Publications by authors named "Stephan Neudecker"

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Diagnosis and Clinical Development of Sporadic Inclusion Body Myositis and Polymyositis With Mitochondrial Pathology: A Single-Center Retrospective Analysis.
Maren Winkler, Christina von Landenberg, Karin Kappes-Horn, Stephan Neudecker, Cornelia Kornblum

J Neuropathol Exp Neurol· November 2021

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Isolated bilateral blindness as the sole manifestation of transient ischaemic attacks.
Michael Krasnianski, Viktoria Bau, Stephan Neudecker, Alfred Lindner, Stephan Zierz

Acta Ophthalmol Scand· June 2006

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Call-Fleming postpartum angiopathy in the puerperium: a reversible cerebral vasoconstriction syndrome.
Stephan Neudecker, Karsten Stock, Michael Krasnianski

Obstet Gynecol· February 2006

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Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
Tobias Müller, Marcus Deschauer, Stephan Neudecker, Stephan Zierz

Acta Neuropathol· October 2005

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Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies.
Anna Krasnianski, Marcus Deschauer, Stephan Neudecker, Frank N Gellerich, Tobias Müller

Brain· August 2005

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Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.
Stephan Neudecker, Michael Krasnianski, Erik Bahn, Stephan Zierz

Acta Neuropathol· September 2004

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Alfred Hauptmann, Siegfried Thannhauser, and an endangered muscular disorder.
Michael Krasnianski, Uwe Ehrt, Stephan Neudecker, Stephan Zierz

Arch Neurol· July 2004

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Magnetic resonance angiography in a patient with Crohn's disease associated cerebral vasculitis.
Andreas Schluter, Michael Krasnianski, Mirko Krivokuca, Rolf P Spielmann, Stephan Neudecker

Clin Neurol Neurosurg· March 2004

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Yawning despite trismus in a patient with locked-in syndrome caused by a thrombosed megadolichobasilar artery.
Michael Krasnianski, Charly Gaul, Stephan Neudecker, Curd Behrmann, Andreas Schlüter

Clin Neurol Neurosurg· December 2003

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Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
Michael Krasnianski, Katharina Eger, Stephan Neudecker, Sibylle Jakubiczka, Stephan Zierz

Arch Neurol· October 2003

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Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion.
Michael Krasnianski, Stephan Neudecker, Katharina Eger, Sibylle Jakubiczka, Stephan Zierz

J Neurol· September 2003

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Babinski-Nageotte's syndrome and Hemimedullary (Reinhold's) syndrome are clinically and morphologically distinct conditions.
Michael Krasnianski, Stephan Neudecker, Andreas Schluter, Stephan Zierz

J Neurol· August 2003

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Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy.
Michal Vytopil, Enzo Ricci, Antonio Dello Russo, Frank Hanisch, Stephan Neudecker

Neuromuscul Disord· December 2002

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Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.
Frank Norbert Gellerich, Marcus Deschauer, Ying Chen, Tobias Müller, Stephan Neudecker

Biochim Biophys Acta· October 2002

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