The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Intrauterine Growth Restriction: Antenatal and Postnatal Aspects
Open accessAbstract
Intrauterine growth restriction (IUGR), a condition that occurs due to various reasons, is an important cause of fetal and neonatal morbidity and mortality. It has been defined as a rate of fetal growth that is less than normal in light of the growth potential of that specific infant. Usually, IUGR and small for gestational age (SGA) are used interchangeably in literature, even though there exist minute differences between them. SGA has been defined as having birth weight less than two standard deviations below the mean or less than the 10th percentile of a population-specific birth weight for specific gestational age. These infants have many acute neonatal problems that include perinatal asphyxia, hypothermia, hypoglycemia, and polycythemia. The likely long-term complications that are prone to develop when IUGR infants grow up includes growth retardation, major and subtle neurodevelopmental handicaps, and developmental origin of health and disease. In this review, we have covered various antenatal and postnatal aspects of IUGR.
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Cites
The origins of the developmental origins theory
Barker, D. J. P. (2007) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2007.01809.x · Cited by 2,955
INFANT MORTALITY, CHILDHOOD NUTRITION, AND ISCHAEMIC HEART DISEASE IN ENGLAND AND WALES
BARKER, D. (1986) · The Lancet · doi:10.1016/s0140-6736(86)91340-1 · Cited by 2,892
Fetal and placental size and risk of hypertension in adult life.
Barker, D. J., Bull, A. R., Osmond, C., & Simmonds, S. J. (1990) · BMJ · doi:10.1136/bmj.301.6746.259 · Cited by 1,728
Bhutta, Z. A., Das, J. K., Bahl, R., Lawn, J. E., Salam, R. A., Paul, V. K., Sankar, M. J., Blencowe, H., Rizvi, A., Chou, V. B., et al. (2014) · The Lancet · doi:10.1016/s0140-6736(14)60792-3 · Cited by 1,367
The GRIT Study Group, & article, P. A. L. A. T. E. O. T. (2003) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1046/j.1471-0528.2003.02014.x · Cited by 305
Baschat, A. A., Gembruch, U., Weiner, C. P., & Harman, C. R. (2003) · Ultrasound in Obstetrics & Gynecology · doi:10.1002/uog.149 · Cited by 166
Systematic review and meta-analysis of middle cerebral artery Doppler to predict perinatal wellbeing
Morris, R. K., Say, R., Robson, S. C., Kleijnen, J., & Khan, K. S. (2012) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2012.07.027 · Cited by 70
Cited by
Cutland, C. L., Lackritz, E. M., Mallett-Moore, T., Bardají, A., Chandrasekaran, R., Lahariya, C., Nisar, M. I., Tapia, M. D., Pathirana, J., Kochhar, S., et al. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.01.049 · Cited by 459
Neonatal Morbidities of Fetal Growth Restriction: Pathophysiology and Impact
Malhotra, A., Allison, B. J., Castillo-Melendez, M., Jenkin, G., Polglase, G. R., & Miller, S. L. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00055 · Cited by 453
Hirschsprung disease — integrating basic science and clinical medicine to improve outcomes
Heuckeroth, R. O. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2017.149 · Cited by 304
Fetal growth restriction and stillbirth: Biomarkers for identifying at risk fetuses
King, V. J., Bennet, L., Stone, P. R., Clark, A., Gunn, A. J., & Dhillon, S. K. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.959750 · Cited by 52
Alves, M. B., Laureano, D. P., Dalle Molle, R., Machado, T. D., Salvador, A. P. D. A., Miguel, P. M., Lupinsky, D., Dalmaz, C., & Silveira, P. P. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.03.010 · Cited by 30
Metadata
- Authors
- Sharma, D., Shastri, S., & Sharma, P.
- Venue
- Clinical Medicine Insights: Pediatrics
- Publisher
- SAGE Publications
- Published
- 2016-01
- Volume
- 10
- Pages
- 67-83
- ISSN
- 1178-220X (ISSN-L)
- 1179-5565
- OpenAlex
- W2463560934
- Cited by
- 860
- References
- 7
- FWCI
- 57.90
- Type
- journal article
- Language
- en
- Open access
- gold
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