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Books > Medicine > Clinical & internal medicine > Haematology
Offering a concise overview of transfusion medicine, including best
practices for specific clinical settings, this practical resource
by Dr. Robert W. Maitta covers the key information you need to
know. Holistic, multidisciplinary coverage and a succinct,
easy-to-read format make it essential reading for transfusion
specialists, as well as practitioners in other specialties whose
patients undergo blood transfusions. Covers the latest advancements
in transfusion therapies, hematopoietic stem cells, infectious and
non-infectious complications of transfusions, and future directions
in transfusion medicine. Discusses special populations, including
organ transplant patients; pediatric, obstetric, and geriatric
patients; and patients undergoing emergency care. Consolidates
fundamental clinical concepts and current practice of transfusion
medicine into one convenient resource.
This issue of Clinics in Laboratory Medicine, edited by David M.
Dorfman, will cover Flow Cytometry. Topics covered in this issue
include: Flow cytometric evaluation of primary immunodeficiencies;
Flow cytometry of B cell neoplasms; Flow cytometry of T cell
neoplasms; Flow cytometry of acute myeloid leukemias; AML minimal
residual disease (MRD) assessment by flow cytometric analysis;
Acute lymphoblastic leukemia minimal residual disease (MRD)
assessment by flow cytometric analysis; Flow cytometric assessment
of myelodysplasia and myeloproliferative neoplasms; Flow cytometry
of plasma cell neoplasms, including MRD testing; Paroxysmal
nocturnal hemoglobinuria (PNH) assessment by flow cytometric
analysis; Mast cell disease assessment by flow cytometric analysis;
Flow cytometry in pediatric hematopathology; Clinical applications
of mass cytometry; Automated analysis of clinical flow cytometry
data; and Cost-effective flow cytometric testing strategies.
This issue of Hematology/Oncology Clinics, edited by Dr. Frits van
Rhee and Dr. Nikhil C. Munshi, focuses on Castleman's Disease.
Topics include, but are not limited to, Epidemiology; Pathogenesis;
Role of Interleukin 6 in Castleman Disease; Pathology, Diagnosis;
Unicentric Castleman Disease; Treatment of HHV8 related
Multicentric Castleman Disease; Treatment of HHV8 negative
Castleman Disease; TAFRO Syndrome; POEMS; and more.
This issue of Hematology/Oncology Clinics will focus on The
Treatment of Myeloid Malignancies with Kinase Inhibitors. Articles
will focus on: Targeting aberrant signaling in myeloid
malignancies: promise versus reality; The development and use of
imatinib for the treatment of chronic myelogenous leukemia;
Mechanisms of resistance to ABL kinase inhibition in CML and the
development of next generation ABL kinase inhibitors; Tyrosine
kinase inhibitors in the treatment of systemic mastocytosis and
hypereosinophilic syndrome; The development and use of JAK2
inhibitors for the treatment of myeloproliferative neoplasms (MPN);
Mechanisms of resistance to JAK2 inhibitors in MPN; Kinase
inhibitor screening in myeloid malignancies; and more!
This issue of Hematology/Oncology Clinics is devoted to New
Anticoagulant and Antithrombotic Agents and will include articles
such as: Development and Pharmacology; Post Orthopedic Joint
Replacement Surgery VTE Prophylaxis; Use for Afib; Treatment of
Acute VTE; Extended Treatment of VTW; Bleeding Risks: Use in
Special Poplulations; Monitoring Anticoagulant Effect, and many
more articles surrounding this important title.
This issue of Hematology/Oncology Clinics will cover aggressive
B-Cell Lymphoma and articles to be included are: State of the art
therapy for advanced stage DLBCL; DLBCL: Should limited stage
patients be treated differently; Role of PET in DLBCL; Management
of relapsed DLBCL; The spectrum of double-hit lymphoma; Optimizing
outcomes in primary mediastinal B cell lymphoma; The grey zone of
unclassifiable lymphomas; as well as many more.
This issue of Hematology/Oncology Clinics of North America is
devoted to Imaging of Neurological complications in Hematological
disorders and will include articles on Blood Dyscriasis:
Classification and Clinical Neurological Presentations, Imaging
Manifestation of Anemia, CNS Complications of Hemorrhagic and
Coagulation Disorders, Neurological and Head and Neck Manifestation
of Sickle Cell Disease, Neuroimaging in Lymphoma, and many more!
