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109 results
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Correlation between Weakness and Axonal Loss in Patients with CMT1A.
Krajewski K, Turansky C, Lewis R, Garbern J, Hinderer S, Kamholz J, Shy ME. Krajewski K, et al. Among authors: garbern j. Ann N Y Acad Sci. 1999 Oct;883(1):490-492. doi: 10.1111/j.1749-6632.1999.tb08618.x. Ann N Y Acad Sci. 1999. PMID: 29086958 No abstract available.
Persistent CNS dysfunction in a boy with CMT1X.
Siskind C, Feely SM, Bernes S, Shy ME, Garbern JY. Siskind C, et al. J Neurol Sci. 2009 Apr 15;279(1-2):109-13. doi: 10.1016/j.jns.2008.12.031. Epub 2009 Feb 3. J Neurol Sci. 2009. PMID: 19193385
Peripheral neuropathy caused by proteolipid protein gene mutations.
Garbern JY, Cambi F, Lewis R, Shy M, Sima A, Kraft G, Vallat JM, Bosch EP, Hodes ME, Dlouhy S, Raskind W, Bird T, Macklin W, Kamholz J. Garbern JY, et al. Ann N Y Acad Sci. 1999 Sep 14;883:351-65. Ann N Y Acad Sci. 1999. PMID: 10586260
Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations.
Garbern JY, Cambi F, Lewis R, Shy M, Sima A, Kraft G, Vallat JM, Bosch EP, Hodes ME, Dlouhy S, Raskind W, Bird T, Macklin W, Kamholz J. Garbern JY, et al. Ann N Y Acad Sci. 1999 Oct;883(1):351-365. doi: 10.1111/j.1749-6632.1999.tb08597.x. Ann N Y Acad Sci. 1999. PMID: 29086946
109 results