eurowilson.org - Report a new case - Latest News
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Asociación española de familiares y enfermos de Wilson. Apoyo a pacientes y familias. En la actualidad existen varias investigaciones relacionadas con la enfermedad de Wilson. Esta Asociación quiere recabar datos sobre el mayor número de enfermos posible con la única intención de aportar un. 8211; Recabar la máxima información de la enfermedad de Wilson, facilitada por los pacientes.
Studien aus der ganzen Welt verdeutlichen den unzureichenden Vitamin D-Status in der Bevölkerung. Wir tragen Sorge für Menschen mit der seltenen Kupferspeicherkrankheit. Wir bieten medizinische Hilfe bei Vergiftungen mit Schwermetallen und Kontaminationen mit Radionukliden. Vitamine sind unverzichtbar für viele lebenswichtige Funktionen des menschlichen Körpers. Diese organischen Verbindungen kann .
Big thinking for people with rare diseases. 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. Compliance - our guiding principles. Private section for Healthcare Professionals.
Swiss Association for the Study of the Liver. Tel 043 268 79 64. IBAN CH85 0900 0000 3000 8596 4. SASL Day of the Liver. 2 Dec 2015, 1100h-1800h. 2nd Swiss Hepatology Postgraduate Course. November 26th to 28th 2015. Wolfsberg Executive Development Center CH 8272 Ermatingen. SASL School Number 9, Monday, 31 Aug 2015, 1730h-1900h. David Semela, Kantonsspital St. SASL School Number 10, Monday, 14 Dec 2015, 1730h-1900h.
It affects about one in thirty thousand people worldwide. Saturday, March 19, 2005.
WilsonPatientforeningen støtter patienter og deres pårørende ved at informere og oplyse om sygdommen og via gensidig erfaringsudveksling. Vi arbejder for den højest mulige kvalitet i diagnostik og behandling af alle Wilsonpatienter. Specielt nydiagnosticerede og deres familier kan have mange problemer og spørgsmål, som kan være vanskelige at overskue.
WDSG-UK was granted charitable status by HMRC in 2010 and is recognised as a charitable company. As such, WDSG-UK is entitled to claim Gift Aid back on donations, where appropriate. If you wish to make a donation to WDSG-UK and to Gift Aid it, please complete this form. If you are at all interested, please join. WDSG-UK - A support group for all. This is the official website. WDSG-UK was founded in the year .
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Living with wilsons disease. The EuroWilson website contains information about Wilson disease that we. Believe might be of interest to patients, family members and health care. Professionals. We strive to ensure that the contents are correct and up-to-date. The website is under the responsibility of a scientific committee whose members all have expertise in Wilson disease. Its object is to disseminate information, but not to be a substitute for consultation with healthcare professionals.PARSED CONTENT
The web page states the following, "The EuroWilson website contains information about Wilson disease that we." We saw that the web site said " Believe might be of interest to patients, family members and health care." It also said " We strive to ensure that the contents are correct and up-to-date. The website is under the responsibility of a scientific committee whose members all have expertise in Wilson disease. Its object is to disseminate information, but not to be a substitute for consultation with healthcare professionals."SEEK SUBSEQUENT BUSINESSES
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