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Cited by in CrossRef
For: Wu ZY, Li YL, Chang B. Pituitary stalk interruption syndrome and liver changes: From clinical features to mechanisms. World J Gastroenterol 2020; 26(44): 6909-6922 [PMID: 33311939 DOI: 10.3748/wjg.v26.i44.6909]
URL: https://www.wjgnet.com/1007-9327/full/v26/i44/6909.htm
Number Citing Articles
1
Geoanna Bautista. Overview of Congenital Hypopituitarism for the NeonatologistNeoReviews 2022; 23(5): e300 doi: 10.1542/neo.23-5-e300
2
Qiuxuan Guo, Jing Zhao, Shuang Yu. Clinical Features and Analysis in Pituitary Stalk Interruption SyndromeInternational Journal of Endocrinology 2024; 2024: 1 doi: 10.1155/2024/2493083
3
Huan He, Dong Mei Li. One Case of Pituitary Stalk Interruption Syndrome Associated with Liver CirrhosisEndocrine, Metabolic & Immune Disorders - Drug Targets 2023; 23(9): 1229 doi: 10.2174/1871530323666230228110650
4
Rongqian Wu, Jixiong Xu. Pituitary Stalk Interruption Syndrome with Excessive Height Growth Combined with Congenital Absence of the Uterus and Ovaries: A Rare Case Report and Review of the LiteratureDiabetes, Metabolic Syndrome and Obesity 2024; : 1739 doi: 10.2147/DMSO.S456678
5
Qibin Huang, Hongli Xu, Xi Wang, Jiangfeng Mao, Bingqing Yu, Yiyi Zhu, Rui Zhang, Bang Sun, Junyi Zhang, Wen Ji, Wanlu Ma, Min Nie, Xueyan Wu. Relationship between growth hormone deficiency and nonalcoholic fatty liver disease in patients with pituitary stalk interruption syndromeClinical Endocrinology 2022; 97(5): 612 doi: 10.1111/cen.14732
6
El Mehdi Mniai, Abderrahim Bourial, Siham Salam, Mohamed Mahi, Amal Rami. Short Stature: Think About the Pituitary Stalk Interruption SyndromeCureus 2023;  doi: 10.7759/cureus.35700
7
Rana Bilal Idrees, Mariam Malik, Faisal Ehsan Cheema, Maham Khalid, Farwa Malik, Muhammad Hamid Chaudhary. Lost Connection: A Case Report of Interrupted Pituitary Stalk SyndromeCureus 2024;  doi: 10.7759/cureus.60232
8
Ekaterina Iausheva, Sara Mohamed, Elizabeth Littlejohn, Tarek Mohamed, Mohammed Abdulmageed. Critical Hypoglycemia in a Newborn with Pituitary Stalk Interruption Syndrome in Conjunction with 16p11.2 Deletion Syndrome and Duplication of Xp22.33/Yp11.32Journal of Neonatology 2024; 38(1): 153 doi: 10.1177/09732179231172274