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         Proteus Syndrome:     more detail
  1. Proteus syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Lisa, MS, CGC Andres, 2005
  2. The Elephant Man : A Study in Human Dignity by Ashley Montagu, 2001-08
  3. The Elephant Man by Frederick Drimmer, 1985-09-16
  4. The Elephant Man by Michael Howell, Peter Ford, 1983-11
  5. The True History of the Elephant Man: The Definitive Account of the Tragic and Extraordinary Life of Joseph Carey Merrick by Peter Ford, Michael Howell, 2010-04-01
  6. Articulating the Elephant Man: Joseph Merrick and His Interpreters (Parallax: Re-visions of Culture and Society) by Professor Peter W. Graham, Professor Fritz H. Oehlschlaeger, 1992-02-01
  7. The True History of the Elephant Man by Michael Howells, Peter Ford, 2001-08-15
  8. The Elephant Man: A Play by Bernard Pomerance, 1979-09
  9. The elephant man and other reminiscences by Frederick Treves, 1923-01-01
  10. The Brink of Tomorrow by Ken Gullekson, 2010-02-10

81. Proteus Syndrome Articles, Support Groups, And Resources
proteus syndrome articles, support groups, and resources for patients from MedHelp International (www.medhelp.org)
http://www.medhelp.org/HealthTopics/Proteus_Syndrome.html
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82. Journal Of Bronchology - UserLogin
Hemoptysis in proteus syndrome Case Report and Topic Review We report apatient with proteus syndrome who presented with massive hemoptysis.
http://www.bronchology.com/pt/re/jbronch/fulltext.00128594-200507000-00015.htm
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83. British Library Direct: Order Details
Order from the British Library Vascular anomalies in proteus syndrome ClinicalAnd Experimental Dermatology.
http://direct.bl.uk/research/50/39/RN148744901.html
This is an article from British Library Direct, a new service that allows you to search across 20,000 journals for free and order full text using your credit card. Article details Article title Vascular anomalies in Proteus syndrome Author Hoeger, P. H. Martinez, A. Maerker, J. Harper, J. I. Journal title CLINICAL AND EXPERIMENTAL DERMATOLOGY Bibliographic details 2004, VOL 29; NUMBER 3, pages 222-230 Publisher Blackwell Publishing Ltd Country of publication Great Britain ISBN ISSN Language English Pricing To buy the full text of this article you pay:
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To see the abstract, point to the 'A' icon Abstract: Summary Proteus syndrome (PS) is a complex hamartomatous disorder defined by local overgrowth (macrodactyly or hemihypertrophy), subcutaneous tumours and various bone, cutaneous and/or vascular anomalies (VA). VA are manifold in PS, but their prevalence is unknown so far. In order to further characterize PS, we studied the prevalence of VA in 22 PS patients presenting to our outpatient clinic and reviewed 100 PS patients previously reported between 1983 and 2001. The diagnosis of vascular abnormalities was made on clinical grounds and supported with imaging studies and/or histology in 12 and seven patients out of 22, respectively. Thirty-five VA were identified in 22/22 (100%) of our patients, and more than one type of VA were present in 10 of them. Vascular tumours, portwine stains (PWS),...

84. The Lantern Online
might have actually suffered from a rare affliction known as proteus syndrome.proteus syndrome was first discovered in 1979 and named after the Greek
http://www.thelantern.com/news/2003/08/07/Campus/Elephant.Man.Mystery.Unsolved-4
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Elephant man mystery unsolved
By Mandy Heth Published: Thursday, August 7, 2003 It would take more than the "Mystery Van" and a lovable dog sidekick for one Ohio State researcher to solve a 112-year-old mystery.
Dr. Charis Eng, Director of the Division of Human Genetics, was sought out by Dr. Paul Trotman, a producer for New Zealand Natural History TV, to help him with a documentary. Trotman wanted Eng to test his theory about what caused the strange deformities of Joseph Merrick.
Merrick, commonly referred to as "the elephant man," was once believed to have suffered from elephantiasis. That diagnosis changed in later years to neurofibramatosis, a very common neurological disorder that causes an enlarged head, optic nerve tumors, spots of discoloration, as well as bumps and nerve tumors.
"These tumors can be very significant, even life threatening, and grow anywhere in the body," said Kevin Sweet, genetic counselor at the James Cancer Center. "These tumors form on nerves throughout the body, thus the name neurofibromatosis, and can affect the development of bones and skin, resulting in disfigurement."

