cystinose.nl cystinose.nl

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Home - Cystinose

Alles over cystinose vind je op de website van CGN - CystinoseGroep Nederland. Dus: wat wil je weten?

http://www.cystinose.nl/

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Home - Cystinose | cystinose.nl Reviews
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Alles over cystinose vind je op de website van CGN - CystinoseGroep Nederland. Dus: wat wil je weten?
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1 over cgn
2 wat is cystinose
3 tips
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7 cystinosis
8 zoek
9 cystinose groep nederland
10 cystinose video
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Home - Cystinose | cystinose.nl Reviews

https://cystinose.nl

Alles over cystinose vind je op de website van CGN - CystinoseGroep Nederland. Dus: wat wil je weten?

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cystinose.nl cystinose.nl
1

Kennisbank - Cystinose

https://cystinose.nl/htdocs/artikelen.asp

In deze kennisbank staan door CGN geselecteerde brochures en artikelen, die voor patiënten, hun familie, zorgverleners en belangstellenden van belang kunnen zijn. Als er naar aanleiding van deze documenten vragen of opmerkingen zijn, neem dan contact op met Cystinosegroep Nederland. Nederlandstalige brochure over Cystinose. Nephropathic cystinosis: an international consensus document – Emma et al. 2014. Over Cystinose Groep Nederland. Cystinose Groep Nederland is onderdeel van VKS.

2

Wat is Cystinose? - Cystinose

https://cystinose.nl/htdocs/wat_is_cystinose.asp

Cystinose is een zeldzame stofwisselingsziekte. Cystinose kenmerkt zich door een stapeling van het aminozuur cystine in verschillende organen van het lichaam, zoals: nieren, ogen, spieren, alvleesklier en hersenen. Niet alle organen worden tegelijkertijd en in dezelfde mate aangetast. In de meest voorkomende vorm, nefropatische cystinose, worden de nieren als eerste aangetast. Hoe wordt cystinose veroorzaakt? Hoe heeft mijn kind deze ziekte gekregen? Over Cystinose Groep Nederland.

3

Nieuws - Cystinose

https://cystinose.nl/htdocs/nieuws.asp

Sorry, no posts matched your criteria. Over Cystinose Groep Nederland. Cystinose Groep Nederland is onderdeel van VKS.

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elsinosis.com elsinosis.com

Cystinosis Resources | Elsinosis: Living with Cystinosis

https://elsinosis.com/cystinosis-resources

Elsinosis: Living with Cystinosis. A real life account of beautiful Elsie and how she lives with cystinosis. Australian Cystinosis Support Group. Cystinose Selbsthilfe e.V. Grupo de Suporte à Cistinose Nordeste do Brasil. CRF 2014 Hope Through Research. Day in the Life with Cystinosis. Living with Cystinosis: A Closer Look. Know Cystinosis Whiteboard Animation. What is Nephropathic Cystinosis. Cystinosis Family Canada – Famille cystinose Canada. Parents Of Children With Cystinosis Support. Address never ...

cistinosis.org.mx cistinosis.org.mx

Asociación Mexicana de Cistinosis A.C.

http://www.cistinosis.org.mx/interes.html

Asociación Mexicana de Cistinosis. Nuestro Deseo es Ayudarte. Cystinosis Foundation USA - www.cystinosisfoundation.org. Cystinosis Research Foundation - www.natalieswish.org. Cystinosis Research Network - www.cystinosis.org. Cystinosis Foundation UK - www.cystinosis.org.uk. Cystinosis Australia - www.cystinosis.com.au. Cystinosis Alemania - www.leben-eben.com. Cystinosis Foundation Ireland - www.cystinosis.ie. Cystionosis Nederland - www.cystinose.nl. Cystinosis Francia - www.cystinose.org.

rareconnect.org rareconnect.org

Cystinosis, the Community - RareConnect

https://www.rareconnect.org/en/community/cystinosis

Connecting rare disease patients globally. Search and join a community. Search or start a discussion. Living with a rare disease. Discuss with other patients. Welcome - Cystinosis Community. Cystinosis is a lysosomal storage disease characterized by the abnormal accumulation of the amino acid cystine. Source: Participating patient organizations visible below. Published about 1 month ago. 31 years ago I had the good fortune of giving birth to my first daughter, the most beautiful girl in the world, to me!

