T. Deinlein
doi : 10.1111/jdv.17141
Volume 35, Issue 3 p. 566-566
The clinical and dermoscopic differentiation between early melanomas and atypical naevi remains challenging, especially in patients with multiple pigmented lesions and in lesions with worrisome clinical and/or dermoscopic features. Several (site-related) melanoma-specific criteria and standardized algorithms are described and increased early melanoma recognition remarkably. However, none of these approaches considered the lesion’s location and the amount of sun exposure as important factors on their clinical and dermoscopic appearance.1, 2
T. Shiohara
doi : 10.1111/jdv.17138
Volume 35, Issue 3 p. 567-568
Severe adverse drug reactions (ADRs) encompass two distinct clinical entities, the most common being drug-induced hypersensitivity syndrome (DiHS)/drug reaction with eosinophilia and systemic symptoms (DRESS). Another one is Stevens–Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN). The two forms of severe ADRs likely exhibit individually distinctive pathogenic mechanisms, although some of causative drugs are common. DiHS/DRESS is characterized by sequential reactivations of herpesviruses associated with further progression of defects of regulatory T cells (Tregs),1 while SJS/TEN is characterized by aberrant activation of effector T cells.2 Wen-Hung Chung et al.3 have found a striking association between HLA-B*33:03 allele and strontium ranelate (SR)-induced SJS. Previous studies, however, demonstrated that many sensitive carriers with a specific HLA phenotype are unlikely to develop severe ADRs upon drug intake. These findings suggest that multiple factors, other than HLA allele, which modulate immune responses, may determine the disease phenotype. Consistent with this view, the clinical phenotype may vary with time and some patients with a mild form of ADRs have been reported to evolve into SJS/TEN. Indeed, evidence has linked the specific HLA alleles with the subsequent risk of developing ADRs, but not specific to DiHS/DRESS or SJS/TEN. In this regard, we demonstrated that HLA-A*31:01 has been linked to carbamazepine (CBZ)-induced ADRs in Japanese,4 northern Europeans and southern Chinese populations. Thus, the HLA-A*31:01 appears to be a specific marker for CBZ-induced ADRs but not necessarily a specific marker for CBZ-induced SJS or DiHS/DRESS.
J. Uitto
doi : 10.1111/jdv.17142
Volume 35, Issue 3 p. 569-571
N. Kluger
doi : 10.1111/jdv.16937
Volume 35, Issue 3 p. 572-573
M. Janier, M. Unemo, N. Dupin, G.S. Tiplica, M. Poto?nik, R. Patel
doi : 10.1111/jdv.16946
Volume 35, Issue 3 p. 574-588
The 2020 edition of the European guideline on the management of syphilis is an update of the 2014 edition.
H.C. Lee, C.L. Goh
doi : 10.1111/jdv.16925
Volume 35, Issue 3 p. 589-596
The COVID-19 pandemic has enveloped the world and there has been a high incidence of occupational dermatoses related to Personal Protective Equipment (PPE) amongst healthcare workers (HCWs) during this period. Prevention and management of these conditions will not only improve staff morale and quality of life, but will also minimize the risk of breaching PPE protocol due to such symptoms. The tropical climate in Singapore predisposes HCWs to more skin damage and pruritus due to intense heat, high humidity and sun exposure. The effects of friction, occlusion, hyperhidrosis and overheating on the skin in the tropics should not be neglected. Preventive measures can be taken based on our recommendations, and the working environment can be made more conducive for frontline HCWs. We review the literature and discuss various preventive and management strategies for these occupational skin diseases for our frontline HCWs, especially those working in less controlled working environments beyond the hospital in Singapore. Shorter shifts and frequent breaks from PPE are recommended. Duration of continuous PPE-usage should not exceed 6 h, with breaks in non-contaminated areas every 2–3 h to hydrate and mitigate the risk of skin reactions. Other strategies, such as teledermatology, should be considered so that consultations can remain accessible, while ensuring the safety and well-being of our clinical staff.
