121. Hydrops Fetalis With Polymalformative Syndrome Medical report on two consecutive pregnancies with this diagnoses, as well as intrauterine growth retardation and Dysmorphic syndrome. http://www.hydropsfetalis.org/index.html

HYDROPS FETALIS FRANÇAIS My both pregnancies ended in non immune hydrops fetalis because of possible cardiomyopathy. The first case report describes a polymalformative syndrome. Some congenital malformations could be attributed to Seckel syndrome. The following address we refer you to will give you a good idea of this complex phenomenon called hydrops fetalis : Universal edema of the newborn Our site is intended for : physicians (gynecologists, geneticists, pathologists ) who have a real passion for uncommon and complex mechanisms before birth, who love caring for patients with humanity, who can question their knowledge and proceed like detectives paying attention to each detail ; couples whose pregnancy was affected who look for information desperately because no scientist was able to answer their questions. After your visit, you will know that you are not alone. We are most grateful to the specialists who really helped us in our search : Dr Raymonde Bouvier, Edouard Herriot Hospital in Lyon (France) Dr Géraldine Viot, Cochin Hospital Complex, Port-Royal in Paris (France)

122. CHARGE Syndrome Foundation Home Page Provides information about CHARGE syndrome, related disorders, therapies and outcome. http://www.chargesyndrome.org/

CHARGE Syndrome Foundation Inc. CHARGE Syndrome Foundation, Inc. 2004 Parkade Boulevard Columbia, MO 65202-3121 Phone: (800) 442-7604 or (573) 499-4694 Contact: Marion Norbury Marion Norbury: (Executive Director) marion@chargesyndrome.org Meg Hefner (Genetic Counselor): m e g@chargesyndrome.org For information on the 200 CHARGE Syndrome Conference in Miami please contact Susy Morales -Conference Chair): conference@chargesyndrome.org CHARGE SyndromeRelated Terms: CHARGE Syndrome - Choanal Atresia, Posterior Coloboma, Heart defect, choanal Atresia, Retardation, Genital and Ear anomalies. CHARGE Syndrome refers to children with a specific set of birth defects. "CHARGE" originally came from the first letter of some of the most common features seen in these children: C = coloboma, H = heart defects, A = atresia of the choanae, R = retardation of growth and development, G = genital and urinary abnormalities, E = ear abnormalities and/or hearing loss. The diagnosis of CHARGE is based on finding several of these and possibly other features in a child. The diagnosis should be made by a medical geneticist who has ruled out other disorders with overlapping findings. FEATURES C = Coloboma A coloboma is a cleft or failure to close of the eyeball. This can result in a keyhole shaped pupil and/or abnormalities in the retina or optic nerve. Colobomas of the retina or optic nerve may result in significant vision loss, especially visual field defects in the upper half of the visual field. Visual acuity may also be affected, resulting in nearsightedness or farsightedness. Surgery cannot correct ocular colobomas, but glasses often help with visual acuity. Children with CHARGE Syndrome are often very sensitive to light. Many are more comfortable with sunglasses, even indoors.

123. Treatment Of Polycystic Ovary Syndrome With Insulin Lowering Medications by Dr. Mark Perloe of the Atlanta Reproductive Health Center. http://www.ivf.com/pcostreat.html

Polycystic Ovary Syndrome... Treatment with Insulin Lowering Medications by Mark Perloe, M.D. INTRODUCTION: Polycystic ovary syndrome is characterized by anovulation (irregular or absent menstrual periods) and hyperandrogenism (elevated serum testosterone and androstenedione) . Patients with this syndrome may complain of abnormal bleeding, infertility, obesity, excess hair growth, hair loss and acne. In addition to the clinical and hormonal changes associated with this condition, vaginal ultrasound shows enlarged ovaries with an increased number of small (6-10mm) follicles around the periphery (Polycystic Appearing Ovaries or PAO) . While ultrasound reveals that polycystic appearing ovaries are commonly seen in up to 20% of women in the reproductive age range, P oly C ystic O vary S yndrome (PCOS) is a estimated to affect about half as many or approximately 6-10% of women. The condition appears to have a genetic component and those effected often have both male and female relatives with adult-onset diabetes, obesity, elevated blood triglycerides, high blood pressure and female relatives with infertility, hirsutism and menstrual problems. As of yet, we do not understand why one woman who demonstrates polycystic appearing ovaries on ultrasound has regular menstrual cycles and no signs of excess androgens while another develops PCOS. One of the major biochemical features of polycystic ovary syndrome is insulin resistance accompanied by compensatory

