Accessing Article OR microscopic polyangiitis IMPLICATIONS FOR THE SURGICAL PATHOLOGIST. of Wegener s granulomatosis (WG) and microscopic polyangiitis (MPA) in 27 http://www.nature.com/modpathol/journal/v15/n11/full/3880682a.html
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Journal References For Drug Information Support and information for people fighting microscopic polyangiitis. microscopic polyangiitis clinical and laboratory findings in eightyfive patients http://www.users.fast.net/~rcb1/mpa/MPA_Information/Drugs/References/references.
Extractions: Allison AC, Eugui EM. Immunosuppressive and other effects of mycophenolic acid and an ester prodrug, mycophenolate mofetil. Immunol Rev 1993;136:528. Brijker F, Magee CC, Cohen Tervaert JW, ONeill S, Walshe JJ. Outcome analysis of patients with vasculitis associated with antineutrophil cytoplasmic antibodies. Clin Nephrol 1999;52:34451. Falk RJ, Hogan S, Carey TS, Jennette JC. Clinical course of anti-neutrophil cytoplasmic autoantibody-associated glomerulonephritis and systemic vasculitis: the Glomerular Disease Collaborative Network. Ann Intern Med 1990;113:65663. Falk RJ, Jennette JC. Anti-neutrophil cytoplasmic autoantibodies with specificity for myeloperoxidase in patients with systemic vasculitis and idiopathic necrotizing and crescentic glomerulonephritis. N Engl J Med 1988;318:165157. Jennette JC, Falk RJ. Small-vessel vasculitis. N Engl J Med 1997;337:151223. Jennette JC, Falk RJ, Andrassy K, et al. Nomenclature of systemic vasculitides: proposal of an international consensus conference. Arthritis Rheum 1994;37:18792. Guillevin L, Druand Gasselin D, Cevallos R, et al. Microscopic polyangiitis: clinical and laboratory findings in eighty-five patients. Arthritis Rheum 1999;42:42130.
Extractions: This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Download to citation manager Search for citing articles in: British Society for Rheumatology F. Weber E. Kowald M. Schmuth and N. Sepp Department of Dermatology and Venereology, University of Innsbruck, Anichstrasse 35, 6020 Innsbruck, Austria S IR , We report a 40-yr-old female patient in whom relapsing polychondritis was associated with systemic vasculitis affecting the skin, kidneys and lungs.
Extractions: This Article Full Text Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Download to citation manager Search for citing articles in: ISI Web of Science (1) Request Permissions PubMed PubMed Citation Articles by Weber, F. Articles by Sepp, N. Related Collections Connective tissue disease Rheumatology 2001; 40: 233-235 F. Weber E. Kowald M. Schmuth and N. Sepp Department of Dermatology and Venereology, University of Innsbruck, Anichstrasse 35, 6020 Innsbruck, Austria The first 10% of the full text of this article appears below. S IR , We report a 40-yr-old female patient in whom relapsing polychondritis was associated with systemic vasculitis affecting the skin, kidneys and lungs.
British Library Direct: Order Details Order from the British Library Asbestosis and probable microscopic polyangiitisCanadian Respiratory Journal. http://direct.bl.uk/research/50/2B/RN155615290.html
Extractions: This is an article from British Library Direct, a new service that allows you to search across 20,000 journals for free and order full text using your credit card. Article details Article title Asbestosis and probable microscopic polyangiitis Author Philteos, G. S. R. Coverett, K. Chibbar, R. Ward, H. A. Cockcroft, D. W. Journal title CANADIAN RESPIRATORY JOURNAL Bibliographic details 2004, VOL 11; NUMB 5, pages 359-362 Publisher PULSUS GROUP INC Country of publication Canada ISBN ISSN Language English Pricing To buy the full text of this article you pay:
Jornal Brasileiro De Pneumologia - microscopic polyangiitis is a form of AntiNeutrophil Cytoplasmic Antibody The case of a 66-year-old man with microscopic polyangiitis presenting with http://www.scielo.br/scielo.php?pid=S1806-37132004000200013&script=sci_arttext&t
Sao Paulo Medical Journal - microscopic polyangiitis and Wegener?s granulomatosis, concerning a 10 year Wegener s granulomatosis and microscopic polyangiitis.6 We focus the http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802001000100008
Vasculitis Clinical Research Consortium - Learn More What causes microscopic polyangiitis? microscopic polyangiitis is thought to bean autoimmune disease for which there is no known cause. http://rdcrn.epi.usf.edu/vcrc/learnmore/definitions.htm
Extractions: What is the VCRC? Information for Patients: Learn More Introduction to Vasculitis Disease Definitions Useful Links ... Learn More Please Choose from the Menu below: Who gets Wegener's Granulomatosis? What causes Wegener's Granulomatosis? Wegener's granulomatosis is thought to be an auto-immune disease for which there is no known cause. How is Wegener's Granulomatosis diagnosed? What is the treatment for Wegener's Granulomatosis? Treatment of Wegener's granulomatosis usually includes a combination of glucocorticoids and an immunosuppressive drug such as cyclophosphamide, methotrexate, or azathioprine. If diagnosed promptly, treatment can bring about early remission and prevent organ failure. It is a chronic disease, and although remission of symptoms is usually achieved, the relapse rate remains high. Join the Contact Registry for this Disorder Find a Study Advocacy Groups for this Disease Back to Top What is Microscopic Polyangiitis?
