T. Nijsten, J. Silverberg, P. Gisondi, C. Vestergaard, L. Hollestein, M. Wakkee
doi : 10.1111/bjd.20393
Volume185, Issue1,Pages 1-2
J. Kottner, J. Schmitt
doi : 10.1111/bjd.19836
Volume185, Issue1,Pages 3-4
The development and use of Core Outcome Sets (COS) is increasingly recognized as an important aspect to improve the quality and usefulness of clinical trial evidence. In dermatology, several COS have been published or are under development.1 The Cochrane Skin-Core Outcome Set Initiative (CS-COUSIN, http://cs-cousin.org/) supports the development of COS in dermatology and offers guidance and support for COS development groups. Currently, 21 COS groups are affiliated with CS-COUSIN, among them the Acne Core Outcomes Research Network (ACORN). In COS development, the selection and prioritization of critical outcome domains is a crucial first step which is followed by the selection of outcome measurement instruments (OMIs) per domain. Guidance on how to best select core outcome domains is available to support this complex and challenging process.2 However, the appropriate selection of OMIs is at least as challenging as selecting core domains.3
F. Coyer
doi : 10.1111/bjd.19873
Volume185, Issue1,Pages 4-5
no abstract
B. Volc-Platzer
doi : 10.1111/bjd.20057
Volume185, Issue1,Pages 5-6
L.A.V. Orenstein
doi : 10.1111/bjd.19886
Volume185, Issue1,Pages 6-7
G. Becher, A.D. Burden
doi : 10.1111/bjd.20055
Volume185, Issue1,Pages 7-8
The COVID-19 pandemic has presented clinicians managing immune-mediated inflammatory diseases (IMIDs) such as psoriasis, with many challenges. Patients with severe psoriasis have an increased prevalence of risk factors for severe COVID-19 including obesity, hypertension, diabetes and male sex.1 Moreover, many systemic treatments for psoriasis are known to increase the risk of severe infection. Therefore, it is understandable that in the early stages of the pandemic, patients on conventional targeted systemic therapies were considered to be at higher risk of severe COVID-19 infection. In addition to risk-mitigating behaviours such as social distancing recommended by the World Health Organization, those who were thought to be more vulnerable, for instance those on immunosuppressants, were advised to adopt stricter measures of social isolation including distancing themselves from other members of their household.2, 3 There was a pressing need to establish whether patients on immunosuppressive or immunomodulatory medications should continue on their medications.
E.K. Johansson
doi : 10.1111/bjd.20394
Volume185, Issue1,Pages 8-9
It is well-known that children with atopic dermatitis (AD) have a reduced health-related quality of life that is of a similar magnitude to children with cerebral palsy and diabetes mellitus.1, 2 It is also known that children with AD have an increased risk of attention deficit hyperactivity disorder (ADHD).3 Less is known about other psychiatric comorbidities in children with AD.
J. Wiggins, D. Polsky
doi : 10.1111/bjd.20396
Volume185, Issue1,Pages 9-10
P. S. Mortimer
doi : 10.1111/bjd.20047
Volume185, Issue1,Pages 10-11
Cellulitis (also known as erysipelas) is a common infection of the skin and subcutaneous tissues, and therefore falls within the domain of dermatologists. Cellulitis, which can often be recurrent, is among the top 10 reasons for admission to hospital, with patients receiving treatment from many specialties including emergency care, general practitioners, general medicine, surgery, tissue viability and dermatology.1
M. Linder
doi : 10.1111/bjd.20395
Volume185, Issue1,Pages 11-12
In their article in this issue, Droitcourt et al. investigate the risk of some systemic infections leading to hospitalization in children with atopic dermatitis (AD) compared with sex- and age-matched comparators in Denmark.1 Studied outcomes were upper and lower respiratory tract, gastrointestinal tract, musculoskeletal tract, urinary tract, heart and central nervous system infections and sepsis. Infections treated in hospitals were regarded as serious infections, and AD was defined as at least one recorded diagnosis of AD, but an algorithm may have captured more children with AD.2
A.W.M. Evers, S. van Beugen
doi : 10.1111/bjd.20397
Volume185, Issue1,Pages 12-13
The reciprocal relationship between stress and skin diseases is well known, showing that for example many chronic skin diseases induce moderate-to-severe stress responses,1, 2 such as subjective levels of psychological distress and a physiological stress response of altered hypothalamic–pituitary–adrenal (HPA) axis activity, that in turn might trigger a worsened disease course or progression.3 Although there is considerable evidence showing that stress is a common psychological consequence of skin conditions,1 there is much less ‘hardcore’ evidence from prospective studies about the possible causal effects of stress on the origin or course of a skin disease.4 There are at least three ways through which stress can affect the skin that all ask for different designs.
