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20231120112226.0 |
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170425s2017 enk ob 001 0 eng d |
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|a 984561635
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|z 0128114835
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|a (OCoLC)984236594
|z (OCoLC)984561635
|z (OCoLC)993989866
|z (OCoLC)1011199780
|z (OCoLC)1024278127
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|z (OCoLC)1105170694
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|a MED
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|2 bisacsh
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0 |
4 |
|a 618.9245
|2 23
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| 100 |
1 |
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|a Hindmarsh, P. C.
|q (Peter C.)
|
| 245 |
1 |
0 |
|a Congential adrenal hyperplasia :
|b a comprehensive guide /
|c Peter C. Hindmarsh, Kathy Geertsma.
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| 260 |
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|a London :
|b Academic Press,
|c 2017.
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| 300 |
|
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|a 1 online resource
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| 336 |
|
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
|
| 338 |
|
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|a online resource
|b cr
|2 rdacarrier
|
| 505 |
0 |
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|6 880-01
|a Cover; Title page; Copyright page; Contents; Review; Personal Story; A Medical View; Introduction; Section One -- Congenital Adrenal Hyperplasia-Introduction; Chapter 1 -- Physiology of the Adrenal Glands: How Does It Work?; Glossary; Introduction; The hypothalamus and pituitary gland; What are steroids?; Regulation of cortisol release; The circadian rhythm of cortisol-the natural production of cortisol; Renin-angiotensin system; Adrenal androgens; The backdoor pathway for adrenal androgen formation; Conclusions; Further reading; Chapter 2 -- How Males and Females Develop; Glossary; General.
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| 505 |
8 |
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|a Genes making males or femalesExternal appearances-the role of male hormones; Assessing these changes; Further reading; Chapter 3 -- Genetics of Congenital Adrenal Hyperplasia; Glossary; General; Understanding the genetics of congenital adrenal hyperplasia; Antenatal diagnosis and treatment; Further reading; Chapter 4 -- Common Forms of Congenital Adrenal Hyperplasia; Glossary; General; CLASSICAL CAH -- 21-Hydroxylase deficiency or CYP21 deficiency; Salt-wasting Congenital Adrenal Hyperplasia (SWCAH); Classical CAH-Salt-wasting Congenital Adrenal Hyperplasia (SWCAH): Summary.
|
| 505 |
8 |
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|a Simple Virilising Congenital Adreanl Hyperplasia (SVCAH)Simple Virilising Congenital Adrenal Hyperplasia: Summary; Non-Classical Congenital Adrenal Hyperplasia (NCCAH) also known as Late-Onset Congenital Adrenal Hyperplasia (LOCAH); Non-Classical Congenital Adrenal Hyperplasia: Summary; 11-Hydroxylase or CYP11B1 deficiency; 11-Hydroxylase (CYP11B1) Deficiency: Classical summary; 11-Hydroxylase (CYP11B1) Deficiency: Non-classical summary; Further reading; Chapter 5 -- Other Blocks in the Pathway Causing Congenital Adrenal Hyperplasia; Glossary; General.
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| 505 |
8 |
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|a When should the first bone age X-ray be taken?Conclusions; Further reading; Chapter 7 -- Puberty; Glossary; General; Hormonal control of puberty; How we measure the stages of puberty; Sex steroid production; Order of puberty; What happens in CAH when the adrenals make too many adrenal androgens; Symptoms and signs of precocious puberty; Both genders; Boys; Girls; Conclusions; Further reading; Chapter 8 -- Biochemical Tests Used for Diagnosis; Glossary; General; Blood measurements; Urine samples; Saliva sampling; Stimulation tests; Genetic confirmation of the diagnosis.
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| 504 |
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|a Includes bibliographical references and index.
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| 650 |
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0 |
|a Adrenogenital syndrome.
|
| 650 |
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0 |
|a Hydrocortisone.
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| 650 |
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2 |
|a Adrenal Hyperplasia, Congenital
|0 (DNLM)D000312
|
| 650 |
|
2 |
|a Hydrocortisone
|0 (DNLM)D006854
|
| 650 |
|
4 |
|a Adrenal Hyperplasia, Congenital.
|
| 650 |
|
4 |
|a Adrenogenital syndrome.
|
| 650 |
|
4 |
|a Hydrocortisone.
|
| 650 |
|
6 |
|a Syndrome g�enito-surr�enal.
|0 (CaQQLa)201-0077272
|
| 650 |
|
6 |
|a Hydrocortisone.
|0 (CaQQLa)201-0023811
|
| 650 |
|
7 |
|a MEDICAL
|x Gynecology & Obstetrics.
|2 bisacsh
|
| 650 |
|
7 |
|a Adrenogenital syndrome
|2 fast
|0 (OCoLC)fst00797178
|
| 650 |
|
7 |
|a Hydrocortisone
|2 fast
|0 (OCoLC)fst00964880
|
| 655 |
|
0 |
|a Electronic books.
|
| 655 |
|
4 |
|a Internet Resources.
|
| 655 |
|
4 |
|a Charts.
|
| 700 |
1 |
|
|a Geertsma, Kathy.
|
| 776 |
0 |
8 |
|i Print version:
|z 0128114835
|z 9780128114834
|w (OCoLC)960895745
|
| 856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128114834
|z Texto completo
|
| 880 |
8 |
|
|6 505-01/(S
|a 17α-Hydroxylase/17, 20-lyase (P450C17) or CYP17 deficiency3BETA-Hydroxysteroid dehydrogenase type-2 (3β-HSD 2) deficiency; 3Beta-hydroxysteroid dehydrogenase type-2: Summary; Congenital lipoid adrenal hyperplasia (lipoid CAH) (StAR deficiency); StAR Deficiency: Summary; Most severe form of CAH; Milder form; P450 oxidoreductase deficiency; P450 Oxidoreductase Deficiency: Summary; Further reading; Chapter 6 -- Growth; Glossary; General; The process; Growth; How to estimate genetic height potential; Growth in childhood; Growth in puberty; Weight; Body mass index; Bone age; How bone age is done.
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