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Books > Medicine > Clinical & internal medicine > Endocrinology > General
Responding to a renewed interest in the growing problem of iodine
deficiency worldwide, Drs. Charles Oxnard and Peter Obendorf, along
with experienced translator and anatomist John Dennison, take a
fresh look at the classic text, Der endemische Kretinismus,
published in 1936 by Springer. Translated here for the first time
into English, this landmark text will be a welcome resource for
researchers confronting the problem of iodine deficiency. Oxnard
and Obendorf point out that there is very little detailed knowledge
or numerical data on cretinism available in the English-speaking
world. In addition, highly-renowned Professor Basil S. Hetzel,
recently-retired World Health Organization Chairman of the
International Council for Control of Iodine Deficiency Disorders,
published in 2009 with Dr Chen Zu-pei on the resurgence of iodine
deficiency in China. Indeed, throughout the entire developing world
there may be as many as two billion people at risk to iodine
deficiency; perhaps three quarters of a billion have goiter, and
ten million may be cretins. Even in developed countries, iodine
deficiency is re-emerging (as in New South Wales in 19% of
children) with the result of significantly reduced numbers of
gifted children (though this is not cretinism per se). Certain to
be of significant interest to a wide range of researchers, health
providers and professionals, including government health
administrators, this English translation of Endemic Cretinism is a
major contribution to the literature.
2022 Endocrine Case Management: Meet The Professor Reference
Edition is your source for the latest updates in the diagnosis and
management of a wide range of endocrine disorders. This valuable
resource allows you to evaluate your knowledge and gain insight
into the strategies used by clinical experts. Updated annually.
Regulation of Insulin Secretion.- Impaired Glucose-Induced Insulin
Secretion: Studies in Animal Models with Spontaneous NIDDM.-
Perturbation of Islet Metabolism and Insulin Release in NIDDM.-
Regulation of Cytoplasmic Free Ca2+ in Insulin-Secreting Cells.-
The ss-Cell Sulfonylurea Receptor.- Insulin, Insulin Receptors and
Glucose Transporters.- Regulation of Glucose Transporters and the
Na/K-ATPase by Insulin in Skeletal Muscle.- Insulin Receptor:
Aspects of Its Structure and function.- The Diabetogenes Concept of
NIDDM.- Molecular Genetics of NIDDM and the Genes for Insulin and
Insulin Receptor.- Autoregulation of Glucose Transport: Effects of
Glucose on Glucose Transporter Expression and Cellular Location in
Muscle.- Insulin Action in NIDDM.- Insulin Resistance and the
Pathogenesis of Non-Insulin Dependent Diabetes Mellitus: Cellular
and Molecular Mechanisms.- Indirect Effects of Insulin in
Regulating Glucose Fluxes.- The Insulin-Antagonistic Effect of the
Counterregulatory Hormones - Clinical and Mechanistic Aspects.- On
Insulin Action in Vivo: The Single Gateway Hypothesis.-
Gluconeogenesis.- Acute Hormonal Regulation of Gluconeogenesis in
the Conscious Dog.- Estimating Gluconeogenic Rates in NIDDM.-
Glucose Metabolism during Physical Exercise in Patients with
Noninsulin-Dependent (Type II) Diabetes.- Substrates and the
Regulation of Hepatic Glycogen Metabolism.- Gluconeogenesis in Type
2 Diabetes.- Obesity, Lipoproteins, Atherogenesis, and NIDDM.-
Regulation of Adipose Tissue Lipolysis, Importance for the
Metabolic Syndrome.- Cellular and Molecular Factors in Adipose
Tissue Growth and Obesity.- Regional Obesity and NIDDM.-
Hyperinsulinemia and VLDL Kinetics.- Hyperinsulinism and
Dyslipidemias as Coronary Heart Disease Risk Factors in NIDDM.-
Potential Impact of New Concepts In NIDDM on Delivery of Care to
Diabetic Populations.- A Paradigm to Link Clinical Research to
Clinical Practice: The Challenge in Non-Insulin Dependent Diabetes
Mellitus.
