Comparative aspects of the brain growth spurt

Quantitative growth and development of human brain

Dobbing, J., & Sands, J. (1973) · Archives of Disease in Childhood · doi:10.1136/adc.48.10.757 · Cited by 1,442

The later development of the brain and its vulnerability

Dobbing, J. (1982) · Journal of Inherited Metabolic Disease · doi:10.1007/bf01805569 · Cited by 391

Scientific Foundations of Paediatrics

Polani, P. E. (1974) · Archives of Disease in Childhood · doi:10.1136/adc.49.11.914-a · Cited by 290

Scientific Foundations of Paediatrics

Haworth, J. C. (1975) · JAMA · doi:10.1001/jama.1975.03240140055034 · Cited by 284

Vulnerability of Developing Brain. IX. The Effect of Nutritional Growth Retardation on the Timing of the Brain Growth-Spurt

Dobbing, J., & Sands, J. (2009) · Biology of the Neonate · doi:10.1159/000240430 · Cited by 275

Prenatal and postnatal growth and development of the central nervous system of the pig

Dickerson, J. W. T., & Dobbing, J. (1967) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1967.0002 · Cited by 269

Growth and development of the brain and spinal cord of the guinea pig

Dobbing, J., & Sands, J. (1970) · Brain Research · doi:10.1016/0006-8993(70)90311-2 · Cited by 244

Growth and Development of the Rabbit Brain

Harel, S., Watanabe, K. S., Linke, I., & Schain, R. J. (2009) · Biology of the Neonate · doi:10.1159/000240527 · Cited by 121

Fetal and Postnatal Cellular Growth

(1976) · Archives of Disease in Childhood · doi:10.1136/adc.51.6.487 · Cited by 77

A comparison of the albino rat with man in respect to the growth of the brain and of the spinal cord

Donaldson, H. H. (1908) · Journal of Comparative Neurology and Psychology · doi:10.1002/cne.920180402 · Cited by 69

Murine Models for the Study of Fetal Alcohol Spectrum Disorders: An Overview

Almeida, L., Andreu-Férnández, V., Navarro‐Tapia, E., Aras‐López, R., Serra-Delgado, M., Martínez, L., García‐Algar, Ó., & Gómez‐Roig, M. D. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.00359 · Cited by 73

Developmental neurotoxic effects of two pesticides: Behavior and biomolecular studies on chlorpyrifos and carbaryl

Lee, I., Eriksson, P., Fredriksson, A., Buratovic, S., & Viberg, H. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.08.014 · Cited by 67

Early postnatal chronic intermittent hypoxia modifies hypoxic respiratory responses and long-term phrenic facilitation in adult rats

Reeves, S. R., Mitchell, G. S., & Gozal, D. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00851.2005 · Cited by 67

Early Postnatal Ethanol Exposure Has Long-Term Effects on the Performance of Male Rats in a Delayed Matching-to-Place Task in the Morris Water Maze

Girard, T. A., Xing, H.-C., Ward, G. R., & Wainwright, P. E. (2000) · Alcoholism Clinical and Experimental Research · doi:10.1097/00000374-200003000-00007 · Cited by 67

Neonatal sevoflurane anesthesia induces long-term memory impairment and decreases hippocampal PSD-95 expression without neuronal loss.

Wang, S.-Q., Fang, F., Xue, Z.-G., Cang, J., & Zhang, X.-G. (2013) · PubMed · Cited by 67

Behavioral Characterization of Seizures in Rats

Velı́šková, J. (2006) · Elsevier eBooks · doi:10.1016/b978-012088554-1/50050-5 · Cited by 67

Neuropathology in intrauterine growth restricted newborn piglets is associated with glial activation and proinflammatory status in the brain

Wixey, J. A., Lee, K. M., Miller, S. M., Goasdoué, K., Colditz, P. B., Bjorkman, S. T., & Chand, K. K. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1392-1 · Cited by 67

Neonatal glucocorticoids and the developing brain: short-term treatment with life-long consequences?

