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Pediatric Endocrine Society
Formerly Named in Honor of Lawson Wilkins
The Lawson Wilkins Pediatric Endocrine Society founded in 1972 has officially changed its name to Pediatric Endocrine Society. This important step to change the organization’s name comes as a result of a strategic planning exercise in which the membership of the Society has redefined itself beyond prior boundaries, a change in identity that will accompany this change in name.
The Mission of Society is to advance the care of children and adolescents with endocrine disorders. The vision of the Society is to become the North American medical organization in the field of pediatric endocrinology that is:
The Society has reorganized its internal committee structure and engaged a
team of experienced association management professionals to assist the Society
and its membership in meeting these challenging Strategic Objectives. The membership
overwhelmingly voted to approve the name change in order that PES might more
easily be identified by other professional societies, governmental agencies,
industry manufacturers and parents.
Our new site is underdevelopment and will be ready by July 2010.
2010 Officer Elections
The results of the 2010 Elections are:
President Elect - Janet Silverstein
Secretary - Peter Lee
Director - Stephen Rosenthal
Thank you to all who voted.
Study Network of Pediatric Endocrinology (SNoPE)
After a 24 month gestation, we are proud to announce the delivery of SNoPE (Study Network of Pediatric Endocrinology) on the members only portion of the PES website http://www.lwpes.org/professionals/snope/index.cfm. SNoPE is an exciting and potentially useful creation which will grow and develop with time. All the parts seem to be working well. SNoPE is there for you to use for collaborative interactions among centers, investigators and fellows. SNoPE lives in the “Gateway” within the PES website and contains:
1. SNoPE sponsored studies to which you are invited to join (currently 2).
a. Predictors of Stress, Parental Overprotection and Perceived Child Vulnerability among Parents of Children Affected by Disorders of Sex Development (DSDs), Steven Chernausek and Amy Wisniewski (PIs)
b. SNoPE Multicenter Study of the Outcomes of Estrogen Replacement in Pubertal-Aged Girls with Turner Syndrome, Judy Ross (PI)
2. Protocols initiated by individuals which you can join or you can initiate
your own collaborative study (ies). The current listed protocols
are:
a)Investigator Initiated Study in rhGH treated patients with Turner Syndrome comparing two low doses of estradiol by patch to induce puberty - Dr. Robert Rosenfield, PI
b
) a study of the effect of beta cell
rest in adolescents and young adults with type 2 diabetes with
Kristina Rother as PI and
c)
the Neonatal Diabetes Mellitus Registry with Louis Philipson
as PI.
3. A search engine on the Gateway for protocols by investigator(s), topic,
and title.
NIH Launches New Web Site for Parents on Medical Research
The National Heart, Lund and Blood Institute (NHLBI), in
partnership with other NIH Institutes, has created a comprehensive
website designed to give parents and healthcare providers
alike the information needed to understand clinical research
in children and make informed decisions about participating
in a study.
In a format geared to all educational levels, the website combines text, graphics, and documentary film interviews with experts, parents, and children themselves to give viewers an "inside view" of pediatric clinical research. It can assist caregivers in answering patients' questions about research. Families who are contemplating enrolling their child in a clinical study can use the information to augment their understanding and complement the informed consent process. The site has sufficient content to be used as an educational tool for trainees and junior faculty about the key concepts of pediatric clinical research. Based on focus groups, we organized the information into easily-accessible chapters for locating information quickly, something often needed in emergency research. The content is not copy-writed and the DVD-based documentaries may be downloaded to run in waiting rooms or hospital libraries.
The "No More Hand-Me-Downs: Research Designed for
Children" theme of the website represents the thinking
of our many colleagues across NIH, DHHS, the research community.
Please visit the site at:
www.ChildrenAndClinicalStudies.nhlbi.nih.gov
Please contact the NHLBI directly if you have any questions or comments.