Works matching DE "PALMOPLANTAR keratoderma"

Results: 731

Demographic, clinical, and scintigraphic comparison of patients affected by palmoplantar pustulosis and severe acne: a retrospective study.

Published in:

Clinical Rheumatology, 2020, v. 39, n. 6, p. 1989, doi. 10.1007/s10067-019-04904-8

By:

Li, Yueting;
Li, Chen;
Wu, Nan;
Li, Feng;
Wu, Zhihong;
Sun, Xiaochuan;
Li, Qiyi;
Li, Li

Publication type:

Article

Sistemik isotretinoin ile başarılı bir şekilde tedavi edilen idiyopatik palmoplantar filiform hiperkeratozis.

Published in:

Turkish Archives of Dermatology & Venerology / Turkderm, 2019, v. 53, n. 3, p. 119, doi. 10.4274/turkderm.galenos.2018.34466

By:

Korkmaz, Selma;
Erturan, İjlal;
Filiz, Başak;
Karahan, Nermin;
Ciriş, İbrahim Metin;
Yıldırım, Mehmet

Publication type:

Article

A Novel Heterozygous Desmoplakin Variant Causes Cardiocutaneous Syndrome with Arrhythmogenic Cardiomyopathy and Palmoplantar Keratosis.

Published in:

2023

By:

Çimen, Tolga;
Medeiros-Domingo, Argelia;
Kolios, Antonios;
Akdiş, Deniz;
Anwer, Shehab;
Tanner, Felix C.;
Brunckhorst, Corinna;
Duru, Firat;
Saguner, Ardan M.

Publication type:

Case Study

Topographic Differential Diagnosis of Chronic Plaque Psoriasis: Challenges and Tricks.

Published in:

Journal of Clinical Medicine, 2020, v. 9, n. 11, p. 3594, doi. 10.3390/jcm9113594

By:

Gisondi, Paolo;
Bellinato, Francesco;
Girolomoni, Giampiero

Publication type:

Article

Keratolytic Winter Erythema: An Update.

Published in:

Dermatopathology, 2019, v. 6, n. 2, p. 126, doi. 10.1159/000496338

By:

Ramsay, Michèle;
Ngcungcu, Thandiswa;
Grayson, Wayne

Publication type:

Article

Treatment of a chronic skin lesion in the lower limb in Meleda disease.

Published in:

Journal of Wound Care, 2022, v. 31, n. 3, p. 224, doi. 10.12968/jowc.2022.31.3.224

By:

Nebbioso, Giuseppe;
Nebbioso, Viviana;
Petrella, Francesco

Publication type:

Article

Pack-year cigarette smoking affects the course of palmoplantar pustulosis.

Published in:

Advances in Clinical & Experimental Medicine, 2021, v. 30, n. 2, p. 189, doi. 10.17219/acem/131750

By:

Putra-Szczepaniak, Magdalena;
Reich, Adam;
Jankowska-Konsur, Alina;
Czarnecka, Anna;
Bagłaj-Oleszczuk, Marta;
Hryncewicz-Gwóźdź, Anita

Publication type:

Article

Palmoplantar pustulosis: Factors causing and influencing the course of the disease.

Published in:

Advances in Clinical & Experimental Medicine, 2020, v. 29, n. 1, p. 157, doi. 10.17219/acem/112613

By:

Putra-Szczepaniak, Magdalena;
Maj, Joanna;
Jankowska-Konsur, Alina;
Czarnecka, Anna;
Hyncewicz-Gwóźdź, Anita

Publication type:

Article

Cutaneous adverse events associated with BRAF and MEK inhibitors: a systematic review and meta-analysis.

Published in:

2025

By:

Qian, Junhui;
Wan, Jinlong;
Yao, Qin;
Chen, Yin;
Ling, Tao;
Zhang, Yuejuan;
Tang, Zhihua

Publication type:

Literature Review

A real-world pharmacovigilance study of Sorafenib based on the FDA Adverse Event Reporting System.

Published in:

Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1442765

By:

Zhang, Dongdong;
Cai, Ying;
Sun, Yixin;
Zeng, Peiji;
Wang, Wei;
Wang, Wenhui;
Jiang, Xiaohua;
Lian, Yifan

Publication type:

Article

Involvement of palms and soles in patients with autoimmune bullous diseases: a comparative analysis of a diagnostically relevant localization.

Published in:

Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1227855

By:

Jałowska, Magdalena;
Spałek, Maciej;
Bowszyc-Dmochowska, Monika;
Porowska, Justyna Gornowicz;
Dmochowski, Marian

Publication type:

Article

Dental prosthetic rehabilitation of Papillon-Lefèvre syndrome: a case report.

