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Pain
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September 1, 1996
Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II
Gudarz 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 albinism
Stav 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 aniridia
Dikla 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 cells
Dan Deutsch, Nechama Silverstein, Dekel Shilo, et al.
Plos One
|
January 17, 2024
Visual acuity improvement in children with albinism beyond the first decade of life
Claudia 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 Family
Claudia 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 families
Ada 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 disease
Arthur 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 Israel
Claudia Yahalom, Ron Braun, Rani Patal, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Pain
|
September 1, 1996
Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II
Gudarz 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 albinism
Stav 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 aniridia
Dikla 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 cells
Dan Deutsch, Nechama Silverstein, Dekel Shilo, et al.
Plos One
|
January 17, 2024
Visual acuity improvement in children with albinism beyond the first decade of life
Claudia 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 Family
Claudia 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 families
Ada 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 disease
Arthur 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 Israel
Claudia Yahalom, Ron Braun, Rani Patal, et al.
Page
of 5