Literature DB >> 8676631

Systemic sclerosis: current pathogenetic concepts and future prospects for targeted therapy.

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Abstract

Although there is no cure for systemic sclerosis, the disease is certainly treatable. And the more that is understood of its pathogenesis, the better the prospects for treatment. Excessive collagen deposition in the skin and viscera is responsible for the morbidity and mortality. The immune system plays a critical role in setting up the fibrotic process, but impaired regulation of collagen gene expression probably underlies the persistence of fibrosis. The development of effective antifibrotic drugs, in particular agents that inhibit transcription factors involved in the activation of type I collagen genes, is likely to be the way forward for treatment of the later stages of diffuse systemic sclerosis, with immunomodulatory therapy for the earlier stages.

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Year:  1996        PMID: 8676631

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  17 in total

1.  How can treatment of systemic sclerosis be improved?. By setting up a national database of all cases and entering patients into trials. UK Scleroderma Study Group.

Authors: 
Journal:  BMJ       Date:  1998-08-01

2.  Ligand-dependent genetic recombination in fibroblasts : a potentially powerful technique for investigating gene function in fibrosis.

Authors:  Bing Zheng; Zhaoping Zhang; Carol M Black; Benoit de Crombrugghe; Christopher P Denton
Journal:  Am J Pathol       Date:  2002-05       Impact factor: 4.307

Review 3.  Novel therapeutic strategies in scleroderma.

Authors:  C P Denton; C M Black
Journal:  Curr Rheumatol Rep       Date:  1999-10       Impact factor: 4.592

4.  Proximal stomach function in systemic sclerosis: relationship with autonomic nerve function.

Authors:  P Iovino; G Valentini; C Ciacci; A De Luca; F Tremolaterra; F Sabbatini; E Tirri; G Mazzacca
Journal:  Dig Dis Sci       Date:  2001-04       Impact factor: 3.199

5.  Renal Crisis as the Initial Manifestation of Scleroderma.

Authors:  Ronak Gandhi; Aparna Das; Daniel Gonzalez; Vijaya Murthy
Journal:  Cureus       Date:  2022-06-11

6.  Resolution of pansclerotic morphea after treatment with antithymocyte globulin.

Authors:  Philip Song; Christopher Gocke; Fredrick M Wigley; Francesco Boin
Journal:  Nat Rev Rheumatol       Date:  2009-09       Impact factor: 20.543

Review 7.  T and NK Cell Phenotypic Abnormalities in Systemic Sclerosis: a Cohort Study and a Comprehensive Literature Review.

Authors:  Isabel Almeida; Sara Vieira Silva; Ana Raquel Fonseca; Ivone Silva; Carlos Vasconcelos; Margarida Lima
Journal:  Clin Rev Allergy Immunol       Date:  2015-12       Impact factor: 8.667

8.  Serum homocystein level in patients with scleroderma.

Authors:  Mohammadali Nazarinia; Mesbah Shams; Eskandar Kamali Sarvestani; Saeede Shenavande; Maryam Khademalhosseini; Zeinab Khademalhosseini
Journal:  Iran Red Crescent Med J       Date:  2013-01-05       Impact factor: 0.611

9.  Increased Risk of Valvular Heart Disease in Systemic Sclerosis: An Underrecognized Cardiac Complication.

Authors:  Reto D Kurmann; Edward A El-Am; Yasser A Radwan; Avneek S Sandhu; Cynthia S Crowson; Eric L Matteson; Kenneth J Warrington; Rekha Mankad; Ashima Makol
Journal:  J Rheumatol       Date:  2021-01-15       Impact factor: 5.346

10.  Prothrombotic effects of tumor necrosis factor alpha in vivo are amplified by the absence of TNF-alpha receptor subtype 1 and require TNF-alpha receptor subtype 2.

Authors:  Joachim Pircher; Monika Merkle; Markus Wörnle; Andrea Ribeiro; Thomas Czermak; Yvonn Stampnik; Hanna Mannell; Markus Niemeyer; Volker Vielhauer; Florian Krötz
Journal:  Arthritis Res Ther       Date:  2012-10-18       Impact factor: 5.156

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