3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Hirsutism & acne • Infertility ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology
Melanoma of the Foot - The physical examination revealed a well-defined, fleshy, reddish plaque measuring 2
#Clinical #Derm ... #Podiatry #Honc ... #AmelanoticMelanoma ... Melanoma #Foot #NEJM
Immunosuppressive Strategies for the Prevention or Treatment of Acute GVHD. Panel A shows several classic immunosuppressive
are in routine clinical ... been tested in clinical ... #Pathophysiology ... #IM #Honc #Pharm ... Immunosuppression #NEJM