Bakker, J. M., van Bel, F., & Heijnen, C. J. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01948-2 · Cited by 67

Maternal dietary 22: 6n-3 is more effective than 18: 3n-3 in increasing the 22: 6n-3 content in phospholipids of glial cells from neonatal rat brain

Bowen, R. A. R., & Clandinin, M. T. (2005) · British Journal Of Nutrition · doi:10.1079/bjn20041390 · Cited by 67

Cooling the newborn after asphyxia — physiological and experimental background and its clinical use

Thoresen, M. (2000) · Seminars in Neonatology · doi:10.1053/siny.1999.0118 · Cited by 67

Effects of Methyl Mercury in Postnatal Developing Rats

Sakamoto, M., Nakano, A., Kajiwara, Y., Naruse, I., & Fujisaki, T. (1993) · Environmental Research · doi:10.1006/enrs.1993.1048 · Cited by 67

Effects of early life exposure to traffic-related air pollution on brain development in juvenile Sprague-Dawley rats

Patten, K. T., González, E. A., Valenzuela, A. E., Berg, E. L., Wallis, C., Garbow, J. R., Silverman, J. L., Bein, K. J., Wexler, A. S., & Lein, P. J. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-0845-3 · Cited by 66

Topical Review: Animal Models of Germinal Matrix Hemorrhage

Balasubramaniam, J., & Bigio, M. R. D. (2006) · Journal of Child Neurology · doi:10.1177/08830738060210050201 · Cited by 66

Neurodevelopmental and neurofunctional outcomes in children with congenital diaphragmatic hernia

Danzer, E., & Hedrick, H. L. (2011) · Early Human Development · doi:10.1016/j.earlhumdev.2011.05.005 · Cited by 66

The Neurobiological Foundations of Giftedness

Mrázik, M., & Dombrowski, S. C. (2010) · Roeper Review · doi:10.1080/02783193.2010.508154 · Cited by 75

Long‐lasting effects of neonatal dexamethasone treatment on spatial learning and hippocampal synaptic plasticity. Involvement of the NMDA receptor complex

Kamphuis, P. J. G. H., Gardoni, F., Kamal, A., Croiset, G., Bakker, J. M., Cattabeni, F., Gispen, W. H., van Bel, F., Luca, M. D., & Wiegant, V. M. (2003) · The FASEB Journal · doi:10.1096/fj.02-0333fje · Cited by 66

An examination of sex differences in the effects of early-life opiate and alcohol exposure

Terasaki, L. S., Gomez, J., & Schwarz, J. M. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0123 · Cited by 66

Glutamate and GABA receptor dysfunction in the fetal alcohol syndrome

Olney, J. W., Wozniak, D. F., Jevtović‐Todorović, V., Farber, N. B., Bittigau, P., & Ikonomidou, C. (2002) · Neurotoxicity Research · doi:10.1080/1029842021000010875 · Cited by 66

Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies

Galanopoulou, A. S., & Moshé, S. L. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.04.015 · Cited by 65

Rescuing the neonatal brain from hypoxic injury with autologous cord blood

Liao, Y., Cotten, M., Tan, S., Kurtzberg, J., & Cairo, M. S. (2012) · Bone Marrow Transplantation · doi:10.1038/bmt.2012.169 · Cited by 65

In Vivo Monitoring of Sevoflurane-induced Adverse Effects in Neonatal Nonhuman Primates Using Small-animal Positron Emission Tomography

Zhang, X., Liu, S., Newport, G. D., Paule, M. G., Callicott, R. J., Thompson, J., Liu, F., Patterson, T. A., Berridge, M. S., Apana, S. M., et al. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001154 · Cited by 65

