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Mohammed H. Hassan

Publications (10)

Genetic Aspects in Congenital Heart Diseases in Infant of Diabetic Mother: A Review Article

Mohammed H. Hassan, Amany Abdelaty Hassany, Nagwan I. Rashwan & Ahmed El-Abd Ahmed · Asian Journal of Pediatric Research · 2022

Background: The pathogenesis and effects of maternal diabetes on their infants is still not entirely understood, but it's likely to have several teratogenic mechanisms. The fetal heart is anatomically and physiologically altered by diabetes mellitus. About 400 genes are thought t...

Open access Research Article 10.9734/ajpr/2022/v8i130236

Diagnostic Utility of Plasma Chitotriosidase, Total Acid Phosphatase Activity, Ferritin and Globulin Levels in Screening for Gaucher Disease

Mohammed H. Hassan, Ayat A. Sayed, Ahmed El-Abd Ahmed & Tahia H. Saleem · International Journal of Biochemistry Research & Review · 2017

Aims: Gaucher disease "GD" is one of the most common glycolipid storage disorders. Several circulating molecules thought to be secreted by Gaucher cells have been studied as biological markers of disease. We investigate and compare the validity of using plasma chitotriosidase "Ch...

Open access Research Article 10.9734/IJBCRR/2017/32782

Effect of Enzyme Replacement Therapy on Disease Burden Biomarkers in Gaucher's Disease

Mohammed H. Hassan, Ayat A. Sayed, Ahmed El-Abd Ahmed, Tahia H. Saleem, Khalid I. Elsayh & Norhan B. B. Mohammed · International Journal of Biochemistry Research & Review · 2017

Aims: We evaluate the effect of enzyme replacement therapy "ERT" on the plasma levels of some biochemical markers of the disease burden, in pediatric patients with Gaucher's disease "GD", in the form of plasma chitotriosidase "ChT", total acid phosphatase activity, ferritin and g...

Open access Research Article 10.9734/IJBCRR/2016/30768

Blood Gases, Plasma Ammonia Levels and Urine Analysis; a Potential for Early Detection of Some Inborn Errors of Metabolism

Tahia H. Saleem, Mohammed H. Hassan, Ghaleb Oriquat, Amal A. S. Soliman, Aliaa A. Youssef & Wesam G. Ammari · International Journal of Biochemistry Research & Review · 2017

Aims: Inborn errors of metabolism (IEM) constitute a group of inherited disorders that cause significant morbidity and mortality. This diverse group of diseases present with different clinical manifestations that make the diagnosis a real challenge. The current work aimed to inve...

Open access Research Article 10.9734/IJBCRR/2016/31021

Frequency of Janus Kinas 2V617F (JAK2V617F) Mutation among Children with Type 1 Diabetes Mellitus

Nadia Farouk Zekry, Omyma Galal, Mohammed H. Hassan, Hala M. Sakhr & Rana Toghan · Asian Journal of Biochemistry, Genetics and Molecular Biology · 2020

Background and Objectives: Type 1 Diabetes mellitus (T1DM) is a disorder of glucose homeostasis results from the destruction of β- cells of the pancreas with subsequent insulin deficiency and hyperglycemia. Acquired mutation (V617F) affecting the JAK2 gene disrupts the auto-inhib...

Open access Research Article 10.9734/ajbgmb/2020/v4i130096

Carotid Intima-media Thickness as a Non-invasive Predictive Imaging Tool for Occurrence and Severity of Coronary Artery Disease: Correlations with Lipid Profile

Hossam-Eldin M. Mahmoud, Ghada Abdelrazek & Mohammed H. Hassan · Asian Journal of Cardiology Research · 2019

Background: It is important to identify patients at risk of developing cardiovascular events to enable preventive interventions and promote lifestyle modifications. Carotid intima–media thickness (CIMT) is an important marker for cardiovascular disease and can be easily measured...

Open access Research Article

Correlation between Anthropometric Measures, Lipid Profile and Serum Adiponectin and Steatosis in Nondiabetic Nonalcoholic Fatty Liver Disease

Hasan S. Mahmoud, Mohamad M. Helal, Mohammed H. Hassan & Mahmoud F. Sherif · Journal of Advances in Medicine and Medical Research · 2015

Aims: To assess the relation between the grade of steatosis and anthropometric measures, lipid profile and serum adiponectin in non-diabetic patients with nonalcoholic fatty liver. Study Design: Cross sectional study. Place and Duration of Study: Department of Tropical Medicine a...

Open access Research Article 10.9734/BJMMR/2015/16594

Biochemical and Genetic Markers in Neurological Trauma and Tumors: Review Article

Omyma Ashraf, Tahia H. Saleem, Bakheet E. M. Elsadek, Ali R. Hamdan & Mohammed H. Hassan · Asian Journal of Biochemistry, Genetics and Molecular Biology · 2022

CNS traumas and tumors are major health problems. They lead to serious health and economic burdens. They are major causes of disability, or death all over the world. Nowadays, the order of causes of trauma-related death has beenchanged from multiorgan affection to CNS trauma. Ass...

Open access Research Article 10.9734/ajbgmb/2022/v11i230260

Macrophage Migration Inhibitory Factor in Vitiligo: Pathogenesis and Potential Therapeutic Aspects

Hassan Mohammed Ibrahim, Essam El-din Abd El-Aziz Nada, Soheir Abdel-Hamid Ali, Eisa Mohamed Hegazy & Mohammed H. Hassan · Asian Journal of Biochemistry, Genetics and Molecular Biology · 2021

Vitiligo is an acquired skin disorder that is characterized by a gradual loss of skin pigmentation when melanocytes, the skin's pigment-producing cellsis lost. Pathogenicmechanisms are not well understood. Genetic, abnormal biochemical pathways, autoimmune, melanocyte adhesion de...

Open access Research Article 10.9734/ajbgmb/2021/v8i230189

Correlations of Plasma Biotinidase Levels with Hepatic Synthetic Functions in Children with Chronic Liver Diseases

Tahia H. Saleem, Hamdy N. Eltalawy, Ahmed El-Abd Ahmed, Nagla H. Abu-Faddan, Mohammed H. Hassan, Ayat A. Sayed & Hussein M. Eldeeb · International Journal of Biochemistry Research & Review · 2017

Aims: Certain liver diseases can cause decreased synthesis of liver proteins or enzymes, including biotinidase, thereby reducing biotinidase activity in serum. The present study aimed to assess plasma biotinidase level in pediatric patients with compensated and decompensated chro...

Open access Research Article 10.9734/IJBCRR/2017/32764