Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

110 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mutations in alpha-B-crystallin cause autosomal dominant axonal Charcot-Marie-Tooth disease with congenital cataracts.
Cortese A, Currò R, Ronco R, Blake J, Rossor AM, Bugiardini E, Laurà M, Warner T, Yousry T, Poh R, Polke J, Rebelo A, Dohrn MF, Saporta M, Houlden H, Zuchner S, Reilly MM. Cortese A, et al. Among authors: rossor am. Eur J Neurol. 2024 Jan;31(1):e16063. doi: 10.1111/ene.16063. Epub 2023 Sep 29. Eur J Neurol. 2024. PMID: 37772343 Free PMC article.
Strachan's syndrome and riboflavin deficiency.
Kramarz C, McHugh J, Rossor A. Kramarz C, et al. Pract Neurol. 2024 Mar 19;24(2):121-128. doi: 10.1136/pn-2023-003822. Pract Neurol. 2024. PMID: 38290841 Review.
Trigeminal neuropathy from root entry zone infarction.
Farag M, Kafiabadi S, Roy A, Rossor AM, Holmes P. Farag M, et al. Among authors: rossor am. Pract Neurol. 2023 Nov 23;23(6):523-524. doi: 10.1136/pn-2023-003823. Pract Neurol. 2023. PMID: 37524437 No abstract available.
Digenic FLNA and UCHL1 variants resulting in a complex phenotype.
Pernice HF, O'Donnell LF, Rossor AM, Laura M, Record CJ, Skorupinska M, Blake J, Poh R, Polke J, Reilly MM. Pernice HF, et al. Among authors: rossor am. J Peripher Nerv Syst. 2024 Mar;29(1):111-115. doi: 10.1111/jns.12611. Epub 2024 Jan 7. J Peripher Nerv Syst. 2024. PMID: 38131667
Nutritional peripheral neuropathies.
Kramarz C, Murphy E, Reilly MM, Rossor AM. Kramarz C, et al. Among authors: rossor am. J Neurol Neurosurg Psychiatry. 2023 Dec 14;95(1):61-72. doi: 10.1136/jnnp-2022-329849. J Neurol Neurosurg Psychiatry. 2023. PMID: 37536924 Review.
Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.
Record CJ, Skorupinska M, Laura M, Rossor AM, Pareyson D, Pisciotta C, Feely SME, Lloyd TE, Horvath R, Sadjadi R, Herrmann DN, Li J, Walk D, Yum SW, Lewis RA, Day J, Burns J, Finkel RS, Saporta MA, Ramchandren S, Weiss MD, Acsadi G, Fridman V, Muntoni F, Poh R, Polke JM, Zuchner S, Shy ME, Scherer SS, Reilly MM; Inherited Neuropathies Consortium—Rare Disease Clinical Research Network. Record CJ, et al. Among authors: rossor am. Brain. 2023 Oct 3;146(10):4336-4349. doi: 10.1093/brain/awad187. Brain. 2023. PMID: 37284795 Free PMC article.
Toxic neuropathies: a practical approach.
Smyth D, Kramarz C, Carr AS, Rossor AM, Lunn MP. Smyth D, et al. Among authors: rossor am. Pract Neurol. 2023 Apr;23(2):120-130. doi: 10.1136/pn-2022-003444. Epub 2023 Jan 25. Pract Neurol. 2023. PMID: 36697225 Review.
110 results