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Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects

Kanter, J., Smith, W. R., Desai, P. C., Treadwell, M., Andemariam, B., Little, J., Nugent, D., Claster, S., Manwani, D. G., Baker, J., Strouse, J. J., Osunkwo, I., Stewart, R. W., King, A., Shook, L. M., Roberts, J. D., & Lanzkron, S.

Mechanisms of Bone Impairment in Sickle Bone Disease

Giordano P, Urbano F, Lassandro G, & Faienza MF
Sickle Cell Disease

Provider Attitudes and Practices Regarding Intrauterine System (IUS) Insertion in Adolescents With and Without Bleeding Disorders for Management of Heavy Menstrual Bleeding

O’Flynn O’Brien K, Wheeler AP, Borzutzky C, Haley KM, Kouides P, and Adeymei-Fowode O
Bleeding Disorders Heavy Menstrual Bleeding LAN Developed

Updated Guidelines for Treatment of von Willebrand Disease

James, P.D., Connell, N.T., Ameer, B., Di Paola, J., Eikenbook, J., Giraud, N., et al.
Von Willebrand Disease

Laboratory misdiagnosis of von Willebrand disease in post-menarchal females: A multi-center study

Jaffray J, Staber JM, Malvar J, Sidonio R, Haley KM, Stillings A, Weyand A, Hege K, Jain S, Gupta S, Agnew C, Wheeler A, Pawar A, Sharma M, Chitlur M, OʼBrien SH, Kouides P.
Von Willebrand Disease

Women and girls with haemophilia and bleeding tendencies: Outcomes related to menstruation, pregnancy, surgery and other bleeding episodes from a retrospective chart review

Chaudhury A, Sidonio R Jr, Jain N, Tsao E, Tymoszczuk J, Oviedo Ovando M, Kulkarni R.
Acquired Hemophilia Bleeding Disorders Pregnancy and Postpartum