Pheochromocytoma (PHEO) and Paraganglioma (PGL)

This book outlines some new advances in genetics, clinical evaluation, localization, therapy (newly including immunotherapy) of pheochromocytoma and paraganglioma including their metastatic counterparts. Well-known and experienced clinicians and scientists contributed to this book to include some no...

Ամբողջական նկարագրություն

Պահպանված է:
Մատենագիտական մանրամասներ
Հիմնական հեղինակներ: Pacak, Karel, Taïeb, David
Ձևաչափ: Online
Լեզու:անգլերեն
Հրապարակվել է: MDPI - Multidisciplinary Digital Publishing Institute 2021
Խորագրեր:
n/a
GTV
PGL
dog
HIF
NF1
NET
PCC
VHL
PET
Առցանց հասանելիություն:42657
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author Pacak, Karel
Taïeb, David
author_browse Pacak, Karel
Taïeb, David
author_facet Pacak, Karel
Taïeb, David
author_sort Pacak, Karel
collection Directory of Open Access Books
description This book outlines some new advances in genetics, clinical evaluation, localization, therapy (newly including immunotherapy) of pheochromocytoma and paraganglioma including their metastatic counterparts. Well-known and experienced clinicians and scientists contributed to this book to include some novel approaches to these tumors. This book will serve to various health care professionals from different subspecialties, but mainly oncologists, endocrinologists, endocrine surgeons, pediatricians, and radiologists. This book shows that the field of pheochromocytoma/paraganglioma is evolving and a significant progress has been made in last 5 years requiring that health care professionals and scientists will learns new information and implement it in their clinical practice or scientific work, respectively. This book should not be missed by anybody who is focusing on neuroendocrine tumors, their newest evaluation and treatment.
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institution Directory of Open Access Books
language eng
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher MDPI - Multidisciplinary Digital Publishing Institute
publisherStr MDPI - Multidisciplinary Digital Publishing Institute
record_format ojs
spelling doab-20.500.12854ir-561552024-03-31T13:10:10Z Pheochromocytoma (PHEO) and Paraganglioma (PGL) Pacak, Karel Taïeb, David R5-920 polycythemia peptide receptor radiotherapy n/a vasculogenesis catecholamines neuroendocrine GTV adaptive immunity therapy resistance histology transgenic mice cryoablation spheroids energy metabolism somatostatinoma angiogenesis pheochromocytoma SDHD percutaneous ethanol injection metanephrines SDHB global longitudinal strain mutation normetanephrines catecholamine PASS PGL 177Lu-DOTATATE chromosomal alteration speckle-tracking echocardiography lL-6 dog percutaneous ablation stem-like tumor cells EPAS1 neural crest fluorescence imaging neutrophil xenograft inflammation head and neck weighted standard deviation FGF21 calorimetry HIF average real variability next-generation sequencing adrenocortical carcinoma carotid body hypoxia-inducible factor paraganglioma succinate dehydrogenase blood pressure variability arrhythmia mortality NF1 toll-like receptor GAPP NET subclinical systolic dysfunction pheochromocytoma and paraganglioma PET-CT pan-cancer analysis mouse pheochromocytoma cells innate immunity neurogenesis neuroendocrine tumor obesity hypotension hypoxia CNV detection 18F-FDOPA comparative genomics adrenomedullary function PCC pathogen-associated molecular patterns adrenal tumor radiotherapy 11C-hydroxy-ephedrine radiofrequency ablation PPGL minimally invasive procedure sporadic diabetes mellitus adrenal incidentaloma germline mutation immunotherapy VHL immunohistochemistry metastatic OR malignant pheochromocytoma erythropoietin postoperative targeted therapy PRRT metastatic mitochondria T cell TCA cycle meta-analysis pseudohypoxia ectopic secretion radiosensitization chromogranin A hereditary hypertension PET phosphorylation tyrosine hydroxylase thema EDItEUR::M Medicine and Nursing This book outlines some new advances in genetics, clinical evaluation, localization, therapy (newly including immunotherapy) of pheochromocytoma and paraganglioma including their metastatic counterparts. Well-known and experienced clinicians and scientists contributed to this book to include some novel approaches to these tumors. This book will serve to various health care professionals from different subspecialties, but mainly oncologists, endocrinologists, endocrine surgeons, pediatricians, and radiologists. This book shows that the field of pheochromocytoma/paraganglioma is evolving and a significant progress has been made in last 5 years requiring that health care professionals and scientists will learns new information and implement it in their clinical practice or scientific work, respectively. This book should not be missed by anybody who is focusing on neuroendocrine tumors, their newest evaluation and treatment. 2021-02-11T22:47:21Z 2021-02-11T22:47:21Z 2019-12-09 11:49:16 2019 book 42657 9783039216550 9783039216543 https://directory.doabooks.org/handle/20.500.12854/56155 eng application/octet-stream Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/1816 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-03921-655-0 10.3390/books978-3-03921-655-0 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783039216550 9783039216543 380 open access
spellingShingle R5-920
polycythemia
peptide receptor radiotherapy
n/a
vasculogenesis
catecholamines
neuroendocrine
GTV
adaptive immunity
therapy resistance
