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         Lupus:     more books (103)
  1. The Lupus Book: A Guide for Patients and Their Families by Daniel J Wallace, 2008-12-02
  2. The Lupus Recovery Diet: A Natural Approach to Autoimmune Disease That Really Works by Jill Harrington, 2007-05-01
  3. Despite Lupus: How to Live Well with a Chronic Illness by Sara Gorman, 2009-06-15
  4. ABC of Asthma, Allergies and Lupus: Eradicate Asthma - Now! by F. Batmanghelidj, 2000-08
  5. The First Year--Lupus: An Essential Guide for the Newly Diagnosed by Nancy C. Hanger, 2003-10-02
  6. Lupus Handbook for Women: Up-to-Date Information on Understanding and Managing the Disease Which Affects by Robin Dibner, 1994-10-01
  7. New Hope for People with Lupus: Your Friendly, Authoritive Guide to the Latest in Traditional and Complementary Solutions by Theresa Foy Digeronimo, 2002-04
  8. Living with Lupus: The Complete Guide, Second Edition by Sheldon Paul Blau, Dodi Schultz, 2004-09-08
  9. Lupus: Alternative Therapies That Work by Sharon Moore, 2000-09
  10. Coping With Lupus: A Practical Guide to Alleviating the Challenges of Systemic Lupus Erythematosus by Robert H. Phillips, 2001-06-04
  11. Healing Lupus: Steps in a Personal Journey by Waverly Evans, 2008-05-27
  12. Lupus: The Essential Clinician's Guide (Oxford American Rheumatology Library)
  13. Lupus Q + A (Revised Edition) by Robert G. Lahita, 2004-06-03
  14. Dubois' Lupus Erythematosus

1. Lupus Foundation Of America, Inc.
Resources, advocacy center, directory of local chapters, and calendar of upcoming events.Category Health Conditions and Diseases lupus Organizations...... Donate by Mail or Fax Check, Debit, or Credit Card Memorialor Honorary Gifts Donate in memory or honor of a person with lupus.
Enter a search term: Choose a Section - Education - Support - LFA Research - What's New - LFA in Action - News -Research -Awareness Lupus Disease - Cutaneous (skin) - Drug-Induced - Neonatal - Overlap - Systemic About LFA Get Involved Donate Now! Mailing List ... Home document.write(""+doClock("M1","%20","D1",",%20","Y0")+"");

Lupus Facts and Overview

Information and Publications

Links and Resources
Lupus News
Lupus Foundation of
America, Inc.
1300 Piccard Drive, Suite 200
Rockville, MD 20850-4303
Phone 301-670-9292 Fax 301-670-9486 Contact Us Words of Caution Donate Now! Donate Online Visa, MasterCard, AMEX and Discover. Donate by Mail or Fax Check, Debit, or Credit Card

2. Hamline University Lupus Home Page

3. Hamline University Lupus Home Page
Disease facts, symptoms, treatment and coping strategies hosted by Hamline University. Link to the Category Health Conditions and Diseases Connective Tissue lupus......

4. Lupus Canada-Welcome/Bienvenue
Translate this page lupus Canada. Working together. To conquer lupus.Travailler ensemble. Pour vaincre le lupus.
Lupus Canada
Working together. To conquer Lupus. Travailler ensemble. Pour vaincre le lupus. English

5. Lupus (SLE) Resource
Features information on lupus (SLE), which includes symptoms, diagnosis, tests and treatment. Also has message boards and newsletter. lupus (SLE) is an autoimmune disease that can affect virtually any system in the body.
You are using a non-frames capable browser, Click here for clinical overview and index.

6. LUPUS - Welcome To The Official Lupus Website Of St.Thomas' Lupus Trust
A patient information and support website for those with lupus/lupus variant autoimmune connective tissue diseases, including Hughes' (antiphospholipid) Syndrome lupus Patients Understanding Support has been rated among the top three for the award of Best Consumer Medical Site
LUPUS - Welcome to the official Lupus website of St Thomas' Lupus Trust
St Thomas' Lupus Trust
The Rayne Institute
St Thomas' Hospital
London SE1 7EH
ph: 020 7922 8197 The St Thomas' Lupus Trust is the charity that funds lupus research at St Thomas' Hospital. Results from the Lupus Research Unit have made a major contribution to the increased survival rate of patients with this complex disease.
We aim to continue this vital and pioneering work until one day a cure is found.
"Who Wants To Be A Millionaire" in aid of St Thomas' Lupus Trust due to be aired April/May 03 Trek Peru 2003 Dr Graham Hughes, Head of the St Thomas' Lupus Unit, St Thomas' Hospital oversees this website

