The splenic platelet reservoir in sickle cell anemia

Integrin α6 and EGFR signaling converge at mechanosensitive calpain 2.

Biomaterials·2018

Do ryanodine receptors regulate transmitter release at the neuromuscular junction of rat?

Neuroscience letters·1999

Placental echolucencies: does their presence influence outcome following genetic amniocentesis?

Military medicine·1996

Factor XI deficiency in an Ashkenazi Jewish child, causing severe postoperative hemorrhage.

Journal of pediatric surgery·1995

Infection in major sickle hemoglobinopathies: should management strategies change?

Maryland medical journal (Baltimore, Md. : 1985)·1993

Thalassemia screening in Baltimore.

Maryland medical journal (Baltimore, Md. : 1985)·1992

Vasculopathy in the Forecast: Biophysically Altered Red Cells Act as Hemodynamic Hail to Trigger Endothelial Dysfunction.

Blood·2026

Nipocalimab for warm autoimmune hemolytic anemia: results from the phase 2/3 randomized, double-blind ENERGY study.

Blood·2026

Inhibition of nucleoporin 214 depletes leukemia stem cells by promoting heme catabolism and lipid peroxidation.

Blood·2026

International Consensus Criteria for the Diagnosis, Treatment Initiation, and Response Assessment for T-LGL Leukemia.

Blood·2026

Epigenetic markers expand genetic risk estimation in acute myeloid leukemia.

Blood·2026

Phase 1 Trial with Soquelitinib, a Selective ITK Inhibitor for Treatment of Relapsed/Refractory T Cell Lymphomas.

Blood·2026

Long-term outcome of pediatric anti-complement factor H antibody-associated atypical hemolytic uremic syndrome receiving abbreviated plasma exchange: a retrospective study from a single center.

Journal of nephrology·2026

[Therapeutic apheresis in first-line treatment of hematological disorders - an evidence-based review].

Therapeutische Umschau. Revue therapeutique·2026

Same-day rescue plerixafor during leukapheresis is safe and effective in allogeneic donors suboptimally responding to granulocyte colony-stimulating factor mobilization.

Transfusion·2026

Platelet-erythrocyte complex production is exacerbated by histones and protected by small polyanion histone neutralizing compounds.

Platelets·2026

Changing the treatment paradigm in beta thalassemia.

Folia medica·2026

Noninvasive Thrombus Imaging in Patients With Ischemic Stroke.

Circulation·2026

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The splenic platelet reservoir in sickle cell anemia

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Integrin α6 and EGFR signaling converge at mechanosensitive calpain 2.

Do ryanodine receptors regulate transmitter release at the neuromuscular junction of rat?

Placental echolucencies: does their presence influence outcome following genetic amniocentesis?

Factor XI deficiency in an Ashkenazi Jewish child, causing severe postoperative hemorrhage.

Infection in major sickle hemoglobinopathies: should management strategies change?

Thalassemia screening in Baltimore.

Vasculopathy in the Forecast: Biophysically Altered Red Cells Act as Hemodynamic Hail to Trigger Endothelial Dysfunction.

Nipocalimab for warm autoimmune hemolytic anemia: results from the phase 2/3 randomized, double-blind ENERGY study.

Inhibition of nucleoporin 214 depletes leukemia stem cells by promoting heme catabolism and lipid peroxidation.

International Consensus Criteria for the Diagnosis, Treatment Initiation, and Response Assessment for T-LGL Leukemia.

Epigenetic markers expand genetic risk estimation in acute myeloid leukemia.

Phase 1 Trial with Soquelitinib, a Selective ITK Inhibitor for Treatment of Relapsed/Refractory T Cell Lymphomas.

Long-term outcome of pediatric anti-complement factor H antibody-associated atypical hemolytic uremic syndrome receiving abbreviated plasma exchange: a retrospective study from a single center.

[Therapeutic apheresis in first-line treatment of hematological disorders - an evidence-based review].

Same-day rescue plerixafor during leukapheresis is safe and effective in allogeneic donors suboptimally responding to granulocyte colony-stimulating factor mobilization.

Platelet-erythrocyte complex production is exacerbated by histones and protected by small polyanion histone neutralizing compounds.

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The splenic platelet reservoir in sickle cell anemia

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