In this issue of Critical Care Clinics, guest editors Drs. Robert M. Kliegman and Brett J. Bordini bring their considerable expertise to the topic of Undiagnosed and Rare Diseases in Critical Care. Top experts in the field cover key topics such as critical genetic arrhythmia disorders, uncommon causes of rhabdomyolysis, status epilepsy syndromes, autoimmune encephalitis, rapid-onset paralysis and weakness, and more.
Undiagnosed and Rare Diseases in Critical Care: The Role of Diagnostic Access Rapid Exome and Genome Sequencing in the Intensive Care Unit Diagnostic Time-Outs to Improve Diagnosis Subtypes and Mimics of Sepsis All that Wheezes is not Asthma or Bronchiolitis Recognition and Management Considerations of Cardiac Channelopathies in the Intensive Care Unit Undiagnosed and Rare Diseases in Critical Care: Severe Mucocutaneous Medication Reactions Uncommon Causes of Rhabdomyolysis Common Presentations of Rare Drug Reactions and Atypical Presentations of Common Drug Reactions in the Intensive Care Unit Pediatric Acute Liver Failure Uncommon Causes of Acute Kidney Injury Zebras Seize the Day: Rare Causes of Status Epilepticus Across the Continuum of Critical Care Primary Causes of Hypertensive Crisis Autoimmune Encephalitis: Distinguishing Features and Specific Therapies Rapid Onset of Neuromuscular Paralysis or Weakness Uncommon Etiologies of Shock Genetic Defects that Predispose to Serious Viral Infections
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