Geometry.Net - the online learning center
Home  - Health_Conditions - Ehlers-danlos Syndrome Bookstore
Page 1     1-20 of 103    1  | 2  | 3  | 4  | 5  | 6  | Next 20
A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

         Ehlers-danlos Syndrome:     more books (33)
  1. Issues and Management of Joint Hypermobility: A Guide for the Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome by Brad T. Tinkle, 2008-09-30
  2. Joint Hypermobility Handbook-A Guide for the Issues & Management of Ehlers-Danlos Syndrome Hypermobility Typeand the Hypermobility Syndrome by Brad T Tinkle, 2010-07-12
  3. The Official Patient's Sourcebook on Ehlers-Danlos Syndrome: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-08
  4. Ehlers-Danlos Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-28
  5. Ehlers-Danlos syndrome, classical type: case management.(Disease Management): An article from: Dermatology Nursing by Sara E. Whitelaw, 2004-10-01
  6. 2009 Conquering Ehlers-Danlos Syndrome (Cutis Elastica) - The Empowered Patient's Complete Reference - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-04-10
  7. Ehlers-Danlos syndrome
  8. 21st Century Ultimate Medical Guide to Ehlers-Danlos Syndrome (Cutis Elastica) - Authoritative, Practical Clinical Information for Physicians and Patients, Treatment Options (Two CD-ROM Set) by PM Medical Health News, 2009-04-10
  9. Ehlers-Danlos Syndrome (Cutis Elastica) Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-04-10
  10. Name that syndrome: JHS or EDS-HM?(LETTERS)(joint hypermobility syndrome)(Ehlers-Danlos syndrome-hypermobility type)(Letter to the editor): An article from: Internal Medicine News by Gale Reference Team, 2006-08-01
  11. Contortion: Ehlers-Danlos Syndrome, Hypermobility, Whiplash, Joint Dislocation, Frontbend
  12. 21st Century Complete Medical Guide to Ehlers-Danlos Syndrome (EDS), Hypermobility, Authoritative Federal Government Clinical Data and Practical Information for Patients and Physicians by PM Medical Health News, 2004-04
  13. Ehlers-Danlos syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Judith Sims, Java, M.S. Solis, 2006
  14. Ehlers-Danlos Syndrome - A Medical Dictionary, Bibliographynd Annotated Research Guide to Internet References, 2004 publication by various, 2004-01-01

1. Ehlers-danlos
Represents people who suffer from a group of rare, inherited disorders which mainly affect the skin and joints. With an overview of the disorder and selfhelp details.
Ehlers-Danlos Support Group
Support for the New Millenium
EDS Search Page
Welcome to the Ehlers-Danlos Syndrome UK Support Group
You are Visitor No.
Ehlers-Danlos Syndrome (EDS) is the name given to a group of heritable connective tissue disorders. EDS can affect the skin, ligaments, and internal organs.
Review of the 2002 Conference
Information Sheets ...
View our message board
Web address:
Designed with
Contact Information
UK 01252 690 940 (please leave a message if asked - we will try to get back to you as soon as we can!)
World +44 1252 690 940
(UK Office Hours ONLY please!
Postal address:
The Director Ehlers-Danlos Support Group.
P. O. Box 335 FARNHAM Surrey. GU10 1XJ England Electronic mail
General Information:
Message Board View our message board MEDICAL ADVISORY PANEL
Dr. F. M. Pope, Honorary Professor and Consultant in Medical Genetics, MD. FRCP. Mr. A. P. Barabas, MD. FRCS.
Mr A. I. Attwood MBBS FRCS (Ed), D. Merrild. MD. MPH. Mr N. Burrows, MD MRCP

2. EDNF - Home Page Of The Ehlers-Danlos National Foundation EDNF
Provides support and information to those affected by ehlers-danlos syndrome and their families.Category Health Conditions and Diseases ehlers-danlos syndrome...... Providing emotional support and the latest information to those affectedby ehlersdanlos syndrome and their families since 1985. March 14, 2003.
~ Together we will find a brighter day ~. Ehlers-Danlos National Foundation
You are Visitor
since June 26th 2002 Navigation Member Login
Join the EDNF

