Works matching DE "DOWLING-Degos disease"

Results: 37

Dowling-degos Disease: A Case Report.

Published in:

2021

By:

Erhan, Selma Şengiz;
Yüksel, Tülin;
Zerk, Pınar Engin

Publication type:

Case Study

Una nueva visión clínica y etiopatogénica de la enfermedad de Dowling-Degos.

Published in:: 2014
Publication type:: Case Study

Dowling-Degos disease and malignant melanoma: Association or mere coincidence?

Published in:

2015

By:

Gupta, Vishal;
Sahni, Kanika;
Khute, Prakash;
Sharma, Vinod K.;
Ali, Mohammad Firdaus

Publication type:

Case Study

Follicular Dowling Degos disease: A rare variant of an evolving dermatosis.

Published in:

2013

By:

Singh, Saurabh;
Khandpur, Sujay;
Verma, Parul;
Singh, Manoj

Publication type:

Case Study

Clinico-pathological correlation of localised Dowling-Degos disease.

Published in:

Saudi Journal for Health Sciences, 2015, v. 4, n. 1, p. 129, doi. 10.4103/2278-0521.157892

By:

Warpe, Bhushan Malhari

Publication type:

Article

Progesterone Receptor Status and Ki-67 Index May Predict Early Relapse in Luminal B/HER2 Negative Breast Cancer Patients: A Retrospective Study.

Published in:

PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0095629

By:

Zong, Yu;
Zhu, Li;
Wu, Jiayi;
Chen, Xiaosong;
Huang, Ou;
Fei, Xiaochun;
He, Jianrong;
Chen, Weiguo;
Li, Yafen;
Shen, Kunwei

Publication type:

Article

Successful Management of Dowling-Degos Disease with Combination of Q-switched Nd: YAG and Fractional Carbon Dioxide Laser.

Published in:

2017

By:

Tambe, Swagata Arvind;
Patil, Priyanka Deelip;
Saple, Dattatray Gopal

Publication type:

Case Study

Progressive cribriform and zosteriform hyperpigmentation: a histologic mimicker of Dowling-Degos disease?

Published in:

Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2022, v. 39, n. 5, p. 986, doi. 10.5114/ada.2022.120889

By:

Cong Liu;
Hui-Hui JI;
Cheng Tan

Publication type:

Article

Middle of the breasts pigmentation in a pedigree with POFUT1-related Dowling-Degos disease, expansion of the phenotype.

Published in:

2021

By:

Yingda Wu;
Wanlu Zhang;
Jianbing Wu;
Yiping Ma;
Pangen Cui;
Chengrang Li

Publication type:

Case Study

Retraction: Acropigmentation of Kitamura with immigration delay disease: A rare entity.

Published in:: 2016
Publication type:: Correction Notice

Atypical cases of Dowling-Degos disease.

Published in:

2016

By:

Naveen, Kikkeri Narayanshetty;
Athaniker, Sharatchandra B.;
Hegde, Spandana P.;
Shetty, Rahul;
Radha, Hanumanthayya;
Parinitha, Sadashivappa Sangam

Publication type:

Case Study

Dowling-Degos disease with reticulate acropigmentation of Kitamura: Extended spectrum of a single entity.

Published in:

2016

By:

Rathoriya, Shyam Govind;
Soni, Sumit S. L.;
Asati, Dinesh

Publication type:

Case Study

Acral freckling with palmar pits.

Published in:

2015

By:

Adya, Keshavmurthy A.;
Inamadar, Arun C.;
Palit, Aparna

Publication type:

Case Study

Acropigmentation of Kitamura with immigration delay disease: A rare entity.

Published in:

2015

By:

Kumar, Sumir;
Mahajan, Bharat Bhushan;
Kamra, Nidhi;
Bhoyar, Pritish A.

Publication type:

Case Study

Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa.

