C. Taylor

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Clinical Practice Guidelines for the management of atypical Haemolytic Uraemic Syndrome in the United Kingdom

S. Wigmore, S. Machin, T. Goodship, 2010, British journal of haematology.

Prognosis, treatment and outcome of childhood mesangiocapillary (membranoproliferative) glomerulonephritis.

D. Milford, M. Saleem, S. Hulton, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

1,25-DIHYDROXYCHOLECALCIFEROL IN HYPOPARATHYROIDISM

L. F. Hill, S. Stanbury, C. Taylor, 1977, The Lancet.

Clinical limitations of the estimation of glomerular filtration rate from height/plasma creatinine ratio: a comparison with simultaneous 51Cr edetic acid slope clearance.

R. White, J. Davies, C. Taylor, 1982, Archives of disease in childhood.

Simplified quantification of urinary protein excretion in children.

P. Griffiths, R. White, C. Taylor, 1988, Clinical nephrology.

Antibody Cross-Linking of Myelin Oligodendrocyte Glycoprotein Leads to Its Rapid Repartitioning into Detergent-Insoluble Fractions, and Altered Protein Phosphorylation and Cell Morphology

S. Pfeiffer, T. Coetzee, C. Taylor, 2003, The Journal of Neuroscience.

Partial purification of a 5.7K glycoprotein from bovine vitreous which inhibits both angiogenesis and collagenase activity.

J. Weiss, C. Taylor, 1985, Biochemical and biophysical research communications.

Urinary L-lactate excretion is increased in renal Fanconi syndrome.

D. Milford, R. Gilbert, S. Hulton, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Failure of formation of 1,25-dihydroxycholecalciferol in chronic renal insufficiency.

E. Mawer, S. Stanbury, C. Taylor, 1973, Lancet.

TREATMENT OF HYPOPARATHYROIDISM WITH 1,25‐DIHYDROXYCHOLECALCIFEROL

L. F. Hill, S. Stanbury, C. Taylor, 1976, Clinical endocrinology.

Literature abstracts

D. Milford, M. Breuning, B. Rowe, 2004, Pediatric Nephrology.

A simple method to determine whole cell uptake of radiolabelled oestrogen and progesterone and their subcellular localization in breast cancer cell lines in monolayer culture.

D. Zava, C. Taylor, B. Blanchard, 1984, Journal of steroid biochemistry.

Effects of 24,25-dihydroxy-vitamin D3 on its plasma level in man.

J. Kanis, T. Cundy, R. Russell, 1981, Metabolic bone disease & related research.

Plasma levels of vitamin D metabolites in diphosphonate-treated rats.

J. Eisman, H. Fleisch, J. Bonjour, 1981, Clinical science.

Influence of prostaglandins and of cyclic nucleotides on the metabolism of 25-hydroxyvitamin D3 in primary chick kidney cell culture.

H. Fleisch, J. Bonjour, U. Trechsel, 1980, Biochemical and biophysical research communications.

1,25-Dihydroxycholecalciferol in human serum and its relationship with other metabolites of vitamin D-3.

E. Mawer, C. Taylor, J. Wallace, 1979, Clinica chimica acta; international journal of clinical chemistry.

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.

V. Sheffield, E. Stone, D. Schorderet, 1996, Archives of ophthalmology.

Effect of verocytotoxins (Shiga-like toxins) on human neutrophils in vitro

C. Savage, J. Holle, L. Harper, 2005, Pediatric Nephrology.

Advances in haemolytic uraemic syndrome

L. Monnens, C. Taylor, 1998, Archives of disease in childhood.

Renal histopathology in fatal cases of diarrhoea-associated haemolytic uraemic syndrome

D. Milford, A. Howie, C. Taylor, 1997, Pediatric Nephrology.

Verocytotoxin-producing Escherichia coli and the haemolytic uraemic syndrome.

C. Taylor, 1995, The Journal of infection.

Verocytotoxin-1 induces apoptosis in vero cells.

D. Milford, P. Rose, C. Taylor, 1995, The Journal of infection.

Iron overload and iron-chelating therapy in hemoglobin E-beta thalassemia.

G. Brittenham, D. Weatherall, N. Olivieri, 2000, Journal of pediatric hematology/oncology.

Epiphyseal growth plate cartilage and chondrocytes in mineralising cultures produce a low molecular mass angiogenic procollagenase activator.

