61. FastDates.com Pit Lane News - November 2002 Page 1 The Colin has been suffering from microscopic polyangiitis since the end of August. Microscopicpolyangiitis is a form of vasculitis which is extremely rare. http://www.fastdates.com/PitLaneNews2002.11.1.HTM

FastDates.com November 2002 Superbike, MotoGP, Calendar Girls Official Calendar of the SBK World Superbike Championship Sponsor of AMA 750cc Supersport Champs EBSCO Corona Extra Suzuki This Week's Starting Grid: Superbike Winter Testing SBK 2002 Superbike Championship Final at Imola The most exciting Championship final ever, Edwards retakes title. MotoGP 2002 Valentino Rossi takes first MotoGP Championship title in Brazil HERE . Alex Barros wins Valencia season final HERE AMA 2002 National Season Finals Nicky Hayden on top. FastDates.com Corona Suzuki wins its 2nd 750cc SuperSport title! Editorial The AMA 2003 Superbike Rules Fiasco? British Superbike 2002 Final Steve Hislop wins title then dumped! LA Calendar Bike Show Weekend British Sportbike magazines exposed! Taking over America! Ducati 999R Superbike The best of ther best, plus

62. Final Diagnosis -- Case 59 DIAGNOSIS Spinal subarachnoid hemorrhage secondary to microscopic polyangiitis(Idiopathic lateonset cerebellar ataxia). DISCUSSION http://path.upmc.edu/divisions/neuropath/bpath/cases/case59/dx.html

Brain Pathology Case of the Month - February 2001 DIAGNOSIS: Spinal subarachnoid hemorrhage secondary to microscopic polyangiitis (Idiopathic late-onset cerebellar ataxia) DISCUSSION: Spinal SAH was an unexpected postmortem finding in this elderly man. In the past, he had been investigated for 20 years of (non-familial) progressive ataxia, receiving a diagnosis of sporadic cerebellar degeneration. His neurodegenerative disorder had prompted a neuropathological referral, a diagnosis of idiopathic late-onset cerebellar ataxia being made. His terminal illness had been characterised by renal failure and laboratory evidence of an immunogenic disorder. Spinal SAH usually presents with intense back pain and spinal rigidity, to be followed by the consequences of damage to the spinal cord and nerve roots. This presentation was not apparent, but may have been obscured by other clinical problems. Histological examination revealed non-granulomatous inflammation of arcuate and interlobular arteries in the kidney and small arteries and venules in the spinal leptomeninges. A diagnosis of microscopic polyangiitis (MPA) is consistent with these findings and the immunology results (1, 2). Wegener's granulomatosis (WG), another small vessel vasculitis, and polyarteritis nodosa (PAN) comprise the differential diagnosis. According to modern classifications (1), PAN is excluded on the basis that it affects predominantly medium-sized vessels and not venules, and is rarely associated with ANCA. WG may appear histologically similar to MPA, and both may affect the respiratory system. However, WG usually displays granulomatous inflammation, and is associated much more with cANCA than pANCA (1, 3).

63. Health Waikato ICU - General - Presentations Asthma 95%, Pulmonary infiltrates 70%, Renal up to 49%. microscopic polyangiitisSystemic Necrotizing vasculitis that affects small vessels without granulomas. http://anaes-icu-waikato.org.nz/ICU/general/presentations.php?cat=anca

64. PUBLICATIONS INTERNATIONALES DU GERM"O"P Translate this page microscopic polyangiitis with alveolar hemorrhage. A clinical and follow-upstudy of 32 cases. microscopic polyangiitis with alveolar hemorrhage. http://germop.univ-lyon1.fr/fr/germop/publications.htm

