For: | Li MZ, Yuan L, Zhuo ZQ. Gene diagnosis of infantile neurofibromatosis type I: A case report. World J Clin Cases 2020; 8(22): 5678-5683 [PMID: 33344560 DOI: 10.12998/wjcc.v8.i22.5678] |
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URL: | https://www.wjgnet.com/2307-8960/full/v8/i22/5678.htm |
Number | Citing Articles |
1 |
Ming Gao, Haokun Liu, Qiying Sun, Guang Yang. The gene diagnosis of neurofibromatosis type I with headache as the main symptom: A case report and review of the literature. Frontiers in Neurology 2022; 13 doi: 10.3389/fneur.2022.874613
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2 |
Shahram Savad, Mohammad-Hossein Modarressi, Sarang Younesi, Mahnaz Seifi-Alan, Niusha Samadaian, Mona Masoomy, Mehdi Dianatpour, Shima Norouzi, Saloomeh Amidi, Amirreza Boroumand, Mahmoud Reza Ashrafi, Alireza Ronagh, Maryam Eslami, Maryam Hashemnejad, Shahab Nourian, Sanaz Mohammadi, Mohammad Mahdi Taheri Amin, Morteza Heidari, Mahin Seifi-Alan, Hossein Shojaaldini Ardakani, Fatemeh Aghamahdi, Sheyda Khalilian, Soudeh Ghafouri-Fard. A Comprehensive Overview of NF1 Mutations in Iranian Patients. NeuroMolecular Medicine 2024; 26(1) doi: 10.1007/s12017-024-08790-5
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