X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Endocrine tumor syndromes and their genetics / (2013)
    Basel :Karger,
    Details
    UID:
    almafu_9959076710102883
    Format: 1 online resource (202 p.)
    ISBN: 3-318-02331-0
    Series Statement: Frontiers of hormone research, volume 41
    Content: In these times, a book should aspire to present the most significant advances in the field, reflect the themes of the moment, and provide a useful compendium for future reference. This book accomplishes all three objectives by discussing the changing world of modern genetics in endocrine tumors and its impact on clinical practice. Clinicians have to incorporate modern genetics and systems biology in their daily practice. Educators and researchers have to introduce molecular pathways and their genetic variability in their teaching, as well as understanding of classic physiology and pathophysiology. Taking these aspects into account, the chapters in this book cover both the classic multiple endocrine neoplasia (MEN) syndromes, as well as newly described ones, such as Carney triad and Carney-Stratakis syndrome. Furthermore, the genetics of paragangliomas as well as thyroid, parathyroid, and pituitary tumors are examined. Outlining the latest research and its obvious implications for our understanding the genetics of endocrine tumor formation and molecular biology of cancer and their potential therapeutic implications, this book is not only useful for researchers but even more so for practicing clinicians, in particular internists, endocrinologists, oncologists, pediatricians, surgeons, pathologists, geneticists, and genetic counselors.
    Note: Description based upon print version of record. , Multiple endocrine neoplasia type 1 / Agarwal, S.K. -- Multiple endocrine neoplasia type 2 / Lodish, M. -- Von Hippel-Lindau syndrome / Chou, A. ... [et al.] -- Carney complex -- Espiard, S., Bertherat, J. -- Multiple endocrine neoplasia type 4 / Lee, M., Pellegata, N.S. -- Novel hereditary forms of pheochromocytomas and paragangliomas / Dahia, P.L.M. -- Carney triad / Carney, J.A. -- Genetics of pituitary adenomas / Gadelha, M.R. ... [et al.] -- Clinical behavior and genetics of nonsyndromic, familial nonmedullary thyroid cancer / Bauer, A.J. -- Genetic defects associated with familial and sporadic hyperparathyroidism / Hendy, G.N., Cole, D.E.C. -- Endocrine tumors associated with neurofibromatosis type 1, Peutz-Jeghers syndrome, and other familial neoplasia syndromes / Kalkan, E., Waguespack, S.G. , English
    Additional Edition: ISBN 3-318-02330-2
    Language: English
    Keywords: Aufsatzsammlung
    URL: Volltext
    URL: lizenzpflichtig
    URL: Inhaltsverzeichnis
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Online Access
    Stabi Berlin
    UB Potsdam
    Charité
    MPI Bildungsforschung
  • 2
    Online Resource
    Online Resource
    Sperling pediatric endocrinology / (2021)
    Philadelphia, PA :Elsevier,
    Details
    UID:
    almahu_9949606756902882
    Format: 1 online resource (xii, 1021 pages) : , illustrations (chiefly color)
    Edition: Fifth edition.
    ISBN: 0-323-62521-5 , 978-0-323-62520-3
    Content: An ideal resource for both pediatricians and endocrinologists, Sperling's Pediatric Endocrinology, 5th Edition, brings you fully up to date with accelerating research; new discoveries in metabolic, biochemical and molecular mechanisms; and the resulting advances in today's clinical care. The editorial team of world-renowned pediatric endocrinologists led by Dr. Mark Sperling, as well as expert contributing authors, cover comprehensive and current aspects of both basic science and clinical practice. Whether you're preparing for certification or have extensive clinical experience, this detailed, authoritative reference helps you increase your knowledge and determine the best possible course for every patient. Delivers trusted guidance in every area of the field: including Endocrine Disorders of the Newborn, Endocrine Disorders of Childhood and Adolescence, and Laboratory Tests. Features new topics such as transgender issues in children and adolescents and endocrinology of pregnancy, the fetus and the placenta. Offers expert coverage of hot topics such as disorders of sexual development, molecular basis of endocrine disorders, hypoglycemia in newborns and infants; neonatal and other monogenic forms of diabetes; Type I and Type II diabetes and their treatment with new insulins together with the progress in an artificial pancreas and new medications for T2DM in adolescents; the obesity epidemic and role of bariatric surgery; and advances toward personalized medicine. Includes easy-to-follow algorithms and numerous quick-reference tables and boxes in every clinical chapter, plus interactive questions online for self-assessment. Offers state-of-the-art information and fresh perspectives from new and award-winning authors in such areas as disorders of growth, multiple endocrine tumors, and puberty and its disorders in girls and boys. Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.
