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Connective tissue and it heritable disorders [[electronic resource] ] : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Connective tissue and it heritable disorders [[electronic resource] ] : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Wiley-Liss, c2002
Descrizione fisica 1 online resource (1221 p.)
Disciplina 616.77042
Altri autori (Persone) RoycePeter M
SteinmannBeat U
Soggetto topico Connective tissues - Diseases - Genetic aspects
Connective tissues - Diseases - Molecular aspects
Soggetto genere / forma Electronic books.
ISBN 1-280-36667-2
9786610366675
0-470-35006-7
0-471-46117-2
0-471-22192-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CONNECTIVE TISSUE AND ITS HERITABLE DISORDERS SECOND EDITION; Contents; Preface; Acknowledgments; Preface to the First Edition; Contributors; Introduction Research on Collagen in the Author's Laboratory, 1952-1982; Introduction Heritable Disorders of Connective Tissue: A Personal Account of the Origins, Evolution, Validation, and Expansion of a Concept; BIOLOGY OF EXTRACELLULAR MATRIX; Chapter 1 Morphology and Chemical Composition of Connective Tissue; Part I Structure of the Skin and Tendon; Part II Cartilage; Part III Bone; Part IV The Cardiovascular System; Part V The Eye
Chapter 2 CollagenPart I The Collagen Family: Structure, Assembly, and Organization in the Extracellular Matrix; Part II Gene Structure; Chapter 3 Elastin and the Microfibrillar Apparatus; Chapter 4 Glycosylated Matrix Proteins; Chapter 5 Adhesive Glycoproteins; Chapter 6 Keratins; Chapter 7 Extracellular Matrix Degradation; HERITABLE DISORDERS OF CONNECTIVE TISSUE; Chapter 8 Osteogenesis Imperfecta; Chapter 9 The Ehlers-Danlos Syndrome; Chapter 10 Cutis Laxa and Premature Aging Syndromes; Chapter 11 Pseudoxanthoma Elasticum; Chapter 12 The Marfan Syndrome and Other Microfibrillar Disorders
Chapter 13 The HomocystinuriasChapter 14 Menkes Disease and the Occipital Horn Syndrome; Chapter 15 Epidermolysis Bullosa; Chapter 16 Prolidase Deficiency; Chapter 17 a(1)-Antitrypsin Deficiency; Chapter 18 Heritable Forms of Rickets and Osteomalacia; Chapter 19 Osteopetrosis; Chapter 20 Alkaptonuria; Chapter 21 Fibrodysplasia Ossificans Progressiva; Chapter 22 Disorders of Lysosomal Enzymes; Part I General Considerations; Part II Clinical Phenotypes; Chapter 23 Skeletal Dysplasias; Part I Chondrodysplasias: General Concepts and Diagnostic and Management Considerations
Part II Chondrodysplasias: Disorders of Cartilage Matrix ProteinsPart III Skeletal Dysplasias Related to Defects in Sulfate Metabolism; Part IV Craniosynostosis Syndromes and Skeletal Dysplasias Caused by Mutations in Fibroblast Growth Factor Receptor Genes; Part V Defects in Skeletal Morphogenesis; Chapter 24 Disorders of Keratinization; Chapter 25 Alport Syndrome; Chapter 26 Miscellaneous Disorders; Part I Corneal Dystrophies Due to Mutations in the Kerato-Epithelin Gene (big-h3); Part II Progressive Pseudorheumatoid Dysplasia
Part III The Camptodactyly-Arthropathy-Coxa Vara-Pericarditis SyndromePart IV Bruck Syndrome; Part V Osteoporosis-Pseudoglioma Syndrome; Part VI Myopathies Due to Defects in Collagen VI; Part VII Knobloch Syndrome; Appendix I International Nomenclature of Constitutional Disorders of Bone: Osteochondrodysplasias; Appendix II Extracellular Collagen Metabolites in Body Fluids; Index
Record Nr. UNINA-9910143216403321
New York, : Wiley-Liss, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Connective tissue and it heritable disorders [[electronic resource] ] : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Connective tissue and it heritable disorders [[electronic resource] ] : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Wiley-Liss, c2002
Descrizione fisica 1 online resource (1221 p.)
