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         Lupus:     more books (103)
  1. The London Lupus Centre, Book of Lupus: A Patients' Guide by Graham Hughes, 2008-12-15
  2. Lupus Underground: A Patient's Case for a Long-Ignored, Drug-Free, Non-Patentable, Counter-Intuitive Therapy That Actually Works - UVA1 Phototherapy by Anthony DeBartolo, 2004-11-30
  3. Lupus Nephritis: Frontiers and Challenges by Hussein A. Sheashaa, Tarek M. Abbas, et all 2010-07
  4. Positive Options for Living with Lupus: Self-Help and Treatment (Positive Options for Health) by Philippa Pigache, 2006-08-30
  5. Lupus: A Patient's Guide to Diagnosis, Treatment, and Lifestyle by Iris Quintero Del RioMD, 2007-10-01
  6. LUPUS NOVICE: Toward Self Healing by Laura Chester, 1999-08-01
  7. Lupus: Everything You Need to Know (Your Personal Health)
  8. Pumpkin: A Young Woman's Struggle With Lupus by Patricia M. Fagan, 1994-04
  9. Lupus: My Search for a Diagnosis by Radziunas, 1993-01-05
  10. Coping with Lupus: A Guide to Living With Lupus for You and Your Family by Robert H. Phillips, 1984-07-01
  11. Lupus, My Doctor and Me: A Sacred Dialogue by Anita A. Fricklas, Stuart S. Kassan, 2010-07-01
  12. Living Without Pain: Stomach & Digestive Disorders, Arthritis, Fibromyalgia, Lupus, Chronic Fatigue Syndrome, Headaches and More-- by Harvey Diamond, 2007-01
  13. LIVING WITH THE WOLF and Surviving Lupus by Liz Shaw-Stabler, 2010-07-31
  14. Taking Charge of Lupus:: How to Manage the Disease and Make the Most of Your LIfe by Maureen Pratt, David Hallegua, et all 2002-09-03

21. Fundación Mexicana De Lupus, AC
Gu­a para pacientes y familiares. Caracter­sticas de esta enfermedad, grados de afectaci³n, adelantos cient­ficos, tratamiento y pron³stico.

Lupus: Guia de Pacientes y Familiares

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Que es Lupus [ Teorias acerca de la probable causa ] ... [ e-mail ]
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22. Lupus
Written by a nurse who is also a lupus patient, this topic provides information,news, support and community to lupies and their families.
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Note: We are actively seeking a new Feature Writer to adopt this Retired Topic. If interested, please Contact Member Services for more information.
By Karyn Moran Holton Welcome Page My Articles Discussions for You ... Community Bookstore Subscribe to My Topic Related Subject(s): Systemic lupus erythematosus Welcome Message
Welcome to the Lupus pages! When I was first diagnosed with

23. Lupus Canada-Welcome/Bienvenue
A primary source of information about lupus including current research with information on the organization, membership, the immune system and

24. Lupus Canada-Welcome
A source of information about lupus Canada, its member organizations and thedisease lupus of interest to people with lupus, their family and friends,
Welcome to the
Lupus Canada Website!
This site is provided as a source of information about Lupus Canada , its Member Organizations , and lupus. We hope it is of interest to people with lupus, their family and friends, health care professionals and the general public. To improve understanding of this chronic disease, Introduction to Lupus provides an overview. To learn more about lupus, the symptoms, how it is diagnosed, what medications are used to treat it and coping with the disease, read the Lupus Canada publication "Lupus: The disease with 1000 faces" . Topics of interest are presented in Articles About Lupus and further information can be found through the Related Sites
What's New at Lupus Canada? Symposium 2006 Announcement - Mark your calender for June 10, 2006 Wear your support for lupus - Announcing Lupus Canada wristbands Volunteer position - Volunteer Resources Coordinator Symposium - Learning to Live Well with Lupus 2005 - Summary Report Lupus, The Disease with a Thousand Faces
Endorsed by the Canadian Medical Association, the recently released book is a very important resource for people living with lupus, especially due to a limited availability of Canadian information about the disease. World Lupus Day
World Lupus Day is an opportunity to increase awareness and understanding of this puzzling disease. Please share lupus information with family, friends, and co-workers and help make a difference in the lives of people living with lupus.