The role of matrix metalloproteinases in infant traumatic brain injury

Sifringer, M., Stefovska, V. G., Zentner, I., Hansen, B., Stepulak, A., Knaute, C., Marzahn, J., & Ikonomidou, C. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.10.019 · Cited by 68

Lasting Effects of Developmental Dexamethasone Treatment on Neural Cell Number and Size, Synaptic Activity, and Cell Signaling: Critical Periods of Vulnerability, Dose–Effect Relationships, Regional Targets, and Sex Selectivity

Kreider, M. L., Tate, C. A., Cousins, M. M., Oliver, C. A., Seidler, F. J., & Slotkin, T. A. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300783 · Cited by 65

Correlation between level of (n − 3) polyunsaturated fatty acids in brain phospholipids and learning ability in rats. A multiple generation study

Jensen, M. M., Skarsfeldt, T., & Høy, C. (1996) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(96)00007-0 · Cited by 65

Development and Plasticity

Gollin, E. S. (1981) · Elsevier eBooks · doi:10.1016/b978-0-12-289620-0.50017-9 · Cited by 66

Ketamine-induced apoptosis in cultured rat cortical neurons

Takadera, T., Ishida, A., & Ohyashiki, T. (2005) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2005.10.005 · Cited by 64

Altered Mitochondrial Dynamics Contributes to Propofol-induced Cell Death in Human Stem Cell–derived Neurons

Twaroski, D. M., Yan, Y., Žaja, I., Clark, E., Bosnjak, Z. J., & Bai, X. (2015) · Anesthesiology · doi:10.1097/aln.0000000000000857 · Cited by 64

Variability of brain lesions in rats administered methylmercury at various postnatal development phases

Wakabayashi, K., Kakita, A., Sakamoto, M., Su, M., Iwanaga, K., & Ikuta, F. (1995) · Brain Research · doi:10.1016/0006-8993(95)01208-7 · Cited by 64

Glucose affects the severity of hypoxic-ischemic brain injury in newborn pigs.

LeBlanc, M. H., Huang, M. H., VIG, V., Patel, D. M., & Smith, E. E. (1993) · Stroke · doi:10.1161/01.str.24.7.1055 · Cited by 64

Anesthetic Neurotoxicity in Newborns

Anand, K. J. S. (2007) · Anesthesiology · doi:10.1097/01.anes.0000268484.05444.35 · Cited by 64

Domoic Acid Epileptic Disease

Ramsdell, J. S., & Gulland, F. M. D. (2014) · Marine Drugs · doi:10.3390/md12031185 · Cited by 63

Developmental changes in the expression of creatine synthesizing enzymes and creatine transporter in a precocial rodent, the spiny mouse

Ireland, Z., Russell, A. P., Wallimann, T., Walker, D. W., & Snow, R. J. (2009) · BMC Developmental Biology · doi:10.1186/1471-213x-9-39 · Cited by 63

Low-level Gestational Lead Exposure Alters Dendritic Spine Plasticity in the Hippocampus and Reduces Learning and Memory in Rats

Zhao, Z., Zheng, G., Wang, T., Du, K., Han, X., Luo, W., Shen, X., & Chen, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-21521-8 · Cited by 64

Alcohol as an early life stressor: Epigenetics, metabolic, neuroendocrine and neurobehavioral implications

Ciafrè, S., Ferraguti, G., Greco, A., Polimeni, A., Ralli, M., Ceci, F. M., Ceccanti, M., & Fiore, M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.08.018 · Cited by 64

Deficiency of neuronal nitric oxide synthase (nNOS) worsens alcohol-induced microencephaly and neuronal loss in developing mice

Bonthius, D. J., Tzouras, G., Karaçay, B., Mahoney, J. C., Hutton, A. M., McKim, R., & Pantazis, N. J. (2002) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00458-3 · Cited by 63

Pentoxifylline Attenuates Hypoxic-Ischemic Brain Injury in Immature Rats

Eun, B., Liu, X.-H., & Barks, J. (2000) · Pediatric Research · doi:10.1203/00006450-200001000-00014 · Cited by 63