124. MARFAN'S SYNDROME Includes a survey for study and links to useful sites. http://www.ucl.ac.uk/~ucahywc/

Clinical Operational Research Unit University College London The timing of Elective Aortic Root Replacement in the Marfan's Syndrome: Computerized decision support Introduction to the project International Marfan Syndrome Survey (English) Questionario di studio sulla Sindrome di Marfan (Versione Italiana) Cuestionario (Español) Other useful links: Clinical Operational Research Unit, University College London Marfan Association UK National Marfan Foundation (USA) Canadian Marfan Association ... St. George's Hospital Medical School For further information, please contact Dr Terence Chow on ucahywc@ucl.ac.uk This Marfan Syndrome Info Ring site is owned by Dr Terence Chow Want to join the Marfan Syndrome Info Ring? Skip Prev Prev Next ... List Sites This project is funded by the British Heart Foundation Tel: ++44 0207 935 0185 Fax: ++44 0207 486 5820 E-mail: http://www.bhf.org.uk/ 14 Fitzhardinge street, London W1H 4DH, UK You are visitor number :

125. Prevent Shaken Baby Syndrome American Academy of Pediatrics provides information on preventing shaken baby syndrome. Defining how the serious injuries can occur when an infant or toddler is severely or violently shaken. http://www.aap.org/family/preshake.htm

126. Fibromyalgia Information, Treatments And Research News Resource Research and treatment news, support, free email bulletins http://www.fibromyalgiasyndromenews.com

Fibromyalgia News and Fibromyalgia Treatment Information Your Fibromyalgia resource for breaking research and treatment news. This site is updated daily with the latest Fibromyalgia news to help you learn the latest information to manage Fibromyalgia. Simply click on any of the links below to read the complete Fibromyalgia information. Fibromyalgia Recent Fibromyalgia Treatment news and Research Treating Fibromyalgia: The Muscle Pain Epidemic According to Leon Chaitow, N.D., D.O., M.R.O., "Manual therapy, nutrition, stress reduction, breathing and postural reeducation, exercise (in some cases), acupuncture, non-specific immune system modulation such as hydrotherapy, medication (herbal, homeopathic and standard), among other things, have all been useful in encouraging recovery from fibromyalgia." Research: Glucosamine Boosts NSAID for More Effective Pain Relief (Fibromyalgia News) The nutritional supplement glucosamine boosts the pain relieving power of ibuprofen, according to a new study by Temple University researchers in the Journal of Pharmacology and Experimental Therapeutics (JPET). This new drug combination could one day allow patients to take a lower dose and get the same pain relief with fewer unwanted side effects. Increased Free Radical Levels May Cause Fibromyalgia Fibromyalgia may be an oxidative disorder as indicated by the increased levels of malondialdehyde (MDA) and decreased levels of superoxide dismutase (SOD) in patients with this disease, reports a study from Turkey.

127. Rett Syndrome Resources Facts and various information containing links. http://expage.com/page/curerettnow

Rett Syndrome Race for the cure! Please see the "The Great Mississippi River Race for Rett Syndrome" at http://www.dreamkeeper.org to see the World's longest non stop canoe/kayak race for Rett Syndrome. Or check out "The Great Mississippi River Race for Rett Syndrome" at http://www.mississippichallenge.org to see how we smashed a World Record for best time down the Mississippi River - The Mississippi Challenge for Rett Syndrome and Leukodystrophy! This Time It's Personal.....

