Lobna Mansour

MA, K., M. L, and S. RA, "Screening for galactose is : is there a place for it ? ", Int J Gen Med , vol. 12, issue May 2019 , pp. 193 - 205 , Submitted.

, "Biallelic loss of human CTNNA2 ,encoding alpha N- - catering, leads to ARP2/3 complex over activity and disordered cortical neuronal migration ", Nature genetics , vol. 50, issue August 2018 , pp. 1093- 1101 , 2018.

, "Pilot study of classic galactosemia: Neurodevelopemental impact and other complications urge neonatal screening in egypt.", j.jare, 2018.

, "Polymorphisms of Immunoglobulin G Fc Receptors in Pediatric Guillain–Barré Syndrome", Neruropediatrics, vol. 47, pp. 151-156, 2016.

, "Genotype-phenotype relationship among Egyptian children with Rett syndrome", J Egypt Public Health Assoc, vol. 90, issue 3, pp. 133-137, 2015.

, "Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis", Clinical Genetics, vol. 88, pp. 95-97, 2015.

TJ, D. - S., S. JL, U. N, S. J, B. S, S. AE, O. J, B. V, Z. MS, A. - S. GH, et al., "Exome sequencing can improve diagnosis and alter patient management.", Sci Transl Med, vol. 13;4, issue 138, pp. 138ra78. doi: 10.1126, 2012.

G, N., F. AG, Z. MS, H. M, S. JL, H. AD, A. M, R. B, S. E, and M. L, "Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders", Science. , vol. 31;343, issue 6170, pp. 506-11. doi: 10.1126, 2014.