Make a Donation On-line

Admin Login

Ehlers-Danlos National Foundation Providing emotional support and the latest information to those affected by Ehlers-Danlos syndrome and their families since 1985 March 28, 2003 NEWS UPDATE What is EDS? What is the EDNF? Welcome to the website. It has been designed to deliver the information you need as quickly and efficiently as possible. In line with the majority of requests for information, the site is broken into 4 main areas. If this is your first visit to the Ehlers-Danlos National Foundation Website, please take a minute to read the following The site is continually expanding and improving, if you have any comments, suggestions or ideas that you think would help, please let us know by e-mail at

3. Ehlers-Danlos Syndrome
a CHORUS notecard document about ehlersdanlos syndrome ehlers-danlos syndrome. autosomal dominant. connective-tissue disorder
CHORUS Collaborative Hypertext of Radiology Musculoskeletal system

Ehlers-Danlos syndrome
  • autosomal dominant
  • connective-tissue disorder:
  • vascular lesions:
    • aortic dissection
    • aneurysms
    • rarely: tortuous arch, ectatic pulmonary aa.
    • tissue fragility ==> hematomas, aortic rupture after angio
  • clinical types:
    • gravis, mitis, benign hypermobile, ecchymotic, X-linked
  • a/w ** medullary sponge kidney
Charles E. Kahn, Jr., MD - 2 February 1995
Last updated 14 March 2001

Medical College of Wisconsin

4. Ehlers-Danlos Syndrome - About Ehlers-Danlos Syndrome
A brief description of EDS and how it is inherited. Edited by Frederick Matsen III MD Chairman, Departmen Category Health Conditions and Diseases ehlers-danlos syndrome...... ehlersdanlos syndrome. Edited by Frederick A. Matsen, III, MD and Gregory C. Gardner,MD Last updated August 31, 2001 About ehlers-danlos syndrome. What is it?
Home About Us Clinics Physicians ... Contact Us
Table of contents About Ehlers-Danlos syndrome Causes ... View article with questions
External links
  • Ehlers-Danlos National Foundation March of Dimes
  • [Top]
    Ehlers-Danlos Syndrome
    Edited by Frederick A. Matsen, III, M.D. and Gregory C. Gardner, M.D.
    Last updated August 31, 2001
    About Ehlers-Danlos syndrome
    What is it?
    Ehlers-Danlos syndrome (EDS) is a group of hereditary disorders that affects mainly the skin and joints, but other organs as well. EDS results in weakness and/or excessive flexibility of the connective tissues of the body. People with EDS are born without the ability to make certain components of the normal connective tissue of the body.
    Incidence and risk factors
    EDS is a relatively rare disorder, occurring in fewer than 1 in 20,000 people. The various forms of EDS are characterized by abnormalities in the chemical structure of the body's connective tissues (for example, skin, muscles, tendons and ligaments). As a result, skin may become fragile and joints unstable.
    This article is rated out of 5 stars (1477 ratings).

    5. The Ehlers Danlos Foundation Of New Zealand
    Support for sufferers of the ehlersdanlos syndrome and related Hypermobility Syndrome and provides some information for the medical profession and general public.
    [ Home ] Contents Search Ehlers-Danlos Foundation of New Zealand
    The Ehlers Danlos Foundation of New Zealand began as a support group in May 1995 when it was believed there were only twelve families in the country with the condition. Of course this proved a remarkable underestimation of the number of people within New Zealand who actually have EDS. Also catering for people with Hypermobility Syndrome the group achieved charitable status in early 2000. The aim of the organization is to provide emotional support for sufferers of the Ehlers-Danlos Syndrome and HMS, their spouses and family members. Also to create awareness of these conditions by the distribution of information amongst the medical profession and general public. Therefore a newsletter "Loosely Speaking" is published three times a year. It contains both medical information on EDS and personal stories written by the members of the EDFNZ. Individuals with Ehlers-Danlos Syndrome can be affected differently with a variation in the severity and range of symptoms. Because they so often look "normal" it is often difficult to have the condition taken seriously by the medical profession and even within their circle of family and friends. Therefore it can also be an isolating condition and the general lack of awareness and understanding can lead to feelings of frustration, stress and depression. If you're interested in either making a donation or in joining the EDFNZ as a member or Friend of the Foundation please feel free to e-mail or write to the address below. For $10.00 NZ you will receive a copy of Loosely Speaking, the Foundation's newsletter, three times a year.

