Lauren M. Pachman mainly investigates Dermatomyositis, Juvenile dermatomyositis, Internal medicine, Immunology and Connective tissue disease. He interconnects Polymyositis, Autoimmune disease, Muscle weakness and Physical therapy in the investigation of issues within Dermatomyositis. The Autoimmune disease study combines topics in areas such as Inflammatory myopathy, Pathogenesis and Immunopathology.
His work deals with themes such as Juvenile, El Niño and Rash, which intersect with Juvenile dermatomyositis. Lauren M. Pachman has included themes like Gastroenterology, Endocrinology and Surgery in his Internal medicine study. As a part of the same scientific study, he usually deals with the Connective tissue disease, concentrating on Systemic disease and frequently concerns with Cohort study.
Lauren M. Pachman mainly focuses on Juvenile dermatomyositis, Immunology, Internal medicine, Dermatomyositis and Pathology. His Juvenile dermatomyositis study is associated with Disease. His research in Internal medicine intersects with topics in Gastroenterology, Endocrinology and Surgery.
His Dermatomyositis research is multidisciplinary, incorporating perspectives in Polymyositis, Autoimmune disease, Connective tissue disease and Juvenile. His study in Connective tissue disease is interdisciplinary in nature, drawing from both Systemic disease, Immunopathology and Inflammation. His Juvenile rheumatoid arthritis research includes themes of El Niño and Rheumatoid arthritis.
The scientist’s investigation covers issues in Juvenile dermatomyositis, Internal medicine, Immunology, Dermatomyositis and Pathology. His Juvenile dermatomyositis study is concerned with Disease in general. His Internal medicine research incorporates elements of Gastroenterology, Endocrinology and Surgery.
His Dermatomyositis research is multidisciplinary, incorporating elements of Muscle biopsy, Connective tissue disease, Genome-wide association study and Genetic predisposition. Many of his research projects under Pathology are closely connected to Nominal group and Outcomes research with Nominal group and Outcomes research, tying the diverse disciplines of science together. His Autoimmune disease research includes elements of Family aggregation and Autoimmunity.
His main research concerns Juvenile dermatomyositis, Dermatomyositis, Internal medicine, Immunology and Disease. His studies in Juvenile dermatomyositis integrate themes in fields like Diagnostic marker, Neopterin and Myositis. His Dermatomyositis research is multidisciplinary, relying on both Tumor necrosis factor alpha, Polymyositis and Connective tissue disease.
His Internal medicine study incorporates themes from Gastroenterology and Surgery. The various areas that Lauren M. Pachman examines in his Surgery study include White blood cell and Immunopathology. The study of Immunology is intertwined with the study of Genome-wide association study in a number of ways.
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Quantification of keratan sulfate in blood as a marker of cartilage catabolism.
Eugene J‐ M. A. Thonar;Mary Ellen Lenz;Gordon K. Klintworth;Bruce Caterson.
Arthritis & Rheumatism (1985)
Juvenile dermatomyositis and other idiopathic inflammatory myopathies of childhood
Brian M Feldman;Lisa G Rider;Ann M Reed;Lauren M Pachman.
The Lancet (2008)
US incidence of juvenile dermatomyositis, 1995-1998: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry.
Eduardo P. Mendez;Rebecca Lipton;Rosalind Ramsey-Goldman;Phil Roettcher.
Arthritis Care and Research (2003)
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration
Marina Bakay;Zuyi Wang;Zuyi Wang;Gisela Melcon;Louis Schiltz.
Combined immunodeficiency disease associated with adenosine deaminase deficiency. Report on a workshop held in Albany, New York, October 1, 1973.
H.J. Meuwissen;B. Pollara;R.J. Pickering;A. Ammann.
The Journal of Pediatrics (1975)
Mutations in the Mu Heavy-Chain Gene in Patients with Agammaglobulinemia
Leman Yel;Yoshiyuki Minegishi;Elaine Coustan-Smith;Rebecca H. Buckley.
The New England Journal of Medicine (1996)
Gene Expression Profiling in DQA1*0501+ Children with Untreated Dermatomyositis: A Novel Model of Pathogenesis
Zivana Tezak;Eric P. Hoffman;Jennica L. Lutz;Tamara O. Fedczyna.
Journal of Immunology (2002)
Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies: II. The Childhood Myositis Assessment Scale (CMAS): A quantitative tool for the evaluation of muscle function
Daniel J. Lovell;Carol B. Lindsley;Robert M. Rennebohm;Susan H. Ballinger.
Arthritis & Rheumatism (1999)
International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease.
D. A. Isenberg;E. Allen;V. Farewell;M. R. Ehrenstein.
TNFα-308A allele in juvenile dermatomyositis: Association with increased production of tumor necrosis factor α, disease duration, and pathologic calcifications
Lauren M. Pachman;Lauren M. Pachman;Margaret R. Liotta-Davis;David K. Hong;T. Randall Kinsella.
Arthritis & Rheumatism (2000)
Profile was last updated on December 6th, 2021.
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