85. DMFR -- Sign In Page
proteus syndrome is a rare condition that involves atypical growth of the bones The authors present a case of a 7year-old girl with proteus syndrome in
http://dmfr.birjournals.org/cgi/content/full/34/4/251

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Dentomaxillofacial imaging in Proteus syndrome
Korbmacher et al. Dentomaxillofac Radiol.
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86. Massive Hemoptysis Secondary To Proteus Syndrome -- Daniels Et Al. 126 (4): 940S
proteus syndrome is a rare, sporadic, congenital disorder characterized by overgrowth Previous reports of pulmonary involvement in proteus syndrome are
http://meeting.chestjournal.org/cgi/content/abstract/126/4/940S-a
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This Article Full Text (PDF) Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Daniels, C. E. Articles by Edell, E. S.
Airway I
Monday, October 25, 2004 4:15 PM - 5:45 PM
Massive Hemoptysis Secondary to Proteus Syndrome
Craig E. Daniels, MD* Mark E. Wylam, MD David J. Driscoll, MD and Eric S. Edell, MD Mayo Clinic, Rochester, MN INTRODUCTION: We report a case of recurrent massive hemoptysis in a 27-year-old man with Proteus syndrome. Proteus Syndrome is a rare, sporadic, congenital disorder characterized by overgrowth of multiple tissues [1]. It is caused by the sporadic genetic mutation of a somatic gene, which distributes in a mosaic pattern. This mutation results in sporadic growth of varying body tissues occurring primarily in the postnatal period [2]. The phenotypic presentation is varied, depending on the mosaic distribution

87. Proteus Syndrome: Diagnostic Criteria, Differential Diagnosis, And Patient Evalu
Workshop on proteus syndrome Diagnostic Criteria, Differential Diagnosis, andPatient Evaluation cosponsored by the Office of Rare Diseases at NIH.
http://rarediseases.info.nih.gov/html/workshops/workshops/proteus980319.html
National Human Genome Research Institute (NHGRI)
Proteus Syndrome: Diagnostic Criteria, Differential Diagnosis, and Patient Evaluation
March 19-20, 1998
Agenda
Thursday, March 19
12:00 p.m.
Welcome and Orientation
Leslie Biesecker and Anita Pikus 12:30 p.m. Overview of Proteus Syndrome
M. Michael Cohen, Jr. 1:30 p.m. Clinical Evaluation of 18 Patients Referred with a Diagnosis of Proteus Syndrome
Leslie Biesecker 2:45 p.m. The South African Experience with Proteus and Related Syndromes
Denis Viljoen 3:45 p.m. The Mosaicism Hypothesis
Rudolph Happle Friday, March 20 8:00 a.m. Molecular Genetics of Overgrowth Disorders Rosanna Weksberg 9:00 a.m. Lipomas and Spinal Lesions John M. Graham, Jr. 10:15 a.m. Vascular Malformations and Tumors John Mulliken 11:15 a.m. Diagnostic Criteria for Proteus syndrome The charge for the group is to develop a consensus on the clinical manifestations necessary for diagnosis of Proteus syndrome and the distinction of Proteus and overlapping conditions. 1:00 p.m. Diagnostic Criteria for Proteus Syndrome (continued) 2:30 p.m.

88. Lipomatosis Of The Colon Complicating Proteus Syndrome -- Mackay Et Al. 86 (4):
A 12 year old boy with proteus syndrome (macrodactyly, plantar/palmar cerebriformhyperplasia, lipomata, verroucous naevi, macrocephaly, and/or vascular
http://adc.bmjjournals.com/cgi/content/full/86/4/265

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Images in paediatrics
Lipomatosis of the colon complicating Proteus syndrome
G Mackay L Spitz and K McHugh Department of Paediatric Surgery, Great Ormond Street Hospital for Children NHS Trust, Great Ormond Street, London WC1N 3JH, UK;
Department of Radiology, Great Ormond Street Hospital for Children NHS Trust A 12 year old boy with Proteus syndrome (macrodactyly, plantar/palmar cerebriform hyperplasia, lipomata, verroucous naevi, macrocephaly

89. Germline Mutation Of The Tumour Suppressor PTEN In Proteus Syndrome -- Smith Et
proteus syndrome (PS, OMIM 176920) is a hamartomatous disorder CutaneousManifestations of proteus syndrome Correlations With General Clinical Severity
http://jmg.bmjjournals.com/cgi/content/extract/39/12/937