Morphological changes in white matter astrocytes in response to hypoxia/ischemia in the neonatal pig

Sullivan, S. M., Björkman, S. T., Miller, S. M., Colditz, P. B., & Pow, D. V. (2010) · Brain Research · doi:10.1016/j.brainres.2010.01.010 · Cited by 63

Altered organization of cortical interneurons in rats exposed to ethanol during neonatal life

Granato, A. (2005) · Brain Research · doi:10.1016/j.brainres.2005.11.024 · Cited by 62

Controversies in Neonatal Seizure Management

Glass, H. C., & Wirrell, E. C. (2009) · Journal of Child Neurology · doi:10.1177/0883073808327832 · Cited by 62

Glucose given after hypoxic ischemia does not affect brain injury in piglets.

LeBlanc, M. H., Huang, M. H., Patel, D. M., Smith, E. E., & Devidas, M. (1994) · Stroke · doi:10.1161/01.str.25.7.1443 · Cited by 62

Propofol-Induced Changes in Neurotrophic Signaling in the Developing Nervous System In Vivo

Popić, J., Pešić, V., Milanović, D., Todorovic, S. T., Kanazir, S., Jevtović‐Todorović, V., & Ruždijić, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034396 · Cited by 62

The effects of ethanol on the developing cerebellum and eyeblink classical conditioning

Green, J. T. (2004) · The Cerebellum · doi:10.1080/14734220410017338 · Cited by 62

Neonatal ethanol produces cerebellar deep nuclear cell loss and correlated disruption of eyeblink conditioning in adult rats

Green, J. T., Tran, T. D., Steinmetz, J. E., & Goodlett, C. R. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03561-8 · Cited by 62

Short- and long-term effects of perinatal asphyxia on monoamine, amino acid and glycolysis product levels measured in the basal ganglia of the rat

Chen, Y., Engidawork, E., Loidl, C. F., Dell’Anna, E., Goiny, M., Lübec, G., Andersson, K., & Herrera‐Marschitz, M. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00131-4 · Cited by 62

The effects of neonatal ethanol and/or cocaine exposure on isolation-induced ultrasonic vocalizations

Barron, S., Segar, T. M., Yahr, J. S., Baseheart, B. J., & Willford, J. A. (2000) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(00)00304-x · Cited by 62

The Colostrum-Deprived Piglet as a Model for Study of Infant Lipid Nutrition

Innis, S. M. (1993) · Journal of Nutrition · doi:10.1093/jn/123.suppl_2.386 · Cited by 62

SIGNAL TRANSDUCTION IN ENVIRONMENTAL NEUROTOXICITY

Costa, L. G. (1998) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.38.1.21 · Cited by 62

Ethanol causes and lithium prevents neuroapoptosis and suppression of pERK in the infant mouse brain

Young, C., Straiko, M. M. W., Johnson, S. A., Creeley, C. E., & Olney, J. W. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.05.009 · Cited by 61

Postnatal development of the amygdala: A stereological study in rats

Chareyron, L. J., Lavenex, P. B., & Lavenex, P. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23132 · Cited by 64

Effects of hyperglycemia or hypoglycemia on brain cell membrane function and energy metabolism during the immediate reoxygenation–reperfusion period after acute transient global hypoxia–ischemia in the newborn piglet

Park, W. S., Chang, Y. S., & Lee, M. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02295-8 · Cited by 61

Central neuropeptide systems and respiratory control during development

Moss, I. R., & Laferrière, A. (2002) · Respiratory Physiology & Neurobiology · doi:10.1016/s1569-9048(02)00034-4 · Cited by 61

Effects of Repeated Oral Postnatal Exposure to Chlorpyrifos on Cholinergic Neurochemistry in Developing Rats

Richardson, J. R. (2005) · Toxicological Sciences · doi:10.1093/toxsci/kfi081 · Cited by 61

Does transferrin have a special role in the nervous system?

