Search Results - Lohse, Peter
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1
Risk factors for AA amyloidosis in Germany by Blank, Norbert (Author) , Hegenbart, Ute (Author) , Lohse, Peter (Author) , Beimler, Jörg (Author) , Röcken, Christoph (Author) , Ho, Anthony Dick (Author) , Lorenz, Hanns-Martin (Author) , Schönland, Stefan (Author) ,
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Skeletal scintigraphy indicates disease severity of cardiac involvement in patients with senile systemic amyloidosis by Kristen, Arnt (Author) , Haufe, Sabine (Author) , Schönland, Stefan (Author) , Hegenbart, Ute (Author) , Schnabel, Philipp Albert (Author) , Röcken, Christoph (Author) , Hardt, Stefan (Author) , Lohse, Peter (Author) , Ho, Anthony Dick (Author) , Haberkorn, Uwe (Author) , Dengler, Thomas (Author) , Altland, Klaus (Author) , Katus, Hugo (Author) ,
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Amyloid in endomyocardial biopsies by Kieninger, Barbara (Author) , Eriksson, Magdalena (Author) , Kandolf, Reinhard (Author) , Schnabel, Philipp Albert (Author) , Schönland, Stefan (Author) , Kristen, Arnt (Author) , Hegenbart, Ute (Author) , Lohse, Peter (Author) , Röcken, Christoph (Author) ,
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4
Leptin gene (TTTC)n microsatellite polymorphism as well as leptin receptor R223Q and PPARγ2 P12A substitutions are not associated with hypertensive disorders in pregnancy by Wiedemann, Annette Lucia (Author) , Vocke, Franziska (Author) , Fitzgerald, Justine S. (Author) , Markert, Udo R. (Author) , Jeschke, Udo (Author) , Lohse, Peter (Author) , Toth, Bettina (Author) ,
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5
Severe TNF receptor-associated periodic syndrome due to 2 TNFRSF1A mutations including a new F60V substitution by Haas, Stephan (Author) , Lohse, Peter (Author) , Schmitt, Wilhelm (Author) , Hildenbrand, Ralf (Author) , Karaorman, Mevlüt (Author) , Singer, Manfred V. (Author) , Böcker, Ulrich (Author) ,
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AL
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Amyloid
Amyloidosis
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familial Mediterranean fever
hypertensive disorders in pregnancy
leptin gene
leptin receptor
polymorphism
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serum amyloid-A protein