Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Amr S. Gouda"'
Autor:
Hala M. Sakhr, Mohammed H. Hassan, Ahmed El-Abd Ahmed, Nagwan I. Rashwan, Rehab H. Abdel-Aziz, Amr S. Gouda, Rana Toghan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Nutritional status assessment, including amino acids, carnitine, and acylcarnitine profile, is an important component of diabetes care management, influencing growth and metabolic regulation. A designed case–control research included 100 E
Externí odkaz:
https://doaj.org/article/8b4f5cc34c494161a8cc8abd558d22f3
Autor:
Aly A. Aboulnasr, Khaled R. Gaber, Gamal Abdel Sameea, Amr S. Gouda, Mona M. Ibrahim, Taghreed A. Shalabi, Amr Elnouri
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Mucopolysaccharidosis VI (MPS VI) or Maroteaux–Lamy syndrome is an autosomal recessive lysosomal storage disorder. Clinical manifestations are related to progressive accumulation of dermatan sulfate (DS). Two-dimensional electro
Externí odkaz:
https://doaj.org/article/466717b4dfbe44e99656183ff89a8c29
Autor:
Amr S. Gouda, Walaa S. Nazim
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Phenylketonuria (PKU), inborn error of metabolism, results from phenylalanine hydroxylase deficiency. PKU leads to neurological manifestations, intellectual disability, and mental disorders. Treatment depends on phenylalanine-rest
Externí odkaz:
https://doaj.org/article/738fe6743fd04cf89a059de8098bdba0
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 379-385 (2014)
Background: Inborn errors of metabolism (IEM) are single gene disorders responsible for abnormalities in the synthesis or catabolism of proteins, carbohydrates and fats by means of defective enzymes or transport proteins which results in a block of t
Externí odkaz:
https://doaj.org/article/f4c2d465c6bd4bcc98da6aa0b967f60e
Autor:
Nagwa A. Meguid, Maha Hemimi, Said A. S. Ghozlan, Wafaa A. Kandeel, Adel F. Hashish, Amr S. Gouda, Walaa S. Nazim, Magda F. Mohamed
Publikováno v:
Journal of Diabetes & Metabolic Disorders. 21:1491-1497
Obesity is more prevalent among people with Down Syndrome (DS) compared to general population. In this pilot study, we investigated the effect of cystathionine beta-synthase (CBS) overdosage on the regulation of transsulfuration pathway and the obesi
Autor:
Manal A. Mohsen, Mai M. Youssef, Ebtissam M. Salah El-Din, Samar M. E. Salem, Hala Mohamed Salah El Din Megahed, Mones M. AbuShady, Dalia Medhat, Amr S. Gouda, Walaa Nazim, Manal A. Shehata
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 10:674-680
BACKGROUND: Childhood obesity is considered a risk factor for chronic diseases later in life. Phthalates (phthalate acid esters), predominant constituents of plasticizers, are well-thought-out global environmental contaminants. AIM: This study aims t
Autor:
Aly A. Aboulnasr, Amr Elnouri, Gamal Abdel Sameea, Amr S. Gouda, Mona M. Ibrahim, Taghreed A. Shalabi, Khaled R. Gaber
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 48:682-687
To introduce a quantitative determination of heparan sulfate and dermatan sulfate by mass spectrometry and to compare it with two-dimensional electrophoresis of the glycosaminoglycans in the amniotic fluid for the prenatal diagnosis of mucopolysaccha
Autor:
Manal Shehata, Ebtissam Salah, Mai M. Youssef, Mones Mahmoud Abu Shady, Inas El-Alameey, Engy Ashaat, Amr S. Gouda, Walaa Nazim
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 9:1640-1646
Background: Evidence supporting environmental risk factors of autism spectrum disorder (ASD) is rising. Phthalates are assumed to contribute to this risk due to their extensive use in daily life as plasticizers and additives in numerous customer prod
Publikováno v:
Azhar International Journal of Pharmaceutical and Medical Sciences.
The study aimed to diagnose type 1 and 2 of neuronal ceroid lipofuscinoses (NCLs) using leukocytes and dried blood spot samples. A hundred subjects divided equally to patient and control groups of matching age and sex were included. The patient group
Autor:
Samy M. Saleh, Ekram M. Fateen, Amr S. Gouda, Sonia A. El-Saiedi, Nesrine S. Elfeel, Hala S. Hamza, Mai A. Youssef Ismail, Dina M. Abo-el Matty
Publikováno v:
Middle East Journal of Medical Genetics. 6:75-81