Monteros, A. E. D. L., Peña, L. A., & de Vellis, J. (1989) · Journal of Neuroscience Research · doi:10.1002/jnr.490240202 · Cited by 61

A systematic review of therapeutic ketamine use in children and adolescents with treatment-resistant mood disorders

Kim, S. W., Rush, B. S., & Rice, T. (2020) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-020-01542-3 · Cited by 62

Deficits in trace fear conditioning in a rat model of fetal alcohol exposure: dose–response and timing effects

Hunt, P. S., Jacobson, S. E., & Torok, E. J. (2009) · Alcohol · doi:10.1016/j.alcohol.2009.08.004 · Cited by 60

Acute oligodendrocyte loss with persistent white matter injury in a third trimester equivalent mouse model of fetal alcohol spectrum disorder

Newville, J., Valenzuela, C. F., Li, L., Jantzie, L. L., & Cunningham, L. A. (2017) · Glia · doi:10.1002/glia.23164 · Cited by 70

Ketamine induces hippocampal apoptosis through a mechanism associated with the caspase-1 dependent pyroptosis

Ye, Z., Li, Q., Guo, Q., Xiong, Y., Guo, D., Hong, Y., & Shu, Y. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.09.035 · Cited by 60

Vasopressin excites interneurons to suppress hippocampal network activity across a broad span of brain maturity at birth

Spoljaric, A., Seja, P., Spoljaric, I., Virtanen, M. A., Lindfors, J., Uvarov, P., Summanen, M., Crow, A., Hsueh, B., Puskarjov, M., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717337114 · Cited by 60

Neuroanesthesiology Update

Pasternak, J. J., & Lanier, W. L. (2009) · Journal of Neurosurgical Anesthesiology · doi:10.1097/ana.0000000000000048 · Cited by 61

Use of Pup in a Cup Model to Study Brain Development

West, J. R. (1993) · Journal of Nutrition · doi:10.1093/jn/123.suppl_2.382 · Cited by 60

The identification and long term effects of fetal growth restriction

Pryor, J. E. (1997) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.1997.tb10933.x · Cited by 60

Cortico-thalamic connectivity is vulnerable to nicotine exposure during early postnatal development through α4/β2/α5 nicotinic acetylcholine receptors

Heath, C. J., King, S. L., Gotti, C., Marks, M. J., & Picciotto, M. R. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.130 · Cited by 59

Paracetamol (Acetaminophen) and the Developing Brain

Bührer, C., Endesfelder, S., Scheuer, T., & Schmitz, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011156 · Cited by 62

Perinatal Hyperoxia and Developmental Consequences on the Lung‐Brain Axis

Obst, S., Herz, J., Alcazar, M. A. A., Endesfelder, S., Möbius, M. A., Rüdiger, M., Felderhoff‐Müser, U., & Bendix, I. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/5784146 · Cited by 60

Effect of Propofol in the Immature Rat Brain on Short- and Long-Term Neurodevelopmental Outcome

Karen, T., Schlager, G. W., Bendix, I., Sifringer, M., Herrmann, R., Pantazis, C., Enot, D. P., Keller, M., Kerner, T., & Felderhoff‐Mueser, U. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064480 · Cited by 61

Postnatal day 7 ethanol treatment causes persistent reductions in adult mouse brain volume and cortical neurons with sex specific effects on neurogenesis

Coleman, L. G., Oğuz, İ., Lee, J., Styner, M. A., & Crews, F. T. (2012) · Alcohol · doi:10.1016/j.alcohol.2012.01.003 · Cited by 59

Dose-dependent effects of methylmercury administered during neonatal brain spurt in rats

Sakamoto, M., Kakita, A., de Oliveira, R. B., Pan, H. S., & Takahashi, H. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2004.06.016 · Cited by 60

