Sperfeld AD - Search Results

1

Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis.

Dorst J, Kühnlein P, Hendrich C, Kassubek J, Sperfeld AD, Ludolph AC. Dorst J, et al. Among authors: sperfeld ad. J Neurol. 2011 Apr;258(4):613-7. doi: 10.1007/s00415-010-5805-z. Epub 2010 Dec 3. J Neurol. 2011. PMID: 21128082

2

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: sperfeld ad. Neurology. 2004 Aug 24;63(4):724-6. doi: 10.1212/01.wnl.0000134608.83927.b1. Neurology. 2004. PMID: 15326253

3

CSF glial markers correlate with survival in amyotrophic lateral sclerosis.

Süssmuth SD, Sperfeld AD, Hinz A, Brettschneider J, Endruhn S, Ludolph AC, Tumani H. Süssmuth SD, et al. Among authors: sperfeld ad. Neurology. 2010 Mar 23;74(12):982-7. doi: 10.1212/WNL.0b013e3181d5dc3b. Neurology. 2010. PMID: 20308682

4

The advanced glycation end-product N epsilon-(carboxymethyl)lysine level is elevated in cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

Kaufmann E, Boehm BO, Süssmuth SD, Kientsch-Engel R, Sperfeld A, Ludolph AC, Tumani H. Kaufmann E, et al. Neurosci Lett. 2004 Nov 23;371(2-3):226-9. doi: 10.1016/j.neulet.2004.08.071. Neurosci Lett. 2004. PMID: 15519762

5

Widespread white matter changes in Kennedy disease: a voxel based morphometry study.

Kassubek J, Juengling FD, Sperfeld AD. Kassubek J, et al. Among authors: sperfeld ad. J Neurol Neurosurg Psychiatry. 2007 Nov;78(11):1209-12. doi: 10.1136/jnnp.2006.112532. Epub 2007 Mar 1. J Neurol Neurosurg Psychiatry. 2007. PMID: 17332050 Free PMC article.

6

Amygdala size reduction is associated with memory deficits in complicated hereditary spastic paraparesis: an MRI study.

Pinkhardt EH, Sperfeld AD, Uttner I, Ludolph AC, Kassubek J. Pinkhardt EH, et al. Among authors: sperfeld ad. Eur Neurol. 2010;64(2):117-23. doi: 10.1159/000316773. Epub 2010 Jul 22. Eur Neurol. 2010. PMID: 20664204

7

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation.

Sperfeld AD, Collatz MB, Baier H, Palmbach M, Storch A, Schwarz J, Tatsch K, Reske S, Joosse M, Heutink P, Ludolph AC. Sperfeld AD, et al. Ann Neurol. 1999 Nov;46(5):708-15. doi: 10.1002/1531-8249(199911)46:5<708::aid-ana5>3.0.co;2-k. Ann Neurol. 1999. PMID: 10553987

8

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. Brain. 2002 May;125(Pt 5):996-1004. doi: 10.1093/brain/awf115. Brain. 2002. PMID: 11960890

9

Proton magnetic resonance spectroscopy in Kennedy syndrome.

Karitzky J, Block W, Mellies JK, Träber F, Sperfeld A, Schild HH, Haller P, Ludolph AC. Karitzky J, et al. Arch Neurol. 1999 Dec;56(12):1465-71. doi: 10.1001/archneur.56.12.1465. Arch Neurol. 1999. PMID: 10593301

10

Different regional brain volume loss in pure and complicated hereditary spastic paraparesis: a voxel-based morphometric study.

Kassubek J, Juengling FD, Baumgartner A, Unrath A, Ludolph AC, Sperfeld AD. Kassubek J, et al. Among authors: sperfeld ad. Amyotroph Lateral Scler. 2007 Dec;8(6):328-36. doi: 10.1080/17482960701500718. Epub 2007 Jul 30. Amyotroph Lateral Scler. 2007. PMID: 17852008

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