Published in:

Clinics & Practice, 2020, v. 10, n. 3, p. 78, doi. 10.4081/cp.2020.1285

By:

Patil, Shweta M.;
Metkari, Suryakant B.;
Shetty, Shilpa;
Thakkannavar, Savita;
Sarode, Sachin C.;
Sarode, Gargi S.;
Sengupta, Namrata;
Patil, Shankargouda

Publication type:

Article

Baricitinib rapidly improves mechanic's hands and hiker's feet in anti-synthetase syndrome.

Published in:

2024

By:

Hu, Hongming;
Wang, Shasha

Publication type:

Case Study

Successful treatment of severe pityriasis rubra pilaris with secukinumab in a 3‐year‐old boy.

Published in:

Clinical & Experimental Dermatology, 2022, v. 47, n. 11, p. 2043, doi. 10.1111/ced.15353

By:

Xu, Yong‐Hui;
Dong, Dan‐Dan;
Lin, Yu‐Feng;
Wang, Qian;
Huang, Liang‐Mei;
Shi, Jian‐Qiang

Publication type:

Article

Ichthyosis follicularis syndromes in patients with mutations in GJB2.

Published in:

Clinical & Experimental Dermatology, 2022, v. 47, n. 8, p. 1561, doi. 10.1111/ced.15217

By:

Youssefian, Leila;
Naji, Mahtab;
Park, Jason S.;
Rajabi, Fateme;
Abdollahimajd, Fahimeh;
Mahmoudi, Hamidreza;
Kamyab‐Hesari, Kambiz;
Ghalamkarpour, Fariba;
Zabihi, Masoud;
Teimoorian, Mehrdad;
Youssefian, Laya;
Zeinali, Sirous;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Identification of clinically useful predictive genetic variants in pachyonychia congenita.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 5, p. 867, doi. 10.1111/ced.14569

By:

Samuelov, L.;
Sarig, O.;
Adir, N.;
Pavlovsky, M.;
Smith, F. J.;
Schwartz, J.;
Hansen, C. D.;
Sprecher, E.

Publication type:

Article

Molecular epidemiology of pachyonychia congenita in the Israeli population.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 4, p. 663, doi. 10.1111/ced.14509

By:

Pavlovsky, M.;
Peled, A.;
Samuelov, L.;
Malki, L.;
Malovitski, K.;
Assaf, S.;
Mohamad, J.;
Meijers, O.;
Eskin‐Schwartz, M.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Chalk‐white fluorescence under Wood light in a case of terra firma‐forme dermatosis.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 1, p. 165, doi. 10.1111/ced.14354

By:

Ozturk Durmaz, E.

Publication type:

Article

Palmoplantar keratoderma caused by a missense variant in CTSB encoding cathepsin B.

Published in:

Clinical & Experimental Dermatology, 2021, v. 46, n. 1, p. 103, doi. 10.1111/ced.14384

By:

Mohamad, J.;
Samuelov, L.;
Malki, L.;
Peled, A.;
Pavlovsky, M.;
Malovitski, K.;
Taiber, S.;
Adir, N.;
Rabinowitz, T.;
Shomron, N.;
Milner, J. D.;
Lestringant, G.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

A unique 'hand in bucket' sign in a case of acquired unilateral aquagenic syringeal acrokeratoderma.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 8, p. 1100, doi. 10.1111/ced.14338

By:

Narang, I.;
Mohandas, P.;
Hawari, R.;
Nambi, R.

Publication type:

Article

A novel frameshift truncation mutation in the V2 tail domain of KRT1 causes mild ichthyosis hystrix of Curth–Macklin.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 6, p. 719, doi. 10.1111/ced.14193

By:

Yang, Z.;
Xu, Z.;
Zhang, N.;
Ma, L.

Publication type:

Article

Identification of putative genetic modifying factors that influence the development of Papillon–Lefévre or Haim–Munk syndrome phenotypes.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 5, p. 555, doi. 10.1111/ced.14171

By:

Pap, É. M.;
Farkas, K.;
Tóth, L.;
Fábos, B.;
Széll, M.;
Németh, G.;
Nagy, N.

Publication type:

Article

An unusual manifestation of X‐linked hypohidrotic ectodermal dysplasia with palmoplantar keratoderma.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 3, p. 352, doi. 10.1111/ced.14096

By:

De Brito, M.;
Ferguson, L.;
Mansour, S.;
Khan, I.

