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         Alport Syndrome:     more detail
  1. Molecular Pathology and Genetics of Alport Syndrome (Contributions to Nephrology)
  2. Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  3. Gale Encyclopedia of Medicine: Alport syndrome by Carol A. Turkington, 2002-01-01
  4. The Molecular Genetics of X-Linked Alport Syndrome (Acta Biomedica Lovaniensia) by Caiying Guo, 1995-11
  5. Alport Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Carol Turkington, 2006
  6. Hereditary nephropathy with hearing loss: "Alport's syndrome" (Acta paediatrica Scandinavica : Supplement) by Ulla Marianne Iversen, 1974
  7. Hereditary hearing loss with nephropathy (Alport's syndrome); (Acta oto-laryngologica. Supplement[um]) by John Sidney Turner, 1970
  8. Familial nephritis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Maria, PhD Basile, 2005

81. Syndrome D'Alport
Les informations d'Orphanet   propos de cette maladie rare. Signes de la maladie, associations de patients, projets de recherche.
http://orphanet.infobiogen.fr/Site/data/OC_Pat_data.php?Asb=Pat&PatId=630&am

82. Alport's Syndrome
MediFocus Guide. alport's syndrome. The Medifocus Guide on alport's syndrome. provides answers to the following important
http://www.yourbargainsite.com/med/Alports_Syndrome.html
MediFocus™ Guide
Alport's Syndrome
The Medifocus Guide on Alport's Syndrome
provides answers to the following important questions and medical issues:
  • What are the most common symptoms of Alport's Syndrome? Are there any recognized risk factors for developing Alport's Syndrome? What kinds of medical tests are used to establish the diagnosis of Alport's Syndrome? What is the current standard of care for the treatment of Alport's Syndrome? What treatment options are available for the management of Alport's Syndrome? Are there any promising new developments or potential breakthroughs in treatment? Who are the most notable medical authorities who specialize in Alport's Syndrome? Where are the leading hospitals and centers of research for Alport's Syndrome? What are the most important questions to ask my doctor about Alport's Syndrome?
At Medifocus.com

83. Alport's Syndrome -- ECureMe.com
alport s syndrome, more about alport s syndrome, alport s syndrome is a common cause of hematuria (blood in the urine). It
http://www.ecureme.com/emyhealth/Pediatrics/Alport's_Syndrome.asp
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Alport's Syndrome
more about Alport's Syndrome

  • Alport's syndrome is a common cause of hematuria (blood in the urine). It is responsible for about 15% of childhood cases of hematuria.
    Microscopic hematuria: Blood cells in the urine visible only under the microscope, are usually first noticed on routine checks during a routine physical examination.

84. THE MERCK MANUALSECOND HOME EDITION, Alport S Syndrome In Ch.
alport s syndrome. alport s syndrome (hereditary alport s syndrome can affect organs other than the kidneys. Hearing problems, usually
http://www.merck.com/mrkshared/mmanual_home2/sec11/ch146/ch146n.jsp

85. Bbc.co.uk - Health - Ask The Doctor Alport's Syndrome
Ask the Doctor. Q alport s syndrome. I am trying to find out some information about alport s syndrome, can you help? What is it, is it curable? Gillian.
http://www.bbc.co.uk/health/ask_doctor/alports_syndrome.shtml
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Q: Alport's Syndrome I am trying to find out some information about Alport's Syndrome, can you help? What is it, is it curable? Gillian Dr Trisha Macnair responds Alport's Syndrome is a rare inherited problem which has a combination of the effects. Most commonly the kidneys are affected, with nephritis (inflammation) and the gradual development of kidney failure. But hearing may also be affected (there is nerve deafness - i.e. it is the nerves which detect hearing which are to blame rather than structures in the ear or brain). Very rarely there may also be problems with the platelets in the blood, which are tiny cells that normally control the 'stickiness' and clotting of blood. It's much more common in boys Because it is inherited , several people in one family may have the same problem. Alport's is unusual because it is one of the few problems thought to be carried on the X chromosome (the 'female" chromosome). Girls are protected to a degree because they carry two X chromosomes and so may have a normal copy of the gene as well as the faulty one. However, boys carry one X and one Y chromosome, and so those who carry a faulty gene have no normal X to protect them. This is why men develop Alport's Syndrome more often than women. But there are several different types of Alport's Syndrome and the exact way in which it is inherited is still under debate.

