Congenital heart disease: molecular genetics, principles of diagnosis and treatment ; 43 tables
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Basel [u.a.]
Karger
2015
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| Physical Description: | XIV, 326 S. zahlr. Ill., graph. Darst. |
| ISBN: | 9783318030037 |
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| 245 | 1 | 0 | |a Congenital heart disease |b molecular genetics, principles of diagnosis and treatment ; 43 tables |c ed. Maximilian Muenke ... |
| 264 | 1 | |a Basel [u.a.] |b Karger |c 2015 | |
| 300 | |a XIV, 326 S. |b zahlr. Ill., graph. Darst. | ||
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CONTENTS
XI PREFACE
MUENKE, M.; KRUSZKA, P.S. (BETHESDA, MD.);
SABLE, C.A.
(WASHINGTON, D.C.); BELMONT, J.W. (HOUSTON,TEX.)
XIII FOREWORD
NOONAN, J.A. (LEXINGTON, KY.)
OVERVIEW
2
CONGENITAL CARDIOVASCULAR ANOMALIES:
A HISTORICAL OVERVIEW
MOLLER, J.H. (MINNEAPOLIS, MINN.)
2 ABSTRACT
3 EARLY DESCRIPTIONS OF ANOMALIES
3 CORRELATING ANATOMIC AND CLINICAL FEATURES
4 DIAGNOSTIC PROCEDURES
4 EXTRACARDIAC OPERATIONS
6 INTRACARDIAC OPERATIONS
8 INTERVENTIONAL CATHETERIZATION PROCEDURES
9 OTHER ADVANCES
9 REFERENCES
11 NORMAL DEVELOPMENT OF THE HEART
SYLVA, M.;
MOORMAN, A.F.M. (AMSTERDAM)
11 ABSTRACT
11 FORMATION OF THE LINEAR HEARTTUBE
11 ORIGIN OF THE CARDIAC MESODERM
12 FOLDING OF THE EMBRYO AND FORMATION OF THE HEART
TUBE
12 GROWTH OF THE LINEAR HEARTTUBE
15 FROM ONE TUBE TO FOUR CHAMBERS
15 THE BALLOONING MODEL OF CHAMBER FORMATION
15 FORMATION OF THE ATRIAL CHAMBERS
17 FORMATION OF THE VENTRICULAR CHAMBERS
18 BUILDING THE ECG
18 THE EARLIEST ECG RECORDINGS
18 SINUS NODE
18 ATRIOVENTRICULAR NODE
18 PERIPHERAL VENTRICULAR CONDUCTION SYSTEM
19 SEPTATION
19 ATRIAL SEPTATION
19 VENTRICULAR SEPTATION
19 SEPTATION OF THE ATRIOVENTRICULAR CANAL AND PRIMARY
FORAMEN
21 SEPARATION OF THE OUTFLOW TRACT
21 THE CARDIAC CONNECTIVE TISSUES
21 DEVELOPMENT OF THE CARDIAC VASCULATURE
21 THE INSULATING PLANE
22 DEVELOPMENT OF THE VALVES
22 UNIDIRECTIONAL FLOW IN THE PRIMITIVE HEART
22 THE ATRIOVENTRICULAR VALVES
22 THE SEMILUNAR VALVES
22 REMODELING OF THE EMBRYONIC VALVES
22 FUTURE PERSPECTIVE
24 REFERENCES
2 EPIDEMIOLOGY
28 EPIDEMIOLOGY AND PREVENTION OF
CONGENITAL HEART DEFECTS
BOTTO, L.D. (SALT LAKE CITY, UTAH)
28 ABSTRACT
29 UNDERSTANDING THE PROBLEM
29 COMMON, COSTLY, AND CRITICAL: EPIDEMIOLOGY AS AN
INCENTIVE FOR ACTION
29 HOW COMMON ARE CONGENITAL HEART DEFECTS?
30 WHAT DRIVES THE VARIATIONS IN REPORTED BIRTH
PREVALENCE?