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Vol Page [Advanced] This Article Full Text Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Smith, J M Articles by Marsh, D J Related Collections Cancer:other
Genetics
Journal of Medical Genetics
LETTER TO JMG
Germline mutation of the tumour suppressor PTEN in Proteus syndrome
J M Smith E P E Kirk G Theodosopoulos G M Marshall J Walker M Rogers M Field J J Brereton and D J Marsh
Kolling Institute of Medical Research, Royal North Shore Hospital, and Department of Molecular Medicine, University of Sydney, St Leonards, NSW 2065, Australia
Visiting Medical Officer, Wollongong Hospital, Crown Street, Wollongong, NSW 2500, Australia Correspondence to:
Dr D J Marsh, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards, NSW 2065, Australia;

90. PTEN Mutations Are Uncommon In Proteus Syndrome -- Barker Et Al. 38 (7): 480 --
Cutaneous Manifestations of proteus syndrome Correlations With General Clinical Germline mutation of the tumour suppressor PTEN in proteus syndrome
http://jmg.bmjjournals.com/cgi/content/extract/38/7/480

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Letters to the editor
PTEN mutations are uncommon in Proteus syndrome
K Barker a , A Martinez b , R Wang c , S Bevan a , V Murday a , J Shipley c , R Houlston a , J Harper b a Cancer Genetics Section, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK, b Department of Dermatology, Great Ormond Street Hospital for Children NHS Trust, Great Ormond Street, London WC1N 3JH, UK, c Molecular Carcinogenesis Section, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK

91. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/
proteus syndrome Foundation Support and education for families and professionals The CaF Directory - A definition of proteus syndrome, its inheritance
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis
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UF Scientist Finds Unexpected Link Between Cat And Human AIDS Viruses (September 9, 2005) full story Mayo Clinic Develops New Coma Measurement System (September 8, 2005) full story Nitric Oxide Could Extend Fertility (September 8, 2005) Biochemistry , an American Chemical Society journal. full story Flipped, Expelled, Copied, And Shrunk: Researchers Document Dramatic Genome Alterations During Primate Evolution (September 6, 2005) Genome Research presents a series of studies that provide insight into the evolution and variation of primate genomes. The issue will appear online and in print on September 1, concomitant with the publication of the chimpanzee genome sequence in the journal Nature full story Discovery Will Aid Identification Of Misregulated Genes In Rett Syndrome (September 4, 2005) Molecular Cell that the "Rett Syndrome protein", MeCP2, only binds to genes with a specific sequence of nucleotide bases. This knowledge will aid in the identification of the genes that are regulated by the gene MECP2. This work was supported, in part, by the Rett Syndrome Research Foundation (RSRF).

92. OSU Geneticist Turns Sleuth In Elephant Man Mystery : College Of Medicine & Publ
proteus syndrome, named after the Greek god who could change his shape at He hypothesized Merrick might have suffered from proteus syndrome and NF 1.
http://medicine.osu.edu/news/article.cfm?ID=1352

93. Proteus Family Network (UK) - Patient UK
To create a network of families affected by proteus syndrome. To raiseawareness of proteus syndrome with other professionals.
http://www.patient.co.uk/showdoc/26739866/
Proteus Family Network (UK)
31 Baswich Lane
Weeping Cross
Stafford
Tel: 01785 254953
Web: www.proteus-uk.org
Best time to telephone: any reasonable time.
Proteus Syndrome is a very rare congenital condition. The Proteus Family Network UK is a network for families and individuals affected by the syndrome to enable them to have contact with other families in similar circumstances. The Network has information on a clothing and footwear database. The aims of the Network are as follows.
  • To create a network of families affected by Proteus Syndrome.
  • To help and encourage contact between the children.
  • To collate current information on Proteus Syndrome.
  • To raise awareness of Proteus Syndrome with other professionals.
  • To help and encourage any research work being done into Proteus Syndrome.
  • To offer mutual support and friendship to affected families.
The Network publish newsletters which are also available to download from their website. They also work with and are supported by a Medical Advisory Board drawn from Great Ormond Street Hospital.
Checked: October 2004
Sponsored links and adverts Patient UK has no control of the content of the following links. Inclusion does not imply endorsement by Patient UK.