86. Alport, Syndrome : Sites Et Documents Francophones
Translate this page Néphropathie familiale avec surdité . Arborescence(s) du thesaurus MeSH contenant le mot-clé alport, syndrome nephritis, hereditary
http://www.chu-rouen.fr/ssf/pathol/alportsyndrome.html
Alport, syndrome Menu général CISMeF Synonyme(s) CISMeF Alport lié à l'X, syndrome d' ; Alport type dominant, syndrome d' ; Alport type récessif, syndrome d' ; Surdité-néphropathie, type Alport .
Synonyme(s) MeSH Néphrite hématurique familiale avec surdité ; Néphropathie familiale avec surdité
Arborescence(s) Alport, syndrome nephritis, hereditary
maladies appareil génital féminin et complications grossesse
maladies et malformations congénitales, héréditaires et néonatales maladies urologiques et appareil génital mâle Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources :
guide ressources
  • Alport, syndrome d' - synonyme(s) et inclusion(s) : Alport lié à l'X, syndrome d' ; Alport type dominant, syndrome d' ; Alport type récessif, syndrome d' ; surdité-néphropathie, type Alport
    [Par Pr Niaudet P.

87. Alport, Syndrome : Arborescences MeSH
Translate this page alport, syndrome arborescences MeSH. Menu général CISMeF. Vous pouvez aussi consulter toutes les arborescences des mots clés
http://www.chu-rouen.fr/navimesh/A/navialportsyndrome.html
Alport, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF

88. ORPHANET - Maladies Rares - Médicaments Orphelins
alport lié à l X, syndrome d alport type dominant
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=63

89. Alport's Syndrome (www.whonamedit.com)
alport s syndrome A very rare hereditary syndrome characteriszed by progressive renal failure, nerve deafness and abnormities of the lense of the eye.
http://www.whonamedit.com/synd.cfm/337.html

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Alport's syndrome Also known as:
Dickinson's hereditary deafness nephropathy
Dickinson’s syndrome Synonyms: Congenital hereditary hematuria, hematuria nephropathy-deafness syndrome, hematuric familial nephropathy, hematuric hereditary nephritis, hemorrhagic familial nephritis, hereditäres Nephropathie-Taubheits-Syndrom (German), hereditary familial congenital hemorrhagic nephritis, hereditary nephritis, hereditary nephritis-deafness syndrome, hereditary nephropathy-deafness syndrome, néphropathie héréditaire avec surdité (French), Nephropathie mit Innenohrschwerhörigkeit (German), progressive hereditary nephritis. Associated persons: Arthur Cecil Alport William Howship Dickinson Description: The main characteristics of this very rare hereditary syndrome are progressive renal failure, nerve deafness and abnormities of the lense of the eye. Male/female relationship 1:1. Men are earlier and more severely affected than women. It is thought to be due to an autosomal inherited defect of the glomerular basement membrane of the kidneys. Death usually occurs before middle age.

90. UK NKF - Alports Syndrome.
What is alport s syndrome? alport s syndrome is an inherited kidney disease (it runs in families). GoTo top of page (2K). Why it is called alport s syndrome?
http://www.kidney.org.uk/Medical-Info/alports/
Alport's Syndrome
What is Alport's Syndrome?
Why it is called Alport's Syndrome?
What Causes Alport's Syndrome?
How is Alport's Syndrome diagnosed?
Is Alport's Syndrome common?
Is there any treatment to prevent kidney failure?
What about ear and eye damage - is this serious?
Does everyone with Alport's Syndrome develop kidney failure?
Can people with Alport's Syndrome have dialysis or a kidney transplant?
Should members of the family have tests to look for Alport's syndrome?
What is Alport's Syndrome?
Alport's syndrome is an inherited kidney disease (it runs in families). Men are more severely affected than women, and people can develop deafness as well as kidney failure.
Why it is called Alport's Syndrome?
Alport's syndrome is named after Dr A. Cecil Alport, who recognised families with the syndrome in 1927. He was born in 1880 in South Africa, and graduated as a doctor in Edinburgh. At first he worked in Johannesburg (owning a small gold mine). After the First World War he moved to St Mary's Hospital, Paddington, London, where he was working when he described the syndrome of hereditary renal failure and deafness. Later he worked in Cairo, and died in 1959.
What Causes Alport's Syndrome, and differences between men and women?