128. Le Syndrome De Turner http://www.aaa.dk/TURNER/French/tur_syn.htm

Le Syndrome de Turner Les groupes d'Amitié-Turner Une information par Johannes Nielsen et des membres des groupes d'Amitié-Turner Traduit par Bernard Noel Publié par I'Association nationale des groupes d'Amitié-Turner du Danemark © 1987 par les auteurs et l'Association nationale des Groupes d'Amitié-Turner du Danemark Le Centre Turner Skovagervej 2 DK-8240 Risskov Danemark Tél. 45 77 89 36 84 ISBN 87 982104 Traduction en français du texte anglais: Bernard Noel Layout: Harald Nymark Composition: Jens Erik Thygesen La publication de l'édition française a été possible grâce aux donations de KabiVitrum, Suède. Sommaire Préface Origine de la dénomination, syndrome de Turner Fréquence du syndrome de Turner Quelle en est la cause? ... À continuer

129. PAS: An Age-Old Custody Problem Paper by Michael R. Walsh and J. Michael Bone in the Florida Bar Journal. http://www.deltabravo.net/custody/pas-walsh.htm

Ad-Free Signup Ad-Free Login PAS: An Age-Old Custody Problem You can double-click any word on this page to do a search on that word. THE FLORIDA BAR JOURNAL, JUNE 1997 Parental Alienation Syndrome: An Age-Old Custody Problem by Michael R. Walsh and J. Michael Bone The term parental alienation syndrome (PAS), first described by Richard Gardner, is also sometimes referred to as "brainwashing."( ) Its concept and dynamics include a complex network of involvement and motives on the part of all members acting in this family drama. Furthermore, each of them usually takes his or her role in the alienation process well before the dissolution or separation process begins. Additionally, one should be mindful that in some instances a child does not reject a parent immediately following a parental separation but rather based upon actual or true life experiences. Thus, this syndrome affects intact, as well as divided, families. PAS, in its most extreme form, refers to a disturbance in which a child is preoccupied with viewing one parent as all "good" and the other as all "bad." The former is loved and idealized, while the other is hated and verbally vilified. The PAS hostility expressed by the child is generally characterized without any outward expression of guilt, embarrassment, or ambivalence. Accordingly, this conduct may be especially puzzling, even to a trained observer, if there is no apparent factual basis to justify the depth of the emotions involved.

130. Syndrome Frontal http://pro.wanadoo.fr/jerome.grondin/syndfron.htm

Frontal Troubles du comportement moteur test de Stroop Troubles des conduites verbales Troubles des conduites visuelles Troubles cognitifs anticipations choix de solution Ce sont les fonctions qui permettent finalement l'autonomie cognitive et sociale. SOMMAIRE NOUS ECRIRE

131. A Guide For The Patient (aka "the Dr. Fox Paper") From Scripps Clinic and Research Foundation http://www.dry.org/ss95gui.html

A Guide for the Patient (aka "the Dr. Fox Paper") Click here for the "Dr. Fox Paper, 2002 edition" Click here for the "Dr. Fox Paper, 1995 edition" Or click here for: Sjogren's Syndrome: New approaches to treatment by Dr. Robert I Fox (Continuing education for medical professionals) Dry.Org Home Contact Dry.Org

132. TROUBLES FACTICES / SYNDROME DE MUNCHAUSEN AVEC MANIFESTATIONS PSYCHIATRIQUES http://perso.club-internet.fr/andreisz/index_fr.html

english version Troubles factices (syndrome de Munchausen) avec signes et symptômes psychologiques Les troubles factices représentent la production ou feinte intentionnelle de signes ou symptômes somatiques ou psychologiques en absence de motivations externes significatives. Table des matières Introduction : Les troubles factices peuvent prendre l'apparence de n'importe quelle maladie somatique ou psychiatrique soulevant ainsi la question du diagnostic différentiel. Malgré l'importance évidente de ce diagnostic différentiel pour le psychiatre, en clinique comme dans la recherche, les données concernant le syndrome de Munchausen à manifestations psychiatriques sont très limitées. Cette situation ne peut être améliorée que par des études portant sur un nombre important de cas cliniques détaillés et contenant des informations homogènes. Etant donné la difficulté de recueillir un nombre suffisant de cas par un seul clinicien (ou équipe de cliniciens), je propose ici la création d'une base de données concernant le syndrome de Munchausen avec signes et symptômes psychologiques. retour au début de la page Introduction Contenu du site Menu de navigation Ecrivez-moi!

