LNA - Association Lesch-Nyhan Action
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The Association of Italian families involved. In the fight against the Lesch-Nyhan. SUPPORT THE INITIATIVES OF FAMILIES. Lesch-Nyhan Syndrome is a very rare disease that has severe implications on affected people and their families life. Books, thesis and articles. In this section you can download theses, books and articles on the Lesch-Nyhan syndrome. Reserved Area for the families. Please enter your username and password.
ESTE BLOG FOI CRIADO PARA INFORMAR A TODOS QUE O VISITEM QUEM É JOAQUIM E O QUE PODE SER FEITO PARA AJUDÁ-LO. A SUPERAR AS CONSEQUÊNCIAS DE UM PARTO COM COMPLICAÇÕES. INFORME-SE SOBRE NOSSA CAMPANHA, AJUDE A DIVULGÁ-LA E CONTRIBUA. Quarta-feira, 23 de outubro de 2013. Tudo bem com todo mundo? Comigo, tudo ótimo! E com um nome esquisito. É! Na França, há uma.
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Association Francaise Lesch-Nyhan Action Maladie Genetique
Administrateur Web LNA
8, rue Andre Malraux
Saint-Sever, 40500
FR
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Site de lAssociation Française Lesch-Nyhan Action.Pour le soutien aux familles et à la recherche médicale sur la maladie de Lesch-Nyhan.CONTENT
This web site lesch-nyhan-action.org had the following in the homepage, "Journée Internationale des Maladies Rares." We noticed that the website stated " Dans le cadre de la." It also said " Journée Internationale des Maladies Rares. 28 Février, nous vous proposons de renouveler votre adhésion à lassociation Lesch-Nyhan Action LNA. La cotisation est de 20 EUR et elle est assimilable à un don vous recevrez donc un reçu fiscal vous permettant den déduire 66 de vos impôts. Merci à tous nos adhérents, anciens et nouveaux! Nous esp."SEEK SIMILAR WEBSITES
The Association of Italian families involved. In the fight against the Lesch-Nyhan. SUPPORT THE INITIATIVES OF FAMILIES. Lesch-Nyhan Syndrome is a very rare disease that has severe implications on affected people and their families life. Books, thesis and articles. In this section you can download theses, books and articles on the Lesch-Nyhan syndrome. Reserved Area for the families. Please enter your username and password.
Official website of the Lesch-Nyhan Disease International Study Group. The content is written for everyone, at all levels of experience. Each section starts with general information that is written for patients, family members and caretakers. More detailed information, intended for physicians and researchers, can be accessed via submenus and links from the introductory section. If necessary, feel free to contact the authors. HAJ and JEV 2006 2018.
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