R. Brown, B. Mclaughlin, J. Weiss, 1987, Bone and mineral.

Prognostic significance of proteinuria one year after onset of diarrhea-associated hemolytic-uremic syndrome.

D. Milford, R. White, C. Taylor, 1991, The Journal of pediatrics.

Risk of hypertension in children with multicystic dysplastic kidney.

C. Taylor, 2006, Archives of disease in childhood.

Renal length and inulin clearance in the radiologically normal single kidney

W. Wong, P. Davies, C. Taylor, 2003, Pediatric Nephrology.

What’s new in haemolytic uraemic syndrome?

S. Johnson, C. Taylor, Sally Johnson, 2008, European Journal of Pediatrics.

Enterohaemorrhagic Escherichia coli and Shigella dysenteriae type 1-induced haemolytic uraemic syndrome

C. Taylor, 2008 .

Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome

G. Ariceta, D. Landau, S. Johnson, 2009, Pediatric Nephrology.

Prostacyclin in diarrhoea-associated haemolytic uraemic syndrome

C. Taylor, C. Lote, C. Taylor, 1993, Pediatric Nephrology.

The expression of blood group P1 in post-enteropathic haemolytic uraemic syndrome

T. C. Roy, D. Milford, B. Rowe, 2004, Pediatric Nephrology.

PATHOGENESIS OF HAEMOLYTIC URAEMIC SYNDROME

P. Rose, C. Taylor, J. Kavi, 1988, The Lancet.

Prognostic markers in diarrhoea-associated haemolytic-uraemic syndrome: initial neutrophil count, human neutrophil elastase and von Willebrand factor antigen.

D. Milford, F. Hill, J. Dawes, 1991, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Changes in the postenteropathic form of the hemolytic uremic syndrome in children.

B. Rowe, C. Taylor, T. Marshall, 1991, Clinical nephrology.

A comparison of the effects of verocytotoxin-1 on primary human renal cell cultures.

D. Milford, J. Williams, C. Lingwood, 1999, Toxicology letters.

Haemolytic-uraemic syndrome: clinical experience of an outbreak in the West Midlands.

B. Rowe, R. White, C. Taylor, 1986, British medical journal.

Tauroursodeoxycholic acid binds to the G‐protein site on light activated rhodopsin

Christina M. Taylor, G. Marshall, C. Taylor, 2018, Experimental eye research.

Renal function following liver transplantation for unresectable hepatoblastoma

D. Milford, R. Grundy, P. McKiernan, 2003, Pediatric transplantation.

Further evidence of lipid peroxidation in post-enteropathic haemolytic-uraemic syndrome

R. D. Situnayake, B. Crump, D. Thurnham, 1991, Pediatric Nephrology.

The effects of retinoid treatment and antiestrogens on the growth of T47D human breast cancer cells.

C. Taylor, N. Wetherall, 1986, European journal of cancer & clinical oncology.

Homeostatic regulation of zinc absorption and endogenous losses in zinc-deprived men.

J. Bacon, C. Taylor, P. Aggett, 1991, The American journal of clinical nutrition.

Increased procollagenase activating angiogenic factor in the vitreous humour of oxygen treated kittens.

A. Garner, B. Mclaughlin, J. Weiss, 1988, The British journal of ophthalmology.

kittens . vitreous humour of oxygen treated activating angiogenic factor in the Increased procollagenase

A. Garner, B. Mclaughlin, J. Weiss, 2022 .

Parathyroid hormone-independent regulation of 1,25(OH)2D in response to inhibition of bone resorption.

H. Fleisch, J. Bonjour, U. Trechsel, 1988, The American journal of physiology.

Unilateral nephrectomy and 1,25-dihydroxyvitamin D3.

H. Fleisch, J. Bonjour, U. Trechsel, 1983, Kidney international.

Assay of 24R,25-dihydroxycholecalciferol in human serum.

C. Taylor, 1980, Methods in enzymology.

Matrix integrity and the control of angiogenesis.

C. Taylor, J. M. Thompson, J. Weiss, 1991, International journal of radiation biology.

End-stage renal failure in adolescence with Sjögren’s syndrome autoantibodies SSA and SSB

S. Hulton, S. Johnson, M. Brundler, 2007, Pediatric Nephrology.

Highly specific binding of 1,25-dihydroxycholecalciferol in bone cytosol.