    6. Ehlers Danlos, Syndrome : Sites Et Documents Francophones
    Le mot clé Ehlers Danlos, syndrome ehlersdanlos syndrome est présent au sein de plusieurs arborescences du
    Ehlers Danlos, Syndrome Menu général CISMeF Voir aussi réticuline
    Arborescence(s) Ehlers Danlos, syndrome Ehlers-Danlos syndrome
    appareil cardiovasculaire, maladies
    hémopathies et maladies lymphatiques maladies et malformations congénitales, héréditaires et néonatales maladies peau et tissu conjonctif Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources :
    patient 20 janvier 2003
    Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

    7. NORD - Ehlers-Danlos Syndrome
    EDS disease information from the National Organization for Rare Disorders.

    8. What Is EDS?
    EhlersDanlos National Foundation. What is ehlers-danlos syndrome?
    ~ Together we will find a brighter day ~. Ehlers-Danlos National Foundation Navigation Member Login
    Join the EDNF

    Make a Donation On-line

    Admin Login

    Ehlers-Danlos National Foundation What is Ehlers-Danlos Syndrome? Symptoms Types Nosology Prevalence ... Prognosis Individuals with EDS have a defect in their connective tissue, the tissue which provides support to many body parts such as the skin, muscles and ligaments. The fragile skin and unstable joints found in EDS are the result of faulty collagen. Collagen is a protein which acts as a "glue" in the body, adding strength and elasticity to connective tissue.
    Ehlers–Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders, characterized by articular(joint) hypermobility, skin extensibility and tissue fragility.There are six major types of EDS. The different types of EDS are classified according to their manifestations of signs and symptoms.Each type of EDS is a distinct disorder that "runs true"in a family. This means that an individual with Vascular Type EDS will not have a child with Classical Type ED

    9. Booklets2000
    Please help us by taking these surveys and explain your experiences with Connective Tissue Disorders like ehlersdanlos syndrome, Marfan's Syndrome, Stickler Involved Syndrome, and Fibromyalgia.
    WHO HAS IT? Connective Tissue Disorders do not appear to favor one set of genes over another. People from every age, gender, race, religion, and hemisphere are candidates. DOES IT EFFECT YOUR LIFE? Can people with C.T.D. still contribute? You bet they can!
    with Connective Tissue Disorder. LIFE DOES GO ON . . . Focusing on the pace – not on the hurdles – makes life more worthwhile. There are ways to improve your condition:
    "Quality of Life" can always be improved!
    Medical breakthroughs,
    personal support systems,
    new medications and treatments,
    – appear on the scene every day. Review advice from others who share your
    symptoms. Share your thoughts
    and experiences. Find a good doctor in your area. Take Survey

    10. EDS_Booklet
    ehlersdanlos syndrome Edited by Professor HA Bird. Mr P. Cuckow, Mr. M. HawthorneThis is a 30 page, A5, Illustrated Booklet on ehlers-danlos syndrome (EDS).
    Ehlers-Danlos Support Group
    Support for the New Millenium
    EDS Search Page
    Edited by: Professor H.A. Bird
    Authors: - Professor P. Beighton, Prof. A. C. Bird, Prof. R. Grahame, Mr. A. P. Barabas, Dr. F. M. Pope, Dr. I.P. Hunter. Mr P. Cuckow, Mr. M. Hawthorne
    This is a 30 page, A5, Illustrated Booklet on Ehlers-Danlos Syndrome (EDS). It has 20 different Sections; these cover various aspects of EDS. At the beginning the sections cover an introduction to EDS, explain what exactly Collagen is, the different types of collagen and the abnormality in EDS as well as how EDS is diagnosed. The different Types of EDS are stated and also the Hereditary patterns for each one. Other Sections include: Skin Features; The Rheumatological Symptoms; Orthopaedic Complications; Vascular Complications; Gastrointestinal Complications; EDS and the Eye; Hearing Impairment; Pregnancy; The Urinary Tract; Complications of EDS in Childhood; The Dental Aspects; Is there a Cure? Treatment; Surgery in EDS; and Anaesthesia.
    Available from Ehlers-Danlos Support Group.