Marchand E., Raynaud-Gaubert M.,Lauque D., Wallaert B., Cordier J.F., Tonnel A.B., and the Groupe d’Etudes et de Recherche sur les Maladies "Orphelines" Pulmonaires. Chronic eosinophilic pneumonia (CEP). A clinical and follow-up study of 61 cases. Am J Respir Crit Care Med 1997 ; 155 : A329 Crestani B., Valeyre D., Bayle J.Y., Wallaert B., Cordier J.F. and the Groupe d’Etudes et de Recherche sur les Maladies "Orphelines" Pulmonaires. Bronchiolitis obliterans organizing pneumonia primed by radiation therapy for breast carcinoma. A report of 15 patients. Am J Respir Crit Care Med 1997 ; 155 : A332 Marchand E., Reynaud-Gaubert M., Lauque D., Durieu J., Tonnel A.B., Cordier J.F., and the Groupe d’Etudes et de Recherche sur les Maladies "Orphelines" Pulmonaires (GERM"O"P). Idiopathic chronic eosinophilic pneumonia. A clinical and follow-up study of 62 cases. Medicine 1998 ; 77 : 299-312 Crestani B., Valeyre D., Roden S., Wallaert B., Dalphin J.C., Cordier J.F., and the Groupe d’Etudes et de Recherche sur les Maladies Orphelines Pulmonaires (GERM"O"P). Bronchiolitis obliterans organizing pneumonia syndrome primed by radiation therapy to the breast Am J Respir Crit Care Med 1998 ; 158 : 1929-35

65. Abstract: Mortality And Morbidity In Peripheral Neuropathy Associated Churg-Stra ChurgStrauss syndrome (CSS) and microscopic polyangiitis (MPA) are commonly characterizedby systemic necrotizing vasculitis and frequent occurrence of axonal http://www.jrheum.com/abstracts/abstracts02/1408.html

Search the Journal Home Current Issue Archives Guidelines for Authors ... Contact Info Mortality and Morbidity in Peripheral Neuropathy Associated Churg-Strauss Syndrome and Microscopic Polyangiitis NAOKI HATTORI, KEIKO MORI, KENICHIRO MISU, HARUKI KOIKE, MIYUKI ICHIMURA, and GEN SOBUE Objective. Churg-Strauss syndrome (CSS) and microscopic polyangiitis (MPA) are commonly characterized by systemic necrotizing vasculitis and frequent occurrence of axonal neuropathy. We investigated whether the neuropathy in these 2 diseases reveals differences in clinicopathologic features and predicts survival and functional outcome. We compared 30 patients with CSS associated neuropathy with 26 patients with MPA associated neuropathy in terms of clinical, laboratory, electrophysiologic, and outcome data. MPA cases showed a significantly higher age at onset, a higher male/female ratio, and more extensive systemic organ involvement than CSS. Inflammatory markers including antimyeloperoxidase antibody titers were also significantly higher in MPA. Both CSS and MPA showed similar neuropathic symptoms, electrophysiologic findings, and sural nerve biopsy findings representing acute axonal changes. Functional disability assessed by modified Rankin score, muscle strength, and nerve conduction variables were similar in CSS and MPA, both in the acute peak phase and during longterm followup. However, survival was significantly worse in MPA than CSS. Neuropathy associated CSS and MPA shared common neuropathic features throughout the course, but systemic organ involvement, inflammatory marker concentrations, and relapse rates were significantly higher in MPA, which showed a poorer survival rate. (J Rheumatol 2002;29:1408-14)

66. Florida State University College Of Medicine Digital Library microscopic polyangiitis Access document. Noble Textbook of Primary Care Medicine,3rd Ed.2001 (MD Consult) Table of contents - Medical Library subscription http://fsumed-dl.slis.ua.edu/clinical/rheumatology/autoimmune/vasculitides/syste