    Note: Overview and principles of pediatric endocrinology -- Molecular endocrinology, endocrine genetics, and precision medicine -- Receptor transduction pathways mediating hormone action -- Endocrinology laboratory testing -- Fetal-maternal endocrinology and parturition -- Ambiguous genitalia -- Hypoglycemia in the newborn and infant -- Disorders of the thyroid in the newborn and infant -- Disorders of mineral metabolism: normal homeostasis -- Monogenic diabetes mellitus: neonatal diabetes and maturity-onset diabetes of the young -- Disorders of childhood growth -- Disorders of the posterior pituitary -- Thyroid disorders in children and adolescents -- The adrenal cortex and its disorders -- Pheochromocytoma/paraganglioma, medullary thyroid carcinoma, and hereditary endocrine neoplasia syndromes -- Puberty in the female and its disorders -- Turner syndrome -- Puberty and its disorders in the male -- Care of transgender/gender nonconforming youth -- Disorders of mineral metabolism ii. Abnormalities of mineral homeostasis in the newborn, infant, child, and adolescent -- Diabetes mellitus -- Autoimmune polyglandular syndromes -- Hypoglycemia in the toddler and child -- Obesity, metabolic syndrome and disorders of energy balance -- Lipid disorders in children and adolescents.
    Additional Edition: ISBN 0-323-62520-7
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    HU Berlin
    FU Berlin
    Charité
  • 3
    Online Resource
    Online Resource
    Gigantism and acromegaly : genetics, diagnosis, and treatment (2021)
    London, England ; : Elsevier,
    Details
    UID:
    almahu_9949697894702882
    Format: 1 online resource (312 pages)
    ISBN: 0-12-814538-2
    Content: "Gigantism and Acromegaly brings together pituitary experts, taking readers from bench research, to genetic analysis, clinical analysis, and new therapeutic approaches. This book serves as a reference for growth hormone over-secretion and its diagnosis and treatment for endocrinologists, pediatricians, internists, and neurosurgeons, and for geneticists. Pharmaceutical companies may use it as a reference for drug development and research. Students, residents and fellows in medicine and endocrinology and genetics will also find it valuable as it provides a single up-to-date review of the molecular biology of gigantism and acromegaly as well as recommended approaches to evaluation and management. Acromegaly is a rare pituitary disorder that slowly changes its adult victim's appearance over time: larger hands and feet, bigger jaw, forehead, nose, and lips. Generally, a benign pituitary tumor is the cause and symptoms of acromegaly can vary from patient to patient, making a diagnosis difficult and prolonging suffering for years. Early detection is key in the management of acromegaly as the pathologic effects of increased growth hormone (GH) production are progressive and can be life-threatening as the result of associated cardiovascular, cerebrovascular, and respiratory disorders and malignancies"--
    Additional Edition: ISBN 0-12-814537-4
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    HU Berlin
    FU Berlin
    Charité
  • 4
    Book
    Book
    Protein kinase A and human disease : [... result of a conference entitled Protein kinase A and human disease ... held on September 10, 2001 in Bethesda, Maryland] (2002)
    New York, N.Y. : The New York Academy of Sciences
    Details
    UID:
    gbv_347710557
    Format: VII, 271 S. , Ill., graph. Darst.
    ISBN: 1573314129 , 1573314137
    Series Statement: Annals of the New York Academy of Sciences 968
    Note: This volume is the result of a conference - Includes bibliographical references and index
    Language: English
    Keywords: Pathophysiologie ; Kongress ; Proteinkinase A ; Pathobiochemie ; Adenylatcyclase ; Zelle ; Signaltransduktion ; Proteinkinasen ; Konferenzschrift ; Konferenzschrift
    URL: Inhaltsverzeichnis
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Book
    Stabi Berlin get availability status
    Akademie d. Wiss. get availability status
  • 5
    Online Resource
    Online Resource
    Endocrine tumor syndromes and their genetics / (2013)
    Basel :Karger,
    Details
    UID:
    edoccha_9959076710102883
    Format: 1 online resource (202 p.)