cystinosis.com.au cystinosis.com.au

Australian Cystinosis Support Group » Links

http://www.cystinosis.com.au/project/links

Larr; Family contacts. What is Cystinosis →. We’ve collated some of the leading websites from around the world that deal with topics relating to the treatment of Cystinosis and and support for families living with the condition. The Cystinosis Foundation, France. Cystinose-Selbsthilfe (Cystinosis Self Help, Germany). CARE: Cystinosis Awareness and Research Effort. Canadian based charity supporting research to improve the quality of life for Cystinosis patients. A USA based charity for Cystinosis research.

cystinosisindia.org cystinosisindia.org

Cystinosis Chapter of India

http://www.cystinosisindia.org/Resources.html

What can we do about it? What YOU can do about it? Http:/ www.cystinosis.org/. Http:/ www.cystinosisfoundation.org/. Http:/ www.natalieswish.com/. Http:/ www.cystinosis.org.uk/. Cystinose-Selbsthilfe (Cystinosis Self Help, Germany). Http:/ www.cystinose-selbsthilfe.de/. Http:/ www.cistinosi.it/. Http:/ www.cystinose.nl/. Http:/ www.charitysa.co.za/cystinosis-support-group-south-africa.html. Http:/ www.cystinosislife.com.

orphan-europe.com orphan-europe.com

Nephropathic cystinosis | Orphan Europe

http://www.orphan-europe.com/patients-and-families/nephropathic-cystinosis

Skip to main content. Big thinking for people with rare diseases. A growing international presence. At the forefront of rare disease policy. Hyperammonaemia due to NAGS, IVA, MMA or PPA. Vitamin E deficiency in chronic cholestasis. Foods for Special Medical Purposes. Urea Cycle Disorders Consortium. Orphan Europe Volunteer Programme. Support to patient organisations. Compliance - our guiding principles. With proper treatment, Nephropathic cystinosis progression can be halted or symptoms can be reduced.

sanne-eijken.nl sanne-eijken.nl

Klanten - Sanne Eijken Kwalitatief Marktonderzoek : Sanne Eijken Kwalitatief Marktonderzoek

http://www.sanne-eijken.nl/referenties

Sanne Eijken Kwalitatief Marktonderzoek. Ik heb mijn sporen in kwalitatief marktonderzoek verdiend aan bureauzijde en besloot in 2010 om zelfstandig verder te groeien. Sindsdien heb ik voor een uiteenlopende klantenkring gewerkt in sectoren als telecom. En de publieke sector. En Dittmeijers’ Research. Tot slot werk ik met veel plezier voor patiëntenorganisaties (bijv. Cystinose Groep Nederland. En culturele instellingen (bijv. Organisatie Oude Muziek. Wat mijn klanten over mij zeggen:.

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Ce nom de domaine n'est pas disponible. Il a été enregistré via gandi.net. More information about the owner. Enregistrer votre nom de domaine. Chez Gandi, vous avez le choix sur plus d'une centaine d'extensions et vous bénéficiez de tous les services inclus (mail, redirection, ssl.). Rechercher un nom de domaine. Votre site dans le cloud? Découvrez Simple Hosting, notre cloud en mode PaaS à partir de 4 HT par mois (-50% la première année pour les clients domaine). It is currently being parked by the owner.

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cystinol.de cystinol.de

Cystinol - bei Blasenentzündungen, wiederkehrenden Blasenerkrankungen & Reizblase

Bei Blasenentzündung and Reizblase. Pflanzlich, schnell, antibakteriell. Wirkt schonend und ursächlich. Vermindert das erneute Aufsteigen von Keimen. Beugt weiteren Entzündungen der Harnwege vor. Zur Akut-Therapie bei Reizblase. Lindert die Beschwerden, löst Krämpfe, wirkt durchspülend. Was ist eigentlich eine Blasenentzündung? Bei einer Zystitis (Blasenentzündung) können Hausmittel bei der Therapie helfen: Es kann helfen ausreichend zu trinken um die Erreger auszuspülen. Nässe, Frost und Blasenschmerzen.

cystinose-selbsthilfe.de cystinose-selbsthilfe.de

Willkommen - Leben-eben! Cystinose-Selbsthilfe e.V.

