Medical school approach to manage the current COVID-19 crisis

بواسطة Samarasekera, DD, Goh, DLM, Lau, TC
منشور في 2021

Urea cycle disorder presenting as bilateral mesial temporal sclerosis - An unusual cause of seizures: A case report and review of the literature

بواسطة Wang F.S., Goh D.L.M., Ong H.T.
منشور في 2019

Clinical and laboratory barriers to the timely diagnosis of sulphite oxidase deficiency

بواسطة Choong, C.T., Hart, C., Tan, E.S., Goh, D.L.M.
منشور في 2016

Resurgence of measles in Singapore: Profile of hospital cases

بواسطة Goh, D.L.M., Chew, F.T., Khor, S.H., Lee, B.W.
منشور في 2013

Novel CFTR gene mutation in a patient with CBAVD

بواسطة Goh, D.L.M., Zhou, Y., Chong, S.S., Ngiam, N.S.P., Goh, D.Y.T.
منشور في 2011

Edible 'bird's nest' - induced anaphylaxis: An under-recognized entity?

بواسطة Goh, D.L.M., Chew, F.-T., Chua, K.-Y., Chay, O.-M., Lee, B.-W.
منشور في 2014

Ethnic differences in genetic susceptibility to atopy and asthma in Singapore

بواسطة Shek, L.P.C., Tay, A.H.N., Goh, D.L.M., Lee, B.W.
منشور في 2014

Genetic susceptibility to asthma and atopy among Chinese in Singapore - Linkage to markers on chromosome 5q31-33

بواسطة Shek, L.P.-C., Tay, A.H., Chew, F.T., Goh, D.L.M., Lee, B.W.
منشور في 2013

Identification and characterization of novel mouse PDE4D isoforms: Molecular cloning, subcellular distribution and detection of isoform-specific intracellular localization signals

بواسطة Chandrasekaran, A., Toh, K.Y., Low, S.H., Tay, S.K.H., Brenner, S., Goh, D.L.M.
منشور في 2016

Identification and characterization of novel mouse PDE4D isoforms: Molecular cloning, subcellular distribution and detection of isoform-specific intracellular localization signals

بواسطة Chandrasekaran, A., Toh, K.Y., Low, S.H., Tay, S.K.H., Brenner, S., Goh, D.L.M.
منشور في 2011

Changes in PDE4D isoforms in the hippocampus of a patient with advanced Alzheimer disease [1]

بواسطة McLachlan, C.S., Chen, M.L., Lynex, C.N., Goh, D.L.M., Brenner, S., Tay, S.K.H.
منشور في 2014

Characterization of the human gene encoding α-aminoadipate aminotransferase (AADAT)

بواسطة Goh, D.L.M., Patel, A., Thomas, G.H., Salomons, G.S., Schor, D.S.M., Jakobs, C., Geraghty, M.T.
منشور في 2014

Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance

بواسطة Loscalzo, M.L., Goh, D.L.M., Loeys, B., Kent, K.C., Spevak, P.J., Dietz, H.C.
منشور في 2016

Unusually mild phenotype of AADC deficiency in 2 siblings

بواسطة Tay, S.K.H., Poh, K.S., Pang, Y.W., Low, P.S., Goh, D.L.M., Ong, H.T., Hyland, K.
منشور في 2011

Ethnic differences in genetic susceptibility to atopy and asthma

بواسطة Tay, A.H.N., Chew, F.T., Goh, D.L.M., Shek, L.P.C., Lee, B.W., Tan, E.C.
منشور في 2013

UGT1A1 haplotype mutation among Asians in Singapore

بواسطة Zhou, Y.Y., Lee, L.Y., Ng, S.Y., Hia, C.P.P., Low, K.T., Chong, Y.S., Goh, D.L.M.
منشور في 2016

Immunochemical characterization of edible bird's nest allergens

بواسطة Goh, D.L.M., Chua, K.Y., Chew, F.T., Seow, T.K., Ou, K.L., Yi, F.C., Lee, B.W.
منشور في 2013

Endotoxin levels in rural Thai and urban Singaporean homes

بواسطة Lee, A., Tan, T.-N., Shek, L.P., Goh, D.L.M., Van, Bever H., Lee, B.W., Ho, B., Ma, S., Sangsupawanich, P.
منشور في 2011

cMET and Refractive Error Progression in Children

بواسطة Khor, C.C., Grignani, R., Ng, D.P.K., Toh, K.Y., Chia, K.-S., Tan, D., Goh, D.L.M., Saw, S.-M.
منشور في 2014

Support for TGFB1 as a susceptibility gene for high myopia in individuals of Chinese descent

بواسطة Khor, C.C., Fan, Q., Goh, L., Tan, D., Young, T.L., Li, Y.-J., Seielstad, M., Goh, D.L.M., Saw, S.M.
منشور في 2014