Low-Dose Ionizing Radiation Rapidly Affects Mitochondrial and Synaptic Signaling Pathways in Murine Hippocampus and Cortex

Kempf, S. J., Moertl, S., Sepe, S., von Toerne, C., Hauck, S. M., Atkinson, M. J., Mastroberardino, P. G., & Tapio, S. (2015) · Journal of Proteome Research · doi:10.1021/acs.jproteome.5b00114 · Cited by 59

Perinatal exposure to concentrated ambient particulates results in autism-like behavioral deficits in adult mice

Church, J. S., Tijerina, P. B., Emerson, F. J., Coburn, M. A., Blum, J. L., Zelikoff, J. T., & Schwartzer, J. J. (2018) · NeuroToxicology · doi:10.1016/j.neuro.2017.10.007 · Cited by 59

Pig Brains Have Homologous Resting-State Networks with Human Brains

Simchick, G. A., Shen, A., Campbell, B., Park, H. J., West, F. D., & Zhao, Q. C. (2019) · Brain Connectivity · doi:10.1089/brain.2019.0673 · Cited by 63

Therapeutic motor training ameliorates cerebellar effects of postnatal binge alcohol

Klintsova, A. Y., Goodlett, C. R., & Greenough, W. T. (2000) · Neurotoxicology and Teratology · doi:10.1016/s0892-0362(99)00052-5 · Cited by 59

Is Docosahexaenoic Acid Necessary in Infant Formula? Evaluation of High Linolenate Diets in the Neonatal Rat

Woods, J., Ward, G. R., & Salem, N. (1996) · Pediatric Research · doi:10.1203/00006450-199611000-00007 · Cited by 59

Fetal Glucocorticoid Exposure and Hypothalamo‐Pituitary‐Adrenal (HPA) Function After Birth

Matthews, S. G., Owen, D., Kalabis, G. M., Banjanin, S., Setiawan, E. B., Dunn, E. A., & Andrews, M. H. (2004) · Endocrine Research · doi:10.1081/erc-200044091 · Cited by 59

The effects of dietary fatty acid composition combined with environmental enrichment on brain and behavior in mice

Wainwright, P. E., Huang, Y. S., Bulman‐Fleming, B., Lévesque, S., & McCutcheon, D. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90139-2 · Cited by 59

Relationship between circulating IGF-1 levels and traumatic brain injury-induced hippocampal damage and cognitive dysfunction in immature rats

Ozdemir, D., Baykara, B., Aksu, I., Kiray, M., Sisman, A. R., Cetin, F., Dayi, A., Gurpinar, T., Uysal, N., & Arda, M. N. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2011.11.059 · Cited by 58

Behavioral assessment of cognitive function using a translational neonatal piglet model

Dilger, R. N., & Johnson, R. W. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.05.008 · Cited by 58

Sex-specific consequences of early life seizures

Akman, Ö., Moshé, S. L., & Galanopoulou, A. S. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.05.021 · Cited by 58

Chronic postnatal DE-71 exposure: Effects on learning, attention and thyroxine levels

Driscoll, L. L., Gibson, A., & Hieb, A. (2008) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2008.11.003 · Cited by 58

Effect of general anesthetics on the developing brain

Reddy, S. (2012) · Journal of Anaesthesiology Clinical Pharmacology · doi:10.4103/0970-9185.92426 · Cited by 58

Neuroprotection provided by isoflurane pre-conditioning and post-conditioning

Sun, Y.-Z., Chen, G., Jiang, M., Sun, L., Feng, D., Yu, Z., & Gao, R. (2017) · Medical Gas Research · doi:10.4103/2045-9912.202910 · Cited by 58

Is neuronal death required for seizure-induced epileptogenesis in the immature brain?