Y. Mostmans, B. Richert, V. Badot, C. Nagant, V. Smith, O. Michel
doi : 10.1111/jdv.16813
Volume 35, Issue 3 p. 597-606
Since the field around morphea and systemic sclerosis (SSc) is evolving rapidly, this review approaches conventional as well as more recent clinical developments from a dermatological point of view. Skin manifestations are critical in sub-classifying these diseases ensuring a correct prognosis for these patients. They can be discretely present, and therefore, diagnosis can be challenging sometimes, implicating a thorough dermatological examination is mandatory. Furthermore, a growing amount of dermatologists perform nailfold videocapillaroscopy (NVC), a more recent reliable non-invasive imaging technique used for in vivo assessment of the microcirculation at the nailfold. After all, specific NVC-changes are present in a majority of patients with SSc. This way, dermatologists not only take part in the diagnosis process through clinical investigation but also through the use of a modern state of the art imaging technique that is becoming the golden standard in SSc multidisciplinary workup. In this review, current understandings for NVC in morphea and SSc are revised. So far, the role of NVC in the diagnosis/prognosis/classification of morphea patients has not been thoroughly investigated to make proper conclusions. As for SSc, it is well known that NVC contributes to the diagnosis and can make a fundamental difference especially when obvious clinical SSc signs are absent. This review emphasizes the (somewhat underestimated) role of dermatologists in the process of diagnosis and follow-up, and thus, the difference we can make for our patients and fellow colleagues in the multidisciplinary workup of SSc and morphea.
I. Torres-Navarro, B. de Unamuno-Bustos, R. Botella-Estrada
doi : 10.1111/jdv.16894
Volume 35, Issue 3 p. 607-614
Severe cutaneous adverse reactions (SCARs) [Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug rash with eosinophilia and systemic syndrome (DRESS), acute generalized exanthematous pustulosis (AGEP), and generalized bullous fixed eruption (GBFE)] are severe drug reactions that often require hospitalization and could be fatal. BRAF and MEK inhibitors (BRAF/MEKi) are a standard of care in patients with BRAF-mutated metastatic melanomas. These agents are administered until disease progression or unacceptable toxicity occurs. This review has focus on BRAF/MEKi-induced SCARs. A systematic search of the following terms: ‘vemurafenib’, ‘cobimetinib’, ‘dabrafenib’, ‘trametinib’, ‘encorafenib’, ‘binimetinib’, ‘Acute Generalized Exanthematous Pustulosis’, ‘Stevens Johnson syndrome’, ‘Toxic Epidermal Necrolysis’, ‘Generalized Bullous Fixed Eruption’ ‘Drug Hypersensitivity Syndrome’, and ‘DRESS’ in simple combination (every drug with each disease) and all in combination, was performed on MEDLINE, EMBASE, Web of Knowledge and The Cochrane Library repositories, with no restriction on language, for original studies. One hundred sixty-eight original articles were found, 26 (retrospective series, case reports and conference abstracts) were selected, and 21 were included in the qualitative synthesis. A total of 31 SCAR cases (23 DRESS and 8 SJS/TEN – 1 SJS and 7 TEN –) were identified. Vemurafenib was the culprit drug in all but one case, which was dabrafenib-induced. Mean time to SCAR onset from drug intake was 15.5 and 11.4 days, for SJS/TEN and DRESS, respectively. For the DRESS cases, hepatic involvement occurred in 96% and renal alterations in 87% of patients. Overall, BRAF/MEKi-induced SCARs are rare. Among them, vemurafenib is the drug that requires more close monitoring for SCARs. Prior immunotherapy can favour SCARs. Vemurafenib DRESS is likely to occur within the first fifteen days of treatment accompanied by hepatic and renal involvement. Following vemurafenib-induced SCAR resolution, switching to dabrafenib seems to be a safe alternative for these patients’ treatment.
