Severe Congenital Dysfibrinogenemia (Fibrinogen-Riyadh): A Family Study | Citedby Results | Acta Haematologica | Karger Publishers

Skip to Main Content

Skip Nav Destination

Severe Congenital Dysfibrinogenemia (Fibrinogen-Riyadh): A Family Study

Acta Haematol (1992) 88 (4): 194–197.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

Evaluating for Suspected Child Abuse: Conditions That Predispose to Bleeding

Shannon L. Carpenter
Thomas C. Abshire
Emily Killough
James D. Anderst

Pediatrics (2022) 150 (4)

Evaluating for Suspected Child Abuse: Conditions That Predispose to Bleeding

Shannon L. Carpenter
Thomas C. Abshire
James D. Anderst
Shannon L. Carpenter
Thomas C. Abshire
James D. Anderst
Jeffrey Hord
Gary Crouch
Gregory Hale
Brigitta Mueller
Zora Rogers
Patricia Shearer
Eric Werner
Stephen Feig
Eric Kodish
Alan Gamis

Pediatrics (2013) 131 (4): e1357.

A review of long‐term prophylaxis in the rare inherited coagulation factor deficiencies

T. TODD
D. J. PERRY

Haemophilia (2010) 16 (4): 569.

Hematopoietic stem cell transplantation for Hodgkin’s disease in a patient with dysfibrinogenemia and thrombosis

Apar Kishor Ganti
Julie M. Vose
William D. Haire

Journal of Thrombosis and Thrombolysis (2007) 23 (2): 155.

Cephalhaematoma in a child with acute promyelocytic leukaemia

Michael Goldman
Chaim Kaplinsky

Pediatric Radiology (2002) 32 (9): 695.

Hereditary Bleeding Disorders in Riyadh, Saudi Arabia

Ibrahim M. Al-Fawaz
Abdeljalil M.A. Gader
Hassan M. Bahakim
Fahad Al-Mohareb
Abdulkarim K. Al-Momen
Mohamed S. Harakati

Annals of Saudi Medicine (1996) 16 (3): 257.