32 HOW MANY PEOPLE ARE LIVING WITH CONGENITAL HEART
DEFECTS - INCLUDING ADULTS?
32 HOW COSTLY ARE CONGENITAL HEART DEFECTS?
33 SHORT-TERM ASSESSMENT: CROSS-SECTIONAL COSTS
HTTP://D-NB.INFO/1070033227
34 LONG-TERM VIEW: LIFETIME COSTS
34 HOW CRITICAL ARE HEART DEFECTS?
34 PREVENTION: EVIDENCE AND STRATEGIES
35 INTEGRATING INTERVENTIONS
35 WHEN TO START PREVENTING?
35 WHAT PROPORTION OF HEART DEFECTS CAN BE
PREVENTED?
36 ESTIMATING HOW MANY CASES CAN BE PREVENTED
37 MAXIMIZING THE IMPACT
38 CASE STUDY: MATERNAL DIABETES
39 CASE STUDY: FOLIC ACID/MULTIVITAMINS
40 PUTTING EVERYTHING TOGETHER: HEALTHY HEART,
HEALTHY CHILD, AND HEALTHY PARENTS
41 EPIDEMIOLOGY AND PREVENTION:TRENDS AND FUTURE
43 CONCLUSIONS
43 REFERENCES
46 CLINICAL EPIDEMIOLOGY AND MANAGEMENT OF
CONGENITAL HEART DEFECTS IN A DEVELOPING
COUNTRY
EKURE, E.N. (LAGOS);
ADEYEMO, A.A. (BETHESDA, MD.)
46 ABSTRACT
47 TYPES OF CONGENITAL HEART DEFECTS SEEN IN NIGERIA
49 ETIOLOGY OF CONGENITAL HEART DEFECTS IN NIGERIA
50 AGE AT DIAGNOSIS
51 CLINICAL PRESENTATION
52 MANAGEMENT OF CONGENITAL HEART DEFECTS IN NIGERIA
54 OUTCOME
54 CHALLENGES AND OPPORTUNITIES
55 REFERENCES
57 MATERNAL NONGENETIC RISK FACTORS FOR
CONGENITAL HEART DEFECTS
RIEHLE-COLARUSSO, TJ. (ATLANTA, GA.);
PATEL, S.S. (AURORA, COLO.)
57 ABSTRACT
58 UNDERSTANDING RISK FACTORS FOR CONGENITAL HEART
DEFECTS
58 MEASUREMENTS OF ASSOCIATIONS FOR RISK FACTORS WITH
CONGENITAL HEART DEFECTS
59 CHALLENGES OF STUDYING RISK FACTORS FOR CONGENITAL
HEART DEFECTS
59 SELECT RISK FACTORS
60 MATERNAL SOCIODEMOGRAPHIC CHARACTERISTICS
60 MATERNAL HEALTH CONDITIONS
65 MATERNAL THERAPEUTIC MEDICATIONS
66 MATERNAL NONTHERAPEUTIC DRUGS
66 CONCLUSION
67 REFERENCES
70 ADULTS WITH CONGENITAL HEART DISEASE
NIWA, K. (TOKYO)
70 ABSTRACT
70 FREQUENCY OF ADULT CONGENITAL HEART DISEASE
71 TREATMENT FACILITIES AND HUMAN RESOURCES
72 CURRENT STATUS AND FUTURE PROSPECTS OF ADULT
CONGENITAL HEART DISEASE
72 COMMON PROBLEMS AND SPECIFIC PATHOPHYSIOLOGICAL
ISSUES IN ADULT CONGENITAL HEART DISEASE
72 CARDIAC FAILURE
73 ARRHYTHMIAS
74 PULMONARY HYPERTENSION
75 PREGNANCY AND DELIVERY
76 PSYCHOSOCIAL ISSUES
76 POSSIBILITY OF ACQUIRED CARDIOVASCULAR DISEASE
77 AORTOPATHY
77 CONCLUSION
78 REFERENCES
^ CHROMOSOMAL DISORDERS
82 DOWN SYNDROME
KRUSZKA, P.S. (BETHESDA, MD.)
