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diagnosis ultrasound signs neurology symptoms echocardiogram management transverse lung a4c cardiology em pcc pediatrics peds pulmonary radiology sonostuff trachea video
Regulation of Core Body Temperature #Pathophysiology #Thermoregulation #Body #Temperature #Core #Thermoregulatory ** GrepMed Recommended Text: Hutchison's Clinical Methods
Regulation of Core ... Temperature #Pathophysiology ... #Temperature #Core ... Text: Hutchison's Clinical
Acute Spinal Cord Injuries: Pathogenesis and clinical findings • Anterior Cord Syndrome -> Anterior spinal artery
Acute Spinal Cord ... Pathogenesis and clinical ... findings • Anterior Cord ... Syndrome ->Cord ... Syndromes #diagnosis #pathophysiology
Cor Triatriatum on Echocardiogram - EchoTalk Echocardiography @echotalk Cor Triatriatum (or triatrial heart) is a congenital heart defect
Cor Triatriatum ... the left atrium (cor ... right atrium (cor ... Echocardiogram #A4C #POCUS ... #Clinical #Congenital
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 Primary Hyperthyroidism - Pathogenesis and Clinical Findings Note: Although rare, gestational diseases can lead to thyrotoxicosis due
Pathogenesis and Clinical ... Hyperthyroidism #endocrinology ... #pathophysiology
Graves’ Disease: Pathogenesis and Clinical Findings B & T lymphocyte mediated autoimmunity attack TSH receptor -> Continuous
Pathogenesis and Clinical ... GravesDisease #pathophysiology ... #endocin #endocrinology
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
of the spinal cord ... monophasic Pathophysiology ... against the spinal cord ... Transverse Myelitis - Clinical ... to the spinal cord
Ventricular Fibrillation in Real Time This was recorded at the conclusion of a swine experiment prior to
Cory M. ... #VFib #Video #Clinical ... #POCUS #openheart
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 Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
Pathogenesis and clinical ... share the same pathophysiology ... signs #symptoms #endocrinology ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... , sleep apnea, cor ... Syndrome #genetics #pathophysiology
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