Loss of opportunities in the diagnosis and treatment of primary obstetric antiphospholipid syndrome (POAPS): from theory to reality
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10067-023-06846-8.pdf
Reference19 articles.
1. Meroni PL, Borghi MO, Grossi C, Chighizola CB, Durigutto P, Tedesco F (2018) Obstetric and vascular antiphospholipid syndrome: same antibodies but different diseases? Nat Rev Rheumatol 14(7):433–440. https://doi.org/10.1038/s41584-018-0032-6
2. Radin M, Foddai SG, Barinotti A, Cecchi I, Rubini E, Sciascia S et al (2021) Reducing the diagnostic delay in antiphospholipid syndrome over time: a real world observation. Orphanet J Rare Dis 16(1):280. https://doi.org/10.1186/s13023-021-01906-1
3. Faviez C, Chen X, Garcelon N, Neuraz A, Knebelmann B, Salomon R et al (2020) Diagnosis support systems for rare diseases: a scoping review. Orphanet J Rare Dis 15(1):94. https://doi.org/10.1186/s13023-020-01374-z
4. Miyakis S, Lockshin MD, Atsumi T, Branch DW, Brey RL, Cervera R et al (2006) International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thrombosis Haemostasis : JTH 4(2):295–306. https://doi.org/10.1111/j.1538-7836.2006.01753.x
5. Bulletins--Obstetrics ACoP. (2002) ACOG practice bulletin. Diagnosis and management of preeclampsia and eclampsia. Number 33, January 2002. Obstetrics and gynecology. 99(1):159–67. https://doi.org/10.1016/s0029-7844(01)01747-1.
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