RCMI Coordinating Center (RCMI CC) Header Logo

Search Results (9)

MatchTypeWhy
Coexistence of congenital giant melanocytic nevus of the scalp with cranial defect, poliosis, and hair loss.Academic Article Why?
Dual Efficacy of Upadacitinib in 2 Patients With Concomitant Severe Atopic Dermatitis and Alopecia Areata.Academic Article Why?
Androgenetic alopecia at various ages and prostate cancer risk in an equal-access multiethnic case-control series of veterans.Academic Article Why?
The human orthologue of murine Mpzl3 with predicted adhesive and immune functions is a potential candidate gene for immune-related hereditary hair loss.Academic Article Why?
Evidence of hair loss after subacute exposure to 2-chloroethyl ethyl sulfide, a mustard analog, and beneficial effects of N-acetyl cysteine.Academic Article Why?
Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart.Academic Article Why?
Rapid hair regrowth induced by dupilumab in a patient affected by alopecia totalis of 28?years' duration: Clinical and dermoscopic features.Academic Article Why?
AlopeciaConcept Why?
Alopecia AreataConcept Why?
Psoriasis onset under dupilumab treatment in two patients affected by atopic dermatitis and one patient affected by alopecia areata: Clinical and dermoscopic patterns.Academic Article Why?
Alfano, Robert R.Person Why?
Csiszar, KatalinPerson Why?
Moon, KeePerson Why?
Analysis of patient experiences with gestational trophoblastic neoplasia reported on Instagram social media.Academic Article Why?
Das, SalilPerson Why?
Per Page    Page  of 1
Next
Prev
Search Criteria
  • Alopecia
Filter by Type
_
Click "Why?" to see why an item matched the search.
RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

For technical support please contact support