Extractions: What is the VCRC? Information for Patients: Learn More Take Action Information for Physicians About the VCRC ... Home Information for Physicians Please Choose from the Menu below: Microscopic Polyangiitis (MPA) Churg-Strauss Syndrome (CSS) Polyarteritis Nodosa (PAN) Takayasu's Arteritis (TAK) ... Back to Top Join the Contact Registry for this Disorder Find a Study Back to Top Churg Strauss Syndrome (CSS) Join the Contact Registry for this Disorder Find a Study Back to Top Join the Contact Registry for this Disorder Find a Study Back to Top Join the Contact Registry for this Disorder Find a Study Back to Top Join the Contact Registry for this Disorder Find a Study Back to Top Join the Contact Registry for this Disorder Find a Study Back to Top Home ...
Journal Of Clinical Gastroenterology - UserLogin Focal Rectal Capillaritis microscopic polyangiitis Presenting as Painless We report the case of a 59year-old woman with microscopic polyangiitis http://www.jcge.com/pt/re/jclngastro/fulltext.00004836-200208000-00008.htm
Entrez PubMed Varicella in childhood is usually a selflimiting illness with few complications.Varicella nephriti http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Entrez PubMed microscopic polyangiitis diagnosed at hysterectomy. Gran JT, Berner A, KlosterJensenA, Bostad L. Department of Rheumatology University Hospital of Tromso, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Extractions: Text Size A A A Front Page ... Auto-Immune : Microscopic Polyangiitis Hurricane Winds Carried Ocean Salt And Plankton Far Inland (August 29, 2005) full story Microscopic Brain Imaging In The Palm Of Your Hand (August 25, 2005) full story Temperature Control Improves NIST X-ray Detector (August 21, 2005) full story Diamonds Are A Scientist's Best Friend (August 11, 2005) full story Patient's Genes Can Predict Response To Chemotherapy For Breast Cancer (August 10, 2005) Journal of Translational Medicine , researchers sampled primary tumour tissue from eighty-three breast cancer patients, and found fifty-seven 'predictor genes' that could be used to predict patients' response to preoperative systemic chemotherapy in all cases of partial remission, and nearly three quarters of cases of complete remission. full story New Technology Shows Our Ancestors Ate ... Everything!
American Thoracic Society - About ATS microscopic polyangiitis (microscopic polyarteritis). Semin Diagn Pathol 2001;183 13. Churg J, Strauss L. Allergic granulomatosis, allergic angiitis and http://www.thoracic.org/aboutats/vignettes/Vignette8.asp
Extractions: Churg-Strauss Syndrome Andrew Churg, M.D. Dean Schraufnagel has asked me to write about the history of the syndrome first described by my father and Lotte Strauss. Churg-Strauss syndrome (CSS) is best understood in the context of the history of vasculitis. The first report of vasculitis is generally credited to Kussmaul and Maier, who in 1866 described periarteritis nodosa, a name later recast as polyarteritis nodosa (PAN). PAN usually affected medium-sized arteries and frequently produced small aneurysms. Although the initial description of PAN was fairly specific, for most of the next 100 years every case of vasculitis tended to be called PAN, even if the sizes and types of vessels involved were completely different and there was no evidence of aneurysm formation. Wegener F. Uber eiene eigenartrige rhinogene Granulomatose mit besonderer Beteiligung des Arterienesystems und er Nieren.
Extractions: Background The differential diagnosis of chronic progressive multifocal asymmetric neuropathies is challenging. Vasculitic neuropathies, multifocal forms of chronic inflammatory demyelinating polyneuropathy, multifocal motor neuropathies, and asymmetric lower motor neuron disorders are important considerations. Case presentation We report a patient with an unusually long 12-year course of nonsystemic vasculitic neuropathy prior to the development of systemic manifestations.
