國立虎尾科技大學 |

Hypoparathyroidism

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Hypoparathyroidism/ edited by Maria Luisa Brandi, Edward Meigs Brown.
其他作者:	Brandi, Maria Luisa.
面頁冊數:	XVII, 429 p. 67 illus., 37 illus. in color.online resource. :
Contained By:	Springer Nature eBook
標題:	Endocrinology . -
電子資源:	https://doi.org/10.1007/978-88-470-5376-2
ISBN:	9788847053762

Hypoparathyroidism
Hypoparathyroidism[electronic resource] /edited by Maria Luisa Brandi, Edward Meigs Brown. - 1st ed. 2015. - XVII, 429 p. 67 illus., 37 illus. in color.online resource.

Preface -- Part I ANATOMY AND PHYSIOLOGY OF THE PARATHYROID GLANDS -- 1 The History: from Fuller Albright to the sequence of Parathyroid Hormone -- 2 Embryology of the parathyroid glands -- 3 PTH and PTH-related peptides -- 4 PTH assays and their clinical significance -- 5 Calcium-control of PTH secretion -- 6 Phosphate control of PTH secretion -- 7 Role of magnesium in Parathyroid Physiology -- 8 The vitamin D/FGF23/PTH axis -- 9 The PTH receptorsome and transduction pathways -- 10 G protein Gsα and GNAS imprinting -- 11 PTH actions on bone and kidney -- 12 PTH and PTHrp: non‐classical target -- 13 In vitro cellular models of parathyroid cells -- II CONDITIONS OF HYPOPARATHYROIDISM -- 14 Epidemiology of hypoparathyropidism -- 15 Clinical Presentation of Hypoparathyroidism -- 16 Isolated, Familial Hypoparathyroidism -- 17 Autoimmune Hypoparathyroidism -- 18 DiGeorge Syndrome (M. Tarsitano) -- 19 Hypoparathyroidism, Deafness and renal dysplasia syndrome -- 20 Hypoparathyroidism, dwarfism, Medullary stenosis of long bones and eye abnormalities (Kenny- Caffey) Syndrome and hypoparathyroidism, retardation and dysmorphism (Sanjad-Sakati) Syndrome -- 21 Hypoparathyroidism in mitochondrial disorders -- 22 Postoperative hypoparathyroidism -- 23 Hypoparathyroidism during pregnancy, lactation, and fetal/neonatal development -- 24 Other forms of acquired hypoparathyroidism (radiation‐induced, infiltrative disorders, heavy‐metal storage disorders, post burn, maternal hyperparathyroidism) -- 25 Refractory hypoparathyroidism -- 26 Bone features in hypoparathyroidism -- 27 Management of acute hypocalcemia -- 28 Conventional Treatment in chronic hypoparathyroidism -- 29 Follow‐up in chronic hypoparathyroidism -- 30 Replacement therapy with PTH1-34 -- 31 Replacement Therapy with PTH1-84 -- III FUNCTIONAL HYPOPARATHYROIDISM -- 32 Classification of pseudohypoparathyroidism and differential diagnosis -- 33 Pseudohypoparathyroidism type Ia, Pseudopseudohypoparathyroidism and Albright Hereditary Osteodystrophy -- 34 Pseudohypoparathyroidisms other than Ia -- 35 Genetic testing in pseudo-hypoparathyroidism -- 36 Blomstrand’s chondrodystrophy -- 37 Hypoparathyroidism during magnesium deficiency or excess -- IV ADVOCATING FOR HYPOPARATHYROIDISM -- 38. Advocating For Hypoparathyroidism.

Hypoparathyroidism, a condition in which insufficient parathyroid hormone (PTH) is produced to maintain normocalcemia is associated with a variety of acute and chronic symptoms and complications due to hypocalcemia. Replacement therapy utilizing PTH has long been awaited, and this book is new and very timely as it coincides with the publication of results on the role of the PTH molecule in the pharmacological management of this disorder. This advance is sparking renewed interest in hypoparathyroidism, which is attributable to neck surgery in most cases and to inherited disorders in a minority. Hypoparathyroidism has been written by acknowledged experts in the field and provides essential, up-to-date information on the pathology, diagnosis, and treatment of the condition. It opens by addressing in detail the anatomy and physiology of the parathyroids and describing the epidemiology and clinical presentation of hypoparathyroidism. The full range of hypoparathyroid disorders are then discussed, including the various genetic forms, postoperative hypoparathyroidism, and other forms of acquired hypoparathyroidism. Individual chapters focus on refractory disease, the impact of the condition on bone, and the management of acute hypocalcemia. Both conventional treatment for hypoparathyroidism and the novel replacement therapy with PTH peptides are then thoroughly examined. Pseudohypoparathyroidism is also extensively discussed, with information on the various forms, differential diagnosis, and genetic testing. This book will be of interest to all endocrinologists, and also to surgeons and internal medicine physicians. .

