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Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
September 3, 2014
[Indocyanine green elimination for the evaluation of liver function: prognostic value in patients with community-acquired sepsis]
S A Kaulen, C Hübner, J Mieth, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 2009
Insertion of short transmembrane helices by the Sec61 translocon
Simon Jaud, Mónica Fernández-Vidal, Ingmarie Nilsson, et al.
The American Journal of Pathology
|
October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A
L V Anderson, K Davison, J A Moss, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
B Kerst, D Mennerich, M Schuelke, et al.
Genomics
|
July 1, 1993
Multipoint mapping of the central core disease locus
S Schwemmle, K Wolff, L M Palmucci, et al.
The EMBO Journal
|
March 17, 2001
Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2 Cl(-) channel disruption
M R Bösl, V Stein, C Hübner, et al.
Pediatric Research
|
September 1, 1996
Wheat kernel ingestion protects from progression of muscle weakness in mdx mice, an animal model of Duchenne muscular dystrophy
C Hübner, H A Lehr, R Bodlaj, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 1, 1994
P-selectin mediates the interaction of circulating leukocytes with platelets and microvascular endothelium in response to oxidized lipoprotein in vivo
H A Lehr, A M Olofsson, T E Carew, et al.
Neurology
|
April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children
M Henneke, N Preuss, V Engelbrecht, et al.
Neuromuscular Disorders : NMD
|
December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis
M von der Hagen, J Schallner, A M Kaindl, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
September 3, 2014
[Indocyanine green elimination for the evaluation of liver function: prognostic value in patients with community-acquired sepsis]
S A Kaulen, C Hübner, J Mieth, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 8, 2009
Insertion of short transmembrane helices by the Sec61 translocon
Simon Jaud, Mónica Fernández-Vidal, Ingmarie Nilsson, et al.
The American Journal of Pathology
|
October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A
L V Anderson, K Davison, J A Moss, et al.
Neuromuscular Disorders : NMD
|
October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
B Kerst, D Mennerich, M Schuelke, et al.
Genomics
|
July 1, 1993
Multipoint mapping of the central core disease locus
S Schwemmle, K Wolff, L M Palmucci, et al.
The EMBO Journal
|
March 17, 2001
Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2 Cl(-) channel disruption
M R Bösl, V Stein, C Hübner, et al.
Pediatric Research
|
September 1, 1996
Wheat kernel ingestion protects from progression of muscle weakness in mdx mice, an animal model of Duchenne muscular dystrophy
C Hübner, H A Lehr, R Bodlaj, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
September 1, 1994
P-selectin mediates the interaction of circulating leukocytes with platelets and microvascular endothelium in response to oxidized lipoprotein in vivo
H A Lehr, A M Olofsson, T E Carew, et al.
Neurology
|
April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children
M Henneke, N Preuss, V Engelbrecht, et al.
Neuromuscular Disorders : NMD
|
December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis
M von der Hagen, J Schallner, A M Kaindl, et al.
Page
of 10