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- [1] De Novo CSNK2B Mutations in Five Cases of Poirier-Bienvenu Neurodevelopmental SyndromeFRONTIERS IN NEUROLOGY, 2022, 13Yang, Qi论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaZhang, Qinle论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaYi, Shang论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaQin, Zailong论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaShen, Fei论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaOu, Shang论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaLuo, Jingsi论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R ChinaHe, Sheng论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Dept Genet & Metab Cent Lab, Nanning, Peoples R China Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Guangxi Key Lab Birth Defects Res & Prevent, Guangxi Key Lab Reprod Hlth & Birth Defects Preve, Nanning, Peoples R China
- [2] Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2BMOLECULAR GENETICS & GENOMIC MEDICINE, 2024, 12 (01):Li, Danyang论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Univ Tradit Chinese Med, Sch Publ Hlth, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaZhou, Bingbo论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaTian, Xinyuan论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Univ Tradit Chinese Med, Sch Publ Hlth, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaChen, Xue论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaWang, Yupei论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaHao, Shengju论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaZhang, Chuan论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Med Genet Ctr, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Lanzhou 730050, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R ChinaHui, Ling论文数: 0 引用数: 0 h-index: 0机构: Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China Gansu Univ Tradit Chinese Med, Sch Publ Hlth, Lanzhou, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Med Genet Ctr, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Lanzhou 730050, Gansu, Peoples R China Gansu Prov Matern & Child Care Hosp, Gansu Prov Clin Res Ctr Birth Defects & Rare Dis, Med Genet Ctr, Lanzhou, Gansu, Peoples R China
- [3] Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutationNEUROGENETICS, 2021, 22 (04) : 323 - 332Yang, Sai论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaWu, Liwen论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaLiao, Hongmei论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaLu, Xiulan论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaZhang, Xiao论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaKuang, Xiaojun论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R ChinaYang, Liming论文数: 0 引用数: 0 h-index: 0机构: Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China Hunan Childrens Hosp, Dept Neurol, Ziyuan Rd & 86, Changsha 410001, Hunan, Peoples R China
- [4] Poirier-Bienvenu neurodevelopmental syndrome: A report of a patient with a pathogenic variant in CSNK2B with abnormal linear growthAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (02) : 539 - 543Selvam, Pavalan论文数: 0 引用数: 0 h-index: 0机构: Atwal Clin Genom & Personalized Med, Palm Beach, FL USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USAJain, Angita论文数: 0 引用数: 0 h-index: 0机构: Atwal Clin Genom & Personalized Med, Palm Beach, FL USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USACheema, Anvir论文数: 0 引用数: 0 h-index: 0机构: Atwal Clin Genom & Personalized Med, Palm Beach, FL USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USAAtwal, Herjot论文数: 0 引用数: 0 h-index: 0机构: Atwal Clin Genom & Personalized Med, Palm Beach, FL USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USAForghani, Irman论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn, Dept Human Genet, Miami, FL 33136 USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USAAtwal, Paldeep S.论文数: 0 引用数: 0 h-index: 0机构: Atwal Clin Genom & Personalized Med, Palm Beach, FL USA Atwal Clin Genom & Personalized Med, Palm Beach, FL USA
- [5] Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutationneurogenetics, 2021, 22 : 323 - 332Sai Yang论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyLiwen Wu论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyHongmei Liao论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyXiulan Lu论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyXiao Zhang论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyXiaojun Kuang论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of NeurologyLiming Yang论文数: 0 引用数: 0 h-index: 0机构: Hunan Children’s Hospital,Department of Neurology
