Loading...
Images of Elon Pras
(0 from 0 )1
0
0
News
NaturalNewsBlogs Brain development requires asparagine for normal...
naturalnewsblogs.com
... James O. McNamara, Guy A. Rouleau, Debra L. Silver, Doron Lancet, Elon Pras, Grant A. Mitchell, Jacques L. Michaud, David B. Goldstein.
Telephone & Addresses
Elon Pras, 58, Rockville, US, Congressional Ln, Apt T3
View Elon's social profiles and photos on Facebook, MySpace, and +40 Networks.
Elon Pras, Rockville, US, Rollins Ave
View Elon's social profiles and photos on Facebook, MySpace, and +40 Networks.
Network Profiles
Pras Elon - publications and coauthors
scicurve.com
Overview of Pras Elon research, his coauthors and publications
Interests
Scientists identify a gene causing a fatal heart condition, common in...
www.eurekalert.org
... Dr. Elon Pras, decided to approach Weizmann Institute scientists for help. At the Institute Drs. Olender and Avidan initially had little success, ...
New genetic cause of Coats plus syndrome -- ScienceDaily
www.sciencedaily.com
A team of Israeli researchers has discovered that mutations in STN1, a gene that helps maintain the ends of chromosomes, cause the rare, inherited disorder...
Breakthrough Genetic Test For WomenÂs Hair Loss Now Available
www.prweb.com
... Head of the Crown Human Genome Center at the Department of Molecular Genetics, Weizmann Institute of Science, Dr Elon Pras, Director of ...
Business Profiles
patentbuddy: Elon Pras
Ramat Efal, IL, US
Just a moment...
www.zoominfo.com
View Elon Pras's business profile as Associate Professor Position at Sackler School of Medicine and see work history, affiliations and more.
Books & Literature
Search | IOVS | ARVO Journals
iovs.arvojournals.org
Almogit Abu; Moshe Frydman; Dina Marek; Eran Pras; Chaim Stolovitch; Ayala Aviram-Goldring; Shlomit Rienstein; Haike Reznik-Wolf; Elon Pras. TAGS: dna ...
Advanced Search | American Society of Nephrology
jasn.asnjournals.org
No information is available for this page.
Molecular Vision: Articles by the Authors
www.molvis.org
Articles by the Authors. Articles by Emre Zafer. Articles by Jeanne Meck. Articles by Liora Gerrad. Articles by Elon Pras. Articles by Moshe Frydman
Manufacturing Engineering: and Beyond - Google Books
books.google.co.uk
CLINICAL HETEROGENEITY IN FAMILIAL MEDITERRANEAN FEVER Eran Pras1, Avi Livneh1,2, James E.Balow Jr.3, Elon Pras\ Daniel L. Kastner3. Mordechai Pras1 2. Pnina Langevitz1'2,. Department of Medicine 'F and 4C. 2Heller Institute for Medical Research. Sheba Medical Center, Tel-Hashomer, Israel. 3Arthritis ...
Related Documents
CiteSeerX — © Molecular Vision Cone-rod dystrophy and a...
citeseerx.ist.psu.edu
© Molecular Vision Cone-rod dystrophy and a frameshift mutation in the PROM1 gene . Cached , Elon Pras Summary; Active Bibliography; Co-citation; …
ELON PRAS M.D. CURRICULUM VITAE - Hemophilia
www.hemophilia.co.il
1 ELON PRAS M.D. CURRICULUM VITAE Name: Elon Pras M.D. Passport No: Place of work: Department of Medicine C Tel No:
Analysis of the Three Most Common MEFV Mutations in 412 Patients ...
www.semanticscholar.org
Elon Pras MD. 2 and Avi Livneh MD Heller Institute of Medical Research and2Danek Gartner Institute of Human Genetics, Sheba Medical Center, Tel Hashomer, Israel. Affiliated to Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel. Key words: familial Mediterranean fever, MEFV gene, mutations, ...
