Aneurysms-osteoarthritis syndrome : SMAD3 gene mutations created by Denise van der Linde, Bart L. Loeys and Jolien W. Roos-Hesselink

By:

Linde, Denise van der [author, MD, MSc, PhD, Department of Cardiology, Erasmus University Medical Center, Rotterdam, The Netherlands]

Contributor(s):

Loeys, Bart L [author - MD, PhD, Center of Medical Genetics, Antiwerp University Hospital, Antiwerp, Belgium; and the Department of Human Genetics, Radboud University Medical Center Nijmegen, The Netherlands]
Roos-Hesselink, Jolien W [author, MD, PhD, Department of Cardiology, Erasmus University Medical Center, Rotterdam, The Netherlands]

Material type: Text

TextLanguage: English Publication details: Amsterdam Elsevier/Academic Press 2017Description: 163 pages col. ill. 23 cmISBN:

9780128027080 (pbk)

Subject(s):

LOC classification:

RC693 LIN

Contents:

1. Genetics (the discovery, broadened to include aspects as genotype/phenotype correlations, functional role of SMAD3, insights into the role of TGFbeta signaling in aortic disease) 2. Cardiovascular phenotype 3. Systemic features (skeletal, joints, auto-immune, craniofacial features) 4. Differential diagnosis heritable thoracic aortic diseases 5a. Marfan 5b. Loeys-Dietz 5c. Ehlers-Danlos 5d. Bicuspid aortic valve 5e. Turner Syndrome 6. Cardiovascular imaging 7. Treatment options 7a. Optimal cardiovascular medical treatment (Losartan etc.) 7b. Cardiothoracic surgical experience 7c. Vascular interventions and surgical experience 7d. Orthopedic treatment options 7e. Genetic counseling 7f. Approach to clinical management (including proposed clinical follow-up chart)

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Holdings
Item type	Current library	Call number	Copy number	Status	Barcode
Book	Medical School Open Shelf	RC693 LIN (Browse shelf(Opens below))	147400	Available	BK133972
Book	Medical School Open Shelf	RC693 LIN (Browse shelf(Opens below))	148262	Available	BK135100
Book	Medical School Open Shelf	RC693 LIN (Browse shelf(Opens below))	147372	Available	BK133862

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Previous	RC687 PER Perloff's clinical recognition of congenital heart disease	RC691.6.A53 IMA Image-guided interventions /	RC691.6.I52 HUT Aortic diseases:	RC693 LIN Aneurysms-osteoarthritis syndrome : SMAD3 gene mutations	RC693 LIN Aneurysms-osteoarthritis syndrome : SMAD3 gene mutations	RC693 LIN Aneurysms-osteoarthritis syndrome : SMAD3 gene mutations	RC694.3 BRI Manual of chronic total occlusion interventions : a step by step approach /	Next

Includes bibliographical references and index

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