Literature DB >> 7712636

Neurofibromatosis.

K L Roos1, M Muckway.   

Abstract

The neurofibromatoses are defined by the presence of café-au-lait macules and neurofibromas and are associated with central and peripheral nervous system tumors. Individuals with neurofibromatosis 1 are at risk for optic nerve gliomas, nerve root and plexi neurofibromas and schwannomas, spinal cord tumors, benign and malignant peripheral nerve sheath tumors, and pheochromocytomas. Individuals with neurofibromatosis 2 are at risk for presenile cataracts, vestibular schwannomas, intracranial and intraspinal meningiomas, and intramedullary spinal cord ependymomas.

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Mesh:

Year:  1995        PMID: 7712636

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  2 in total

Review 1.  Genetic basis of intramedullary spinal cord tumors and therapeutic implications.

Authors:  A T Parsa; A J Fiore; P C McCormick; J N Bruce
Journal:  J Neurooncol       Date:  2000-05       Impact factor: 4.130

2.  Survival of Human Neurofibroma in Immunodeficient Mice and Initial Results of Therapy With Pirfenidone.

Authors:  Dusica Babovic-Vuksanovic; Lydia Petrovic; Bruce E. Knudsen; Timothy B. Plummer; Joseph E. Parisi; Srdan Babovic; Jeffrey L. Platt
Journal:  J Biomed Biotechnol       Date:  2004
  2 in total

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