Results 171 to 180 of about 20,018 (209)
Prevalence of Oral Alterations and Correlation Between Oral and Cutaneous Neurofibromas in Neurofibromatosis Type 1: A Retrospective Case-Control Study. [PDF]
J Oral Pathol Medde Pinho Montovani P +3 more
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Solitary Fibrous Tumors of the Submandibular Gland: A Case Report. [PDF]
Clin Case RepGarousi M +5 more
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Immortalization and characterization of Schwann cell lines derived from NF1-associated cutaneous neurofibromas. [PDF]
PLoS OneLi H +20 more
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Nipple-Areolar Complex Neurotization Following Nipple-sparing Mastectomy and Breast Reconstruction for Solitary Breast Neurofibroma. [PDF]
Plast Reconstr Surg Glob OpenAhmed S +5 more
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RadioGraphicsJournal of the European Academy of Dermatology and Venereology, EarlyView.
Shehbaz Ansari +4 more
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Insight - the Journal of the American Society of Ophthalmic Registered Nurses, 1996
Although neurofibroma is a rare orbital tumor, ophthalmic nurses may have the first opportunity to observe patients with this tumor. These patients may first be seen with normal visual acuity, proptosis, or affected ocular motility. An interesting patient who was diagnosed with an orbital neurofibroma is presented.
C A, Servodidio +2 more
openaire +2 more sources
Although neurofibroma is a rare orbital tumor, ophthalmic nurses may have the first opportunity to observe patients with this tumor. These patients may first be seen with normal visual acuity, proptosis, or affected ocular motility. An interesting patient who was diagnosed with an orbital neurofibroma is presented.
C A, Servodidio +2 more
openaire +2 more sources
Histopathology, 1977
At rare intervals in the literature, reports have appeared of a skin tumour containing structures resembling Pacinian corpuscles. Four such tumours collected over the course of 20 years are described and the literature reviewed.
D M, MacDonald, E, Wilson-Jones
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At rare intervals in the literature, reports have appeared of a skin tumour containing structures resembling Pacinian corpuscles. Four such tumours collected over the course of 20 years are described and the literature reviewed.
D M, MacDonald, E, Wilson-Jones
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Otolaryngology–Head and Neck Surgery, 1980
A neurofibroma in the larynx is quite unusual and is more likely to appear as a solitary, isolated lesion rather than a concomitant finding in von Recklinghausen's disease. A case is presented of a patient with residual endolaryngeal neurofibroma despite eight attempts at removal.
J S, Supance, D J, Quenelle, J, Crissman
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A neurofibroma in the larynx is quite unusual and is more likely to appear as a solitary, isolated lesion rather than a concomitant finding in von Recklinghausen's disease. A case is presented of a patient with residual endolaryngeal neurofibroma despite eight attempts at removal.
J S, Supance, D J, Quenelle, J, Crissman
openaire +2 more sources