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ISPAD Newsletter Spring 2003

Dear members
The contents of this letter are very important so please take time to read them and respond to the requests by the appropriate deadline dates.

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ISPAD Newsletter 2002

The past three years have been exciting times for ISPAD. The new Constitution will come in to force in September opening the Society to all health professionals committed to research, clinical care and advocacy in all forms of childhood diabetes.

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ISPAD Newsletter 2001

Dear Friends
The next ISPAD's scientific meeting will be held in Siena, September 19th-22nd 2001. This will be a very important meeting. The proposed changes to the ISPAD Constitution will be voted on and will determine the direction of the Society.

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ISPAD Newsletter 2000

ISPAD has started the new millenium with growth and an optimistic vision for the future. The membership has increased in all parts of the world, the new website has improved communication, the new Consensus Guidelines for the Management of Diabetes in Children and Adolescents are finalized, the ISPAD Science School is starting, and the future Annual Meetings are well planned...

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ISPAD Newsletter 1998

Seasonal Greetings to all members!
By the end of 1998 ISPAD is still growing stronger. By 1. November we had 431 members. We have welcomed 64 new members the last year...

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ISPAD Newsletter Summer 2012

Click the link and read ISPAD Newsletter: Spring/Summer 2012

Dear ISPAD member,
On behalf of the ISPAD Steering Committee I wish to update you on the recent (Summer 2012) developments.

 

The EURO-WABB project

The EURO-WABB project is a European rare disease registry for Wolfram, Alstrom, Bardet Biedl (WABB), Thiamin responsive megaloblastic anaemia, and Wolcott Rollison syndromes. The ISPAD contact persons are Prof Timothy Barrett
(t.g.barrett@bham.ac.uk) and Prof Wojciech Mlynarski (Wojciech.Mlynarski@joslin.harvard.edu).

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The International Wolfram Registry

The International Wolfram Registry is led from Washington University, St Louis, USA by Prof Alan Permutt. The registry is open to patients from all over the world. The ISPAD contact person for this registry is Prof Neil White (White_N@kids.wustl.edu).

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ISPAD Rare Diabetes

The ISPAD Rare Diabetes in Exeter led by Prof. Andrew Hattersley (andrew.hattersley@pms.ac.uk) is the central clearing house for all enquiries from ISPAD members about rare diabetes. It is a resource for information about all forms of diabetes, and offers molecular genetic testing on most monogenic forms of diabetes. If the person (even if an adult today) was diagnosed with diabetes before age 6 months, this analysis is done for free (except for shipping costs).

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