    ISBN: 3-318-02331-0
    Series Statement: Frontiers of hormone research, volume 41
    Content: In these times, a book should aspire to present the most significant advances in the field, reflect the themes of the moment, and provide a useful compendium for future reference. This book accomplishes all three objectives by discussing the changing world of modern genetics in endocrine tumors and its impact on clinical practice. Clinicians have to incorporate modern genetics and systems biology in their daily practice. Educators and researchers have to introduce molecular pathways and their genetic variability in their teaching, as well as understanding of classic physiology and pathophysiology. Taking these aspects into account, the chapters in this book cover both the classic multiple endocrine neoplasia (MEN) syndromes, as well as newly described ones, such as Carney triad and Carney-Stratakis syndrome. Furthermore, the genetics of paragangliomas as well as thyroid, parathyroid, and pituitary tumors are examined. Outlining the latest research and its obvious implications for our understanding the genetics of endocrine tumor formation and molecular biology of cancer and their potential therapeutic implications, this book is not only useful for researchers but even more so for practicing clinicians, in particular internists, endocrinologists, oncologists, pediatricians, surgeons, pathologists, geneticists, and genetic counselors.
    Note: Description based upon print version of record. , Multiple endocrine neoplasia type 1 / Agarwal, S.K. -- Multiple endocrine neoplasia type 2 / Lodish, M. -- Von Hippel-Lindau syndrome / Chou, A. ... [et al.] -- Carney complex -- Espiard, S., Bertherat, J. -- Multiple endocrine neoplasia type 4 / Lee, M., Pellegata, N.S. -- Novel hereditary forms of pheochromocytomas and paragangliomas / Dahia, P.L.M. -- Carney triad / Carney, J.A. -- Genetics of pituitary adenomas / Gadelha, M.R. ... [et al.] -- Clinical behavior and genetics of nonsyndromic, familial nonmedullary thyroid cancer / Bauer, A.J. -- Genetic defects associated with familial and sporadic hyperparathyroidism / Hendy, G.N., Cole, D.E.C. -- Endocrine tumors associated with neurofibromatosis type 1, Peutz-Jeghers syndrome, and other familial neoplasia syndromes / Kalkan, E., Waguespack, S.G. , English
    Additional Edition: ISBN 3-318-02330-2
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Charité
  • 6
    Online Resource
    Online Resource
    Sperling pediatric endocrinology / (2021)
    Philadelphia, PA :Elsevier,
    Details
    UID:
    edocfu_9961352660802883
    Format: 1 online resource (xii, 1021 pages) : , illustrations (chiefly color)
    Edition: Fifth edition.
    ISBN: 0-323-62521-5 , 978-0-323-62520-3
    Content: An ideal resource for both pediatricians and endocrinologists, Sperling's Pediatric Endocrinology, 5th Edition, brings you fully up to date with accelerating research; new discoveries in metabolic, biochemical and molecular mechanisms; and the resulting advances in today's clinical care. The editorial team of world-renowned pediatric endocrinologists led by Dr. Mark Sperling, as well as expert contributing authors, cover comprehensive and current aspects of both basic science and clinical practice. Whether you're preparing for certification or have extensive clinical experience, this detailed, authoritative reference helps you increase your knowledge and determine the best possible course for every patient. Delivers trusted guidance in every area of the field: including Endocrine Disorders of the Newborn, Endocrine Disorders of Childhood and Adolescence, and Laboratory Tests. Features new topics such as transgender issues in children and adolescents and endocrinology of pregnancy, the fetus and the placenta. Offers expert coverage of hot topics such as disorders of sexual development, molecular basis of endocrine disorders, hypoglycemia in newborns and infants; neonatal and other monogenic forms of diabetes; Type I and Type II diabetes and their treatment with new insulins together with the progress in an artificial pancreas and new medications for T2DM in adolescents; the obesity epidemic and role of bariatric surgery; and advances toward personalized medicine. Includes easy-to-follow algorithms and numerous quick-reference tables and boxes in every clinical chapter, plus interactive questions online for self-assessment. Offers state-of-the-art information and fresh perspectives from new and award-winning authors in such areas as disorders of growth, multiple endocrine tumors, and puberty and its disorders in girls and boys. Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.
