Member of the Association of American Physicians
Paul H. Plotz focuses on Internal medicine, Immunology, Myositis, Dermatomyositis and Polymyositis. His Internal medicine research incorporates elements of Gastroenterology, Lupus erythematosus and Endocrinology. His Endocrinology study integrates concerns from other disciplines, such as Acid alpha-glucosidase, Glycogen storage disease type II, Mononuclear phagocyte system and Immune system.
The Immunology study combines topics in areas such as Myocyte and Skeletal muscle. Paul H. Plotz is interested in Inclusion body myositis, which is a branch of Myositis. His studies in Dermatomyositis integrate themes in fields like Physical therapy, Albumin and Apheresis.
His primary scientific interests are in Immunology, Internal medicine, Myositis, Molecular biology and Dermatomyositis. Dermatology and Pathogenesis is closely connected to Disease in his research, which is encompassed under the umbrella topic of Immunology. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Lupus erythematosus and Endocrinology.
His work focuses on many connections between Endocrinology and other disciplines, such as Glycogen storage disease type II, that overlap with his field of interest in Autophagy, Myopathy and Biochemistry. His Myositis research includes elements of Inflammation, Muscle biopsy and Connective tissue disease. He focuses mostly in the field of Dermatomyositis, narrowing it down to topics relating to Polymyositis and, in certain cases, Surgery, Etiology and Muscle weakness.
Paul H. Plotz mainly investigates Immunology, Skeletal muscle, Glycogen storage disease type II, Autophagy and Myositis. His studies examine the connections between Immunology and genetics, as well as such issues in Disease, with regards to Pathogenesis and Catabolism. Paul H. Plotz has researched Skeletal muscle in several fields, including Glycogen, Myopathy, Muscle contraction and Enzyme replacement therapy.
His study explores the link between Glycogen storage disease type II and topics such as Cardiac muscle that cross with problems in Respiratory failure and Molecular biology. His study in Myositis is interdisciplinary in nature, drawing from both Polymyositis, Dermatomyositis and Muscle biopsy. His Internal medicine study frequently links to related topics such as Gastroenterology.
His primary areas of study are Skeletal muscle, Immunology, Glycogen storage disease type II, Cell biology and Autophagy. His biological study spans a wide range of topics, including Myocyte and Myositis. The Inclusion body myositis research Paul H. Plotz does as part of his general Myositis study is frequently linked to other disciplines of science, such as Face validity, therefore creating a link between diverse domains of science.
His research investigates the connection between Glycogen storage disease type II and topics such as Glycogen that intersect with problems in Lysosomal storage disease. His research integrates issues of Biochemistry, Lysosomal storage disorders and Microautophagy in his study of Cell biology. His work deals with themes such as Cardiac muscle and Myopathy, which intersect with Autophagy.
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Therapy of lupus nephritis. Controlled trial of prednisone and cytotoxic drugs.
H. A. Austin;J. H. Klippel;J. E. Balow;N. G.H. Le Riche.
The New England Journal of Medicine (1986)
A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patient groups.
Lori A. Love;Richard L. Leff;David D. Fraser;Ira N. Targoff.
Medicine (1991)
Defective Reticuloendothelial System Fc-Receptor Function in Systemic Lupus Erythematosus
Michael M. Frank;Max I. Hamburger;Thomas J. Lawley;Robert P. Kimberly.
The New England Journal of Medicine (1979)
Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease
Nina Raben;Victoria Hill;Lauren Shea;Shoichi Takikita.
Human Molecular Genetics (2008)
Enhanced autoantigen expression in regenerating muscle cells in idiopathic inflammatory myopathy
Livia Casciola-Rosen;Kanneboyina Nagaraju;Paul Plotz;Kondi Wang.
Journal of Experimental Medicine (2005)
Current concepts in the idiopathic inflammatory myopathies: polymyositis, dermatomyositis, and related disorders.
Paul H. Plotz;Marinos Dalakas;Richard L. Leff;Lori A. Love.
Annals of Internal Medicine (1989)
Controlled trial of plasma exchange and leukapheresis in polymyositis and dermatomyositis.
Frederick W. Miller;Susan F. Leitman;Mary E. Cronin;Jeanne E. Hicks.
The New England Journal of Medicine (1992)
Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease.
Tokiko Fukuda;Lindsay Ewan;Martina Bauer;Robert J. Mattaliano.
Annals of Neurology (2006)
Drug therapy of the idiopathic inflammatory myopathies: predictors of response to prednisone, azathioprine, and methotrexate and a comparison of their efficacy
Marshall M. Joffe;Lori A. Love;Richard L Leff;David D. Fraser.
The American Journal of Medicine (1993)
Conditional up-regulation of MHC class I in skeletal muscle leads to self-sustaining autoimmune myositis and myositis-specific autoantibodies.
Kanneboyina Nagaraju;Nina Raben;Lisa Loeffler;Tomasina Parker.
Proceedings of the National Academy of Sciences of the United States of America (2000)
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