- [6] Splicing Interruption by Intron Variants in CSNK2B Causes Poirier-Bienvenu Neurodevelopmental Syndrome: A Focus on Genotype-Phenotype CorrelationsFRONTIERS IN NEUROSCIENCE, 2022, 16Zhang, Wen论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Clin Res Ctr Children Neurodev Disabil Hunan Prov, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R ChinaYe, Fanghua论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R ChinaChen, Shimeng论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Clin Res Ctr Children Neurodev Disabil Hunan Prov, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Clin Res Ctr Children Neurodev Disabil Hunan Prov, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R ChinaPang, Nan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Clin Res Ctr Children Neurodev Disabil Hunan Prov, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R ChinaYin, Fei论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Clin Res Ctr Children Neurodev Disabil Hunan Prov, Changsha, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha, Peoples R China
- [7] De novo pathogenic variants in CSNK2B cause a new intellectual disability-craniodigital syndrome distinguished from Poirier-Bienvenu neurodevelopmental syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 129 - 130Asif, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Inst Biochem 1, Fac Med, Cologne, Germany Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyKaygusuz, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Inst Biochem 1, Fac Med, Cologne, Germany Univ Med Ctr Gottingen, Inst Human Genet, Gottingen, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyShinawi, M.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, Dept Pediat, Div Genet & Genom Med, St Louis, MO 63110 USA Univ Cologne, Cologne Ctr Genom, Cologne, GermanyNickelsen, A.论文数: 0 引用数: 0 h-index: 0机构: Westphalian Wilhelms Univ, Inst Pharmaceut & Med Chem, Munster, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyHochscherf, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Biochem, Dept Chem, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyLindenblatt, D.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Inst Biochem, Dept Chem, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyNoegel, A. A.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyTinschert, S.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Zentrum Med Genet, Innsbruck, Austria Univ Cologne, Cologne Ctr Genom, Cologne, Germany论文数: 引用数: h-index:机构:Fortugno, P.论文数: 0 引用数: 0 h-index: 0机构: Ist Dermopat Immacolata IDI IRCCS, Rome, Italy Univ Cologne, Cologne Ctr Genom, Cologne, GermanyJose, J.论文数: 0 引用数: 0 h-index: 0机构: Westphalian Wilhelms Univ, Inst Pharmaceut & Med Chem, Munster, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyBrancati, F.论文数: 0 引用数: 0 h-index: 0机构: Ist Dermopat Immacolata IDI IRCCS, Rome, Italy Univ Aquila, Dept Life Hlth & Environm Sci, Med Genet, Laquila, Italy Univ Cologne, Cologne Ctr Genom, Cologne, GermanyNuernberg, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, GermanyHussain, M. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Inst Biochem 1, Fac Med, Cologne, Germany Univ Cologne, Ctr Mol Med Cologne, Cologne, Germany Univ Cologne, Cologne Ctr Genom, Cologne, Germany
- [8] Case report: Novel deletions in the 6p21.33 involving the CSNK2B gene in patients with Poirier-Bienvenu neurodevelopmental syndrome and literature reviewFRONTIERS IN MEDICINE, 2024, 11Zhang, Xuan论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R ChinaLu, Hongjuan论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R ChinaJi, Yichen论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R ChinaSun, Wei论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R China Capital Med Univ, Xuanwu Hosp, Dept Neurol, Beijing, Peoples R China
- [9] Characterization of Epilepsy and Neurodevelopmental disorders in familiar and sporadic cases of Poirier-Bienvenu Neurodevelopmental SyndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 99 - 99Stregapede, Fabrizia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyTerracciano, Allessandra论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyMicalizzi, Alessia论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyTrivisano, Marina论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyDe Dominicis, Angela论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyDentici, Marialisa论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyQuintavalle, Chiara论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyCappelletti, Simona论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalySpecchio, Nicola论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, ItalyNovelli, Antonio论文数: 0 引用数: 0 h-index: 0机构: IRCCS Bambino Gesu Childrens Hosp, Rome, Italy IRCCS Bambino Gesu Childrens Hosp, Rome, Italy
- [10] Case report: Two cases of Poirier-Bienvenu neurodevelopmental syndrome and review of literatureFRONTIERS IN PEDIATRICS, 2023, 11Chen, Xiaolan论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R ChinaHan, Yunli论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R ChinaLi, Xing论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R ChinaHuang, Shiqin论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R ChinaYuan, Hai论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R ChinaQin, Yuanhan论文数: 0 引用数: 0 h-index: 0机构: Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China Guangxi Med Univ, Dept Pediat, Affiliated Hosp 1, Nanning, Peoples R China