Skalej M - Search Results

1

Delayed resolution of white matter changes following therapy of B burgdorferi encephalitis.

Steinbach JP, Melms A, Skalej M, Dichgans J. Steinbach JP, et al. Among authors: skalej m. Neurology. 2005 Feb 22;64(4):758-9. doi: 10.1212/01.WNL.0000152048.34121.E1. Neurology. 2005. PMID: 15728315 No abstract available.

2

Teaching NeuroImage: thromboembolic stroke in ICA stenosis.

Isenmann S, Skalej M, Dichgans J. Isenmann S, et al. Among authors: skalej m. Neurology. 2005 Oct 11;65(7):E16. doi: 10.1212/01.wnl.0000178887.74545.0d. Neurology. 2005. PMID: 16217044 No abstract available.

3

Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.

Bürk K, Fetter M, Skalej M, Laccone F, Stevanin G, Dichgans J, Klockgether T. Bürk K, et al. Among authors: skalej m. J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):662-4. doi: 10.1136/jnnp.62.6.662. J Neurol Neurosurg Psychiatry. 1997. PMID: 9219762 Free PMC article.

4

Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.

Klockgether T, Skalej M, Wedekind D, Luft AR, Welte D, Schulz JB, Abele M, Bürk K, Laccone F, Brice A, Dichgans J. Klockgether T, et al. Among authors: skalej m. Brain. 1998 Sep;121 ( Pt 9):1687-93. doi: 10.1093/brain/121.9.1687. Brain. 1998. PMID: 9762957

5

Magnetic resonance imaging-based volumetry differentiates idiopathic Parkinson's syndrome from multiple system atrophy and progressive supranuclear palsy.

Schulz JB, Skalej M, Wedekind D, Luft AR, Abele M, Voigt K, Dichgans J, Klockgether T. Schulz JB, et al. Among authors: skalej m. Ann Neurol. 1999 Jan;45(1):65-74. Ann Neurol. 1999. PMID: 9894879

6

Sporadic cerebellar ataxia associated with gluten sensitivity.

Bürk K, Bösch S, Müller CA, Melms A, Zühlke C, Stern M, Besenthal I, Skalej M, Ruck P, Ferber S, Klockgether T, Dichgans J. Bürk K, et al. Among authors: skalej m. Brain. 2001 May;124(Pt 5):1013-9. doi: 10.1093/brain/124.5.1013. Brain. 2001. PMID: 11335703 Review.

7

Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging.

Klockgether T, Zühlke C, Schulz JB, Bürk K, Fetter M, Dittmann H, Skalej M, Dichgans J. Klockgether T, et al. Among authors: skalej m. Neurology. 1996 Jan;46(1):118-21. doi: 10.1212/wnl.46.1.118. Neurology. 1996. PMID: 8559357

8

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

Bürk K, Abele M, Fetter M, Dichgans J, Skalej M, Laccone F, Didierjean O, Brice A, Klockgether T. Bürk K, et al. Among authors: skalej m. Brain. 1996 Oct;119 ( Pt 5):1497-505. doi: 10.1093/brain/119.5.1497. Brain. 1996. PMID: 8931575

9

Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.

Bürk K, Stevanin G, Didierjean O, Cancel G, Trottier Y, Skalej M, Abele M, Brice A, Dichgans J, Klockgether T. Bürk K, et al. Among authors: skalej m. J Neurol. 1997 Apr;244(4):256-61. doi: 10.1007/s004150050081. J Neurol. 1997. PMID: 9112595

10

Central nervous system Hodgkin's lymphoma without systemic manifestation: case report and review of the literature.

Herrlinger U, Klingel K, Meyermann R, Kandolf R, Kaiserling E, Kortmann RD, Melms A, Skalej M, Dichgans J, Weller M. Herrlinger U, et al. Among authors: skalej m. Acta Neuropathol. 2000 Jun;99(6):709-14. doi: 10.1007/s004010051185. Acta Neuropathol. 2000. PMID: 10867808

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