I.M. Mukovozov, D.E. Morra, D. Giustini, M. Tadrous, A.M. Cheung, A.M. Drucker
doi : 10.1111/jdv.16895
Volume 35, Issue 3 p. 615-628
Atopic dermatitis (AD) is associated with systemic inflammation and systemic corticosteroid use which can lead to poor bone health. The aim of this systematic review is to investigate the relationship between AD and bone mineral density (BMD), osteoporosis and fractures. We searched Web of Science, Cochrane Database of Systematic Reviews, MEDLINE and Embase. Title, abstract and full-text screening, and data extraction were done in duplicate. Quality appraisal was performed using the Agency for Healthcare Research and Quality Methodology Checklist (cross-sectional studies) and Newcastle-Ottawa Scale (cohort studies). We screened 3800 abstracts and included fifteen studies (twelve cross-sectional, three cohort). In cross-sectional studies, AD was associated with decreased BMD and increased fractures. In cross-sectional studies and a cohort study, AD was associated with a higher prevalence of osteoporosis compared to controls. There was inconsistency across studies, with some finding no association. In a large cohort study, AD was associated with increased risk of fractures of the hip (HR: 1.06, 95% CI: 1.02 to 1.11), spine (HR: 1.14, 95% CI: 1.06 to 1.23) and wrist (HR: 1.06, 95% CI: 1.01 to 1.10), with further increased risk with more severe AD. Differences between studies precluded quantitative synthesis. There is some evidence supporting an association between AD and poor bone health. Research is needed to clarify this association, underlying mechanisms and develop strategies to improve bone health of individuals with AD.
A. Alessandrini, F. Bruni, B.M. Piraccini, M. Starace
doi : 10.1111/jdv.17079
Volume 35, Issue 3 p. 629-640
The field of hair disorders is constantly growing. The most important hair diseases are divided in non- cicatricial and cicatricial ones. Non-cicatricial alopecia are more frequent than cicatricial alopecia. The first step is to obtain a good history and physical examination. Laboratory testing is often unnecessary, while trichoscopy is fundamental for all hair diseases. Scalp biopsy is strongly suggested in cicatricial alopecia and in doubtful cases. Androgenetic alopecia, alopecia areata, telogen effluvium, trichotillomania are common causes of non- cicatricial alopecia. Frontal fibrosing alopecia, discoid lupus erythematosus, lichen planopilaris, follicullitis decalvans are some of the most common forms of cicatricial hair loss. Many treatments are available, and a prompt diagnosis is very important for the prognosis.
T. Steeb, E.A.T. Koch, A. Wessely, L.G. Wiest, L. Schmitz, C. Berking, M.V. Heppt
doi : 10.1111/jdv.16844
Volume 35, Issue 3 p. 641-649
Actinic keratosis (AK) is a common precancerous lesion of the skin that may be treated with chemical peelings. Despite their long-standing usage and clinical experience, no evidence-based recommendation regarding the efficacy and safety of chemical peelings for AK exists.
L. Tognetti, A. Cartocci, E. Cinotti, E. Moscarella, F. Farnetani, A. Lallas, D. Tiodorovic, C. Carrera, C. Longo, S. Puig, J.L. Perrot, G. Argenziano, G. Pellacani, G. Cataldo, A. Balistreri, G. Cevenini, P. Rubegni
doi : 10.1111/jdv.16847
Volume 35, Issue 3 p. 650-657
The anatomical location of atypical melanocytic skin lesion (aMSL) was never combined into an algorithm for discriminating early melanomas (EM) from atypical nevi (AN).
W. Kempf, C. Mitteldorf, M. Battistella, R. Willemze, L. Cerroni, M. Santucci, E. Geissinger, P. Jansen, M.H. Vermeer, M. Marschalko, E. Papadavid, M.A. Piris, P.L. Ortiz-Romero, M. Novelli, M. Paulli, P. Quaglino, A. Ranki, J.L. Rodr?guez Peralto, M. Wobser, B. Auschra, A. Robson
doi : 10.1111/jdv.16969
Volume 35, Issue 3 p. 658-668
Cutaneous peripheral T-cell lymphoma, not otherwise specified (PTL NOS) is an aggressive, but poorly characterized neoplasm.
B. Park, C.H. Bang, C. Lee, J.H. Han, W. Choi, J. Kim, G.S. Park, J.W. Rhie, J.H. Lee, C. Kim
doi : 10.1111/jdv.16985
Volume 35, Issue 3 p. 669-676
The Breslow depth is an important parameter to determine the excision margin and prognosis of melanoma. However, it is difficult to accurately determine the actual Breslow depth before surgery using the existing ocular micrometer and biopsy technique.
