Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum
Ibrahim, Doaa M A, Ali, Ola S M, Nasr, Hala, Fateen, Ekram, AbdelAleem, Alice
Published in Orphanet journal of rare diseases (13.03.2023)
Published in Orphanet journal of rare diseases (13.03.2023)
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Journal Article
Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum
Amr, Khalda, Fateen, Ekram, Mansour, Lobna, Tosson, Angie MS, Zaki, Maha S., Salam, Ghada MH. Abdel, Mohamed, Ahmed Nabil, El-Bassyouni, Hala T.
Published in Journal of molecular neuroscience (01.05.2021)
Published in Journal of molecular neuroscience (01.05.2021)
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Journal Article
Biochemical diagnosis of Sanfilippo disorder types A and B
Nosier, Soha S., El Nakeeb, Seham M. S., Ibrahim, Mona M., El-Gammal, Mona, Fateen, Ekram M.
Published in Journal of Genetic Engineering and Biotechnology (01.12.2023)
Published in Journal of Genetic Engineering and Biotechnology (01.12.2023)
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Journal Article
Molecular study of Pompe disease in Egyptian infants
Essawi, Mona, ElBagoury, Nagham, Ashaat, Engy, Sharaf-Eldin, Wessam, Fateen, Ekram
Published in Egyptian Journal of Medical Human Genetics (19.11.2021)
Published in Egyptian Journal of Medical Human Genetics (19.11.2021)
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Journal Article
Quaternary diagnostics scheme for mucolipidosis II and detection of novel mutation in GNPTAB gene
Essawi, Mona L., Fateen, Ekram M., Atia, Hanan A., Eissa, Noura R., Aboul-Ezz, Eman H., Ibrahim, Mona M., Hassan, Heba A., Temtamy, Samia A.
Published in Journal of Genetic Engineering and Biotechnology (03.08.2021)
Published in Journal of Genetic Engineering and Biotechnology (03.08.2021)
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Journal Article
Mucopolysaccharidoses diagnosis in the era of enzyme replacement therapy in Egypt
Fateen, Ekram, Abdallah, Zeinab Y., Nazim, Walaa S., Ibrahim, Mona, Radwan, Amira
Published in Heliyon (01.08.2021)
Published in Heliyon (01.08.2021)
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Journal Article
Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion
El-Beshlawy, Amal, Tantawy, Azza A. G., Shawky, Rabah M., Elsayed, Solaf M., Marzouk, Iman M., Elgawhary, S., Abdelghaffar, Hadeer, Safy, Usama El, Eid, Khaled, EISayh, Khalid I., Megahed, Ahmed, Adly, Amira, Sherif, Eman M., Youssef, Mervat A. M., Fathy, Manar Mohamed, Salah, Nouran Yousef, Elzeiny, Sherine M., EI Bakky, Eslam Rabie Abdel Aziz, Fateen, Ekram
Published in Egyptian Journal of Medical Human Genetics (31.07.2024)
Published in Egyptian Journal of Medical Human Genetics (31.07.2024)
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Journal Article
Effect of diode laser on antioxidant enzymes of salivary glands in diabetic rats
El-Sadek, Hoda, El-Hadidi, Sahar M.A., Aboul-Ezz, Eman H.A., Fateen, Ekram M., Sobhy, Amr G., Rashed, Laila A., Yehia, Hussein
Published in Middle East Journal of Medical Genetics (01.01.2017)
Published in Middle East Journal of Medical Genetics (01.01.2017)
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Journal Article
Fifteen years experience: Egyptian metabolic lab
Fateen, Ekram M., Gouda, Amr S., Ibrahim, Mona M., Abdallah, Zeinab Y.
Published in The Egyptian journal of medical human genetics (01.10.2014)
Published in The Egyptian journal of medical human genetics (01.10.2014)
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Journal Article
Biochemical study of glycogen storage disease type II (Pompe disease) in Egyptian infants
Fateen, Ekram M., Hamza, Hala S., Abo-el Matty, Dina M., Gouda, Amr S., El-Saiedi, Sonia A., Saleh, Samy M., Sobhy Elfeel, Nesrine M., Youssef Ismail, Mai A.
Published in Middle East Journal of Medical Genetics (01.07.2017)
Published in Middle East Journal of Medical Genetics (01.07.2017)
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Journal Article
Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses
Gaber, Khaled R., Ibrahim, Mona M., Farag, Mona K., Abdallah, Zeinab Y., Eldessouky, Sara H., Fateen, Ekram M.
Published in The Egyptian journal of medical human genetics (01.04.2015)
Published in The Egyptian journal of medical human genetics (01.04.2015)
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Journal Article
Biochemical diagnosis of mucopolysaccharidoses over 11 years: the Egyptian experience
Fateen, Ekram M., Ibrahim, Mona M., Gouda, Amr S., Youssef, Zienab A.
Published in Middle East Journal of Medical Genetics (01.01.2014)
Published in Middle East Journal of Medical Genetics (01.01.2014)
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