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Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.
Journal of Clinical Pathology|May 1, 1996
Anti-GM1 antibodies in polyneuropathies of unknown originJ Finsterer, W Muellbacher, W M Halbmayer, et al.
The Medical Journal of Malaysia|July 30, 2020
Periodic weakness of the diaphragm as the sole manifestation of bulbar onset myastheniaJ Finsterer, C A Scorza, F A Scorza, et al.
European Journal of Pediatrics|October 17, 1998
Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyM Huemer, A Muehl, K Wandl-Vergesslich, et al.
Current Neurology and Neuroscience Reports|March 24, 2018
Takotsubo Syndrome: Clinical Features, Pathogenesis, Treatment, and Relationship with Cerebrovascular DiseasesM Ranieri, J Finsterer, G Bedini, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 11, 2000
The genetic background modifies the effects of the obesity mutation, 'fatty', on apolipoprotein gene regulation in rat liverE Schuller, N Patel, C Item, et al.
Human Mutation|January 1, 1997
Molecular heterogeneity of classical and Duarte galactosemia: mutation analysis by denaturing gradient gel electrophoresisS Greber-Platzer, P Guldberg, S Scheibenreiter, et al.
Journal of Lipid Research|July 1, 1995
Thyroid hormone influences conditional transcript elongation of the apolipoprotein A-I gene in rat liverY C Lin-Lee, S M Soyal, A Surguchov, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 11, 2001
Intramyocardial hematoma mimicking abnormal left ventricular trabeculationC Stöllberger, J Finsterer, F R Waldenberger, et al.
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