Clinical Resources by Topic: Cardiovascular Disorders Polyangiitis Overlap Syndrome Clinical Resources Atlases Pathology Clinical Guidelines Miscellaneous Resources See also: General Cardiovascular Disorders Clinical Resources Polyangiitis Overlap Syndrome Patient/Family Resources Harrison's Principles of Internal Medicine 15th Ed.-2001: Table of contents Medical Library subscription INFO Chapter 317: The Vasculitis Syndromes Table of contents Definition: Access document Classification of Vasculitic Syndromes: Access document Pathophysiology and Pathogenesis: Access document Approach to the Patient: Access document Systemic Necrotizing Vasculitis: Access document Polyangiitis Overlap Syndrome: Access document Principles of Treatment: Access document Goldman: Cecil Textbook of Medicine 21st Ed.-2000 (MD Consult): Table of contents Medical Library subscription INFO Chapter 292 - The Vasculitic Syndromes: Access document Chapter 293 - Polyarteritis Nodosa Group: Access document Ruddy: Kelly's Textbook of Rheumatology 6th Ed.-2001 (MD Consult): Table of contents Medical Library subscription INFO Chapter 77 - Classification of Vasculitis Access document Chapter 79 - Vasculitis Associated with Antineutrophil Cytoplasmic Antibody Access document Microscopic Polyangiitis Access document Feldman: Sleisenger and Fordtran's Gastrointestinal and Liver Disease 7th Ed.-2002 (MD Consult):

67. Cordier226-243.html Wegener's granulomatosis, microscopic polyangiitis, and ChurgStrauss syndromeare the three biggest vasculitides with pulmonary manifestations. http://www.personal.u-net.com/~ersj/ERM/Monograph files/14 summaries/cordier226-

Summary Pulmonary vasculitis often remains difficult to recognize, especially because this type of pulmonary "orphan" disease is seldom encountered by pulmonary physicians. Wegener's granulomatosis, microscopic polyangiitis, and Churg-Strauss syndrome are the three biggest vasculitides with pulmonary manifestations. All three are associated with antineutrophil cytoplasmic antibodies, which have become a major biological diagnostic tool. Early diagnosis of pulmonary vasculitis is necessary to start treatment with corticosteroids and immunosuppressors without delay. Keywords: Churg-Strauss syndrome, microscopic polyangiitis, pulmonary vasculitis; Wegener's granulomatosis. Back to Contents

68. P990820a - Polyarteritis Nodosa Title Treatment of polyarteritis nodosa and microscopic polyangiitis. Title Polyarteritisnodosa, microscopic polyangiitis, and ChurgStrauss syndrome. http://www.emory.edu/WHSCL/grady/amreport/litsrch99/p990820a.html

Polyarteritis Nodosa (Lubin) Question: What is polyarteritis nodosa? Fulltext Available in MDConsult using Journal Search and the search term: Unique Identifier: 99086413 Authors: Guillevin L. Lhote F. Institution: Hopital Avicenne, Universite Paris-Nord, Bobigny, France. Title: Treatment of polyarteritis nodosa and microscopic polyangiitis. [Review] [49 refs] Unique Identifier: 96160004 Authors: Lhote F. Guillevin L. Institution: Hopital Delafontaine, Saint-Denis, France. Title: Polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndrome. Clinical aspects and treatment. [Review] [132 refs] Source: Rheumatic Diseases Clinics of North America. 21(4):911-47, 1995 Nov. Abstract: In this article, three systemic vasculitidespolyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndromeare reviewed, focusing on advances in the understanding of the pathogenesis, new classification nomenclature, and major clinical features of these vasculitides. Distinguishing criteria between polyarteritis nodosa and microscopic polyangiitis are also presented in detail, and recent advances in the clinical management of these diseases according to appropriate therapeutic strategies are recommended. [References: 132] Morning Report Emory University School of Medicine 1999 Edition Participating Faculty: Daniel Stephens MD / Donald Brady MD dbrady@emory.edu

69. Baylor College Medicine Monthly Summary Hotline Aids - Social Issues - Health Medicine - AIDS/HIV microscopic polyangiitis- microscopic polyangiitis (MPA) is vasculitis of small vessels. http://www.fizgigs.com/page.php?page=baylor college medicine monthly summary

70. INFLAMMATORY MYOPATHIES IN THE 21ST CENTURY The largest case series reported to date included 14 patients with Wegener's granulomatosis,11 patients with microscopic polyangiitis, and a patient with http://www.rheuma21st.com/archives/cutting_edge_immunoglobulin.html

