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diagnosis management treatment ics laba lama pediatrics peds pulmonary 21hydroxylasedeficiency 21ohd adrenal cah causes congenitaladrenalhyperplasia covid19 diabetes exacerbations genetics gold2017
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
ADH (SIADH) - Comparison ... Insipidus #SIADH #Comparison ... #Table #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Lung Ultrasound in COVID 19 symptoms and a history of COPD FAMUS @FAMUSultrasound #Lung #Ultrasound #COVID19 #POCUS #COPD
Ultrasound in COVID 19 symptoms ... and a history of COPD ... COVID19 #POCUS #COPD ... #Algorithm #Comparison
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
The goals of #COPD #treatment include recognizing the impact that both #symptoms and #exacerbations have on
The goals of #COPD ... impact that both #symptoms ... discusses the need for COPD ... #management #algorithm ... #pharmacology
Hyperparathyroidism - Primary vs Secondary vs Tertiary Lab Comparison: • Primary Hyperparathyroidism: ↑→PTH, ↑Calcium, ↑Vitamin D,
Tertiary Lab Comparison ... Phosphate Physical Symptoms ... pain Psychiatric Symptoms ... Hyperparathyroidism #diagnosis #endocrinology ... Secondary #Tertiary #pathophysiology
Medical Treatment Algorithm for Chronic Obstructive Pulmonary Disease Initial medical treatment of chronic obstructive pulmonary disease (COPD)
Medical Treatment Algorithm ... of obstruction, symptom ... control persistent symptoms ... #Algorithm #Management ... SABA #SAMA #ICS #Pharmacology
Pharmacologic treatment algorithms by Global Initiative for Chronic Obstructive Lung Disease grade. Highlighted boxes and arrows
Pharmacologic treatment ... algorithms by Global ... perceived level of symptoms ... Management #Pulmonary #COPD
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
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