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Bone Marrow Failure / edited by Gary M. Kupfer, Gregory H. Reaman, Franklin O. Smith.

Colaborador(es): Kupfer, Gary M, editor literario | Reaman, Gregory H, editor literario | Smith, Franklin O, editor literario | SpringerLink (Online service).
Tipo de material: materialTypeLabelE-bookSeries (Pediatric Oncology,, 1613-5318); (Medicine (Springer-11650)).Editor: Cham : Springer International Publishing : Imprint: Springer, 2018Descripción: 1 recurso en línea (IX, 214 páginas, 19 ilustraciones, 12 ilustraciones a color).ISBN: 9783319614212.Tema: Médula ósea -- EnfermedadesRecursos en línea: Acceso a este recurso digital (usuarios Universidad Europea de Valencia)Digital Resources
Contenidos:
1. The Cellular and Molecular Mechanisms of Hematopoiesis -- 2. Acquired Aplastic Anemia -- 3. Pediatric Myelodysplastic Syndromes -- 4. Fanconi Anemia: A Pathway of Hematopoeisis and Cancer Predisposition -- 5. Ribosomopathies Through a Diamond Lens -- 6. Dyskeratosis Congenita and the Telomere Biology Disorders -- 7. Diamond Blackfan Anemia -- 8. Shwachman-Diamond Syndrome -- 9. Hematopoietic Cell Transplantation for the Treatment of Patients with Bone Marrow Failure Syndromes -- 10. Inherited Neutropenias and Their Insights into Cellular and Developmental Biology -- 11. Inherited Thrombocytopenias.
Resumen: This book presents the latest scientific knowledge on inherited and acquired bone marrow failure syndromes, describing the advances in understanding of genetics and pathophysiology that have been achieved as a result of high-throughput DNA sequencing, RNA expression studies, and modern biochemistry techniques. The full range of relevant conditions is covered, including acquired aplastic anemia, Fanconi anemia, ribosomopathies, telomeropathies, dyskeratosis congenita, Shwachman-Diamond syndrome, Diamond-Blackfan anemia, and congenital neutropenias and thrombocytopenias. In addition, it is explained how the study of these rare diseases has uncovered important new science and elucidated the pathophysiology of more common hematological and oncological diseases. A treatment-specific chapter describes options ranging from the conventional to the cutting edge. Bone Marrow Failure will be of value for both trainee and practicing hematologists and oncologists.
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Existencias
Tipo de ítem Biblioteca actual Colección Signatura topográfica Estado Fecha de vencimiento Código de barras Reserva de ítems
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Valencia Digital Acceso Electrónico (UEV) Ciencias de la Salud RC645.7 .B66 2018 EB (Navegar estantería(Abre debajo)) Acceso electrónico
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1. The Cellular and Molecular Mechanisms of Hematopoiesis -- 2. Acquired Aplastic Anemia -- 3. Pediatric Myelodysplastic Syndromes -- 4. Fanconi Anemia: A Pathway of Hematopoeisis and Cancer Predisposition -- 5. Ribosomopathies Through a Diamond Lens -- 6. Dyskeratosis Congenita and the Telomere Biology Disorders -- 7. Diamond Blackfan Anemia -- 8. Shwachman-Diamond Syndrome -- 9. Hematopoietic Cell Transplantation for the Treatment of Patients with Bone Marrow Failure Syndromes -- 10. Inherited Neutropenias and Their Insights into Cellular and Developmental Biology -- 11. Inherited Thrombocytopenias.

This book presents the latest scientific knowledge on inherited and acquired bone marrow failure syndromes, describing the advances in understanding of genetics and pathophysiology that have been achieved as a result of high-throughput DNA sequencing, RNA expression studies, and modern biochemistry techniques. The full range of relevant conditions is covered, including acquired aplastic anemia, Fanconi anemia, ribosomopathies, telomeropathies, dyskeratosis congenita, Shwachman-Diamond syndrome, Diamond-Blackfan anemia, and congenital neutropenias and thrombocytopenias. In addition, it is explained how the study of these rare diseases has uncovered important new science and elucidated the pathophysiology of more common hematological and oncological diseases. A treatment-specific chapter describes options ranging from the conventional to the cutting edge. Bone Marrow Failure will be of value for both trainee and practicing hematologists and oncologists.

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