    11. DermIS / Main Menu / DOIA / Ehlers-Danlos Syndrome / Images
    ehlersdanlos syndrome / images
    HOME DOIA PeDOIA Skincancer ... DOIA Ehlers-Danlos Syndrome images
    images for the diagnosis 'Ehlers-Danlos Syndrome'
    sitesearch: DermIS - Dermatology Information System

    12. Ehlers-Danlos Syndrome - Coping With EDS
    Previous, ehlersdanlos syndrome. Edited by Frederick A. Matsen, III, MD andGregory C. Gardner, MD Last updated December 7, 2001 Coping with EDS. Coping.
    Home About Us Clinics Physicians ... Contact Us
    Table of contents About Ehlers-Danlos syndrome Causes Symptoms and diagnosis Management and treatment ... View article with questions
    External links
  • American Juvenile Arthritis Organization (AJAO)
  • [Top]
    Ehlers-Danlos Syndrome
    Edited by Frederick A. Matsen, III, M.D. and Gregory C. Gardner, M.D.
    Last updated December 7, 2001
    Coping with EDS
    If you or your child has EDS, you know that it may present many challenges. Adults and children may initially react with feelings of fear, anger or depression. Children may also feel self-conscious about having the disorder. Try to remember that it often takes time to adjust to having a chronic (long-lasting) disorder, but that many people with Ehlers-Danlos syndrome are able to live full, relatively active lives. If you have EDS you might have concerns about managing pain , maintaining independence, financial strain or family worries. Discussing your problems and learning new ways to manage daily activities will help you cope more effectively. Your family may be one of your best sources of support. Discuss these issues with them, and ask for their support. It is important that parents discuss their child's symptoms with teachers, neighbors, relatives, baby-sitters and friends. They need to understand that cuts and bruises are common features of the Ehlers-Danlos syndromes, and not signs of child abuse. They also need to know about the following:

    13. Michiana Branch Of The Ehlers-Danlos National Foundation
    Support group for individuals and families from Michigan and Indiana who have ehlersdanlos syndrome (EDS), a genetic connective-tissue disorder. Meetings are held in South Bend, Indiana.

    14. Genetic/Metabolic - Ehlers-Danlos Syndrome
    Genetic/Metabolic Disorders. ehlersdanlos syndrome. Ehlers-Danlossyndromes (EDS) comprise a heterogenous group of connective tissue

    PIDL Home/ Contents
    Development Nutrition Acute Illness ... Psychosocial
    Genetic/Metabolic Disorders
    EHLERS-DANLOS SYNDROME Ehlers-Danlos syndromes (EDS) comprise a heterogenous group of connective tissue disorders that share, as fundamental features, alterations of the integrity of the supporting structures of the body and inheritance in a simple Mendelian fashion. The cardinal manifestations of EDS are hyperextensible skin, hypermobile joints, easy bruisability, and generalized fragility of various connective tissues. The spectrum of severity ranges from almost imperceptible findings to severe debilitating illness. EDS results from the molecular abnormality of the connective tissues, and the clinical and genetic heterogeneity are, in part, a reflection of an underlying biochemical heterogenity. Four varieties of EDS have this far been found to be due to different abnormalities in the biogenesis of the collagens. Joint hypermobility is a cardinal feature. Typically, joint hypermobility involves both large and small joints. Joint effusions may be relatively frequent and hemarthrosis may occur. Congenital club foot is also not uncommon.