    Note: Overview and principles of pediatric endocrinology -- Molecular endocrinology, endocrine genetics, and precision medicine -- Receptor transduction pathways mediating hormone action -- Endocrinology laboratory testing -- Fetal-maternal endocrinology and parturition -- Ambiguous genitalia -- Hypoglycemia in the newborn and infant -- Disorders of the thyroid in the newborn and infant -- Disorders of mineral metabolism: normal homeostasis -- Monogenic diabetes mellitus: neonatal diabetes and maturity-onset diabetes of the young -- Disorders of childhood growth -- Disorders of the posterior pituitary -- Thyroid disorders in children and adolescents -- The adrenal cortex and its disorders -- Pheochromocytoma/paraganglioma, medullary thyroid carcinoma, and hereditary endocrine neoplasia syndromes -- Puberty in the female and its disorders -- Turner syndrome -- Puberty and its disorders in the male -- Care of transgender/gender nonconforming youth -- Disorders of mineral metabolism ii. Abnormalities of mineral homeostasis in the newborn, infant, child, and adolescent -- Diabetes mellitus -- Autoimmune polyglandular syndromes -- Hypoglycemia in the toddler and child -- Obesity, metabolic syndrome and disorders of energy balance -- Lipid disorders in children and adolescents.
    Additional Edition: ISBN 0-323-62520-7
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    FU Berlin
  • 7
    Online Resource
    Online Resource
    Sperling pediatric endocrinology / (2021)
    Philadelphia, PA :Elsevier,
    Details
    UID:
    edoccha_9961352660802883
    Format: 1 online resource (xii, 1021 pages) : , illustrations (chiefly color)
    Edition: Fifth edition.
    ISBN: 0-323-62521-5 , 978-0-323-62520-3
    Content: An ideal resource for both pediatricians and endocrinologists, Sperling's Pediatric Endocrinology, 5th Edition, brings you fully up to date with accelerating research; new discoveries in metabolic, biochemical and molecular mechanisms; and the resulting advances in today's clinical care. The editorial team of world-renowned pediatric endocrinologists led by Dr. Mark Sperling, as well as expert contributing authors, cover comprehensive and current aspects of both basic science and clinical practice. Whether you're preparing for certification or have extensive clinical experience, this detailed, authoritative reference helps you increase your knowledge and determine the best possible course for every patient. Delivers trusted guidance in every area of the field: including Endocrine Disorders of the Newborn, Endocrine Disorders of Childhood and Adolescence, and Laboratory Tests. Features new topics such as transgender issues in children and adolescents and endocrinology of pregnancy, the fetus and the placenta. Offers expert coverage of hot topics such as disorders of sexual development, molecular basis of endocrine disorders, hypoglycemia in newborns and infants; neonatal and other monogenic forms of diabetes; Type I and Type II diabetes and their treatment with new insulins together with the progress in an artificial pancreas and new medications for T2DM in adolescents; the obesity epidemic and role of bariatric surgery; and advances toward personalized medicine. Includes easy-to-follow algorithms and numerous quick-reference tables and boxes in every clinical chapter, plus interactive questions online for self-assessment. Offers state-of-the-art information and fresh perspectives from new and award-winning authors in such areas as disorders of growth, multiple endocrine tumors, and puberty and its disorders in girls and boys. Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.
    Note: Overview and principles of pediatric endocrinology -- Molecular endocrinology, endocrine genetics, and precision medicine -- Receptor transduction pathways mediating hormone action -- Endocrinology laboratory testing -- Fetal-maternal endocrinology and parturition -- Ambiguous genitalia -- Hypoglycemia in the newborn and infant -- Disorders of the thyroid in the newborn and infant -- Disorders of mineral metabolism: normal homeostasis -- Monogenic diabetes mellitus: neonatal diabetes and maturity-onset diabetes of the young -- Disorders of childhood growth -- Disorders of the posterior pituitary -- Thyroid disorders in children and adolescents -- The adrenal cortex and its disorders -- Pheochromocytoma/paraganglioma, medullary thyroid carcinoma, and hereditary endocrine neoplasia syndromes -- Puberty in the female and its disorders -- Turner syndrome -- Puberty and its disorders in the male -- Care of transgender/gender nonconforming youth -- Disorders of mineral metabolism ii. Abnormalities of mineral homeostasis in the newborn, infant, child, and adolescent -- Diabetes mellitus -- Autoimmune polyglandular syndromes -- Hypoglycemia in the toddler and child -- Obesity, metabolic syndrome and disorders of energy balance -- Lipid disorders in children and adolescents.
