A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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im Januar 2009 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в січні 2009

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A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

@en

A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

@en

A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

@nl

P1476

A rare association between neurofibromatosis type I and Cogan's syndrome: Case report

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P2093

Donato Gianfelice

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Francesca Forli

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Stefano Berrettini

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P2860

The protein product of the neurofibromatosis type 1 gene is expressed at highest abundance in neurons, Schwann cells, and oligodendrocytes

Cogan syndrome: a retrospective review of 60 patients throughout a half century

Clinical manifestations and management of neurofibromatosis type 1.

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update.

Pathophysiology of neurofibromatosis type 1.

Middle-ear development. V: Development of umbo sensitivity in the gerbil.

Neurofibromatosis 1 in childhood.

Cochlear implantation in patients with Cogan's syndrome: a review of four cases.

Use of "unidentified bright objects" on MRI for diagnosis of neurofibromatosis 1 in children.

Neurofibromatosis type I involving the external auditory canal.

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241-245

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scholarly article

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10.3109/16513860903076407

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P433

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P478

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Emanuele Neri

Susanna Passetti

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2009-01-01T00:00:00Z

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