Results 81 to 90 of about 31,072 (141)
This dataset supports the findings in the manuscript "Efficacy of Baricitinib in Moderate Alopecia Areata, Severe Alopecia Areata, Alopecia Totalis, and Alopecia Universalis: A Real-world Comparative Study." The dataset includes:Demographic and baseline ...
Jiang, Guan
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Three mutations in SASH1 cause the pathogenesis of dyschromatosis universalis hereditaria (DUH) [PDF]
, 2011 Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis characterized by hyper- and hypopigmented macules which form a reticulate or mottled pattern.
Zhiyun Wei, Qinghe Xing, Dingan Zhou
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Alopecia areata universalis showing excellent response to combination treatment modalities
, 2022 Alopecia areata (AA) is a non-scarring alopecia with mainly an autoimmune etiopathogenesis. The most severe AA variant is alopecia areata universalis (AAU), characterized by a total loss of scalp and body hair. AAU poses a significant psychosocial impact
Noer Kamila +4 more
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, 2012 Alopecia areata is among the most prevalent autoimmune diseases, yet compared with other autoimmune conditions, it is not well studied. This in part results from limitations in the C3H/HeJ mouse and DEBR rat model systems most commonly used to study the ...
Alli, Rajshekhar +4 more
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Complete remission of alopecia universalis after allogeneic hematopoietic stem cell transplantation.
, 2005 This case report is on a 40-year-old male patient with chronic myeloid leukemia (CML) receiving an allogeneic hematopoietic stem cell transplantation (HSCT) in first chronic phase from an HLA-identical sibling brother.
Gratwohl A +7 more
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Actas Dermo-SifiliográficasAlopecia areata (AA) is a dermatological disease of immune origin characterized by partial or total hair loss of the scalp (alopecia totalis) or the whole body (alopecia universalis).
S. Vañó-Galván +5 more
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Molecular signatures define alopecia areata subtypes and transcriptional biomarkers
EBioMedicine, 2016 Alopecia areata (AA) is an autoimmune disease typified by nonscarring hair loss with a variable clinical course. In this study, we conducted whole genome gene expression analysis of 96 human scalp skin biopsy specimens from AA or normal control subjects.
Ali Jabbari +9 more
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Of Hairless Mice and Men: The Genetic Basis of Congenital Alopecia Universalis/Congenital Atrichia
, 1999 Background: Mouse models of human diseases help identify gene defects. Objective: The methods of homozygosity mapping and mouse/human homology to identify genes are reviewed.
Sherri J. Bale
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Frontiers in ImmunologyBackgroundAlopecia areata (AA) is a common autoimmune disorder causing patchy hair loss. Epidemiological observations and molecular studies collectively suggest an underrecognized interplay between AA and cardiovascular disease (CVD).
Jiawei Lu +4 more
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, 2011 ObjectiveTo evaluate the reason of major behavioral problems in alopecia universalis patients, we tried to examine by way of MCMI- III whether these signs are transient, developmental or ingrained.Methods279 patients with alopecia universalis were ...
K.K. Pirkalani, Z. Talaee Rad
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