Beate Schlotter-Weigel

Beate Schlotter-Weigel

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Beate Schlotter-Weigel

Beate Schlotter-Weigel

Publications by authors named "Beate Schlotter-Weigel"

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22Publications

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[Immune-mediated / inflammatory and hereditary neuropathies - overview and diagnostic algorithm].

Fortschr Neurol Psychiatr 2018 09 24;86(9):566-574. Epub 2018 Sep 24.

Friedrich-Baur-Institut, Neurologische Klinik und Poliklinik, Klinikum der LMU München.

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http://dx.doi.org/10.1055/a-0655-7659DOI Listing
September 2018

HIV-Associated Cerebellar Dysfunction and Improvement with Aminopyridine Therapy: A Case Report.

Case Rep Neurol 2017 May-Aug;9(2):121-126. Epub 2017 May 16.

Department of Neurology, University Medical Centre Mannheim, Mannheim, Germany.

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http://dx.doi.org/10.1159/000475544DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471757PMC
May 2017

Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness.

Neurology 2016 Jul 11;87(3):295-8. Epub 2016 May 11.

From Newborn Screening and Metabolic Diagnostics (Z.L., P.N.C.), University Medical Center Hamburg-Eppendorf, Hamburg; Friedrich-Baur Institute, Department of Neurology (S.W., B.S.-W., M.C.W., P.R., T.K., B.S.), and Department of Neuropediatrics, Dr. Von Haunersche Kinderklinik (W.M.-F.), Ludwig Maximilian University of Munich, Germany; The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust (T.A.W.), Oswestry; Institute of Genetic Medicine (T.E., M.G., V.S.), Newcastle University; Salford Royal NHS Foundation Trust (M.R.), Salford; UCL Institute of Neurology and National Hospital (R.Q.), Queen Square, London; Department of Neurology (D.H.-J.), Oxford University Hospital, UK; and Department of Neurology (S.Z., M.D.), Halle University, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000002758DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955273PMC
July 2016

The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy.

Neuromolecular Med 2016 Mar 16;18(1):81-90. Epub 2015 Nov 16.

Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, Haartmaninkatu 8, 00290, Helsinki, Finland.

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http://dx.doi.org/10.1007/s12017-015-8379-1DOI Listing
March 2016

Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients.

Neuromuscul Disord 2007 Oct 23;17(9-10):698-706. Epub 2007 Jul 23.

Haunersche Kinderklinik, Childrens Hospital, Ludwig-Maximilians-University, Lindwurmstr. 4, 80337 Munich, Germany.

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http://dx.doi.org/10.1016/j.nmd.2007.06.002DOI Listing
October 2007

Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy.

Neuromuscul Disord 2006 Jul 26;16(7):432-6. Epub 2006 May 26.

Department of Neurology, Friedrich-Baur-Institute, Lab. for Molecular Myology, Ludwig-Maximilians-University, Marchioninistr. 17, 81377 Munich, Germany.

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https://linkinghub.elsevier.com/retrieve/pii/S09608966060012
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http://dx.doi.org/10.1016/j.nmd.2006.04.006DOI Listing
July 2006

Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.

Neuromuscul Disord 2005 Jan;15(1):40-4

Friedrich-Baur-Institute, Gene Center and Department of Neurology, Ludwig-Maximilians-University of Munich, Munich, Germany.

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http://dx.doi.org/10.1016/j.nmd.2004.09.007DOI Listing
January 2005

The long-term outcome of anti-Jo-1-positive inflammatory myopathies.

J Neurol 2004 Jul;251(7):859-64

Friedrich-Baur-Institut, Department of Neurology, University of Munich, Ziemssenstr. 1a, 80336, Germany.

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http://dx.doi.org/10.1007/s00415-004-0449-5DOI Listing
July 2004