Sperm DNA damage is common and has been associated with reduced
rates of conception, impaired embryonic development and increased
risk of miscarriage. Although the exact causes of sperm DNA damage
are unknown, it is clear that infertile men possess substantially
higher levels of sperm DNA damage than do fertile men. Written by
leading, internationally renowned clinicians and basic scientists
with expertise in sperm DNA, Sperm Chromatin: Biological and
Clinical Applications in Male Infertility and Assisted Reproduction
provides readers with a thoughtful and comprehensive review of the
biological and clinical significance of sperm DNA damage. The work
covers the fundamental principles of sperm chromatin architecture
and function, the proposed modes of DNA damage and repair, the
tests of sperm DNA damage, the clinical aspects of DNA damage and
the impact of DNA damage on reproductive outcome. Unlike any other
title on the topic, Sperm Chromatin: Biological and Clinical
Applications in Male Infertility and Assisted Reproduction is an
invaluable addition to the literature and will serve as an
indispensable resource for basic scientists with an interest in
sperm biology and for urologists, gynecologists, reproductive
endocrinologists, and embryologists working in the field of
infertility.
This practice-oriented book provides a comprehensive and up-to-date
review of the history, surgical anatomy, etiology, pathogenesis,
clinical presentation and treatment of primary, secondary, and
tertiary hyperparathyroidism. The coverage is wide ranging,
encompassing, for example, innovations in both medical and surgical
treatment, current indications for parathyroidectomy, the role and
performance of minimally invasive surgery, the value of
intraoperative parathyroid hormone monitoring and guidance on
reoperations. Individual chapters are devoted to particular
conditions and disease settings, including multiple endocrine
neoplasia types 1 and 2 and parathyroid carcinoma, with provision
of information on genetic testing, clinical manifestations and
therapy. All aspects of secondary hyperparathyroidism in
predialysis and dialysis patients are discussed. The book is
endorsed by the Italian Society of Surgery. It will be of great
value for endocrine surgeons and endocrinologists and will also be
of interest to specialists in internal medicine, nephrologists,
urologists, gynecologists and radiologists.
Historically the field of endocrine research has always been at the
forefront of scientific endeavors. The investigators of these
important breakthroughs in research have been rewarded by numerous
Nobel awards. In the field of diabetes alone, Nobel prizes have
been awarded to researchers who discovered insulin, characterized
the protein and invented radioimmunoassays using insulin as a
paradigm. Not surprisingly, biomedical researchers have always been
attracted by the endocrine system and other similar systems of
intercellular communication.
Over the past two decades, endocrine research has developed rapidly
and adapted modern molecular and cellular biology techniques for
its specific use. These changes have allowed researchers in the
field to maintain their edge. Thus, endocrine disease-related genes
have been characterized and mutations in these genes have helped
explain common and
less common endocrine disorders. Our understanding of the
regulation of gene expression has been greatly enhanced by
molecular techniques.
In an attempt to bring investigators up to date with the recent
advances in this exploding field we have decided to publish a
series entitled Advances in Molecular and Cellular Endocrinology.
Internationally famous investigators have agreed to participate and
their contributions are appreciated.
Volume 1 has focused on aspects of the hypothalamic-pituitary axis
including GnRH and GH gene regulation, molecular aspects of
insulin, insulin-like growth factors and glucagon. In addition,
reviews on the recently cloned calcium receptor and steroid
receptor interactions with DNA are presented.
In this fascinating book, Jacques Balthazart presents a simple
description of the biological mechanisms that are involved in the
determination of sexual orientation in animals and also presumably
in humans. Using scientific studies published over the last few
decades, he argues that sexual orientation, both homosexual and
heterosexual, is under the control of embryonic endocrine and
genetic phenomena in which there is little room for individual
choice. The author begins with animal studies of the hormonal and
neural mechanisms that control the so-called instinctive behaviors
and analyzes how this animal work may potentially apply to humans.
The book does not focus exclusively on homosexuality, however.
Instead, the book acts as a broader guide to the biological basis
of sexual orientation, and also discusses important gender
differences that may influence sexual orientation. While firmly
grounded in the scientific literature, this text is developed for a
broader audience and will be of interest to psychologists,
researchers, students, and anyone interested in the biological
factors that determine our sexuality.
