Respiratory control abnormalities in necdin-null mice and in mice lacking Mecp2 gene have provided new insights into the developmental origins of the respiratory disorders seen in Prader-Willi and Rett syndromes, respectively. Genetic Basis for Respiratory Control Disorders emphasizes the potent synergy between human studies and mouse models of genetic disorders underlying respiratory control anomalies.
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The overview of current research presented in this book opens up the field to the development of new therapeutic strategies, especially in newborns and infants, who are the primary target of respiratory control disorders. This book is addressed to pediatricians, neonatologists, pulmonologists, respiratory physiologists as well as geneticists. Convert currency.
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Genetic Basis for Respiratory Control Disorders
Customer satisfaction our priority. Genetic Basis for Respiratory Control Disorders. Publisher: Springer , This specific ISBN edition is currently not available. Genetic Basis for Respiratory Control Disorders. Respiratory control disorders: from genes to patients and back. Pages Hereditary aspects of respiratory control in health and disease in humans. Phox2b and the homeostatic brain. Congenital central hypoventilation syndrome: from patients to gene discovery. Structural and functional brain abnormalities in Congenital Central Hypoventilation Syndrome. Ronald M. Harper, Mary A.
Woo, Paul M. Macey, Rajesh Kumar. Sudden infant death syndrome: study of genes pertinent to cardiorespiratory and autonomic regulation.
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