Search Results - Yunus, Zabedah Md

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  1. 1
    Clinical and Mutational Analysis of the GCDH Gene in Malaysian Patients with Glutaric Aciduria Type 1

    Clinical and Mutational Analysis of the GCDH Gene in Malaysian Patients with Glutaric Aciduria Type 1 by Lock Hock, Ngu, Huey Yin, Leong, Md Yunus, Zabedah, Abdul Azize, Nor Azimah, Yakob, Yusnita, Abdul Wahab, Siti Aishah, Mohd Khalid, Mohd Khairul Nizam

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  2. 2
    Challenges identified in the management of patients with inherited metabolic disorders – A five year experience from Pakistan

    Challenges identified in the management of patients with inherited metabolic disorders – A five year experience from Pakistan by Afroze, Bushra, Lakhani, Laila, Naz, Farah, Somani, Sana, Yunus, Zabedah Md, Brown, Nick

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  3. 3
    Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance

    Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance by Habib, Anasufiza, Md Yunus, Zabedah, Azize, Nor Azimah, Ch’ng, Gaik-Siew, Ong, Winnie PeiTee, Chen, Bee-Chin, Hsu, Ho-Torng, Wong, Ke-Juin, Pitt, James, Ngu, Lock-Hock

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  4. 4
    Serum N-Glycan Profiling in Congenital Disorder of Glycosylation by Mass Spectrometry

    Serum N-Glycan Profiling in Congenital Disorder of Glycosylation by Mass Spectrometry by Rahman, Salina Abdul, Wahab, Siti Aishah Abdul, Yunus, Zabedah Md

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  5. 5
    Inherited metabolic disorders presenting as hypoxic ischaemic encephalopathy: A case series of patients presenting at a tertiary care hospital in Pakistan

    Inherited metabolic disorders presenting as hypoxic ischaemic encephalopathy: A case series of patients presenting at a tertiary care hospital in Pakistan by Zahid, Maya, Khan, Aysha Habib, Yunus, Zabedah Md, Chen, Bee Chin, Steinmann, Beat, Johannes, Haberle, Afroze, Bushra

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  6. 6
    Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients

    Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients by Ali, Ernie Zuraida, Khalid, Mohd Khairul Nizam Mohd, Yunus, Zabedah Md, Yakob, Yusnita, Chin, Chen Bee, Latif, Kartikasalwah Abd, Hock, Ngu Lock

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  7. 7
    Neonatal intrahepatic cholestasis associated with citrin deficiency (NICCD): a case series of 11 Malaysian patients

    Neonatal intrahepatic cholestasis associated with citrin deficiency (NICCD): a case series of 11 Malaysian patients by Chew, Hui Bein, Ngu, Lock Hock, Zabedah, Md Yunus, Keng, Wee Teik, Balasubramaniam, Shanti, Hanifah, Mohd Jamil M., Kobayashi, Keiko

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  8. 8
    Clinical and Mutational Analysis of the GCDH Gene in Malaysian Patients with Glutaric Aciduria Type 1

    Clinical and Mutational Analysis of the GCDH Gene in Malaysian Patients with Glutaric Aciduria Type 1 by Wahab, Siti Aishah Abdul, Yakob, Yusnita, Azize, Nor Azimah Abdul, Yunus, Zabedah Md, Yin, Leong Huey, Khalid, Mohd Khairul Nizam Mohd, Hock, Ngu Lock

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  9. 9
    Alpha-fucosidosis – Two brothers presenting with dysostosis multiplex

    Alpha-fucosidosis – Two brothers presenting with dysostosis multiplex by Shaukat, Rimshah, Raza, Syed Musa, Yuns, Zabedah Md, Omar, Affandi, Afroze, Bushra

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