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diagnosis peds cardiogenic management genetics neurology pharmacology syndrome 21hydroxylasedeficiency 21ohd abcdes acute acutecoronarysyndrome adhd als alzheimersdisease amyotrophic arthropathy attentiondeficithyperactivedisorder atypical
Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
Cardiogenic Shock ... complications and clinical ... #pathophysiology ... #cardiology #diagnosis ... #signs #symptoms
Acute Coronary Syndrome - Diagnostic Likelihood Ratios for Symptoms and Physical Examination. Source: Does This
Likelihood Ratios for Symptoms ... : The Rational Clinical ... EBM #Diagnosis #Cardiology ... #ACS #AcuteCoronarySyndrome ... #Symptoms #Signs
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... of shock from dehydration ... #PhysicalExam #Signs ... #Symptoms #Shock ... Dehydration #Peds #Pediatrics
SCAI Pyramid of Cardiogenic Shock Classification E - Extremis - A patient experiencing cardiac arrest with ongoing
of Cardiogenic Shock ... patient who has clinical ... currently experiencing signs ... or symptoms of ... ABCDEs #diagnosis #cardiology
Pathophysiology and Clinical Manifestations of Shock #Shock #Manifestations #Cardiogenic #Hypovolemic #Signs #Symptoms
Pathophysiology ... and Clinical Manifestations ... of Shock #Shock ... #Hypovolemic #Signs ... #Symptoms
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Pathogenesis and Clinical ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #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 ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... fasciculations Common Symptoms ... Exam: clinical evidence
Heart failure with Reduced Ejection Fraction (HFrEF) Clinical Presentation 1. Typical symptoms: dyspnea, orthopnea paroxysmal noctumal dyspnea, fatigue,
Fraction (HFrEF) Clinical ... Typical symptoms ... Less Typical Symptoms ... Pharmacology: • ACE ... diagnosis #management #cardiology
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