Published in:

2017

By:

Ralser, Damian J.;
Basmanav, F. Buket Ü.;
Tafazzoli, Aylar;
Wititsuwannakul, Jade;
Delker, Sarah;
Danda, Sumita;
Thiele, Holger;
Wolf, Sabrina;
Busch, Michélle;
Pulimood, Susanne A.;
Altmüller, Janine;
Nürnberg, Peter;
Lacombe, Didier;
Hillen, Uwe;
Wenzel, Jörg;
Frank, Jorge;
Odermatt, Benjamin;
Betz, Regina C.

Publication type:

journal article

Successful treatment of Dowling- Degos disease using intense pulsed light.

Published in:

Australasian Journal of Dermatology, 2015, v. 56, n. 3, p. e63, doi. 10.1111/ajd.12232

By:

Gupta, Aakriti;
Huilgol, Shyamala C

Publication type:

Article

Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura.

Published in:

Journal of Investigative Dermatology, 2015, v. 135, n. 2, p. 615, doi. 10.1038/jid.2014.406

By:

Basmanav, F Buket;
Fritz, Günter;
Lestringant, Gilles G;
Pachat, Divya;
Hoffjan, Sabine;
Fischer, Johannes;
Wehner, Maria;
Wolf, Sabrina;
Thiele, Holger;
Altmüller, Janine;
Pulimood, Susanne A;
Rütten, Arno;
Kruse, Roland;
Hanneken, Sandra;
Frank, Jorge;
Danda, Sumita;
Bygum, Anette;
Betz, Regina C

Publication type:

Article

Reflectance confocal microscopy for the diagnosis of Galli-Galli disease.

Published in:

International Journal of Dermatology, 2017, v. 56, n. 12, p. 1501, doi. 10.1111/ijd.13677

By:

Coelho de Sousa, Vírginia;
El‐Shabrawi‐Caelen, Laila;
Mendes‐Bastos, Pedro;
Oliveira, André

Publication type:

Article

Dowling-Degos disease: a classic presentation of a rare disease.

Published in:

Pigment International, 2025, v. 12, n. 1, p. 57, doi. 10.4103/pigmentinternational_26_22

By:

Das, Abhijit;
Dhabal, Arunima;
Malakar, Arpita;
Kar, Chinmay

Publication type:

Article

Speckled acral hypopigmentation in an adolescent.

Published in:

Pediatric Dermatology, 2018, v. 35, n. 1, p. e57, doi. 10.1111/pde.13341

By:

Rutt, Veronica L.;
Quinn, Kelly B.;
Zaenglein, Andrea

Publication type:

Article

Vesicular variant of Dowling–Degos disease.

Published in:

2018

By:

Linke, M.;
Orouji, A.;
Géraud, C.

Publication type:

Case Study

Novel <italic>POFUT1</italic> mutation associated with hidradenitis suppurativa–Dowling–Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors.

Published in:

2018

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Hafner, A.;
Sprecher, E.

Publication type:

Letter to the Editor

A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. e160, doi. 10.1111/bjd.16285

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Malchin, N.;
Bochner, R.;
Mohamad, J.;
Gat, A.;
Peled, A.;
Hafner, A.;
Sprecher, E.

Publication type:

Article

Concurrent hidradenitis suppurativa and Dowling–Degos disease taken down a ‘Notch’.

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. 328, doi. 10.1111/bjd.16068

By:

McGrath, J. A.

Publication type:

Article

A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.

Published in:

British Journal of Dermatology, 2018, v. 178, n. 2, p. 502, doi. 10.1111/bjd.16000

By:

Pavlovsky, M.;
Sarig, O.;
Eskin‐Schwartz, M.;
Malchin, N.;
Bochner, R.;
Mohamad, J.;
Gat, A.;
Peled, A.;
Hafner, A.;
Sprecher, E.

Publication type:

Article

Updated review of genetic reticulate pigmentary disorders.

Published in:

British Journal of Dermatology, 2017, v. 177, n. 4, p. 945, doi. 10.1111/bjd.15575

By:

Zhang, J.;
Li, M.;
Yao, Z.

Publication type:

Article

Mutations in POGLUT1 in Galli-Galli/Dowling-Degos disease.

