An infant with Cushing syndrome

por Sng, Andrew, Loke, Kah Yin, Lim, Yvonne, Ho, Cindy
Publicado 2015

Pamidronate therapy for hypercalcemia of childhood malignancy

por Sng, Andrew, Loke, Kah Yin, Lim, Yvonne, Ho, Cindy
Publicado 2015

A novel de novo androgen receptor nonsense mutation in a sex-reversed 46,XY infant

por Poon, Kok-Siong, Tan, Karen Mei-Ling, Loke, Kah Yin
Publicado 2021

Clinical and mutational spectrum of patients with congenital lipoid adrenal hyperplasia in Southeast Asia

por Ariyawatkul, Kansuda, Yeetong, Patra, Jaruratanasirikul, Somchit, Loke, Kah Yin, Nakavachara, Pairunyar, Kongkanka, Chawkaew, Sahakitrungruang, Taninee
Publicado 2015

Genetic Testing Confirmed the Early Diagnosis of X-Linked Hypophosphatemic Rickets in a 7-Month-Old Infant

por Poon, Kok Siong, Sng, Andrew Anjian, Ho, Cindy Weili, Koay, Evelyn Siew-Chuan, Loke, Kah Yin
Publicado 2015

In-vitro function of upstream visfatin polymorphisms that are associated with adverse cardiometabolic parameters in obese children

por Ooi, Delicia Shu Qin, Ong, Siong Gim, Heng, Chew Kiat, Loke, Kah Yin, Lee, Yung Seng
Publicado 2016

Sirolimus therapy in a child with partially diazoxide-responsive hyperinsulinaemic hypoglycaemia

por Loke, Kah-Yin, Anjian, Andrew Sng, Yijuan, Yvonne Lim, Ho Wei Li, Cindy, Güemes, Maria, Hussain, Khalid
Publicado 2016