Noonan Syndrome
Links shared publicly online about this topic
Pediatrics and Medicine: Noonan Syndrome
pedmedicine.blogspot.com — “Health News by an Assistant Professor at University of Chicago, Internist and Allergist” View full resource at pedmedicine.blogspot.com
Most Recently Shared on October 8, 2010 at 5:12 am By:
Ves Dimov, M.D. Allergist, Physician, Doctor, and Internist
Noonan Syndrome http://t.co/qfJcK5S
Noonan Syndrome: eMedicine Pediatrics: Genetics and Metabolic Disease
emedicine.medscape.com — “Overview: Noonan syndrome was first recognized as a unique entity in 1963 when Noonan and Ehmke described a series of patients with unusual facies and multiple malformations, including congenital heart disease. These patients were previously thought to ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 16, 2010 at 9:23 pm By:
Medscape Pediatrics Health Site and Pediatrics
We've updated our Noonan Syndrome article at http://bit.ly/b4v8vy. #pediatrics #genetics #geneticdisease
Possible New Drug Targets For The Genetic Disorder Noonan Syndrome
medicalnewstoday.com — “Noonan syndrome is a relatively common genetic disorder characterized by short stature, unique facial features, and heart defects. About 10%-15% of affected individuals have mutations in their SO” View full resource at medicalnewstoday.com
Most Recently Shared on November 2, 2010 at 5:05 pm By:
Possible New Drug Targets For The Genetic Disorder Noonan Syndrome http://mnt.to/3LYk #genetics
Noonan Syndrome-Findings from University Children\'s Hospital broaden unders...
newsrx.com — “World's Largest Source of Health Information. Health, Medical, Biotech, Legal, Business & Clinical Research News for Professionals and Knowledgeable Consumers.” View full resource at newsrx.com
Most Recently Shared on May 18, 2009 at 1:01 pm By:
NewsRx Medical News Health News
Findings from University Children's Hospital broaden understanding of Noonan syndrome in...http://bit.ly/cYrnb
Medical News: ENDO: GH Therapy Adds Inches in Noonan Syndrome - in Meeting Coverage, ENDO from MedPage Today
medpagetoday.com — “SAN DIEGO -- Children with the autosomal dominant congenital disorder Noonan syndrome may benefit from treatment with growth hormone, researchers said here.” View full resource at medpagetoday.com
Most Recently Shared on June 25, 2010 at 10:05 am By:
Endocrinology Wisdom OW Health
ENDO: GH Therapy Adds Inches in Noonan Syndrome (CME/CE): SAN DIEGO (MedPage Today) -- Children with the autosomal... http://bit.ly/9Wop9z
JCI - Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome–like phenotype and hyperactivated MAPK signaling in humans and mice
jci.org — “JCI - Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome–like phenotype and hyperactivated MAPK signaling in humans and mice” View full resource at jci.org
Most Recently Shared on August 2, 2011 at 8:47 pm By:
Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactiv... http://bit.ly/qed4CO #adhd
Ulerythema: eMedicine Dermatology
emedicine.medscape.com — “Overview: Ulerythema ophryogenes, a rare cutaneous disorder, is characterized by inflammatory keratotic facial papules that may result in scars, atrophy, and alopecia. This disorder has been described in association with other congenital anomalies such as Noonan syndrome, ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:18 pm By:
Julie Bohlen Health Executive and Active Health Library
Ulerythema ophryogenes is a relatively infrequent disorder that mainly affects children and young adults. Learn causes. http://bit.ly/aewdJc
News From The Journal Of Clinical Investigation: Feb. 21, 2011
medicalnewstoday.com — “CARDIOLOGY: Possible new approach to treating two related multi-organ syndromesLEOPARD syndrome and Noonan syndrome are two genetic conditions caused by mutations that affect the” View full resource at medicalnewstoday.com
Most Recently Shared on February 22, 2011 at 2:29 pm By:
MedicalNewsToday: News From The Journal Of Clinical Investigation: Feb. 21, 2011 http://bit.ly/fHLIqi Full http://bit.ly/i4Xgju
News From The Journal Of Clinical Investigation : August 1, 2011 - QualityPoint Technologies
qualitypointtech.net — “CARDIOLOGY: New mechanism underlying Noonan-like syndrome Noonan syndrome is an inherited disorder characterized by the abnormal development of several parts of the body, including the heart. Genetic mutations that lead to hyperactivation of the RAS/MAPK signaling pathway have been shown to cause the condition in the majority of patients. A team of researchers, led by Christian Thiel, at Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, has now identified the genetic cause of disease ” View full resource at qualitypointtech.net
Most Recently Shared on August 3, 2011 at 8:45 am By:
News From The Journal Of Clinical Investigation : August 1, 2011: CARDIOLOGY: New mechanism underlying Noonan-like... http://bit.ly/p8PFN6
ROCK off: Study establishes molecular link between genetic defect and heart malformation — News Room - UNC Health Care
news.unchealthcare.org — “The study also shows that treatment with a drug that regulates cell shape rescues the cardiac defect, pointing to therapeutic avenues that could one day benefit Noonan syndrome patients.” View full resource at news.unchealthcare.org
Most Recently Shared on February 6, 2012 at 7:45 pm By:
ROCK off: Study establishes molecular link between #genetic defect and #heart malformation. http://t.co/pGrMwSlc
CGC Genetics Introduces Test For Molecular Diagnosis Of Noonan And Other Genetically Related Syndromes
medicalnewstoday.com — “CGC Genetics offers a broad menu of over 1,500 molecular diagnostic, cytogenetic and clinical genomic CLIA laboratory tests that cover all the major disciplines of medicine. One of the company's” View full resource at medicalnewstoday.com
Most Recently Shared on December 6, 2010 at 2:11 pm By:
Drugs and Devices OW OW Health
CGC Genetics Introduces Test For Molecular Diagnosis Of Noonan And Other Genetically Related Syndrome... http://mnt.to/f/3NBg #MedDevice
Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations - Capalbo - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
onlinelibrary.wiley.com — “Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations - Capalbo - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library” View full resource at onlinelibrary.wiley.com
Most Recently Shared on March 15, 2012 at 10:31 am By:
Noonan‐like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurologic... http://t.co/BoLcyWce
The Top 3 resources shared on this topic. More resources.
Key stats and trends about this topic
Related WisdomCards
Related Health Centers
Featuring the top 3 experts for this topic
-
Ves Dimov, M.D.
Assistant Professor at University of Chicago, Allergist/Immunologist, Internist. Former Cleveland Clinic Assistant Professor and NEJM Advisory Panel Member.
-
Medscape Pediatrics
Latest medical news, articles, and features from Medscape Pediatrics
-
MNT Genetics News
The latest genetics news published daily. Articles from research centers, universities and prestigious journals.
Advertisement