INTRAVENOUS IMMUNOGLOBULIN (IVIG) THERAPY IN AUTOIMMUNE DISEASES - SLE, ANTIPHOSPHOLIPID SYNDROME, VASCULITIS What Is New? by Yaniv Sherer, MD, Yair Levy, MD, and Yehuda Shoenfeld, MD Department of Medicine 'B' and the Research Unit of Autoimmune Diseases, Sheba Medical Center, Tel-Hashomer, and Sackler Faculty of Medicine, Tel-Aviv University, Israel published 9. September 1999 Download As A PDF File : To read and print PDF files, you will need free Adobe Acrobat Reader Correspondence to: Y. Shoenfeld, M.D., Department of Medicine 'B', Sheba Medical Center, Tel-Hashomer, 52621, Israel. Tel: 972-3-5302652. Fax: 972-3-5352855. E-mail: Shoenfel@post.tau.ac.il The first use of intravenous immunoglobulin (IVIg) was for patients with various immunodeficiency states. Currently, it is also an accepted treatment in some autoimmune diseases, such as polymyositis/dermatomyositis, Guillain-Barre syndrome, and immune thrombocytopenic purpura. The use of IVIg and its beneficial role in other autoimmune conditions is not yet established, and, in some cases, is even controversial. In this cutting edge article, the main reports of IVIg use in three groups of human autoimmune diseases will be discussed: systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), and autoimmune vasculitis. IVIg in SLE Several case-reports of IVIg use in human SLE have been reported

71. Investigations Specificity and sensitivity of ANCA serology testing for Wegener's granulomatosisand microscopic polyangiitis (adapted from Hagen et al, Kidney Int 1998;53 http://www.wellclosesquare.co.uk/rheum/invest.htm

Investigations X-Rays RA Hands and feet Jointspace narrowing, erosions OA Inter-bone distance Ank spondy AP pelvis Pseudowidening/blurring of lower 2/3 of SI joint. Erosion of vertebral end-plates ("squared off"). Psoriatic arthropathy Asymmetrical small joint erosions (DIP) and periosteal reaction. Chondrocalcinosis AP knees Chronic tophaceous gout "Punched-out" sclerotic erosions RA: acute phase Inflammation results in release of soluble mediators (cytokines, including interleukins 1-6 and TNF) which results in: C-reactive protein (CRP) raised ++ Serum amyloid A (SSA) raised ++ Albumin reduced WBC N/raised Platelets raised Hb reduced Plasma viscoscity raised ESR raised C3, C4 raised Alk phos raised Antibodies Anti nuclear antibody ( ANA +ve in Systemic lupus erythematosus (active) 99% Systemic lupus erythematosus (inactive) 95% Drug induced lupus 99% Mixed connective tissue disease 99% Rheumatoid arthritis 32% Juvenile rheumatoid arthritis 76% Chronic active hepatitis 75% % Sjorgen's syndrome 68% Progressive systemic sclerosis 64% "Normal" controls 0-2% (Increase with age - 20% at 70yrs)

72. Medicalseek - Search Engine For The Healthcare Industry Conditions and DiseasesImmune DisordersAutoImmunemicroscopic polyangiitis MicroscopicPolyangiitis in a Pediatric Patient From Archives of Family Medicine http://www.medicalseek.net/Conditions_and_Diseases_Immune_Disorders_Auto_Immune_

CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Auto-Immune Microscopic Polyangiitis Featured Site Immunity Support.com Immunity Products and alternative treatments. Immune Advantage™ is a natural, concentrated source of immunoglobulin and other immuno-proteins that promote a natural resistance to illness and infection. Just as colostrum passes immunity from mother to child, Immune Advantage™ utilizes concentrated blood serum, the precursor to colostrum, to help boost immunity and support the body against invading pathogens. Conditions and Diseases:Immune Disorders:Auto-Immune:Microscopic Polyangiitis Microscopic Polyangiitis in a Pediatric Patient From Archives of Family Medicine, a description of this disorder, followed by a case study. archfami.ama-assn.org/issues/current/abs/fb... Rachael's MPA Support Site Support and information for people fighting Microscopic Polyangiitis. Frequently asked questions and dealing with doctors are a few of the topics discussed. users.fast.net/~rcb1/mpa/ Savvy Medinfo for Patients and Doctors A description of Microscopic Polyangiitis along with a look at the diagnosing. blackandwhite.org/micro/index.shtml