Childhood acute leukemias are one of the main causes of death in
children aged 1 to 14 years in some countries; and unfortunately,
we have been unable to prevent it. Certainly, a good parcel of it
is due to the poor understanding about its etiology. This book aims
to describe the most important theories and hypothesis regarding
childhood acute leukemia. Written by the most outstanding
researchers in the field, this book intends to contribute to a
greater understanding of the etiology of this disease. It goes
beyond the simple and common analysis of risk factors, which hardly
allows us to draw definite conclusions. By addressing the etiology
of the disease, discussing from molecular biology until
epidemiology and clinical manifestations, this book will guide
present and future approaches, contributing for a better clinical
management of leukemia in children. The knowledge regarding
etiology is a crucial step for a better evaluation, prevention and
treatment of a disease. Thus, this book finally intends to provide
such knowledge, allowing physicians and practitioners to a better
manage of childhood acute leukemias.
Dr. George Fedoriw leads the second issue presented in the Surgical
Pathology Clinics on Hematopathology. Topics in this issue include:
Evidence-based, high-value hematopathology; The expanding spectrum
of follicular lymphoma; Lymphoid proliferations in the
immunocompromised host; Reporting clinically relevant biomarkers of
intermediate/high grade B-cell lymphomas; Transformation of
lymphomas; T-cell lymphoproliferations: distinguishing benign from
malignant; Lymphoma microenvironment and immunotherapy;
Differentiating low grade lymphomas with non-specific
immunophenotype; Molecular markers of myeloid leukemias and
myelodysplastic syndromes; Update of myeloproliferative neoplasms;
Mimics of myeloid neoplasms; Therapy effect: impact on bone marrow
morphology. Each topic is written by a leader in pathology with
expertise in hematopathology. The focus on these articles, as all
in the series, is on Differential Diagnosis, with histologic images
and tips for working with the most challenging aspects of these
pathologies.
This issue of the Clinics in Laboratory Medicine on
"Pharmacogenomics" is being edited by Drs. Roland Valdes and
Kristen Reynolds and will cover a wide variety of topics, including
but not limited to, fundamentals of pharmacology, a review of
pharmacogenetics guidelines, pharmacogenetic testing in pain
management, pharmacogenetics of pain management, clinical and
economic impact of pharmacogenetic genotyping analysis, exosome
analysis in lab medicine, and implementation of pharmacogenetics in
developing countries.
This issue will focus on the global state of hematology and will
include articles such as: The Global Burden of Anemia, Iron
Deficiency Anemia: Problems in Diagnosis and Therapy, Progress
Towards the Control and Management of the Thalassemias, Problems
and Approaches for Blood Transfusion in the Developing Countries,
and many more!
Recent advances in protein structural biology, coupled with new
developments in human genetics, have opened the door to
understanding the molecular basis of many metabolic, physiological,
and developmental processes in human biology. Medical pathologies,
and their chemical therapies, are increasingly being described at
the molecular level. For single-gene diseases, and some multi-gene
conditions, identification of highly correlated genes immediately
leads to identification of covalent structures of the actual
chemical agents of the disease, namely the protein gene products.
Once the primary sequence of a protein is ascertained, structural
biologists work to determine its three-dimensional, biologically
active structure, or to predict its probable fold and/or function
by comparison to the data base of known protein structures.
Similarly, three-dimensional structures of proteins produced by
microbiological pathogens are the subject of intense study, for
example, the proteins necessary for maturation of the human HIV
virus. Once the three-dimensional structure of a protein is known
or predicted, its function, as well as potential binding sites for
drugs that inhibit its function, become tractable questions. The
medical ramifications of the burgeoning results of protein
structural biology, from gene replacement therapy to "rational"
drug design, are well recognized by researchers in biomedical
areas, and by a significant proportion of the general population.
The purpose of this book is to introduce biomedical scientists to
important areas of protein structural biology, and to provide an
insightful orientation to the primary literature that shapes the
field in each subject.
The chapters in this volume cover aspects of protein structural
biology which have led to the recognition of fundamental
relationships between protein structure and function.
This issue of Hematology/Oncology Clinics of North America is
devoted to Congenital and Acquired Disorders of Macrophages and
Histiocytes. Guest Editors Nancy Berliner, MD and Barrett Rollins,
MD have assembled a group of expert authors to review the following
topics: Nosology of Langerhans Cell Histiocytosis (LCH); Cell of
Origin of LCH; Genomic Changes in LCH; Clinical Treatment of LCH;
Neurodegeneration in LCH; Pathogenesis of Hemophagocytic
Lymphohistiocytosis (HLH); Familial HLH; HLH in Adults; Macrophage
Activation Syndrome; and Stem Cell Transplant for HLH.
Recent advances in neonatal hematology, largely made by the authors
of these chapters, are likely to generate wide spread and long-term
improvements in outcomes, as well as reductions in costs of care.