Disciplina 616.77042
Altri autori (Persone) RoycePeter M
SteinmannBeat U
Soggetto topico Connective tissues - Diseases - Genetic aspects
Connective tissues - Diseases - Molecular aspects
ISBN 1-280-36667-2
9786610366675
0-470-35006-7
0-471-46117-2
0-471-22192-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CONNECTIVE TISSUE AND ITS HERITABLE DISORDERS SECOND EDITION; Contents; Preface; Acknowledgments; Preface to the First Edition; Contributors; Introduction Research on Collagen in the Author's Laboratory, 1952-1982; Introduction Heritable Disorders of Connective Tissue: A Personal Account of the Origins, Evolution, Validation, and Expansion of a Concept; BIOLOGY OF EXTRACELLULAR MATRIX; Chapter 1 Morphology and Chemical Composition of Connective Tissue; Part I Structure of the Skin and Tendon; Part II Cartilage; Part III Bone; Part IV The Cardiovascular System; Part V The Eye
Chapter 2 CollagenPart I The Collagen Family: Structure, Assembly, and Organization in the Extracellular Matrix; Part II Gene Structure; Chapter 3 Elastin and the Microfibrillar Apparatus; Chapter 4 Glycosylated Matrix Proteins; Chapter 5 Adhesive Glycoproteins; Chapter 6 Keratins; Chapter 7 Extracellular Matrix Degradation; HERITABLE DISORDERS OF CONNECTIVE TISSUE; Chapter 8 Osteogenesis Imperfecta; Chapter 9 The Ehlers-Danlos Syndrome; Chapter 10 Cutis Laxa and Premature Aging Syndromes; Chapter 11 Pseudoxanthoma Elasticum; Chapter 12 The Marfan Syndrome and Other Microfibrillar Disorders
Chapter 13 The HomocystinuriasChapter 14 Menkes Disease and the Occipital Horn Syndrome; Chapter 15 Epidermolysis Bullosa; Chapter 16 Prolidase Deficiency; Chapter 17 a(1)-Antitrypsin Deficiency; Chapter 18 Heritable Forms of Rickets and Osteomalacia; Chapter 19 Osteopetrosis; Chapter 20 Alkaptonuria; Chapter 21 Fibrodysplasia Ossificans Progressiva; Chapter 22 Disorders of Lysosomal Enzymes; Part I General Considerations; Part II Clinical Phenotypes; Chapter 23 Skeletal Dysplasias; Part I Chondrodysplasias: General Concepts and Diagnostic and Management Considerations
Part II Chondrodysplasias: Disorders of Cartilage Matrix ProteinsPart III Skeletal Dysplasias Related to Defects in Sulfate Metabolism; Part IV Craniosynostosis Syndromes and Skeletal Dysplasias Caused by Mutations in Fibroblast Growth Factor Receptor Genes; Part V Defects in Skeletal Morphogenesis; Chapter 24 Disorders of Keratinization; Chapter 25 Alport Syndrome; Chapter 26 Miscellaneous Disorders; Part I Corneal Dystrophies Due to Mutations in the Kerato-Epithelin Gene (big-h3); Part II Progressive Pseudorheumatoid Dysplasia
Part III The Camptodactyly-Arthropathy-Coxa Vara-Pericarditis SyndromePart IV Bruck Syndrome; Part V Osteoporosis-Pseudoglioma Syndrome; Part VI Myopathies Due to Defects in Collagen VI; Part VII Knobloch Syndrome; Appendix I International Nomenclature of Constitutional Disorders of Bone: Osteochondrodysplasias; Appendix II Extracellular Collagen Metabolites in Body Fluids; Index
Record Nr. UNINA-9910676612303321
New York, : Wiley-Liss, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Connective tissue and it heritable disorders : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Connective tissue and it heritable disorders : molecular, genetic, and medical aspects / / edited by Peter M. Royce and Beat Steinmann
Edizione [2nd ed.]