91. UK NKF - How Is Alport's Syndrome Diagnosed?
alport s syndrome. How is alport s syndrome diagnosed? alport s syndrome causes small amounts of blood to appear in the urine from a very early age.
http://www.kidney.org.uk/Medical-Info/alports/diagnosis.html
Alport's Syndrome
How is Alport's Syndrome diagnosed?
  • Family screening
    An explanation of which family members should be screened is given later ( click here ). If someone is to be screened because of a family history, it may only be necessary to check the urine for blood. This can be done by taking a small sample of urine and dipping into it on a small plastic stick. Alport's syndrome causes small amounts of blood to appear in the urine from a very early age. This test is not completely foolproof - a negative urine test may need to be repeated several times to be sure there is no blood, and blood can be present for other reasons, such as a urine infection.
    Kidney biopsy
    Alport's syndrome causes a unique appearance when the kidney is examined under the microscope. The membrane that filters blood to make urine is split into several layers. Splitting is generally seen in men and in some women. Sometimes the membrane may just be very thin, which can make it more difficult to diagnose Alport's syndrome.
    If someone with a known family history of Alport's syndrome has blood in the urine, it is usually not necessary to perform a kidney biopsy. However, in some cases where the diagnosis is not proven, it may be necessary. Kidney biopsy carries a small risk of bleeding. For more information
  • 92. MediFocus MedCenter Preview For Alport's Syndrome
    MediFocus MedCenter ® Back to Directory alport s syndrome (NK001) Introduction. What are the most common symptoms of alport s syndrome?
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    Alport's Syndrome
    Introduction
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

    93. ALPORT'S SYNDROME
    Terms of Use. alport S syndrome. Specialty Definition alport S syndrome. Domain, Definition. Medicine. Top. Modern Translation alport S syndrome.
    http://www.websters-online-dictionary.org/definition/english/Al/Alport's_syndrom
    Philip M. Parker, INSEAD.
    ALPORT'S SYNDROME
    Specialty Definition: ALPORT'S SYNDROME
    Domain Definition
    Medicine
    Hereditary progressive nephropathy with albuminuria and hematuria and progressive bilateral nerve deafness, mostly affecting males. Source: European Union. references Source: compiled by the editor from various references ; see credits. Top
    Modern Translation: ALPORT'S SYNDROME
    Language Translations for "ALPORT'S SYNDROME"; alternative meanings/domain in parentheses.
    Danish
    Alport's syndrom (Alport syndrome, hereditary nephropathy-deafness syndrome), nephropathia hereditaria (Alport syndrome, hereditary nephropathy-deafness syndrome). ( various references
    French
    syndrome d'Alport (Alport syndrome), n©phropathie h©maturique familiale avec surdit© de Dickinson (Alport syndrome). ( various references
    German
    Alport-Syndrom (Alport syndrome, hereditary nephropathy-deafness syndrome), otookulorenales Syndrom (Alport syndrome, hereditary nephropathy-deafness syndrome), Nephropathie-Taubheitssyndrom (Alport syndrome, hereditary nephropathy-deafness syndrome), heredit¤re Nephritis (Alport syndrome, hereditary nephropathy-deafness syndrome). (

