Titre:nspku | the national society for phenylketonuria
La description :jump to navigation the national society for phenylketonuria www.nspku.org the national society for phenylketonuria -- home information what is pku? what is the nspku? faqs how to join mailing list his...
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L'adresse IP principale: 91.146.108.148,Votre serveur United Kingdom,Maidenhead ISP:UK Webhosting Ltd TLD:org Code postal:gb
Ce rapport est mis à jour en 05-Aug-2018
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Latitude: | 51.522789001465 |
Longitude: | -0.71986001729965 |
Pays: | United Kingdom (gb) |
Ville: | Maidenhead |
Région: | England |
ISP: | UK Webhosting Ltd |
domaine | Titre |
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nspku.org | nspku | the national society for phenylketonuria |
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jump to navigation the national society for phenylketonuria www.nspku.org the national society for phenylketonuria -- home information what is pku? what is the nspku? faqs how to join mailing list history news dietary information events publications general events conferences members society & groups publications dietary information news & views newsletters booklets leaflets conferences travel forms resources maternal recipes contact general enquiries emergency contacts council of management links other organisations manufacturers members web sites chat forum donate join membership twitter facebook news pku in the news... posted thursday 2nd august 2018 link to article by journalist sara royle in the westmorland gazette - august... read more general prescription problems posted tuesday 15th may 2018 event scott jepson - spartan race posted wednesday 1st august 2018 general new nspku research grants posted tuesday 17th july 2018 dietary discontinued mevalia products posted friday 6th july 2018 general my pku story posted monday 9th april 2018 new parent? if your baby has just been diagnosed with pku, we suggest that you read the what is pku and frequently asked question pages before exploring the rest of the site. what is the nspku? the national society for phenylketonuria exists to help and support people with pku and their families. read more what is pku? phenylketonuria is a rare inherited condition which can be treated with a low protein diet. read more publications management of pku the child with pku news & views 151 dietary information please note the treatment of pku varies for each individual. no patient should alter their treatment as a result of anything written on this or any site without first consulting their doctor or dietitian. copyright © 2004-2011 national society for phenylketonuria . charity 273670 . company 1256124.
http://www.nspku.org/copyright
http://www.nspku.org/contact
http://www.nspku.org/publications/publication/child-pku
http://www.nspku.org/events/members
http://www.nspku.org/recipes
http://www.nspku.org/publications/leaflets
http://www.nspku.org/news/story/discontinued-mevalia-products
http://www.nspku.org/news/dietaryinformation
http://www.nspku.org/donate
http://www.nspku.org/#main-menu
http://www.nspku.org/contact/general
http://www.nspku.org/contact/emergency
http://www.nspku.org/publications/dietaryinformation
http://www.nspku.org/news/story/new-nspku-research-grants
http://www.nspku.org/information/whatispku
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