Leben eben Cystinose Selbsthilfe e.V. Herzlich willkommen bei der Cystinose-Selbsthilfe e.V. Herzlich willkommen - im Leben eben! Mit dieser Seite möchten wir Ihnen möglichst viele Informationen zum Thema Cystinose zur Verfügung stellen. Das Ziel dieser Seite ist, alle Betroffenen, Eltern, Ärzte, Apotheker - kurz jeden, der sich für Cystinose interessiert - auf dem Laufenden zu halten. Durch nationale und internationale Kontakte versuchen wir. Fragen aus dem Alltag zu beantworten. Die gibt es hier. Dass ...

cystinose.fr cystinose.fr

Cystinose France, maladie métabolique caractérisée par l’accumulation anormale d’un acide aminé, la cystine, dans plusieurs organes tels que les reins, les yeux, les muscles, le pancréas et le cerveau | Cystinose France Cystinose.fr

Break' not in the 'loop' or 'switch' context in /homepages/3/d359133160/htdocs/cystinose.fr/modules/imageapi/imageapi gd.module.

cystinose.nl cystinose.nl

Home - Cystinose

Cystinose is een zeldzame stofwisselingsziekte. De aandoening is erfelijk, waarbij ouders meestal niet weten dat ze drager zijn. Informatie omtrent symptomen, erfelijkheid en behandeling hebben we samengebracht op de pagina ‘Wat is cystinose? Presentaties, wetenschappelijke artikelen en andere documenten over cystinose hebben we verzameld in de Kennisbank. Zelf zoeken is niet meer nodig, relevante kennis staat hier. In deze video (2014) vertellen zijn ouders wat voor effect dit heeft op hun gezin.

cystinose.org cystinose.org

Cystinose Will Change Your Business - Starting tips that Matters

Cystinose Will Change Your Business. Starting tips that Matters. February 20, 2018. February 20, 2018. Small Business Tips – How To Cut Your Costs. October 18, 2017. October 18, 2017. Things Not To Do While Hiring Movers Company For Home. October 18, 2017. October 18, 2017. Cases Handled By Criminal Lawyers In Toronto. September 19, 2017. September 20, 2017. Features To Look For When Searching For Tradesman Insurance. September 18, 2017. September 18, 2017. How Can I Show My Talent To People? July 6, 2017.

cystinose.skyrock.com cystinose.skyrock.com

cystinose's blog - ma vie a 10ans - Skyrock.com

Ma vie a 10ans. Bonjour à tous je m'appelle florian rodriguez, j'ai dix ans et je suis atteint d'une maladie, qui se nomme la (CYSTINOSE). Ce blog est fait pour touts les parents qui on envie de suivre mon évolution il sera mis à jour régulièrement au fil de l'évolution de ma maladie. Longue vie à vous tout, et bonne visite dans ma vie.florian. Besançon,Doubs,france (25). 19/07/2007 at 6:04 AM. 30/08/2012 at 2:26 AM. Subscribe to my blog! Please enter the sequence of characters in the field below. Don't ...

cystinosis-thestorysofar.blogspot.com cystinosis-thestorysofar.blogspot.com

Cystinosis - The Story So Far.

Cystinosis - The Story So Far. The journey so far. There was an error in this gadget. Monday, 4 March 2013. Well sorry I haven't posted in a while. Had no laptop but then remembered can use the app on iPhone lol. Trying to remember everything that's happened lately. Mostly it's been good stuff really. Few colds for both girls but have manage to keep them out of hospital! She's back in 2 weeks to be checked again and see if its improved with a patch. Apart from all that she's doing well! She loves all the...

cystinosis.com cystinosis.com

Cystinosis Foundation - Founded in 1983 - Serving Families for Over 25 Years

The Cystinosis Foundation has been hosting family conferences in the U.S. and Europe since 1983. Read about our 9th International Conference and more in the latest Newsletter by. Would you like to participate in the next Cystinosis Clinic at UCSD/ Rady Children's Hospital in San Diego, Ca? To schedule appointments, patients should call. Delayed-release capsules - oral therapy for vital organs. The treatment of Corneal Crystals in Cystinosis Patients. Join Our Email List. A Guide for Parents, Patients,.