Publication type:

Article

Molecular detection of fungal and bacterial DNA from pustules in patients with palmoplantar pustulosis: special focus on Malassezia species.

Published in:

Clinical & Experimental Dermatology, 2020, v. 45, n. 1, p. 36, doi. 10.1111/ced.14026

By:

Matsumoto, Y.;
Harada, K.;
Maeda, T.;
Egusa, C.;
Hirano, H.;
Okubo, Y.;
Tsuboi, R.

Publication type:

Article

A systematic review of reported cases of pachyonychia congenita tarda.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 6, p. 606, doi. 10.1111/ced.13980

By:

Tatiane, A.;
Slape, D.;
Lawless, R.;
Frew, J. W.

Publication type:

Article

Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 5, p. 528, doi. 10.1111/ced.13800

By:

Smith, F. J. D.;
Kreuser‐Genis, I. M.;
Jury, C. S.;
Wilson, N. J.;
Terron‐Kwiatowski, A.;
Zamiri, M.

Publication type:

Article

Loricrin palmoplantar keratoderma: full‐thickness skin grafting for pseudoainhum.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 4, p. 444, doi. 10.1111/ced.13770

By:

Zamiri, M.;
Watson, S.

Publication type:

Article

Palmoplantar keratoderma Bothnia type with acrokeratoelastoidosis‐like features due to AQP5 mutations.

Published in:

Clinical & Experimental Dermatology, 2019, v. 44, n. 1, p. 88, doi. 10.1111/ced.13747

By:

Pan, Y.;
Men, Y.;
Lin, Z.

Publication type:

Article

A novel frameshift SERPINB7 mutation in a Chinese case with Nagashima‐type palmoplantar keratosis: case report and review of the literature.

Published in:

2018

By:

Hua, S.;
Miao, X.;
Mao, W.;
Hua, L.;
Chen, J.;
Li, B.

Publication type:

Case Study

Inherited palmoplantar keratodermas: the heart of the matter.

Published in:

2018

By:

Thomas, L. J.;
Freeman, A.;
O'Toole, E. A.;
McGrath, J. A.;
Perrett, C. M.

Publication type:

Case Study

Erythema elevatum diutinum presenting with palmoplantar keratoderma.

Published in:

Clinical & Experimental Dermatology, 2017, v. 42, n. 5, p. 573, doi. 10.1111/ced.13103

By:

Kamyab, K.;
Balighi, K.;
Azizpour, A.;
Khani, S.;
Safar, F.

Publication type:

Article

Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma.

Published in:

Clinical & Experimental Dermatology, 2017, v. 42, n. 3, p. 316, doi. 10.1111/ced.13049

By:

Dinani, N.;
Ali, M.;
Liu, L.;
McGrath, J.;
Mellerio, J.

Publication type:

Article

Clinical and molecular characterization of two patients with palmoplantar keratoderma-congenital alopecia syndrome type 2.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 6, p. 632, doi. 10.1111/ced.12857

By:

Castori, M.;
Morlino, S.;
Sana, M. E.;
Paradisi, M.;
Tadini, G.;
Angioni, A.;
Malacarne, M.;
Grammatico, P.;
Iascone, M.;
Forzano, F.

Publication type:

Article

Malignant melanoma in a patient with mal de Meleda.

Published in:

Clinical & Experimental Dermatology, 2016, v. 41, n. 4, p. 437, doi. 10.1111/ced.12791

By:

Vilas‐Sueiro, A.;
Rosón, E.;
Suárez‐Peñaranda, J.‐M.;
Vázquez‐Osorio, I.;
Sánchez‐Aguilar, D.;
Vázquez‐Veiga, H.

Publication type:

Article

Olmsted syndrome in an Iranian boy with a new de novo mutation in TRPV3.

Published in:

Clinical & Experimental Dermatology, 2014, v. 39, n. 4, p. 492, doi. 10.1111/ced.12318

By:

Kariminejad, A.;
Barzegar, M.;
Abdollahimajd, F.;
Pramanik, R.;
McGrath, J. A.

Publication type:

Article

A novel splice-site mutation in the AAGAB gene segregates with hereditary punctate palmoplantar keratoderma and congenital dysplasia of the hip in a large family.

Published in:

Clinical & Experimental Dermatology, 2014, v. 39, n. 2, p. 182, doi. 10.1111/ced.12213

By:

Eytan, O.;
Sarig, O.;
Israeli, S.;
Mevorah, B.;
Basel‐Vanagaite, L.;
Sprecher, E.