    94. NEJM -- Alport's Syndrome, Goodpasture's Syndrome, And Type IV Collagen
    Review Article from The New England Journal of Medicine alport s syndrome, Goodpasture s syndrome, and Type IV Collagen. alport s syndrome. Genetics.
    http://content.nejm.org/cgi/content/short/348/25/2543
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    Previous Volume 348:2543-2556 June 19, 2003 Number 25 Next Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen
    Billy G. Hudson, Ph.D., Karl Tryggvason, M.D., Ph.D., Munirathinam Sundaramoorthy, Ph.D., and Eric G. Neilson, M.D. Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.
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    Basement membranes form a complex surface on which epithelial cells reside. These membranes provide morphogenic cues that determine the fate of cells, the polarization of subcellular constituents, and the location of cell receptors and transporters. Basement membranes are assembled through an interweaving of type IV collagen (collagen IV) with laminins, nidogen, and sulfated proteoglycans. Collagen IV belongs to a family of collagenous proteins that has at least 25 distinct members. The and genes Full Text of this Article Structure and Distribution of Type IV Collagen Alport's Syndrome Genetics Pathogenesis Clinical Presentation Findings on Kidney Biopsy Treatment Goodpasture's Syndrome Genetics Pathogenesis Clinical Presentation Findings on Kidney Biopsy Treatment Summary
    This article has been cited by other articles:
    • Zeisberg, M., Muller, G. A., Kalluri, R. (2004). Are there endogenous molecules that protect kidneys from injury? The case for bone morphogenic protein-7 (BMP-7).

    95. Alport (syndrome D' -)
    alport (syndrome d -) alport (syndrome d -) Le syndrome d’alport est une maladie
    http://www.frm.org/informez/info_ressources_maladies_fiche.php?id=121

    96. HealingWell.com - Medifocus Guides - Alports Syndrome
    HealingWell Medcenter Medifocus Guide. alport s syndrome. Nephritis is a general term for inflammation of the kidneys. There are
    http://www.healingwell.com/medcenter/alports_syndrome.asp
    Search Site: Search Web: HealingWell Medcenter Medifocus Guide
    Alport's Syndrome

    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

    97. Alport's Syndrome, Kidney
    alport s syndrome, kidney,. Print this article, (Arthur alport, 18801959, English physician), a syndrome consisting of hereditary
    http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 2/ALPORTS SYNDROM
    Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Alport's syndrome, kidney, (Arthur Alport, 18801959, English physician), a syndrome consisting of hereditary chronic nephritis, deafness and ocular abnormalities. Inheritance is usually autosomal dominant. Both sexes are affected, but the disease starts earlier in males and has a more rapid course. Clinical features include intermittent haematuria, progressive renal failure, and progressive high-frequency nerve deafness. Nephrotic syndrome is rare. Ocular abnormalities include posterior cataracts, lens dislocation, corneal dystrophy, nystagmus and myopia. Pathologically, the kidneys are small with patchy interstitial fibrosis. Foam cells in the vicinity of the corticomedullary junction are a distinctive microscopic finding. Intravenous urography or CT show small kidneys with impaired contrast excretion. Nephrocalcinosis may be present.
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    98. MediFocus MedCenter Preview For Alport's Syndrome
    31. MediFocus MedCenter © alport s syndrome (NK001). Introduction. Nephritis issues What are the most common symptoms of alport s syndrome?
    http://www.virtualquincy.com/quincy/health/MedFocus/NK001.HTM
    MediFocus MedCenter
    Alport's Syndrome
    Introduction
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

    99. Treatment & Condition - MediFocus MedCenter Preview For Alport's Syndrome
    alport s syndrome (NK001) Introduction. The Medifocus Guide on alport s syndrome provides answers to the following important questions and medical issues
    http://funandmagic.com/Nk001.htm
    Magic Mike's audio tour of the site Alport's Syndrome
    Introduction
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    The cause of AS is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people. Treatment requires medication, and often, kidney transplant.

    100. Alports Syndrome
    MediFocus MedCenter © alport s syndrome (NK001). Order the Full Guide. Introduction. What are the most common symptoms of alport s syndrome?
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    Introduction
    Nephritis is a general term for inflammation of the kidneys. There are several hereditary forms of nephritis. Alport's syndrome (AS) is one of these but is unique because of the additional symptom of hearing loss in the presence of kidney failure. The disorder causes chronic glomerulonephritis with destruction of the glomeruli. The eventual result is end stage renal disease (ESRD) requiring dialysis (or transplantation) develops between adolescence and age 40.
    AS affects the basement membranes which are the supporting layers of epithelial and endothelial tissues that make up much of the body's surfaces. The cause is a mutation in a gene for collagen. The disorder is uncommon, affecting about 2 out of 10,000 people.

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