    Additional Edition: ISBN 0-323-62520-7
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Charité
  • 8
    Online Resource
    Online Resource
    Gigantism and acromegaly : genetics, diagnosis, and treatment (2021)
    London, England ; : Elsevier,
    Details
    UID:
    edoccha_9960074101202883
    Format: 1 online resource (312 pages)
    ISBN: 0-12-814538-2
    Content: "Gigantism and Acromegaly brings together pituitary experts, taking readers from bench research, to genetic analysis, clinical analysis, and new therapeutic approaches. This book serves as a reference for growth hormone over-secretion and its diagnosis and treatment for endocrinologists, pediatricians, internists, and neurosurgeons, and for geneticists. Pharmaceutical companies may use it as a reference for drug development and research. Students, residents and fellows in medicine and endocrinology and genetics will also find it valuable as it provides a single up-to-date review of the molecular biology of gigantism and acromegaly as well as recommended approaches to evaluation and management. Acromegaly is a rare pituitary disorder that slowly changes its adult victim's appearance over time: larger hands and feet, bigger jaw, forehead, nose, and lips. Generally, a benign pituitary tumor is the cause and symptoms of acromegaly can vary from patient to patient, making a diagnosis difficult and prolonging suffering for years. Early detection is key in the management of acromegaly as the pathologic effects of increased growth hormone (GH) production are progressive and can be life-threatening as the result of associated cardiovascular, cerebrovascular, and respiratory disorders and malignancies"--
    Additional Edition: ISBN 0-12-814537-4
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Charité
  • 9
    Online Resource
    Online Resource
    Gigantism and acromegaly : genetics, diagnosis, and treatment (2021)
    London, England ; : Elsevier,
    Details
    UID:
    edocfu_9960074101202883
    Format: 1 online resource (312 pages)
    ISBN: 0-12-814538-2
    Content: "Gigantism and Acromegaly brings together pituitary experts, taking readers from bench research, to genetic analysis, clinical analysis, and new therapeutic approaches. This book serves as a reference for growth hormone over-secretion and its diagnosis and treatment for endocrinologists, pediatricians, internists, and neurosurgeons, and for geneticists. Pharmaceutical companies may use it as a reference for drug development and research. Students, residents and fellows in medicine and endocrinology and genetics will also find it valuable as it provides a single up-to-date review of the molecular biology of gigantism and acromegaly as well as recommended approaches to evaluation and management. Acromegaly is a rare pituitary disorder that slowly changes its adult victim's appearance over time: larger hands and feet, bigger jaw, forehead, nose, and lips. Generally, a benign pituitary tumor is the cause and symptoms of acromegaly can vary from patient to patient, making a diagnosis difficult and prolonging suffering for years. Early detection is key in the management of acromegaly as the pathologic effects of increased growth hormone (GH) production are progressive and can be life-threatening as the result of associated cardiovascular, cerebrovascular, and respiratory disorders and malignancies"--
    Additional Edition: ISBN 0-12-814537-4
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    FU Berlin
  • 10
    Online Resource
    Online Resource
    Endocrine tumor syndromes and their genetics / (2013)
    Basel :Karger,
    Details
    UID:
    almahu_BV040926162
    Format: 1 Online-Ressource (XI, 187 Seiten).
    ISBN: 978-3-318-02331-2
    Series Statement: Frontiers of hormone research Vol. 41
    Content: In our days, a book should aspire to present the most significant advances in the field, reflect the theme of the moment, and provide a useful compendium for the future. This book accomplishes all three points by discussing the changing world of modern genetics in endocrine tumors and its impact on clinical practice. Clinicians have to incorporate modern genetics and systems biology in their daily practice. Educators and researchers have to introduce molecular pathways and their genetic variability in their teaching and understanding of classic physiology and pathophysiology.Taking these aspects into account, the chapters in this book cover both the classic multiple endocrine neoplasia (MEN) syndromes, as well as newly described ones, such as Carney triad and Carney-Stratakis syndrome. Furthermore, the genetics of paragangliomas as well as thyroid, parathyroid, and pituitary tumors are examined. Outlining the latest research and its obvious implications for our understanding the genetics of endocrine tumor formation and molecular biology of cancer and their potential therapeutic implications, this book is not only useful for researchers but even more so for practicing clinicians, in particular internists, endocrinologists, oncologists, pediatricians, surgeons, pathologists, geneticists, and genetic counselors
    Note: From classic MEN syndromes to various germline and somatic mutations in sporadic tumors
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 978-3-318-02330-5
    Language: English
    Subjects: Medicine
    RVK:
    YC 3700
    RVK:
    XF 1227
    Keywords: Hormonaktiver Tumor ; Erbkrankheit ; Aufsatzsammlung
    DOI: 10.1159/isbn.978-3-318-02331-2
    URL: Volltext
    Author information: Stratakis, Constantine A.
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Online Resource
    Online Access
    Open Access Request
    HU Berlin
Nothing or not found what you are looking for? Please check your search query or use the Interlibrary Loan Search.
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages