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Abbreviation : DDD
Long Form : Dowling-Degos disease
No. Year Title Co-occurring Abbreviation
2019 Full ablative versus fractional ablative laser therapy for Dowling-Degos disease. ---
2018 A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN. HS
2018 Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features. EGF, Pofut1
2017 Galli-Galli Disease Presenting as a Lentigo-like Eruption: A Further Clinical Feature in the Wide Spectrum of Reticulate Pigment Disorders. GGD, RPD
2017 Mutations in gamma-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa. AI, KRT5, Pofut1, POGLUT1
2017 PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) andDowling-Degos Disease (DDD): IsAIorDDD the Subphenotype? AI
2016 Atypical cases of Dowling-Degos disease. ---
2016 Dowling-Degos disease co-presenting with Darier disease. DD, GGD, KRT5, Pofut1, POGLUT1
2016 Dowling-Degos disease with reticulate acropigmentation of Kitamura: Extended spectrum of a single entity. RAK
10  2015 Successful treatment of Dowling-Degos disease using intense pulsed light. ---
11  2014 Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease. ---
12  2014 Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli disease. GGD
13  2014 Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease. WT
14  2013 Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis. AC, FF, HS, IBD, KID, PAPA Syndrome, SAPHO
15  2013 Generalized dowling-degos disease: case reports. ---
16  2013 Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease. hpf, KRT5
17  2013 Treatment of Dowling-Degos disease with fractional Er:YAG laser. ---
18  2013 Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease. RAK
19  2012 A novel heterozygous nonsense mutation of keratin 5 in a Chinese family with Dowling-Degos disease. KRT5
20  2012 The spectrum of reticulate pigment disorders of the skin revisited. GGD, HS, RAD
21  2011 A case of dowling-degos disease on the vulva. ---
22  2011 Coexistence of reticulate acropigmentation of Kitamura and Dowling-Degos disease. RAK
23  2011 Dowling-Degos disease: classic clinical and histopathological presentation. ---
24  2010 Dowling-Degos disease. DSH, DUH, RAPK
25  2010 Dowling-Degos disease: case report and review of the literature. ---
26  2010 Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. GGD, KRT5
27  2009 Changing a concept--controversy on the confusing spectrum of the reticulate pigmented disorders of the skin. GGD
28  2007 A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease. ---
29  2007 Generalized Dowling-Degos disease. ---
30  2006 Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease. KRT5
31  2005 A study of immunohistochemical and electron microscopic changes in Dowling-Degos disease. ---
32  2004 Hidradenitis suppurativa, Dowling-Degos and multiple epidermal cysts: a new follicular occlusion triad. HS
33  2000 A case of Dowling-Degos disease suggesting an evolutional sequence. RAK
34  1999 Dowling-Degos disease (reticulate pigmented anomaly of the flexures): a clinical and histopathologic study of 6 cases. ---
35  1998 Overlap of reticulate acropigmentation of Kitamura, acropigmentation of Dohi and Dowling-Degos disease in four generations. APD, RAPK
36  1994 Spectrum of reticulate flexural and acral pigmentary disorders in northern India. RAPK
37  1993 Reticulate acropigmentation of Kitamura: two case reports. RAK