au.\*:("MAHER, E. R")
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Inherited renal cell carcinomaMAHER, E. R.British journal of urology (Print). 1996, Vol 78, Num 4, pp 542-545, issn 0007-1331Article
Genetics of urological cancersMAHER, E. R.British medical bulletin. 1994, Vol 50, Num 3, pp 698-707, issn 0007-1420Article
Intrapericardial instillation of bleomycin in malignant pericardial effusionMAHER, E. R; BUCKMAN, R.The American heart journal. 1986, Vol 111, Num 3, pp 613-614, issn 0002-8703Article
Beckwith-Wiedermann syndromeELLIOTT, M; MAHER, E. R.Journal of medical genetics. 1994, Vol 31, Num 7, pp 560-564, issn 0022-2593Article
Von Hippel-Lindau diseaseMAHER, E. R; MOORE, A. T.British journal of ophthalmology. 1992, Vol 76, Num 12, pp 743-745, issn 0007-1161Article
Choroid plexus papilloma : A new presentation of von Hippel-Lindau (VHL) diseaseBLAMIRES, T. L; MAHER, E. R.Eye (London. 1987). 1992, Vol 6, pp 90-92, issn 0950-222X, 1Article
Calcific aortic stenosis: a complication of chronic uraemiaMAHER, E. R; PAZIANAS, M; CURTIS, J. R et al.Nephron. 1987, Vol 47, Num 2, pp 119-122, issn 0028-2766Article
The VHL tumour-suppressor gene paradigmKAELIN, W. G; MAHER, E. R.Trends in genetics (Regular ed.). 1998, Vol 14, Num 10, pp 423-426, issn 0168-9525Article
Familial renal cell carcinoma : clinical and molecular genetic aspectsMAHER, E. R; YATES, J. R. W.British journal of cancer. 1991, Vol 63, Num 2, pp 176-179, issn 0007-0920, 4 p.Article
Serum ferritin in haemodialysis patients: is there a relationship to haemochromatosis alleles HLA A3, B7, B14?MAHER, E. R; CURTIS, J. R.Nephron. 1986, Vol 43, Num 1, pp 43-44, issn 0028-2766Article
The clinical features and natural history of the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)MAHER, E. R; LEES, A. J.Neurology. 1986, Vol 36, Num 7, pp 1005-1008, issn 0028-3878Article
Epigenetic inactivation of the RASSF10 candidate tumor suppressor gene is a frequent and an early event in gliomagenesisHILL, V. K; UNDERHILL-DAY, N; LATIF, F et al.Oncogene (Basingstoke). 2011, Vol 30, Num 8, pp 978-989, issn 0950-9232, 12 p.Article
Epigenotype—phenotype correlations in Silver—Russell syndromeWAKELING, E. L; ABU AMERO, S; MOORE, G. E et al.Journal of medical genetics. 2010, Vol 47, Num 11, pp 760-768, issn 0022-2593, 9 p.Article
Assisted reproductive therapies and imprinting disorders : a preliminary British surveySUTCLIFFE, A. G; PETERS, C. J; BOWDIN, S et al.Human reproduction (Oxford. Print). 2006, Vol 21, Num 4, pp 1009-1011, issn 0268-1161, 3 p.Article
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the α-subunit of cone specific transducin (GNAT2)MICHAELIDES, M; ALIGIANIS, I. A; HOLDER, G. E et al.British journal of ophthalmology. 2003, Vol 87, Num 11, pp 1317-1320, issn 0007-1161, 4 p.Article
Genetic and functional analysis of the von Hippel-Lindau (VHL) tumour suppressor gene promoterZATYKA, M; MORRISSEY, C; KUZMIN, I et al.Journal of medical genetics. 2002, Vol 39, Num 7, pp 463-472, issn 0022-2593Article
Detailed mapping of a congenital heart disease gene in chromosome 3p25GREEN, E. K; PRIESTLEY, M. D; WATERS, J et al.Journal of medical genetics. 2000, Vol 37, Num 8, pp 581-587, issn 0022-2593Article
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic provides Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationLAM, W. W. K; HATADA, I; OHISHI, S et al.Journal of medical genetics. 1999, Vol 36, Num 7, pp 518-523, issn 0022-2593Article
Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutationWEBSTER, A. R; MAHER, E. R; MOORE, A. T et al.Archives of ophthalmology (1960). 1999, Vol 117, Num 3, pp 371-378, issn 0003-9950Article
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeCATCHPOOLE, D; LAM, W. W. K; VALLER, D et al.Journal of medical genetics. 1997, Vol 34, Num 5, pp 353-359, issn 0022-2593Article
Somatic inactivation of the VHL gene in von Hippel-Lindau disease tumorsPROWSE, A. H; WEBSTER, A. R; RICHARDS, F. M et al.American journal of human genetics. 1997, Vol 60, Num 4, pp 765-771, issn 0002-9297Article
Phenotypic expression in von Hippel-Lindau disease : correlations with germline VHL gene mutationsMAHER, E. R; WEBSTER, A. R; RICHARDS, F. M et al.Journal of medical genetics. 1996, Vol 33, Num 4, pp 328-332, issn 0022-2593Article
Age at onset in Huntington's disease and methylation at D4S95REIK, W; MAHER, E. R; MORRISON, P. J et al.Journal of medical genetics. 1993, Vol 30, Num 3, pp 185-188, issn 0022-2593Article
Atherosclerotic renovascular disease causing renal impairment. A case for treatmentSCOBLE, J. E; MAHER, E. R; HAMILTON, G et al.Clinical nephrology. 1989, Vol 31, Num 3, pp 119-122, issn 0301-0430Article
Neutropenia and plasma free radical reaction products during haemodialysisMAHER, E. R; WICKENS, D. G; GRIFFIN, J. F. A et al.Nephrology, dialysis, transplantation (Print). 1988, Vol 3, Num 3, pp 277-283, issn 0931-0509Article
