Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E Eyal

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Bioinformatics (Oxford, England)|April 13, 2001
MutaProt: a web interface for structural analysis of point mutationsE Eyal, R Najmanovich, V Sobolev, et al.
Harefuah|December 15, 1980
[Comparison of bioavailability of pilocarpine]E Eyal, P Nemet, A D Korczyn, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 1, 1988
The influence of maternal hypnosis on fetal movements in anxious pregnant womenE Z Zimmer, B A Peretz, E Eyal, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|June 9, 2001
Spontaneous ruptured lumbar artery in a chronic renal failure patientM Halak, M Kligman, Z Loberman, et al.
International Journal of Cardiology|July 1, 1991
A correlation between the structure of myocardial cells and prolonged Q-T interval in young ratsA Fein, Z Hecht, D Varon, et al.
Annales De Biologie Animale, Biochimie, Biophysique|January 1, 1973
The effect of the ratio of dilution of ram semen in different diluents on the conception rateD Amir, H Schindler, E Eyal, et al.
Technology in Cancer Research & Treatment|September 5, 2013
Standardization of radiological evaluation of dynamic contrast enhanced MRI: application in breast cancer diagnosisE Furman-Haran, M Shapiro Feinberg, D Badikhi, et al.
Clinical Genetics|March 21, 2017
Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic typeE Reinstein, V Drasinover, R Lotan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|April 13, 2001
MutaProt: a web interface for structural analysis of point mutationsE Eyal, R Najmanovich, V Sobolev, et al.
Harefuah|December 15, 1980
[Comparison of bioavailability of pilocarpine]E Eyal, P Nemet, A D Korczyn, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|February 1, 1988
The influence of maternal hypnosis on fetal movements in anxious pregnant womenE Z Zimmer, B A Peretz, E Eyal, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|June 9, 2001
Spontaneous ruptured lumbar artery in a chronic renal failure patientM Halak, M Kligman, Z Loberman, et al.
International Journal of Cardiology|July 1, 1991
A correlation between the structure of myocardial cells and prolonged Q-T interval in young ratsA Fein, Z Hecht, D Varon, et al.
Annales De Biologie Animale, Biochimie, Biophysique|January 1, 1973
The effect of the ratio of dilution of ram semen in different diluents on the conception rateD Amir, H Schindler, E Eyal, et al.
Technology in Cancer Research & Treatment|September 5, 2013
Standardization of radiological evaluation of dynamic contrast enhanced MRI: application in breast cancer diagnosisE Furman-Haran, M Shapiro Feinberg, D Badikhi, et al.
Clinical Genetics|March 21, 2017
Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic typeE Reinstein, V Drasinover, R Lotan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavinG Heimer, E Eyal, X Zhu, et al.
Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.
Pageof 2