Publication type:

Article

Recurrent splice-site mutation in MBTPS2 underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patient.

Published in:

Clinical & Experimental Dermatology, 2014, v. 39, n. 2, p. 158, doi. 10.1111/ced.12248

By:

Wang, H. J.;
Tang, Z. L.;
Lin, Z. M.;
Dai, L. L.;
Chen, Q.;
Yang, Y.

Publication type:

Article

Papules on the hands and feet.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 8, p. 949, doi. 10.1111/ced.12142

By:

Sharma, A.;
Goulding, J. M. R.

Publication type:

Article

Ectodermal dysplasia-skin fragility syndrome: a novel mutation in the PKP1 gene.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 7, p. 787, doi. 10.1111/ced.12109

By:

Hernández‐Martín, A.;
Torrelo, A.;
Ciria, S.;
Colmenero, I.;
Aguilar, A.;
Grimalt, R.;
González‐Sarmiento, R.

Publication type:

Article

Multiple palmoplantar angiokeratomas.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 6, p. 670, doi. 10.1111/ced.12043

By:

Smith, V. M.;
Lyon, C. C.

Publication type:

Article

Collodion baby and loricrin keratoderma: a case report and mutation analysis.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 2, p. 147, doi. 10.1111/j.1365-2230.2012.04426.x

By:

Yeh, J. M.;
Yang, M. H.;
Chao, S. C.

Publication type:

Article

Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9.

Published in:

Clinical & Experimental Dermatology, 2013, v. 38, n. 2, p. 189, doi. 10.1111/ced.12059

By:

Fuchs‐Telem, D.;
Padalon‐Brauch, G.;
Sarig, O.;
Sprecher, E.

Publication type:

Article

Resolution of paraneoplastic palmoplantar keratoderma after treating mixed serous neuroendocrine tumor of the pancreas: a case report and literature review.

Published in:

Dermatology Reports, 2024, v. 16, n. 4, p. 32, doi. 10.4081/dr.2024.9906

By:

Alotaibi, Hend M.;
Alluhaybi, Abdulrahman;
Nagshabandi, Khalid Nabil;
Barakeh, Maha M.

Publication type:

Article

Resolution of paraneoplastic palmoplantar keratoderma after treating mixed serous neuroendocrine tumor of the pancreas: a case report and literature review.

Published in:

2024

By:

Alotaibi, Hend M.;
Alluhaybi, Abdulrahman;
Nagshabandi, Khalid Nabil;
Barakeh, Maha M.

Publication type:

Case Study

Genetic analysis of seven patients with inherited ichthyosis and Nagashima‑type palmoplantar keratoderma.

Published in:

2024

By:

Zhang, Jing;
Yao, Yue;
Tan, Ya;
Hu, Hua-Ying;
Zeng, Lin-Xi;
Zhang, Guo-Qiang

Publication type:

Case Study

Nagashima-type palmoplantar keratosis in a Chinese Han population.

Published in:

Molecular Medicine Reports, 2016, v. 14, n. 5, p. 4049, doi. 10.3892/mmr.2016.5757

By:

JIA ZHANG;
GUOLONG ZHANG;
CHENG NI;
RUHONG CHENG;
JIANYING LIANG;
MING LI;
ZHIRONG YAO

Publication type:

Article

Papillon-Lefèvre Syndrome and Basal Cell Carcinoma: A Case Study.

Published in:

Case Reports in Oncology, 2019, v. 12, n. 2, p. 411, doi. 10.1159/000500502

By:

Alsaif, Fahad M.;
Arafah, Maria A.;
Alenazi, Rasha T.;
Alotaibi, Ghadah F.

Publication type:

Article

A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the<bold><italic> R-spondin1 </italic></bold>Gene Associated with Familial 46,XX DSD.

Published in:

Sexual Development, 2017, v. 11, n. 5/6, p. 269, doi. 10.1159/000485393

By:

Naasse, Yassine;
Bakhchane, Amina;
Charoute, Hicham;
Jennane, Farida;
Bignon-Topalovic, Joelle;
Malki, Abderrahim;
Bashamboo, Anu;
Barakat, Abdelhamid;
Rouba, Hassan;
McElreavey, Ken

Publication type:

Article

Thickened nails.

Published in:: Journal of Paediatrics & Child Health, 2023, v. 59, n. 4, p. 703, doi. 10.1111/jpc.1_16057
Publication type:: Article

A young girl with curly hair.

Published in:: 2020
Publication type:: journal article