EBSCOhost | | The D1152H cystic fibrosis mutation in...
web.b.ebscohost.com
screening, patients and prenatal diagnosis. Leah Peleg, Mazal Karpati, Silvia Bronstein, Michal Berkenstadt, Moshe Frydman,. Hagith Yonath and Elon Pras.
Scientific Publications
Genomic Organization ofSLC3A1,a Transporter Gene Mutated in...
www.sciencedirect.com
Genomic Organization ofSLC3A1,a Transporter Gene Mutated in Cystinuria. Elon Pras a, 1, Raman Sood b, Nina Raben b, Ivona Aksentijevich b, Xiang Chen b,
NIAMS Scientists Map Gene for Cystinuria
nihsearch.cit.nih.gov
"It was a truly serendipitous situation," says Daniel Kastner, senior investigator at NIAMS, of his foray into cystinuria with Elon Pras, his postdoctoral fellow.
Cone-rod dystrophy and a frameshift mutation in the PROM1 gene
www.ncbi.nlm.nih.gov
· Eran Pras, 1, 4, 5 Almogit Abu, 2 Ygal Rotenstreich, 3, 5 Isaac Avni, 1, 5 Orit Reish, 4, 5 Yair Morad, 1, 5 Haike Reznik-Wolf, 2 and Elon Pras 2, 5
A Priori Attitudes Predict Amniocentesis Uptake in Women of Advan...:...
www.ingentaconnect.com
Briscoe, Elon Pras & Dena Towner (2015) A Priori Attitudes Predict Amniocentesis Uptake in. Women of Advanced Maternal Age: A Pilot Study, ...
Publications
Analysis of allelic association between D6S461 marker and multiple...
link.springer.com
Analysis of allelic association between D6S461 marker ... Yael Shinar, Elon Pras, ... Analysis of allelic association between D6S461 marker and multiple ...
Cone-rod dystrophy and a frameshift mutation in the PROM1 gene - CORE
core.ac.uk
By Eran Pras, Almogit Abu, Ygal Rotenstreich, Isaac Avni, Orit Reish, Yair Morad, Haike Reznik-Wolf and Elon Pras
Evidence for linkage of the gene causing familial Mediterranean fever...
link.springer.com
Familial Mediterranean fever (FMF) is an autosomal recessive disorder of unknown pathogenesis, ... Elon Pras Affiliated with Arthritis and Rheumatism Branch, ...
Reports & Statements
Whole-exome sequencing in undiagnosed genetic diseases: interpreting...
www.nature.com
Original Research Article
Miscellaneous
Clinical disease among FMF heterozygotes , Elon Pras - M.D
www.e-med.co.il
Clinical disease among FMF heterozygotes , Elon Pras - M.D. תאריך: כותרת: Clinical disease among FMF heterozygotes , Elon Pras - M.D תיאור:
(PDF) Autosomal Recessive Catecholamine or Exercise-Induced...
www.academia.edu
Autosomal Recessive Catecholamine or Exercise-Induced Polymorphic Ventricular Tachycardia
A nonsense mutation in IKBKB causes combined immunodeficiency | Blood...
ashpublications.org
... Dr Doron Lancet, Dr Elon Pras, Arthur Holden, Dr Elijah Behr, Dr Annapurna Poduri, Dr Patricia Lugar, Dr Rasheed Gbadegesin, Dr Michelle Winn, Dr Robert ...
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and...
www.cambridge.org
FMR1 CGG allele length in Israeli BRCA1/BRCA2 mutation carriers and the general population display distinct distribution patterns - Volume 96
Factors that affect the decision to undergo amniocentesis in women...
metatoc.com
... , Elon Pras. Health Expectations. Published online on May 12, Abstract. Background Risk for foetal Down syndrome (DS) increases as maternal age increases.
Pacemaker endocarditis: Report of 44 cases and review of the...
miami.pure.elsevier.com
Nadir Arber, Elon Pras, Yitschak Copperman, Jonathan M. Schapiro, Vardiela Meiner, Izidore S. Lossos, Arie Militianu, David Hassin, Eran Pras, Avi Shai, Menachem ...
