Ramsden R - Search Results

1

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.

Astuti D, Hart-Holden N, Latif F, Lalloo F, Black GC, Lim C, Moran A, Grossman AB, Hodgson SV, Freemont A, Ramsden R, Eng C, Evans DG, Maher ER. Astuti D, et al. Among authors: ramsden r. Clin Endocrinol (Oxf). 2003 Dec;59(6):728-33. doi: 10.1046/j.1365-2265.2003.01914.x. Clin Endocrinol (Oxf). 2003. PMID: 14974914

2

Incidence of vestibular schwannoma and neurofibromatosis 2 in the North West of England over a 10-year period: higher incidence than previously thought.

Evans DG, Moran A, King A, Saeed S, Gurusinghe N, Ramsden R. Evans DG, et al. Among authors: ramsden r. Otol Neurotol. 2005 Jan;26(1):93-7. doi: 10.1097/00129492-200501000-00016. Otol Neurotol. 2005. PMID: 15699726

3

Further genotype--phenotype correlations in neurofibromatosis 2.

Selvanathan SK, Shenton A, Ferner R, Wallace AJ, Huson SM, Ramsden RT, Evans DG. Selvanathan SK, et al. Among authors: ramsden rt. Clin Genet. 2010 Feb;77(2):163-70. doi: 10.1111/j.1399-0004.2009.01315.x. Epub 2009 Nov 23. Clin Genet. 2010. PMID: 19968670

4

Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.

Wu CL, Thakker N, Neary W, Black G, Lye R, Ramsden RT, Read AP, Evans DG. Wu CL, et al. Among authors: ramsden rt. J Med Genet. 1998 Dec;35(12):973-7. doi: 10.1136/jmg.35.12.973. J Med Genet. 1998. PMID: 9863591 Free PMC article.

5

Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma.

Evans DG, Lye R, Neary W, Black G, Strachan T, Wallace A, Ramsden RT. Evans DG, et al. Among authors: ramsden rt. J Neurol Neurosurg Psychiatry. 1999 Jun;66(6):764-7. doi: 10.1136/jnnp.66.6.764. J Neurol Neurosurg Psychiatry. 1999. PMID: 10329751 Free PMC article.

6

Paediatric presentation of type 2 neurofibromatosis.

Evans DG, Birch JM, Ramsden RT. Evans DG, et al. Among authors: ramsden rt. Arch Dis Child. 1999 Dec;81(6):496-9. doi: 10.1136/adc.81.6.496. Arch Dis Child. 1999. PMID: 10569966 Free PMC article.

7

Diagnostic issues in a family with late onset type 2 neurofibromatosis.

Evans DG, Bourn D, Wallace A, Ramsden RT, Mitchell JD, Strachan T. Evans DG, et al. Among authors: ramsden rt. J Med Genet. 1995 Jun;32(6):470-4. doi: 10.1136/jmg.32.6.470. J Med Genet. 1995. PMID: 7666400 Free PMC article.

8

Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas.

Mohyuddin A, Neary WJ, Wallace A, Wu CL, Purcell S, Reid H, Ramsden RT, Read A, Black G, Evans DG. Mohyuddin A, et al. Among authors: ramsden rt. J Med Genet. 2002 May;39(5):315-22. doi: 10.1136/jmg.39.5.315. J Med Genet. 2002. PMID: 12011146 Free PMC article.

9

Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplification.

Evans DG, Ramsden RT, Shenton A, Gokhale C, Bowers NL, Huson SM, Pichert G, Wallace A. Evans DG, et al. Among authors: ramsden rt. J Med Genet. 2007 Jul;44(7):424-8. doi: 10.1136/jmg.2006.047753. Epub 2007 Feb 16. J Med Genet. 2007. PMID: 17307835 Free PMC article.

10

Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosis.

Evans DG, Wallace AJ, Wu CL, Trueman L, Ramsden RT, Strachan T. Evans DG, et al. Among authors: ramsden rt. Am J Hum Genet. 1998 Sep;63(3):727-36. doi: 10.1086/512074. Am J Hum Genet. 1998. PMID: 9718334 Free PMC article.

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