The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.

[1]  D. Louis,et al.  Optic pathway gliomas in children with neurofibromatosis 1: Consensus statement from the nf1 optic pathway glioma task force , 1997, Annals of neurology.

[2]  D. Gutmann,et al.  Juvenile Xanthogranuloma, Neurofibromatosis 1, and Juvenile Chronic Myeloid Leukemia , 1996 .

[3]  M. Kaiser-Kupfer,et al.  Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities. , 1996, American journal of human genetics.

[4]  S. Pulst,et al.  A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes , 1996, Neurology.

[5]  R. Weksberg,et al.  Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. , 1996, American journal of human genetics.

[6]  B. Moore,et al.  Neuropsychological significance of areas of high signal intensity on brain MRIs of children with neurofibromatosis , 1996, Neurology.

[7]  S. Pulst,et al.  The neuroimaging and clinical spectrum of neurofibromatosis 2. , 1996, Neurosurgery.

[8]  B. Korf,et al.  Neurobehavioral profiles of children with neurofibromatosis 1 referred for learning disabilities are sex-specific. , 1996, American journal of medical genetics.

[9]  M. Short,et al.  Schwannomatosis , 1996, Neurology.

[10]  C. R. Abernathy,et al.  Somatic mosaicism in a patient with neurofibromatosis type 1. , 1996, American journal of human genetics.

[11]  B. Korf,et al.  Deletion of the entire NF1 gene detected by the FISH: four deletion patients associated with severe manifestations. , 1995, American journal of medical genetics.

[12]  D. Abeliovich,et al.  Familial café au lait spots: a variant of neurofibromatosis type 1. , 1995, Journal of medical genetics.

[13]  J. Charrow,et al.  Optic pathway tumors in children: the effect of neurofibromatosis type 1 on clinical manifestations and natural history. , 1995, The Journal of pediatrics.

[14]  S. Pulst,et al.  Ocular Abnormalities in Neurofibromatosis 2 , 1995 .

[15]  G. Annéren,et al.  Noonan syndrome with café‐au‐lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus , 1995, Clinical genetics.

[16]  A. Zvulunov,et al.  Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia. World statistical analysis. , 1995, Archives of dermatology.

[17]  E. Zackai,et al.  Neurofibromatosis type 1: pathologic substrate of high-signal-intensity foci in the brain. , 1995, Radiology.

[18]  D. Evans,et al.  Diagnostic issues in a family with late onset type 2 neurofibromatosis. , 1995, Journal of medical genetics.

[19]  K. Hoang-Xuan,et al.  Screening for germ‐line mutations in the NF2 Gene , 1995, Genes, chromosomes & cancer.

[20]  N. Zigmond.  Models for Delivery of Special Education Services to Students with Learning Disabilities in Public Schools , 1995, Journal of child neurology.

[21]  R. Briggs,et al.  Comprehensive management of bilateral acoustic neuromas. Current perspectives. , 1994, Archives of otolaryngology--head & neck surgery.

[22]  A. Paller,et al.  Familial multiple cafe au lait spots. , 1994, Archives of dermatology.

[23]  M I Kaiser-Kupfer,et al.  Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity. , 1994, American journal of medical genetics.

[24]  T. Strachan,et al.  Germline mutations in the neurofibromatosis type 2 tumour suppressor gene. , 1994, Human molecular genetics.

[25]  K. North,et al.  Specific learning disability in children with neurofibromatosis type 1 , 1994, Neurology.

[26]  R. Bryan,et al.  Neurofibromatosis type 1: the cognitive phenotype. , 1994, The Journal of pediatrics.

[27]  S. Green,et al.  What is segmental neurofibromatosis? , 1994, The British journal of dermatology.

[28]  K. North.  Neurofibromatosis Type 1: Review of the First 200 Patients in an Australian Clinic , 1993, Journal of child neurology.

[29]  S. Pulst,et al.  Familial meningioma is not allelic to neurofibromatosis 2 , 1993, Neurology.

[30]  S. Pulst,et al.  Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 , 1993, Nature.

[31]  M. Prados,et al.  Carboplatin and vincristine for recurrent and newly diagnosed low-grade gliomas of childhood. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[32]  J. Haines,et al.  A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor , 1993, Cell.

