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Isotopes in Environmental and Health Studies
|
September 7, 2011
Mineral- und heilwässer in sachsen - eine isotopenanalytische charakterisierung
K 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 DM2
T 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 aura
T 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 mutation
M 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 disorders
C Gaul, R Eismann, T Schmidt, et al.
European Journal of Pediatrics
|
November 1, 1993
Mutation analysis in the diagnosis of cystic fibrosis
T Deufel, H Rabe, T Wieser, et al.
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of 2
Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 charakterisierung
K 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 DM2
T 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 aura
T 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 mutation
M 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 disorders
C Gaul, R Eismann, T Schmidt, et al.
European Journal of Pediatrics
|
November 1, 1993
Mutation analysis in the diagnosis of cystic fibrosis
T Deufel, H Rabe, T Wieser, et al.
Page
of 2