41. 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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42. 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.

Allison AC, Eugui EM. Immunosuppressive and other effects of mycophenolic acid and an ester prodrug, mycophenolate mofetil. Immunol Rev 1993;136:5–28. Brijker F, Magee CC, Cohen Tervaert JW, O’Neill S, Walshe JJ. Outcome analysis of patients with vasculitis associated with antineutrophil cytoplasmic antibodies. Clin Nephrol 1999;52:344–51. 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;113:656–63. 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;318:1651–57. Jennette JC, Falk RJ. Small-vessel vasculitis. N Engl J Med 1997;337:1512–23. Jennette JC, Falk RJ, Andrassy K, et al. Nomenclature of systemic vasculitides: proposal of an international consensus conference. Arthritis Rheum 1994;37:187–92. Guillevin L, Druand Gasselin D, Cevallos R, et al. Microscopic polyangiitis: clinical and laboratory findings in eighty-five patients. Arthritis Rheum 1999;42:421–30.

43. Microscopic Polyangiitis In A Patient With Relapsing Polychondritis -- Weber Et In microscopic polyangiitis, haemorrhagic capillaritis is a very serious andoften lifethreatening complication and the course of glomerulonephritis http://rheumatology.oxfordjournals.org/cgi/content/full/40/2/233

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: 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: 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 British Society for Rheumatology Letters to the Editor Microscopic polyangiitis in a patient with relapsing polychondritis 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.

44. Microscopic Polyangiitis In A Patient With Relapsing Polychondritis -- Weber Et microscopic polyangiitis in a patient with relapsing polychondritis. F. Weber , E.Kowald , M. Schmuth and N. Sepp. Department of Dermatology and http://rheumatology.oxfordjournals.org/cgi/content/extract/40/2/233

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: 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 Letters to the Editor Microscopic polyangiitis in a patient with relapsing polychondritis 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.

45. 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

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. Buy this article Search British Library Direct Return to Google 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: service charge Abstract: By using this site you agree to our terms and conditions Privacy policy We welcome your comments

46. 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

47. 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

48. 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

What is the VCRC? Information for Patients: Learn More Introduction to Vasculitis Disease Definitions Useful Links ... Learn More Disease Definitions Please Choose from the Menu below: Microscopic Polyangiitis (MPA) Churg-Strauss Syndrome (CSS) Polyarteritis Nodosa (PAN) Takayasu's Arteritis (TAK) ... Polymyalgia Rheumatica 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 Microscopic Polyangiitis (MPA) What is Microscopic Polyangiitis?

49. Vasculitis Clinical Research Consortium - Information For Physicians Wegener’s Granulomatosis (WG); microscopic polyangiitis (MPA); ChurgStrauss Syndrome microscopic polyangiitis (MPA) is a systemic form of vasculitis http://rdcrn.epi.usf.edu/vcrc/physicians/

What is the VCRC? Information for Patients: Learn More Take Action Information for Physicians About the VCRC ... Home Information for Physicians Disease Definitions Please Choose from the Menu below: Microscopic Polyangiitis (MPA) Churg-Strauss Syndrome (CSS) Polyarteritis Nodosa (PAN) Takayasu's Arteritis (TAK) ... Back to Top Microscopic Polyangiitis (MPA) Join the Contact Registry for this Disorder Find a Study Back to Top Churg-Strauss Syndrome (CSS) Churg Strauss Syndrome (CSS) Join the Contact Registry for this Disorder Find a Study Back to Top Polyarteritis Nodosa (PAN) Join the Contact Registry for this Disorder Find a Study Back to Top Takayasu's Arteritis (TAK) Join the Contact Registry for this Disorder Find a Study Back to Top Giant Cell (Temporal) Arteritis (GCA) Join the Contact Registry for this Disorder Find a Study Back to Top Polymyalgia Rheumatica (PMR) Join the Contact Registry for this Disorder Find a Study Back to Top Home ... Return to RDCRN Main Page

50. 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

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51. 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

52. 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

53. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Immune_Disorders/A full story. More news about microscopic polyangiitis . Error We did not findany matches for your request. More books about microscopic polyangiitis http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Immune_Diso

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Auto-Immune : Microscopic Polyangiitis Subtopics See Also: Health: Conditions and Diseases: Rare Disorders Search Google: Microscopic Polyangiitis News Books Links ... 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!

