Hanemann CO - Search Results

1

Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time.

Sperfeld AD, Kassubek J, Crosby AH, Winner B, Ludolph AC, Uttner I, Hanemann CO. Sperfeld AD, et al. Among authors: hanemann co. J Neurol. 2004 Oct;251(10):1285-7. doi: 10.1007/s00415-004-0562-5. J Neurol. 2004. PMID: 15503116 No abstract available.

2

Hereditary motor neuropathies and motor neuron diseases: which is which.

Hanemann CO, Ludolph AC. Hanemann CO, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Dec;3(4):186-9. doi: 10.1080/146608202760839003. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12710507 Review.

3

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

Münch C, Rosenbohm A, Sperfeld AD, Uttner I, Reske S, Krause BJ, Sedlmeier R, Meyer T, Hanemann CO, Stumm G, Ludolph AC. Münch C, et al. Among authors: hanemann co. Ann Neurol. 2005 Nov;58(5):777-80. doi: 10.1002/ana.20631. Ann Neurol. 2005. PMID: 16240349

4

Laryngospasm: an underdiagnosed symptom of X-linked spinobulbar muscular atrophy.

Sperfeld AD, Hanemann CO, Ludolph AC, Kassubek J. Sperfeld AD, et al. Among authors: hanemann co. Neurology. 2005 Feb 22;64(4):753-4. doi: 10.1212/01.WNL.0000151978.74467.E7. Neurology. 2005. PMID: 15728312

5

MR-pathologic comparison of the upper spinal cord in different motor neuron diseases.

Sperfeld AD, Bretschneider V, Flaith L, Unrath A, Hanemann CO, Ludolph AC, Kassubek J. Sperfeld AD, et al. Among authors: hanemann co. Eur Neurol. 2005;53(2):74-7. doi: 10.1159/000084650. Epub 2005 Mar 22. Eur Neurol. 2005. PMID: 15785072

6

Motor protein diseases of the nervous system.

Hanemann CO, Ludolph AC. Hanemann CO, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Dec;6(4):197-201. doi: 10.1080/14660820510035360. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005. PMID: 16319022 Review.

7

Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2.

Sperfeld AD, Hein C, Schröder JM, Ludolph AC, Hanemann CO. Sperfeld AD, et al. Among authors: hanemann co. Brain. 2002 May;125(Pt 5):996-1004. doi: 10.1093/brain/awf115. Brain. 2002. PMID: 11960890

8

ALS/MND meeting of the European AlS/MND group Reisensburg Castle 30 January - 1 February 2003.

Hanemann CO, Ludolph AC. Hanemann CO, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Jun;4(2):121-2. doi: 10.1080/14660820310004221. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 14506945 No abstract available.

9

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

Münch C, Sedlmeier R, Meyer T, Homberg V, Sperfeld AD, Kurt A, Prudlo J, Peraus G, Hanemann CO, Stumm G, Ludolph AC. Münch C, et al. Among authors: hanemann co. Neurology. 2004 Aug 24;63(4):724-6. doi: 10.1212/01.wnl.0000134608.83927.b1. Neurology. 2004. PMID: 15326253

10

X-linked bulbospinal neuronopathy: Kennedy disease.

Sperfeld AD, Karitzky J, Brummer D, Schreiber H, Häussler J, Ludolph AC, Hanemann CO. Sperfeld AD, et al. Among authors: hanemann co. Arch Neurol. 2002 Dec;59(12):1921-6. doi: 10.1001/archneur.59.12.1921. Arch Neurol. 2002. PMID: 12470181

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