39 results
HINTS Exam - Abnormal Head Impulse Test = Peripheral Cause

This video demonstrates:
1) Normal Head Impulse Test
HINTS Exam - Abnormal ... patient with vertigo symptoms ... , this abnormal ... #PhysicalExam #Clinical ... #Video #Neurology
HINTS Exam - Abnormal Test of Skew (Abnormal Vertical Skew)

In a patient with vertigo symptoms, this
HINTS Exam - Abnormal ... Test of Skew (Abnormal ... patient with vertigo symptoms ... #PhysicalExam #Clinical ... #Video #Neurology
HINTS Exam - Abnormal Head Impulse Test = Peripheral Cause

This video demonstrates:
1) Normal Head Impulse Test
HINTS Exam - Abnormal ... patient with vertigo symptoms ... , this abnormal ... #PhysicalExam #Clinical ... #Video #Neurology
HINTS Exam - Normal Test of Skew (Normal Vertical Skew)

In a patient with vertigo symptoms, this
HINTS Exam - Normal ... Test of Skew (Normal ... patient with vertigo symptoms ... #PhysicalExam #Clinical ... #Video #Neurology
HINTS Exam - Normal Head Impulse Test = Central Cause

This patient as a normal head impulse
HINTS Exam - Normal ... patient with vertigo symptoms ... , this normal finding ... #PhysicalExam #Clinical ... #Video #Neurology
The asphyxia escape reflex is assessed by placing the child in the prone position on the
#PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics ... #Normal #Primitive
Lyme Disease: Early and Late Clinical manifestations
Stage 1. Localized
 • EM appears 7-14 days at the
Disease: Early and Late ... Clinical manifestations ... • Heralded by neurologic ... impairment - Normal ... diagnosis #signs #symptoms
Aphasia - Pathophysiology and Clinical Findings
Broca's Aphasia - Expressive language impairment: non-Fluent
 - Sensory speech areas
Aphasia - Pathophysiology ... and Clinical Findings ... deficits #Aphasia #Pathophysiology ... diagnosis #signs #symptoms ... Brocas #Wernickes #neurology
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
#PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics ... #Normal #Primitive
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds