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Undiagnosed and Rare Diseases,An Issue of Clinics in Perinatology

Om Undiagnosed and Rare Diseases,An Issue of Clinics in Perinatology

In collaboration with Consulting Editor, Dr. Lucky Jain, Drs. Robert Kliegman and Bret Bordini  have put together topics that provide a current clinical update on the treatment and management of undiagnosed and rare diseases in the neonate.  Expert authors have contributed clinical review articles on the following topics:  Neonatal Liver Failure; Neonatal Autoinflammatory Disorders; Rare or Unusual Dermatologic Disorders In Neonates; Neonatal Immune Deficiency; Congenital Diarrhea Syndromes; Nonimmune Hydrops; DNA Depletion Syndromes; Genomic Approach to Dysmorphology Syndromes; Nonimmune Anemias; Severe Metabolic Crisis (Metabolic Acidosis, Unresponsive Hypoglycemia, Hyperammonemia); Heterotaxia Syndromes; Neonatal Appendicitis; Avoiding Diagnostic Errors in Neonatology; and Differentiating Congenital Myopathy from Congenital Muscular Dystrophy.  Readers will come away with the information they need to improve outcomes in the neonate.

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  • Språk:
  • Engelska
  • ISBN:
  • 9780323711432
  • Format:
  • Inbunden
  • Sidor:
  • 240
  • Utgiven:
  • 3. februari 2020
  • Mått:
  • 152x229x0 mm.
  • Vikt:
  • 520 g.
  Fri leverans
Leveranstid: 2-4 veckor
Förväntad leverans: 30. december 2024
Förlängd ångerrätt till 31. januari 2025

Beskrivning av Undiagnosed and Rare Diseases,An Issue of Clinics in Perinatology

In collaboration with Consulting Editor, Dr. Lucky Jain, Drs. Robert Kliegman and Bret Bordini  have put together topics that provide a current clinical update on the treatment and management of undiagnosed and rare diseases in the neonate.  Expert authors have contributed clinical review articles on the following topics:  Neonatal Liver Failure; Neonatal Autoinflammatory Disorders; Rare or Unusual Dermatologic Disorders In Neonates; Neonatal Immune Deficiency; Congenital Diarrhea Syndromes; Nonimmune Hydrops; DNA Depletion Syndromes; Genomic Approach to Dysmorphology Syndromes; Nonimmune Anemias; Severe Metabolic Crisis (Metabolic Acidosis, Unresponsive Hypoglycemia, Hyperammonemia); Heterotaxia Syndromes; Neonatal Appendicitis; Avoiding Diagnostic Errors in Neonatology; and Differentiating Congenital Myopathy from Congenital Muscular Dystrophy.  Readers will come away with the information they need to improve outcomes in the neonate.

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