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ANU College of Medicine, Biology and Environment. Raquo; more academic areas. ANU College of Medicine, Biology and Environment. The John Curtin School of Medical Research. The Centre for Personalised Immunology. National Centre for Indigenous Genomics. Morning tea to raise the profile of rare disease.
ASOCIACION DE FAMILIAS CON PERTHES. La enfermedad de Perthes es una necrosis avascular en la cabeza del fémur.
Perthesin tauti on lasten lonkkasairaus, jossa verenkiertohäiriö aiheuttaa reisiluun pään pehmenemisen ja lonkkanivelen vaurioitumisen. Lue lisää Perthesin taudista täältä. Suomen Perthes ry edistää Perthesin taudin tunnettavuutta sekä antaa tietoa ja tukea potilaille ja heidän läheisilleen. Vertaistukea on tarjolla niin sairauden kohdanneille lapsiperheille kuin jo aikuistuneille Perthes-potilaille. Suomen Perthes ry on Invalidiliiton.
I decided to write this blog, as I thought it would be helpful to other families who have a child with Perthes Disease. It is an honest diary of events and feelings. Monday, 20 July 2009. Annabel is so well after her operation. To have her pins and plates removed. Everything went really smoothly before up to. The op, compared to the last one. Friday, 26 June 2009.
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Perthes disease - a place for parents and professionalsPARSED CONTENT
The web page has the following on the web page, "Access How to join us." I viewed that the web page also said " Our Store Support Perthes! Helping children with Osteochondritis PERTHES ASSOCIATION is an entirely Voluntary Organisation, founded in Birmingham in 1976 and was registered as a charity in 1977; in 1991 the charity moved to Guildford in Surrey and became a National Charity." They also said " Our registered charity Number is 326161. 5 per 100,000 children mainly boys between the ages of 2 and 15 years."ANALYZE SUBSEQUENT WEB SITES
Miércoles, 23 de abril de 2008. No ha caminado aun esta web, pero no importa, ya tendremos la oportunidad de tener testimonios, y comentar lo que vivimos en este minuto, en mayo, el 15 tennemos control con Adolfo, y debo llevar ese dia, un Rx que le tomaremos, les comentare como nos va, fuera de eso, le pedire ayuda al doctor para que nos ayude a llegar a mas personas. Martes, 8 de abril de 2008. Sábado, 5 de abril de 2008. Por favor, recuerden promov.
I decided to write this blog, as I thought it would be helpful to other families who have a child with Perthes Disease. It is an honest diary of events and feelings. Monday, 20 July 2009. Annabel is so well after her operation. To have her pins and plates removed. Everything went really smoothly before up to. The op, compared to the last one. Friday, 26 June 2009.
Wednesday, 11 February 2009. My son Joe has Perthes. He has just turned five and was diagnosed around two years ago after he started limping and favouring his left leg. Having done a fair bit of research on the subject and attended several appointments with our specialist I thought that I would put my experiences down on paper to reassure other parents. Firstly, what is Perthes disease? I remember one conversation with Joe recently when.
Deviant since Apr 27, 2005. This is the place where you can personalize your profile! By moving, adding and personalizing widgets. You can drag and drop to rearrange. You can edit widgets to customize them.