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For: Hellmund A, Berg C, Geipel A, Müller A, Gembruch U. Prenatal diagnosis of fetal akinesia deformation sequence (FADS): a study of 79 consecutive cases. Arch Gynecol Obstet 2016;294:697-707. [DOI: 10.1007/s00404-016-4017-x] [Cited by in Crossref: 17] [Cited by in F6Publishing: 12] [Article Influence: 2.8] [Reference Citation Analysis]
Number Citing Articles
1 Reischer T, Liebmann-Reindl S, Bettelheim D, Balendran-Braun S, Streubel B. Genetic diagnosis and clinical evaluation of severe fetal akinesia syndrome. Prenat Diagn 2020;40:1532-9. [PMID: 32779773 DOI: 10.1002/pd.5809] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
2 Niles KM, Blaser S, Shannon P, Chitayat D. Fetal arthrogryposis multiplex congenita/fetal akinesia deformation sequence (FADS)-Aetiology, diagnosis, and management. Prenat Diagn 2019;39:720-31. [PMID: 31218730 DOI: 10.1002/pd.5505] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 4.7] [Reference Citation Analysis]
3 Sileo FG, Kulkarni A, Branescu I, Homfray T, Dempsey E, Mansour S, Thilaganathan B, Bhide A, Khalil A. Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosis. Ultrasound Obstet Gynecol 2020;56:416-21. [PMID: 32196790 DOI: 10.1002/uog.22019] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 Busack B, Ott CE, Henrich W, Verlohren S. Prognostic significance of prenatal ultrasound in fetal arthrogryposis multiplex congenita. Arch Gynecol Obstet 2021;303:943-53. [PMID: 33090266 DOI: 10.1007/s00404-020-05828-4] [Reference Citation Analysis]
5 Correa ARE, Naini K, Mishra P, Dadhwal V, Agarwal R, Shukla R, Kabra M, Gupta N. Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis. Prenat Diagn 2021. [PMID: 34302381 DOI: 10.1002/pd.6022] [Reference Citation Analysis]
6 Toshimitsu M, Nagaoka S, Kobori S, Ogawa M, Suzuki F, Kato T, Miyai S, Kawamura R, Inagaki H, Kurahashi H, Murotsuki J. Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome. Case Rep Obstet Gynecol 2019;2019:6753184. [PMID: 31662930 DOI: 10.1155/2019/6753184] [Reference Citation Analysis]
7 Tjon JK, Tan-Sindhunata GM, Bugiani M, Witbreuk MM, van der Sluijs JA, Weiss MM, van de Pol LA, van Weissenbruch MM, van der Knoop BJ, de Vries JI. Fetal akinesia deformation sequence, arthrogryposis multiplex congenita, and bilateral clubfeet: Is motor assessment of additional value for in utero diagnosis? A 10-year cohort study. Prenat Diagn 2019;39:219-31. [PMID: 30578734 DOI: 10.1002/pd.5411] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
8 Tjon JK, Lakeman P, van Leeuwen E, Waisfisz Q, Weiss MM, Tan-Sindhunata GMB, Nikkels PGJ, van der Voorn PJP, Salomons GS, Burchell GL, Linskens IH, van der Knoop BJ, de Vries JIP. Fetal akinesia deformation sequence and massive perivillous fibrin deposition resulting in fetal death in six fetuses from one consanguineous couple, including literature review. Mol Genet Genomic Med 2021;9:e1827. [PMID: 34636181 DOI: 10.1002/mgg3.1827] [Reference Citation Analysis]
9 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]
10 Dempsey E, Homfray T, Simpson JM, Jeffery S, Mansour S, Ostergaard P. Fetal hydrops – a review and a clinical approach to identifying the cause. Expert Opinion on Orphan Drugs 2020;8:51-66. [DOI: 10.1080/21678707.2020.1719827] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
11 Sparks TN, Thao K, Lianoglou BR, Boe NM, Bruce KG, Datkhaeva I, Field NT, Fratto VM, Jolley J, Laurent LC, Mardy AH, Murphy AM, Ngan E, Rangwala N, Rottkamp CAM, Wilson L, Wu E, Uy CC, Valdez Lopez P, Norton ME; University of California Fetal–Maternal Consortium (UCfC). Nonimmune hydrops fetalis: identifying the underlying genetic etiology. Genet Med 2019;21:1339-44. [PMID: 30410095 DOI: 10.1038/s41436-018-0352-6] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 4.3] [Reference Citation Analysis]
12 van Bosse HJP. Orthopaedic care of the child with arthrogryposis: a 2020 overview. Curr Opin Pediatr 2020;32:76-85. [PMID: 31743218 DOI: 10.1097/MOP.0000000000000847] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
13 Akalin M, Demirci O, Bolat G, Kahramanoglu O, Eric Ozdemir M, Karaman A. Foetal thoracic hypoplasia: concomitant anomalies and neonatal outcomes. J Obstet Gynaecol 2021;:1-6. [PMID: 34579606 DOI: 10.1080/01443615.2021.1945014] [Reference Citation Analysis]
14 Carneiro-Sampaio M, Moreira-Filho CA, Bando SY, Demengeot J, Coutinho A. Intrauterine IPEX. Front Pediatr 2020;8:599283. [PMID: 33330291 DOI: 10.3389/fped.2020.599283] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]