Organic acidurias in Egyptian children: The urge for high‐risk screening
Mehaney, Dina A., Seliem, Zeinab S., Selim, Laila A., Khalil, Mona S., Abou‐Youssef, Hazem S., Elsayed, Elham M., Abdou, Doaa M., Rizzo, Cristiano, Dioniasi‐Vici, Carlo, Abdelazim, Aya M., Elkady, Sherihan H.
Published in Pediatrics international (01.01.2023)
Published in Pediatrics international (01.01.2023)
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Journal Article
Serum Vitamin D and Vitamin D Receptor Gene Polymorphism in Mycosis Fungoides Patients: A Case Control Study
Rasheed, Hoda, Hegazy, Rehab A, Gawdat, Heba I, Mehaney, Dina A, Kamel, Marwa M, Fawzy, Marwa M, Nooh, Mohammed M, Darwish, Hebatallah A
Published in PloS one (23.06.2016)
Published in PloS one (23.06.2016)
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Journal Article
Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study
Hassan, Fayza A, El-Mougy, Fatma, Sharaf, Sahar A, Mandour, Iman, Morgan, Marian F, Selim, Laila A, Hassan, Sawsan A, Salem, Fadia, Oraby, Azza, Girgis, Marian Y, Mahmoud, Iman G, El-Badawy, Amira, El-Nekhely, Ibrahim, Moharam, Nadia, Mehaney, Dina A, Elmonem, Mohamed A
Published in Journal of medical screening (01.09.2016)
Published in Journal of medical screening (01.09.2016)
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Journal Article
Analysis of oxidative stress status, catalase and catechol-O-methyltransferase polymorphisms in Egyptian vitiligo patients
Mehaney, Dina A, Darwish, Hebatallah A, Hegazy, Rehab A, Nooh, Mohammed M, Tawdy, Amira M, Gawdat, Heba I, El-Sawalhi, Maha M
Published in PloS one (10.06.2014)
Published in PloS one (10.06.2014)
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Journal Article
Interleukins 17 and 10 in a sample of Egyptian relapsing remitting multiple sclerosis patients
Tawfik, Tarek Z., MD, Gad, Adel H., MD, Mehaney, Dina A., MD, El Nahrery, Eslam, MD, Shehata, Hatem S., MD, Hashem, Hebatalla, MD, Ghaffar, Nawal F. Abdel, Ms, Shalaby, Nevin Mohieldin, MD
Published in Journal of the neurological sciences (15.10.2016)
Published in Journal of the neurological sciences (15.10.2016)
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Journal Article
Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children
Mehaney, Dina A., Haghighi, Alireza, Embaby, Amira K., Zeyada, Reham A., Darwish, Rania K., Elfeel, Nesrine S., Abouelhoda, Mohamed, El-Saiedi, Sonia A., Gohar, Nadida A., Seliem, Zeinab S.
Published in Cardiology in the young (01.02.2022)
Published in Cardiology in the young (01.02.2022)
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Journal Article
Genetic study of pediatric hypertrophic cardiomyopathy in Egypt
Darwish, Rania K., Haghighi, Alireza, Seliem, Zeinab S., El-Saiedi, Sonia A., Radwan, Nora H., El-Gayar, Dina F., Elfeel, Nesrine S., Abouelhoda, Mohamed, Mehaney, Dina A.
Published in Cardiology in the young (01.12.2020)
Published in Cardiology in the young (01.12.2020)
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Journal Article
Association of chitotriosidase enzyme activity and genotype with the risk of nephropathy in type 2 diabetes
Elmonem, Mohamed A., Amin, Hanan S., El-Essawy, Riham A., Mehaney, Dina A., Nabil, Malak, Kamel, Laila N., Farid, Ibtisam M.
Published in Clinical biochemistry (01.04.2016)
Published in Clinical biochemistry (01.04.2016)
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Journal Article
Lysosomal Storage Disorders in Egyptian Children
Elmonem, Mohamed A., Mahmoud, Iman G., Mehaney, Dina A., Sharaf, Sahar A., Hassan, Sawsan A., Orabi, Azza, Salem, Fadia, Girgis, Marian Y., El-Badawy, Amira, Abdelwahab, Magy, Salah, Zeinab, Soliman, Neveen A., Hassan, Fayza A., Selim, Laila A.
Published in Indian journal of pediatrics (01.08.2016)
Published in Indian journal of pediatrics (01.08.2016)
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Journal Article
Concerning the article “Interleukins 17 and 10 in a sample of Egyptian relapsing remitting multiple sclerosis patients”
Tawfik, Tarek Z, Gad, Adel H, Mehaney, Dina A, El Nahrery, Eslam, Shehata, Hatem S, Hashem, Hebatalla, Abdel Ghaffar, Nawal F, Shalaby, Nevin
Published in Journal of the neurological sciences (15.07.2017)
Published in Journal of the neurological sciences (15.07.2017)
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Journal Article
Profile of cystic fibrosis in a single referral center in Egypt
El-Falaki, Mona M., Shahin, Walaa A., El-Basha, Noussa R., Ali, Aliaa A., Mehaney, Dina A., El-Attar, Mona M.
Published in Journal of advanced research (01.09.2014)
Published in Journal of advanced research (01.09.2014)
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Journal Article
Biochemical and genetic analysis of Leigh syndrome with complex I deficiency
Mehaney⁎, Dina A., Hassan, Fayza A., Selim, Laila A., Hassan, Sawsn A., Bertini, Enrico, Santorelli, Fillipo, Fattori, Fabiana, Sabry, Randa, Zeyada, Reham
Published in Mitochondrion (01.07.2011)
Published in Mitochondrion (01.07.2011)
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Journal Article
Genetic variants of Pompe disease among a sample of Egyptian pediatric patients
Darwish, Rania K., Rabie, Walaa A., El Abd, Dina M., Selim, Laila A., Seliem, Zeinab S., Lotfy, Sarah A., Mehaney, Dina A.
Published in Gene reports (01.06.2022)
Published in Gene reports (01.06.2022)
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Journal Article
Profile of cystic fibrosis
Mona M. El-Falaki, Walaa A. Shahin, Noussa R. El-Basha, Aliaa A. Ali, Dina A. Mehaney, Mona M. El-Attar
Published in Journal of advanced research (01.09.2014)
Published in Journal of advanced research (01.09.2014)
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Journal Article