[33]  J. Charrow,et al.  Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage. , 1993, American journal of medical genetics.

[34]  E. R. Kandel,et al.  Synaptic transmission: A bidirectional and self-modifiable form of cell-cell communication , 1993, Cell.

[35]  B. Korf.  Diagnostic outcome in children with multiple café au lait spots. , 1992, Pediatrics.

[36]  D. Evans,et al.  A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity. , 1992, Journal of medical genetics.

[37]  B. Cohen.  Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, 2nd Ed. , 1992 .

[38]  N. Cohen,et al.  Cochlear implants in the management of bilateral acoustic neuromas. , 1992, The American journal of otology.

[39]  V. Riccardi,et al.  Neurofibromatosis: Phenotype, Natural History and Pathogenesis , 1992 .

[40]  J. Flickinger,et al.  Tumor control after stereotactic radiosurgery in neurofibromatosis patients with bilateral acoustic tumors. , 1992, Neurosurgery.

[41]  W. Burke,et al.  Large de novo DNA deletion in a patient with sporadic neurofibromatosis 1, mental retardation, and dysmorphism. , 1992, Journal of medical genetics.

[42]  R A Levine,et al.  Preservation of hearing and facial nerve function in resection of acoustic neuroma , 1992, The Laryngoscope.

[43]  D. Evans,et al.  A clinical study of type 2 neurofibromatosis. , 1992, The Quarterly journal of medicine.

[44]  L. Lunsford,et al.  Stereotactic radiosurgery in the treatment of patients with acoustic tumors. , 1992, Otolaryngologic clinics of North America.

[45]  M. Burch,et al.  A clinical study of Noonan syndrome. , 1992, Archives of disease in childhood.

[46]  J. Allanson,et al.  Watson syndrome: is it a subtype of type 1 neurofibromatosis? , 1991, Journal of medical genetics.

[47]  V. Riccardi.  Neurofibromatosis: past, present, and future. , 1991, The New England journal of medicine.

[48]  R. Miyamoto,et al.  Preservation of Hearing in Neurofibromatosis 2 , 1990, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[49]  B. Brownstein,et al.  Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. , 1990, Science.

[50]  P. O'Connell,et al.  Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus , 1990, Cell.

[51]  P. O'Connell,et al.  A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations , 1990, Cell.

[52]  M. Kaiser-Kupfer,et al.  NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update. , 1990, Annals of internal medicine.

[53]  E. Zackai,et al.  The diagnosis of neurofibromatosis-1 in the child under the age of 6 years. , 1989, American journal of diseases of children.

[54]  D. Shucard,et al.  The significance of MRI abnormalities in children with neurofibromatosis , 1989, Neurology.

[55]  S. Huson,et al.  Von Recklinghausen neurofibromatosis: a clinical and population study in south-east Wales , 1988 .

[56]  J. Bader.  Neurofibromatosis and Cancer , 1986, Annals of the New York Academy of Sciences.

[57]  N. J. Thompson,et al.  Plexiform (multinodular) schwannoma. A tumor simulating the plexiform neurofibroma. , 1983, The American journal of surgical pathology.

[58]  R. Eldridge,et al.  Central neurofibromatosis with bilateral acoustic neuroma , 1980, Neurology.

[59]  G. H. Watson.  Pulmonary stenosis, café-au-lait spots, and dull intelligence. , 1967, Archives of disease in childhood.

[60]  F. Crowe.  AXILLARY FRECKLING AS A DIAGNOSTIC AID IN NEUROFIBROMATOSIS. , 1964, Annals of internal medicine.

[61]  R. Tenconi,et al.  Headache in Patients With Neurofibromatosis Type 1 , 1996, Headache.

[62]  R. Heim,et al.  Screening for truncated NF1 proteins , 1994, Nature Genetics.

[63]  R. Hughes,et al.  The Neurofibromatoses : a pathogenetic and clinical overview , 1994 .

[64]  D. Fretzin,et al.  Genetic counseling in segmental neurofibromatosis. , 1990, Journal of the American Academy of Dermatology.