ASAH1‐related disorders: Description of 15 novel pediatric patients and expansion of the clinical phenotype
Mahmoud, Iman G., Elmonem, Mohamed A., Zaki, Maha S., Ramadan, Areef, Al‐Menabawy, Nihal M., El‐Gamal, Aya, Mansour, Lobna, Issa, Mahmoud Y., Abdel‐Hamid, Mohamed S., Abdel‐Hady, Sawsan, Khalifa, Iman, Ibrahim, Ahmed, Solyom, Alexander, Rolfs, Arndt, Selim, Laila
Published in Clinical genetics (01.12.2020)
Published in Clinical genetics (01.12.2020)
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Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease
Sayed Amr, Khalda, El-Bassyouni, Hala T, Abdel Hady, Sawsan, Mostafa, Mostafa I, Mehrez, Mennat I, Coviello, Domenico, El-Kamah, Ghada Y
Published in Genes (29.09.2021)
Published in Genes (29.09.2021)
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Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: A 5year report
Selim, Laila A., Hassan, Sawsan Abdel-Hady, Salem, Fadia, Orabi, Azza, Hassan, Fayza A., El-Mougy, Fatma, Mahmoud, Iman Gamal-Eldin, El-Badawy, Amira, Girgis, Marian Y., Elmonem, Mohamed A., Mehaney, Dina
Published in Clinical biochemistry (01.06.2014)
Published in Clinical biochemistry (01.06.2014)
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Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt
Eid, Ola M, Abdel Hady, Sawsan, El-Kotoury, Ahmed, Said, Khalda A, Rafat, Karima, El-Bassyouni, Hala T
Published in Ophthalmic genetics (03.09.2017)
Published in Ophthalmic genetics (03.09.2017)
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Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report
Selim, Laila A, Hassan, Sawsan Abdel-Hady, Salem, Fadia, Orabi, Azza, Hassan, Fayza A, El-Mougy, Fatma, Mahmoud, Iman Gamal-Eldin, El-Badawy, Amira, Girgis, Marian Y, Elmonem, Mohamed A, Mehaney, Dina
Published in Clinical biochemistry (01.06.2014)
Published in Clinical biochemistry (01.06.2014)
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Merosin deficient congenital muscular dystrophy: Clinical, neuroimaging and immunohistochemical study of 8 Egyptian pediatric patients
Selim, Laila Abdel moteleb, Mehaney, Dina Ahmed, Hassan, Fayza Abdel Hamid, Hassan, Sawsan Abdel Hady, Gamaleldin, Iman, Sabry, Randa, Bertini, Enrico
Published in Journal of Genetic Engineering and Biotechnology (01.06.2013)
Published in Journal of Genetic Engineering and Biotechnology (01.06.2013)
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Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt
Eid, Ola M., Abdel Hady, Sawsan, El-Kotoury, Ahmed, Said, Khalda A., Rafat, Karima, El-Bassyouni, Hala T.
Published in Ophthalmic Genetics (03.09.2017)
Published in Ophthalmic Genetics (03.09.2017)
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Effect of Fluorophenylalanine on Bacteriophage MS2 Replication
Wray, G W, Gimlin, D M, Abdel-Hady, S N, Sherard, S K, Leach, F R
Published in Journal of Virology (01.02.1970)
Published in Journal of Virology (01.02.1970)
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An effect of fluorophenylalanine on MS-2 RNA replicase
Abdel-Hady, S N, Leach, F R, Henderson, L M
Published in Proceedings of the Society for Experimental Biology and Medicine (01.04.1972)
Published in Proceedings of the Society for Experimental Biology and Medicine (01.04.1972)
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