Search research articles
Contact Us
Filters
Showing results (1-10 of 13) with videos related to
Page
of 2
Sort By:
The Egyptian Journal of Medical Human Genetics
|
July 31, 2023
Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship
Heba Saed El-Amawy, Heba Dawoud
Journal of Nutrition and Metabolism
|
October 5, 2020
Clinical Course and Nutritional Management of Propionic and Methylmalonic Acidemias
Amira Mobarak, Heba Dawoud, Hanaa Nofal, et al.
Molecular Biology Reports
|
May 20, 2026
Reversible high-fat ketogenic formula-induced hypertriglyceridemia in a child with NALCN mutation on a ketogenic diet: a case report
Amany Elbarky, Heba Dawoud, Khalid Elsayed Elballat, et al.
Pediatric Research
|
May 18, 2023
Lipid profile after omega-3 supplementation in neonates with intrauterine growth retardation: a randomized controlled trial
Mai Elsheikh, Doaa El Amrousy, Heba El-Mahdy, et al.
Urolithiasis
|
May 20, 2025
Safety and efficacy of Silodosin as medical expulsive therapy after shock wave lithotripsy in paediatric patients with renal stones
Mohammed Lotfi Amer, Mohamed Essam Elkholefy, Heba Dawoud, et al.
Congenital Anomalies
|
December 28, 2021
Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations
Rasha Moheb Elhossini, Mohamed S Abdel-Hamid, Engy Ashaat, et al.
International Journal of Pediatrics
|
December 9, 2020
Propionic and Methylmalonic Acidemias: Initial Clinical and Biochemical Presentation
Amira Mobarak, Heba Dawoud, Wesam A Mokhtar, et al.
Molecular Biology Reports
|
June 14, 2024
Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients
Nesma M Elaraby, Hoda A Ahmed, Heba Dawoud, et al.
Scientific Reports
|
November 29, 2025
A multicenter study on clinico-epidemiological profile of phenylketonuria in Egyptian children
Sohier Yahia, Abdel-Hady El-Gilany, Rofaida M Magdy, et al.
European Journal of Endocrinology
|
April 15, 2026
Severe Osteogenesis Imperfecta Due to Homozygous Glycine Substitutions in COL1A1 and COL1A2
Alexandra Blaschitz, Rodrigo Montero-Lopez, Tamer A El-Sobky, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
The Egyptian Journal of Medical Human Genetics
|
July 31, 2023
Lysosomal storage diseases in the era of COVID-19: a report of an Egyptian case of alpha-fucosidosis and a summary of the lysosomal storage diseases-COVID-19 relationship
Heba Saed El-Amawy, Heba Dawoud
Journal of Nutrition and Metabolism
|
October 5, 2020
Clinical Course and Nutritional Management of Propionic and Methylmalonic Acidemias
Amira Mobarak, Heba Dawoud, Hanaa Nofal, et al.
Molecular Biology Reports
|
May 20, 2026
Reversible high-fat ketogenic formula-induced hypertriglyceridemia in a child with NALCN mutation on a ketogenic diet: a case report
Amany Elbarky, Heba Dawoud, Khalid Elsayed Elballat, et al.
Pediatric Research
|
May 18, 2023
Lipid profile after omega-3 supplementation in neonates with intrauterine growth retardation: a randomized controlled trial
Mai Elsheikh, Doaa El Amrousy, Heba El-Mahdy, et al.
Urolithiasis
|
May 20, 2025
Safety and efficacy of Silodosin as medical expulsive therapy after shock wave lithotripsy in paediatric patients with renal stones
Mohammed Lotfi Amer, Mohamed Essam Elkholefy, Heba Dawoud, et al.
Congenital Anomalies
|
December 28, 2021
Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations
Rasha Moheb Elhossini, Mohamed S Abdel-Hamid, Engy Ashaat, et al.
International Journal of Pediatrics
|
December 9, 2020
Propionic and Methylmalonic Acidemias: Initial Clinical and Biochemical Presentation
Amira Mobarak, Heba Dawoud, Wesam A Mokhtar, et al.
Molecular Biology Reports
|
June 14, 2024
Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients
Nesma M Elaraby, Hoda A Ahmed, Heba Dawoud, et al.
Scientific Reports
|
November 29, 2025
A multicenter study on clinico-epidemiological profile of phenylketonuria in Egyptian children
Sohier Yahia, Abdel-Hady El-Gilany, Rofaida M Magdy, et al.
European Journal of Endocrinology
|
April 15, 2026
Severe Osteogenesis Imperfecta Due to Homozygous Glycine Substitutions in COL1A1 and COL1A2
Alexandra Blaschitz, Rodrigo Montero-Lopez, Tamer A El-Sobky, et al.
Page
of 2