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Abnormal Heartbeats May Have Genetic Roots
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Variant changes heart muscle control, study finds
Researchers Make Progress in Understanding Devastating Childhood...
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Researchers identify a second mutation that causes a rare but severe form of childhood cardiac arrhythmia.
Gene variant linked to arrhythmia in African Americanswww.genomenewsnetwork.org/articles/08_02/arrhythmia.shtml
www.genomenewsnetwork.org
"The SCN5A gene has been implicated in several types of arrhythmias," says Igor Splawski, also of Harvard Medical School and Children's ...
Wipo Publishes Patent of Mark Anthony Rutz, Katrin Ulrike...
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GENEVA, June Publication No. WO was published on June 12.Title of the... | Article from US Fed News Service, Including US State News June 13,...
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Igor Splawski, San Francisco, Cook St
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Igor Splawski's Phone & Address | PeopleByName
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Igor Splawski 36 Queensberry St Boston, MA Age 56 (Born Jan 1960). Background Check - Available. Record ID: Igor Splawski E
Network Profiles
WikiGenes - Igor Splawski
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Igor Splawski. Howard Hughes Medical Institute. Department of Cardiology. and Genomics Program and Division of Genetics. Children's Hospital. USA.
Interests
Rare childhood genetic syndrome identified | EurekAlert! Science News
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The study was led by Igor Splawski, PhD, in the Cardiovascular Research Division at Children's Hospital Boston in collaboration with the ...
New Cardiac Arrhythmia Syndrome Identified -- ScienceDaily
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Other members of the team are: Igor Splawski, Leah Sharpe and Mark Keating of the HHMI and Harvard Medical School; Carlo Napolitano, ...
Arrhythmia gene in people of African descent
www.medscape.com
Dr Igor Splawski (Harvard Medical School, Boston, MA) et al looked specifically at the SCN5A gene, a gene known to be implicated in sodium ...
Igor Splawski - Patents
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Igor Splawski patents Recent bibliographic sampling of Igor Splawski patents listed/published in the public domain by the USPTO (USPTO Patent Application #,Title):
Business Profiles
patentbuddy: Igor Splawski
NOVARTIS AG, Winchester, MA, US
Books & Literature
Search | IOVS | ARVO Journals
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Andrew A. Nguyen; Kehao Zhao; Michael Twarog; Elizabeth Deweerd; Jirong Bai; Yiqin Wang; Yong-in Kim; Bijan Etemad-Gilbertson; Igor Splawski; Joy G.
Cardiac Electrophysiology: From Cell to Bedside E-Book: Expert...
books.google.de
... Igor Splawski, Raffaella Bloise, and Carlo Napolitano Chapter 73 Idiopathic Ventricular Fibrillation Rainer Schimpf, Christian Wolpert, and Martin Borggrefe ...
ECG Masters’ Collection: Favorite ECGs from Master Teachers Around ...
books.google.de
Short-coupled TdP is another variant. We would like to acknowledge Dr. G. Michael Vincent, Dr. Shuyan Li, Dr. Igor Splawski, and Dr. Bortolo Martini for each of ...
Ion Channels and Genetic Diseases - Society of General Physiologists...
books.google.de
Acknowledgements The molecular genetic work described in this manuscript was performed in my laboratory by Changan Jiang, Mark Curran, Igor Splawski, ...
Related Documents
The so Called Brugada Syndrome The True History
www.slideshare.net
The syndrome of sudden Death, right bundle branch block and ST elevation was firstly described by A.Nava and B. Martini in , and only five years later…
CiteSeerX — Compound mutations: a common cause of severe long-QT...
citeseerx.ist.psu.edu
BibTeX @MISC{Westenskow_compoundmutations:, author = {Peter Westenskow and Igor Splawski and Katherine W. Timothy and Mark T. Keating and Michael C and …
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder...
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CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism Igor Splawski, Katherine W. Timothy, Leah M. Sharpe, Niels...
Scientific Publications
A molecular basis for cardiac arrhythmia: HERG mutations cause long...
www.sciencedirect.com
, Copyright by Cell Press A Molecular Basis for Cardiac Arrhythmia: HERG Mutations Cause Long QT Syndrome Mark E. Curran,*t Igor Splawski,*t ...
Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac...
www.jstor.org
Every year, ~450,000 individuals in the United States die suddenly of cardiac arrhythmia. We identified a variant of the cardiac sodium channel gene SCN5A that...
Mutations in Danish patients with long QT syndrome and the...
bmcmedgenet.biomedcentral.com
Dr. Igor Splawski, Novartis Institutes for Biomedical Research and Professor Mike Sanguinetti, University of Utah, are thanked for help with information the p.
