Prevalence and significance of cranial nerve imaging abnormalities in patients with hereditary neuropathies: Clinical implications at the skull base-Reference-Cited by-同舟云学术

Prevalence and significance of cranial nerve imaging abnormalities in patients with hereditary neuropathies: Clinical implications at the skull base

Published:2020-01-10 Issue:1 Volume:5 Page:11-18
ISSN:2378-8038
Container-title:Laryngoscope Investigative Otolaryngology
language:en
Short-container-title:Laryngoscope Investigative Otolaryngology

Author:

Bartholomew Ryan A.¹^ORCID,Zamani Amir A.²,Kim Grace S.³,Alyono Jennifer C.³,Steinert Haley⁴,Fridman Vera⁴,Sadjadi Reza⁵^ORCID,Jackler Robert K.³^ORCID,Corrales C. Eduardo¹

Affiliation:

1. Division of Otolaryngology‐Head and Neck SurgeryHarvard Medical School, Brigham and Women's Hospital Boston Massachusetts

2. Division of NeuroradiologyHarvard Medical School, Brigham and Women's Hospital Boston Massachusetts

3. Department of Otolaryngology‐Head and Neck Surgery, Division of Otology & Neurotology, StanfordStanford University School of Medicine California

4. Department of NeurologyUniversity of Colorado School of Medicine Aurora Colorado

5. Department of NeurologyHarvard Medical School, Massachusetts General Hospital Boston Massachusetts

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/lio2.343

Reference13 articles.

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3. Bilateral Facial and Trigeminal Nerve Hypertrophy in a Patient With Polyneuropathy

4. A novel mutation of the myelin P0 gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening

5. A familial Charcot‐Marie‐Tooth disease type 1B (CMTD1B) manifesting a new mutation of myelin P0 gene;Mitsui Y;Clin Neurol,1994

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