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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1979 1
1993 2
1995 4
1996 1
1998 2
1999 1
2000 1
2001 2
2002 5
2003 2
2004 4
2005 4
2006 7
2007 5
2008 6
2009 10
2010 13
2011 26
2012 33
2013 24
2014 22
2015 27
2016 22
2017 26
2018 22
2019 29
2020 34
2021 29
2022 28
2023 31
2024 29

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387 results

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Page 1
Genetic pain loss disorders.
Lischka A, Lassuthova P, Çakar A, Record CJ, Van Lent J, Baets J, Dohrn MF, Senderek J, Lampert A, Bennett DL, Wood JN, Timmerman V, Hornemann T, Auer-Grumbach M, Parman Y, Hübner CA, Elbracht M, Eggermann K, Geoffrey Woods C, Cox JJ, Reilly MM, Kurth I. Lischka A, et al. Among authors: reilly mm. Nat Rev Dis Primers. 2022 Jun 16;8(1):41. doi: 10.1038/s41572-022-00365-7. Nat Rev Dis Primers. 2022. PMID: 35710757 Review.
Blood biomarkers of peripheral neuropathy.
Rossor AM, Reilly MM. Rossor AM, et al. Among authors: reilly mm. Acta Neurol Scand. 2022 Oct;146(4):325-331. doi: 10.1111/ane.13650. Epub 2022 May 25. Acta Neurol Scand. 2022. PMID: 35611606 Free PMC article. Review.
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease.
Yiu EM, Bray P, Baets J, Baker SK, Barisic N, de Valle K, Estilow T, Farrar MA, Finkel RS, Haberlová J, Kennedy RA, Moroni I, Nicholson GA, Ramchandren S, Reilly MM, Rose K, Shy ME, Siskind CE, Yum SW, Menezes MP, Ryan MM, Burns J. Yiu EM, et al. Among authors: reilly mm. J Neurol Neurosurg Psychiatry. 2022 May;93(5):530-538. doi: 10.1136/jnnp-2021-328483. Epub 2022 Feb 9. J Neurol Neurosurg Psychiatry. 2022. PMID: 35140138 Review.
Differentiating lower motor neuron syndromes.
Garg N, Park SB, Vucic S, Yiannikas C, Spies J, Howells J, Huynh W, Matamala JM, Krishnan AV, Pollard JD, Cornblath DR, Reilly MM, Kiernan MC. Garg N, et al. Among authors: reilly mm. J Neurol Neurosurg Psychiatry. 2017 Jun;88(6):474-483. doi: 10.1136/jnnp-2016-313526. Epub 2016 Dec 21. J Neurol Neurosurg Psychiatry. 2017. PMID: 28003344 Free PMC article. Review.
Nutritional peripheral neuropathies.
Kramarz C, Murphy E, Reilly MM, Rossor AM. Kramarz C, et al. Among authors: reilly mm. 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.
RFC1 CANVAS / Spectrum Disorder.
Cortese A, Reilly MM, Houlden H. Cortese A, et al. Among authors: reilly mm. 2020 Nov 25. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2020 Nov 25. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 33237689 Free Books & Documents. Review.
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: reilly mm. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
387 results