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headct management choosingwisely em aliem older2 over2 under2 younger2 21hydroxylasedeficiency 21ohd ddxof differential disease endocrinology epiglottitis evaluation genetics head incomplete
PECARN Pediatric Blunt Head Trauma Algorithm - Under Age 2 #Diagnosis #Management #Peds #Pediatrics #HeadTrauma #HeadCT
PECARN Pediatric ... - Under Age 2 #Diagnosis ... #Management #Peds ... #Pediatrics #HeadTrauma ... #HeadCT #PECARN
PECARN Pediatric Blunt Head Trauma Algorithm - Under Age 2 #Diagnosis #Management #Peds #Pediatrics #HeadTrauma #HeadCT
PECARN Pediatric ... - Under Age 2 #Diagnosis ... #Management #Peds ... #Pediatrics #HeadTrauma ... #HeadCT #PECARN
PECARN Pediatric Blunt Head Trauma Algorithm - Age 2 and Up #Diagnosis #Management #Peds #Pediatrics #HeadTrauma
PECARN Pediatric ... Age 2 and Up #Diagnosis ... #Management #Peds ... #Pediatrics #HeadTrauma ... #HeadCT #PECARN
PECARN Pediatric Blunt Head Trauma Algorithm - Age 2 and Up #Diagnosis #Management #Peds #Pediatrics #HeadTrauma
PECARN Pediatric ... Age 2 and Up #Diagnosis ... #Management #Peds ... #Pediatrics #HeadTrauma ... #HeadCT #PECARN
PATIENT AGE >2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
AGE >2 Years - Pediatric ... Study) #Diagnosis ... #Management #Peds ... #EM #Algorithm ... #HeadTrauma #HeadCT
PATIENT AGE <2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
AGE <2 Years - Pediatric ... Study) #Diagnosis ... #Management #Peds ... #EM #Algorithm ... #HeadTrauma #HeadCT
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the ... Evaluation of Pediatric ... Need for Head CT #Diagnosis ... Management #EM #Peds ... Evaluation #Head #HeadTrauma
Epiglottitis - Swollen inflamed epiglottis Clinical (Rapid onset) • Fever • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
if they have no clinical ... purposes of this algorithm ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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