The second edition of this work continues to address the intimate
pathophysiologic relationship between hypertension and stroke. The
editors and authors clearly and concisely synthesize our developing
knowledge of this relationship and place epidemiologic and
physiologic information into a practical clinical context.
Comprehensive chapters present the evidence supporting strategies
for stroke prevention and care, including blood pressure lowering
therapies, anti-coagulation, and management of other
cerebrovascular risk factors. In addition to prescriptive measures
for first stroke prevention, the book illuminates current regimens
for care immediately after acute stroke and for the prevention of
recurrent stroke. This latest edition also features extensively
updated chapters from the previous edition, as well as new chapters
on the effects of hypertension and stroke on the cerebral
vasculature, blood pressure management in subarachnoid hemorrhage,
and blood pressure variability, antihypertensive therapy, and
stroke risk. Written by experts in the field, Hypertension and
Stroke: Pathophysiology and Management, Second Edition is of great
utility for specialists in neurology and cardiovascular medicine
and a valuable practical resource for all physicians caring for
older adults and hypertensive patients.
The American Cancer Society recently estimated that about 45,000
new cases of thyroid cancer will be diagnosed in the United States,
with three-quarters occurring in women. The overall 5-year survival
rate is about 97%, making it one of the least lethal cancers. We
are experiencing an epidemic of well-differentiated thyroid cancer,
in part due to the widespread use of imaging modalities that detect
thyroid nodules and microcarcinomas. Concurrently, there have been
a number of recent advances in surgical treatment, as well as
diagnostic modalities that allow us to detect small amounts of
residual local and metastatic disease. Additionally, a
reexamination of past treatment regimens has led to new
recommendations regarding the use of radioactive iodine, and to new
therapeutic options, such as targeted therapy which have supplanted
the use of more toxic chemotherapy for metastatic cancer. Multiple
academic organizations have developed consensus guidelines for the
management of thyroid cancer, occasionally with conflicting
recommendations. In Thyroid Cancer, a renowned group of authors
presents a broad overview of the pathology, pathophysiology,
diagnosis, and management of thyroid cancer, with an emphasis on
recent evidence-based information. State-of-the-art and a
significant contribution to the literature, Thyroid Cancer is an
invaluable reference for endocrinologists, oncologists, nuclear
medicine physicians, radiation oncologists, primary care
physicians, and surgeons who deal with head and neck cancer.
The mature T and NK cell lymphomas are rare, comprising
approximately 10% of all malignant lymphomas. The incidence of T-
cell lymphoma is variable around the world, with a higher incidence
compared to B-cell lymphomas in the Asian basin. While the overall
incidence of B-cell lymphomas has begun to decline in the United
States, the incidence of T-cell lymphomas continues to rise. Over
the last decade, a number of novel agents have been developed which
target T-cell lymphomas and studies have identified novel genes and
pathways associated with lymphomagenesis in T-cells. This
comprehensive volume examines the clinical and biological aspects
of the T-cell lymphoproliferative disorders in adults and children.
The book includes an overview of both the cutaneous and the
systemic T-cell malignancies and addresses the classification of
T-cell lymphomas, the clinical features of each subtype, and the
relevant molecular and genetic studies. Clinical outcomes and
treatment strategies are discussed with an emphasis on the
development of novel biological and targeted therapies. An
outstanding resource for hematologists and oncologists, this book
gathers insights from experts in the field and provides the most
up-to-date information on all of the T-cell lymphoma subgroups and
current and emerging therapies.
Jacques Barzun, the noted Columbia University historian of ideas
and culture, once described the feeling that some people experience
when they come upon a new reference book. He wrote: "Hand over to
one of us a new Dictionary, "Companion," or Guide, and our eyes
first light up and then turn dreamy: we have seized the volume and
are off, arm in arm with the guide i or companion. ..." The book
now in your hands made my eyes light up. Thyroid Disorders with
Cutaneous Manifestations is that kind of book. Heymann, who has
been fascinated by this sometimes controversial subject for
decades, has brought not only his own expertise, but that of many
experts from the fields of the skin and the thyroid gland. Steven
Jay Gould wrote about overlapping and nonoverlapping
magisteria-this book demonstrates just how much important overlap
there is. But it also covers the basics in such a way that
dermatologists can find what they need to know about the thyroid
and thyroidologists can find what they need to know about the skin.
