Li J - Search Results

1

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.

Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium. Tao F, et al. Among authors: li j. J Neuromuscul Dis. 2019;6(2):201-211. doi: 10.3233/JND-190377. J Neuromuscul Dis. 2019. PMID: 30958311 Free PMC article.

2

Hereditary neuropathy with liability to pressure palsy: the electrophysiology fits the name.

Li J, Krajewski K, Shy ME, Lewis RA. Li J, et al. Neurology. 2002 Jun 25;58(12):1769-73. doi: 10.1212/wnl.58.12.1769. Neurology. 2002. PMID: 12084875

3

Asymmetric flaccid paralysis: a neuromuscular presentation of West Nile virus infection.

Li J, Loeb JA, Shy ME, Shah AK, Tselis AC, Kupski WJ, Lewis RA. Li J, et al. Ann Neurol. 2003 Jun;53(6):703-10. doi: 10.1002/ana.10575. Ann Neurol. 2003. PMID: 12783415

4

Motor unit number estimate of distal and proximal muscles in Charcot-Marie-Tooth disease.

Lewis RA, Li J, Fuerst DR, Shy ME, Krajewski K. Lewis RA, et al. Among authors: li j. Muscle Nerve. 2003 Aug;28(2):161-7. doi: 10.1002/mus.10419. Muscle Nerve. 2003. PMID: 12872319 Clinical Trial.

5

Phenotypic clustering in MPZ mutations.

Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J. Shy ME, et al. Among authors: li j. Brain. 2004 Feb;127(Pt 2):371-84. doi: 10.1093/brain/awh048. Epub 2004 Jan 7. Brain. 2004. PMID: 14711881 Review.

6

Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies.

Li J, Krajewski K, Lewis RA, Shy ME. Li J, et al. Muscle Nerve. 2004 Feb;29(2):205-10. doi: 10.1002/mus.10521. Muscle Nerve. 2004. PMID: 14755484

7

Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.

Li J, Bai Y, Ghandour K, Qin P, Grandis M, Trostinskaia A, Ianakova E, Wu X, Schenone A, Vallat JM, Kupsky WJ, Hatfield J, Shy ME. Li J, et al. Brain. 2005 May;128(Pt 5):1168-77. doi: 10.1093/brain/awh483. Epub 2005 Mar 17. Brain. 2005. PMID: 15774502

8

T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.

Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. Shy ME, et al. Among authors: li j. Ann Neurol. 2006 Feb;59(2):358-64. doi: 10.1002/ana.20777. Ann Neurol. 2006. PMID: 16437560

9

Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.

Li J, Bai Y, Ianakova E, Grandis M, Uchwat F, Trostinskaia A, Krajewski KM, Garbern J, Kupsky WJ, Shy ME. Li J, et al. J Comp Neurol. 2006 Sep 10;498(2):252-65. doi: 10.1002/cne.21051. J Comp Neurol. 2006. PMID: 16856127

10

Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes.

Bai Y, Ianokova E, Pu Q, Ghandour K, Levinson R, Martin JJ, Ceuterick-de Groote C, Mazanec R, Seeman P, Shy ME, Li J. Bai Y, et al. Among authors: li j. Arch Neurol. 2006 Dec;63(12):1787-94. doi: 10.1001/archneur.63.12.1787. Arch Neurol. 2006. PMID: 17172621

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

177,415 results

Search Page