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Cited by in CrossRef
For: Awad AW, Aleck KA, Bhardwaj RD. Concomitant achondroplasia and Chiari II malformation: A double-hit at the cervicomedullary junction. World J Clin Cases 2014; 2(11): 711-716 [PMID: 25405196 DOI: 10.12998/wjcc.v2.i11.711]
URL: https://www.wjgnet.com/2307-8960/full/v2/i11/711.htm
Number Citing Articles
1
Aldesia Provenzano, Andrea La Barbera, Mirko Scagnet, Angelica Pagliazzi, Giovanna Traficante, Marilena Pantaleo, Lucia Tiberi, Debora Vergani, Nehir Edibe Kurtas, Silvia Guarducci, Sara Bargiacchi, Giulia Forzano, Rosangela Artuso, Viviana Palazzo, Ada Kura, Flavio Giordano, Daniele di Feo, Marzia Mortilla, Claudio De Filippi, Gianluca Mattei, Livia Garavelli, Betti Giusti, Lorenzo Genitori, Orsetta Zuffardi, Sabrina Giglio. Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genesHuman Genetics 2021; 140(4): 625 doi: 10.1007/s00439-020-02231-6
2
Luca Massimi, Massimo Caldarelli, Concezio Di Rocco. Textbook of Pediatric Neurosurgery2018; : 1 doi: 10.1007/978-3-319-31512-6_9-1
3
Luca Massimi, Massimo Caldarelli, Concezio Di Rocco. Textbook of Pediatric Neurosurgery2020; : 243 doi: 10.1007/978-3-319-72168-2_9
4
Alessio Coi, Michele Santoro, Ester Garne, Anna Pierini, Marie‐Claude Addor, Jean‐Luc Alessandri, Jorieke E. H. Bergman, Fabrizio Bianchi, Ljubica Boban, Paula Braz, Clara Cavero‐Carbonell, Miriam Gatt, Martin Haeusler, Kari Klungsøyr, Jennifer J. Kurinczuk, Monica Lanzoni, Nathalie Lelong, Karen Luyt, Olatz Mokoroa, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary T. O'Mahony, Isabelle Perthus, Judith Rankin, Anke Rissmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Katarzyna Wisniewska, Nataliia Zymak‐Zakutnia, Ingeborg Barišić. Epidemiology of achondroplasia: A population‐based study in EuropeAmerican Journal of Medical Genetics Part A 2019; 179(9): 1791 doi: 10.1002/ajmg.a.61289
5
Claude Stoll, Yves Alembik, Beatrice Dott, Marie-Paule Roth. Associated anomalies in cases with achondroplasiaEuropean Journal of Medical Genetics 2022; 65(11): 104612 doi: 10.1016/j.ejmg.2022.104612
6
Claude G. Stoll, Yves Alembik, Marie Paule Roth. Associated Anomalies in Cases with AchondroplasiaSSRN Electronic Journal 2022;  doi: 10.2139/ssrn.4170102