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Ngu, Lock Hock
102
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Online (102)
Mediatypes
Articles (Online) (65)
Bookchapter (Online) (2)
OpenAccess-fulltext (35)
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1
Corrigendum to: Prevalence of DDC genotypes in patients wit..:
Himmelreich, Nastassja
;
Bertoldi, Mariarita
;
Alfadhel, Majid
...
Molecular Genetics and Metabolism. 139 (2023) 4 - p. 107647 , 2023
Link:
https://doi.org/10.1016/..
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2
Prevalence of DDC genotypes in patients with aromatic L-ami..:
Himmelreich, Nastassja
;
Bertoldi, Mariarita
;
Alfadhel, Majid
...
Molecular Genetics and Metabolism. 139 (2023) 3 - p. 107624 , 2023
Link:
https://doi.org/10.1016/..
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3
Myoclonus‐Ataxia Syndrome Associated with Hyperprolinemia T..:
Ong, Tien Lee
;
Lau, Yue Hui
;
Ngu, Lock Hock
...
Movement Disorders Clinical Practice. 10 (2023) S3 - p. , 2023
Link:
https://doi.org/10.1002/..
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4
Molecular, Biochemical, and Clinical Characterization of Th..:
Abdul Wahab, Siti Aishah
;
Yakob, Yusnita
;
Mohd Khalid, Mohd Khairul Nizam
...
Genetics Research. 2022 (2022) - p. 1-7 , 2022
Link:
https://doi.org/10.1155/..
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5
Long-term clinical outcomes of patients treated with elosul..:
Mitchell, John
;
Ramaswami, Uma
;
Longo, Nicola
...
Molecular Genetics and Metabolism. 129 (2020) 2 - p. S112 , 2020
Link:
https://doi.org/10.1016/..
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6
Long-term treatment with elosulfase alfa has an acceptable ..:
Burton, Barbara
;
Guffon, Nathalie
;
Ramaswami, Uma
...
Molecular Genetics and Metabolism. 129 (2020) 2 - p. S36 , 2020
Link:
https://doi.org/10.1016/..
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7
Clinical, biochemical and genetic profiles of patients with..:
Leong, Huey Yin
;
Abdul Azize, Nor Azimah
;
Chew, Hui Bein
...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
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8
Identification of mutations in Malaysian patients with argi..:
Ali, Ernie Zuraida
;
Yakob, Yusnita
;
Ngu, Lock Hock
Molecular Genetics and Metabolism Reports. 21 (2019) - p. 100525 , 2019
Link:
https://doi.org/10.1016/..
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9
Mutation Study of Malaysian Patients with Ornithine Transca..:
Ali, Ernie Zuraida
;
Zakaria, Yuslina
;
Mohd Radzi, Mohd Amran
..
BioMed Research International. 2018 (2018) - p. 1-15 , 2018
Link:
https://doi.org/10.1155/..
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10
Fructose-1,6-bisphosphatase deficiency as a cause of recurr..:
Moey, Lip Hen
;
Abdul Azize, Nor Azimah
;
Yakob, Yusnita
...
Pediatrics & Neonatology. 59 (2018) 4 - p. 397-403 , 2018
Link:
https://doi.org/10.1016/..
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11
Mutations in mitochondrial complex I assembly factor NDUFAF..:
Baertling, Fabian
;
Sánchez-Caballero, Laura
;
Timal, Sharita
...
Molecular Genetics and Metabolism. 120 (2017) 3 - p. 243-246 , 2017
Link:
https://doi.org/10.1016/..
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12
Two Novel Gross Deletions of TSC2 in Malaysian Patients wit..:
Ismail, Nur Farrah Dila
;
Nik Abdul Malik, Nik Mohd Ariff
;
Mohseni, Jafar
...
Japanese Journal of Clinical Oncology. 44 (2014) 5 - p. 506-511 , 2014
Link:
https://doi.org/10.1093/..
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13
Mutational Analyses on X-Linked Adrenoleukodystrophy Reveal..:
Hung, Kun-Long
;
Wang, Jinn-Shyan
;
Keng, Wee Teik
...
Pediatric Neurology. 49 (2013) 3 - p. 185-190 , 2013
Link:
https://doi.org/10.1016/..
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14
A catalytic defect in mitochondrial respiratory chain compl..:
Ngu, Lock Hock
;
Nijtmans, Leo G.
;
Distelmaier, Felix
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822 (2012) 2 - p. 168-175 , 2012
Link:
https://doi.org/10.1016/..
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15
Neonatal intrahepatic cholestasis associated with citrin de..:
Chew, Hui Bein
;
Ngu, Lock Hock
;
Zabedah, Md Yunus
...
Journal of Inherited Metabolic Disease. 33 (2010) S3 - p. 489-495 , 2010
Link:
https://doi.org/10.1007/..
1-15