    15. MEDLINEplus: Ehlers-Danlos Syndrome
    Topics. ehlersdanlos syndrome. Contents Organizations. Search MEDLINEfor recent research articles on • ehlers-danlos syndrome. You
    Skip navigation
    Other health topics: A B C D ... List of All Topics
    Ehlers-Danlos Syndrome
    Contents of this page:
    From the NIH




    Search MEDLINE for recent research articles on
    Ehlers-Danlos Syndrome
    You may also be interested in these MEDLINEplus related pages:
    Connective Tissue Disorders

    Skin Diseases (General)
    Bones, Joints and Muscles Genetics/Birth Defects From the National Institutes of Health
  • Questions and Answers About Heritable Disorders of Connective Tissue (National Institute of Arthritis and Musculoskeletal and Skin Diseases)
  • General/Overviews
  • Ehlers-Danlos Syndrome (EDS) (Arthritis Foundation) What is Ehlers-Danlos Syndrome? (Ehlers-Danlos National Foundation)
  • Diagnosis/Symptoms
  • Ehlers-Danlos Syndrome: Symptoms and Diagnosis (University of Washington, Dept. of Orthopaedics and Sports Medicine)
  • Disease Management
  • Coping with EDS (University of Washington, Dept. of Orthopaedics and Sports Medicine)
  • Treatment
  • Ehlers-Danlos Syndrome: Management and Treatment (University of Washington, Dept. of Orthopaedics and Sports Medicine)
  • Genetics
  • Ehlers-Danlos Syndrome: Causes (University of Washington) Hereditary Patterns (Ehlers-Danlos National Foundation)
  • Organizations
  • Ehlers-Danlos National Foundation National Institute of Arthritis and Musculoskeletal and Skin Diseases
  • Information from the Medical Encyclopedia:
  • Ehlers-Danlos Syndrome
  • Health services in North Carolina Other states coming - learn more The primary NIH organization for research on Ehlers-Danlos Syndrome

    16. Hypermobility & Fibromyalgia Support Site
    Information about joint hypermobility (ehlersdanlos syndrome), fibromyalgia and chronic fatigue syndrome.

    About This Site
    Hypermobility Syndrome Info Fibromyalgia Syndrome Info Ehlers-Danlos Syndrome Info ... Search this Site Welcome to the original Support Site for people with joint hypermobility and Fibromyalgia!
    This site is dedicated to providing information and support for people with both joint hypermobility (including Ehlers-Danlos and Benign Joint Hypermobility Syndromes, or any form of Hypermobility Syndrome) and Fibromyalgia or Chronic Fatigue Syndrome (aka Chronic Fatigue Immune Dysfunction Syndrome, or Myalgic Encephalopathy in the U.K. and Australia). It is the first of its kind and provides information on these conditions, and also links to many sites with much more detailed information. It's important to note that this is an amateur site, not an official local, national or international support or information group. Hopefully, however, small individual endeavours like this will pave the way for such official groups to emerge. In addition, the Hypermobility & Fibromyalgia Group (hm-ed-fm) is the only discussion/support group online for people with both of these conditions. All are welcome! Click on the "Support: Talk to Others" link in the navigation bar on the left to learn more about the mailing list, as well as the vibrant Webforum and Chat Room. Join The List!

    17. MEDLINEplus Medical Encyclopedia: Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. Causes, incidence, and risk factors. Ehlers-Danlossyndrome involves abnormal formation of connective tissue.
    Skip navigation
    Medical Encyclopedia
    Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z
    Ehlers-Danlos syndrome
    Contents of this page: Definition An inherited disorder characterized by excessive looseness (laxity) of the joints, hyperelastic skin that is fragile and bruises easily, easily damaged blood vessels and rarely, rupture on internal organs. Causes, incidence, and risk factors Ehlers-Danlos syndrome involves abnormal formation of connective tissue. This condition, occurs in different forms, most of which result from defects in different genes. Symptoms range from mild to severe. Symptoms
    • Joint dislocation or subluxation, including congenital Increased joint mobility, joints popping, early arthritis Double-jointedness, flat feet Easily damaged, bruised and stretchy skin Easy scarring and poor wound healing Premature rupture of membranes or births Very stretchy skin Visual difficulties Peg teeth
    Signs and tests Examination by the health care provider may show:
    • Excess joint laxity and joint hypermobility Soft, thin or hyperextensible skin

