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Mona Mohamed Hafez
Observed names:
Hafez M,
M HAFEZ,
M Hafez,
M. Hafez,
M.M. Hafez,
Mona Hafez,
Mona M. Hafez
show all 7
Observed institutions:
Ain Shams University,
Kafrelsheikh University,
Cairo University,
Mansoura University,
King Abdulaziz University,
National Research Centre,
Electronics Research Institute,
Cairo University hospitals,
Alexandria University
show all 9
OpenAlex ID:
A5111643182
Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients
2010
·
Laurent Maimoun
, Pascal Philibert
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
216
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
2017
·
Ahmed Khattab
, Shozeb Haider
, et al.
·
Proceedings of the National Academy of Sciences
·
156
PDF
Human Prop‐1: cloning, mapping, genomic structure
1998
·
Philippe Duquesnoy
, Anne Roy
, et al.
·
FEBS Letters
·
123
PDF
Preconcentration and separation of total mercury in environmental samples using chemically modified chloromethylated polystyrene-PAN (ion-exchanger) and its determination by cold vapour atomic absorption spectrometry
2001
·
M Hafez
·
Talanta
·
87
Molecular analysis of 5α‐reductase type 2 gene in eight unrelated egyptian children with suspected 5α‐reductase deficiency: prevalence of the G34R mutation
2003
·
Inas Mazen
, Yehia Z. Gad
, et al.
·
Clinical Endocrinology
·
64
Country-Specific Prevalence and Incidence of Youth-Onset Type 2 Diabetes: A Narrative Literature Review
2020
·
Jane L. Lynch
, Margarita Barrientos-Pérez
, et al.
·
Annals of Nutrition and Metabolism
·
47
Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients
2020
·
Safa Meshaal
, Rabab El Hawary
, et al.
·
Journal of Clinical Immunology
·
30
Monogenic leptin deficiency in early childhood obesity
2019
·
Gehan ElSaeed
, Noha Mousa
, et al.
·
Pediatric Obesity
·
29
A Novel Mutation of the 5α-Reductase Type 2 Gene in Two Unrelated Egyptian Children with Ambiguous Genitalia
2003
·
I. Mazen
, M. Hafez
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
22
Timing and Outcome Concerns regarding Feminizing Genitoplasty from the Perspective of Egyptian Families of Girls with Virilized External Genitalia
2015
·
Mahmoud M. Marei
, Ahmed E. Fares
, et al.
·
Hormone Research in Paediatrics
·
20
A New Mutation of 5-Alpha-Reductase Type 2 (A62E) in a Large Egyptian Kindred
2003
·
Mona Hafez
, Inas Mazen
, et al.
·
Hormone Research in Paediatrics
·
19
The role of anti-Mullerian and inhibin B hormones in the evaluation of 46,XY disorders of sex development
2014
·
Mona Hafez
, Soha M. Abd El Dayem
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
16
Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia
2007
·
Mohammad Hafez
, Youssef Al-Tonbary
, et al.
·
Hematology
·
14
PDF
Sanjad Sakati Syndrome: Case reports from Egypt
2017
·
Mona Hafez
, Ghada M. Anwar
, et al.
·
Egyptian Pediatric Association Gazette
·
13
PDF
Relationship between visceral obesity and plasma fibrinogen in obese children
2015
·
Mona Hafez
, Sahar El-Masry
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
12
Evaluation of carotid artery access in comparison with femoral artery access in neonatal percutaneous stenting of ductus arteriosus
2021
·
Gehan A. Alsawah
, Hala Elmarsafawy
, et al.
·
Cardiology in the Young
·
10
Copy Number Variations in Genetic Diagnosis of Congenital Adrenal Hyperplasia Children
2022
·
Aisha Tolba
, Iman Mandour
, et al.
·
Frontiers in Genetics
·
8
PDF
Genetic profiling of CAH Egyptian children: rapid guide to clinical interpretation of common mutations
2020
·
F. Elmougy
, M. Elsharkawy
, et al.
·
Journal of Endocrinological Investigation
·
8
Effect of metformin on clinical and biochemical hyperandrogenism in adolescent girls with type 1 diabetes
2019
·
Mona Hafez
, Noha Musa
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
7
Guiding Program for Mothers to Improve the Quality of Life of Their Children With Congenital Heart Disease
2020
·
Neama EL-Gendy
, Rabab Hassan
, et al.
·
Mansoura Nursing Journal
·
6
High frequency of splice site mutation in 21-hydroxylase deficiency children
2014
·
S. Sharaf
, M. Hafez
, et al.
·
Journal of Endocrinological Investigation
·
6
Plasma and red cell iron turnover in protein calorie malnutrition.
1969
·
M. Khalil
, H. Awwad
, et al.
·
Archives of Disease in Childhood
·
6
PDF
CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge
2017
·
Fatma Elmougy
, Sahar Sharaf
, et al.
·
Annals of the New York Academy of Sciences
·
5
Upregulation of CD40/CD40L system in rheumatic mitral stenosis with or without atrial fibrillation
2012
·
Hanan Azzam
, Nashwa K. Abousamra
, et al.
·
Platelets
·
5
ALJP: An Arabic Legal Judgment Prediction in Personal Status Cases Using Machine Learning Models
2024
·
Salwa Abbara
, Mona Hafez
, et al.
·
Research Square
·
4
PDF
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Works count:
70
Citation count:
966
H-index:
13
I10-index:
16
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