Double trouble: Complement-mediated thrombotic microangiopathy in patients with hemoglobinopathies after stem cell transplantation.

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Double trouble: Complement-mediated thrombotic microangiopathy in patients with hemoglobinopathies after stem cell transplantation.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Double trouble: Complement-med ...... ter stem cell transplantation.

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Double trouble: Complement-med ...... ter stem cell transplantation.

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label

Double trouble: Complement-med ...... ter stem cell transplantation.

@en

Double trouble: Complement-med ...... ter stem cell transplantation.

@nl

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Double trouble: Complement-med ...... ter stem cell transplantation.

@en

Double trouble: Complement-med ...... ter stem cell transplantation.

@nl

P1476

Double trouble: Complement-med ...... ter stem cell transplantation.

@en

P2093

Sonata Jodele

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P2860

Pulmonary arterial hypertension in pediatric patients with hematopoietic stem cell transplant-associated thrombotic microangiopathy.

Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults

Abnormal echocardiography 7 days after stem cell transplantation may be an early indicator of thrombotic microangiopathy.

Histologic Features of Intestinal Thrombotic Microangiopathy in Pediatric and Young Adult Patients after Hematopoietic Stem Cell Transplantation

Variable Eculizumab Clearance Requires Pharmacodynamic Monitoring to Optimize Therapy for Thrombotic Microangiopathy after Hematopoietic Stem Cell Transplantation.

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy.

New approaches in the diagnosis, pathophysiology, and treatment of pediatric hematopoietic stem cell transplantation-associated thrombotic microangiopathy.

The role of complement activation in thrombosis and hemolytic anemias.

Severe transplant-associated thrombotic microangiopathy in patients with hemoglobinopathies.

Atypical haemolytic uraemic syndrome in a patient with sickle cell disease, successfully treated with eculizumab

P31

scholarly article

P356

10.1002/PBC.26566

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P433

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P478

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P577

2017-04-27T00:00:00Z

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P698

28449196

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