133. NOMID Home Page Resource for parents and patients suffering from Neonatal Onset Multiinflammatory Disease Chronic, or Infantile, Neurologic, Cutaneous and Articular syndrome. Site maintained by patients, parents and friends for their counterparts worldwide. Email support group at eGroups. http://pweb.netcom.com/~jkbarton/nomid/Html/nomid_home_page.htm

Welcome to the NOMID / CINCA web site! By patients, families and friends, For patients, families and friends What's new? Click here for summary of website updates. Most recent update: 23 May 2004 Contents: Egroups discussion board List of contacts Photo gallery Personal stories ... What's New on the website? ..... Happy Birthday Miranda Putvin ..... 9 years old on 10 May ! ..... and, new contact, Isabela Condé .... also 9 on 6 May ! ..... Number of hits since 6 Aug 2000 s="na";c="na";j="na";f=""+escape(document.referrer) Return to NOMID / CINCA home page Children's Chronic Arthritis Association (CCAA) Online, point-and-click, illustrated medical dictionary Paedriatric Rheumatolgy European Society (PRES) ... NIH Children's Inn Page owner: John Barton, jkbarton@ix.netcom.com This page last updated: 24 May 2004

134. Welcome To AboutBFS.com An Online Community For Those Suffering From BFS (Benign Information on Benign Fasciculation syndrome. http://www.aboutbfs.com

An online community for those suffering from Benign Fasciculation Syndrome Frequently Asked Questions Articles Message Forums Web Links Welcome to AboutBFS.com AboutBFS.com is an Online Community for people suffering from BFS - Benign Fasciculation Syndrome, and those who wish to know more about the illness. It is my desire to be a place to find support, get information, have your questions answered, and raise awareness about this illness. I am always striving to make this site better, so please visit the forums and give me any suggestions or comments you may have about the site. I certainly welcome your input. Please help me to make this the best place to find information about Benign Fasciculation Syndrome on the Web! Have you been recently diagnosed with BFS or are expriencing it's symptoms? Make sure you check out the Frequently Asked Questions section for answers about BFS. Also, the Featured Articles Section has more in depth information. If you have a question that hasn't been answered in the FAQ section, you can post it in the Forums and someone is sure to help.

135. Home Support group for people with PostPolio syndrome in the Phoenix, AZ area. There is information on the local chapters and their activities and speakers as well as updated articles and events to come. http://polioecho.org

PolioEcho, Inc of Arizona Serving AZ Polio Survivors since 1985 We are Polio Survivors with needs just like other Polio Survivors. Polio Echo, Inc.- a tax exempt, non profit organization certified under United Way and supported by Easter Seal Society of Arizona and Arizona Chapter of March of Dimes - strives to service these needs by offering information, services, equipment and "support" by professionals and most importantly, by those who are walking in your shoes! Chapters meet monthly, General Membership meetings are held bi-annually.. To subscribe to the Polio Echo Newsletter E-mail the Treasurer Ed Crawford at: janwec94@earthlink.net Read on to learn about us and how we can assist YOU! We have a lot of fun along with doing a lot of good. What We Have to Offer Besides having meetings featuring guest speakers who keep us informed, we have a bi-monthly newsletter called " Polio Echo News " , an Assistive Equipment Loan program, a library full of informative books and videos, a message line to call for questions you may have, informational packets on Post-Polio, and get-togethers such as parties and field trips. The information on this site is not to be considered as medical advice. It is posted merely as informational and the user should always consult their physician prior to trying any suggestions gleaned from this site and/or any of its web links.

136. THE MERCK MANUAL, Sec. 17, Ch. 224, Glomerular Diseases A description of nephritic syndrome with a look at its acute stage, the etiology, signs, symptoms, diagnosis, prognoses and treatment. Also includes crescentic glomerulonephritis and chronic nephritic syndrome. http://www.merck.com/pubs/mmanual/section17/chapter224/224b.htm

This Publication Is Searchable The Merck Manual of Diagnosis and Therapy Section 17. Genitourinary Disorders Chapter 224. Glomerular Diseases Topics [General] Nephritic Syndrome Nephrotic Syndrome Nephritic Syndrome The classic nephritic syndrome includes hematuria, hypertension, renal insufficiency, and edema. Frequently, individual components of the syndrome are absent. Nephritic syndrome may be acute and transient (eg, postinfectious GN), fulminant with rapid renal failure (eg, rapidly progressive glomerulonephritis [RPGN]), or indolent (eg, IgA nephropathy). Pathologic changes, and therefore clinical manifestations, often vary over time. ACUTE NEPHRITIC SYNDROME (Acute Glomerulonephritis; Postinfectious Glomerulonephritis) A syndrome characterized pathologically by diffuse inflammatory changes in the glomeruli and clinically by abrupt-onset hematuria with RBC casts, mild proteinuria, and, often, hypertension, edema, and azotemia. Etiology The prototype of an acute nephritic syndrome is poststreptococcal glomerulonephritis (PSGN) due to infection with certain nephritogenic strains of group A Pathology and Pathogenesis Lesions are confined mainly to the glomeruli, which become enlarged and hypercellular, initially with neutrophils or eosinophils and later with mononuclear cells. Epithelial cell hyperplasia is a common early, transient feature. Microthrombosis may occur; if damage is severe, hemodynamic changes produce oliguria, frequently accompanied by epithelial crescents (formed within Bowman's space from epithelial cell hyperplasia, probably mediated by growth factors from stimulated macrophages). Endothelial and mesangial cells increase in number, and the mesangial regions often are greatly expanded by edema and contain neutrophils, dead cells, cellular debris, and subepithelial deposits of electron-dense material.

137. Bmj.com Yunus And Aldag 312 (7042): 1339 British Medical Journal article, 1996 a controlled study. http://www.bmj.com/cgi/content/full/312/7042/1339

Home Help Search/Archive Feedback ... Respond to this article Read responses to this article PubMed citation Related articles in PubMed Download to Citation Manager This article has been cited by other articles Search Medline for articles by: Yunus, M. B Aldag, J. C Alert me when: New articles cite this article BMJ Papers Restless legs syndrome and leg cramps in fibromyalgia syndrome: a controlled study Muhammad B Yunus professor of medicine, section of rheumatology a Jean C Aldag associate professor of preventive medicine in medicine a a Department of Medicine, University of Illinois College of Medicine at Peoria, Box 1649, Peoria, IL 61656, USA Correspondence to: Professor Yunus. Restless legs syndrome is characterised by an unpleasant, difficult-to-describe sensation in the legs that produces an invariable urge to move them frequently. This symptom typically occurs at rest or before sleep and is alleviated by activity. Restless legs syndrome may occur without or with an associated condition, such as rheumatoid arthritis. We investigated the prevalence of restless legs syndrome and of leg cramps in patients with fibromyalgia syndrome, a common condition with widespread musculoskeletal

138. PETIT LEXIQUE DE TERMES MEDICAUX syndrome de sevrage. http://www.biam2.org/dico.html

et en italique Termes Signification foie , poumons, cerveau, etc.) furoncles abdomen ventre aberrant abrasion abricot fruit aux vertus fortifiantes abstinence 1) abstinence (pop) - 2) continence acathisie entraîne malaise, paralysie, coma accomodation utilise le cristallin pomme chez l'adulte substance chimique renfermant une fonction acide et une fonction amine ( idem aminoacide acide gras acide urique goutte calculs urinaires sentiment de brûlure et d' irritation accumulation dan le sang de substances acides complication du acidose acidose lactique accumulation d' acide lactique provoquant notamment des crampes musculaires, des troubles digestifs ou de la fatigue complication , des boissons alcooliques, un jeûne sensation auditive anormale acrosyanose bleuissement des mains et des pieds finesse de perception de l'oeil/de l'oreille additif infection inflammation des ganglions lymphatiques augmentation du volume de la prostate, tumeur qui parasite une glande adjuvant hormone ), dont l'action physiologique son effet dilatation des coronaires dilatation sympathique sympathique qui supprime les effets de adsorption micro-organisme agalactie absence de lait agalaxie absence de lait absence / insuffisance de gammaglobulines plasmatiques agitation (motrice + mentale) trouble du comportement alliant excitation mentale et motrice agoniste agranulocytose diminution importante ou disparition de certains globules blancs ail plante stimulant de certains microbes, a un

139. Follow The White Rabbit... The author David Rodgerson, offers information about a condition called XLP, XLinked Lymphoproliferative Disease. http://torch.cs.dal.ca/~rodgerso/xlp/

David Rodgerson 's xlp home has moved here

140. Antiphospholipid Syndrome A case study as well as indepth look at this disease discussing treatment, diagnosis, ocular and systemic manifestations. Written by Erik Letko, M.D. http://www.uveitis.org/Enhanced/MD_info/antiphospholipid_syndrome.htm

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