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Anat Blumenfeld

Showing results (1-10 of 46) with videos related to

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Pain|September 1, 1996
Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type IIGudarz Davar, Christo Shalish, Anat Blumenfeld, et al.
Harefuah|March 28, 2018
[FROM THE LAB BENCH TO THE PATIENT - CAN INJURED SKELETAL TISSUES REGENERATE?]Amir Haze, Josh Schroeder, Anat Blumenfeld, et al.
European Journal of Ophthalmology|October 3, 2023
The prevalence of autism among children with albinismStav Gunz, Irit Rozen-Knisbacher, Anat Blumenfeld, et al.
Molecular Vision|March 13, 2008
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridiaDikla Bandah, Ada Rosenmann, Anat Blumenfeld, et al.
European Journal of Oral Sciences|January 17, 2012
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cellsDan Deutsch, Nechama Silverstein, Dekel Shilo, et al.
Plos One|January 17, 2024
Visual acuity improvement in children with albinism beyond the first decade of lifeClaudia Yahalom, Ana Navarrete, Atara Juster, et al.
Ophthalmic Genetics|February 18, 2015
Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a FamilyClaudia Yahalom, Dror Sharon, Eli Dalia, et al.
Prenatal Diagnosis|July 24, 2009
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli familiesAda Rosenmann, Idit Bejarano-Achache, Dalia Eli, et al.
European Heart Journal|February 20, 2004
Association of oestrogen receptor alpha gene polymorphism with the angiographic extent of coronary artery diseaseArthur Pollak, Ariel Rokach, Anat Blumenfeld, et al.
Eye (London, England)|August 24, 2021
Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in IsraelClaudia Yahalom, Ron Braun, Rani Patal, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Pain|September 1, 1996
Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type IIGudarz Davar, Christo Shalish, Anat Blumenfeld, et al.
Harefuah|March 28, 2018
[FROM THE LAB BENCH TO THE PATIENT - CAN INJURED SKELETAL TISSUES REGENERATE?]Amir Haze, Josh Schroeder, Anat Blumenfeld, et al.
European Journal of Ophthalmology|October 3, 2023
The prevalence of autism among children with albinismStav Gunz, Irit Rozen-Knisbacher, Anat Blumenfeld, et al.
Molecular Vision|March 13, 2008
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridiaDikla Bandah, Ada Rosenmann, Anat Blumenfeld, et al.
European Journal of Oral Sciences|January 17, 2012
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cellsDan Deutsch, Nechama Silverstein, Dekel Shilo, et al.
Plos One|January 17, 2024
Visual acuity improvement in children with albinism beyond the first decade of lifeClaudia Yahalom, Ana Navarrete, Atara Juster, et al.
Ophthalmic Genetics|February 18, 2015
Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a FamilyClaudia Yahalom, Dror Sharon, Eli Dalia, et al.
Prenatal Diagnosis|July 24, 2009
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli familiesAda Rosenmann, Idit Bejarano-Achache, Dalia Eli, et al.
European Heart Journal|February 20, 2004
Association of oestrogen receptor alpha gene polymorphism with the angiographic extent of coronary artery diseaseArthur Pollak, Ariel Rokach, Anat Blumenfeld, et al.
Eye (London, England)|August 24, 2021
Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in IsraelClaudia Yahalom, Ron Braun, Rani Patal, et al.
Pageof 5