ISBN: 9788847053762

Standard No.: 10.1007/978-88-470-5376-2doiSubjects--Topical Terms:

1254221
Endocrinology .

LC Class. No.: RC648-665.2

Dewey Class. No.: 616.4

Hypoparathyroidism
LDR:05262nam a22003975i 4500 001 969092
003 DE-He213
005 20200702061855.0
007 cr nn 008mamaa
008 201211s2015 it | s |||| 0|eng d
020 $a 9788847053762 $9 978-88-470-5376-2
024 7 $a 10.1007/978-88-470-5376-2 $2 doi
035 $a 978-88-470-5376-2
050 4 $a RC648-665.2
072 7 $a MJG $2 bicssc
072 7 $a MED027000 $2 bisacsh
072 7 $a MJG $2 thema
082 0 4 $a 616.4 $2 23
245 1 0 $a Hypoparathyroidism $h [electronic resource] / $c edited by Maria Luisa Brandi, Edward Meigs Brown.
250 $a 1st ed. 2015.
264 1 $a Milano : $b Springer Milan : $b Imprint: Springer, $c 2015.
300 $a XVII, 429 p. 67 illus., 37 illus. in color. $b online resource.
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
347 $a text file $b PDF $2 rda
505 0 $a Preface -- Part I ANATOMY AND PHYSIOLOGY OF THE PARATHYROID GLANDS -- 1 The History: from Fuller Albright to the sequence of Parathyroid Hormone -- 2 Embryology of the parathyroid glands -- 3 PTH and PTH-related peptides -- 4 PTH assays and their clinical significance -- 5 Calcium-control of PTH secretion -- 6 Phosphate control of PTH secretion -- 7 Role of magnesium in Parathyroid Physiology -- 8 The vitamin D/FGF23/PTH axis -- 9 The PTH receptorsome and transduction pathways -- 10 G protein Gsα and GNAS imprinting -- 11 PTH actions on bone and kidney -- 12 PTH and PTHrp: non‐classical target -- 13 In vitro cellular models of parathyroid cells -- II CONDITIONS OF HYPOPARATHYROIDISM -- 14 Epidemiology of hypoparathyropidism -- 15 Clinical Presentation of Hypoparathyroidism -- 16 Isolated, Familial Hypoparathyroidism -- 17 Autoimmune Hypoparathyroidism -- 18 DiGeorge Syndrome (M. Tarsitano) -- 19 Hypoparathyroidism, Deafness and renal dysplasia syndrome -- 20 Hypoparathyroidism, dwarfism, Medullary stenosis of long bones and eye abnormalities (Kenny- Caffey) Syndrome and hypoparathyroidism, retardation and dysmorphism (Sanjad-Sakati) Syndrome -- 21 Hypoparathyroidism in mitochondrial disorders -- 22 Postoperative hypoparathyroidism -- 23 Hypoparathyroidism during pregnancy, lactation, and fetal/neonatal development -- 24 Other forms of acquired hypoparathyroidism (radiation‐induced, infiltrative disorders, heavy‐metal storage disorders, post burn, maternal hyperparathyroidism) -- 25 Refractory hypoparathyroidism -- 26 Bone features in hypoparathyroidism -- 27 Management of acute hypocalcemia -- 28 Conventional Treatment in chronic hypoparathyroidism -- 29 Follow‐up in chronic hypoparathyroidism -- 30 Replacement therapy with PTH1-34 -- 31 Replacement Therapy with PTH1-84 -- III FUNCTIONAL HYPOPARATHYROIDISM -- 32 Classification of pseudohypoparathyroidism and differential diagnosis -- 33 Pseudohypoparathyroidism type Ia, Pseudopseudohypoparathyroidism and Albright Hereditary Osteodystrophy -- 34 Pseudohypoparathyroidisms other than Ia -- 35 Genetic testing in pseudo-hypoparathyroidism -- 36 Blomstrand’s chondrodystrophy -- 37 Hypoparathyroidism during magnesium deficiency or excess -- IV ADVOCATING FOR HYPOPARATHYROIDISM -- 38. Advocating For Hypoparathyroidism.
520 $a Hypoparathyroidism, a condition in which insufficient parathyroid hormone (PTH) is produced to maintain normocalcemia is associated with a variety of acute and chronic symptoms and complications due to hypocalcemia. Replacement therapy utilizing PTH has long been awaited, and this book is new and very timely as it coincides with the publication of results on the role of the PTH molecule in the pharmacological management of this disorder. This advance is sparking renewed interest in hypoparathyroidism, which is attributable to neck surgery in most cases and to inherited disorders in a minority. Hypoparathyroidism has been written by acknowledged experts in the field and provides essential, up-to-date information on the pathology, diagnosis, and treatment of the condition. It opens by addressing in detail the anatomy and physiology of the parathyroids and describing the epidemiology and clinical presentation of hypoparathyroidism. The full range of hypoparathyroid disorders are then discussed, including the various genetic forms, postoperative hypoparathyroidism, and other forms of acquired hypoparathyroidism. Individual chapters focus on refractory disease, the impact of the condition on bone, and the management of acute hypocalcemia. Both conventional treatment for hypoparathyroidism and the novel replacement therapy with PTH peptides are then thoroughly examined. Pseudohypoparathyroidism is also extensively discussed, with information on the various forms, differential diagnosis, and genetic testing. This book will be of interest to all endocrinologists, and also to surgeons and internal medicine physicians. .
650 0 $a Endocrinology . $3 1254221
650 0 $a Surgery. $3 644132
650 0 $a Internal medicine. $3 644638
650 0 $a Human physiology. $3 636012
650 1 4 $a Endocrinology. $3 645497
650 2 4 $a Internal Medicine. $3 668583
650 2 4 $a Human Physiology. $3 668349
700 1 $a Brandi, Maria Luisa. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1066810
700 1 $a Brown, Edward Meigs. $4 edt $4 http://id.loc.gov/vocabulary/relators/edt $3 1066811
710 2 $a SpringerLink (Online service) $3 593884
773 0 $t Springer Nature eBook
776 0 8 $i Printed edition: $z 9788847053779
776 0 8 $i Printed edition: $z 9788847053755
776 0 8 $i Printed edition: $z 9788847058651
856 4 0 $u https://doi.org/10.1007/978-88-470-5376-2
912 $a ZDB-2-SME
912 $a ZDB-2-SXM
950 $a Medicine (SpringerNature-11650)
950 $a Medicine (R0) (SpringerNature-43714)