73. CCHS Clinical Digital Library microscopic polyangiitis Access document. Feldman Sleisenger and Fordtran's Gastrointestinaland Liver Disease 7th Ed.2002 (MD Consult) Table of contents http://cchs-dl.slis.ua.edu/clinical/rheumatology/autoimmune/vasculitides/systemi

Clinical Resources by Topic: Cardiovascular Disorders Polyangiitis Overlap Syndrome Clinical Resources Atlases Pathology Clinical Guidelines Miscellaneous Resources See also: General Cardiovascular Disorders Clinical Resources Polyangiitis Overlap Syndrome Patient/Family Resources Harrison's Principles of Internal Medicine 15th Ed.-2001: Table of contents Health Sciences Library subscription INFO Chapter 317: The Vasculitis Syndromes Table of contents Definition: Access document Classification of Vasculitic Syndromes: Access document Pathophysiology and Pathogenesis: Access document Approach to the Patient: Access document Systemic Necrotizing Vasculitis: Access document Polyangiitis Overlap Syndrome: Access document Principles of Treatment: Access document Goldman: Cecil Textbook of Medicine 21st Ed.-2000 (MD Consult): Table of contents Health Sciences Library subscription INFO Chapter 292 - The Vasculitic Syndromes: Access document Chapter 293 - Polyarteritis Nodosa Group: Access document Ruddy: Kelly's Textbook of Rheumatology 6th Ed.-2001 (MD Consult): Table of contents Health Sciences Library subscription INFO Chapter 77 - Classification of Vasculitis Access document Chapter 79 - Vasculitis Associated with Antineutrophil Cytoplasmic Antibody Access document Microscopic Polyangiitis Access document Feldman: Sleisenger and Fordtran's Gastrointestinal and Liver Disease 7th Ed.-2002 (MD Consult):

74. Microscopic Polyangiitis microscopic polyangiitis Rachael's MPA Support Site http//www.users.fast.netSupport and information for people fighting microscopic polyangiitis. http://www.medlina.com/microscopic_polyangiitis.htm

Academic Medicine Addiction Aging AIDS-HIV ... Women's Health The Web MEDLINA.com (partial) CDC WHO FDA NIH CATEGORIES Search: All Products Books Magazines Popular Music Classical Music Video DVD Baby Electronics Software Outdoor Living Wireless Phones Keywords: Home Up Marfan Syndrome Melorheostosis ... Meckel-Gruber Syndrome Microscopic Polyangiitis Machado Joseph Syndrome Mannosidosis Microscopic Polyangiitis Microscopic Polyangiitis in a Pediatric Patient - http://archfami.ama-assn.org From Archives of Family Medicine, a description of this disorder, followed by a case study. Savvy Medinfo for Patients and Doctors - http://www.blackandwhite.org A description of Microscopic Polyangiitis along with a look at the diagnosing. Rachael's MPA Support Site - http://www.users.fast.net Support and information for people fighting Microscopic Polyangiitis. Frequently asked questions and dealing with doctors are a few of the topics discussed. SUBCATEGORIES Up powered by A merica M edica, I nc. info@medlina.com New York City

75. Blood Vessels (9/25) PANCA (perinuclear) act against myeloperoxidase in the neutrophils and areassociated with microscopic polyangiitis and Churg-Strauss syndrome. http://www.med.uiuc.edu/m2/Pathology/bloodtwo.htm