94. Alex Hoag Run For Sunshine 5K Run - Home Page - The Proceeds From This Run Benef
The Proteus Foundation The proteus syndrome Foundation is a worldwide support The cause of proteus syndrome is unknown, the effects of proteus syndrome
http://www.alexhoagrun.org/
In honor of Alex's memory his family and friends will continue to battle Proteus Syndrome until a cure can be found.
The Proteus Syndrome Foundation is a worldwide support group founded by Alex Hoag's mom in 1991. It supports research to find the cause of and cure for this disease. It also provides family support by helping families unite and by giving grants to families helping them buy much needed medical supplies such as wheelchairs, shoes, hospital beds, etc. More race pictures added Check out your results of the 2005 Alex Hoag Run for Sunshine!
Three time Olympian and three time British National Champion Steeplechaser Justin Chaston has joined the Alex Hoag Run For Sunshine as the 2005 Honorary Chairman. Justin is a native of Wales Great Britain and has lived and trained in the U.S. for nearly 15 years. Justin has lived in Colorado Springs for over two years with his wife, Stacey, and two children, Thomas and Emily. In addition to his training, he also works as a real estate agent for Prudential. Justin has participated in the Alex Hoag Run For Sunshine for the last two years. He and Stacey both hold the Male and Female course records, respectively. Justin's world class athletic success coupled with his business experience will greatly contribute to raising international awareness for the Proteus Syndrome Foundation.
The syndrome became widely known by the movie and Broadway play 'The Elephant Man'.

95. BBC NEWS | Health | Elephant Man Mystery Unravelled
Tests suggested he may have suffered from NF1 or proteus syndrome, or maybe evenboth. proteus syndrome is present at birth and can cause overgrowth in
http://news.bbc.co.uk/2/hi/health/3084483.stm
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... Newswatch Last Updated: Monday, 21 July, 2003, 17:32 GMT 18:32 UK E-mail this to a friend Printable version Elephant man mystery unravelled

A computer image of how Merrick may have looked The notorious "elephant man" may have suffered from two rare disorders, according to scientists. They believe Joseph Merrick, who lived in Britain more than 100 years ago, could have suffered from type 1 neurofibromatosis (NF1) and Proteus syndrome. They believe both conditions may have combined to trigger his severe physical deformities. Their claim, which is featured in a new series on the Discovery Health channel, follows DNA tests on the man's hair and bones. 'Fairground freak' Merrick, who was born in Leicester in 1862, showed signs of deformity from the age of five. By the time he was a teenager, he was completely deformed and had been rejected by his community and his own parents. How Merrick may have looked without his affliction He was a member of a travelling circus and became widely known for his role as a fairground freak. In his mid-20s, he met a surgeon who arranged for him to be admitted to the Royal London Hospital, where he died at the age of 27.

96. Proteus' Syndrome (www.whonamedit.com)
proteus syndrome A congenital syndrome characterised by a variety of abnormalitiesAlso known as Wiedemann s syndrome.
http://www.whonamedit.com/synd.cfm/997.html

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Proteus' syndrome Also known as: Wiedemann's syndrome Synonyms: Proteiform syndrome. Associated persons: Proteus Proteus Hans-Rudolf Wiedemann Description: A congenital syndrome characterised by a variety of abnormalities, most commonly by asymmetry of the arms and legs with partial enlargement of the hands and/or feet, hemihypertrophy - overgrowth of one side of the face, body, or limbs - thickening of the skin and subcutaneous tissues, subcutaneous masses, vascular disorders, epidermal naevi, and macrodactyly; accelerated growth during early years, cystiform pulmonary abnormalities, visceral manifestations from abdominal and pelvic lipomatosis, macrocephaly or asymmetry of the skull with bony prominences due to hemihypertrophy, scoliosis and kyphosis, muscle atrophy, and convulsions. Aetiology unknown. Reported cases have been isolated occurrences in families, suggesting that the condition is not hereditary. It affects both sexes equally, and has no particular racial, geographical or ethnic distribution.

97. Syndrome, Proteus Definition - Medical Dictionary Definitions Of Popular Medical
Online Medical Dictionary and glossary with medical definitions.
http://www.medterms.com/script/main/art.asp?articlekey=5662

98. Syndrome De Fatigue Chronique - PasseportSanté.net
Translate this page syndrome de fatigue chronique description médicale, symptômes, facteurs derisque, prévention, traitements médicaux, traitements non conventionnels,
http://www.reseauproteus.net/fr/Maux/Problemes/Fiche.aspx?doc=syndrome_fatigue_c

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