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Low-Level Human Equivalent Gestational Lead Exposure Produces Supernormal Scotopic Electroretinograms, Increased Retinal Neurogenesis, and Decreased Retinal Dopamine Utilization in Rats

Fox, D. A., Kala, S. V., Hamilton, W. R., Johnson, J. E., & O'Callaghan, J. P. (2008) · Environmental Health Perspectives · doi:10.1289/ehp.11268 · Cited by 37

Neuroprotective effect of acid-sensing ion channel inhibitor psalmotoxin-1 after hypoxia–ischemia in newborn piglet striatum

Yang, Z.-J., Ni, X., Carter, E. L., Kibler, K. K., Martin, L. J., & Koehler, R. C. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.04.018 · Cited by 37

Fetal asphyctic preconditioning protects against perinatal asphyxia-induced behavioral consequences in adulthood

Strackx, E., van den Hove, D., Prickaerts, J., Zimmermann, L. J. I., Steinbusch, H. W. M., Blanco, C. E., Gavilanes, A. W. D., & Vles, J. S. H. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.11.040 · Cited by 37

Neonatal exposure to propofol affects BDNF but not CaMKII, GAP-43, synaptophysin and tau in the neonatal brain and causes an altered behavioural response to diazepam in the adult mouse brain

Pontén, E., Fredriksson, A., Gordh, T., Eriksson, P., & Viberg, H. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.04.019 · Cited by 37

Standards for preclinical research and publications in developmental anaesthetic neurotoxicity: expert opinion statement from the SmartTots preclinical working group

Chinn, G. A., Pearn, M. L., Vutskits, L., Mintz, C. D., Loepke, A. W., Lee, J., Chen, J., Bosnjak, Z. J., Brambrink, A. M., Jevtović‐Todorović, V., et al. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.01.011 · Cited by 38

Effects of antiepileptic drugs on mRNA levels of BDNF and NT-3 and cell neogenesis in the developing rat brain

Shi, X.-Y., Wang, J., Cui, H., Li, B., Lei, G.-F., & Sun, R. (2009) · Brain and Development · doi:10.1016/j.braindev.2009.03.012 · Cited by 37

Maturation‐Dependent Alcohol Resistance in the Developing Mouse: Cerebellar Neuronal Loss and Gene Expression During Alcohol‐Vulnerable and ‐Resistant Periods

Karaçay, B., Li, S., & Bonthius, D. J. (2008) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2008.00720.x · Cited by 37

Short-Term Memory Impairment and Reduced Hippocampal c-Fos Expression in an Animal Model of Fetal Alcohol Syndrome

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Prenatal measurement of the fetal cerebellum and cisterna cerebellomedullaris by ultrasound

Smith, P. A., Johansson, D., Tzannatos, C. A., & Campbell, S. C. (1986) · Prenatal Diagnosis · doi:10.1002/pd.1970060209 · Cited by 37

GABAB receptor antagonism abolishes the learning impairments in rats with chronic atypical absence seizures

Chan, K. F. Y., Burnham, W. M., Jia, Z., Cortez, M. A., & Snead, O. C. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.04.012 · Cited by 37

Participation of microRNA 124-CREB pathway: a parallel memory enhancing mechanism of standardised extract of Bacopa monniera (BESEB CDRI-08)

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Disproportionate Intrauterine Growth Intervention Trial At Term: DIGITAT

Boers, K. E., Bijlenga, D., Mol, B. W., le Cessie, S., Birnie, E., van Pampus, M. G., Stigter, R. H., Bloemenkamp, K. W. M., van Meir, C. A., van der Post, J., et al. (2007) · BMC Pregnancy and Childbirth · doi:10.1186/1471-2393-7-12 · Cited by 37

Duration of fetoscopic spina bifida repair does not affect the central nervous system in fetal lambs

Vergote, S., Joyeux, L., Basurto, D., Bleeser, T., Valenzuela, I. J., Valentyn, B., Emam, D., Watananirun, K., Bie, F. R. D., Aertsen, M., et al. (2023) · American Journal of Obstetrics & Gynecology MFM · doi:10.1016/j.ajogmf.2023.101156 · Cited by 3

43 Adding fetal surgery to general anesthesia does not impair brain development in the rabbit model

der Veeken, L. V., Emam, D., Bleeser, T., Valenzuela, I. J., Rex, S., & Deprest, J. A. (2021) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2020.12.119

Longitudinal evolution of central nervous system anomalies in fetuses with open spina bifida fetoscopic repair and correlation with neurologic outcome

Trigo, L., Eixarch, E., Faig, F., Gómez‐Chiari, M., Rebollo, M., Dalaqua, M., Gratacós, E., & Lapa, D. (2023) · American Journal of Obstetrics & Gynecology MFM · doi:10.1016/j.ajogmf.2023.100932 · Cited by 10

Neuroprotection is improved by watertightness of fetal spina bifida repair in the sheep model

Joyeux, L., van der Merwe, J., Aertsen, M., Patel, P. A., Khatoun, A., da Cunha, M. G. M. C. M., Vleeschauwer, S. D., Parra, J., Danzer, E., Laughlin, M. M., et al. (2022) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.24907 · Cited by 14

Safety and efficacy of fetal surgery techniques to close a spina bifida defect in the fetal lamb model: A systematic review

Joyeux, L., Bie, F. R. D., Danzer, E., Mieghem, T. V., Flake, A. W., & Deprest, J. A. (2018) · Prenatal Diagnosis · doi:10.1002/pd.5222 · Cited by 27