Thyroid Disorders with Cutaneous Manifestations falls neatly into
the tra- tion of medical monographs that become standards. They
fulfill the roles of gathering, digesting, and synthesizing current
knowledge, and they do so in a way that review articles cannot
approach and that the scientific literature is not designed to
accomplish.
SocialBonding,aProductofEvolution: anIntroductiontotheVolume
Mechanisms underlying reproductive and maternal functions or coping
represent the
initialstructuringforcebehindmanysocialbehaviors.Theyareaccompaniedbysel-
tivehormonalenvironmentsaimedatfacilitatingor
stabilizingthem.Sexandadrenal steroids are major players in the
regulation of reproductive functions and coping challenges, but
other hormones also participate in a variety of social behaviors
(in
particular,oxytocinandvasopressin,twophylogeneticallyveryoldmoietiesoriginally
associated with maternal care and water balance) and are receiving
increasing att- tion. Their role is highlighted in the present
volume, which gathers contributions to
theColloqueMedicineetRecherche"HormonesandSocialBehavior"organizedbythe
FondationIPSENinDecember 2007.
Whatisthekeytounderstandingtherationaleofhormonalsubstratesofbehavior?
Evolution, of course. Higher manifestations of social behavior have
evolved from -
productivebehavior,characterizedbyErnstMayras"theleadingedgeofevolutionary
change." As formulated by one contributor to thisvolume, however,
"the evolutionary increase in neocortex seen in primates has
induced a signi?cant emancipation of - havior from hormonal
determinants, and in parallel, an increasing role for intelligent
socialstrategies"(Keverne 2008). In so-called "lower" mammalian
animals, many social behaviors are closely - pendent upon the
olfactory system, a component of autonomous regulation of such
importancethatitexpressesalargeproportionofallreceptorgenespresentinthebrain.
Whenonelooksat"higher"mammalssuchasprimates,olfactorycontrolbecomesless
stringent. Olfactory structures exhibit the same number of receptor
genes, but a large number are transformed into non-coding
"pseudogenes." In parallel, hormones i- tially targeted on
physiological functions become increasingly associated with more
diversi?edcognitivefunctions.
Cushings syndrome is a rare disorder that is associated with many
co-morbidities such as systemic hypertension, diabetes,
osteoporosis, impaired immune function, and psychiatric disease,
all of which severely reduce quality of life and life expectancy.
This book reviews the role of cortisol in the human body, focusing
on the effects of excess cortisol due to Cushing's syndrome as well
as the role of the HPA axis in metabolism, inflammation, and
neuropsychiatric function. The volume will cover basic mechanistic
data, clinical outcomes data, and novel therapies. Also discussed
are everything from abnormalities of the HPA axis, to the role of
the HPA axis in the development of neuropsychiatric disorders and
metabolic disorders, to new definitions of Cushing's remission and
recurrence. The Hypothalamic Pituitary Adrenal Axis in Health and
Disease will provide a comprehensive and multi-disciplinary review
of the pathophysiology and outcomes of excess cortisol in the human
body and brain as well as the role of the HPA axis in other disease
states.
Tamoxifen is a pioneering medicine for the treatment and prevention
of breast cancer. It is the first drug targeted therapy in cancer
to be successful. Tamoxifen targets the tumor estrogen receptor.
The therapy is known to have saved the lives of millions of women
over the past 40 years. This monograph, written by V. Craig Jordan
- known as the "father of tamoxifen" - and his Tamoxifen Team at
the Georgetown University Washington DC, illustrates the journey of
this milestone in medicine. It includes a personal interview with
V. Craig Jordan about his four decades of discovery in breast
cancer research and treatment. V. Craig Jordan was there for the
birth of tamoxifen as he is credited for reinventing a "failed
morning after contraceptive" to become the "gold standard" for the
treatment of breast cancer. He contributed to every aspect of
tamoxifen application in therapeutics and all aspects of
tamoxifen's pharmacology. He discovered the selective estrogen
receptor modulators (SERMs) and explored the new biology of
estrogen-induced apoptosis.