54. 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

ATS Centennial ATS Historic Retrospectroscope "I remember..." ... Articles 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.

55. BioMed Central | Full Text | P-ANCA Vasculitic Neuropathy With 12-year Latency B Keywords Vasculitic neuropathy, microscopic polyangiitis, Multifocal neuropathy.Abstract. Background. The differential diagnosis of chronic progressive http://www.biomedcentral.com/1471-2377/2/10

home journals A-Z subject areas advanced search ... Volume 2 Viewing options Abstract Full text PDF Associated material: Pre-publication history PubMed record Related literature: Articles citing this article on Google Scholar Other articles by authors Greenberg SA ... Similar articles (PubMed) Tools: E-mail to a friend Download references Post a comment Key E-mail Corresponding author Case report P-ANCA vasculitic neuropathy with 12-year latency between onset of neuropathy and systemic symptoms Steven A Greenberg From the Department of Neurology, Division of Neuromuscular Disease, Brigham and Women's Hospital and Harvard Medical School, Boston, USA BMC Neurology The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2377/2/10 Received Accepted Published Keywords: Vasculitic neuropathy, Microscopic polyangiitis, Multifocal neuropathy Abstract 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.

56. 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

Phil Seo, M.D. Treatment Abstract 601: Cyclosporin A in GCA Abstract 602: IV Glucocorticoid as Initial Treatment in GCA Abstract 1719: Wegener's Etanercept Trial Abstract 605: Rituximab in Severe ANCA-associated Vasculitis Pathophysiology Abstract 603 Targets of Anti-Endothelial Cell Antibodies Clinical Aspects Abstract 604 Association of Serologic Markers with Disease Activity in WG Abstract 606 Epidemiology of Primary Systemic Vasculitis Treatment Abstract 601: No Additional Steroid Sparing Effect of Cyclosporin A in Patients with Giant Cell Arteritis 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.

57. Johns Hopkins Arthritis ACR Highlights 1999 patients were grouped into one of 4 types of AAV (Wegener’s granulomatosis,microscopic polyangiitis, ChurgStrauss syndrome, and pauci-immune http://www.hopkins-arthritis.som.jhmi.edu/edu/college_of_rhuematology/vasculitis

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 Wegener’s Granulomatosis.

58. 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

59. JN 2004; Vol.17 N.S8: 3-9 microscopic polyangiitis, Wegener s granulomatosis and ChurgStrauss syndrome were Do the names Wegener’s granulomatosis, microscopic polyangiitis and http://www.sin-italy.org/jnonline/Vol17 Suppl 8n/S2.html

Table of Contents Review J NEPHROL 2004; 17: 3-9 Thoughts about the classification of small vessel vasculitis R.J. Falk , J.C. Jennette Division of Nephrology and Hypertension, The University of North Carolina at Chapel Hill, Chapel Hill, NC - USA 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, Wegener’s granulomatosis, the Churg-Strauss syndrome and pauciimmune necrotizing and crescentic glomerulonephritis. Key Words.

60. Mycophenolate Mofetil For Maintenance Therapy Of Wegener's Granulomatosis And Mi Maintenance Therapy of Wegener s Granulomatosis and microscopic polyangiitis granulomatosis (WG) (n = 9) and microscopic polyangiitis (MPA) (n = 2). http://www.jasn.org/cgi/content/abstract/10/9/1965

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: 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 American Society of Nephrology REGULAR ARTICLES Mycophenolate Mofetil for Maintenance Therapy of Wegener's Granulomatosis and Microscopic Polyangiitis A Pilot Study in 11 Patients with RenalInvolvement RAINER NOWACK PIETER KLOOKER OLAF HERGESELL KONRAD ANDRASSY and FOKKO J. VAN DER WOUDE 5th Medical Clinic (Nephrology, Endocrinology), University-Clinic Mannheim, Faculty of Clinical Medicine of the University of Heidelberg, Mannheim, Germany Medical Clinic (Nephrology, Hypertension), Faculty of Clinical Medicine of the Humboldt University Berlin, Campus Buch, Berlin, Germany Klinikum der Stadt Ludwigshafen, Medizinische Klinik A, Ludwigshafen, Germany

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