82 ABSTRACT
82 EPIDEMIOLOGY
83 GENETICS
84 EMBRYOGENESIS
85 CLINICAL PRESENTATION
85 CARDIAC PHENOTYPE
87 TREATMENT
88 PROGNOSIS
88 GENE THERAPY FOR FUTURE DIRECTIONS
88 REFERENCES
91 CONGENITAL CARDIOVASCULAR DEFECTS IN
MONOSOMY X OR TURNER SYNDROME
BONDY, C. (BETHESDA, MD.)
91 ABSTRACT
92 SPECTRUM OF CONGENITAL CARDIOVASCULAR MALFORMATIONS
IN TURNER SYNDROME
92 AORTIC VALVE
93 AORTIC DILATION
93 AORTIC ARCH
94 PARTIAL ANOMALOUS PULMONARY VENOUS RETURN
94 OTHER CARDIOVASCULAR DEFECTS
94 THEORIES ON THE CAUSE OF CONGENITAL CARDIOVASCULAR
DEFECTS IN TURNER SYNDROME
94 ASSOCIATION WITH FETAL LYMPHEDEMA
95 NEURAL CREST
95 PARALLELS WITH THE 22Q 11.2 DELETION (DIGEORGE
SYNDROME)
96 GENES IMPLICATED IN TURNER SYNDROME
97 X-CHROMOSOME GENOMIC IMPRINTING
97 CONCLUSION
97 REFERENCES
1 OO
THE 22Q
11
.2 DELETION SYNDROME
GOLDMUNTZ, E. (PHILADELPHIA, PA.)
100 ABSTRACT
101 MOLECULAR CHARACTERISTICS OF THE 22Q11.2 DELETION
SYNDROME
101 CLINICAL CHARACTERISTICS OF THE 22Q11.2 DELETION
SYNDROME
101 CONGENITAL HEART DISEASE IN THE 22Q11.2 DELETION
SYNDROME
VI
CONTENTS
103 NONCARDIAC MANIFESTATIONS OF THE 22Q11.2 DELETION
SYNDROME
104 THE 22Q11.2 DELETION SYNDROME AND CONGENITAL HEART
DISEASE
104 22Q11.2 DELETIONS IN CONOTRUNCAL DEFECTS
105 IDENTIFYING THE CARDIAC PATIENT WITH A 22Q 11.2
DELETION
106 CLINICAL OUTCOME
108 CLINICAL MANAGEMENT OF THE CARDIAC PATIENT WITH A
22Q11.2 DELETION
108 REFERENCES
112
OTHER GENOMIC DISORDERS CAUSING
CONGENITAL CARDIOVASCULAR MALFORMATIONS
LALANI, S.R. (HOUSTON,
TEX.)
112 ABSTRACT
114 GENOMIC REARRANGEMENTS
114 COPY NUMBER VARIATIONS IN CONGENITAL CARDIOVASCULAR
MALFORMATIONS
115 1P36 DELETION
115 8P23.1 DELETION/DUPLICATION
115 WILLIAMS-BEUREN SYNDROME
115 KLEEFSTRA SYNDROME
116 SMITH-MAGENIS SYNDROME/POTOCKI-LUPSKI
SYNDROME
116 KOOLEN-DE VRIES SYNDROME
116 WOLF-HIRSCHHORN SYNDROME
117 JACOBSEN SYNDROME
117 OTHER GENOMIC REARRANGEMENTS
117 LESS FREQUENT CVM-ASSOCIATED GENOMIC DISORDERS
118 CONCLUSION
118 REFERENCES
^ SINGLE GENE DISORDERS
122
NOONAN SYNDROME AND OTHER RAS/MAPK
PATHWAY SYNDROMES
GELB, B.D. (NEW YORK,
N.Y.); ROBERTS, A.E.
