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Stephan Zierz

Showing results (41-50 of 123) with videos related to

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Archives of Neurology|October 22, 2003
Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletionMichael Krasnianski, Katharina Eger, Stephan Neudecker, et al.
Clinical Chemistry and Laboratory Medicine|April 23, 2003
Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testingThomas Wieser, Christoph Mueller, Stefan Evers, et al.
Medizinische Klinik (Munich, Germany : 1983)|September 20, 2005
[Hypokalemic thyrotoxic periodic paralysis (HTPP). Rare differential diagnosis in case of acute tetraparesis in Europe]Charly Gaul, Georg Leonhardt, Antje Spens, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 27, 2020
Basilar artery thrombosis during sexual intercourseAndreas Posa, Tobias Mueller, Olga Ungurs, et al.
Journal of Neurology|September 25, 2003
Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletionMichael Krasnianski, Stephan Neudecker, Katharina Eger, et al.
Orphanet Journal of Rare Diseases|April 15, 2018
Decreased outlet angle of the superior cerebellar artery as indicator for dolichoectasia in late onset Pompe diseaseOle Hensel, Ilka Schneider, Mathias Wieprecht, et al.
Journal of Medical Case Reports|January 6, 2018
Foodborne botulism due to ingestion of home-canned green beans: two case reportsDorothea Hellmich, Katja E Wartenberg, Stephan Zierz, et al.
Acta Ophthalmologica Scandinavica|May 18, 2006
Isolated bilateral blindness as the sole manifestation of transient ischaemic attacksMichael Krasnianski, Viktoria Bau, Stephan Neudecker, et al.
Biochimica Et Biophysica Acta|May 30, 2002
The quantitation of ADP diffusion gradients across the outer membrane of heart mitochondria in the presence of macromoleculesFrank Norbert Gellerich, Fanny Dorine Laterveer, Stephan Zierz, et al.
International Journal of Molecular Sciences|March 23, 2019
Normal FGF-21-Serum Levels in Patients with Carnitine Palmitoyltransferase II (CPT II) DeficiencyLeila Motlagh Scholle, Diana Lehmann, Pushpa Raj Joshi, et al.
Pageof 13

Showing results (41-50 of 123) with videos related to

Sort By:
Pageof 13
Archives of Neurology|October 22, 2003
Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletionMichael Krasnianski, Katharina Eger, Stephan Neudecker, et al.
Clinical Chemistry and Laboratory Medicine|April 23, 2003
Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testingThomas Wieser, Christoph Mueller, Stefan Evers, et al.
Medizinische Klinik (Munich, Germany : 1983)|September 20, 2005
[Hypokalemic thyrotoxic periodic paralysis (HTPP). Rare differential diagnosis in case of acute tetraparesis in Europe]Charly Gaul, Georg Leonhardt, Antje Spens, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 27, 2020
Basilar artery thrombosis during sexual intercourseAndreas Posa, Tobias Mueller, Olga Ungurs, et al.
Journal of Neurology|September 25, 2003
Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletionMichael Krasnianski, Stephan Neudecker, Katharina Eger, et al.
Orphanet Journal of Rare Diseases|April 15, 2018
Decreased outlet angle of the superior cerebellar artery as indicator for dolichoectasia in late onset Pompe diseaseOle Hensel, Ilka Schneider, Mathias Wieprecht, et al.
Journal of Medical Case Reports|January 6, 2018
Foodborne botulism due to ingestion of home-canned green beans: two case reportsDorothea Hellmich, Katja E Wartenberg, Stephan Zierz, et al.
Acta Ophthalmologica Scandinavica|May 18, 2006
Isolated bilateral blindness as the sole manifestation of transient ischaemic attacksMichael Krasnianski, Viktoria Bau, Stephan Neudecker, et al.
Biochimica Et Biophysica Acta|May 30, 2002
The quantitation of ADP diffusion gradients across the outer membrane of heart mitochondria in the presence of macromoleculesFrank Norbert Gellerich, Fanny Dorine Laterveer, Stephan Zierz, et al.
International Journal of Molecular Sciences|March 23, 2019
Normal FGF-21-Serum Levels in Patients with Carnitine Palmitoyltransferase II (CPT II) DeficiencyLeila Motlagh Scholle, Diana Lehmann, Pushpa Raj Joshi, et al.
Pageof 13