Calcific aortic stenosis: a complication of chronic uraemia. by Maher, E, Pazianas, M, Curtis, JR

Infratentorial immature teratoma of congenital origin can be associated with a 20-year survival outcome: a case report and review of literature by Yazid Maghrabi, Maher E. Kurdi, Saleh S. Baeesa

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Familial paraganglioma: a novel presentation of a case and response to therapy with radiolabelled MIBG. by Lawrence, J, Maher, E, Sheaves, R, Grossman, AB

Effectiveness of sunflower seed husk biochar for removing copper ions from wastewater: a comparative study by Maher E. SALEH, Ahmed A. EL-REFAEY, Amal H. MAHMOUD

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Klinefelter-like phenotype and primary infertility in a male with a paracentric Xq inversion. by Németh, A, Gallen, I, Crocker, M, Levy, E, Maher, E

Novel multiple-colour fluorescence in situ hybridisation technology for the simultaneous identification of the 24 human metaphase chromosomes on a single slide: applications in the... by Crooks, K, Brown, T, Maher, E, Houghton, J, Lawrie, M, Cardy, D

The interaction between the von Hippel-Lindau gene product (pVHL) and hypoxia-inducible factor 1 is disrupted by disease-causing pVHL mutants. by Maher, E, Clifford, S, Maxwell, P, Wiesener, MS, Chang, G, Ratcliffe, P

The pVHL-associated SCF ubiquitin ligase complex: molecular genetic analysis of elongin B and C, Rbx1 and HIF-1alpha in renal cell carcinoma. by Clifford, S, Astuti, D, Hooper, L, Maxwell, P, Ratcliffe, P, Maher, E

Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas. by Dahia, P, Toledo, S, Mulligan, L, Maher, E, Grossman, AB, Eng, C

Fluorescence in situ hybridisation of multiple probes on a single microscope slide. by Larin, Z, Fricker, M, Maher, E, Ishikawa-Brush, Y, Southern, E

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map. by Markie, D, Huson, S, Maher, E, Davies, A, Tomlinson, I, Bodmer, W

Germline mutation in DOK7 associated with fetal akinesia deformation sequence. by Vogt, J, Morgan, N, Marton, T, Maxwell, S, Harrison, B, Beeson, D, Maher, E

Potential bioremediation of lead and phenol by sunflower seed husk and rice straw-based biochar hybridized with bacterial consortium: a kinetic study by Eman H. El-Gamal, Mohamed Rashad, Maher E. Saleh, Sahar Zaki, Marwa Eltarahony

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A legacy of tinnitus: multiple head and neck paragangliomas. by Tan, T, Hatfield, E, Thakker, R, Maher, E, Meeran, K, Martin, N, Turner, J

Interaction between the von Hippel-Lindau gene product (pVHL) and hypoxia-inducible factor 1 is disrupted by disease causing pVHL mutants by Clifford, S, Maxwell, P, Wiesener, MS, Chang, G, Smallwood, A, Ratcliffe, P, Maher, E

Molecular genetic evidence that endometriosis is a precursor of ovarian cancer. by Prowse, A, Manek, S, Varma, R, Liu, J, Godwin, A, Maher, E, Tomlinson, I, Kennedy, S

Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. by Knight, S, Horsley, S, Regan, R, Lawrie, N, Maher, E, Cardy, D, Flint, J, Kearney, L

Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease. by Clifford, S, Cockman, M, Smallwood, A, Mole, D, Woodward, E, Maxwell, P, Ratcliffe, P, Maher, E

Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11) by Baumber, L, Patel, S, Kinning, E, Critchley, P, Nemeth, A, Talbot, K, Maher, E, Trembath, R

Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment. by Menko, F, Maher, E, Schmidt, L, Middelton, L, Aittomäki, K, Tomlinson, I, Richard, S, Linehan, WM