sharron-harrysstory blogspot.com

Atypical Progeria Syndrome Harrys story

Atypical Progeria Syndrome Harrys story. Meet Harry Crowther our 16 year old son who has an extremely rare genetic disorder known as Atypical Progeria Syndrome Non Classical Progeria whereby Harry has a defect with the LAMIN AC gene LMNA. Though not to be confused with the classical Hutchinson Guilford Progeria Syndrome HGPS - both are Premature Aging Disorders. Harry was diagnosed in the USA aged 7 years old. Monday, 3 August 2015. Monday, 6 April 2015. Memories to last a lifetime. In April Harr.

OVERVIEW

This web page sharron-harrysstory.blogspot.com currently has a traffic ranking of zero (the lower the superior). We have explored nineteen pages inside the domain sharron-harrysstory.blogspot.com and found forty-nine websites referring to sharron-harrysstory.blogspot.com. We were able to observe two social web platforms linked to this website.
Pages Crawled
19
Links to this site
49
Social Links
2

SHARRON-HARRYSSTORY.BLOGSPOT.COM RANKINGS

This web page sharron-harrysstory.blogspot.com has seen a fluctuation levels of traffic within the past the year.
Traffic for sharron-harrysstory.blogspot.com

Date Range

1 week
1 month
3 months
This Year
Last Year
All time
Traffic ranking (by month) for sharron-harrysstory.blogspot.com

Date Range

All time
This Year
Last Year
Traffic ranking by day of the week for sharron-harrysstory.blogspot.com

Date Range

All time
This Year
Last Year
Last Month

LINKS TO WEB SITE

progeria family circle

Researchers, parents and patients meet in Marseille. On Jan 16, the Italian and French research groups that work on Laminopathies met in Marseille. It was a combined meeting for doctors and patients, including parents of children with progeria. Dr De Sandre-Giovannoli explained what steps should all be taken before one can start with a trial.

Progeria Family Circle

Les chercheurs, les parents et les patients se sont rencontrés à Marseille. Le 16 janvier dernier les chercheurs italiens et français qui étudient les laminopathies se sont rencontrés à Marseille. Les laminopathies comprennent toutes les maladies, incluant la progéria, causées par un fonctionnement anormal du gène LMNA qui produit les lamines A et C.

progeria el síndrome de Hutchinson-Gilford

Cuando Néstor se acercó hasta el laboratorio de Carlos López Otín en Oviedo, todo indicaba que el tipo de envejecimiento prematuro que sufría sería del tipo Hutchinson-Gilford, el mismo que el investigador asturiano estaba estudiando tratar dentro de un ensayo internacional. Describen un nuevo tipo de envejecimiento acelerado.

WHAT DOES SHARRON-HARRYSSTORY.BLOGSPOT.COM LOOK LIKE?

Desktop Screenshot of sharron-harrysstory.blogspot.com Mobile Screenshot of sharron-harrysstory.blogspot.com Tablet Screenshot of sharron-harrysstory.blogspot.com

SHARRON-HARRYSSTORY.BLOGSPOT.COM HOST

Our parsers identified that a lone page on sharron-harrysstory.blogspot.com took one thousand six hundred and thirty-two milliseconds to come up. We could not find a SSL certificate, so our crawlers consider sharron-harrysstory.blogspot.com not secure.
Load time
1.632 secs
SSL
NOT SECURE
Internet Protocol
74.125.228.234

WEBSITE IMAGE

SERVER OS AND ENCODING

I found that this domain is operating the GSE server.

PAGE TITLE

Atypical Progeria Syndrome Harrys story

DESCRIPTION

Atypical Progeria Syndrome Harrys story. Meet Harry Crowther our 16 year old son who has an extremely rare genetic disorder known as Atypical Progeria Syndrome Non Classical Progeria whereby Harry has a defect with the LAMIN AC gene LMNA. Though not to be confused with the classical Hutchinson Guilford Progeria Syndrome HGPS - both are Premature Aging Disorders. Harry was diagnosed in the USA aged 7 years old. Monday, 3 August 2015. Monday, 6 April 2015. Memories to last a lifetime. In April Harr.

CONTENT

This web page sharron-harrysstory.blogspot.com states the following, "Meet Harry Crowther our 16 year old son who has an extremely rare genetic disorder known as Atypical Progeria Syndrome Non Classical Progeria whereby Harry has a defect with the LAMIN AC gene LMNA." We saw that the webpage said " Though not to be confused with the classical Hutchinson Guilford Progeria Syndrome HGPS - both are Premature Aging Disorders." It also said " Harry was diagnosed in the USA aged 7 years old. Monday, 3 August 2015. Monday, 6 April 2015. Memories to last a lifetime."

SEEK SIMILAR DOMAINS

E business and E marketing

Accessorise Your Dreams With The Ultimate Wealth Complex. Hello everybody my name is Sharon and welcome to my blog. The purpose of this blog is to show amateurs and professionals new ways of working from home. I am always looking out for new ways to generate income or incentives and i hope you find something that tickles your interest and eventually suit at least one of your needs! Please leave a comment, all is welcome. What do you think of this blog? .

Sharron Angle Reno, NV 89507

Join me in my battle against Politics As Usual. Website paid for by Our Voice PAC.