M.-A. Richard, J.-P. Lacour, M.-P. Konstantinou, M. Ruer-Mulard, P. Joly, S. Aractingi, P. Auquier, B. Pelvet, M.L. Augustin, E. Mahé, R.J.G. Chalmers
doi : 10.1111/jdv.16893
Volume 35, Issue 3 p. 677-684
The utility of the Simplified Psoriasis Index (SPI), a recently developed multidomain tool for assessing psoriasis, was investigated in a study assessing response to secukinumab.
M. ?ychowska, A. Reich, J. Maj, A. Jankowska-Konsur, J. C. Szepietowski
doi : 10.1111/jdv.16930
Volume 35, Issue 3 p. 685-692
Psoriasis is a chronic skin condition that in one third of cases starts in the first two decades of life. The disease might impact the quality of life (QoL) of the affected children and their caregivers. The issue of gender differences in the assessment of psychological burden of dermatological conditions has been the subject of few studies with contradictory results.
M.C. Fargnoli, M. Esposito, P. Dapavo, A. Parodi, M. Rossi, R. Tiberio, S. Dastoli, A.M. Offidani, G. Argenziano, P. Gisondi, A. Lo Schiavo, F. Loconsole, P. Pella, F. Bardazzi, F. Cusano, M. Gattoni, M. Nacca, S.P. Cannav?, C. Pellegrini, A. Costanzo, BRILLIANT Working Group
doi : 10.1111/jdv.16931
Volume 35, Issue 3 p. 693-700
Brodalumab was efficacious and safe in moderate-to-severe plaque-type psoriasis in the AMAGINE trials; published reports under real-life conditions are limited.
A. Pinter, M. Hoffmann, K. Reich, M. Augustin, K. Kaplan, S.D. Gudj?nsd?ttir, T. Delvin, U. Mrowietz, on behalf of the CHANGE investigator group
doi : 10.1111/jdv.16932
Volume 35, Issue 3 p. 701-711
Brodalumab is a fully human monoclonal immunoglobulin IgG2 antibody that binds to the human IL-17 receptor subunit A and by that inhibits the biologic action of IL-17A, IL-17F, IL-17C and IL-17E. Therapy with fumaric acid esters (FAE) is a well established and widely used first-line systemic treatment for subjects with moderate-to-severe plaque psoriasis.
C.-B. Chen, Y.-E. Chen, M.-T. Chu, C.-W. Wang, R. C.-Y. Hui, C.-W. Lu, Y.-P. Hsiao, C.-Y. Chu, M.M. Chang, C. M.-t. Cheung, C.-Y. Cheng, Y.-W. Wang, Y.-J. Lin, C.-J. Chang, S.-I. Hung, W.-H. Chung, the Taiwan Severe Cutaneous Adverse Reaction Consortium
doi : 10.1111/jdv.16924
Volume 35, Issue 3 p. 712-720
There is increasing use of anti-osteoporotic agents (AOA) worldwide for prevention or management of patients with osteoporosis. However, there have been reports of severe cutaneous adverse reactions (SCAR) induced by AOA. A recent study showed weak association between HLA and strontium ranelate (SR)-SCAR.
K. Weller, A. Giménez-Arnau, C. Grattan, R. Asero, P. Mathelier-Fusade, M. Bizjak, M. Hanna, M. Maurer, on behalf of the CURE Investigators
doi : 10.1111/jdv.16947
Volume 35, Issue 3 p. 721-729
Chronic urticaria (CU) is a common disease, characterized by the recurrent appearance of wheals, angioedema or both for more than 6 weeks. Its underlying biology is not well understood, and many patients do not obtain sufficient relief from recommended treatments. Patient registries are rapidly growing as a form of research, because they can provide powerful, data-driven insights about the epidemiology of diseases, real-world effectiveness of treatments, rare patient types, safety monitoring, healthcare costs and opportunities for quality improvement of healthcare delivery.
C. Svedman, M. Bruze, A. Antelmi, N. Hamnerius, I. Hauksson, J. Ulriksdotter, M. Mowitz
doi : 10.1111/jdv.16981
Volume 35, Issue 3 p. 730-737
Medical devices are increasingly being reported to cause contact allergic dermatitis reactions.