BLOOD VESSELS II Lecture Handout Jill Conway, 9/19/00 Important Terms: Fibrinoid necrosis = necrotic tissue has fibrin-like eosinophilic material. This is associated with blood vessel and connective tissue disorders, malignant hypertension, and wound healing. Granuloma = nodular inflammatory lesions associated with immune reaction. Consists of focal area of epithelioid-like macrophages surrounded by a mononuclear infiltrate, mainly of lymphocytes and some plasma cells. Older granulomas develop fibrosis and are firm and nodular. Epithelioid cells may form giant cells with many nuclei arranged peripherally (Langhans-type) or haphazardly (foreign-body type). ESR = erythrocyte sedimentation rate in which blood cells are allowed to settle for one hour in a calibrated tube. Elevated values indicate inflammatory states that may increase fibrinogen in serum that helps RBCs form "rouleaux" which sediment more quickly. Palpable purpura = purpura is hemorrhage into the skin and palpable designates raised lesions Aneurysm shapes: berry = small, spherical about 1.5 cm in diameter.

76. Dr. Rose's Peripheral Brain-VASCULITIS active Wegener's. Perinuclear ANCA (pANCA) is more closely associatedwith microscopic polyangiitis, a smaller-vessel vasculitis; http://faculty.washington.edu/momus/PB/vasculit.htm

VASCULITIDES I. Definitions and pathophysiology Inflammation in blood vessel walls, leading to Tissue ischemia and necrosis Aneurysms and rupture Can occur in any blood vessel Tends to be irregular and segmental May be focal or diffuse, acute or chronic In some forms, associated with immunoglobulin deposition, which presumably leads to complement activation and PMN recruitment Mechanisms of inflammation may vary in different forms of vasculitis Infection, including hep B and C may play a role in some vasculitis syndromes Neoplasms, e.g. lymphomas and hairy cell leukemia may also be associated II. Large artery vasculitides Takayasu's arteritis Pathophysiology Involves the aorta (us. the most severely affected vessel) and its primary branches, including renal and mesenteric aa. Continuous or patchy granulomatous inflammation with lymphocytes, histiocytes, and multinucleated giant cells Can produce either luminal compromise (more common) or dilatation and aneurysms Us. young women, most often Asian or European background, us. onset age 10-30y

77. Health Conditions And Diseases Immune Disorders Auto-Immune Microscopic Polyangi Health Conditions and Diseases Immune Disorders AutoImmunemicroscopic polyangiitis 524278 Polish Yellow Pages YP.pl. http://www.yellowpages.pl/ca/524278/Health/Conditions_and_Diseases/Immune_Disord

>English Version Polskie Firmy: Firmy wg SIC Szukaj firmy Szukaj w Internecie: Polska ¦wiat Katalog Stron Biznes Serwisy YellowPages: Rejestracja DOMEN Strony WWW DNS ZOOM ... Sklep Partner idealo.de NETSPRINT Reporter.pl Portofolio DVD Search TOP CHARTS Webkatalog Multi szukanie - mainSeek Polska - Netsprint ¦wiatowy Katalog Stron Katalog Firm Teleadreson Szukaj domeny TOP Health Auto-Immune Microscopic Polyangiitis in a Pediatric Patient - From Archives of Family Medicine, a description of this disorder, followed by a case study. Rachael's MPA Support Site - Support and information for people fighting Microscopic Polyangiitis. Frequently asked questions and dealing with doctors are a few of the topics discussed. Savvy Medinfo for Patients and Doctors - A description of Microscopic Polyangiitis along with a look at the diagnosing. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor P³atna reklama REJESTRACJA DOMEN KATALOG STRON PROFESJONALNY DNS SKLEP ... e-mail

78. ¤º¬ìÁ`¬d©Ð»PÁ{§É¯f²z°Q½×·|Á¿¸q main target antigen of cANCA, which is seen in Wegener's Granulomatosis, also canbe seen in other immune diseases, eg microscopic polyangiitis, Churg-Strauss http://www.vghtpe.gov.tw/~im/gr97mar/gr5.htm