7. Miller, CyndeeThinking About Creating A Personal Homepage? For Design Ideas See
National Library of Medicine provides links to fact sheets and articles on the symptoms, diagnosis, treatment, and management of the disease. Frequently Asked Questions About lupus (lupus Foundation of America). lupus (Patient Education Institute) - requires
Welcome to Cyndee Miller's Lupus Home Page
Dedicated to Lupus Awareness
COMBINED! Source: Lupus Foundation of America, Inc., Lupus Fact Sheet Lupus is a chronic, autoimmune disease which causes inflammation of various parts of the body, especially the skin, joints, blood, and kidneys. The immune system normally protects the body against viruses, bacteria and other foreign materials. In an autoimmune disease like lupus, the immune system loses its ability to tell the difference between foreign substances and its own cells and tissues. The immune system then makes antibodies directed against "self." Lupus is NOT infectious, rare or cancerous. The Lupus Foundation of America market research data show that between 1.4 million and 2 million people have been diagnosed with lupus. (Study conducted by Bruskin/Goldring Research, 1994.) Although the cause of lupus is unknown, scientists suspect that individuals are genetically predisposed to lupus, and know that environmental factors such as infections, antibiotics, ultraviolet light, extreme stress and certain drugs play a critical role in triggering lupus.

8. SENZA MASCHERA - Sito Dedicato Alle Persone Affette Da 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.
Questo sito e la rivista "Senza Maschera" hanno lo scopo di fornire alle persone affette da Lupus eritematoso sistemico
  • Leggimi : come contribuire allo sviluppo di questa iniziativa LES Associazioni : indirizzi delle sedi delle Associazioni di Malati Reumatici Congressi : programmi dei congressi sul LES organizzati in Italia Links : raccolta di links sul LES Rivista : modalità per abbonarsi alla rivista "Senza Maschera" Forum : spazio riservato alle discussioni L'Esperto Risponde : linea diretta con un pool di medici. E' possibile leggere centinai di domande con le rispettive risposte e porre dei quesiti.

9. Dorough Lupus Foundation - Main
Official site for this nonprofit organization started by Howie Dorough and his family. Aims to aid in research, education of the public, and providing financial assistance to individuals who cannot afford treatment for the disease.
Mission Statement:
The Foundation's goals are to aid in research, education of the public and to provide financial assistance to organizations helping individuals living with Lupus who cannot afford treatment.
The Dorough Lupus Foundation is not affiliated with the Lupus Foundation of America.
Howie D. signing autographs at Chatham-Kent Health Alliance General Hospital. The hospital was presented with a $19,000 (USD) gift from the foundation to the Palliative Care Suite. Join the official DLF mailing list
for future updates! Name: Age: Country: Email Address: Powered by Site best viewed with Internet Explorer. Angelia Herring, Executive Director of the DLF and Howie D., presenting a check for $165,000 to the Arthritis Foundation. (Picture courtesy of the Arthritis Foundation).

10. 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.
The Lupus Foundation of Minnesota provides educational materials; offers a source of hope, strength, empowerment and comfort; and supports research focused on finding the cause of
and cure for lupus.
Research Partially Funded by LFM makes the news! Genetic "Signature" Linked to Severre Lupus Symptoms
We want to provide you with informative and up-to-date educational resources that will help you better understand this disease, and we believe that our programs and support services will be a source of hope, encouragement, strength, empowerment and comfort. Enjoy your stay! Please contact us if there are any other ways in which we can help. To contact the Foundation Staff and Board of Directors Have You Noticed Any Trucks in Your Neighborhood With the Lupus Logo? For More Information About Donating Clothing or Other Household Items, Click on the Truck!! Home Lupus Basics Educational Resources Support Services ... About Us INTERNATIONAL MARKET SQUARE

11. Lupus Site(SLE)- Information On Lupus
Diagnostic information, tests, medications, advice, support, forum, and survey.Category Health Conditions and Diseases Connective Tissue lupus......lupus (SLE), diagnosis, symptoms of lupus, tests, lupus FAQ, tips, forum,chat room more. The lupus Site, Visit our sponsors Entertainment
Home Support this site Site Updates Lupus information ...
(UK customers)
Please help to support this site by visiting our Store Message Board Lupus store Chat Room ... Search The Lupus Site Visit our sponsors:
Entertainment Book

Save up to 50% with the Entertainment Book!
Taking Charge of Lupus

UK customers
Subscribe to Site Updates Bookmark this site Click here to make this site your home page Recommend this site to your friends Visit the message boards , for support and information. If you don't know much about lupus, a good place to start is the Lupus FAQ , which answers many of the most common questions on lupus. The factsheets section contains 18 Lupus UK factsheets. Information on blood tests and medical procedures used can be found in the Diagnosis/Tests section , along with info on how lupus is diagnosed. Butterfly News - free newsletter containing news and articles on lupus - join here now to receive it!

