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020 _a9783030874841
024 7 _a10.1007/978-3-030-87484-1
_2doi
040 _aTR-AnTOB
_beng
_erda
_cTR-AnTOB
041 _aeng
060 _aWS 21
072 7 _aMJ
_2bicssc
072 7 _aMED045000
_2bisacsh
072 7 _aMJ
_2thema
096 _aWS21EBK
100 1 _aBaird, John Scott.
_eauthor.
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
245 1 0 _aDorothy Hansine Andersen
_h[electronic resource] :
_bThe Life and Times of the Pioneering Physician-Scientist Who Identified Cystic Fibrosis /
_cby John Scott Baird.
250 _a1st ed. 2022.
264 1 _aCham :
_bSpringer International Publishing :
_bImprint: Springer,
_c2022.
300 _a1 online resource
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
505 0 _aPart I: Life before Babies Hospital -- Chapter 1: A beginning -- Chapter 2: Orphaned -- Chapter 3: College and medical school -- Chapter 4: False start -- Chapter 5: A reboot -- Part II: Babies Hospital during the McIntosh Era -- Chapter 6: Historical perspectives -- Chapter 7: Synergy -- Chapter 8: Andy’s abandoned farm -- Chapter 9: Scoring the first goal -- Chapter 10: CF firsts -- Chapter 11: “To Dr. Andersen who has pulled me through many a tough year” -- Chapter 12: McIntosh, pediatric pathology, and Columbia University.-Chapter 13: CF sweat and the Matilda Effect -- Chapter 14: Glycogen storage diseases -- Chapter 15: Celiac disease -- Chapter 16: Randomized, controlled trials -- Chapter 17: Babies Hospital siblings -- Chapter 18: A last decade of CF research -- Chapter 19: Pediatric heart diseases -- Part III: Beyond Babies Hospital and the McIntosh Era -- Chapter 20: Time to enjoy the view -- Chapter 21: A foundation and a club for CF -- Chapter 22: The end of an era -- Chapter 23: Cancer.
520 _aThis book chronicles the life and accomplishments of Dorothy Hansine Andersen, a pioneering American pathologist and pediatrician who was the first person to define, diagnose, and treat cystic fibrosis. Divided into three parts, the book begins by detailing Anderson’s early life, including being orphaned as an adolescent, her college career, and her laborious start in the medical field. Part II then examines Andersen’s role in defining the new disease “cystic fibrosis of the pancreas” and her career of active engagement in various clinical pursuits and research, both in pathology and pediatrics. Chapters in this section also discuss the numerous attempts made by others to minimize Andersen’s work through gender bias and the Matilda Effect. The book concludes by reviewing the foundations laid for CF, Andersen’s legacy, and her terminal illness. Featuring an engaging narrative style, Dorothy Hansine Andersen is a historically relevant, invaluable text for anyone interested in the life of Dorothy Anderson and the nascence of cystic fibrosis diagnoses.
650 0 _aInternal medicine.
650 0 _aPediatrics.
650 1 4 _aInternal Medicine.
650 2 4 _aPediatrics.
653 1 _aAndersen, Dorothy H (Dorothy Hansine), 1901-1963
653 0 _aPediatricians
653 6 _aBiography
653 6 _aHistory
710 2 _aSpringerLink (Online service)
856 4 0 _uhttps://doi.org/10.1007/978-3-030-87484-1
_3Springer eBooks
_zOnline access link to the resource
942 _2NLM
_cEBK