Publication of these advances in a single volume will facilitate
dissemination of these techniques and practices. The advances
include neuroprotection from erythropoietic stimulators, improved
guidelines for platelet transfusions, evidence-based guidelines for
FFP administration, improved diagnostic methods for genetic causes
of severe neonatal jaundice, more accurate definitions of
hematological perturbations in necrotizing enterocolitis and
sepsis, and reduction in transfusions and in IVH rates by cord
milking/delayed clamping.
Clinics Collections: Lipid Disorders draws from Elsevier's robust
Clinics Review Articles database to provide multidisciplinary
teams, including general practitioners, cardiologists,
endocrinologists, pathologists, cardiologists, rheumatologists, and
hepatologists, with practical clinical advice and insights on this
highly prevalent condition and its comorbidities. Clinics
Collections: Lipid Disorders guides readers on how to apply current
primary research findings on lipid disorders to everyday practice
to help overcome challenges and complications, keep up with new and
improved treatment methods, and improve patient outcomes. . Areas
of focus include lipids and biomarkers, lipids and pharmacotherapy,
lipids and heart disease, lipids and chronic disease, lipids and
pediatrics, lipids and women's health and special considerations. .
Each article begins with keywords and key points for immediate
access to the most critical information. . Articles are presented
in an easy-to-digest and concisely worded format. Elsevier's
Clinics Collections provide concise reviews of today's most
prevalent conditions and significant medical developments. Other
Clinics Collections titles available include Type II Diabetes
Mellitus, Asthma, Obesity, and Pain Management
This issue of Hematology/Oncology Clinics of North America, guest
edited by Dr. Robert Brodsky, is devoted to Complement-mediated
Hemolytic Anemias. Articles in this outstanding issue include:
Complement: An overview for the clinician; Warm autoimmune
hemolytic anemia; Cold Agglutinin Disease; ABO incompatible blood
transfusions; Paroxysmal cold hemoglobinuria; Paroxysmal nocturnal
hemoglobinuria; Congenital CD59 deficiency; Atypical Hemolytic
Uremic Syndrome (HUS); Typical Hemolytic Uremic Syndrome (HUS);
Thrombotic thrombocytopenic purpura; and Pharmacologic complement
inhibitors.
This issue concentrates on the current evidence and the collected
experience of pediatric oncologists who care for cancer patients.
The individual articles will provide the general pediatrician with
a comprehensive primer on diagnosing and managing various types of
cancers in the child with cancer. A cancer diagnosis is no longer a
death sentence, so management and monitoring is very important and
covered in every article.
Clinical laboratory directors and staff working with blood samples
will benefit from the essential information in this hematology
focused publication in Clinics in Laboratory Medicine. Leading a
field of expert authors are two renown physicians in the field - Dr
Carlo Brugnara and Dr Alexander Kratz. They present topics such as
White Blood Cell Counts: Reference Methodology; Integration of
Automated Heme and Bone Marrow Analysis; Red Cell Dynamics; Red
Cell Diagnosis other than Anemia; Laboratory and Genetic Assessment
of Iron Deficiency in Blood Donors; Body Fluid Cell Counting;
Platelets: The Few, the Young, and the Active; Reticulocytes;
Quality Control of Automated Cell Counters; Digital Image Analysis
of Blood Cells; Blood Cell Counters in Urgent Care Settings; Novel
Parameters in Blood Cell Counters; and the Development and Future
of Automated Blood Cell Counters.
Topics in this clinically focused publication devoted to
Anticoagulants are: Antithrombin clinical applications and
anti-inflammatory effects; Pharmacology and laboratory testing of
oral direct thrombin inhibitor Dabigatran; Pharmacology and
laboratory testing of the oral Xa inhibitors; Clincial use of the
new oral anticoagulants; Pharmacology and safety of new oral
anticoagulants-the challenge of bleeding; Emergency reversal of
Warfarin anticoagulation - prothrombin complex concentrate compared
with plasma; Prothrombin complex concentrate as reversal agent for
new oral anticoagulants - lessons from prelinical models; Bleeding
with new oral anticoagulants - clinical presentation and
management; Treatment of ICH with new oral anticoagulants - a
neurologist's view; Management of anticoagulation agents in trauma
patients; and Anticoagulation and pediatric patients.
This issue of Hematology/Oncology Clinics of North America, devoted
to Multiple Myeloma, is edited by Dr. Kenneth C. Anderson. Articles
in this issue include: Monoclonal Gammopathy of Undetermined
Significance and Smoldering Multiple Myeloma; Diagnosis and Risk
Stratification in Myeloma; Treatment of Newly Diagnosed Transplant
Eligible Patients; Treatment of Newly Diagnosed Transplant
Ineligible Patients; Treatment of Relapsed/Refractory Myeloma;
Maintenance Therapy; Novel Targeted Therapies; Novel Immune-based
Therapies; Allotransplantation in Myeloma; and Waldenstrom's
Macroglobulinemia.
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