Search Results - "DAVIES, A. F"

Epidural infusion or combined femoral and sciatic nerve blocks as perioperative analgesia for knee arthroplasty by Davies, A.F., Segar, E.P., Murdoch, J., Wright, D.E., Wilson, I.H.

“…Peripheral neural blockade appears to provide effective analgesia with potentially less morbidity than central neuraxial techniques. We compared the relative…”
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Evaluation of the HemoCue compared with the Coulter STKS for measurement of neonatal haemoglobin by Rechner, I J, Twigg, A, Davies, A F, Imong, S

“…Objective: To compare the measurement of haemoglobin concentration ([Hb]) using the HemoCue haemoglobinometer with that using the Coulter STKS…”
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Efficacy of microfiltration in decreasing propofol‐induced pain by Davies, A. F., Vadodaria, B., Hopwood, B., Dexter, T., Conn, D.

“…Summary In a randomised, double‐blinded, two‐centre trial we evaluated the effect of a microbiological filter (Supor®, Pall Life Sciences) on propofol…”
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Delineation of two distinct 6p deletion syndromes by DAVIES, A. F, MIRZA, G, RAGOUSSIS, J, SEKHON, G, TURNPENNY, P, LEROY, F, SPELEMAN, F, LAW, C, VAN REGEMORTER, N, VAMOS, E, FLINTER, F

“…Deletions of the short arm of chromosome 6 are relatively rare, the main features being developmental delay, craniofacial malformations, hypotonia, and defects…”
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Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region by Davies, A F, Stephens, R J, Olavesen, M G, Heather, L, Dixon, M J, Magee, A, Flinter, F, Ragoussis, J

“…Orofacial clefting is genetically complex, no single gene being responsible for all forms. It can, however, result from a single gene defect either as part of…”
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Rapid molecular method for prenatal detection of Down's syndrome by Pertl, B, Yau, S C, Sherlock, J, Davies, A F, Mathew, C G, Adinolfi, M

“…We have evaluated a rapid method that allows prenatal detection of Down's syndrome in less than 24 hours. DNA from uncultured amniotic fluid, fetal blood, and…”
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Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting by Davies, A F, Imaizumi, K, Mirza, G, Stephens, R S, Kuroki, Y, Matsuno, M, Ragoussis, J

“…Chromosomal translocations affecting the 6p24 region have been associated with orofacial clefting. Here we present a female patient with cleft palate, severe…”
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The water balance of a sub-Arctic town by Semádeni-Davies, Annette F., Bengtsson, Lars

“…Urban water balances differ from their rural counterparts due to extreme spatial heterogeneity, water imported from outside catchment boundaries and changed…”
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FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs by Davies, A F, Barber, L, Murer-Orlando, M, Bobrow, M, Adinolfi, M

“…Techniques have been reported in which fluorescence in situ hybridisation (FISH) and cosmid probes are used to detect trisomy 21 (and other abnormalities…”
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A 46,XX fetus with external female and internal male genitalia, facial dysmorphic features and mildly dilated lateral ventricles of the brain: a new syndrome? by Becker, K, Seller, M J, Pal, K, Davies, A F

“…The clinical features of a 46,XX fetus with dysmorphic facial features, mild dilatation of the lateral ventricles of the brain, and female external and male…”
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A FISH probe specific for the telomeric region of 6p by Mirza, G, Davies, A F, Ragoussis, J

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A fetus with an X;1 balanced reciprocal translocation and eye disease by Seller, M J, Pal, K, Horsley, S, Davies, A F, Berry, A C, Meredith, R, McCartney, A C

“…A 19 week female fetus is described with a de novo X;1 reciprocal balanced translocation, with the breakpoint on the X chromosome at Xp11.4, and eye pathology…”
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An improved method for the detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization by Davies, A F, Barber, L, Murer-Orlando, M, Bobrow, M, Adinolfi, M

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Representation of Snow in Urban Drainage Models by Semádeni-Davies, Annette F

“…Modeling guidelines of parsimony (simplicity of assumptions), accuracy, modesty, and testability are discussed in terms of urban snowmelt induced runoff…”
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Characterization of terminal chromosome anomalies using multisubtelomere FISH by Davies, Angela F., Kirby, Toby L., Docherty, Zoe, Mackie Ogilvie, Caroline

“…Telomeric repeat sequences (TTAGGG) are known to cap the termini of every human chromosome. Proximal to these repeat sequences are chromosome‐specific repeat…”
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Characterization of a Chromosomally Complex Lung Cancer Cell Line Using Multiwell Fluorescence In Situ Hybridization by Ogilvie, C.Mackie, Shemilt, S, Davies, A.F, Weber-Hall, S, Chuang, C.-Y, Sundaresan, V

“…The chromosomal characterization of a non-small cell lung cancer cell line (NCIH358) is described. This characterization was achieved using a simple, cheap and…”
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Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex by Tripodis, N, Mason, R, Humphray, S J, Davies, A F, Herberg, J A, Trowsdale, J, Nizetic, D, Senger, G, Ragoussis, J

“…We have physically mapped and cloned a 2.5-Mb chromosomal segment flanking the centromeric end of the major histocompatibility complex (MHC). We characterized…”
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Generation of Novel Human MHC Class II Mutant B-Cell Lines by Integrating YAC DNA into a Cell Line Homozygously Deleted for the MHC Class II Region by Fabb, Stewart A., Davies, Angela F., Correa, Isabel, Kelly, Adrian P., Mackie, Caroline, Trowsdale, John, Ragoussis, Jiannis

“…The human B lymphoblastoid cell line (LCL) 721.174 sustains a large homozygous deletion in the major histocompatibility complex (MHC) class II region that…”
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A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome by Davies, A F, Olavesen, M G, Stephens, R J, Davidson, R, Delneste, D, Van Regemorter, N, Vamos, E, Flinter, F, Abusaad, I, Ragoussis, J

“…Deletions of the short arm of chromosome 6 are relatively rare, only 16 cases having been described in the literature so far. Here we present a detailed…”
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An integrated map of human chromosome 6p23 by Olavesen, M G, Davies, A F, Broxholme, S J, Wixon, J L, Senger, G, Nizetic, D, Campbell, R D, Ragoussis, J

“…The human chromosomal band 6p23 is a Giemsa-negative (light) band that may be expected to be relatively gene rich. The genes for spinocerebellar ataxia type 1…”
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