(BOSTON, MASS.);TARTAGLIA, M. (ROME)
122 ABSTRACT
123 RASOPATHY-ASSOCIATED CARDIOVASCULAR INVOLVEMENT
123 THE NOONAN SYNDROME
125 THE NOONAN SYNDROME WITH MULTIPLE LENTIGINES
125 THE CARDIOFACIOCUTANEOUS SYNDROME
125 THE COSTELLO SYNDROME
126 THE NOONAN SYNDROME WITH LOOSE ANAGEN HAIR
126 RASOPATHY GENETICS
127 GENOTYPE-PHENOTYPE ASSOCIATIONS
127 PATHOGENESIS OF CARDIOVASCULAR DISEASE IN THE
RASOPATHIES
127 THE NOONAN SYNDROME
128 THE NOONAN SYNDROME WITH MULTIPLE LENTIGINES
128 THE COSTELLO SYNDROME
128 CONCLUDING REMARKS
128 ACKNOWLEDGMENTS
128 REFERENCES
131 THE HOLT-ORAM SYNDROME AND OTHER
TRANSCRIPTION FACTOR-RELATED HEART
DISEASES
BORLAK, J. (HANNOVER); CIRIBILLI, Y. (MATTARELLO)
131 ABSTRACT
131 THE HOLT-ORAM SYNDROME
132 TRANSCRIPTION FACTORS AND EMBRYOGENESIS
134 GERMLINE MUTATIONS
136 SOMATIC MUTATIONS
138 GENE REPORTER ASSAYS TO EVALUATE THE CLINICAL
SIGNIFICANCE OF MUTATIONS
139 'ISOGENIC NATURE'
140 'CHROMATIN ENVIRONMENT'
140 'REPORTER CONSTRUCTS'
141 'RHEOSTATABLE PROMOTERS'
141 'MUTANT PROTEIN ASSAYS'
142 CONCLUSION
142 REFERENCES
145 CHARGE SYNDROME
CORSTEN-JANSSEN, N.; VAN RAVENSWAAIJ-ARTS, C.M.A.
(GRONINGEN)
145 ABSTRACT
146 DIAGNOSIS
146 CLINICAL DIAGNOSIS
147 MOLECULAR DIAGNOSIS
148 OTHER CAUSES OF THE CHARGE SYNDROME
149 BROAD PHENOTYPIC SPECTRUM OF CHD7 MUTATIONS
149 CLINICAL FEATURES OF PATIENTS WITH A CHD7 MUTATION
149 CHD7 MUTATIONS IN OTHER SYNDROMES
149 GENOTYPE-PHENOTYPE ASSOCIATIONS
150 HEART DEFECTS IN THE CHARGE SYNDROME
151 CHD7 FUNCTION IN THE HEART
152 CLINICAL SURVEILLANCE AND GENETIC COUNSELING
152 CONCLUDING REMARKS
153 REFERENCES
155 ALAGILLE SYNDROME
LIN, H.C.;
FALSEY, A.; KRANTZ,
I.; SPINNER, N.
(PHILADELPHIA, PA.)
155 ABSTRACT
156 PATHOPHYSIOLOGY
156 CLINICAL FEATURES
157 HEPATIC MANIFESTATIONS
158 CARDIAC MANIFESTATIONS
159 MUSCULOSKELETAL MANIFESTATIONS
159 OCULAR MANIFESTATIONS
160 FACIAL FEATURES
160 RENAL MANIFESTATIONS
161 VASCULAR MANIFESTATIONS
161 COGNITIVE FUNCTION
161 DIAGNOSIS
162 MANAGEMENT
163 GENETIC COUNSELING
163 CONCLUSION
163 REFERENCES
CONTENTS
VII
166 HETEROTAXY
LO, C.;
LI, Y.;
YAGI, H.; GABRIEL,
G.; KLENA,
N.; LEMKE, K.
(PITTSBURGH, PA.); LEATHERBURY, L. (WASHINGTON, D.C.)