Baram, T. Z., Eghbal-Ahmadi, M., & Bender, R. A. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)35033-7 · Cited by 58

Embryonic Exposure to Domoic Acid Increases the Susceptibility of Zebrafish Larvae to the Chemical Convulsant Pentylenetetrazole

Tiedeken, J. A., & Ramsdell, J. S. (2007) · Environmental Health Perspectives · doi:10.1289/ehp.10344 · Cited by 58

Postnatal neurogenesis in the dentate gyrus of the guinea pig

Guidi, S., Ciani, E., Severi, S., Contestabile, A., & Bartesaghi, R. (2004) · Hippocampus · doi:10.1002/hipo.20050 · Cited by 59

Molecular Regulation of Acute Ethanol-Induced Neuron Apoptosis

Akhtar, L. N., Klocke, B. J., & Roth, K. A. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.6.490 · Cited by 60

Antenatal corticosteroids: is more better?

Smith, G. N., Kingdom, J. C., Penning, D. H., & Matthews, S. G. (2000) · The Lancet · doi:10.1016/s0140-6736(99)00448-1 · Cited by 58

Unbiased cell quantification reveals a continued increase in the number of neocortical neurones during early post‐natal development in mice

Lyck, L., Krøigård, T., & Finsen, B. R. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05763.x · Cited by 57

Long-term alterations to the brain transcriptome in a maternal voluntary consumption model of fetal alcohol spectrum disorders

Kleiber, M. L., Laufer, B. I., Wright, E., Chater‐Diehl, E., & Singh, S. M. (2012) · Brain Research · doi:10.1016/j.brainres.2012.04.016 · Cited by 59

Developmental Exposure to Manganese Increases Adult Susceptibility to Inflammatory Activation of Glia and Neuronal Protein Nitration

Moreno, J. A., Streifel, K. M., Sullivan, K. A., Legare, M. E., & Tjalkens, R. B. (2009) · Toxicological Sciences · doi:10.1093/toxsci/kfp221 · Cited by 57

Alteration of Gene Expression, DNA Methylation, and Histone Methylation in Free Radical Scavenging Networks in Adult Mouse Hippocampus following Fetal Alcohol Exposure

Chater‐Diehl, E., Laufer, B. I., Castellani, C. A., Alberry, B., & Singh, S. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154836 · Cited by 57

Neurotrophins in the Brain

Boschen, K. E., & Klintsova, A. Y. (2016) · Vitamins and hormones · doi:10.1016/bs.vh.2016.10.008 · Cited by 61

Animal models for neonatal brain injury induced by hypoxic ischemic conditions in rodents

Hamdy, N., Eide, S., Sun, H., & Feng, Z. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113457 · Cited by 61

Determination of nutritional requirements in preterm infants, with special reference to ‘catch-up’ growth

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Fetal dexamethasone exposure alters macromolecular characteristics of rat brain development: A critical period for regionally selective alterations?

Carlos, R. Q., Seidler, F. J., & Slotkin, T. A. (1992) · Teratology · doi:10.1002/tera.1420460108 · Cited by 57

Ethanol-induced alterations of neurotrophin receptor expression on Purkinje cells in the neonatal rat cerebellum

Light, K. E., Brown, D. P., Newton, B. W., Belcher, S. M., & Kane, C. J. M. (2002) · Brain Research · doi:10.1016/s0006-8993(01)03224-3 · Cited by 57

Conversion of alpha-linolenate to docosahexaenoate is not depressed by high dietary levels of linoleate in young rats: tracer evidence using high precision mass spectrometry.

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Long-term behavioral and developmental consequences of pre- and perinatal nicotine

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Prenatal exposure to selective serotonin reuptake inhibitors (SSRI) increases aggression and modulates maternal behavior in offspring mice

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The Epigenetic Role of Vitamin C in Neurodevelopment

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Learning and memory impairment in rats with chronic atypical absence seizures

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Changes in synaptic transmission and protein expression in the brains of adult offspring after prenatal inhibition of the kynurenine pathway

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

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

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

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

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

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