Carrier state for the nebulin exon 55 deletion and abnormal prenatal...
researchportal.helsinki.fi
Hagith Yonath, Haike Reznik-Wolf, Michal Berkenstadt, Shlomit Eisenberg- Barzilai, Vilma-Lotta Lehtokari, Carina Wallgren-Pettersson, Lakshmi Mehta, Reuven Achiron, Yinon Gilboa, Sylvie Polak-Charcon, Thomas Winder, Moshe Frydman, Elon Pras. Haartman Institute · Department of Medical and Clinical Genetics ...
Publications – The Silver Lab
sites.duke.edu
Publications; Contact us. Open Positions; Lab News; Publications William C Wetsel, James O McNamara, Guy A Rouleau, Debra L Silver, Doron Lancet, Elon Pras,
Clinical and diagnostic value of genetic testing in 216 Israeli...
www.jrheum.org
Elon Pras, Debora Zemer, Pnina Langevitz, Mordechai Pras, and Avi Livneh; J Rheumatol January (1): Abstract; Full ...
Subacute thyroiditis in a patient with MS treated with interferon...
n.neurology.org
Yitshak Kreiss, MD, Ohad Cohen, MD, Elon Pras, MD and Anat Achiron, MD, PhD
Table of Contents — April 01, 2010, 37 (4) | The Journal of...
www.jrheum.org
SHAI PADEH, AVI LIVNEH, ELON PRAS, YAEL SHINAR, MERAV LIDAR, OLGA FELD and YACKOV BERKUN The Journal of Rheumatology April , 37 (4) ; DOI: ...
February | | GE2P2 Global :: Publishing & Operations Site
ge2p2-center.net
7 posts published by davidrcurry during February 2014
Functional analysis of mutations in SLC7A9, and genotype-phenotype...
www.scholars.northwestern.edu
Mariona Font, Lídia Feliubadaló, Xavier Estivill, Virginia Nunes, Eliahu Golomb, Yitshak Kreiss, Elon Pras, Luigi Bisceglia, Adamo P. D'Adamo, Leopoldo Zelante, Paolo Gasparini, Maria Teresa Bassi, Alfred L. George, Marta Manzoni, Mirko Riboni, Andrea Ballabio, Giuseppe Borsani, Núria Reig, ...
Molecular Vision: Fundus albipunctatus: novel mutations and...
www.molvis.org
Eran Pras,1 ,5Elon Pras,2 ,5 Haike Reznik-Wolf,2 Dror Sharon,3 Svetlana Raivech,1 Yaniv Barkana,1 ,5 Almogit Abu-Horowitz,2 Ygal ...
Novelties in the field of autoimmunity – 1st Saint Petersburg...
einstein.pure.elsevier.com
Shani Dahan, Yahel Segal, Abdulla Watad, Shir Azrielant, Asaf Shemer, Dror Maymon, Yuri I. Stroev, Polina A. Sobolevskaya, Elena A. Korneva, Miri Blank, Boris Gilburd, Ora Shovman, Howard Amital, Michael Ehrenfeld, Amir Tanay, Shay Kivity, Elon Pras, Joav Chapman, Jan Damoiseaux, Ricard Cervera ...
Scientists Identify A Gene Causing A Fatal Heart Condition, Common In...
wis-wander.weizmann.ac.il
Michael Eldar, Chief of the Heart Institute at the Sheba Medical Center and Dr. Elon Pras of the Danek Gartner Institute of Human Genetics, ...
FMF | FMF & AID
www.fmfandaid.org
For more information on this topic, please refer to this article: Clinical disease among patients heterozygous for familial mediterranean fever by Dina Marek- Yagel, Yackov Berkun, Shai Padeh, Almogit Abu, Haike Reznik-Wolf, Avi Livneh, Mordechai Pras, Elon Pras. http://onlinelibrary.wiley.com/doi art full.
Related search requests for Elon Pras
| Yael Shinar Jeanne Meck Orit Reish | Mordechai Pras Raman Sood |
Person "Pras" (2) Forename "Elon" (132) Name "Pras" (297) |
sorted by relevance / date