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Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
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POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome
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Effect of Strongly Magnetized Electrons and Ions on Heat Flow and Symmetry of Inertial Fusion Implosions
Bose, A, Peebles, J, Walsh, C A, Frenje, J A, Kabadi, N V, Adrian, P J, Sutcliffe, G D, Gatu Johnson, M, Frank, C A, Davies, J R, Betti, R, Glebov, V Yu, Marshall, F J, Regan, S P, Stoeckl, C, Campbell, E M, Sio, H, Moody, J, Crilly, A, Appelbe, B D, Chittenden, J P, Atzeni, S, Barbato, F, Forte, A, Li, C K, Seguin, F H, Petrasso, R D
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Accuracy of retinal thickness measurements obtained with Cirrus optical coherence tomography
Keane, P A, Mand, P S, Liakopoulos, S, Walsh, A C, Sadda, S R
Published in British journal of ophthalmology (01.11.2009)
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The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation
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Published in Journal of medical genetics (01.03.2006)
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Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome
Sheen, V L, Jansen, A, Chen, M H, Parrini, E, Morgan, T, Ravenscroft, R, Ganesh, V, Underwood, T, Wiley, J, Leventer, R, Vaid, R R, Ruiz, D E, Hutchins, G M, Menasha, J, Willner, J, Geng, Y, Gripp, K W, Nicholson, L, Berry-Kravis, E, Bodell, A, Apse, K, Hill, R S, Dubeau, F, Andermann, F, Barkovich, J, Andermann, E, Shugart, Y Y, Thomas, P, Viri, M, Veggiotti, P, Robertson, S, Guerrini, R, Walsh, C A
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A structural basis for reading fluency: white matter defects in a genetic brain malformation
Chang, B S, Katzir, T, Liu, T, Corriveau, K, Barzillai, M, Apse, K A, Bodell, A, Hackney, D, Alsop, D, Wong, S T, Wong, S, Walsh, C A
Published in Neurology (04.12.2007)
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Efficient photodiodes from interpenetrating polymer networks
Halls, J. J. M, Walsh, C. A, Greenham, N. C, Marseglia, E. A, Friend, R. H, Moratti, S. C, Holmes, A. B
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Mode of delivery in pregnancies complicated by major fetal congenital heart disease: a retrospective cohort study
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Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia
Chang, B S, Ly, J, Appignani, B, Bodell, A, Apse, K A, Ravenscroft, R S, Sheen, V L, Doherty, M J, Hackney, D B, O'Connor, M, Galaburda, A M, Walsh, C A
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Expanding the clinical spectrum of biallelic ZNF335 variants
Stouffs, K., Stergachis, A.B., Vanderhasselt, T., Dica, A., Janssens, S., Vandervore, L., Gheldof, A., Bodamer, O., Keymolen, K., Seneca, S., Liebaers, I., Jayaraman, D., Hill, H.E., Partlow, J.N., Walsh, C.A., Jansen, A.C.
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Published in Clinical genetics (01.08.2018)
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Childhood Abuse and Lifetime Psychopathology in a Community Sample
MacMillan, Harriet L., Fleming, Jan E., Streiner, David L., Lin, Elizabeth, Boyle, Michael H., Jamieson, Ellen, Duku, Eric K., Walsh, Christine A., Wong, Maria Y.-Y., Beardslee, William R.
Published in The American journal of psychiatry (01.11.2001)
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