166 ABSTRACT
168 CLASSIFICATION OF HETEROTAXY: ATRIAL ISOMERISMS AND
OTHER LATERALITY DEFECTS
169 ASSOCIATION OF COMPLEX CONGENITAL HEART DISEASE WITH
HETEROTAXY
169 LEFT-RIGHT PATTERNING AND REGULATION OF CARDIAC
LOOPING
171 GENETIC ETIOLOGY OF HETEROTAXY
171 CILIOPATHIES AND HETEROTAXY
172 AIRWAY CILIUM DYSFUNCTION ASSOCIATED WITH PRIMARY
CILIARY DYSKINESIA AND HETEROTAXY
172 RESPIRATORY SYMPTOMS AND DISEASE IN CILIOPATHY AND
HETEROTAXY PATIENTS
173 RESPIRATORY COMPLICATIONS AND WORSE OUTCOME IN
HETEROTAXY PATIENTS
173 SUMMARY AND FUTURE PROSPECTS FOR IMPROVING CLINICAL
CARE AND OUTCOME
175 ACKNOWLEDGMENTS
175 REFERENCES
178 MOLECULAR GENETICS OF ISOLATED
CARDIOVASCULAR MALFORMATIONS
LEE,T.M.; CHUNG, W.K. (NEW YORK,
N.Y.)
178 ABSTRACT
179 MONOGENIC CARDIOVASCULAR MALFORMATIONS
179 ATRIAL SEPTAL DEFECTS
181 VENTRICULAR SEPTAL DEFECTS
181 BICUSPID AORTIC VALVES
181 SUPRAVALVAR AORTIC STENOSES
181 ADDITIONAL LESIONS
182 RECENT ADVANCES
182 COPY NUMBER VARIANTS
182 DE NOVO VARIANTS
182 GENOME-WIDE ASSOCIATION STUDIES
182 CLINICAL GENETIC EVALUATION AND TESTING
183 CONCLUSION
183 REFERENCES
186 OTHER SINGLE-GENE DISORDERS CAUSING
CONGENITAL HEART DISEASE
RUSSELL, M.W.;
HANNIBAL, M. (ANN ARBOR, MICH.)
186 ABSTRACT
186 VACTERL ASSOCIATION
187 DIAGNOSIS/EVALUATION
187 THE KABUKI SYNDROME
188 DIAGNOSIS/EVALUATION
188 THE ELLIS-VAN CREVELD SYNDROME
189 DIAGNOSIS/EVALUATION
189 THE CORNELIA DE LANGE SYNDROME
190 DIAGNOSIS/EVALUATION
190 THE MOWAT-WILSON SYNDROME
190 DIAGNOSIS/EVALUATION
190 THE SMITH-LEMLI-OPITZ SYNDROME
191 DIAGNOSIS/EVALUATION
191 TREATMENT
191 THE RUBINSTEIN-TAYBI SYNDROME
192 DIAGNOSIS/EVALUATION
192 THE CHAR SYNDROME
193 DIAGNOSIS/EVALUATION
193 THE GOLDENHAR SYNDROME
193 DIAGNOSIS/EVALUATION
193 CONCLUSION
193 ACKNOWLEDGMENTS
194 REFERENCES
5
ARRHYTHMIAS, CARDIOMYPATHIES, AND
CONNECTIVE TISSUE DISORDERS
198 GENETIC ARRHYTHMIAS (CHANNELOPATHIES)
MAZZANTI, A.; NG, K. (PAVIA); PRIORI,
S.G.
(PAVIA/NEW YORK, N.Y.)
