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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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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Journal Article
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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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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Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis
Elmonem, Mohamed A, Makar, Samuel H, van den Heuvel, Lambertus, Abdelaziz, Hanan, Abdelrahman, Safaa M, Bossuyt, Xavier, Janssen, Mirian C, Cornelissen, Elisabeth Am, Lefeber, Dirk J, Joosten, Leo Ab, Nabhan, Marwa M, Arcolino, Fanny O, Hassan, Fayza A, Gaide Chevronnay, Héloïse P, Soliman, Neveen A, Levtchenko, Elena
Published in Orphanet journal of rare diseases (19.11.2014)
Published in Orphanet journal of rare diseases (19.11.2014)
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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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Evaluation of the diagnostic efficacy of enzyme colorimetric assay compared to tandem mass spectrometer in neonatal screening for phenylketonuria
Hassan, Fayza A., Morgan, Marianne F., Elgayar, Dina F., Elabd, Dina M., Elessawy, Riham A.
Published in Comparative clinical pathology (01.12.2012)
Published in Comparative clinical pathology (01.12.2012)
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