The laboratory mouse and wild immunology von Viney, M., Lazarou, L., Abolins, S.

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High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis von Mei, D, Lewis, R, Parrini, E, Lazarou, L P, Marini, C, Pilz, D T, Guerrini, R

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Familial Hypercholesterolaemia – a targeted Next Generation Sequencing panel and retrospective analysis of patients with no previously identified pathogenic variant von Willis, E., Wood, M., Hamling, N., Lazarou, L., Morgan, S., Corrin, S., Harris, R., McDowell, I., Haralambos, K., Datta, D.

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Urology residency training in Greece. Results from the first national resident survey von Tzelves, L., Glykas, Lazarou, L., Zabaftis, C., Fragkoulis, C., Leventi, A., Moulavasilis, N., Tzavellas, D., Tsirkas, K., Ntoumas, K., Mourmouris, P., Dellis, A., Varkarakis, Skolarikos, A., Liatsikos, E., Gkialas

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Urology residency training in Greece. Results from the first national resident survey von Tzelves, L., Glykas, I., Lazarou, L., Zabaftis, C., Fragkoulis, C., Leventi, A., Moulavasilis, N., Tzavellas, D., Tsirkas, K., Ntoumas, K., Mourmouris, P., Dellis, A., Varkarakis, I., Skolarikos, A., Liatsikos, E., Gkialas, I.

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Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients von Archer, H L, Whatley, S D, Evans, J C, Ravine, D, Huppke, P, Kerr, A, Bunyan, D, Kerr, B, Sweeney, E, Davies, S J, Reardon, W, Horn, J, MacDermot, K D, Smith, R A, Magee, A, Donaldson, A, Crow, Y, Hermon, G, Miedzybrodzka, Z, Cooper, D N, Lazarou, L, Butler, R, Sampson, J, Pilz, D T, Laccone, F, Clarke, A J

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease von Snell, Russell G, MacMillan, John C, Cheadle, Jeremy P, Fenton, Iain, Lazarou, Lazarus P, Davies, Peter, MacDonald, Marcy E, Gusella, James F, Harper, Peter S, Shaw, Duncan J

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Defining the ideal urology training programme from the trainee’s and professor’s perspective: Is there a concordance in their idea of good training? von Mantica, G., Carrion, D.M., Pang, K.H., Ucar, T., Parodi, S., Tappero, S., Lazarou, L., Glykas, I., Zambaftis, C., Lourenco, M., Gonzalez Padilla, D.A., Ortega Polledo, L.E., Gomez Rivas, J., Esperto, F.

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Molecular analysis and clinical correlations of the Huntington's disease mutation von MacMillan, J.C, Snell, R.G, Tyler, A, Houlihan, G.D, Fenton, I, Cheadle, J.P, Lazarou, L.P, Shaw, J.D, Harper, P.S

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Patient positioning during percutaneous nephrolithotomy: what is the current best practice? von Mourmouris, Panagiotis, Berdempes, Marinos, Markopoulos, Titos, Lazarou, Lazaros, Tzelves, Lazaros, Skolarikos, Andreas

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Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindred von Hateboer, Nick, Buchalter, Maurice, Davies, Sarah J., Lazarou, Lazarus P., Ravine, David

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Early onset seizures and Rett-like features associated with mutations in CDKL5 von EVANS, Julie C, ARCHER, Hayley L, WRIGHT, Michael J, PILZ, Daniela T, LAZAROU, Lazarus, COOPER, David N, SAMPSON, Julian R, BUTLER, Rachel, WHATLEY, Sharon D, CLARKE, Angus J, COLLEY, James P, RAVN, Kirstine, NIELSEN, Jytte Bieber, KERR, Alison, WILLIAMS, Elizabeth, CHRISTODOULOU, John, GECZ, Jozef, JARDINE, Philip E

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Familial phenotype differences in PKD1 von HATEBOER, N, LAZAROU, L. P, WILLIAMS, A. J, HOLMANS, P, RAVINE, D

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Editorial Comment: Does the Use of a Robot Decrease the Complication Rate Adherent to Radical Cystectomy? A Systematic Review and Meta-Analysis of Studies Comparing Open with Robot... von Faria, Eliney F.

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Extraperitoneal laparoscopic radical prostatectomy: Our preliminary experience von Zougkas, K, Kotakidis, G, Petas, A, Lazarou, L, Marantidis, K, Christodoulou, N

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Linkage disequilibrium in Huntington's disease: an improved localisation for the gene von Snell, R G, Lazarou, L P, Youngman, S, Quarrell, O W, Wasmuth, J J, Shaw, D J, Harper, P S

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Formación de la residencia de Urología en Grecia. Resultados de la primera encuesta nacional von Tzelves, L., Glykas, I., Lazarou, L., Zabaftis, C., Fragkoulis, C., Leventi, A., Moulavasilis, N., Tzavellas, D., Tsirkas, K., Ntoumas, K., Mourmouris, P., Dellis, A., Varkarakis, I., Skolarikos, A., Liatsikos, E., Gkialas, I.

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NTNG1 mutations are a rare cause of Rett syndrome von Archer, Hayley L., Evans, Julie C., Millar, David S., Thompson, Peter W., Kerr, Alison M., Leonard, Helen, Christodoulou, John, Ravine, David, Lazarou, Lazarus, Grove, Lucy, Verity, Christopher, Whatley, Sharon D., Pilz, Daniela T., Sampson, Julian R., Clarke, Angus J.

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Presymptomatic Testing for Huntington's Disease in Wales 1987–90 von Tyler, Audrey, Morris, Michael, Lazarou, Lazarus, Meredith, Linda, Myring, Jennifer, Harper, Peter

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Human gene mutations. Gene symbol: PKD1. Disease: Polycystic kidney disease von Daniells, C, Maheshwar, M, Lazarou, L, Davies, F, Coles, G, Ravine, D

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