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For: Dieterich K, Kimber E, Hall JG. Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care. Am J Med Genet C Semin Med Genet 2019;181:345-53. [PMID: 31410997 DOI: 10.1002/ajmg.c.31732] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Hageman G, Nihom J. Fetuses and infants with Amyoplasia congenita in congenital Zika syndrome: The evidence of a viral cause. A narrative review of 144 cases. European Journal of Paediatric Neurology 2022. [DOI: 10.1016/j.ejpn.2022.11.002] [Reference Citation Analysis]
2 Dahan-Oliel N, van Bosse H, Darsaklis VB, Rauch F, Bedard T, Bardai G, James M, Raney E, Freese K, Hyer L, Altiok A, Pellett J, Giampietro P, Hall J, Hamdy RC. Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registry. BMJ Open 2022;12:e060591. [PMID: 36307157 DOI: 10.1136/bmjopen-2021-060591] [Reference Citation Analysis]
3 Dieterich K. PNS or not PNS, a dilemma of the post-genomic era in neurogenic developmental disorders. Eur J Paediatr Neurol 2022;37:A3. [PMID: 35305891 DOI: 10.1016/j.ejpn.2022.03.003] [Reference Citation Analysis]
4 Le Tanno P, Latypova X, Rendu J, Fauré J, Bourg V, Gauthier M, Billy-Lopez G, Jouk PS, Dieterich K. Diagnostic workup in children with arthrogryposis: description of practices from a single reference centre, comparison with literature and suggestion of recommendations. J Med Genet 2021:jmedgenet-2021-107823. [PMID: 34876503 DOI: 10.1136/jmedgenet-2021-107823] [Reference Citation Analysis]
5 Sions JM, Donohoe M, Beisheim EH, Shank TM, Nichols LR. Falls and Associated Factors among Adolescents and Young Adults with Arthrogryposis Multiplex Congenita. Int J Rare Dis Disord 2021;4:035. [PMID: 34723192 DOI: 10.23937/2643-4571/1710035] [Reference Citation Analysis]
6 Piccolo G, d'Annunzio G, Amadori E, Riva A, Borgia P, Tortora D, Maghnie M, Minetti C, Gitto E, Iacomino M, Baldassari S, Fiorillo C, Zara F, Striano P, Salpietro V. Neuromuscular and Neuroendocrinological Features Associated With ZC4H2-Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report. Front Neurol 2021;12:704747. [PMID: 34322088 DOI: 10.3389/fneur.2021.704747] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Langston S, Chu A. Arthrogryposis Multiplex Congenita. Pediatr Ann 2020;49:e299-304. [PMID: 32674167 DOI: 10.3928/19382359-20200624-01] [Reference Citation Analysis]
8 Mis EK, Al-Ali S, Ji W, Spencer-Manzon M, Konstantino M, Khokha MK, Jeffries L, Lakhani SA. The latest FADS: Functional analysis of GLDN patient variants and classification of GLDN-associated AMC as a type of viable fetal akinesia deformation sequence. Am J Med Genet A 2020;182:2291-6. [PMID: 32812332 DOI: 10.1002/ajmg.a.61783] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Seidahmed MZ, Al-Kindi A, Alsaif HS, Miqdad A, Alabbad N, Alfifi A, Abdelbasit OB, Alhussein K, Alsamadi A, Ibrahim N, Al-Futaisi A, Al-Maawali A, Alkuraya FS. Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans. Hum Genet 2020;139:513-9. [PMID: 31960134 DOI: 10.1007/s00439-020-02117-7] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
10 Griffet J, Dieterich K, Bourg V, Bourgeois E. Amyoplasie et arthrogryposes distales. Conférences D'enseignement 2020 2020. [DOI: 10.1016/b978-2-294-77250-4.00013-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]