Hanemann CO - Search Results

1

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

Matsunami N, Smith B, Ballard L, Lensch MW, Robertson M, Albertsen H, Hanemann CO, Müller HW, Bird TD, White R, et al. Matsunami N, et al. Among authors: hanemann co. Nat Genet. 1992 Jun;1(3):176-9. doi: 10.1038/ng0692-176. Nat Genet. 1992. PMID: 1303231

2

Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy.

Hanemann CO, Müller HW. Hanemann CO, et al. Trends Neurosci. 1998 Jul;21(7):282-6. doi: 10.1016/s0166-2236(97)01222-8. Trends Neurosci. 1998. PMID: 9683317 Review.

3

Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot-Marie-Tooth type 1A.

Hanemann CO, D'Urso D, Gabreëls-Festen AA, Müller HW. Hanemann CO, et al. Brain. 2000 May;123 ( Pt 5):1001-6. doi: 10.1093/brain/123.5.1001. Brain. 2000. PMID: 10775544

4

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.

Timmerman V, Nelis E, Van Hul W, Nieuwenhuijsen BW, Chen KL, Wang S, Ben Othman K, Cullen B, Leach RJ, Hanemann CO, et al. Timmerman V, et al. Among authors: hanemann co. Nat Genet. 1992 Jun;1(3):171-5. doi: 10.1038/ng0692-171. Nat Genet. 1992. PMID: 1303230

5

Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies.

Hanemann CO, Stoll G, D'Urso D, Fricke W, Martin JJ, Van Broeckhoven C, Mancardi GL, Bartke I, Müller HW. Hanemann CO, et al. J Neurosci Res. 1994 Apr 1;37(5):654-9. doi: 10.1002/jnr.490370513. J Neurosci Res. 1994. PMID: 8028042

6

Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs.

Hanemann CO, Gabreëls-Festen AA, Stoll G, Müller HW. Hanemann CO, et al. Acta Neuropathol. 1997 Oct;94(4):310-5. doi: 10.1007/s004010050712. Acta Neuropathol. 1997. PMID: 9341930

7

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages.

Hanemann CO, Gabreëls-Fasten AA, Müller HW, Stoll G. Hanemann CO, et al. Brain. 1996 Oct;119 ( Pt 5):1461-9. doi: 10.1093/brain/119.5.1461. Brain. 1996. PMID: 8931571

8

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies.

Stoll G, Gabreëls-Festen AA, Jander S, Müller HW, Hanemann CO. Stoll G, et al. Among authors: hanemann co. Muscle Nerve. 1998 Nov;21(11):1419-27. doi: 10.1002/(sici)1097-4598(199811)21:11<1419::aid-mus9>3.0.co;2-c. Muscle Nerve. 1998. PMID: 9771665

9

PMP22 expression in CMT1a neuropathy.

Hanemann CO, Stoll G, Müller HW. Hanemann CO, et al. Ann Neurol. 1995 Jan;37(1):136. doi: 10.1002/ana.410370127. Ann Neurol. 1995. PMID: 7818248 No abstract available.

10

Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients.

Hanemann CO, Rosenbaum C, Kupfer S, Wosch S, Stoegbauer F, Müller HW. Hanemann CO, et al. Glia. 1998 Jun;23(2):89-98. doi: 10.1002/(sici)1098-1136(199806)23:2<89::aid-glia1>3.0.co;2-z. Glia. 1998. PMID: 9600378

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