C. Zeidler, M.P. Pereira, M. Dugas, M. Augustin, M. Storck, V. Weyer-Elberich, G. Schneider, S. St?nder
doi : 10.1111/jdv.16929
Volume 35, Issue 3 p. 738-743
Chronic prurigo (CPG) is known as a high burdensome disease characterized by severe pruritus and multiple pruriginous lesions. Interestingly, the disease-specific burden is not well established and there are no data which compare the impact of CPG with chronic pruritus (CP) on non-lesional skin (CP-NL).
V.S. Narayan, S.E. Uitentuis, R.M. Luiten, M.W. Bekkenk, A. Wolkerstorfer
doi : 10.1111/jdv.16927
Volume 35, Issue 3 p. 744-748
The treatment of non-segmental vitiligo (NSV) remains a challenge. Current treatments often achieve suboptimal clinical results. To improve these treatment results, several new therapies are being developed and investigated. There is, however, little evidence on the actual need for novel therapies.
S. Meki?, C. Wigmann, D.A. Gunn, L.C. Jacobs, M. Kayser, T. Schikowski, T. Nijsten, L.M. Pardo
doi : 10.1111/jdv.17014
Volume 35, Issue 3 p. 749-754
The severity of facial telangiectasia or red veins is associated with many lifestyle factors. However, the genetic predisposition remains unclear.
E. Casassa, A. Bergeron, A. Maruani, C. Labreze, S. Barbarot, H. Aubert, J. Malloizel-Delaunay, J. Shourick, A. Croiset, I. Dreyfus, J. Mazereeuw-Hautier
doi : 10.1111/jdv.17037
Volume 35, Issue 3 p. 755-761
Very few studies have evaluated the quality of life (QoL) of children suffering from low-flow vascular malformations. This is the first study investigating the influencing factors.
A.K. Langton, J. Ayer, T.W. Griffiths, E. Rashdan, K. Naidoo, M.P. Caley, M.A. Birch-Machin, E.A. O'Toole, R.E.B. Watson, C.E.M. Griffiths
doi : 10.1111/jdv.17063
Volume 35, Issue 3 p. 762-768
Photoageing describes complex cutaneous changes which occur following chronic exposure to solar ultraviolet radiation (UVR). Amongst White Northern Europeans, facial photoageing appears as distinct clinical phenotypes: ‘hypertrophic’ photoageing (HP) and ‘atrophic’ photoageing (AP). Deep, coarse wrinkles predominate in individuals with HP, whereas those with AP have relatively smooth, unwrinkled skin with pronounced telangiectasia. AP individuals have an increased propensity for developing keratinocyte cancers.
L. Fertitta, A. Welfringer-Morin, A. Ouedrani, L. Polivka, S. Chhun, L. Chatenoud, J. Fourgeaud, S. Hadj-Rabia, S. Temmam, M. Eloit, I. Sermet-Gaudelus, C. Bodemer
doi : 10.1111/jdv.16972
Volume 35, Issue 3 p. e164-e167
M. Randolph, A. Al-alola, A. Tosti
doi : 10.1111/jdv.16989
Volume 35, Issue 3 p. e167-e168
K. Hansel, A. Zangrilli, L. Bianchi, K. Peris, A. Chiricozzi, A. Offidani, F. Diotallevi, M.C. Fargnoli, M. Esposito, P. Amerio, G. Gualdi, L. Bianchi, L. Stingeni
