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Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

Journal of Medical Genetics, 2006-04, Vol.43 (4), p.289-294

2006

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Evaluation of clinical diagnostic criteria for neurofibromatosis 2

Neurology, 2002-12, Vol.59 (11), p.1759

2002

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Malignant peripheral nerve sheath tumours in neurofibromatosis 1

Journal of medical genetics, 2002-05, Vol.39 (5), p.311-314

2002

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Management of the patient and family with neurofibromatosis 2: a consensus conference statement

British journal of neurosurgery, 2005-02, Vol.19 (1), p.5-12

2005

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The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

Journal of Medical Genetics, 2005-07, Vol.42 (7), p.540-546

2005

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Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspring

Journal of medical genetics, 2003-06, Vol.40 (6), p.459-463

2003

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Neurofibromatosis type 2

Journal of Medical Genetics, 2000-12, Vol.37 (12), p.897-904

2000

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Multiple meningiomas: differential involvement of the NF2 gene in children and adults

Journal of medical genetics, 2005-01, Vol.42 (1), p.45-48

2005

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Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation

Journal of medical genetics, 2003-11, Vol.40 (11), p.802-806

2003

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Methodological issues in longitudinal studies: vestibular schwannoma growth rates in neurofibromatosis 2

Journal of Medical Genetics, 2005-12, Vol.42 (12), p.903-906

2005

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Age related shift in the mutation spectra of germline and somatic NF2 mutations: hypothetical role of DNA repair mechanisms

Journal of medical genetics, 2005-08, Vol.42 (8), p.630-632

2005

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Evaluation of genotype-phenotype correlations in neurofibromatosis type 1

Journal of medical genetics, 2003-10, Vol.40 (10), p.e109-109

2003

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Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2

Journal of medical genetics, 2004-07, Vol.41 (7), p.529-534

2004

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Age associated increase in the prevalence of chromosome 22q loss of heterozygosity in histological subsets of benign meningioma

Journal of medical genetics, 2006-03, Vol.43 (3), p.285-287

2006

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Neurofibromatosis 2, radiosurgery and malignant nervous system tumours

British journal of cancer, 2000-02, Vol.82 (4), p.998-998

2000

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Neurofibromatosis 2 and malignant mesothelioma

Neurology, 2002-07, Vol.59 (2), p.290

2002

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Ocular Abnormalities in Neurofibromatosis 2

American journal of ophthalmology, 1995-11, Vol.120 (5), p.634-641

1995

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The neuroimaging and clinical spectrum of neurofibromatosis 2

Neurosurgery, 1996-05, Vol.38 (5), p.880-886

1996

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Interindividual differences in the concentration of 1-hydroxypyrene-glucuronide in urine and polycyclic aromatic hydrocarbon-DNA adducts in peripheral white blood cells after charbroiled beef consumption

Carcinogenesis (New York), 1995-05, Vol.16 (5), p.1079-1085

1995

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Genotype-phenotype correlations for cataracts in neurofibromatosis 2

Journal of medical genetics, 2003-10, Vol.40 (10), p.758-760

2003

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Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes

Human genetics, 1996-11, Vol.98 (5), p.534-538

1996

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Predictors of the Risk of Mortality in Neurofibromatosis 2

American journal of human genetics, 2002-10, Vol.71 (4), p.715-723

2002

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The ocular presentation of neurofibromatosis 2

Eye (London), 1997-01, Vol.11 (1), p.12-18

1997

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Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)

Genetic epidemiology, 2002-10, Vol.23 (3), p.245-259

2002

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Neurofibromatosis 2 (NF2) and malignant mesothelioma in a man with a constitutional NF2 missense mutation

Familial cancer, 2005-11, Vol.4 (4), p.321-322

2005

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Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

Evaluation of clinical diagnostic criteria for neurofibromatosis 2

Malignant peripheral nerve sheath tumours in neurofibromatosis 1

Management of the patient and family with neurofibromatosis 2: a consensus conference statement

The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2

Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspring

Neurofibromatosis type 2

Multiple meningiomas: differential involvement of the NF2 gene in children and adults

Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation

Methodological issues in longitudinal studies: vestibular schwannoma growth rates in neurofibromatosis 2

Age related shift in the mutation spectra of germline and somatic NF2 mutations: hypothetical role of DNA repair mechanisms

Evaluation of genotype-phenotype correlations in neurofibromatosis type 1

Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2

Age associated increase in the prevalence of chromosome 22q loss of heterozygosity in histological subsets of benign meningioma

Neurofibromatosis 2, radiosurgery and malignant nervous system tumours

Neurofibromatosis 2 and malignant mesothelioma

Ocular Abnormalities in Neurofibromatosis 2

The neuroimaging and clinical spectrum of neurofibromatosis 2

Interindividual differences in the concentration of 1-hydroxypyrene-glucuronide in urine and polycyclic aromatic hydrocarbon-DNA adducts in peripheral white blood cells after charbroiled beef consumption

Genotype-phenotype correlations for cataracts in neurofibromatosis 2

Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypes

Predictors of the Risk of Mortality in Neurofibromatosis 2

The ocular presentation of neurofibromatosis 2

Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2)

Neurofibromatosis 2 (NF2) and malignant mesothelioma in a man with a constitutional NF2 missense mutation

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