198 ABSTRACT
199 LONG QT SYNDROME
199 EPIDEMIOLOGY
199 GENETIC VARIANTS
199 DIAGNOSIS
201 CLINICAL MANIFESTATIONS
201 RISK STRATIFICATION
202 MANAGEMENT
202 SHORT QT SYNDROME
202 EPIDEMIOLOGY
202 GENETIC VARIANTS
203 DIAGNOSIS
203 CLINICAL MANIFESTATIONS
203 RISK STRATIFICATIONS AND MANAGEMENT
204 BRUGADA SYNDROME
204 EPIDEMIOLOGY
204 GENETIC VARIANTS
204 DIAGNOSIS
204 CLINICAL MANIFESTATIONS
205 RISK STRATIFICATION
205 MANAGEMENT
206 CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR
TACHYCARDIA
206 EPIDEMIOLOGY
206 GENETIC VARIANTS
206 DIAGNOSIS
207 CLINICAL MANIFESTATIONS
207 RISK STRATIFICATIONS
207 MANAGEMENT
208 CONCLUSIONS
208 REFERENCES
210 GENETIC CARDIOMYOPATHIES
TOWBIN, J.A. (MEMPHIS,TENN.)
210 ABSTRACT
211 FINAL COMMON PATHWAYS
211 DILATED CARDIOMYOPATHY
212 GENETICS OF DILATED CARDIOMYOPATHY
216 MUSCLE IS MUSCLE: CARDIOMYOPATHY AND SKELETAL
MYOPATHY GENES OVERLAP
216 HYPERTROPHIC CARDIOMYOPATHY
VIII
CONTENTS
216 GENE IDENTIFICATION IN FAMILIAL HYPERTROPHIC
CARDIOMYOPATHY
217 GENOTYPE-PHENOTYPE CORRELATION IN HYPERTROPHIC
CARDIOMYOPATHY
218 RESTRICTIVE CARDIOMYOPATHY
218 GENETICS
218 LEFT-VENTRICULAR NONCOMPACTION CARDIOMYOPATHY
219 GENETICS
220 ARRHYTHMOGENIC CARDIOMYOPATHIES
220 GENETICS
222 CONCLUSIONS
222 REFERENCES
226 CONGENITAL THORACIC AORTIC ANEURYSM
LINDSAY, M.E.
(BOSTON, MASS.);
DIETZ, H.C. (BALTIMORE, MD.)
226 ABSTRACT
227 GENE DISCOVERY
229 INHERITANCE AND GENETIC COUNSELING
230 CLINICAL FINDINGS AND DIAGNOSES
232 MANAGEMENT AND MOLECULAR PATHOGENESIS
233 CONCLUSIONS
234 REFERENCES
^ EVALUATION
238 THE GENETIC WORKUP FOR CONGENITAL
STRUCTURAL HEART DISEASE: FROM CLINICAL TO
GENETIC EVALUATION
KRUSZKA, P.S. (BETHESDA,
MD.); SABLE, C.A.
(WASHINGTON, D.C.); BELMONT, J.W. (HOUSTON,
TEX.);
MUENKE, M. (BETHESDA, MD.)
238 ABSTRACT
240 GENETIC TESTING ALGORITHM
248 ANEUPLOIDY
248 COPY NUMBER AND STRUCTURAL VARIANTS
250 TARGETED GENE SEQUENCING
252 WHOLE GENOME AND WHOLE EXOME SEQUENCING
254 GENETIC COUNSELING
254 CONCLUDING REMARKS
254 REFERENCES
257 IMAGING OF CONGENITAL HEART DEFECTS FOR
THE NONCARDIOLOGIST
SABLE, C.A.
(WASHINGTON, D.C.)
257 ABSTRACT
257 TYPES OF IMAGING
257 ULTRASOUND PHYSICS
259 ECHOCARDIOGRAPHY EXAMINATION
260 ECHOCARDIOGRAPHY LOGISTICS: WHY, WHEN, WHERE, WHO
260 , INDICATIONS
260 TIMING OF IMAGING
260 WHERE/WHO DOES THE ECHOCARDIOGRAPHY
261 COMMON LESIONS
261 ATRIAL SEPTAL DEFECTS
262 VENTRICULAR SEPTAL DEFECTS
264 ATRIOVENTRICULAR SEPTAL DEFECTS
265 TETRALOGY OF FALLOT
266 PULMONARY VALVE STENOSIS
267 CONCLUDING REMARKS
268 REFERENCES
269 PRENATAL EVALUATION OF CONGENITAL HEART
DEFECTS AND FETAL INTERVENTION
WEINBERG, J.G.;
KRISHNAN, A. (WASHINGTON, D.C.)
