Gino V Hu-A-Ng
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Explore the profile of Gino V Hu-A-Ng including associated specialties, affiliations and a list of published articles.
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4
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10
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Recent Articles
1.
Witkamp D, Oudejans E, Hoogterp L, Hu-A-Ng G, Glaittli K, Stevenson T, et al.
Front Neurosci
. 2024 Feb;
18:1275744.
PMID: 38352041
Vanishing white matter (VWM) is a devastating autosomal recessive leukodystrophy, resulting in neurological deterioration and premature death, and without curative treatment. Pathogenic hypomorphic variants in subunits of the eukaryotic initiation...
2.
Oudejans E, Witkamp D, Hu-A-Ng G, Hoogterp L, van Rooijen-van Leeuwen G, Kruijff I, et al.
Life Sci Alliance
. 2024 Jan;
7(3).
PMID: 38171595
The leukodystrophy vanishing white matter (VWM) is characterized by chronic and episodic acute neurological deterioration. Curative treatment is presently unavailable. Pathogenic variants in the genes encoding eukaryotic initiation factor 2B...
3.
Bugiani M, Abbink T, Edridge A, van der Hoek L, Hillen A, van Til N, et al.
Ann Clin Transl Neurol
. 2023 May;
10(6):904-917.
PMID: 37165777
Objective: Mucopolysaccharidosis type IIIA (MPSIIIA) caused by recessive SGSH variants results in sulfamidase deficiency, leading to neurocognitive decline and death. No disease-modifying therapy is available. The AAVance gene therapy trial...
4.
Witkamp D, Oudejans E, Hu-A-Ng G, Hoogterp L, Krzywanska A, Znidarsic M, et al.
Ann Clin Transl Neurol
. 2022 Jul;
9(8):1147-1162.
PMID: 35778832
Objective: Vanishing white matter (VWM) is a leukodystrophy, characterized by stress-sensitive neurological deterioration and premature death. It is currently without curative treatment. It is caused by bi-allelic pathogenic variants in...