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Loke Kah Yin

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Full Name
Loke Kah Yin
Variants
Loke, K.Y.
Yin, L.K.
Loke, K.-Y.
 
Main Affiliation
 
Faculty
 
Email
paelky@nus.edu.sg
 

Publications

Results 1-20 of 67 (Search time: 0.022 seconds).

Issue DateTitleAuthor(s)
120083rd college of paediatrics and child health lecture - The past, the present and the shape of things to come...Loke, K.Y. ; Lin, J.B.Y.; Mabel, D.-Y.
21-Sep-2019A case of Cushing syndrome in a Wilms' tumourLim, Yvonne Yijuan; Sng, Andrew Anjian; Ng, Nicholas BH; Ho, Wei-li Cindy ; Loke, Kah-yin ; Lee, Yung-seng 
328-Feb-2018A Case of Neonatal Central Diabetes Insipidus in a Premature Infant - Challenges in Diagnosis and ManagementSNG ANJIAN ANDREW ; LOKE KAH YIN ; LIM YIJUAN, YVONNE 
41-Jan-2018A Case of Steroid-Responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT) in a Girl with Newly Diagnosed Hashimoto ThyroiditisLim, Yijuan Yvonne ; Sng, Anjian Andrew ; Ho, Cindy Wei-li ; Lee, Yung-Seng ; Loke, Kah-Yin 
52009A case of X-linked adrenal hypoplasia congenita, central precocious puberty and absence of the DAX-1 gene: Implications for pubertal regulationLoke, K.-Y. ; Poh, L.K.-S.; Lai, P.-S.; Lee, W.W.-R.
62003A distinctive type of metaphyseal chondrodysplasia with characteristic thickening of the distal ulna and radius: Possible metaphyseal chondrodysplasia-RosenbergLee, Y.-S. ; Loke, K.-Y. ; Elliott, A.M.; Lachman, R.S.
71-Dec-2021A novel de novo androgen receptor nonsense mutation in a sex-reversed 46,XY infantPoon, KS; Tan, KML; Loke, KY 
82002A novel melanocortin 3 receptor gene (MC3R) mutation associated with severe obesityLee, Y.-S. ; Poh, L.K.-S.; Loke, K.-Y. 
91999A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasiaSchipani, E.; Hunzelman, J.; Juppner, H.; Juppner, H.; Silve, C.; Le, Merrer M.; Loke, K.Y. ; Dillon, M.J.; Langman, C.
102003Adolescent health - A new perspective in SingaporeLoke, K.Y. 
112000An atypical kindred with X-linked adrenal hypoplasia congenita, normal puberty, and normal Dax-1 promoter and coding sequenceLoke, K.Y. ; Poh, K.S.L.; Tan, J.A.M.A.; Tay, A.H.N.; Walker, A.P.
121997Anti-GAD antibodies in Chinese patients with youth and adult-onset IDDM and NIDDMThai, A.C. ; Ng, W.Y. ; Lui, K.F.; Cheah, J.S. ; Loke, K.Y. ; Lee, W.R.W.
13Mar-2006Aortic aneurysmal disease and cutis laxa caused by defects in the elastin geneSzabo, Z.; Crepeau, M.W.; Mitchell, A.L.; Stephan, M.J.; Puntel, R.A.; Loke, K.Y. ; Kirk, R.C.; Urban, Z.
142008Association of raised liver transaminases with physical inactivity, increased waist hip ratio, and other metabolic morbidities in severely obese childrenLee, Y.S. ; Kek, B.L.K.; Poh, L.K.S.; Loke, K.Y. ; Saw, S.M. 
152009Bilateral facial nerve palsy in Kawasaki diseaseLim, T.C.W.; Yeo, W.S.; Loke, K.Y. ; Quek, S.C. 
161997Can growth hormone treatment improve the growth retardation in children associated with steroid dependent nephrotic syndromeYap, H.K. ; Loke, K.Y. ; Lee, K.O. 
172007Childhood hypopituitarismLoke, K.Y. 
18Dec-2008Clinical applications of molecular genetics: The model of congenital adrenal hyperplasiaLoke, K.Y. 
192008Clinical applications of molecular genetics: the model of congenital adrenal hyperplasia.Loke, K.Y. 
201991Cockayne syndrome--a case report, and a review of the premature aging syndromes in paediatrics.Loke, K.Y.