269 ABSTRACT
269 INDICATIONS FOR FETAL CARDIAC EVALUATION
270 TIMING AND PERFORMANCE OF FETAL ECHOCARDIOGRAPHY
271 PRENATAL DIAGNOSIS OF CONGENITAL HEART DEFECTS
ASSOCIATED WITH SPECIFIC GENETIC DEFECTS
271 FETAL INTERVENTION
275 IMPORTANCE OF FETAL DIAGNOSIS AND OUTCOMES FOLLOW
ING PRENATAL DETECTION OF CONGENITAL HEART DEFECTS
276 REFERENCES
^ TREATMENT
280 SURGICAL MANAGEMENT
COSTELLO, J.P.; JONAS,
R.A.; NATH, D.S.
(WASHINGTON, D.C.)
280 ABSTRACT
280 TRISOMY 21 - DOWN SYNDROME
283 THE 22Q 11.2 DELETION - DIGEORGE SYNDROME
284 TRISOMY 13 (PATAU SYNDROME) AND TRISOMY 18
(EDWARDS SYNDROME)
285 MARFAN SYNDROME
285 TURNER SYNDROME
285 NOONAN SYNDROME
286 OTHER SYNDROMES
286 SPECIAL CONSIDERATIONS
287 REFERENCES
289 INTERVENTIONAL CARDIOLOGY
MORGAN, G.J.; QURESHI, S.A.
(LONDON)
289 ABSTRACT
289 INTERVENTIONAL CARDIAC CATHETERISATION IN PAEDIATRIC
CARDIOLOGY
289 NEONATAL INTERVENTION
290 ATRIAL SEPTOSTOMY
290 AORTIC VALVOPLASTY
291 PULMONARY VALVOPLASTY
292 INFANT AND PAEDIATRIC PROCEDURES
292 ATRIAL SEPTAL DEFECT OCCLUSION
293 VENTRICULAR SEPTAL DEFECT OCCLUSION
294 TRANSCATHETER PULMONARY VALVE IMPLANTATION
294 COARCTATION STENT IMPLANTATION
295 STENT TECHNOLOGY
295 FETAL INTERVENTIONS
295 HYBRID TECHNIQUES
296 HYBRID PALLIATION OF HYPOPLASTIC LEFT HEART DISEASE
296 MUSCULAR VENTRICULAR SEPTAL DEFECT CLOSURE
297 PARAVALVAR LEAK OCCLUSION
CONTENTS
IX
297 CONCLUSION
297 REFERENCES
298 ETHICAL CONSIDERATIONS IN CONGENITAL HEART
DISEASE
BOSS, R.D.; SHAPIRO,
M.C. (BALTIMORE, MD.)
298 ABSTRACT
299 SOCIAL JUSTICE AND CONGENITAL HEART DISEASE RISK
299 PRENATAL DIAGNOSIS: PROMISES AND HARMS
300 A LIFE WORTH LIVING-CAN WE AGREE?
301 SURVIVORS OF CONGENITAL HEART DISEASE AND DEMAND FOR
DESTINATION THERAPIES
302 PALLIATIVE CARE - CLINICIANS' PERSONAL CHOICES VERSUS
PROFESSIONAL RECOMMENDATIONS
303 CONCLUSIONS
303 REFERENCES
306 THE FUTURE OF THERAPEUTICS: STEM CELLS,
TISSUE PLASTICITY, AND TISSUE ENGINEERING
TAO, G.; MARTIN,
J.F. (HOUSTON,TEX.)