doi : 10.1111/jdv.17003
Volume 35, Issue 3 p. e169-e170
K.-K. Lee, C.-C. Lai, C.-M. Chao, H.-J. Tang
doi : 10.1111/jdv.17005
Volume 35, Issue 3 p. e171-e172
H.A. Miot, M. Ianhez, P. Müller Ramos
doi : 10.1111/jdv.17024
Volume 35, Issue 3 p. e172-e173
L.E.M. de Wijs, M.M. Joustra, J.I. Olydam, T. Nijsten, D.J. Hijnen
doi : 10.1111/jdv.17025
Volume 35, Issue 3 p. e173-e176
C. Chaiyabutr, T. Sukakul, C. Pruksaeakanan, J. Thumrongtharadol, W. Boonchai
doi : 10.1111/jdv.17039
Volume 35, Issue 3 p. e176-e178
Y. Zhang, J. Wen, M. Alamgir, J. Xie, H. Jing, M. Fang, J. Wang, M. Zhang, Z. Meng, L. Yang, J. Tao
doi : 10.1111/jdv.17041
Volume 35, Issue 3 p. e179-e181
O.M. Moreno-Arrones, A. Lobato-Berezo, A. Gomez-Zubiaur, S. Arias-Santiago, D. Saceda-Corralo, C. Bernardez-Guerra, R. Grimalt, P. Fernandez-Crehuet, J. Ferrando, R. Gil, A. Hermosa-Gelbard, R. Rodrigues-Barata, D. Fernandez-Nieto, S. Merlos-Navarro, S. Va??-Galv?n
doi : 10.1111/jdv.17045
Volume 35, Issue 3 p. e181-e183
D. Fernandez-Nieto, D. Ortega-Quijano, A. Suarez-Valle, J. Jimenez-Cauhe, P. Jaen-Olasolo, M. Fernandez-Guarino
doi : 10.1111/jdv.17051
Volume 35, Issue 3 p. e183-e185
S. Merhand, L. Misery, V. Delvigne, C. Le Floch, C. Taïeb
doi : 10.1111/jdv.16917
Volume 35, Issue 3 p. e185-e187
T. Gambichler, J. Reuther, M. Stücker, R. Stranzenbach, C. Torres-Reyes, R. Schlottmann, W.E. Schmidt, R. Hayajneh, A. Sriram, J.C. Becker
doi : 10.1111/jdv.16970
Volume 35, Issue 3 p. e187-e189
M.-n. Xu, L. Li, W. Pan, S.-q. Dai, Q. Wang, M.-l. Wang, K. Zeng, X.-w. Huang, K. Eyerich
doi : 10.1111/jdv.16898
Volume 35, Issue 3 p. e189-e192
C. Linder, J. Shourick, A.T Touhouche, F. Giordano-Labadie, M. Severino-Freire, C. Borjesson, C. Richet, M.C. Marguery, M. Tauber, C. Paul
doi : 10.1111/jdv.16900
Volume 35, Issue 3 p. e192-e194
S. Feuchter, M. Kunz, V. Djamei, A.A. Navarini
doi : 10.1111/jdv.16907
Volume 35, Issue 3 p. e194-e195
R. Darlenski, I. Bogdanov, M. Kacheva, D. Zheleva, Z. Demerdjieva, E. Hristakieva, J.W. Fluhr, N. Tsankov
doi : 10.1111/jdv.16908
Volume 35, Issue 3 p. e196-e198
M.C. Aichelburg, A. Pinkowicz, G. Holzer, S. Radakovic, P.-G. Sator, A. Tanew
doi : 10.1111/jdv.16909
Volume 35, Issue 3 p. e198-e200
M.F.R.G. Dias, H. Dutra Rezende, J.R. Furtado Cardoso de Moraes, N. Dlova, C.N. Ekelem, E.A.G. Vilar, R.M. Trüeb
doi : 10.1111/jdv.16918
Volume 35, Issue 3 p. e200-e203
I. Doche, M.M. Rebeis, P. Gerlero, N.Y.S. Valente, M.C. Rivitti-Machado
doi : 10.1111/jdv.16919
Volume 35, Issue 3 p. e203-e205
D. Saceda-Corralo, O.M. Moreno-Arrones, M. Rubio-Lambra?a, R. Gil-Redondo, C. Bern?rdez, ?. Hermosa-Gelbard, P. Jaén-Olasolo, S. Va??-Galv?n
doi : 10.1111/jdv.16920
Volume 35, Issue 3 p. e205-e207