    18. Ehler Danlos
    Personal plea for help from a sufferer in Syria.Category Health Conditions and Diseases ehlers-danlos syndrome...... ehlersdanlos syndrome http// syndrome Menu
    Free Web site hosting -
    Ehler-Danlos Syndrome Hopes T o whom it may concern: I am sending this messages to all physicians and researchers in the medicine world, where there is still a lot diseases with no medicine.. I send this message to every human all over the world, I don’t care about place, all what I care about is reading somebody who can help me and give me some hope. I didn’t find in my country any treatment, even any concern, because my disease is rare. As I’ve been told by some doctors, I am the only with this disease in Syria. I tried some contacts in the U.S. and France but with no result. Let me introduce my self :
    My name is Rawaa Tawileh (a Girl) born in Damascus, Syria in 20/5/1976, I have a disease named (Ehlar-Danlos). The disease was discovered when I was 14 months old, the of this disease are:
    - Fragile tissues, which are not able to get any beat because it will be damaged directly resulting in a wound of 1-3 cm according to the beat and the way the people surrounding deal with it. The wound is like the fish mouth, and it get bigger and bigger with time , and results a very ugly scar.

    19. Family Village -- Ehlers-Danlos Syndrome
    Library E F. ehlers-danlos syndrome. Learn More About It. Ehlers-DanlosSyndrome From the National Organization for Rare Disorders (NORD).
    Ehlers-Danlos Syndrome
    Who to Contact
    Where to Go to Chat with Others

    Learn More About It

    Web Sites
    Search AltaVista for "Ehlers-Danlos Syndrome"
    Who to Contact
    Ehlers-Danlos National Foundation (EDNF)
    6399 Wilshire Boulevard, Suite 510
    Los Angeles, CA 90048
    Fax: (213) 651-1366
    This organization seeks to provide emotional support and updated information to those affected by Ehlers-Danlos syndrome and to their family members. In addition, EDNF serves as a vital information link to and from the medical community. It desires to inspire and support research in the field of connective tissue disorders specifically Ehlers-Danlos syndrome. The Foundation publishes a quarterly newsletter, Loose Connections, which provides current information on medical advances in EDS, as well as a means to share in the everyday experiences of living with EDS. In addition, a computerized database is maintained which allows interested members to communicate with one another. Local Branches and support groups are forming throughout the U.S. These local branches enable members to meet and network with others affected by EDS, thus decreasing the feeling of isolation so many of us know all so well. Learning conferences are held in various locations throughout the country in an effort to allow patients, family members and medical professionals the opportunity to share information about EDS.
    Australian Ehlers-Danlos Syndrome (EDS) Support Group Australia

    20. Arlene Brandeis, Opera Anthology Project Editor
    An expression of the loss of family members to genetic anomalies including ehlersdanlos syndrome, Acute Intermittent Porphyria, and Hypolipoproteinemia. Information provided about each.




    2001 Lyric Opera Of Chicago Production of Vincenzo Bellini's
    I Capuleti e i Montecchi Act I, Scene III
    With Andrea Rost (Giulietta), Vesselina Kasarova (Romeo), Umberto Chiummo (Lorenzo),
    Jeffrey Wells (Capellio), and Fabio Sartori (Tebaldo)
    Photo by Robert Kusel
    ANNOUNCING The Opera Anthology Project ATTENZIONE All Opera Professionals Please share your favorite: On Stage, Back Stage , Off Stage Story in our forthcoming Opera Anthology Publication BEHIND THE OPERA CURTAIN: An Opera Anthology We all have a favorite, funny, touching, and/or interesting story, please share yours. Stories from Opera Superstars to Opera Supernumeraries, Talent from Musical, Artistic, Technical, Production, and Administrative departments will share their experiences. The Who's Who of the Opera World will be represented. Don't exclude yourself or your opera company. Please limit each submission to 1,000 words or less. Story-related photographs are welcomed.

    A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z  

    Page 1     1-20 of 103    1  | 2  | 3  | 4  | 5  | 6  | Next 20

    free hit counter