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Literature DB >> 23598837

Neurofibromatosis: types 1 and 2.

Abstract

Neurofibromatosis types 1 and 2 are a group of neurocutaneous syndromes resulting from disorders in cell regulation. Despite sharing a common name, neurofibromatosis types 1 and 2 are quite distinct phakomatoses, both clinically and genetically.

Entities: Disease Gene

Mesh：

Year: 2013 PMID： 23598837 PMCID： PMC7965224 DOI： 10.3174/ajnr.A3534

Source DB: PubMed Journal: AJNR Am J Neuroradiol ISSN： 0195-6108 Impact factor: 3.825

12 in total

1. Automated detection and volume measurement of plexiform neurofibromas in neurofibromatosis 1 using magnetic resonance imaging.

Authors: Jeffrey Solomon; Katherine Warren; Eva Dombi; Nicholas Patronas; Brigitte Widemann
Journal: Comput Med Imaging Graph Date: 2004-07 Impact factor: 4.790

Review 2. Neuro-ophthalmic features of the neurocutaneous syndromes.

Authors: Jane W Chan
Journal: Int Ophthalmol Clin Date: 2012

Review 3. Neurofibromatosis type 2.

Authors: Ashok R Asthagiri; Dilys M Parry; John A Butman; H Jeffrey Kim; Ekaterini T Tsilou; Zhengping Zhuang; Russell R Lonser
Journal: Lancet Date: 2009-05-22 Impact factor: 79.321

Review 4. Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesis.

Authors: Sebastian Laycock-van Spyk; Nick Thomas; David N Cooper; Meena Upadhyaya
Journal: Hum Genomics Date: 2011-10 Impact factor: 4.639

5. Brainstem lesions in neurofibromatosis type 1.

Authors: Nicole J Ullrich; Ali I Raja; Mira B Irons; Mark W Kieran; Liliana Goumnerova
Journal: Neurosurgery Date: 2007-10 Impact factor: 4.654

6. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis.

Authors: E Legius; D A Marchuk; F S Collins; T W Glover
Journal: Nat Genet Date: 1993-02 Impact factor: 38.330

Neurofibromatosis: types 1 and 2.

1. Automated detection and volume measurement of plexiform neurofibromas in neurofibromatosis 1 using magnetic resonance imaging.

Review 2. Neuro-ophthalmic features of the neurocutaneous syndromes.

Review 3. Neurofibromatosis type 2.

Review 4. Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesis.

5. Brainstem lesions in neurofibromatosis type 1.

6. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis.

7. Whole body MR imaging in neurofibromatosis type 1.

Review 8. Magic but treatable? Tumours due to loss of merlin.

Review 9. Clinical and genetic aspects of neurofibromatosis 1.

Review 10. Nf2/Merlin: a coordinator of receptor signalling and intercellular contact.

Review 1. Diagnosis and differential diagnosis of large-vessel vasculitides.

2. Oculomotor nerve palsy in neurofibromatosis type 2.