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GFMN - Home | galactosemia-mn.com Reviews
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Forums - GFMN
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GFMN Items for Sale. View: normal / recent topics. Over a year ago. 1 topics 1 posts. Last post: over a year ago by xxleannexx.
Photo Gallery - GFMN
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GFMN Items for Sale. 124; Most Commented. 15 Photos Updated November 1, 2015. 4 Photos Updated October 24, 2014. 10 Photos Updated May 25, 2014. 3 Photos Updated October 20, 2013. Newborn Screening 50th Anniversary Traveling Disply. Newborn Screening 50th Anniversary Traveling Di. 5 Photos Updated May 12, 2013. 7 Photos Updated May 12, 2013. 2012 Galactosemia Foundation Conference. 2012 Galactosemia Foundation Conference. 48 Photos Updated October 18, 2012. 17 Photos Updated September 30, 2012.
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GFMN Items for Sale. Oops, you forgot something. The words you entered did not match the given text. Please try again. 9:54 PM on December 2, 2012. Thank you so much for the basket that you put together for me and my son Gavin. Gavin will be turning 1 year old on Saturday and it's very intimidating putting a child that has dairy, egg and peanut allergy on solid foods. Thank you for being an awesome resource!
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Links | GalNet
http://www.galnet.mumc.betawerk.eu/links
European Comission expert on rare diseases. International Rare Disease Research Consortium - IRDiRC. Classic galactosemia or Type I galactosemia. GALK deficiency or Type II galactosemia. GALE deficiency or Type III galactosemia. National Organization for Rare Disorders - NORD:. Classic galactosemia and related disorders. European Galactosaemia Society - EGS. Australian Galactosaemia Support Network - AGSN. Galactosemia Association of Midwest America - GAMA. Galactosemic Families of Minnesota - GFMN.
Links | GalNet
https://www.galactosemianetwork.org/links
European Comission expert on rare diseases. International Rare Disease Research Consortium - IRDiRC. Classic galactosemia or Type I galactosemia. GALK deficiency or Type II galactosemia. GALE deficiency or Type III galactosemia. National Organization for Rare Disorders - NORD:. Classic galactosemia and related disorders. European Galactosaemia Society - EGS. Australian Galactosaemia Support Network - AGSN. Galactosemia Association of Midwest America - GAMA. Galactosemic Families of Minnesota - GFMN.
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galactose (no questions, no lies.) | DeviantArt
Window.devicePixelRatio*screen.width 'x' window.devicePixelRatio*screen.height) :(screen.width 'x' screen.height) ; this.removeAttribute('onclick')". No questions, no lies. No questions, no lies. Deviant for 16 Years. This deviant's full pageview. No questions, no lies. Last Visit: 462 weeks ago. No questions, no lies. 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. Coursing ...
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galactose88's blog - la gactosémie, c'est une maladie génétique... - Skyrock.com
La gactosémie, c'est une maladie génétique. Je vais, tout au long de mon blog, vous présenter ma maladie qui s'appelle la galactosémie.Vous verrez que c'est pas drôle! 31/03/2007 at 10:28 AM. 15/11/2009 at 10:13 AM. Subscribe to my blog! Pour tous ce qui n'ont pas cette maladie:je vais vous la présenter à ma façon! Posted on Sunday, 01 April 2007 at 8:28 AM. Voici un extrait de cette maladie rare :. Posted on Sunday, 01 April 2007 at 8:32 AM. Les signes de la maladie. Les signes cliniques apparaissent da...
galactosemia-biobio.blogspot.com
Galactosemia
A galactosemia é um erro inato do metabolismo (de característica autossômica recessiva), caracterizado por uma inabilidade em converter galactose em glicose da maneira normal. O resultado imediato é o acúmulo de metabólitos da galactose no organismo, que passa a ter níveis circulantes elevados e tóxicos, principalmente para o fígado, cérebro e olhos. Em um fígado normal, a maioria da galactose é convertida em glicose em pouco tempo. Normalmente a via segue a seguinte ordem:. Caso haja algum problema com ...
GFMN - Home
GFMN Items for Sale. Donate now to GFMN. Donate to GALACTOSEMIC FAMILIES OF MINNESOTA. Welcome to Galactosemic Families of MN (GFMN). We are a group of families from Minnesota and the surrounding states living with galactosemia. We were founded in 1998. Why are We Here? One in 80,000 children will be born with galactosemia. The purpose of GFMN is three fold:. To provide support & education information to galactosemic families & interested professionals. Galactosemic Families of MN (GFMN).
Galactosemia
Galactosemia is an inherited disease where the transformation of galactose to glucose is blocked, allowing galactose to increase to toxic levels in the body. If Galactosemia is untreated, high levels of galactose cause vomiting, diarrhea, lethargy, low blood sugar, brain damage, jaundice, liver enlargement, cataracts, susceptibility to infection and death. London, Ontario, Canada. View my complete profile. What is Classic and Duarte Galactosemia? The History of Galactosemia. Books, Phamplets, etc. A pers...
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Galactosemia Foundation
Fundraise by Shopping or Web Searching! Fundraising and Education Events. Fundraise by Shopping or Web Searching! Fundraising and Education Events. Help support research by joining this patient driven database. Mar 3, 2018. Registration is now open for the 2018 Conference! Mar 3, 2018. Mar 3, 2018. Jul 23, 2017. Denver 2018 Conference Planning. Jul 23, 2017. Jul 23, 2017. Mar 4, 2017. 14 Applications for GF Grants. Mar 4, 2017. Mar 4, 2017. We are glad that you found us! Click to learn more.
Galactosemia
Lunes, 14 de enero de 2008. 191;Qué es la galactosemia? La galactosemia es una enfermedad hereditaria cuyo entendimiento precisa del conocimiento de ciertas nociones elementales en relación con una sustancia llamada galactosa. La galactosa es un azúcar simple como también lo es la glucosa. La fuente principal de este azúcar es la lactosa ("azucar de la leche"), otro azúcar más complejo pues resulta de la unión de una galactosa con una glucosa. 191;Qué alimentos contienen lactosa y, por tanto, galactosa?
Galactosemia
Quarta-feira, 3 de dezembro de 2008. Terça-feira, 25 de novembro de 2008. Aqui está um link do depoimento da Stacey Taylor que possui Galactosemia. Ela contas seus sofrimentos e dificuldades durante a vida mas também mostra sua alegria pelo nascimento de seu filho assim como sua esperança de ajudar as pessoas. It has been nearly 30 years of feeling alone, although I have now broken free of those chains it has been 30 years too long.". Vale a pena ler! Segunda-feira, 24 de novembro de 2008. Achei um artig...