Pubbl/distr/stampa New York, : Wiley-Liss, c2002
Descrizione fisica 1 online resource (1221 p.)
Disciplina 616.77042
Altri autori (Persone) RoycePeter M
SteinmannBeat U
Soggetto topico Connective tissues - Diseases - Genetic aspects
Connective tissues - Diseases - Molecular aspects
ISBN 1-280-36667-2
9786610366675
0-470-35006-7
0-471-46117-2
0-471-22192-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CONNECTIVE TISSUE AND ITS HERITABLE DISORDERS SECOND EDITION; Contents; Preface; Acknowledgments; Preface to the First Edition; Contributors; Introduction Research on Collagen in the Author's Laboratory, 1952-1982; Introduction Heritable Disorders of Connective Tissue: A Personal Account of the Origins, Evolution, Validation, and Expansion of a Concept; BIOLOGY OF EXTRACELLULAR MATRIX; Chapter 1 Morphology and Chemical Composition of Connective Tissue; Part I Structure of the Skin and Tendon; Part II Cartilage; Part III Bone; Part IV The Cardiovascular System; Part V The Eye
Chapter 2 CollagenPart I The Collagen Family: Structure, Assembly, and Organization in the Extracellular Matrix; Part II Gene Structure; Chapter 3 Elastin and the Microfibrillar Apparatus; Chapter 4 Glycosylated Matrix Proteins; Chapter 5 Adhesive Glycoproteins; Chapter 6 Keratins; Chapter 7 Extracellular Matrix Degradation; HERITABLE DISORDERS OF CONNECTIVE TISSUE; Chapter 8 Osteogenesis Imperfecta; Chapter 9 The Ehlers-Danlos Syndrome; Chapter 10 Cutis Laxa and Premature Aging Syndromes; Chapter 11 Pseudoxanthoma Elasticum; Chapter 12 The Marfan Syndrome and Other Microfibrillar Disorders
Chapter 13 The HomocystinuriasChapter 14 Menkes Disease and the Occipital Horn Syndrome; Chapter 15 Epidermolysis Bullosa; Chapter 16 Prolidase Deficiency; Chapter 17 a(1)-Antitrypsin Deficiency; Chapter 18 Heritable Forms of Rickets and Osteomalacia; Chapter 19 Osteopetrosis; Chapter 20 Alkaptonuria; Chapter 21 Fibrodysplasia Ossificans Progressiva; Chapter 22 Disorders of Lysosomal Enzymes; Part I General Considerations; Part II Clinical Phenotypes; Chapter 23 Skeletal Dysplasias; Part I Chondrodysplasias: General Concepts and Diagnostic and Management Considerations
Part II Chondrodysplasias: Disorders of Cartilage Matrix ProteinsPart III Skeletal Dysplasias Related to Defects in Sulfate Metabolism; Part IV Craniosynostosis Syndromes and Skeletal Dysplasias Caused by Mutations in Fibroblast Growth Factor Receptor Genes; Part V Defects in Skeletal Morphogenesis; Chapter 24 Disorders of Keratinization; Chapter 25 Alport Syndrome; Chapter 26 Miscellaneous Disorders; Part I Corneal Dystrophies Due to Mutations in the Kerato-Epithelin Gene (big-h3); Part II Progressive Pseudorheumatoid Dysplasia
Part III The Camptodactyly-Arthropathy-Coxa Vara-Pericarditis SyndromePart IV Bruck Syndrome; Part V Osteoporosis-Pseudoglioma Syndrome; Part VI Myopathies Due to Defects in Collagen VI; Part VII Knobloch Syndrome; Appendix I International Nomenclature of Constitutional Disorders of Bone: Osteochondrodysplasias; Appendix II Extracellular Collagen Metabolites in Body Fluids; Index
Record Nr. UNINA-9910877798703321
New York, : Wiley-Liss, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui