NICHD - News Releases

All News releases related to Turner Syndrome

Your search for: All Related News Releases All Years returned the following 53 results:

10/28/09		NIH-Funded Researchers Transform Embryonic Stem Cells Into Human Germ Cells
Researchers funded in part by the National Institutes of Health have discovered how to transform human embryonic stem cells into germ cells, the embryonic cells that ultimately give rise to sperm and eggs. The advance will allow researchers to observe human germ cells—previously inaccessible—in laboratory dishes.

10/19/09		NIH Newborn Screening Research Program Named In Memory of Hunter Kelly
The National Institutes of Health today announced the establishment of a research program to enhance newborn screening, in memory of the son of National Football League Pro Football Hall of Fame quarterback Jim Kelly.

09/21/09		Item of Interest: Public Comment on the DRAFT Intellectual and Developmental Disabilities (IDD) Branch Report to Council
Each component of the NICHD reports its activities to the National Advisory Child Health and Human Development (NACHHD) Council, the federal advisory committee for the NICHD. The NACHHD Council follows all regulations set forth in the Federal Advisory Committee Act.

07/20/09		NIH Issues Research Plan on Fragile X Syndrome and Associated Disorders
The National Institutes of Health has developed a research plan to advance the understanding of fragile X syndrome and its associated conditions, fragile X-associated tremor/ataxia syndrome and fragile X-associated primary ovarian insufficiency. Fragile X syndrome causes intellectual and developmental disabilities and results from a mutation in a gene on the X chromosome.

07/14/09		New Technique Could Sustain Cancer Patients' Fertility
Researchers funded by the National Institutes of Health have completed a critical first step in the eventual development of a technique to retain fertility in women with cancer who require treatments that might otherwise make them unable to have children.

06/19/09		Delay in Diagnosis of Menopause-like Condition in Young Women Linked to Low Bone Density
Women and young girls who experience delays in diagnosing a premature, menopause-like condition face increased risk of low bone density, according to new research by scientists at the National Institutes of Health. A delay in diagnosing the condition, called primary ovarian insufficiency, may make women more susceptible to osteoporosis and fractures later in life, the researchers concluded.

06/11/09		Item of Interest: Public Comment on the DRAFT Endocrinology, Nutrition, and Growth (ENG) Branch Report to Council
A draft of the ENG Branch Report to the NACHHD Council is now available.

05/14/09		Researchers Identify Key Proteins Needed for Ovulation
Researchers from the National Institutes of Health and other institutions have identified in mice two proteins essential for ovulation to take place.

02/05/09		Plan Offers Guidance For Evaluating Menopause-Like Condition in Girls and Young Women
A comprehensive plan to help health care professionals diagnose and treat primary ovarian insufficiency—a menopause-like condition affecting girls and young women that may occur years before normal menopause is expected—has been developed by a scientist at the National Institutes of Health.

08/27/08		Common Treatment to Delay Labor Decreases Preterm Infants' Risk for Cerebral Palsy
Preterm infants born to mothers receiving intravenous magnesium sulfate—a common treatment to delay labor—are less likely to develop cerebral palsy than are preterm infants whose mothers do not receive it, report researchers in a large National Institutes of Health research network.

05/29/08		NIH Researchers Find That Rett Syndrome Gene is Full of Surprises
A study funded by the National Institutes of Health (NIH) has transformed scientists' understanding of Rett syndrome, a genetic disorder that causes autistic behavior and other disabling symptoms. Until now, scientists thought that the gene behind Rett syndrome was an "off" switch, or repressor, for other genes. But the new study, published today in Science1, shows that it is an "on" switch for a startlingly large number of genes.

04/01/08		Newly Awarded Autism Centers of Excellence to Further Autism Research
The National Institutes of Health (NIH) announced on April 1, 2008, the latest recipients of the Autism Centers of Excellence (ACE) program. These grants will support studies covering a broad range of autism research areas, including early brain development and functioning, social interactions in infants, rare genetic variants and mutations, associations between autism-related genes and physical traits, possible environmental risk factors and biomarkers, and a potential new medication treatment.

03/27/08		Gene Variation Predicts Response to Treatment in Common Infertility Disorder
NIH-sponsored researchers have discovered that women who have polycystic ovary syndrome (PCOS) are less likely to ovulate in response to a promising new drug treatment for the condition if they have a variation in a particular gene.

01/29/08		Thin Bones Seen In Boys with Autism and Autism Spectrum Disorder
Results of an early study suggest that dairy-free diets and unconventional food preferences could put boys with autism and autism spectrum disorder (ASD) at higher than normal risk for thinner, less dense bones when compared to a group of boys the same age who do not have autism.

01/22/08		NIH Develops Down Syndrome Research Plan
The National Institutes of Health has developed a research plan to advance understanding of Down syndrome and speed development of new treatments for the condition, the most frequent genetic cause of mild to moderate intellectual disability and associated medical problems. The plan sets research goals for the next 10 years that build upon earlier research advances fostered by the NIH.

Page 1 2 3 4 >

If you are a member of the media and have questions about an NICHD news release or research, or if you would like to schedule an interview with an NICHD scientist or grantee, please contact the Public Information and Communications Branch at 301-496-5133 or by fax at 301-496-7101.