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Saudi Medical Journal
|
August 12, 2008
Shock wave lithotripsy in patients with renal calculi
Abdulmalik M Tayib, Hisham A Mosli, Hasan M Farsi, et al.
The Journal of Comparative Neurology
|
August 12, 1998
Single unit recordings in the auditory nerve of congenitally deaf white cats: morphological correlates in the cochlea and cochlear nucleus
D K Ryugo, B T Rosenbaum, P J Kim, et al.
Journal of Inherited Metabolic Disease
|
November 1, 2002
Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency
D Lev, E Gilad, E Leshinsky-Silver, et al.
Journal of Inherited Metabolic Disease
|
March 21, 2007
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation
R Spiegel, A Shaag, A Gutman, et al.
Scientific Reports
|
August 25, 2025
Advanced integrated strategy for structural and mineralogical exploration of inaccessible regions employing remote sensing and multiscale analysis of aeromagnetic data
Ahmed M Eldosouky, Mohamed A Abd El-Wahed, Mohamed Attia, et al.
Scientific Reports
|
November 4, 2025
A robust edge-detection approach for precise delineation of deep structures from potential field data: Structural insights supported by remote sensing
Ahmed M Eldosouky, Saada A Saada, Sammar A Allam, et al.
Journal of Medical Genetics
|
September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A Saada, A Shaag, S Arnon, et al.
Molecular & Cellular Proteomics : MCP
|
May 13, 2015
Cell Surface Proteomics Provides Insight into Stage-Specific Remodeling of the Host-Parasite Interface in Trypanosoma brucei
Michelle M Shimogawa, Edwin A Saada, Ajay A Vashisht, et al.
American Journal of Medical Genetics
|
July 31, 2001
Antenatal presentation of carnitine palmitoyltransferase II deficiency
O N Elpeleg, C Hammerman, A Saada, et al.
Biochemical and Biophysical Research Communications
|
July 19, 2005
Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene
E Leshinsky-Silver, D Lev, Z Tzofi-Berman, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 59) with videos related to
Sort By:
Page
of 6
Saudi Medical Journal
|
August 12, 2008
Shock wave lithotripsy in patients with renal calculi
Abdulmalik M Tayib, Hisham A Mosli, Hasan M Farsi, et al.
The Journal of Comparative Neurology
|
August 12, 1998
Single unit recordings in the auditory nerve of congenitally deaf white cats: morphological correlates in the cochlea and cochlear nucleus
D K Ryugo, B T Rosenbaum, P J Kim, et al.
Journal of Inherited Metabolic Disease
|
November 1, 2002
Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency
D Lev, E Gilad, E Leshinsky-Silver, et al.
Journal of Inherited Metabolic Disease
|
March 21, 2007
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation
R Spiegel, A Shaag, A Gutman, et al.
Scientific Reports
|
August 25, 2025
Advanced integrated strategy for structural and mineralogical exploration of inaccessible regions employing remote sensing and multiscale analysis of aeromagnetic data
Ahmed M Eldosouky, Mohamed A Abd El-Wahed, Mohamed Attia, et al.
Scientific Reports
|
November 4, 2025
A robust edge-detection approach for precise delineation of deep structures from potential field data: Structural insights supported by remote sensing
Ahmed M Eldosouky, Saada A Saada, Sammar A Allam, et al.
Journal of Medical Genetics
|
September 18, 2007
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A Saada, A Shaag, S Arnon, et al.
Molecular & Cellular Proteomics : MCP
|
May 13, 2015
Cell Surface Proteomics Provides Insight into Stage-Specific Remodeling of the Host-Parasite Interface in Trypanosoma brucei
Michelle M Shimogawa, Edwin A Saada, Ajay A Vashisht, et al.
American Journal of Medical Genetics
|
July 31, 2001
Antenatal presentation of carnitine palmitoyltransferase II deficiency
O N Elpeleg, C Hammerman, A Saada, et al.
Biochemical and Biophysical Research Communications
|
July 19, 2005
Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene
E Leshinsky-Silver, D Lev, Z Tzofi-Berman, et al.
Page
of 6