12. Kollagenose-Ratgeber
Tagebuch von Dorothea Maxin mit Ratgeber, Links und Lexikon.
von Dorothea Maxin Startseite Ratgeber Befundhefte Lexikon Buchbesprechungen ... Kollagenose-Archiv
Verlag für Neue Medizin - Gervinusstr. 47 - D-64287 Darmstadt E-Mail:

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

14. Groupe Taurus Invest
Soci©t© d'©tude et de production ©lectrique, ©lectronique et ©lectrotechnique pour l'industrie a©ronautique, les t©l©communications et les appareils m©dicaux.
Câblages, Bobinages, Intégrations... Appareils médicaux

15. Lupus (SLE) Resource
By H Michael Belmont, MD, Rheumatologist, Specialist in the treatment, research, and the care of affected patients.
You are using a non-frames capable browser, Click here for clinical overview and index.

16. Tuotromedico: Lupus Eritematoso
Descripci³n, s­ntomas, diagn³stico y tratamiento de esta enfermedad.
Otros Temas de Dermatología Acné Candidiasis Cómo Tomar el Sol Condiloma Acuminado Dermoabrasion. Lifting Facial Escabiosis. Sarna Exantemas Infantiles Exantemas por el Sol Fiebre Aftosa Fotosensibilidad a Medicamentos Fotosensibilidad a Plantas Hiperhidrosis. Sudoración Hongos en la Piel Ladillas Lifting Facial Lupus Eritematoso Diseminado Melanoma Molusco Contagioso Pie de Atleta Psoriasis Queloide Reacciones por el Sol Sudoración. Hiperhidrosis Pregunte al doctor Consulte al Especialista LUPUS ERITEMATOSO SISTÉMICO DEFINICION CAUSAS DIAGNOSTICO ... DEFINICIÓN El Lupus Eritematoso Sistémico, también llamado por sus iniciales LES, o simplemente Lupus CAUSAS El LES es una alteración del sistema inmunitario, que es el sistema que, normalmente, protege al organismo frente a infecciones y cánceres. En el LES, dicho sistema inmunitario es hiperactivo, y se producen importantes cantidades de anticuerpos anormales que reaccionan con los tejidos del propio paciente. La causa exacta del Lupus es desconocida, pero juegan un papel importante la herencia, factores del entorno y ciertos cambios hormonales.
Así, la prevalencia del LES varía en los distintos grupos de población, oscilando entre 300 y 400 pacientes por cada 100.000 habitantes. Es más frecuente en ciertos grupos étnicos, especialmente los negros, y más del 90% de los pacientes son mujeres.

17. Homepage Der Deutschen Lupus Erythematodes

18. [L U P U S][2 . 0]
Introductory and exploratory information and articles along with links to other sites, mailing lists and chats. Creative writing competitions.

19. Lupus Canada-Welcome
A source of information about lupus Canada, its member organizations and the diseaselupus of interest to people with lupus, their family and friends, and
Welcome to the
Lupus Canada web site!
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, and health care professionals. 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
Lupus Canada is federally registered (# 11902 5872 RR0001) as a nonprofit charity in Canada. Lupus Canada does not offer medical service or advice. The material found on this web site or accessed through this web site is intended for educational and informational purposes only. Working together. To conquer Lupus.
Lupus Canada
18 Crown Steel DR Suite 209
Markham ON L3R 9X8
Toll Free (in Canada): 1-800-661-1468
Phone: 905-513-0004
Fax: 905-513-9516

20. Notre Association
Informations sur le lupus ©ryth©mateux, ses manifestations et les traitements.
Notre association
Notre association Nos adresses Actualités Le lupus : généralités ... Nous contacter Malades, parents ou amis de malades atteints d'une maladie lupique dont le LUPUS ERYTHEMATEUX DISSEMINE ou SYSTEMIQUE constitue une des formes sévères, nous avons traversé l'épreuve souvent longue et angoissante de l'annonce du diagnostic. La maladie enfin nommée, nous avons cherché à nous informer sur cette maladie assez rare, orpheline, dont l'origine est encore incertaine. Et nous avons mesuré que la simple recherche d'informations était une démarche difficile, jalonnée d'innombrables questions : Où trouver des informations fiables et cependant accessibles au plus grand nombre ? Comment éviter le double danger de dramatiser ou de minimiser une maladie aussi complexe, multiforme et imprévisible ? Comment faire face à la solitude, aux handicaps réels bien que parfois invisibles que la maladie peut générer ? Comment faire comprendre aux malades la nécessité de forger leur propre vigilance ? Comment les mettre en garde contre les charlatans et leurs thérapeutiques dangereuses voire délirantes ? Comment convaincre des médecins qui ne seraient pas encore persuadés que les malades, leurs proches et eux-mêmes ont tout à gagner en organisant une information bien construite, une écoute attentive et une prise en charge bien coordonnée ?

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