, S., Brown, S. A., Kremer, H. P. H., Burgess, M., Meshino, W., Summers, A., Macgregor, D., Buchanan, J., Greenberg, C., Carson, N., Ives, E., Frecker, M., Welch, J. P., Fuller, A., Rosenblatt, D., Miller, S., Dufrasne, S., Roy, M., Andermann, E., Prevost, C., Khalifa, M., Girard, K., Taylor, S., Hunter, A., Goldsmith, C., Whelan, D., Eisenberg, D., Soltan, H., Kane, J., Shokeir, M. H. K., Gibson, A., Cardwell, S., Bamforth, S., Grover, S., Suchowersky, O., Klimek, M., Garber, T., Gardner, H. A., MacLeod, P., Hayden, M. R.
Izdano 1994