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peds diagnosis clinical physicalexam comparison genetics newborn signs algorithm bronchoscopy congenital differential iem inbornerrors infections laryngomalacia laryngoscopy metabolism neonatology nicu
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... of information: Pediatrics ... , UpToDate #Pediatrics ... Neonatology #Peds #Pediatrics ... #Table #IEM #NICU
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... #Table #NICU #Genetics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Congenital TORCH Infections Dr. Natalie Marshall @MicrobeNat #Congenital #Infections #Comparison #Table #pediatrics #diagnosis #symptoms #TORCH
Infections #Comparison #Table ... #pediatrics #diagnosis ... #symptoms #TORCH
Congenital Infections - Comparison Table: Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus Manifestations: Anemia, Bony
Infections - Comparison Table ... Infections #Comparison #Table ... #pediatrics #diagnosis ... #symptoms #TORCH
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings Parasomnias - Micro-arousal episodes during SWS -> Intense activation of
Pediatric Parasomnias ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology ... #symptoms #pharmacology
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... 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
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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