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The Journal of Clinical Investigation
|
February 11, 1992
Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)
H G Klein, P Lohse, P H Pritchard, et al.
Neurology
|
November 26, 2008
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases
T Kümpfel, L-A Hoffmann, H Pellkofer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 30, 2014
Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone
J Staub, N Pfannschmidt, R Strohal, et al.
Journal of Lipid Research
|
November 11, 1992
Familial apolipoprotein E deficiency and type III hyperlipoproteinemia due to a premature stop codon in the apolipoprotein E gene
P Lohse, H B Brewer, M S Meng, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis
|
November 29, 2001
Consistent lowering of clotting factors for the treatment of acute cardiovascular syndromes and hypercoagulability: a different pathophysiological approach
B R Jaeger, P Goehring, J Schirmer, et al.
European Journal of Pediatrics
|
August 21, 2012
Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population
E Lainka, M Bielak, P Lohse, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
August 17, 2001
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester
R Pihusch, T Buchholz, P Lohse, et al.
Annals of the Rheumatic Diseases
|
January 9, 2008
Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment
S Stojanov, C Dejaco, P Lohse, et al.
Bone Marrow Transplantation
|
January 11, 2007
Substitution of cyclophosphamide and busulfan by fludarabine, treosulfan and melphalan in a preparative regimen for children and adolescents with Shwachman-Diamond syndrome
M Sauer, C Zeidler, B Meissner, et al.
Transplantation
|
May 16, 1998
Early loss of renal transplants in patients with thrombophilia
M Fischereder, P Göhring, H Schneeberger, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 90) with videos related to
Sort By:
Page
of 9
The Journal of Clinical Investigation
|
February 11, 1992
Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)
H G Klein, P Lohse, P H Pritchard, et al.
Neurology
|
November 26, 2008
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases
T Kümpfel, L-A Hoffmann, H Pellkofer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 30, 2014
Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsone
J Staub, N Pfannschmidt, R Strohal, et al.
Journal of Lipid Research
|
November 11, 1992
Familial apolipoprotein E deficiency and type III hyperlipoproteinemia due to a premature stop codon in the apolipoprotein E gene
P Lohse, H B Brewer, M S Meng, et al.
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis
|
November 29, 2001
Consistent lowering of clotting factors for the treatment of acute cardiovascular syndromes and hypercoagulability: a different pathophysiological approach
B R Jaeger, P Goehring, J Schirmer, et al.
European Journal of Pediatrics
|
August 21, 2012
Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric population
E Lainka, M Bielak, P Lohse, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
August 17, 2001
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester
R Pihusch, T Buchholz, P Lohse, et al.
Annals of the Rheumatic Diseases
|
January 9, 2008
Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment
S Stojanov, C Dejaco, P Lohse, et al.
Bone Marrow Transplantation
|
January 11, 2007
Substitution of cyclophosphamide and busulfan by fludarabine, treosulfan and melphalan in a preparative regimen for children and adolescents with Shwachman-Diamond syndrome
M Sauer, C Zeidler, B Meissner, et al.
Transplantation
|
May 16, 1998
Early loss of renal transplants in patients with thrombophilia
M Fischereder, P Göhring, H Schneeberger, et al.
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of 9