Acute generalized exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction (SCAR) characterized by sterile non-follicular pustules on an erythematous base that form rapidly after drug exposure. AGEP is mediated …
The Alopecia Areata Consensus of Experts (ACE) Study PART II: Results of an International Expert Opinion on Diagnosis and Laboratory Evaluation for Alopecia Areata.
We previously reported The Alopecia Areata Consensus of Experts (ACE) Study: Results of an International Expert Opinion on Treatments for Alopecia Areata (AA).To report the results of the ACE international …
Development of a Pathogenesis-Based Therapy for Peeling Skin Syndrome Type 1.
Peeling skin syndrome type 1 is a rare and severe autosomal recessive form of congenital ichthyosis. Patients suffer from pronounced erythroderma accompanied by tremendous pruritus and superficial generalised peeling of …
Clinical Presentation and Management of Atypical and Recalcitrant Acute Generalized Exanthematous Pustulosis (AGEP).
Acute generalized exanthematous pustulosis (AGEP) is a severe cutaneous adverse reaction (SCAR) characterized by sterile non-follicular pustules on an erythematous base that form rapidly after drug exposure. AGEP is mediated …
Clinical Outcomes of CoVid-19 in Patients Taking Tumor Necrosis Factor Inhibitors and/or Methotrexate: A Multi-Center Research Network Study.
Data on the impact of biologics and immunomodulators on CoVid-19 related outcomes remains scarce.To determine whether patients on tumor necrosis factor inhibitor (TNFi) and/or methotrexate are at increased risk of …
The Alopecia Areata Consensus of Experts (ACE) Study PART II: Results of an International Expert Opinion on Diagnosis and Laboratory Evaluation for Alopecia Areata.
We previously reported The Alopecia Areata Consensus of Experts (ACE) Study: Results of an International Expert Opinion on Treatments for Alopecia Areata (AA).To report the results of the ACE international …
Development of a Pathogenesis-Based Therapy for Peeling Skin Syndrome Type 1.
Peeling skin syndrome type 1 is a rare and severe autosomal recessive form of congenital ichthyosis. Patients suffer from pronounced erythroderma accompanied by tremendous pruritus and superficial generalised peeling of …