Anti-Neutrophil Cytoplasmic Antibody and Related Diseases ±i¾å¹ç Âå®v April 9, 1997 Overview Case presentation: Case 1. Miss Wen, 20-year-old ¡@¡@¡@¡@Chills, fever, multiple rash over lower legs and forearms for 1 month. ¡@¡@¡@¡@Cough with bloody sputum, oral ulcer noted. ¡@¡@¡@¡@Chest X-Ray: Nodular infiltrate over bilateral lungs. ¡@¡@¡@¡@Lab data: WBC 12800/mm , Hgb 7.3 g/dl, Plat. 303,000/mm ¡@¡@¡@¡@¡@¡@¡@¡@Eos. count 506/mm , IgE 666 ng/dl, RF 244 mg/dl, TB of sputum negative, ¡@¡@¡@¡@¡@¡@¡@¡@ANA negative and all other immunology related examinations are negative. ¡@¡@¡@¡@Skin biopsy (in Kaohsiung Med. School): compatible with anaphylactoid purpura ¡@¡@¡@¡@Bronchoscope (in Kaohsiung M. School): No lesion discovered, cytology negative ¡@¡@¡@¡@CT scan of chest: multiple nodular lesions over both upper and lower lungs with cavity formation. ¡@¡@¡@¡@Serum for ANCA test: strong positive with cANCA pattern. ¡@¡@¡@¡@Treatment was very effective with immune suppressive agents Case 2: A 50-years-old female ¡@¡@¡@¡@C.C.: Nose pain developed treated as sinusitis by antibiotics without effect.

79. BioMed Central | Full Text | Polyarteritis Nodosa And Microscopic Polyangiitis: Welcome guest user, http://www.biomedcentral.com/1523-3774/4/75

Welcome guest user home journals A-Z journals by subject advanced search ... my BioMed Central Although all research articles in Current Rheumatology Reports are available free, most other articles require a subscription Click here to view an abstract of this article Click here to login if you are already a subscriber to Current Rheumatology Reports Subscribe to Current Rheumatology Reports Register for a free online trial Ask your librarian to investigate institutional access Athens users please click here to gain access If you believe you are seeing this page in error, or cannot activate your subscription, e-mail us info@biomedcentral.com Terms and Conditions Privacy statement Information for advertisers ... Contact us

80. References Kandeel A, Ramesh S, Chen Y, Celik C, Jenis E, Ambrus JL Jr. Microscopicpolyangiitis in a pediatric patient. Arch Fam Med. 2000;911891192. http://www.medscape.com/content/2002/00/43/25/432549/432549_ref.html

References for: Crescentic Glomerulonephritis Requiring Hemodialysis and Elevated MPO-ANCA Level and Vasculitis Allergica Cutis in a 21-Year-Old Girl Smith G. Management of childhood nephrotic syndrome. BMJ. 1995;310:530-531. Jennette JC, Falk RJ, Andrassy K, et al. Nomenclature of systemic vasculitides: proposal of an international consensus conference. Arthritis Rheum. 1994;37:187-192. Churg J, Strauss L. Allergic granulomatosis, allergic angiitis, and periarteritis nodosa. Am J Pathol. 1951;27:277-301. Gross WL. Antineutrophil cytoplasmic autoantibody testing in vasculitis. Rheum Dis Clin North Am. 1995;21:987-1011. Niles JL. Antineutrophil cytoplasmic autoantibodies in the classification of vasculitis. Annu Rev Med. 1996;47:303-313. Lesavre P. Antineutrophil cytoplasmic autoantibodies antigen specificity. Am J Kidney Dis. 1991;18:159-163. Watts RA, Scott DGI. Small vessel vasculitis associated with antineutrophil cytoplasmic antibody. BMJ. 1995;310:1128-1132. Kandeel A, Ramesh S, Chen Y, Celik C, Jenis E, Ambrus JL Jr. Microscopic polyangiitis in a pediatric patient. Arch Fam Med. 2000;9:1189-1192. Guillevin L, Lhote F. Distinguishing polyarteritis nodosa from microscopic polyangiitis and implications for treatment. Curr Opin Rheumatol. 1995;7:20-24.

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