S. Manolagas, D. Anderson, C. Taylor, 1979, The Journal of endocrinology.

Competitive protein binding assay for 24,25-dihydroxycholecalciferol.

C. Taylor, S. E. Hughes, C. Taylor, 1976, Biochemical and biophysical research communications.

The effects of a diphosphonate and dietary calcium on the metabolism of vitamin D3 (cholecalciferol) in the chick.

E. Mawer, C. Taylor, A. Reeve, 1975, Clinical science and molecular medicine.

Anti‐idiotypic activity against anti‐myeloperoxidase antibodies in pooled human immunoglobulin

D. Adu, J. Michael, A. Pall, 1994, Clinical and experimental immunology.

Endothelium, myeloperoxidase, anti-myeloperoxidase interaction in vasculitis.

D. Adu, J. Neuberger, R. Thompson, 1993, Advances in experimental medicine and biology.

Endothelium myeloperoxidase-antimyeloperoxidase interaction in vasculitis.

D. Adu, J. Neuberger, R. Thompson, 1992, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The late histologic findings in diarrhea-associated hemolytic uremic syndrome.

D. Milford, N. Moghal, A. Howie, 1998, The Journal of pediatrics.

Comparison of ribosome-inactivating proteins in the induction of apoptosis.

D. Milford, J. Williams, L. Roberts, 1997, Toxicology letters.

Peptides from live yeast cell derivative stimulate wound healing.

T. K. Hunt, B. Halliday, G. H. Davies, 1990, Archives of surgery.

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)

V. Sheffield, E. Stone, J. Fingert, 1997, Archives of ophthalmology.

Vitamin E treatment of haemolytic uraemic syndrome.

R. Walker, C. Taylor, D. McCredie, 1984, Archives of disease in childhood.

Glomerular vascular cell adhesion molecule-1 expression in renal vasculitis.

D. Adu, D. Milford, A. Howie, 1996, Journal of clinical pathology.

New insights into the haemolytic uraemic syndromes.

C. Taylor, D. Milford, 1990, Archives of disease in childhood.

Clinico-pathological findings in diarrhoea-negative haemolytic uraemic syndrome

A. Howie, R. Risdon, C. Taylor, 2004, Pediatric Nephrology.

An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome

G. Ariceta, D. Landau, C. Langman, 2014, Pediatric Nephrology.

Concentrations of endothelial-cell-stimulating angiogenesis factor, a major component of human uterine angiogenesis factor, in human and bovine embryonic tissues and decidua.

N. Maroudas, B. Mclaughlin, J. Weiss, 1992, Journal of reproduction and fertility.

Soluble circulating cell adhesion molecules in haemolytic uraemic syndrome

D. Adu, D. Milford, A. Pall, 1995, Pediatric Nephrology.

A laboratory model of toxin-induced hemolytic uremic syndrome.

D. Milford, F. Raafat, J. Williams, 1999, Kidney international.

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25).

V. Sheffield, E. Stone, E. Héon, 1995, Human molecular genetics.

Estrogen receptor-mediated and cytotoxic effects of the antiestrogens tamoxifen and 4-hydroxytamoxifen.

D. Zava, C. Taylor, B. Blanchard, 1984, Cancer research.

Prostacyclin concentrations in haemolytic uraemic syndrome after acute shigellosis.

C. Taylor, C. Lote, 1992, Archives of disease in childhood.

Peptide synthesis catalyzed by an antibody containing a binding site for variable amino acids.

S. Benkovic, Carol M. Taylor, R. Hirschmann, 1994, Science.

4.02 – Introduction to Computer-Assisted Drug Design – Overview and Perspective for the Future

C. M. Taylor, G. R. Marshall, G. Marshall, 2007 .

Cytomegalovirus infection associated with lower urinary tract symptoms.

R. White, J. Davies, C. Taylor, 1979, British medical journal.

Symptomatic zinc deficiency in experimental zinc deprivation.

H. F. Goode, B. E. Walker, J. Kelleher, 1992, Journal of clinical pathology.

Circulating soluble adhesion molecules in systemic vasculitis.

M. Drayson, D. Adu, J. Michael, 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Linkage of posterior polymorphous corneal dystrophy to 20q11.

Lee M. Alward, V. Sheffield, E. Stone, 1995, Human molecular genetics.

Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci.

V. Sheffield, R. Folberg, E. Stone, 1999, Ophthalmic genetics.

Quantity and carbohydrate content of glycomacropeptide fractions isolated from raw and heat-treated milk

Cheryl Taylor, B. W. Woonton, C. Taylor, 2009 .

Influence of hypoxia on vascular endothelial growth factor and chorionic gonadotrophin production in the trophoblast-derived cell lines: JEG, JAr and BeWo.

C. Taylor, H. Stevens, F. Anthony, 1997, Placenta.

Hormonal modulation of guanyl nucleotide binding to rat luteal membranes.

P. McIlroy, C. Taylor, 1988, Biology of reproduction.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

T. Mansfield, R. Lifton, A. Nayır, 1997, Nature Genetics.

Micturition symptoms and unstable bladder activity in girls with primary vesicoureteric reflux.

J. Corkery, R. White, C. Taylor, 1982, British journal of urology.

19. Unstable Bladder Activity and the Rate of Resolution of Vesico-Ureteric Reflux1

C. Taylor, 1984 .

Unstable bladder activity and the rate of resolution of vesico-ureteric reflux.

C. Taylor, 1984, Contributions to nephrology.

Influence of calcium and calcium regulating hormones on renal compensatory growth.

J. Jobin, J. Bonjour, J. Caverzasio, 1984, Advances in experimental medicine and biology.

The biosynthesis of glycoproteins by cultured bovine tendon fibroblasts.

M. E. Grant, C. Taylor, R. Oelbaum, 1982, Connective tissue research.

Bovine and human pineal glands contain substantial quantities of endothelial cell stimulating angiogenic factor

B. Mclaughlin, J. Weiss, C. Taylor, 2005, Journal of neural transmission.

Effect of oxygen tension on the quantities of procollagenase-activating angiogenic factor present in the developing kitten retina.

A. Garner, C M Taylor, J B Weiss, 1986, The British journal of ophthalmology.

Electron probe analysis for iodine in human thyroid and parathyroid glands, normal and neoplastic.

W. Hammond, P. Grimley, C. Taylor, 1971, Journal of the National Cancer Institute.

Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau Disease.

E. Stone, A. Webster, R. Sui, 2001, Archives of ophthalmology.

Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experience.

R. Gilbert, A. Waters, K. Tullus, 2007, The Journal of pediatrics.

Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland

A. Waters, S. O'Brien, T. Cheasty, 2005 .

Haemolytic uraemic syndromes in the British Isles 1985-8: association with verocytotoxin producing Escherichia coli. Part 1: Clinical and epidemiological aspects.

B Rowe, S M Hall, H. Kleanthous, 1990, Archives of disease in childhood.

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002, Journal of medical genetics.

Novel ATP 6 V 1 B 1 and ATP 6 V 0 A 4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

S. Bianca, C. Morton, V. Tasic, 2002 .

Factor VIII von Willebrand protein in haemolytic uraemic syndrome and systemic vasculitides

P. Rose, M. Robertson, C. Taylor, 1990, The Lancet.

Making sense of the spectrum of glomerular disease associated with complement dysregulation

S. Johnson, E. Wong, C. Taylor, 2014, Pediatric Nephrology.

Dilated cardiomyopathy associated with haemolytic uraemic syndrome.

C. Taylor, J. D. De Giovanni, J. Poulton, 1987, British heart journal.

Haemolytic uraemic syndromes in the British Isles, 1985-8: association with verocytotoxin producing Escherichia coli. Part 2: Microbiological aspects.

H R Smith, B Rowe, D. Milford, 1990, Archives of disease in childhood.

A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.

G. Remuzzi, G. Rizzoni, D. Landau, 2006, Kidney international.

Renal transplantation in HUS patients with disorders of complement regulation

F. Prüfer, C. Loirat, L. Zimmerhackl, 2007, Pediatric Nephrology.

Congenital nephrotic syndrome

V. Iyer, A. Koziell, P. Ramani, 2001, Pediatric Nephrology.

Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.

A. Schinzel, T. Weingeist, E. Messmer, 1995, Archives of ophthalmology.

Type IV Secretion System Components in Vibrio vulnificus

J. Oliver, C. Taylor, 2010 .

Raised levels of latent collagenase activating angiogenesis factor (ESAF) are present in actively growing human intracranial tumours.

R. Lye, J. Weiss, C. Taylor, 1991, British Journal of Cancer.

Clinical significance of antenatal calyceal dilatation detected by ultrasound

J. Corkery, S. Newell, C. Taylor, 1990, The Lancet.

Sudden blindness caused by anterior ischemic optic neuropathy in 5 children on continuous peritoneal dialysis.

E. Haddad, I. Salusky, D. Bremond-Gignac, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Characteristic phenotype in congenital nephrotic syndrome

D. Milford, T. Barrett, C. Taylor, 1995, European Journal of Pediatrics.

Elevated endothelial-cell-stimulating angiogenic factor activity in rodent glycolytic skeletal muscles.

R. Cooper, J. Weiss, C. Taylor, 1991, Clinical science.

D. Milford, S. Hulton, P. Ramani, 2002, Pediatric Nephrology.

Environmental trigger for anti-neutrophil cytoplasmic antibodies?

D. Adu, T. Barrett, A. Pall, 1993, The Lancet.

Cytokines in haemolytic uraemic syndrome associated with verocytotoxin-producing Escherichia coli infection

D. Adu, D. Milford, D Adu, 1997, Archives of disease in childhood.

Little evidence for anti-endothelial cell antibodies in microscopic polyarteritis and Wegener's granulomatosis.

D. Adu, R. Thompson, J. Michael, 1993, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Where next with atypical hemolytic uremic syndrome?

P. Zipfel, M. Noris, T. Jokiranta, 2007, Molecular immunology.

NEUTROPHIL ELASTASES AND HAEMOLYTIC URAEMIC SYNDROME

D. Milford, J. Dawes, C. Taylor, 1989, The Lancet.

Clinical Limitations of the Estimation of Glomerular Filtration Rate From Height/Plasma Creatinine Ratio: a Comparison With Simultaneous 51 Cr Edetic Acid Slope Clearance

R. White, J. Davies, C. Taylor, 1983 .

The absence of 24,25-dihydroxycholecalciferol in anephric patients.

J. Kanis, E. Mawer, R. Russell, 1978, Clinical science and molecular medicine. Supplement.

Vitamin D metabolism and parathyroid function in man.

L. F. Hill, E. Mawer, S. Stanbury, 1975, Clinical science and molecular medicine.

Rapidity of plasma 1,25-dihydroxyvitamin D responses to hypo- and hypercalcemia in steers.

U. Binswanger, W. Born, U. Trechsel, 1983, Endocrinology.

Immunologic therapy for hemolytic-uremic syndrome.

T. C. Roy, D. Milford, P. Rose, 1989, The Journal of pediatrics.

No common final pathogenetic pathway in haemolytic uraemic syndromes.

J. Williams, A. Howie, C. Taylor, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Asian rickets and osteomalacia: patterns of parathyroid response in vitamin D deficiency

P. Adams, S. Stanbury, C. Taylor, 1975, Proceedings of the Nutrition Society.

Myelin associated glycoprotein cross-linking triggers its partitioning into lipid rafts, specific signaling events and cytoskeletal rearrangements in oligodendrocytes.

R. Quarles, S. Cheng, S. Pfeiffer, 2004, Neuron glia biology.

Differing outcomes ofEscherichia coli 0157 colitis in identical twins

D. Milford, C. Taylor, C. Inward, 1993, Pediatric Nephrology.

Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency.

J. Goodship, R. Thompson, A. Howie, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON)

T. Braun, E. Stone, S. Daiger, 2005 .

A case of neonatal Bartter’s syndrome

F. Raafat, S. Hulton, G. Lindop, 1996, Pediatric Nephrology.

RAISED ENDOTHELIAL CELL STIMULATING ANGIOGENIC FACTOR IN DIABETIC RETINOPATHY

J. Weiss, C. Taylor, 1989, The Lancet.

Proceedings: Inhibitory effect of 24,25-dihydroxycholecalciferol on parathyroid hormone secretion in the goat.

M. Peacock, E. Mawer, A. Care, 1975, The Journal of endocrinology.

Recovery of protein from urine specimens collected in cotton wool.

C. Taylor, G. C. Smith, 1992, Archives of disease in childhood.

Competitive protein-binding assay for 24,25-dihydroxycholecalciferol

C. Taylor, S. E. Hughes, P. Silva, 1976, Calcified Tissue Research.