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Genetic malformations of the human cerebral cortex.
Walsh CA. Walsh CA. Neuron. 1999 May;23(1):19-29. doi: 10.1016/s0896-6273(00)80749-7. Neuron. 1999. PMID: 10402190 Review. No abstract available.
Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development.
Ekşioğlu YZ, Scheffer IE, Cardenas P, Knoll J, DiMario F, Ramsby G, Berg M, Kamuro K, Berkovic SF, Duyk GM, Parisi J, Huttenlocher PR, Walsh CA. Ekşioğlu YZ, et al. Among authors: walsh ca. Neuron. 1996 Jan;16(1):77-87. doi: 10.1016/s0896-6273(00)80025-2. Neuron. 1996. PMID: 8562093
Neural development: identical twins separated at birth?
Walsh CA. Walsh CA. Curr Biol. 1996 Jan 1;6(1):26-8. doi: 10.1016/s0960-9822(02)00413-x. Curr Biol. 1996. PMID: 8805214 Review.
Early development of the cerebral cortex.
Reid CB, Walsh CA. Reid CB, et al. Among authors: walsh ca. Prog Brain Res. 1996;108:17-30. doi: 10.1016/s0079-6123(08)62529-7. Prog Brain Res. 1996. PMID: 8979791 Review. No abstract available.
Clonal dispersion and evidence for asymmetric cell division in ferret cortex.
Reid CB, Tavazoie SF, Walsh CA. Reid CB, et al. Among authors: walsh ca. Development. 1997 Jun;124(12):2441-50. Development. 1997. PMID: 9199370
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse.
Ware ML, Fox JW, González JL, Davis NM, Lambert de Rouvroit C, Russo CJ, Chua SC Jr, Goffinet AM, Walsh CA. Ware ML, et al. Among authors: walsh ca. Neuron. 1997 Aug;19(2):239-49. doi: 10.1016/s0896-6273(00)80936-8. Neuron. 1997. PMID: 9292716
Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.
González JL, Russo CJ, Goldowitz D, Sweet HO, Davisson MT, Walsh CA. González JL, et al. Among authors: walsh ca. J Neurosci. 1997 Dec 1;17(23):9204-11. doi: 10.1523/JNEUROSCI.17-23-09204.1997. J Neurosci. 1997. PMID: 9364067 Free PMC article.
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Cell. 1998 Jan 9;92(1):63-72. doi: 10.1016/s0092-8674(00)80899-5. Cell. 1998. PMID: 9489700
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
Fox JW, Lamperti ED, Ekşioğlu YZ, Hong SE, Feng Y, Graham DA, Scheffer IE, Dobyns WB, Hirsch BA, Radtke RA, Berkovic SF, Huttenlocher PR, Walsh CA. Fox JW, et al. Among authors: walsh ca. Neuron. 1998 Dec;21(6):1315-25. doi: 10.1016/s0896-6273(00)80651-0. Neuron. 1998. PMID: 9883725
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
Gleeson JG, Minnerath SR, Fox JW, Allen KM, Luo RF, Hong SE, Berg MJ, Kuzniecky R, Reitnauer PJ, Borgatti R, Mira AP, Guerrini R, Holmes GL, Rooney CM, Berkovic S, Scheffer I, Cooper EC, Ricci S, Cusmai R, Crawford TO, Leroy R, Andermann E, Wheless JW, Dobyns WB, Walsh CA, et al. Gleeson JG, et al. Among authors: walsh ca. Ann Neurol. 1999 Feb;45(2):146-53. doi: 10.1002/1531-8249(199902)45:2<146::aid-ana3>3.0.co;2-n. Ann Neurol. 1999. PMID: 9989615
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