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T Wieser

Showing results (11-20 of 17) with videos related to

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Isotopes in Environmental and Health Studies|September 7, 2011
Mineral- und heilwässer in sachsen - eine isotopenanalytische charakterisierungK V Storch, P Kowski, G Strauch, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A family with PROMM not linked to the recently mapped PROMM locus DM2T Wieser, D Bönsch, K Eger, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 3, 2004
Persistent ocular motor disturbances in migraine without auraT Wieser, R Wolff, K P Hoffmann, et al.
Archives of Neurology|November 16, 2001
Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutationM Deschauer, T Müller, T Wieser, et al.
Neurology|July 26, 2006
Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)C Gaul, T Schmidt, G Windisch, et al.
Cephalalgia : an International Journal of Headache|April 16, 2009
Use of complementary and alternative medicine in patients suffering from primary headache disordersC Gaul, R Eismann, T Schmidt, et al.
European Journal of Pediatrics|November 1, 1993
Mutation analysis in the diagnosis of cystic fibrosisT Deufel, H Rabe, T Wieser, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Isotopes in Environmental and Health Studies|September 7, 2011
Mineral- und heilwässer in sachsen - eine isotopenanalytische charakterisierungK V Storch, P Kowski, G Strauch, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A family with PROMM not linked to the recently mapped PROMM locus DM2T Wieser, D Bönsch, K Eger, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 3, 2004
Persistent ocular motor disturbances in migraine without auraT Wieser, R Wolff, K P Hoffmann, et al.
Archives of Neurology|November 16, 2001
Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutationM Deschauer, T Müller, T Wieser, et al.
Neurology|July 26, 2006
Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)C Gaul, T Schmidt, G Windisch, et al.
Cephalalgia : an International Journal of Headache|April 16, 2009
Use of complementary and alternative medicine in patients suffering from primary headache disordersC Gaul, R Eismann, T Schmidt, et al.
European Journal of Pediatrics|November 1, 1993
Mutation analysis in the diagnosis of cystic fibrosisT Deufel, H Rabe, T Wieser, et al.
Pageof 2