Abbot of Ferrieres, French Benedictine writer, b. in the Diocese of Sens, about 805; d. about 862.
Home Encyclopedia Summa Fathers ... L > Lupus A B C D ... Z
(SERVATUS LUPUS, LOUP) Abbot of Ferrieres, French Benedictine writer, b. in the Diocese of Sens, about 805; d. about 862. He assumed the surname of Servatus in commemoration of his miraculous predestination . He believed in a twofold predestination , not indeed in the sense that God predestined some men to damnation, but that he foreknew the sins of men and foreordained consequent punishment. The closing years of the life of Lupus were saddened by the threatened devastation of his monastery by the invading Normans. He occupies a prominent place in medieval literary history, being one of the most cultured and refined men of the ninth century. His letters, of which we possess 132, are distinguished for literary elegance and valuable historical information. As a hagiographer he has left us a "Life of St. Maximin", Bishop of Trier (d. 349) and a "Life of St. Wigbert", Abbot of Fritzlar in Hesse (d. 747). In the controversy on predestination he wrote his "De tribus quaestionibus", a work which treated of the threefold question of free will, predestination , and the universality of redemption. To illustrate the teaching of the Church on these topics he brought together pertinent passages from the Fathers in his "Collectaneum de tribus quaestionibus."

26. Immunologie - Lupus érythémateux Disséminé
Pr©sente une d©finition de la maladie, sa physiopathologie, les moyens de diagnostic, son ©volution et son traitement.
Nos Fiches Maladies
- Cardiologie

Charte Ethique

Symptomatologie clinique

Diagnostic Positif

Evolution, Pronostic
... Traitement DEFINITION connectivite ADN natif. INTERET Voir tous les livres Autres ressources e-Cardiologie Hypertension Online, Miximage Photos libres de droits. audit et mesure d'audience visiteurs internet par Coup de Coeur "10 ans avant ma mort" Viviali Webmaster Haut de page

27. LUPUS UK Welcome
lupus UK. Coordinating group for local information and support groups for lupus sufferers.

28. LUPUS UK :: Welcome
lupus UK. Coordinating group for local information and support groups for lupussufferers.
Skip Alert Please note:
The content here at LUPUS UK is accessible to every type of browser, however, this browser appears to not support any of the basic Web Standards. To view the site as it is intended please feel free to upgrade your browser to either of the following... Mozilla Opera or Skip to Main Navigation Extract from the LUPUS UK web site at: LUPUS AWARENESS MONTH IS OCTOBER
find out how you can help

LUPUS UK is the only national registered charity supporting people with systemic lupus and discoid lupus and assisting those approaching diagnosis. We presently have over 7,500 Members and 30 Regional Groups who arrange medical talks, publish local newsletters, set up local occasions and organise fundraising events. LUPUS UK also produces an informative national magazine with lupus articles, letters, reports, and photographs, and operates a strong Grant Programme for research purposes and welfare. LUPUS UK's priorities are:
  • to help the lupus patient who may feel alone and isolated to assist those in need as they seek a diagnosis to inform the public and the medical profession about lupus to improve national awareness about lupus and it's impact to maintain a network of Regional Groups and Contacts to fund further research into the causes and towards a cure
Better awareness of Lupus begins with you.

29. Lupus érythémateux Systémique
Fiche dinformation pratique sur le lupus ©ryth©mateux syst©miques,signes de la maladie, autres sites internet, types de consultations adapt©es, laboratoires de diagnostic, projets de recherche en cours,associations de patients , essais cliniques, m©dicaments.
Accès à la base de données Orphanet
Lupus érythémateux systémique
Accès direct aux détails Alias
  • Récepteur 1 du complément, déficit en
Le lupus est une maladie auto-immune chronique dont l'évolution est capricieuse et dont les causes ne sont pas encore connues. Il existe deux formes, le lupus discoïde qui touche plus la peau et peut évoluer vers le lupus disséminé et le lupus érythémateux disséminé qui évolue par poussées et peut toucher le coeur, les poumons et les articulations. Les manifestations cutanées incluent éruption sur les pommettes, photosensibilité et ulcérations buccales. Il existe une prédisposition héréditaire à cette affection.Un gène de susceptibilité a été identifié. Il code pour un immunorécepteur qui régule l'auto-tolérance périphérique des celllules T et B. Les traitements consistent en l'administration d'anti-inflammatoires, d'anti-paludéens de synthèse, de corticothérapie, d'immunosuppresseurs. Ils soulagent mais ne guérissent pas. *Auteur : Equipe Editoriale d'Orphanet (octobre 2002)*.
Traitements du lupus systémique
Mise à jour : 04/09/2005
Accès à la base de données Orphanet

30. Alliance For Lupus Research Prevent, Treat And Cure Lupus Through
April 11, 2005. Our mission is to prevent, treat and cure lupus through medical research. 100% of all donations go to support medical research.

