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1997, International review of child neurology series, ISBN 9781898683131, x, 132
Book
1998, Human molecular genetics series, ISBN 9781859961919, xv, 230
Book
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 04/2019, Volume 71, Issue 4, p. 368
A large number of genetic neurological disorders are accompanied by dermatological manifestations. Among them, neurofibromatosis 1 (NF1, Recklinghausen... 
Neurofibromatosis 2 - pathology | Diagnosis, Differential | Neurofibromatosis 1 - pathology | Neurofibromatosis 2 - diagnosis | Humans | Neurofibromatosis 1 - diagnosis | Cafe-au-Lait Spots - pathology
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2011, Volume 178, Issue 5, pp. 1932 - 1939
Although a mutation in the NF1 gene is the only factor required to initiate the neurocutaneous-skeletal neurofibromatosis 1 (NF1) syndrome, the pathoetiology... 
Pathology | MUTATION ANALYSIS | IN-VITRO | MESSENGER-RNA | TUMOR-SUPPRESSOR PROTEIN | SCHWANN-CELLS | PATHOLOGY | TYPE-1 GENE-PRODUCT | STEADY-STATE LEVELS | NF1 GENE | HUMAN MELANOCYTES | AU-LAIT SPOTS | Multipotent Stem Cells - pathology | Neurofibromatosis 1 - pathology | Phenotype | Animals | Humans | Genotype | Mutation | Neurofibromatosis 1 - genetics | Genes, Neurofibromatosis 1 | Mini-Review
Journal Article
by Kim, JY and Lee, MY and Lee, YC and Shin, HY
MEDICINE, ISSN 0025-7974, 08/2019, Volume 98, Issue 31, p. e16699
Rationale: We report a rare case of neurofibroma in the form of tarsal conjunctival thickening of the eyelid in patients with neurofibromatosis type 1 (NF1),... 
neurofibromatosis type 1 | Lisch nodule | MEDICINE, GENERAL & INTERNAL | neurofibroma | tarsal conjunctiva | Case studies | Diagnosis | Eyelid diseases | Neurofibromatosis
Journal Article