Johns Hopkins Arthritis ACR 2004 Highlights On Vasculitis diseases that includes Wegener s granulomatosis and microscopic polyangiitis) . with various forms of vasculitis (including microscopic polyangiitis, http://www.hopkins-arthritis.som.jhmi.edu/edu/acr2004/vasculitis.html
Extractions: C. Schaufelberger, H. Möllby, J. Bratt, E. Nordborg Background: Giant cell arteritis is a large-vessel vasculitis that can have multiple manifestations, including jaw or upper extremity claudication, polymyalgia rheumatica, fever of unknown origin, and visual loss. Standard therapy for giant cell arteritis utilizes a prolonged course of high-dose glucocorticoids, which have numerous undesirable effects, such as cataracts, avascular necrosis, osteoporosis, hyperglycemia, and mood disorders. Because of the numerous side-effects associated with glucocorticoids (e.g., prednisone), there has been great interest in identifying immunosuppressive agents that might decrease the total amount of glucocorticoid needed to bring this disease under control. This abstract reports the results of a multicenter European trial of 58 patients with biopsy-proven giant cell arteritis randomized to receive adjunctive therapy with cyclosporine A. Study Design: Patients were treated with a standardized glucocorticoid regimen starting with 40 mg of oral prednisone daily for 1 week. Half of these patients were randomized to receive treatment with low dose cyclosporine A, titrated to a goal dosage of 3mg/kg/day. Patients were evaluated at baseline, and 1, 2, 4, 6, 9, and 12 months after enrollment.
Johns Hopkins Arthritis ACR Highlights 1999 patients were grouped into one of 4 types of AAV (Wegeners granulomatosis,microscopic polyangiitis, ChurgStrauss syndrome, and pauci-immune http://www.hopkins-arthritis.som.jhmi.edu/edu/college_of_rhuematology/vasculitis
Extractions: John Stone, M.D., M.P.H. Advances in Diagnosis and Treatment A variety of noteworthy studies pertaining to vasculitis were reported at the 1999 American College of Rheumatology meetings in Boston. The following summary focuses on the major studies related to the diagnosis and treatment of these conditions. Two studies focused on the refinement of testing for anti-neutrophil cytoplasmic antibodies (ANCA) in clinical settings. A common problem encountered in the diagnosis of ANCA-associated Vasculitides (AAV) is that numerous common conditions may mimic the presentation of AAV. The test characteristics of ANCA assays in patients with clinical mimickers of AAV are not well-described. Abstract 627 Prevalence of Antineutrophil Cytoplasmic Antibodies (ANCA) in Patients with Various Pulmonary Diseases or Multi-organ Dysfunction. D Vassilopoulos, JL Niles, A Villa-Forte, AC Arroliga, EJ Sullivan, PA Merkel, GS Hoffman Overview of study: This study evaluated the use of immunofluorescence (IF) and enzyme-linked immunosorbent assays (ELISA) in 3 groups of patients: Group I, 29 Pulmonary Clinic outpatients with a variety of lung conditions (interstitial lung disease, cancer, sarcoidosis, actinomycosis, and bronchiectasis); Group II, 99 Intensive Care Unit patients with multi-organ system dysfunction (including 91 with either pulmonary or renal dysfunction, or both); and Group III, 18 patients with biopsy-proven Wegeners Granulomatosis.
JN - Vol 10 No 1-1997, Pp 30-32 Arteritis Temporalis in a patient with microscopic polyangiitis In contrast,our patient first presented with a microscopic polyangiitis, suggested by http://www.sin-italy.org/jnonline/vol10n1/30.html
JN 2004; Vol.17 N.S8: 3-9 microscopic polyangiitis, Wegener s granulomatosis and ChurgStrauss syndrome were Do the names Wegeners granulomatosis, microscopic polyangiitis and http://www.sin-italy.org/jnonline/Vol17 Suppl 8n/S2.html
Extractions: Department of Pathology and Laboratory of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC - USA ABSTRACT: The classification of small vessel vasculitis has markedly changed over the past 150 years. With the discovery of anti-neutrophil cytoplasmic autoantibodies (ANCA), renewed interest in the field has spawned investigations into the immunopathogenesis of small vessel vasculitis. This review will describe the historical basis of the classification of vasculitis, the current nosology based on the Chapel Hill Nomenclature for vasculitis and then both pathogenic and clinical reasons that support the use of the term ANCA small vessel vasculitis to describe the pauci-immune necrotizing small vessel vasculitides, including microscopic polyangiitis, Wegeners granulomatosis, the Churg-Strauss syndrome and pauciimmune necrotizing and crescentic glomerulonephritis. Key Words.
Extractions: This Article Full Text Full Text (PDF) Alert me when this article is cited ... Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by NOWACK, R. Articles by VAN DER WOUDE, F. J. J Am Soc Nephrol 10:1965-1971, 1999