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Blood Cells, Molecules, and Diseases

Resumen/Descripción – provisto por la editorial en inglés
Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.

Research Areas include:

• Hematolymphopoiesis
• Genetics of Blood Cells and Proteins
• Molecular Biology of Blood Cells and Proteins
• Pathophysiology of Blood Cells and Proteins
• Hematological Malignancies
• Disorders of Blood Cells and Coagulation Proteins

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Palabras clave – provistas por la editorial

No disponibles.

Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde abr. 1995 / hasta dic. 2023 ScienceDirect

Información

Tipo de recurso:

revistas

ISSN impreso

1079-9796

ISSN electrónico

1096-0961

Editor responsable

Elsevier

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

biologia

Ciencias biológicas

medicina-clinica

Medicina clínica

Tabla de contenidos

doi: 10.1006/bcmd.2001.0474

Dixon Quantitative Chemical Shift Imaging Is a Sensitive Tool for the Evaluation of Bone Marrow Responses to Individualized Doses of Enzyme Supplementation Therapy in Type 1 Gaucher Disease

Carla Hollak; Mario Maas; Erik Akkerman; Ard den Heeten; Hans Aerts

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 1005-1012

doi: 10.1016/j.bcmd.2005.07.009

Recombinant glucocerebrosidase uptake by Gaucher disease human osteoblast culture model

M. Lamghari; C.C. Barrias; C. Sá Miranda; M.A. Barbosa

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 348-354

doi: 10.1016/j.bcmd.2010.07.008

Early achievement and maintenance of the therapeutic goals using velaglucerase alfa in type 1 Gaucher disease

D. Elstein; G.M. Cohn; N. Wang; M. Djordjevic; C. Brutaru; A. Zimran

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 119-123

doi: 10.1016/j.bcmd.2012.11.001

Taliglucerase alfa leads to favorable bone marrow responses in patients with type I Gaucher disease

L. van Dussen; A. Zimran; E.M. Akkerman; J.M.F.G. Aerts; M. Petakov; D. Elstein; H. Rosenbaum; D. Aviezer; E. Brill-Almon; R. Chertkoff; M. Maas; C.E.M. Hollak

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 206-211

doi: 10.1016/j.bcmd.2013.04.005

Miglustat therapy in type 1 Gaucher disease: Clinical and safety outcomes in a multicenter retrospective cohort study

David J. Kuter; Atul Mehta; Carla E.M. Hollak; Pilar Giraldo; Derralynn Hughes; Nadia Belmatoug; Monika Brand; Audrey Muller; Berthold Schaaf; Ruben Giorgino; Ari Zimran

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 116-124

doi: 10.1016/j.bcmd.2014.05.005

Heterogeneous pattern of bone disease in adult type 1 Gaucher disease: Clinical and pathological correlates

L. van Dussen; P. Lips; H.W. van Essen; C.E.M. Hollak; N. Bravenboer

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 118-123

doi: 10.1016/j.bcmd.2016.10.004

The utility of magnetic resonance imaging for bone involvement in Gaucher disease. Assessing more than bone crises

Marcio Andrade-Campos; Esther Valero; Mercedes Roca; Pilar Giraldo

Pp. 126-134

doi: 10.1016/j.bcmd.2017.06.003

Skeletal involvement in type 1 Gaucher disease: Not just bone mineral density

M. Baldini; G. Casirati; F.M. Ulivieri; E. Cassinerio; K. Khouri Chalouhi; E. Poggiali; L. Borin; V. Burghignoli; B.M. Cesana; M.D. Cappellini

Palabras clave: Molecular Medicine; Cell Biology; Molecular Biology; Hematology.

Pp. 148-152

doi: 10.1016/j.bcmd.2023.102779

A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country

Nihal Hussien Aly; Mohsen Saleh Elalfy; Safinaz Adel Elhabashy; Nadia Mohamed Mowafy; Roberta Russo; Immacolata Andolfo; Achille Iolascon; Iman Ahmed Ragab

Pp. 102779