Jing Liang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Jing Liang has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Chen Dan-Chun
Department of Pediatrics, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China
1 shared publication - Chun-Kui Shao
Department of Pathology, the Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China
1 shared publication Dan He
1 shared publicationJian-Ning Chen
1 shared publicationJing Zhou
1 shared publication- Li Yin-Ya
Department of Pediatrics, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China
1 shared publication
Latest Publications
- Open Access
- 1 October 2025
- Published by AME Publishing Company in Translational Cancer Research
- Vol. 14 (10) , 6605-6617
Development and validation of a nomogram comprising GLUT1 and clinical characteristics for predicting overall survival in intrahepatic cholangiocarcinoma
Original Article Development and validation of a nomogram comprising GLUT1 and clinical characteristics for predicting overall survival in intrahepatic cholangiocarcinoma Li-Ping Gong, Yulan Weng, Jing Zhou, Xiangqi Huang, Jian-Ning Chen, Dan He, Yi-Wang Zhang, Yongmei Cui, Jing Liang, Chun-Kui Shao
- 1 October 2025
- Published by AME Publishing Company in Translational Cancer Research
- Vol. 14 (10) , 6605-6617
Open AccessDevelopment and validation of a nomogram comprising GLUT1 and clinical characteristics for predicting overall survival in intrahepatic cholangiocarcinoma
Original Article Development and validation of a nomogram comprising GLUT1 and clinical characteristics for predicting overall survival in intrahepatic cholangiocarcinoma Li-Ping Gong, Yulan Weng, Jing Zhou, Xiangqi Huang, Jian-Ning Chen, Dan He, Yi-Wang Zhang, Yongmei Cui, Jing Liang, Chun-Kui Shao
- Open Access
- 1 January 2025
- Published by Wiley in Case Reports in Pediatrics
- Vol. 2025 (1) , 9848886
A Case of Proteus Syndrome, Suspected as Maffucci Syndrome in a Chinese Child
Proteus syndrome (PS) is an exceptionally rare disorder characterized by asymmetric and disproportionate overgrowth of connective tissues. We report the case of an 8‐year‐old female presenting with irregular cranial protrusion, bilateral supraorbital ridge enlargement, overgrowth of the right hand and left foot, and a pelvic MRI revealing an ovarian tumor. Initially, the patient was suspected of having Maffucci syndrome (MS) upon admission. Genetic analysis of a lesion sample from the fifth toe of the left foot identified a heterozygous point mutation, 49G > A (p.Glu17Lys), in the AKT1 gene. The patient met the clinical‐molecular diagnostic criteria established by Leslie G. Biesecker, scoring 15 points, thereby confirming the diagnosis of AKT1‐related PS. This case report contributes to the enhanced understanding of PS diagnosis associated with AKT1 mutations.
- 1 January 2025
- Published by Wiley in Case Reports in Pediatrics
- Vol. 2025 (1) , 9848886
Open AccessA Case of Proteus Syndrome, Suspected as Maffucci Syndrome in a Chinese Child
Proteus syndrome (PS) is an exceptionally rare disorder characterized by asymmetric and disproportionate overgrowth of connective tissues. We report the case of an 8‐year‐old female presenting with irregular cranial protrusion, bilateral supraorbital ridge enlargement, overgrowth of the right hand and left foot, and a pelvic MRI revealing an ovarian tumor. Initially, the patient was suspected of having Maffucci syndrome (MS) upon admission. Genetic analysis of a lesion sample from the fifth toe of the left foot identified a heterozygous point mutation, 49G > A (p.Glu17Lys), in the AKT1 gene. The patient met the clinical‐molecular diagnostic criteria established by Leslie G. Biesecker, scoring 15 points, thereby confirming the diagnosis of AKT1‐related PS. This case report contributes to the enhanced understanding of PS diagnosis associated with AKT1 mutations.