Section One - Regulation Of Cell Growth And Development.- The Role
of Growth Hormone and Prolactin in Beta-Cell Growth and
Regeneration.- The Insulin-Like Growth Factor Family of Peptides,
Binding Proteins and Receptors: Their Potential Role in Tissue
Regeneration.- The Effects of IGF-I and IGF-II on Cell Growth and
Differentiation in the Central Nervous System.- Growth Factor
Expression in Normal and Diabetic Rats During Peripheral Nerve
Regeneration through Silicone Tubes.- Oncogenes and Cell Growth.-
Interferon - A Candidate Mediator of Cell Growth.- Section Two -
Models for the Study of Cell Regeneration.- Islet Beta-Cell
Regeneration and Reg Genes.- Factors Regulating Islet Regeneration
in the Post-Insulinoma NEDH Rat.- Regeneration of Pancreatic
Endocrine Cells in Interferon Gamma Transgenic Mice.- Trophic
Stimulation of the Ductular-Islet Cell Axis: A New Approach to the
Treatment of Diabetes.- Section Three - Induction of Cell Growth
and Mechanisms.- Expression of Insulin-Like Growth Factors (IGFs)
and Their Binding Proteins (IGF BPs) During Pancreatic Development
in Rat, and Modulation of IGF Actions on Rat Islet DNA Synthesis by
IGF BPs.- The Partial Isolation and Characterization of Ilotropin,
A Novel Islet-Specific Growth Factor.- Expression of Growth Factors
in a Pancreatic Islet Regeneration Model.- Role of p21ras in
Hormone Signalling and Cell Growth Transformation.-
Phosphoinositides and Cell Growth.- The Physiological STOP Pathway:
Target Regulation of Axonal Growth.- Cell Calcium Regulation of
Myosin I - A Motor for Membrane Movement.- Section Four -
Pathogenic and Therapeutic Ramifications.- Amylin Expression in the
Pancreatic Beta-Cell.- Studies of Composite Grafts of Fetal
Pancreas (FP) and Fetal Liver (FL) in the Streptozotocin-Induced
Diabetic Rat.- Contributors.
Providing the latest evidence-based information on etiology,
evaluation and treatment, this unique text provides an in-depth,
comprehensive discussion of the epidemiology, genetic and
endocrinologic factors and medical and surgical management of
recurrent pregnancy loss (RPL). Taking a multidisciplinary approach
including psychological treatment and patient perspectives, all
aspects of current RPL prevention and treatment are elucidated.
Detailed chapters provide real-world illustrative material and
cover the set-up and management of RPL clinics and databases,
containing practical tips. Recurrent Pregnancy Loss will be an
excellent resource for OB-GYN specialists, general and reproductive
endocrinologists, radiologists, hematologists, psychiatrists,
psychologists, and any other investigators or clinicians treating
patients confronted with this emotionally and physically trying
condition.
1. The Role of Heat Shock Proteins in the Regulation of Steroid
Receptor Function.- 2. Subcellular and Subnuclear Trafficking of
Steroid Receptors.- 3. Structure and Function of the Steroid and
Nuclear Receptor Ligand-Binding Domain.- 4. Structure and Function
of the Steroid and Nuclear Receptor DNA Binding Domain.- 5.
Modulation of Steroid/Nuclear Receptor Dimerization and DNA Binding
by Ligands.- 6. Molecular Mechanisms of Nuclear-Receptor-Mediated
Transcriptional Activation and Basal Repression.- 7.
Transcriptional Cross-Talk by Steroid Hormone Receptors.- 8.
Chromatin and Steroid-Receptor-Mediated Transcription.- 9.
Regulation of Glucocorticoid and Estrogen Receptor Activity by
Phosphorylation.- 10. Monomeric Nuclear Receptors.- 11. Orphan
Nuclear Receptors and Their Ligands.
This volume, in discussing resistance to ibritumomab, will focus on
the mechanism, hematological aspects, radiological and nuclear
medicine aspects, and medical physics that deal with radiation
dosimetry, and will outline future prospects for overcoming
resistance and enhancing efficacy of ibritumomab.
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