Timothy syndrome - Conditions - GTR - NCBI
www.ncbi.nlm.nih.gov
Timothy syndrome is a multisystem disorder characterized by cardiac, hand/foot, facial, and neurodevelopmental features Igor Splawski Katherine W Timothy
Publications
Publications Authored by Igor Splawski | PubFacts
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Publications by authors named "Igor Splawski". Are you Igor Splawski? Register this Author. 10Publications. 46Reads. -Profile Views ...
Cardiovascular genomics: recent progress, current challenges, future...
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A report from the second Annual Cardiovascular Genomics Meeting, Sponsored by Cambridge Healthtech, Inc., Miami, January 31-February 1,
Reports & Statements
Wikipedia: Syndrome de Timothy — Wikipédia
Le syndrome de Timothy est une canalopathie très rare puisque seulement 15 cas confirmés ... en ) Igor Splawski, Katherine W Timothy, Silvia G Priori, Carlo Napolitano, Timothy Syndrome in GeneTests: Medical Genetics Information ...
Why and how to add Calcium in the diet of a person with Autism...
pursuenatural.wordpress.com
Cells in the brain contain proteins called calcium channels that can regulate Calcium levels within the cells. Calcium levels inside the cells are 10,000 fold...
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence...
www.nature.com
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity ... Igor Splawski 1, 2, 3, Michael H. Lehmann 6, Hua Li 4, ...
Miscellaneous
Igor Splawski - Head, Novartis Biologics Center (NBC), Cambridge ...
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View Igor Splawski's profile on LinkedIn, the world's largest professional community. Igor has 5 jobs listed on their profile. See the complete profile on LinkedIn ...
WO A2 - Common polymorphism in scn5a implicated in...
patents.google.com
The present invention is directed to a specific mutation in SCN5A which causes drug-induced torsade de pointes or ventricular fibrillation. Persons with the...
WO A3 - C5 antigens and uses thereof Google...
patents.google.com
The present invention pertains to the use of a complement component C5 inhibitor in methods of treatment of ocular disorders and the use of a complement...
EP A1 - Compositions et procédés pour des anticorps ciblant une...
patents.google.com
La présente invention porte sur des anticorps ciblant une protéine du complément C5 et sur des compositions et des procédés d'utilisation de ceux-ci....
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder...
slideplayer.com
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism Igor Splawski, Katherine W. Timothy, Leah M. Sharpe, Niels.
Researcher: Igor Splawski in Publications - Dimensions
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Michael J. Ackerman, Igor Splawski, Jonathan C. Makielski, David J. Tester, Melissa L. Will, Katherine W. Timothy, Mark T. Keating, Gregg Jones, Monica ...
Igor Splawski - Patent applications
www.patentsencyclopedia.com
Patent application number, Description, Published , Molecules and Methods for Modulating Complement Component - Compositions that bind to ...
MOLECULAR GENETICS OF THE LONG QT SYNDROME. Igor Splawski - PDF Free...
docplayer.net
MOLECULAR GENETICS OF THE LONG QT SYNDROME by Igor Splawski A dissertation submitted to the faculty of The University of Utah, in partial fulfillment of the ...
AMD: The Biology of the Genetics | IOVS | ARVO Journals
iovs.arvojournals.org
Andrew A. Nguyen, Kehao Zhao, Michael Twarog, Elizabeth Deweerd, Jirong Bai, Yiqin Wang, Yong-in Kim, Bijan Etemad-Gilbertson, Igor Splawski, Joy G. Ghosh, Michael ...
14 patents go to Utah inventors - Deseret News
www.deseret.com
Fourteen patents were awarded to Utah inventors on March 27. U.S. patents are granted each Tuesday.
Calcium Channel Dysfunction Linked To Autism, Arrhythmia | BioSpace
www.biospace.com
... to treat features of the syndrome with calcium channel blocker therapy, lead author Dr. Igor Splawski, at Harvard Medical School in Boston, ...
Gene Variant Linked to Irregular Heartbeat Found Primarily in People...
www.scientificamerican.com
Scientific American is the essential guide to the most awe-inspiring advances in science and technology, explaining how they change our understanding of the...
(PDF) SCN5A mutations associated with an inherited cardiac...
www.academia.edu
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence...
moh-it.pure.elsevier.com
Changan Jiang, Donald Atkinson, Jeffrey A. Towbin, Igor Splawski, Michael H. Lehmann, Hua Li, Katherine Timothy, R. Thomas Taggart, Peter J. Schwartz, ...
compositions and methods for antibodies targeting complement ...
www.gccpo.org
[72] Inventors:1- Beate Diefenbach-Streiber،2- Adina Eberth،3- Braydon Charles Guild،4- Yong-In Kim،5- Michael Roguska،6- Igor Splawski.
17 new patents granted - Deseret News
www.deseret.com
Seventeen patents were awarded to Utah inventors on July 17. U.S. patents are granted each Tuesday. The new patents include:
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