Uttner I - Search Results

1

Emotional adjustment in amyotrophic lateral sclerosis (ALS).

Lulé D, Pauli S, Altintas E, Singer U, Merk T, Uttner I, Birbaumer N, Ludolph AC. Lulé D, et al. Among authors: uttner i. J Neurol. 2012 Feb;259(2):334-41. doi: 10.1007/s00415-011-6191-x. Epub 2011 Aug 2. J Neurol. 2012. PMID: 21808983

2

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: uttner i. J Neurol. 2004 Oct;251(10):1285-7. doi: 10.1007/s00415-004-0562-5. J Neurol. 2004. PMID: 15503116 No abstract available.

3

Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.

Schreiber H, Gaigalat T, Wiedemuth-Catrinescu U, Graf M, Uttner I, Muche R, Ludolph AC. Schreiber H, et al. Among authors: uttner i. J Neurol. 2005 Jul;252(7):772-81. doi: 10.1007/s00415-005-0739-6. Epub 2005 Mar 8. J Neurol. 2005. PMID: 15742104

4

Spastin related hereditary spastic paraplegia with dysplastic corpus callosum.

Alber B, Pernauer M, Schwan A, Rothmund G, Hoffmann KT, Brummer D, Sperfeld AD, Uttner I, Binder H, Epplen JT, Dullinger J, Ludolph AC, Meyer T. Alber B, et al. Among authors: uttner i. J Neurol Sci. 2005 Sep 15;236(1-2):9-12. doi: 10.1016/j.jns.2005.03.040. J Neurol Sci. 2005. PMID: 16009377

5

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: uttner i. Ann Neurol. 2005 Nov;58(5):777-80. doi: 10.1002/ana.20631. Ann Neurol. 2005. PMID: 16240349

6

Primary progressive aphasia accompanied by environmental sound agnosia: a neuropsychological, MRI and PET study.

Uttner I, Mottaghy FM, Schreiber H, Riecker A, Ludolph AC, Kassubek J. Uttner I, et al. Psychiatry Res. 2006 Mar 31;146(2):191-7. doi: 10.1016/j.pscychresns.2005.12.003. Epub 2006 Feb 28. Psychiatry Res. 2006. PMID: 16510269

7

TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Steinacker P, Hendrich C, Sperfeld AD, Jesse S, von Arnim CA, Lehnert S, Pabst A, Uttner I, Tumani H, Lee VM, Trojanowski JQ, Kretzschmar HA, Ludolph A, Neumann M, Otto M. Steinacker P, et al. Among authors: uttner i. Arch Neurol. 2008 Nov;65(11):1481-7. doi: 10.1001/archneur.65.11.1481. Arch Neurol. 2008. PMID: 19001167 Free PMC article.

8

Frontotemporal cognitive function in X-linked spinal and bulbar muscular atrophy (SBMA): a controlled neuropsychological study of 20 patients.

Soukup GR, Sperfeld AD, Uttner I, Karitzky J, Ludolph AC, Kassubek J, Schreiber H. Soukup GR, et al. Among authors: uttner i. J Neurol. 2009 Nov;256(11):1869-75. doi: 10.1007/s00415-009-5212-5. Epub 2009 Jul 2. J Neurol. 2009. PMID: 19572162

9

Concentrations of beta-amyloid precursor protein processing products in cerebrospinal fluid of patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration.

Steinacker P, Hendrich C, Sperfeld AD, Jesse S, Lehnert S, Pabst A, von Arnim CA, Mottaghy FM, Uttner I, Tumani H, Ludolph A, Otto M. Steinacker P, et al. Among authors: uttner i. J Neural Transm (Vienna). 2009 Sep;116(9):1169-78. doi: 10.1007/s00702-009-0271-4. Epub 2009 Aug 1. J Neural Transm (Vienna). 2009. PMID: 19649690

10

A novel presenilin1 mutation (Q223R) associated with early onset Alzheimer's disease, dysarthria and spastic paraparesis and decreased Abeta levels in CSF.

Uttner I, Kirchheiner J, Tumani H, Mottaghy FM, Lebedeva E, Ozer E, Ludolph AC, Huber R, von Arnim CA. Uttner I, et al. Eur J Neurol. 2010 Apr;17(4):631-3. doi: 10.1111/j.1468-1331.2009.02810.x. Epub 2009 Nov 12. Eur J Neurol. 2010. PMID: 19912322

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