Results 121 to 130 of about 54,540 (236)

Acquired von Willebrand Syndrome and Hemolysis in High-Shear States: Time for Cardio-Hematology Collaboration. [PDF]

JACC Asia
Passaniti G, Zhan H, Zheng H.
europepmc   +1 more source

Occurrence of Cold Agglutinin Disease among Patients with Autoimmune Hemolytic Anemia: A Hungarian Single-Center Experience. [PDF]

Transfus Med Hemother
Brugós B, Kerecsenyi M, Simon Z, Illés Á.   +3 more
europepmc   +1 more source

A Rare Case of Neonatal Kaposiform Hemangioendothelioma With Kasabach-Merritt Phenomenon Presenting as an Abdominal Mass Without Cutaneous Manifestations. [PDF]

Case Rep Hematol
Park SY, Halari A, Palacio-Meadows J, Parikh NS, Bentsen D, Puvabanditsin S.   +5 more
europepmc   +1 more source

Is congenital thrombotic thrombocytopenic purpura a risk factor for ischemic osteonecrosis of the hip joint (Legg-Calvé-Perthes disease)? [PDF]

Thromb J
Laemmle A, Lämmle B.
europepmc   +1 more source

Massive Splenomegaly Secondary to Hematologic Dyscrasia. [PDF]

Cureus
Del Bosque J, Salomon D, Verano R, De La Peña DD, Verano R.   +4 more
europepmc   +1 more source

Bartonella quintana endocarditis presenting with severe coombs-positive anemia: a case report. [PDF]

BMC Cardiovasc Disord
Zhang Y, Wangjia P, Yang S, Liu P, Xu X, Han H.   +5 more
europepmc   +1 more source

Fatal Garlic (<i>Allium sativum</i>) Toxicosis in a Dog: Gross and Histopathological Findings in a Rare Case of Systemic Hemolytic Injury. [PDF]

Animals (Basel)
Biasibetti E, Maza V, Tagliati V, Zoppi S, Di Blasio A, Bozzetta E, Pezzolato M.   +6 more
europepmc   +1 more source

Hemolytic Anemia in Liver Disease: A Case of Spur Cell Anemia. [PDF]

Cureus
El Amri H, Reddy AP, Azhar W, Junaid B.
europepmc   +1 more source

High-performance liquid chromatography screening reveals HbS/β+-thalassemia double heterozygosity as a pediatric muscular dystrophy mimic. [PDF]

Lab Med
López-Medina C, Portell-Rigo IM, González-Iribarren V, González-Oller C, Sánchez-Crespo A, Molina-Arrebola MA.   +5 more
europepmc   +1 more source

Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ‐line de novo mutation

American journal of hematology/oncology, 2015
M. Mañú-Pereira, E. González-Roca, W. V. van Solinge, Esther Llaudet-Planas, J. Sevilla, L. Montllor, A. Mensa‐Vilaró, H. K. Ploos van Amstel, R. van Wijk, J. Vives-Corrons   +9 more
semanticscholar   +1 more source