Search research articles
Contact Us
Filters
Showing results (61-70 of 92) with videos related to
Page
of 10
Sort By:
RSC Advances
|
June 13, 2025
Retraction: Effectiveness of some novel heterocyclic compounds as corrosion inhibitors for carbon steel in 1 M HCl using practical and theoretical methods
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
RSC Advances
|
March 26, 2024
Expression of concern: Experimental and surface morphological studies of corrosion inhibition on carbon steel in HCl solution using some new hydrazide derivatives
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
RSC Advances
|
April 28, 2022
Effectiveness of some novel heterocyclic compounds as corrosion inhibitors for carbon steel in 1 M HCl using practical and theoretical methods
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
Neurology
|
January 28, 2012
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
M Anheim, A Elbaz, S Lesage, et al.
BMC Chemistry
|
January 27, 2024
Experimental and theoretical studies of the efficiency of metal-organic frameworks (MOFs) in preventing aluminum corrosion in hydrochloric acid solution
Abd El-Aziz S Fouda, Safaa Eldin H Etaiw, Dina M Abd El-Aziz, et al.
Neurology
|
July 9, 2003
Validity of family history data on PD: evidence for a family information bias
A Elbaz, S K McDonnell, D M Maraganore, et al.
Scientific Reports
|
January 17, 2023
Adult skin fibroblast state change in murine wound healing
Fatma Z Gharbia, Ahmed S Abouhashem, Yomna A Moqidem, et al.
Human Genetics
|
November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)
E Plassart, A Elbaz, J V Santos, et al.
Nature Genetics
|
March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families
B Fontaine, J Vale-Santos, K Jurkat-Rott, et al.
European Journal of Clinical Investigation
|
June 12, 2001
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases
G Hetet, A Elbaz, J Gariepy, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 92) with videos related to
Sort By:
Page
of 10
RSC Advances
|
June 13, 2025
Retraction: Effectiveness of some novel heterocyclic compounds as corrosion inhibitors for carbon steel in 1 M HCl using practical and theoretical methods
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
RSC Advances
|
March 26, 2024
Expression of concern: Experimental and surface morphological studies of corrosion inhibition on carbon steel in HCl solution using some new hydrazide derivatives
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
RSC Advances
|
April 28, 2022
Effectiveness of some novel heterocyclic compounds as corrosion inhibitors for carbon steel in 1 M HCl using practical and theoretical methods
Abd El-Aziz S Fouda, Samir A Abd El-Maksoud, Elsherbiny H El-Sayed, et al.
Neurology
|
January 28, 2012
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
M Anheim, A Elbaz, S Lesage, et al.
BMC Chemistry
|
January 27, 2024
Experimental and theoretical studies of the efficiency of metal-organic frameworks (MOFs) in preventing aluminum corrosion in hydrochloric acid solution
Abd El-Aziz S Fouda, Safaa Eldin H Etaiw, Dina M Abd El-Aziz, et al.
Neurology
|
July 9, 2003
Validity of family history data on PD: evidence for a family information bias
A Elbaz, S K McDonnell, D M Maraganore, et al.
Scientific Reports
|
January 17, 2023
Adult skin fibroblast state change in murine wound healing
Fatma Z Gharbia, Ahmed S Abouhashem, Yomna A Moqidem, et al.
Human Genetics
|
November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)
E Plassart, A Elbaz, J V Santos, et al.
Nature Genetics
|
March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families
B Fontaine, J Vale-Santos, K Jurkat-Rott, et al.
European Journal of Clinical Investigation
|
June 12, 2001
Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases
G Hetet, A Elbaz, J Gariepy, et al.
Page
of 10