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Your search keyword '"Barrow, M"' showing total 35 results
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35 results on '"Barrow, M"'

5. Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders

Author

Ozgen, HM, primary, van Daalen, E, additional, Bolton, PF, additional, Maloney, VK, additional, Huang, S, additional, Cresswell, L, additional, van den Boogaard, MJ, additional, Eleveld, MJ, additional, van ‘t Slot, R, additional, Hochstenbach, R, additional, Beemer, FA, additional, Barrow, M, additional, Barber, JCK, additional, and Poot, M, additional

Published
2009
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28. ChemInform Abstract: METAL COMPLEXES OF NOVEL SULFUR‐ AND PHOSPHORUS‐CONTAINING HETEROCYCLES, PREPARATION AND STRUCTURE OF TRICARBONYL‐ETA(4)‐(1‐PENTAFLUOROPHENYL‐2,3,4,5‐TETRAKISTRIFLUOROMETHYLTHIOPHEN)MANGANESE AND PI‐CYCLOPENTADIENYL‐(1‐HYDROXY‐2,3,4,5‐TETRAKISTRIFLUOROMETHYLPHOSPHOLE‐1‐OXIDE)COBALT

Author

BARROW, M. J., primary, DAVIDSON, J. L., additional, HARRISON, W., additional, SHARP, D. W. A., additional, SIM, G. A., additional, and WILSON, F. B., additional

Published
1973
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33. Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population.

Author

Navti OB, Kinning E, Vasudevan P, Barrow M, Porter H, Howarth E, Konje J, and Khare M

Subjects
Adolescent, Adult, Arthrogryposis diagnosis, Asian People ethnology, Black People ethnology, Family Health, Female, Gestational Age, Hospitals, Teaching, Humans, Infant, Newborn, Pedigree, Pregnancy, Pregnancy Outcome, Prevalence, Retrospective Studies, Ultrasonography, Prenatal, United Kingdom epidemiology, White People ethnology, Young Adult, Arthrogryposis ethnology, Arthrogryposis therapy, Ethnicity
Abstract

Objective: To review the prevalence and perinatal management of cases of arthrogryposis delivering at our hospital over a 6-year period., Methods: This was a retrospective review of cases of arthrogryposis managed at a UK teaching hospital. Cases were identified from the regional congenital anomalies register and departmental databases. Case notes were reviewed and analysed., Results: From 2002 to 2007, there were 27 cases of arthrogryposis. Sixteen (59.3%) were Caucasians, 7(25.9%) Asians and 4(14.8%) Afro-Caribbean; 17(63%) were nulliparous. In eight (29.6%) cases, there was a family history of congenital anomalies. Three had previously affected siblings and in three cases the parents were affected with arthrogryposis. Five (18.5%) were from consanguineous families. Eighteen (66.7%) cases were diagnosed prenatally at a mean gestational age of 21 weeks. Twelve (57%) were delivered by caesarean section. There were 18 live births. Sixteen (59%) cases were reviewed by clinical geneticist. Following detailed review and investigation including post-mortems, 20 (74%) of our cases had a formal diagnosis or likely cause identified., Conclusions: Suspected cases of arthrogryposis require multi-disciplinary management to optimise the possibility of making a diagnosis and providing parents with accurate information to enable them to make informed choices regarding the pregnancy and providing information regarding likelihood of recurrence., (Copyright (c) 2009 John Wiley & Sons, Ltd.)

Published
2010
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34. Familial congenital diaphragmatic hernia: prenatal diagnosis, management, and outcome.

Author

Narayan H, De Chazal R, Barrow M, McKeever P, and Neale E

Subjects
Abnormalities, Multiple diagnostic imaging, Adult, Female, Fetal Diseases genetics, Hernia, Diaphragmatic genetics, Hernias, Diaphragmatic, Congenital, Humans, Infant, Newborn, Lung abnormalities, Male, Obstetric Labor, Premature, Pedigree, Pregnancy, Pregnancy Trimester, Second, Pregnancy Trimester, Third, Fetal Diseases diagnostic imaging, Hernia, Diaphragmatic diagnostic imaging, Pregnancy Outcome, Ultrasonography, Prenatal
Abstract

Congenital diaphragmatic hernia (CDH) is a developmental defect of as yet unknown aetiology which accounts for 8 per cent of all major congenital anomalies and is associated with up to 80 per cent mortality despite optimal postnatal treatment. The risk of recurrence of CDH for future sibs after one affected infant is about 2 per cent. A multifactorial/threshold inheritance pattern with an observed high male:female sex ratio is currently favoured for the rare occurrence of familial CDH, although other modes of inheritance have also been described. We report three cases of familial CDH, two of whom were brother and sister sibs and the third was a first cousin, born within 18 months of each other. The diagnosis was by ultrasound and there were several factors predicting a poor outcome. The mortality in this group was 100 per cent. The prenatal diagnosis, treatment options, the unusual genetic aspects, outcome, and the pathology involved are discussed.

Published
1993
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35. A rapid method for detecting malformations in rat fetuses.

Author

Barrow MV and Taylor WJ

Subjects
Abnormalities, Multiple pathology, Animals, Anophthalmos pathology, Cleft Palate chemically induced, Cleft Palate pathology, Dissection, Female, Fetus, Methods, Microphthalmos pathology, Piperazines, Pregnancy, Rats, Congenital Abnormalities pathology, Histological Techniques
Published
1969
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