Search Results - "MILFORD, D"

Assessing bone mineralisation in children with chronic kidney disease: what clinical and research tools are available? by Lalayiannis, A.D., Crabtree, N.J., Fewtrell, M., Biassoni, L., Milford, D.V., Ferro, C.J., Shroff, R.

“…Mineral and bone disorder in chronic kidney disease (CKD-MBD) is a triad of biochemical imbalances of calcium, phosphate, parathyroid hormone and vitamin D,…”
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A Randomized Trial to Assess the Impact of Early Steroid Withdrawal on Growth in Pediatric Renal Transplantation: The TWIST Study by Grenda, R., Watson, A., Trompeter, R., Tönshoff, B., Jaray, J., Fitzpatrick, M., Murer, L., Vondrak, K., Maxwell, H., Van Damme‐Lombaerts, R., Loirat, C., Mor, E., Cochat, P., Milford, D. V., Brown, M., Webb, N. J. A.

“…Minimizing steroid exposure in pediatric renal transplant recipients can improve linear growth and reduce metabolic disorders. This randomized multicenter…”
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G363 Case reports on serious respiratory complications after renal transplant in obese children: Can these be avoided? by Verma, P, Milford, D

“…Aims To present two obese children who suffered serious post operative respiratory complications after renal transplantation and to discuss strategies we have…”
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A 10‐year longitudinal follow‐up study of a U.K. paediatric transplant population to assess for skin cancer by Foo, S.H., Nightingale, P.G., Gazzani, P., Bader, E., Ogboli, M., Martin‐Clavijo, A., Milford, D.V., Kelly, D.A., Moss, C., Thomson, M.A.

“…Summary Background Our earlier study, published in 2004,found no skin cancer in a cohort of paediatric organ transplant recipients (POTRs) 5–16 years…”
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Distributed expertise: qualitative study of a British network of multidisciplinary teams supporting parents of children with chronic kidney disease by Swallow, V., Smith, T., Webb, N. J. A., Wirz, L., Qizalbash, L., Brennan, E., Birch, A., Sinha, M. D., Krischock, L., van der Voort, J., King, D., Lambert, H., Milford, D. V., Crowther, L., Saleem, M., Lunn, A., Williams, J.

“…Background Long‐term childhood conditions are often managed by hospital‐based multidisciplinary teams (MDTs) of professionals with discipline specific…”
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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome by Gbadegesin, Rasheed A, Adeyemo, Adebowale, Webb, Nicholas J A, Greenbaum, Larry A, Abeyagunawardena, Asiri, Thalgahagoda, Shenal, Kale, Arundhati, Gipson, Debbie, Srivastava, Tarak, Lin, Jen-Jar, Chand, Deepa, Hunley, Tracy E, Brophy, Patrick D, Bagga, Arvind, Sinha, Aditi, Rheault, Michelle N, Ghali, Joanna, Nicholls, Kathy, Abraham, Elizabeth, Janjua, Halima S, Omoloja, Abiodun, Barletta, Gina-Marie, Cai, Yi, Milford, David D, O'Brien, Catherine, Awan, Atif, Belostotsky, Vladimir, Smoyer, William E, Homstad, Alison, Hall, Gentzon, Wu, Guanghong, Nagaraj, Shashi, Wigfall, Delbert, Foreman, John, Winn, Michelle P

“…Steroid-sensitive nephrotic syndrome (SSNS) accounts for >80% of cases of nephrotic syndrome in childhood. However, the etiology and pathogenesis of SSNS…”
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Successful Isolated Liver Transplantation in a Child with Atypical Hemolytic Uremic Syndrome and a Mutation in Complement Factor H by Haller, W., Milford, D. V., Goodship, T. H. J., Sharif, K., Mirza, D. F., McKiernan, P. J.

“…A male infant was diagnosed with atypical hemolytic uremic syndrome (aHUS) at the age of 5.5 months. Sequencing of the gene (CFH) encoding complement factor H…”
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G333(P) Serum biomarkers, but not dual-energy x-ray absorptiometry (DXA), predict bone mineral density in children with chronic kidney disease by Lalayiannis, AD, Crabtree, NJ, Askiti, V, Mitsioni, A, Fewtrell, M, Kaur, A, Milford, DV, Shroff, R

“…IntroductionCurrently available biomarkers and Dual-energy X-ray Absorptiometry (DXA) are thought to be poor predictors of bone mineral density (BMD). The 2017…”
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A Prospective, Randomized, Multicenter Trial of Tacrolimus‐Based Therapy with or without Basiliximab in Pediatric Renal Transplantation by Grenda, R., Watson, A., Vondrak, K., Webb, N. J. A., Beattie, J., Fitzpatrick, M., Saleem, M. A., Trompeter, R., Milford, D. V., Moghal, N. E., Hughes, D., Perner, F., Friman, S., Van Damme‐Lombaerts, R., Janssen, F.

