Dekorationsartikel gehören nicht zum Leistungsumfang.
Sprache:
Englisch
149,79 €
Versandkostenfrei per Post / DHL
Aktuell nicht verfügbar
Kategorien:
Beschreibung
Provides representative case studies and accompanying text
Includes clinical history, muscle/nerve biopsy changes, clinical or instrumental data, and pictures of patients and genetic results, when available, for each case
Revised and expanded to include case studies and literature reviews of additional genetic neuromuscular disorders
Includes clinical history, muscle/nerve biopsy changes, clinical or instrumental data, and pictures of patients and genetic results, when available, for each case
Revised and expanded to include case studies and literature reviews of additional genetic neuromuscular disorders
Provides representative case studies and accompanying text
Includes clinical history, muscle/nerve biopsy changes, clinical or instrumental data, and pictures of patients and genetic results, when available, for each case
Revised and expanded to include case studies and literature reviews of additional genetic neuromuscular disorders
Includes clinical history, muscle/nerve biopsy changes, clinical or instrumental data, and pictures of patients and genetic results, when available, for each case
Revised and expanded to include case studies and literature reviews of additional genetic neuromuscular disorders
Über den Autor
Corrado Angelini, M.D. works at the University of Padua Department of Neuroscience, Italy and also IRCCS S. Camillo Lido, Venice, Italy,
Corrado Angelini trained at the Mayo Clinic where he worked on diagnostic features of metabolic disorders, contributed to the description of late-onset GSD II patients and discovered carnitine deficiency in man. He became Associate and Full Professor in Padova and contributed to the description of beta-sarcoglycanopathy, dysferlinopathy and Limb Girdle 1F.
Zusammenfassung
Provides representative case studies and accompanying text
Includes clinical history, muscle/nerve biopsy changes, clinical or instrumental data, and pictures of patients and genetic results, when available, for each case
Revised and expanded to include case studies and literature reviews of additional genetic neuromuscular disorders
Inhaltsverzeichnis
Muscular Dystrophies.- Congenital Myopathies.- Ion Channel Disorders.- Metabolic Myopathies.- Neurogenic Disorders.
Details
| Erscheinungsjahr: | 2017 |
|---|---|
| Fachbereich: | Andere Fachgebiete |
| Genre: | Mathematik, Medizin, Naturwissenschaften, Technik |
| Rubrik: | Wissenschaften |
| Medium: | Taschenbuch |
| Inhalt: |
xi
433 S. 5 s/w Illustr. 72 farbige Illustr. 433 p. 77 illus. 72 illus. in color. |
| ISBN-13: | 9783319564531 |
| ISBN-10: | 3319564536 |
| Sprache: | Englisch |
| Einband: | Kartoniert / Broschiert |
| Autor: | Angelini, Corrado |
| Auflage: | Second Edition 2018 |
| Hersteller: |
Springer
Birkhäuser Springer International Publishing AG |
| Verantwortliche Person für die EU: | Springer Verlag GmbH, Tiergartenstr. 17, D-69121 Heidelberg, juergen.hartmann@springer.com |
| Maße: | 235 x 155 x 23 mm |
| Von/Mit: | Corrado Angelini |
| Erscheinungsdatum: | 17.10.2017 |
| Gewicht: | 0,756 kg |