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Quoted phrase not found in phrase index: "Peeling skin syndrome 4"
Page 1
Transglutaminase diseases: from biochemistry to the bedside.
FASEB J. 2019 Jan;33(1):3-12. doi: 10.1096/fj.201801544R.
FASEB J. 2019.
PMID: 30593123
In humans, 9 members of the transglutaminase (TG) family have been identified, of which 8 [factor XIII (FXIII)A and TG1-TG7] catalyze post-translational protein-modifying reactions, and 1 does not (protein 4.2). The TG enzymatic activities considered in our discussion of h …
In humans, 9 members of the transglutaminase (TG) family have been identified, of which 8 [factor XIII (FXIII)A and TG1-TG7] catalyze post-t …
Novel TGM5 mutations in acral peeling skin syndrome.
van der Velden JJ, van Geel M, Nellen RG, Jonkman MF, McGrath JA, Nanda A, Sprecher E, van Steensel MA, McLean WH, Cassidy AJ.
van der Velden JJ, et al.
Exp Dermatol. 2015 Apr;24(4):285-9. doi: 10.1111/exd.12650.
Exp Dermatol. 2015.
PMID: 25644735
Acral peeling skin syndrome (APSS, MIM #609796) is a rare autosomal recessive disorder characterized by superficial exfoliation and blistering of the volar and dorsal aspects of hands and feet. ...To confirm their pathogenicity, we performed functional analys …
Acral peeling skin syndrome (APSS, MIM #609796) is a rare autosomal recessive disorder characterized by superficial exf …
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Peeling skin syndrome with hair changes.
Mevorah B, Orion E, de Viragh P, Bergman R, Gat A, Legume C, Van Neste DJ, Brenner S.
Mevorah B, et al.
Dermatology. 1998;197(4):373-6. doi: 10.1159/000018034.
Dermatology. 1998.
PMID: 9873177
A 13-year-old boy with typical peeling skin syndrome (PSS) is described. The clinical picture corresponded to the inflammatory variant of PSS (type B). In addition, the patient had gross and microscopic hair anomalies such as trichorrhexis invaginata-like cha …
A 13-year-old boy with typical peeling skin syndrome (PSS) is described. The clinical picture corresponded to the infla …
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