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Cited by in CrossRef
For: Barada K, El Haddad A, Katerji M, Jomaa M, Usta J. Wilson’s disease in Lebanon and regional countries: Homozygosity and hepatic phenotype predominance. World J Gastroenterol 2017; 23(36): 6715-6725 [PMID: 29085216 DOI: 10.3748/wjg.v23.i36.6715]
URL: https://www.wjgnet.com/1007-9327/full/v23/i36/6715.htm
Number Citing Articles
1
C. Gerosa, D. Fanni, T. Congiu, M. Piras, F. Cau, M. Moi, G. Faa. Liver pathology in Wilson's disease: From copper overload to cirrhosisJournal of Inorganic Biochemistry 2019; 193: 106 doi: 10.1016/j.jinorgbio.2019.01.008
2
Xiaojin Li, Wei Zhang, Donghu Zhou, Tingxia Lv, Anjian Xu, Hejing Wang, Xinyan Zhao, Bei Zhang, Yanmeng Li, Siyu Jia, Yu Wang, Xiaoming Wang, Zhen Wu, Weijia Duan, Qianyi Wang, Yuemin Nan, Jia Shang, Wei Jiang, Yongpeng Chen, Sujun Zheng, Mei Liu, Liying Sun, Hong You, Jidong Jia, Xiaojuan Ou, Jian Huang. Complex ATP7B mutation patterns in Wilson disease and evaluation of a yeast model for functional analysis of variantsHuman Mutation 2019; 40(5): 552 doi: 10.1002/humu.23714
3
Hani Sayed Aboalam, Marwa Khalaf Hassan, Nada El-domiaty, Nagat Faisal Ibrahim, Anwar M. Ali, Wesam Hassan, Esam Ghanem Abu El Wafa, Ashraf Elsaghier, Helal F. Hetta, Mohamed Elbadry, Mohamed El-Kassas. Wilson’s disease clinic at the Assiut Liver Center in Egypt: a real well-established step on the wayEgyptian Liver Journal 2022; 12(1) doi: 10.1186/s43066-022-00205-z
4
Nadia Abbassi, Aicha Bourrahouat, Eduardo Couchonnal Bedoya, Cécile Pagan, Meriem El Qabli, Sana Maidoumi, Abdelouahed Belmalih, Olivier Guillaud, Najib Kissani, Abdelhak Abkari, Imane Chahid, Mohammed Abdoh Rafai, Nezha Mouane, Yamna Kriouile, Saadia Aidi, Moustpha Hida, Mounia Lakhdar Idrissi, Mohammed Faouzi Belahsen, Mohammed El Abkari, Maria Rkain, Zahi Ismaili, Azeddine Sedki, Muriel Bost, Nisrine Aboussair, Alain Lachaux. Phenotype and molecular characterization of Wilson's disease in MoroccoClinics and Research in Hepatology and Gastroenterology 2024; 48(5): 102335 doi: 10.1016/j.clinre.2024.102335
5
Amal Elfatih, Chadi Saad, Said Ismail, Wadha Al-Muftah, Radja Badji, Dima Darwish, Tasnim Fadl, Heba Yasin, Maryem Ennaifar, Rania Abdel-latif, Fatima Alkuwari, Muhammad Alvi, Yasser Al Sarraj, Asmaa Althani, Eleni Fthenou, Fatima Qafoud, Eiman Alkhayat, Nahla Afifi, Sara Tomei, Wei Liu, Stephan Lorenz, Najeeb Syed, Hakeem Almabrazi, Fazulur Rehaman Vempalli, Ramzi Temanni, Tariq Abu Saqri, Mohammed husen Khatib, Mehshad Hamza, Tariq Abu Zaid, Ahmed El Khouly, Tushar Pathare, Shafeeq Poolat, Rashid Al-Ali, Omar M. E. Albagha, Souhaila Al-Khodor, Mashael Alshafai, Ramin Badii, Lotfi Chouchane, Xavier Estivill, Khalid Fakhro, Hamdi Mbarek, Younes Mokrab, Jithesh V. Puthen, Karsten Suhre, Zohreh Tatari, Borbala Mifsud, Hamdi Mbarek. Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variantsEuropean Journal of Human Genetics 2024; 32(11): 1465 doi: 10.1038/s41431-024-01656-1
6
Maryem Sahli, Abdelali Zrhidri, Youssef El Kadiri, Imane Cherkaoui Jaouad, Toufik Meskini, Abdelaziz Sefiani. First application of next-generation sequencing in four families with Wilson disease in MoroccoEgyptian Journal of Medical Human Genetics 2023; 24(1) doi: 10.1186/s43042-023-00437-7
7
Sanay Naha, Sivan Velmathi. A fluorescence turn “on-off” imaging probe for sequential detection of Al3+ and L-Cysteine in HeLa cellsMethods 2024; 221: 27 doi: 10.1016/j.ymeth.2023.11.009
8
Achiya Zvi Amir, Moshe Frydman, Eyal Shteyer. Clinical and Translational Perspectives on WILSON DISEASE2019; : 319 doi: 10.1016/B978-0-12-810532-0.00030-6
9
Jianli Zhou, Qiao Zhang, Yuzhen Zhao, Moxian Chen, Shaoming Zhou, Yongwei Cheng. Early Diagnosis of Wilson’s Disease in Children in Southern China by Using Common ParametersFrontiers in Genetics 2022; 13 doi: 10.3389/fgene.2022.788658