000 03707nam a22004575i 4500
999 _c120811
_d120811
_x1
001 120811
003 ES-MaUEC
005 20230102114101.0
006 a||||fo|||| 00| 0
007 cr nn nnnaamaa
008 200521s2020 gw | s |||| 0|eng d
020 _a9783030423827
024 7 _a10.1007/978-3-030-42382-7
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aRC858.C95
_b2020 EB
245 0 0 _aCystic Fibrosis :
_bA Multi-Organ System Approach
_cedited by Stephanie Duggins Davis, Margaret Rosenfeld, James Chmiel
250 _a1st ed. 2020.
264 1 _aCham
_bSpringer International Publishing :
_bImprint: Humana
_c2020
300 _a1 recurso en línea (XVII, 526 páginas)
_b36 ilustraciones, 26 ilustraciones a color
336 _2rdacontent
_aTexto
_btxt
337 _2rdamedia
_aelectrónico
_bc
338 _2rdacarrier
_arecurso electrónico
_bcr
347 _atext file
_bPDF
_2rda
490 0 _aRespiratory Medicine,
_x2197-7372
490 0 _aMedicine (Springer-11650)
505 0 _aThe Changing Face of CF -- Diagnosing cystic fibrosis -- SECTION I: Pulmonary Manifestations -- Early lung disease -- Pulmonary complications as an adult -- Treating respiratory complications -- Transplant -- SECTION II: Gastrointestinal Manifestations -- Liver disease -- Pancreatic insufficiency and nutritional complications -- SECTION III: Endocrine Manifestations -- Diabetes -- Bone Disease. SECTION IV: Further Comorbidities -- Rheumatologic Manifestations -- Reproductive Issues -- The Impact of CF on the Kidney -- Mental Health.
520 3 _aThis book provides a comprehensive overview of the multisystem disease, cystic fibrosis, for both pediatric and adult patients. Written by experts in the field, the text outlines the progressive nature of CF as well as the impact of this autosomal recessive disease on the respiratory, gastrointestinal, endocrine, rheumatologic, and renal systems, as well as the patient's mental health. The book begins with a chapter describing the history of cystic fibrosis and how the face of this life-shortening disease has changed over the past several decades. The following chapters elucidate the pathophysiology of how cystic fibrosis impacts each organ system. Current management and therapeutics are detailed with step-by-step guidelines for clinicians. This book is unique in that it highlights the entire person, not just the respiratory system, with detailed inclusion of the patient perspectives throughout, informing practice standards and considerations. This is an ideal guide for pediatric and adult physicians who care for patients with cystic fibrosis, as well as respiratory therapists, physical therapists, nurses, nutritionists, and pharmacists who care for these patients.
988 _aSpringer_Medicine_2020
650 7 _2embne
_aFibrosis quística
_9146917
700 1 _aDavis, Stephanie Duggins.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
700 1 _aRosenfeld, Margaret.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
700 1 _aChmiel, James.
_eeditor.
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
710 2 _aSpringerLink (Online service)
_0http://id.loc.gov/authorities/names/no2005046756
_1http://viaf.org/viaf/148105729
776 0 8 _iPrinted edition:
_z9783030423810
776 0 8 _iPrinted edition:
_z9783030423834
776 0 8 _iPrinted edition:
_z9783030423841
830 0 _aRespiratory Medicine,
_x2197-7372
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-030-42382-7
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b09/2020
_dz
_eIG
_zSI