Published in:

British Journal of Dermatology, 2017, v. 176, n. 1, p. 270, doi. 10.1111/bjd.14914

By:

Wilson, N.J.;
Cole, C.;
Kroboth, K.;
Hunter, W.N.;
Mann, J.A.;
McLean, W.H.I.;
Kernland Lang, K.;
Beltraminelli, H.;
Sabroe, R.A.;
Tiffin, N.;
Sobey, G.J.;
Borradori, L.;
Simpson, E.;
Smith, F.J.D.

Publication type:

Article

Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease.

Published in:

British Journal of Dermatology, 2016, v. 174, n. 3, p. 663, doi. 10.1111/bjd.14178

By:

Li, M.;
Wang, J.;
Zhang, J.;
Ni, C.;
Li, X.;
Liang, J.;
Cheng, R.;
Li, Z.;
Yao, Z.

Publication type:

Article

Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.

Published in:

British Journal of Dermatology, 2015, v. 173, n. 2, p. 584, doi. 10.1111/bjd.13702

By:

Kono, M.;
Suganuma, M.;
Takama, H.;
Zarzoso, I.;
Saritha, M.;
Bodet, D.;
Aboobacker, S.;
Kaliaperumal, K.;
Suzuki, T.;
Tomita, Y.;
Sugiura, K.;
Akiyama, M.

Publication type:

Article

Association of Dowling-Degos disease and multiple seborrheic keratosis in a "Christmas tree pattern".

Published in:

Medical Journal of the Islamic Republic of Iran, 2014, v. 28, p. 1

By:

dos Santos, Vitorino Modesto;
dos Santos Pereira, Nayanne Lays;
Silva, Renata Faria;
de Oliveira Silva, Fabio Henrique;
Ferreira da Silva Garcia, Cacilda Joyce;
de Figueiredo Sousa, Maria Aparecida Alves

Publication type:

Article

Galli–Galli disease successfully treated with alitretinoin.

Published in:

2019

By:

Deenen, N.J.;
Damman, J.;
Nijsten, T.E.C.

Publication type:

Case Study

A new nonsense mutation in the POGLUT1 gene in two sisters with Dowling–Degos disease.

Published in:

2018

By:

Duchatelet, S.;
Clerc, H.;
Machet, L.;
Gaboriaud, P.;
Miskinyte, S.;
Kervarrec, T.;
Hovnanian, A.

Publication type:

Case Study

Dowling–Degos disease with mutation in the exon 1 of the keratin 5 gene.

Published in:

2018

By:

Yu, W.;
Gan, L.;
Wu, J.;
Sun, J.;
Jiang, Y.

Publication type:

Case Study

Recognizing syndromic hidradenitis suppurativa: a review of the literature.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 11, p. 1809, doi. 10.1111/jdv.14464

By:

Gasparic, J.;
Theut Riis, P.;
Jemec, G.B.

Publication type:

Article

Pathogenicity of POFUT1 mutations in two Chinese families with Dowling-Degos disease.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2016, v. 30, n. 10, p. e79, doi. 10.1111/jdv.13323

By:

Li, C. ‐ R.;
Brooks, Y.S.;
Jia, W. ‐ X.;
Wang, D. ‐ G.;
Xiao, X. ‐ M.;
Li, Q.;
Li, M.;
Mao, Q. ‐ X.;
Wang, B.

Publication type:

Article

The First Report of KRT5 Mutation Underlying Acantholytic Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family.

Published in:

Indian Journal of Dermatology, 2014, v. 59, n. 5, p. 476, doi. 10.4103/0019-5154.139884

By:

Verma, Shyam;
Pasternack, Sandra M.;
Rütten, Arno;
Ruzicka, Thomas;
Betz, Regina C.;
Hanneken, Sandra

Publication type:

Article

A Case of Reticulate Acropigmentation of Kitamura: Dowling Degos Disease Overlap with Unusual Clinical Manifestations.

Published in:

Indian Journal of Dermatology, 2014, v. 59, n. 3, p. 290, doi. 10.4103/0019-5154.131408

By:

Vasudevan, Biju;
Verma, Rajesh;
Badwal, Sonia;
Pragasam, Vijendran;
Moorchung, Nikhil;
Badad, Ambresh

Publication type:

Article