Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study von 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

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Lysosomal Storage Disorders in Egyptian Children von 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.

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Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report von 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

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Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis von 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

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Molecular copro-prevalence of Cryptosporidium in Egyptian children and evaluation of three diagnostic methods von Fathy, Mona M., Abdelrazek, Noha M., Hassan, Fayza A., El-Badry, Ayman A.

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Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: A 5year report von 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

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Biochemical and genetic analysis of Leigh syndrome with complex I deficiency von Mehaney⁎, Dina A., Hassan, Fayza A., Selim, Laila A., Hassan, Sawsn A., Bertini, Enrico, Santorelli, Fillipo, Fattori, Fabiana, Sabry, Randa, Zeyada, Reham

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Evaluation of the diagnostic efficacy of enzyme colorimetric assay compared to tandem mass spectrometer in neonatal screening for phenylketonuria von Hassan, Fayza A., Morgan, Marianne F., Elgayar, Dina F., Elabd, Dina M., Elessawy, Riham A.

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سياسة الدولة العثمانية تجاه الإمارات الكردية في كردستان (1514-1851م) von حسن ملوك, فائزة

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Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Japanese child: Clinical, radiological and molecular genetic analysis von Selim, Laila, Hassan, Fayza, Mehaney, Dina

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Screening of the most common mitochondrial DNA mutations among Egyptian pediatric patients with mitochondrial disorders: A one year study von Mehaney, Dina, Selim, Laila, Hassan, Fayza

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Lysosomal Storage Disorders in Egyptian Children von Ibrahim, Mohamed, 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

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Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report von 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, Ibrahim, Mohamed, Mehaney, Dina

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Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study von 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, Ibrahim, Mohamed

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Clinical utility of chitotriosidase enzyme in nephropathic cystinosis von Ibrahim, Mohamed, Makar, Samuel H, van den Heuvel, Bert, Abdelaziz, Hanan, Abdelrahman, Safaa M, Bossuyt, Xavier, Janssen, Mirian C, Cornelissen, Elisabeth A.M, Lefeber, Dirk J, Joosten, Leo A.B, Nabhan, Marwa M, Arcolino, Fanny O, Hassan, Fayza A, Gaide Chevronnay, Heloise P, Soliman, Neveen A, Levtchenko, Elena

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Merosin deficient congenital muscular dystrophy: Clinical, neuroimaging and immunohistochemical study of 8 Egyptian pediatric patients von Selim, Laila Abdel moteleb, Mehaney, Dina Ahmed, Hassan, Fayza Abdel Hamid, Hassan, Sawsan Abdel Hady, Gamaleldin, Iman, Sabry, Randa, Bertini, Enrico

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Mitochondrial DNA depletion syndrome presenting with ataxia and external ophthalmoplegia: Case report von Selim, Laila, Mehaney, Dina, Hassan, Fayza, Sabry, Randa, Zeyada, Reham, Hassan, Sawsan, Eldin, Iman Gamal, Bertini, Enrico

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Chitotriosidase enzyme can be used as a screening marker and a therapeutic monitor for NephropathicCystinosis von Elmonem, Mohamed A, Makar, Samuel H, Abdelhamid, Rehab H, van den Heuvel, Bert, Bossuyt, Xavier, Hassan, Fayza A, Soliman, Neveen A, Levtchenko, Elena

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Exploring diatomite as a novel natural resource for ecofriendly-sustainable hybrid cements von Hassan, Hassan Soltan, Shi, Caijun, Hashem, Fayza S., Israde-Alcantara, Isabel, Pfeiffer, Heriberto

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Green Synthesis of Zinc Oxide Nanoparticles Using an Aqueous Extract of Punica granatum for Antimicrobial and Catalytic Activity von Fouda, Amr, Saied, Ebrahim, Eid, Ahmed M, Kouadri, Fayza, Alemam, Ahmed M, Hamza, Mohammed F, Alharbi, Maha, Elkelish, Amr, Hassan, Saad El-Din

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