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Year Number of Results
1960 1
1983 1
1996 1
1998 1
1999 1
2003 1
2004 2
2006 1
2007 1
2009 1
2011 3
2013 1
2015 1
2017 1
2020 1
2023 1
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18 results

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Page 1
Keratosis pilaris: an update and approach to management.
Kodali N, Patel VM, Schwartz RA. Kodali N, et al. Ital J Dermatol Venerol. 2023 Jun;158(3):217-223. doi: 10.23736/S2784-8671.23.07594-1. Epub 2023 May 11. Ital J Dermatol Venerol. 2023. PMID: 37166753 Free article. Review.
Inherited mutations of the FLG gene and ABCA12 gene have been implicated etiologically. KP may be associated with ichthyosis vulgaris and palmar hyperlinearity, but less likely atopic dermatitis. Some potential differential diagnoses for KP include lichen spinulosus …
Inherited mutations of the FLG gene and ABCA12 gene have been implicated etiologically. KP may be associated with ichthyosis vulga …
Ichthyosis: etiology, diagnosis, and management.
DiGiovanna JJ, Robinson-Bostom L. DiGiovanna JJ, et al. Am J Clin Dermatol. 2003;4(2):81-95. doi: 10.2165/00128071-200304020-00002. Am J Clin Dermatol. 2003. PMID: 12553849 Review.
It may be due to mutations in the gene encoding the intermediate filament proteins keratin 1 and 10. Ichthyosis vulgaris is the most common ichthyosis, and is inherited in an autosomal dominant pattern. ...Netherton's syndrome is an autosomal recessive disord …
It may be due to mutations in the gene encoding the intermediate filament proteins keratin 1 and 10. Ichthyosis vulgaris is th …
Ichthyoses: differential diagnosis and molecular genetics.
Oji V, Traupe H. Oji V, et al. Eur J Dermatol. 2006 Jul-Aug;16(4):349-59. Eur J Dermatol. 2006. PMID: 16935789 Review.
Ichthyoses are a heterogeneous group of cornification disorders characterized by a generalized scaling of the skin. Common types such as ichthyosis vulgaris and X-linked recessive ichthyosis manifest after birth. ...This review discusses a broad spectrum of 1 …
Ichthyoses are a heterogeneous group of cornification disorders characterized by a generalized scaling of the skin. Common types such as …
Ichthyosis: clinical manifestations and practical treatment options.
Oji V, Traupe H. Oji V, et al. Am J Clin Dermatol. 2009;10(6):351-64. doi: 10.2165/11311070-000000000-00000. Am J Clin Dermatol. 2009. PMID: 19824737 Review.
Ichthyosis vulgaris and recessive X-linked ichthyosis are common disorders - often of delayed onset, in contrast to congenital ichthyoses, which belong to the group of rare diseases and present at birth with either the features of collodion membrane or congen …
Ichthyosis vulgaris and recessive X-linked ichthyosis are common disorders - often of delayed onset, in contrast to con …
Disorders of keratinization: diagnosis and management.
Shwayder T. Shwayder T. Am J Clin Dermatol. 2004;5(1):17-29. doi: 10.2165/00128071-200405010-00004. Am J Clin Dermatol. 2004. PMID: 14979740 Review.
This paper reviews the major and a few of the rarer ones with a concentration on their therapy. Ichthyosis vulgaris is probably a post-translational defect in pro-filaggrin expression. ...Controlling the odor is an ongoing issue using antibacterial washes, ab …
This paper reviews the major and a few of the rarer ones with a concentration on their therapy. Ichthyosis vulgaris is …
Treatment of ichthyosis vulgaris with a urea-based emulsion: videodermatoscopy and confocal microscopy evaluation.
Benintende C, Boscaglia S, Dinotta F, Lacarrubba F, Micali G. Benintende C, et al. G Ital Dermatol Venereol. 2017 Dec;152(6):555-559. doi: 10.23736/S0392-0488.17.05743-1. G Ital Dermatol Venereol. 2017. PMID: 29050444
BACKGROUND: Ichthyosis vulgaris is a common disorder of keratinization caused by mutations in the filaggrin gene and clinically characterized by variable degree of xerosis. ...CONCLUSIONS: The tested urea-based emulsion represents a valid option for the treatment of …
BACKGROUND: Ichthyosis vulgaris is a common disorder of keratinization caused by mutations in the filaggrin gene and clinicall …
Ichthyoses in everyday practice: management of a rare group of diseases.
Süßmuth K, Traupe H, Metze D, Oji V. Süßmuth K, et al. J Dtsch Dermatol Ges. 2020 Mar;18(3):225-243. doi: 10.1111/ddg.14049. Epub 2020 Mar 2. J Dtsch Dermatol Ges. 2020. PMID: 32115871
A distinction is made between common hereditary ichthyoses (ichthyosis vulgaris and X-linked ichthyosis), which usually manifest themselves in the first year of life, and rare, sometimes severe congenital ichthyoses. ...However, such treatment is frequently t …
A distinction is made between common hereditary ichthyoses (ichthyosis vulgaris and X-linked ichthyosis), which usually …
Use of emollients in the treatment of dry skin conditions.
Dyble T, Ashton J. Dyble T, et al. Br J Community Nurs. 2011 May;16(5):214, 216, 218 passim. doi: 10.12968/bjcn.2011.16.5.214. Br J Community Nurs. 2011. PMID: 21642925 Review.
As a result of this, problems with untreated dry skin can lead to a variety of issues. Conditions such as pruritus and ichthyosis vulgaris can be distressing, while ezcema and psoriasis can lead to more serious consequences such as fissures and infections and can re …
As a result of this, problems with untreated dry skin can lead to a variety of issues. Conditions such as pruritus and ichthyosis …
Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function.
Gruber R, Elias PM, Crumrine D, Lin TK, Brandner JM, Hachem JP, Presland RB, Fleckman P, Janecke AR, Sandilands A, McLean WH, Fritsch PO, Mildner M, Tschachler E, Schmuth M. Gruber R, et al. Am J Pathol. 2011 May;178(5):2252-63. doi: 10.1016/j.ajpath.2011.01.053. Am J Pathol. 2011. PMID: 21514438 Free PMC article.
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier function in ichthyosis vulgaris and atopic dermatitis, the pathomechanism of how FLG deficiency provokes a barrier abnormality in humans is unknown. ...
Although it is widely accepted that filaggrin (FLG) deficiency contributes to an abnormal barrier function in ichthyosis vulgaris …
Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis.
Anton-Lamprecht I. Anton-Lamprecht I. J Invest Dermatol. 1983 Jul;81(1 Suppl):149s-56s. doi: 10.1111/1523-1747.ep12540961. J Invest Dermatol. 1983. PMID: 6345689 Free article. Review.
Most interesting from the morphologic point of view are dominantly inherited skin disorders in the ichthyosis and epidermolysis bullosa groups in which primary structural defects of structural proteins have been demonstrated that seem to be under the direct control of the …
Most interesting from the morphologic point of view are dominantly inherited skin disorders in the ichthyosis and epidermolysis bullo …
18 results