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Journal of Pediatric Genetics
|
May 13, 2017
Overlap between Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly and Fuhrmann's Syndromes in an Egyptian Female Infant
Ebtesam M Abdalla, Ahmed A El-Beheiry
Archives of Andrology
|
January 1, 1979
Methotrexate and fertility in men
A El-Beheiry, E El-Mansy, N Kamel, et al.
Archives of Andrology
|
January 1, 1988
Hyperprolactinemia and impotence
A el-Beheiry, A Souka, A el-Kamshoushi, et al.
BMC Pediatrics
|
June 26, 2025
Point of care ultrasound assessment of the optic nerve sheath diameter in critically ill children
Ahmed A El-Nawawy, Ahmed A El Beheiry, Aya M Abdelaziz, et al.
Archives of Andrology
|
January 1, 1979
The leprous testis
A El-Beheiry, S Abou Zeid, E El-Ghazzawi, et al.
Neurogenetics
|
January 31, 2024
Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families
Sylvia Safwat, Kyle P Flannery, Ahmed A El Beheiry, et al.
HGG Advances
|
December 12, 2025
A homozygous synonymous NOP58 variant causes a neurodevelopmental disorder by impairing maturation of pre-ribosomal RNAs
Loisa D Bonde, Tess Holling, Malik Alawi, et al.
Biochemical and Biophysical Research Communications
|
September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract disease
M Traverso, S Assereto, E Gazzerro, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Journal of Pediatric Genetics
|
May 13, 2017
Overlap between Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly and Fuhrmann's Syndromes in an Egyptian Female Infant
Ebtesam M Abdalla, Ahmed A El-Beheiry
Archives of Andrology
|
January 1, 1979
Methotrexate and fertility in men
A El-Beheiry, E El-Mansy, N Kamel, et al.
Archives of Andrology
|
January 1, 1988
Hyperprolactinemia and impotence
A el-Beheiry, A Souka, A el-Kamshoushi, et al.
BMC Pediatrics
|
June 26, 2025
Point of care ultrasound assessment of the optic nerve sheath diameter in critically ill children
Ahmed A El-Nawawy, Ahmed A El Beheiry, Aya M Abdelaziz, et al.
Archives of Andrology
|
January 1, 1979
The leprous testis
A El-Beheiry, S Abou Zeid, E El-Ghazzawi, et al.
Neurogenetics
|
January 31, 2024
Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families
Sylvia Safwat, Kyle P Flannery, Ahmed A El Beheiry, et al.
HGG Advances
|
December 12, 2025
A homozygous synonymous NOP58 variant causes a neurodevelopmental disorder by impairing maturation of pre-ribosomal RNAs
Loisa D Bonde, Tess Holling, Malik Alawi, et al.
Biochemical and Biophysical Research Communications
|
September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract disease
M Traverso, S Assereto, E Gazzerro, et al.
Page
of 1