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Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Among authors: cross jh. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
Pallister-Killian syndrome: an unusual cause of epileptic spasms.
Sánchez-Carpintero R, McLellan A, Parmeggiani L, Cockwell AE, Ellis RJ, Cross JH, Eckhardt S, Guerrini R. Sánchez-Carpintero R, et al. Among authors: cross jh. Dev Med Child Neurol. 2005 Nov;47(11):776-9. doi: 10.1017/S0012162205001623. Dev Med Child Neurol. 2005. PMID: 16225743 Free article.
Mcm2 labelling of balloon cells in focal cortical dysplasia.
Thom M, Martinian L, Sisodiya SM, Cross JH, Williams G, Stoeber K, Harkness W, Harding BN. Thom M, et al. Among authors: cross jh. Neuropathol Appl Neurobiol. 2005 Dec;31(6):580-8. doi: 10.1111/j.1365-2990.2005.00651.x. Neuropathol Appl Neurobiol. 2005. PMID: 16281906
604 results