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020 _a9783030874841
024 7 _a10.1007/978-3-030-87484-1
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aRJ43.A53
_b2022 EB
100 1 _aBaird, John Scott
_eautor
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
_9685962
245 1 0 _aDorothy Hansine Andersen :
_bThe Life and Times of the Pioneering Physician-Scientist Who Identified Cystic Fibrosis
_cby John Scott Baird
250 _a1st edition 2022
264 1 _aCham
_bSpringer International Publishing
_c2022
300 _a1 recurso en línea (XIV, 198 páginas)
_b28 ilustraciones, 9 ilustraciones a color
336 _atexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
347 _aarchivo de texto
_bPDF
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.
988 _aSpringer_Medicine_2022
600 1 0 _9685963
_aAndersen, Dorothy H.
_q(Dorothy Hansine)
_d1901-1963
650 7 _2embne
_9684892
_aPediatras
_zEstados Unidos
650 7 _2embne
_9146917
_aFibrosis quística
655 7 _2tgfbne
_9684296
_aBiografías
776 0 8 _iPrinted edition:
_z9783030874834
776 0 8 _iPrinted edition:
_z9783030874858
776 0 8 _iPrinted edition:
_z9783030874865
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-030-87484-1
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b01/2023
_dz
_eb
_zSI