P.V. Chernyshov, L. Tomas Aragones, C.M. Salavastru, F. Sampogna, M.J. Boffa, F. Poot, V. Bettoli, N. Pusti?ek, A.W.M. Evers, A. Bewley, S.E. Marron, D. Abeni, A. Svensson, J.S. Szepietowski
doi : 10.1111/jdv.16921
Volume 35, Issue 3 p. e208-e209
G. Richtig, L. Cerroni, H. Schmidt, C. Beham-Schmid, T. Deinlein, C. Vallant, E. Richtig
doi : 10.1111/jdv.16922
Volume 35, Issue 3 p. e209-e211
A.J. Garc?a-Malinis, T. Gracia-Caza?a, D. Planas Linares, P.J. Ag?n-Banzo, Y. Gilaberte
doi : 10.1111/jdv.16935
Volume 35, Issue 3 p. e211-e214
L. Rudnicka, A. Wa?kiel-Burnat
doi : 10.1111/jdv.16936
Volume 35, Issue 3 p. e214-e215
D. Fernandez-Nieto, G. Segurado-Miravalles, A. Gonzalez-Cantero, D. Ortega-Quijano, J. Jimenez-Cauhe, P. Boixeda
doi : 10.1111/jdv.16938
Volume 35, Issue 3 p. e215-e216
C. Hinnen, A. Boonstra, N. Kukutsch, R. van Doorn
doi : 10.1111/jdv.16939
Volume 35, Issue 3 p. e217-e218
J.-P. Lefaucheur, C. Hajj, L. Valeyrie-Allanore, A. Colin, S. Ng Wing Tin, N. de Prost, P. Wolkenstein, O. Chosidow, S. Ingen-Housz-Oro
doi : 10.1111/jdv.16940
Volume 35, Issue 3 p. e218-e221
L.E.M. de Wijs, J.P. Thyssen, C. Vestergaard, H.B. Thio, A.C.M. Kunkeler, T. Biedermann, D.J. Hijnen
doi : 10.1111/jdv.16941
Volume 35, Issue 3 p. e221-e223
L. Vlahova, W. Kempf, M.P. Sch?n, C. Mitteldorf
doi : 10.1111/jdv.16942
Volume 35, Issue 3 p. e223-e225
A. Dondi, A. Di Altobrando, R. Parladori, C. Biagi, C. Balsamo, C. Ghizzi, A. Patrizi, M. Lanari, I. Neri
doi : 10.1111/jdv.16952
Volume 35, Issue 3 p. e225-e227
C. Charpentier, F. Kouby, C. Hua, E. Sbidian, M. Darty, R. Bosc, N. De Prost, C. Gomart, P.-L. Woerther, A. Tazi, J.-W. Decousser, O. Chosidow, Henri Mondor Hospital Necrotizing Fasciitis Group
doi : 10.1111/jdv.16943
Volume 35, Issue 3 p. e227-e228
C. Braegelmann, D. Niebel, J. Wenzel, T. Bieber, A.M. Eis-Hübinger, D. Wilsmann-Theis
doi : 10.1111/jdv.16954
Volume 35, Issue 3 p. e228-e230
H.C. Wulf, S.R. Wiegell
doi : 10.1111/jdv.16957
Volume 35, Issue 3 p. e230-e232
P. O’Reilly, B. Whelan, B. Ramsay, C. Kennedy, P. Meskell, A. Coffey, D.M. Wilson, D.G. Fortune, S. Ryan
doi : 10.1111/jdv.16958
Volume 35, Issue 3 p. e232-e234
A. Rajabi-Estarabadi, F. Garbarino, N.M. Williams, N. Nami, K. Nouri
doi : 10.1111/jdv.16960
Volume 35, Issue 3 p. e234-e236
V. Reynaert, M. Grosber, A. Tache, F. Mana, P. Buydens, P. Lacor, J. Gutermuth
doi : 10.1111/jdv.16961
Volume 35, Issue 3 p. e236-e237
S. Fagotti, M.A. Pizzichetta, P. Corneli, F. Toffolutti, D. Serraino, N. di Meo, I. Zalaudek
doi : 10.1111/jdv.16968
Volume 35, Issue 3 p. e237-e239
G. Schneider, R. Steinbach, S. St?nder, A. Stumpf
doi : 10.1111/jdv.16973
Volume 35, Issue 3 p. e239-e241
M. Granot, S. Yakov, P. Kuperman, G. Yosipovitch, M. Ramon
doi : 10.1111/jdv.16975
Volume 35, Issue 3 p. e241-e242
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