histology
transgenic mice
cryoablation
spheroids
energy metabolism
somatostatinoma
angiogenesis
pheochromocytoma
SDHD
percutaneous ethanol injection
metanephrines
SDHB
global longitudinal strain
mutation
normetanephrines
catecholamine
PASS
PGL
177Lu-DOTATATE
chromosomal alteration
speckle-tracking echocardiography
lL-6
dog
percutaneous ablation
stem-like tumor cells
EPAS1
neural crest
fluorescence imaging
neutrophil
xenograft
inflammation
head and neck
weighted standard deviation
FGF21
calorimetry
HIF
average real variability
next-generation sequencing
adrenocortical carcinoma
carotid body
hypoxia-inducible factor
paraganglioma
succinate dehydrogenase
blood pressure variability
arrhythmia
mortality
NF1
toll-like receptor
GAPP
NET
subclinical systolic dysfunction
pheochromocytoma and paraganglioma
PET-CT
pan-cancer analysis
mouse pheochromocytoma cells
innate immunity
neurogenesis
neuroendocrine tumor
obesity
hypotension
hypoxia
CNV detection
18F-FDOPA
comparative genomics
adrenomedullary function
PCC
pathogen-associated molecular patterns
adrenal tumor
radiotherapy
11C-hydroxy-ephedrine
radiofrequency ablation
PPGL
minimally invasive procedure
sporadic
diabetes mellitus
adrenal incidentaloma
germline mutation
immunotherapy
VHL
immunohistochemistry
metastatic OR malignant pheochromocytoma
erythropoietin
postoperative
targeted therapy
PRRT
metastatic
mitochondria
T cell
TCA cycle
meta-analysis
pseudohypoxia
ectopic secretion
radiosensitization
chromogranin A
hereditary
hypertension
PET
phosphorylation tyrosine hydroxylase
thema EDItEUR::M Medicine and Nursing
Pacak, Karel
Taïeb, David
Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title_full Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title_fullStr Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title_full_unstemmed Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title_short Pheochromocytoma (PHEO) and Paraganglioma (PGL)
title_sort pheochromocytoma pheo and paraganglioma pgl
topic R5-920
polycythemia
peptide receptor radiotherapy
n/a
vasculogenesis
catecholamines
neuroendocrine
GTV
adaptive immunity
therapy resistance
histology
transgenic mice
cryoablation
spheroids
energy metabolism
somatostatinoma
angiogenesis
pheochromocytoma
SDHD
percutaneous ethanol injection
metanephrines
SDHB
global longitudinal strain
mutation
normetanephrines
catecholamine
PASS
PGL
177Lu-DOTATATE
chromosomal alteration
speckle-tracking echocardiography
lL-6
dog
percutaneous ablation
stem-like tumor cells
EPAS1
neural crest
fluorescence imaging
neutrophil
xenograft
inflammation
head and neck
weighted standard deviation
FGF21
calorimetry
HIF
average real variability
next-generation sequencing
adrenocortical carcinoma
carotid body
hypoxia-inducible factor
paraganglioma
succinate dehydrogenase
blood pressure variability
arrhythmia
mortality
NF1
toll-like receptor
GAPP
NET
subclinical systolic dysfunction
pheochromocytoma and paraganglioma
PET-CT
pan-cancer analysis
mouse pheochromocytoma cells
innate immunity
neurogenesis
neuroendocrine tumor
obesity
hypotension
hypoxia
CNV detection
18F-FDOPA
comparative genomics
adrenomedullary function
PCC
pathogen-associated molecular patterns
adrenal tumor
radiotherapy
11C-hydroxy-ephedrine
radiofrequency ablation
PPGL
minimally invasive procedure
sporadic
diabetes mellitus
adrenal incidentaloma
germline mutation
immunotherapy
VHL
immunohistochemistry
metastatic OR malignant pheochromocytoma
erythropoietin
postoperative
targeted therapy
PRRT
metastatic
mitochondria
T cell
TCA cycle
meta-analysis
pseudohypoxia
ectopic secretion
radiosensitization
chromogranin A
hereditary
hypertension
PET
phosphorylation tyrosine hydroxylase
thema EDItEUR::M Medicine and Nursing
topic_facet R5-920
polycythemia
peptide receptor radiotherapy
n/a
vasculogenesis
catecholamines
neuroendocrine
GTV
adaptive immunity
therapy resistance
histology
transgenic mice
cryoablation
spheroids
energy metabolism
somatostatinoma
angiogenesis
pheochromocytoma
SDHD
percutaneous ethanol injection
metanephrines
SDHB
global longitudinal strain
mutation
normetanephrines
catecholamine
PASS
PGL
177Lu-DOTATATE
chromosomal alteration
speckle-tracking echocardiography
lL-6
dog
percutaneous ablation
stem-like tumor cells
EPAS1
neural crest
fluorescence imaging
neutrophil
xenograft
inflammation
head and neck
weighted standard deviation
FGF21
calorimetry
HIF
average real variability
next-generation sequencing
adrenocortical carcinoma
carotid body
hypoxia-inducible factor
paraganglioma
succinate dehydrogenase
blood pressure variability
arrhythmia
mortality
NF1
toll-like receptor
GAPP
NET
subclinical systolic dysfunction
pheochromocytoma and paraganglioma
PET-CT
pan-cancer analysis
mouse pheochromocytoma cells
innate immunity
neurogenesis
neuroendocrine tumor
obesity
hypotension
hypoxia
CNV detection
18F-FDOPA
comparative genomics
adrenomedullary function
PCC
pathogen-associated molecular patterns
adrenal tumor
radiotherapy
11C-hydroxy-ephedrine
radiofrequency ablation
PPGL
minimally invasive procedure
sporadic
diabetes mellitus
adrenal incidentaloma
germline mutation
immunotherapy
VHL
immunohistochemistry
metastatic OR malignant pheochromocytoma
erythropoietin
postoperative
targeted therapy
PRRT
metastatic
mitochondria
T cell
TCA cycle
meta-analysis
pseudohypoxia
ectopic secretion
radiosensitization
chromogranin A
hereditary
hypertension
PET
phosphorylation tyrosine hydroxylase
thema EDItEUR::M Medicine and Nursing
url 42657
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