“…In a 6‐month, multicenter, randomized, controlled, open‐label, parallel‐group trial, we investigated the efficacy and safety of adding basiliximab to a…”
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G440 A Snapshot of acute kidney injury in tertiary paediatric centres in the united kingdom by Verghese, GK, Oni, L, Milford, DV, Holt, RCL

“…BackgroundThe burden of acute kidney injury (AKI) in the paediatric age group is unknown, partly due to the lack of a universally agreed definition in the…”
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ARC syndrome: an expanding range of phenotypes by Eastham, K M, McKiernan, P J, Milford, D V, Ramani, P, Wyllie, J, van't Hoff, W, Lynch, S A, Morris, A A M

“…AIM To describe the clinical phenotype in infants with ARC syndrome, the association of arthrogryposis, renal tubular acidosis, and cholestasis. METHODS The…”
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Dental Abnormalities in Schimke Immuno-osseous Dysplasia by Morimoto, M., Kérourédan, O., Gendronneau, M., Shuen, C., Baradaran-Heravi, A., Asakura, Y., Basiratnia, M., Bogdanović, R., Bonneau, D., Buck, A., Charrow, J., Cochat, P., DeHaai, K.A., Fenkçi, M.S., Frange, P., Fründ, S., Fryssira, H., Keller, K., Kirmani, S., Kobelka, C., Kohler, K., Lewis, D.B., Massella, L., McLeod, D.R., Milford, D.V., Nobili, F., Olney, A.H., Semerci, C.N., Stajić, N., Stein, A., Taque, S., Zonana, J., Lücke, T., Hendson, G., Bonnaure-Mallet, M., Boerkoel, C.F.

“…Described for the first time in 1971, Schimke immuno-osseous dysplasia (SIOD) is an autosomal-recessive multisystem disorder that is caused by bi-allelic…”
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Nodular glomerulosclerosis in a patient with cystic fibrosis, but not diabetes mellitus: A paediatric case by Lalayiannis, A.D, Thompson, C, Malcomson, R, Milford, D.V

“…Abstract Background Nodular glomerulosclerosis is seen in insulin dependent diabetic patients with nephropathy. Kimmelstiel-Wilson nodules on biopsy are…”
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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy by Otto, Edgar A, Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J, Zhou, Weibin, Airik, Rannar, Hurd, Toby W, Ghosh, Amiya K, Wolf, Matthias T, Hoppe, Bernd, Neuhaus, Thomas J, Bockenhauer, Detlef, Milford, David V, Soliman, Neveen A, Antignac, Corinne, Saunier, Sophie, Johnson, Colin A, Hildebrandt, Friedhelm

“…Nephronophthisis associated ciliopathies (NPHP-AC) comprise a group of autosomal recessive cystic kidney diseases that includes nephronophthisis (NPHP),…”
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O6.10 GLIOMA CELL VEGFR-2 EXPRESSION IMPAIRS CHEMOTHERAPEUTIC AND ANTIANGIOGENIC TREATMENTS IN PTEN-DEFICIENT GLIOBLASTOMA by Weiler, M., Kessler, T., Sahm, F., Blaes, J., Osswald, M., Milford, D., Urban, S., Ruiz de Almodovar, C., Heiland, S., Wick, W.

“…BACKGROUND: Given the recent failure of bevacizumab (BEV) in extending overall survival of patients with newly diagnosed glioblastoma, tissue biomarkers…”
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Human Hypertension Caused by Mutations in WNK Kinases by Wilson, Frederick H., Disse-Nicodème, Sandra, Choate, Keith A., Ishikawa, Kazuhiko, Nelson-Williams, Carol, Desitter, Isabelle, Gunel, Murat, Milford, David V., Lipkin, Graham W., Achard, Jean-Michel, Feely, Morgan P., Dussol, Bertrand, Berland, Yvon, Unwin, Robert J., Mayan, Haim, Simon, David B., Farfel, Zvi, Jeunemaitre, Xavier, Lifton, Richard P.

“…Hypertension is a major public health problem of largely unknown cause. Here, we identify two genes causing pseudohypoaldosteronism type II, a Mendelian trait…”
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Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure by Hildebrandt, Friedhelm, Birkenhäger, Ralf, Otto, Edgar, Schürmann, Maria J, Vollmer, Martin, Ruf, Eva-Maria, Maier-Lutz, Irina, Beekmann, Frank, Fekete, Andrea, Omran, Heymut, Feldmann, Delphine, Milford, David V, Jeck, Nicola, Konrad, Martin, Landau, Daniel, Knoers, Nine V.A.M, Antignac, Corinne, Sudbrak, Ralf, Kispert, Andreas

“…Antenatal Bartter syndrome (aBS) comprises a heterogeneous group of autosomal recessive salt-losing nephropathies. Identification of three genes that code for…”
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Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature by BOERKOEL, C. F, O'NEILL, S, FRÜND, S, GEARY, D. F, IESHIMA, A, ILLIES, F, JOSEPH, M. W, KAITILA, I, LAMA, G, LEHEUP, B, LUDMAN, M. D, MCLEOD, D. R, ANDRE, J. L, MEDEIRA, A, MILFORD, D. V, ORMÄLÄ, T, RENER-PRIMEC, Z, SANTAVA, A, SANTOS, H. G, SCHMIDT, B, SMITH, G. C, SPRANGER, J, ZUPANCIC, N, BENKE, P. J, WEKSBERG, R, BOGDANOVIC, R, BULLA, M, BURGUET, A, COCKFIELD, S, CORDEIRO, I, EHRICH, J. H. H

“…Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive spondylo-epiphyseal dysplasia. The characteristic features of SIOD include 1) short…”
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Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene by Stewart, P M, Krozowski, Z S, Gupta, A, Milford, D V, Howie, A J, Sheppard, M C, Whorwood, C B

“…11 beta-hydroxysteroid dehydrogenase (11 beta-HSD) catalyses the interconversion of hormonally active cortisol to inactive cortisone and is vital for dictating…”
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Skin surveillance of a U.K. paediatric transplant population by Thomson, M.A., Suggett, N.R., Nightingale, P.G., Milford, D.V., Baumann, U., Kelly, D.A., Moss, C., Hill, V.A.

“…Summary Background  Solid organ transplant recipients are at increased risk of skin cancer. Melanoma is less common than nonmelanoma skin cancer (NMSC)…”
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