9 results
physicalexam clinical peds video diagnosis meningitis duchenne dystrophy gowers muscular 21hydroxylasedeficiency 21ohd anomalous cardiology comatose genetics hyperparathyroidism management primary pth
Brudzinski's Sign on Physical Exam - Meningitis #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... Meningitis #Brudzinskis ... #Sign #PhysicalExam ... clinical #video #neurology ... #peds #pediatrics
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 Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Josef Brudzinski ... ) Brudzinski's ... While the pathophysiology ... #PhysicalExam #Pediatrics
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 Brudzinski's Sign on Physical Exam - Meningitis via @TheIntern254 #Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... TheIntern254 #Brudzinskis ... #Sign #PhysicalExam ... clinical #video #neurology ... #peds #pediatrics
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 Gowers' Sign on Physical Exam Seen in this patient with Duchenne muscular dystrophy (DMD) #Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... muscular dystrophy (DMD ... ) #Gowers #Sign ... #PhysicalExam #neurology ... clinical #video #pediatrics
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 Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... by Cara Holton, MD ... cardiology #peds #pediatrics
Hyperparathyroidism - Primary vs Secondary vs Tertiary Lab Comparison: • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
Symptoms: Commonly no signs ... Satyendra Dhar, MD ... Hyperparathyroidism #diagnosis #endocrinology ... Secondary #Tertiary #pathophysiology
Gowers' Sign on Physical Exam Indicative of proximal muscle weakness in muscular dystrophy. #Gowers #Sign #PhysicalExam #neurology #clinical
Gowers' Sign on ... #Gowers #Sign #PhysicalExam ... #neurology #clinical ... #video #pediatrics ... muscular #dystrophy #DMD
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
• Mutism Pathophysiology ... • Examine for signs ... Casey Albin MD @ ... #PhysicalExam #neurology
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