31. Lupus/Systemic Lupus Erythematosus (SLE)
lupus involves inflammation (the immune system s response to kill foreign Systemic lupus erythematosus involves chronic inflammation that can affect
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What Is It?
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What Is It? Systemic Lupus Erythematosus (sis-TEM-ick LOO-pus err-ah-theme-ahTOE-sus) is a chronic (long-lasting) rheumatic disease which affects joints, muscles and other parts of the body. Lupus involves inflammation (the immune system's response to kill foreign agents, virus, bacteria). Systemic lupus erythematosus involves chronic inflammation that can affect many parts of the body, including:
  • Heart Lungs Skin Joints Blood-forming organs Kidneys Nervous system
There are several types of lupus:
  • Discoid lupus affects the skin. Drug-induced lupus occurs because of a reaction to drugs. Symptoms, however, disappear once the drugs are discontinued. Crossover, or overlap, syndromes indicate features that overlap with another rheumatic disease.

32. LUPUS Foundation Of Minnesota
Dedicated to support and education of lupus patients, their friends, family and the public and support research to improve the diagnosis and treatment and find a cure for lupus.
Press Lupus Foundation of Minnesota
The Atrium Suite 135
2626 East 82nd Street
Bloomington, MN 55425 Phone Number
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Education Events About Us Home Welcome to the Lupus Foundation of Minnesota. Current Highlights! For information about the Lupus Foundation of Minnesota 8th Annual Walk for Hope Click here for a copy of the Walk brochure ... Click here for online Walk registration The Lupus Foundation of Minnesota is a non-profit charitable organization that provides education, support and service to those affected by lupus. We promote awareness and understanding of lupus to others. We support research that seeks to improve the diagnosis and treatment of lupus as well as to discover its cause and cure. Please contact us if you have any questions that are not answered on our site. What Is Lupus?

33. Patientenratgeber Lupus Erythematodes, Sjögren-Syndrom, Kollagenosen
Tagebuch von Dorothea Maxin mit Ratgeber, Links und Lexikon.
Lupus erythematodes, Sjögren-Syndrom,
Antiphospholipid-Syndrom, Kollagenosen
Patientenratgeber von Dorothea Maxin "Mein Lupus erythematodes Tagebuch" erscheint in der 2., aktualisierten und erweiterten Auflage - - - Mit Patientenverfügung, Antworten auf häufig gestellte Fragen (FAQs) und multilingualem medizinischem Sprachführer - - - Lupus, Sjögren-Syndrom und andere Kollagenosen - - - Aktuelle Liste schubauslösender Medikamente - - - Ausführliches Literaturverzeichnis - - - Leseproben im Internet Startseite Ratgeber Befundhefte Lexikon Buchbesprechungen ... Bestellung Verlag für Neue Medizin - Gervinusstr. 47 - D-64287 Darmstadt - E-Mail: info @

34. St. Thomas' Lupus Trust
Click Now and make money!!! They're here!! lupus Wristbands!! They're here!! lupus Wristbands!! St. Thomas' lupus Trust

35. Hamline University Lupus Home Page

Poduzeće za uzgoj divljači, lovni turizam, poljoprivredu i trgovinu
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Search: Lycos Tripod Dating Search Share This Page Report Abuse Edit your Site ... Next INTERNET STRANICA PODUZEÆA LUPUS JE PREMJEŠTENA NA NOVU LOKACIJU:

37. Hamline University Lupus Home Page
Disease facts, symptoms, treatment and coping strategies hosted by Hamline University.Link to the newsgroup.

38. Sito Dedicato Alle Persone Affette Da Lupus Eritematoso Sistemico (LES)
La cattedra di reumatologia dell'Universit  di Padova e la rivista Senza maschera presentano tutti gli aspetti di questa malattia, i sintomi, le manifestazioni, le cure e le Faq. Offre consulenza online con vari medici specialisti.

39. Lupus Resource Center
H Michael Belmont, MD, Rheumatologist, Specialist in the treatment and investigationof SLE lupus and the compassionate care of affected patients.

40. Pediatric Rheumatology Home Page
A resource for families and physicians caring for children with arthritis, lupus, scleroderma, Kawasaki disease and other rheumatic diseases.
id=13897 All information is provided as a public service and no warranty is expressed or implied.
KEY WORDS: arthritis scleroderma childhood arthritis dermatomyositis JRA juvenile rheumatoid arthritis Kawasaki Disease pediatric rheumatology polyarteritis nodosa SLE systemic lupus erythematosus vasculitis CLICK for Patient and Family Information Information about juvenile rheumatoid arthritis More Information about childhood arthritis Information about systemic lupus ... CLICK for Books on Childhood Arthritis Is your child getting the best care My book
not just growing pains.
A guide to childhood muscle, bone
A guide for parents and professionals
Reviewer’s comments
Dr. Tom Lehman’s experience and compassion are evident on every page of this book, and they help guide the reader—child, parent, and healthcare professional alike – through the world of childhood arthritis. This book is an absolute gem written with a single goal in mind: improve the lives of kids with arthritis. Jack Klippel , M.D. President and CEO of the Arthritis Foundation “Dr. Lehman has given parents and families of children with arthritis the first book that speaks to the parent and child as equals.

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