306 ABSTRACT
306 CARDIAC TISSUE ENGINEERING
307 SUPPORTIVE MATRIX IN FAVOR OF TISSUE FORMATION
307 TISSUE-FORMING CELL POPULATION
308 MECHANICAL LOAD AND ELECTRICAL STIMULATION
308 BIOREACTORS - A BREEDING GROUND FOR ENGINEERED HEART
TISSUE
309 CURRENT CHALLENGES FOR ENGINEERED HEART TISSUE
PRODUCTION
309 CARDIOMYOCYTE MATURATION
310 HOST IMMUNE RESPONSE
310 ISCHEMIA WITHIN ENGINEERED HEART TISSUE
310 DECELLULARIZED HEART AS AN ARTIFICIAL SCAFFOLD FOR
ENGINEERED HEART TISSUE
311 STEM CELLS IN ENGINEERED HEART TISSUE
312 REENTRY OF MATURE CARDIOMYOCYTES INTO THE CELL CYCLE
313 NOVEL POSSIBILITIES FORTREATING HYPERTROPHIC
CARDIOMYOPATHY
313 GENE THERAPY AS EARLY INTERVENING STRATEGIES
314 PERSPECTIVES
314 REFERENCES
317 AUTHOR INDEX
318 SUBJECT INDEX
X
CONTENTS |
| any_adam_object | 1 |
| author_GND | (DE-588)1292270918 |
| building | Verbundindex |
| bvnumber | BV042684193 |
| ctrlnum | (OCoLC)913016946 (DE-599)DNB1070033227 |
| dewey-full | 618.9212043 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 618 - Gynecology, obstetrics, pediatrics, geriatrics |
| dewey-raw | 618.9212043 |
| dewey-search | 618.9212043 |
| dewey-sort | 3618.9212043 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| format | Book |
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| genre | (DE-588)4143413-4 Aufsatzsammlung gnd-content |
| genre_facet | Aufsatzsammlung |
| id | DE-604.BV042684193 |
| illustrated | Illustrated |
| indexdate | 2024-07-20T06:02:57Z |
| institution | BVB |
| isbn | 9783318030037 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-028115999 |
| oclc_num | 913016946 |
| open_access_boolean | |
| owner | DE-12 DE-19 DE-BY-UBM |
| owner_facet | DE-12 DE-19 DE-BY-UBM |
| physical | XIV, 326 S. zahlr. Ill., graph. Darst. |
| publishDate | 2015 |
| publishDateSearch | 2015 |
| publishDateSort | 2015 |
| publisher | Karger |
| record_format | marc |
| spelling | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables ed. Maximilian Muenke ... Basel [u.a.] Karger 2015 XIV, 326 S. zahlr. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Literaturangaben Angeborene Krankheit (DE-588)4331107-6 gnd rswk-swf Herzkrankheit (DE-588)4024663-2 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content Herzkrankheit (DE-588)4024663-2 s Angeborene Krankheit (DE-588)4331107-6 s DE-604 Muenke, Maximilian Sonstige (DE-588)1292270918 oth Erscheint auch als Online-Ausgabe 978-3-318-03004-4 DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=028115999&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables Angeborene Krankheit (DE-588)4331107-6 gnd Herzkrankheit (DE-588)4024663-2 gnd |
| subject_GND | (DE-588)4331107-6 (DE-588)4024663-2 (DE-588)4143413-4 |
| title | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables |
| title_auth | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables |
| title_exact_search | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables |
| title_full | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables ed. Maximilian Muenke ... |
| title_fullStr | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables ed. Maximilian Muenke ... |
| title_full_unstemmed | Congenital heart disease molecular genetics, principles of diagnosis and treatment ; 43 tables ed. Maximilian Muenke ... |
| title_short | Congenital heart disease |
| title_sort | congenital heart disease molecular genetics principles of diagnosis and treatment 43 tables |
| title_sub | molecular genetics, principles of diagnosis and treatment ; 43 tables |
| topic | Angeborene Krankheit (DE-588)4331107-6 gnd Herzkrankheit (DE-588)4024663-2 gnd |
| topic_facet | Angeborene Krankheit Herzkrankheit Aufsatzsammlung |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=028115999&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT muenkemaximilian congenitalheartdiseasemoleculargeneticsprinciplesofdiagnosisandtreatment43tables |