Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hwee-Woon Lim"'
Autor:
Hwee-Woon Lim, Woei-Yuh Saw, Lei Feng, Yuan-Kun Lee, Ratha Mahendran, Irwin Kee-Mun Cheah, Iris Rawtaer, Alan Prem Kumar, Ee-Heok Kua, Rathi Mahendran, Ene-Choo Tan
Publikováno v:
Data in Brief, Vol 18, Iss , Pp 902-912 (2018)
It has been reported that relaxation techniques can improve physical health and cognitive function. A number of studies involving different types of relaxation practices showed changes in expression of genes. We investigated the gene expression patte
Externí odkaz:
https://doaj.org/article/b029837db2964ee887872eb360e17d4a
Autor:
Jerry C. Nagaputra, MBBS, Mark J.A. Koh, MBBS, Maggie Brett, PhD, Eileen C.P. Lim, BSc(Hon), Hwee-Woon Lim, MSc, Ene-Choo Tan, PhD
Publikováno v:
JAAD Case Reports, Vol 4, Iss 4, Pp 318-321 (2018)
Externí odkaz:
https://doaj.org/article/552094a10e7342beaec7ac3786dc1657
Autor:
Yi Zhen Ng, Lynette Wei Yi Wee, Ene-Choo Tan, Cristelle Chow, Ellen Birgitte Lane, Siew-Peng Lee, Hwee-Woon Lim, Te Lu Yap, Priya Bishnoi, John E.A. Common, Christina Ong, Mei Yi Low, Lian Derrick, Yee Hui Mok, Mark Jean Aan Koh, Declan P. Lunny
Publikováno v:
Pediatric Dermatology. 38:908-912
We report a case of junctional epidermolysis bullosa with pyloric atresia (JEB-PA) with minimal skin involvement but severe protein-losing enteropathy and airway involvement. Genetic analysis revealed heterozygous mutations in the ITGB4 gene encoding
Publikováno v:
Singapore Med J
INTRODUCTION Infantile haemangiomas (IH) are the most common vascular tumours in childhood. Over the past decade, treatment of IH has been revolutionised by the discovery of the effectiveness of beta-blockers in its treatment. We review our hospital
Autor:
Mark Jean Aan Koh, Jerry C. Nagaputra, Hwee-Woon Lim, Eileen C.P. Lim, Maggie Brett, Ene-Choo Tan
Publikováno v:
JAAD Case Reports, Vol 4, Iss 4, Pp 318-321 (2018)
JAAD Case Reports
JAAD Case Reports
Publikováno v:
The Cleft Palate-Craniofacial Journal. 54:442-445
Van der Woude syndrome (VWS) is a rare autosomal dominant genetic disorder characterized by orofacial clefting and lip pits. Mutations in the transcription factor interferon regulatory factor 6 gene ( IRF6) have been identified in individuals with VW
Publikováno v:
Neuropsychiatric Disease and Treatment
Ene-Choo Tan,1,2 Hwee-Woon Lim,1 Tze-Ern Chua,2,3 Hui-San Tan,1 Theresa MY Lee,2,3 Helen Y Chen2,3 1KK Research Centre, KK Women’s and Children’s Hospital, Singapore, Singapore; 2Paediatrics Academic Clinical Programme, SingHealth Duke-NUS Medica
Autor:
Mui Ching Tan, Joanne, Hwee Woon Lim, Jean-Aan Koh, Mark, Tan, Joanne Mui Ching, Lim, Hwee Woon, Koh, Mark Jean-Aan
Publikováno v:
Singapore Medical Journal; Mar2021, Vol. 62 Issue 3, p139-142, 4p
Publikováno v:
Cleft Palate Craniofacial Journal; Jul2017, Vol. 54 Issue 4, p442-445, 4p