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Scandinavian Journal of Immunology
|
May 11, 2005
The pathophysiology of acute graft-versus-host disease
M Jaksch, J Mattsson
Neurology
|
September 17, 1999
Age and cause of death in mitochondrial diseases
T Klopstock, M Jaksch, T Gasser
Clinical Biochemistry
|
October 1, 1995
Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis
M Jaksch, K D Gerbitz, C Kilger
The Canadian Journal of Cardiology
|
May 1, 2001
Wolff-Parkinson-White syndrome and isolated left ventricular abnormal trabeculation as a manifestation of Leber's hereditary optic neuropathy
J Finsterer, C Stöllberger, W Kopsa, et al.
European Neurology
|
August 31, 2001
Nail-patella syndrome associated with respiratory chain disorder
J Finsterer, C Stöllberger, J Wanschitz, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2004
Reversion of hypertrophic cardiomyopathy in a patient with deficiency of the mitochondrial copper binding protein Sco2: is there a potential effect of copper?
P Freisinger, R Horvath, C Macmillan, et al.
Blood
|
September 6, 2001
The significance of graft-versus-host disease and pretransplantation minimal residual disease status to outcome after allogeneic stem cell transplantation in patients with acute lymphoblastic leukemia
M Uzunel, J Mattsson, M Jaksch, et al.
Journal of Neuroscience Research
|
March 1, 1992
Nerve growth factor and choline acetyltransferase activity levels in the rat brain following experimental impairment of cerebral glucose and energy metabolism
R Hellweg, R Nitsch, C Hock, et al.
Bone Marrow Transplantation
|
March 7, 2003
Increased levels of immune transcript in patients with acute GVHD after allogeneic stem cell transplantation
M Jaksch, M Uzunel, G Martinez Cangana, et al.
FEBS Letters
|
April 26, 1993
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene
K D Gerbitz, A Paprotta, M Jaksch, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Scandinavian Journal of Immunology
|
May 11, 2005
The pathophysiology of acute graft-versus-host disease
M Jaksch, J Mattsson
Neurology
|
September 17, 1999
Age and cause of death in mitochondrial diseases
T Klopstock, M Jaksch, T Gasser
Clinical Biochemistry
|
October 1, 1995
Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis
M Jaksch, K D Gerbitz, C Kilger
The Canadian Journal of Cardiology
|
May 1, 2001
Wolff-Parkinson-White syndrome and isolated left ventricular abnormal trabeculation as a manifestation of Leber's hereditary optic neuropathy
J Finsterer, C Stöllberger, W Kopsa, et al.
European Neurology
|
August 31, 2001
Nail-patella syndrome associated with respiratory chain disorder
J Finsterer, C Stöllberger, J Wanschitz, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2004
Reversion of hypertrophic cardiomyopathy in a patient with deficiency of the mitochondrial copper binding protein Sco2: is there a potential effect of copper?
P Freisinger, R Horvath, C Macmillan, et al.
Blood
|
September 6, 2001
The significance of graft-versus-host disease and pretransplantation minimal residual disease status to outcome after allogeneic stem cell transplantation in patients with acute lymphoblastic leukemia
M Uzunel, J Mattsson, M Jaksch, et al.
Journal of Neuroscience Research
|
March 1, 1992
Nerve growth factor and choline acetyltransferase activity levels in the rat brain following experimental impairment of cerebral glucose and energy metabolism
R Hellweg, R Nitsch, C Hock, et al.
Bone Marrow Transplantation
|
March 7, 2003
Increased levels of immune transcript in patients with acute GVHD after allogeneic stem cell transplantation
M Jaksch, M Uzunel, G Martinez Cangana, et al.
FEBS Letters
|
April 26, 1993
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene
K D Gerbitz, A Paprotta, M Jaksch, et al.
Page
of 4