D.F. Murrell, C.F. Paul
doi : 10.1111/bjd.20398
Volume185, Issue1,Pages 13-14
R.F.L. O’Shaughnessy
doi : 10.1111/bjd.19888
Volume185, Issue1,Pages 14-15
E.J. Giamarellos-Bourboulis
doi : 10.1111/bjd.20086
Volume185, Issue1,Pages 15-16
R. Hambly, B. Kirby
doi : 10.1111/bjd.20399
Volume185, Issue1,Pages 16-17
Hidradenitis suppurativa (HS) is a chronic, inflammatory skin disease, with multiple systemic comorbidities1 Treatment is challenging and adalimumab [tumour necrosis factor (TNF)-? monoclonal antibody] is the only licensed therapy. It is effective in approximately 50% of patients, based on Hidradenitis Suppurativa Clinical Response results from the phase III trials PIONEER I and II.2
A. Schnuch
doi : 10.1111/bjd.20142
Volume185, Issue1,Pages 17-18
M.H. Vermeer, J.P. Nicolay, J.J. Scarisbrick, P.L. Zinzani
doi : 10.1111/bjd.19669
Volume185, Issue1,Pages 19-25
A. J. Hughes, S. S. Tawfik, K. P. Baruah, E. A. O’Toole, R. F. L. O’Shaughnessy
doi : 10.1111/bjd.19760
Volume185, Issue1,Pages 26-35
E.J. van Zuuren, B.W.M. Arents, M. Miklas, J.W. Schoones, J. Tan
doi : 10.1111/bjd.19675
Volume185, Issue1,Pages 36-51
After dermatitis, acne is the next skin disease to contribute most to the burden of skin diseases worldwide. Recently, seven core outcome domains have been identified, which together form an Acne Core Outcome Set (ACORN). One of these was satisfaction with acne treatment.
D. Beeckman, A. Fourie, C. Raepsaet, N. Van Damme, B. Manderlier, D. De Meyer, H. Beele, S. Smet, L. Demarré, R. Vossaert, A. de Graaf, L. Verhaeghe, N. Vandergheynst, B. Hendrickx, V. Hanssens, H. Keymeulen, K. Vanderwee, J. Van De Woestijne, S. Verhaeghe, A. Van Hecke, I. Savoye, J. Harrison, F. Vrijens, F. Hulstaert
doi : 10.1111/bjd.19689
Volume185, Issue1,Pages 52-61
H. Hamm, D. Wilsmann-Theis, A. Tsianakas, T. Gambichler, K. Taipale, J. Lauterbach, U. Freudensprung, C. Makepeace, the KIFUderm study investigators
doi : 10.1111/bjd.19747
Volume185, Issue1,Pages 62-73
S. Wright, A. Strunk, A. Garg
doi : 10.1111/bjd.19713
Volume185, Issue1,Pages 74-79
S.K. Mahil, M. Yates, S.M. Langan, Z.Z.N. Yiu, T. Tsakok, N. Dand, K.J. Mason, H. McAteer, F. Meynell, B. Coker, A. Vincent, D. Urmston, A. Vesty, J. Kelly, C. Lancelot, L. Moorhead, H. Bachelez, I.N. Bruce, F. Capon, C.R. Contreras, A.P. Cope, C. De La Cruz, P. Di Meglio, P. Gisondi, K. Hyrich, D. Jullien, J. Lambert, H. Marzo-Ortega, I. McInnes, L. Naldi, S. Norton, L. Puig, R. Sengupta, P. Spuls, T. Torres, R.B. Warren, H. Waweru, J. Weinman, C.E.M. Griffiths, J.N. Barker, M.A. Brown, J.B. Galloway, C.H. Smith, on behalf of the PsoProtect, CORE-UK study groups
doi : 10.1111/bjd.19755
Volume185, Issue1,Pages 80-90
I. Vittrup, Y. M. F. Andersen, C. Droitcourt, L. Skov, A. Egeberg, M. C. Fenton, P. Mina-Osorio, S. Boklage, J. P. Thyssen
doi : 10.1111/bjd.19817
Volume185, Issue1,Pages 91-100
C. Dessinioti, A.C. Geller, A. Stergiopoulou, N. Dimou, S. Lo, U. Keim, J.E. Gershenwald, L.E. Haydu, R. Dummer, J. Mangana, A. Hauschild, F. Egberts, R. Vieira, A. Brinca, I. Zalaudek, T. Deinlein, E. Evangelou, J.F. Thompson, R.A. Scolyer, K. Peris, C. Garbe, A.J. Stratigos
doi : 10.1111/bjd.19819
Volume185, Issue1,Pages 101-109
E.A. Burian, T. Karlsmark, P.J. Franks, V. Keeley, I. Quéré, C.J. Moffatt
doi : 10.1111/bjd.19803
Volume185, Issue1,Pages 110-118
C. Droitcourt, I. Vittrup, A. Dupuy, A. Egeberg, J.P. Thyssen
doi : 10.1111/bjd.19825
Volume185, Issue1,Pages 119-129
S.A.J. Schmidt, H.T. S?rensen, S.M. Langan, M. Vestergaard
doi : 10.1111/bjd.19832
Volume185, Issue1,Pages 130-138
K.S. Thomas, C.A. Apfelbacher, J.R. Chalmers, E. Simpson, P.I. Spuls, L.A.A. Gerbens, H.C. Williams, J. Schmitt, M. Gabes, L. Howells, B.L. Stuart, E. Grinich, T. Pawlitschek, T. Burton, L. Howie, A. Gadkari, L. Eckert, T. Ebata, M. Boers, H. Saeki, T. Nakahara, N. Katoh
doi : 10.1111/bjd.19751
Volume185, Issue1,Pages 139-146
J.M. Meyer, E. Lee, A. Celli, K. Park, R. Cho, W. Lambert, M. Pitchford, M. Gordon, K. Tsai, J. Cleaver, S.T. Arron, T.M. Mauro
doi : 10.1111/bjd.19753
Volume185, Issue1,Pages 147-152
M. A. McAleer, I. Jakasa, N. Stefanovic, W. H. I. McLean, S. Kezic, A. D. Irvine
doi : 10.1111/bjd.19703
Volume185, Issue1,Pages 153-163
K. Wolk, T.-C. Brembach, D. ?imait?, E. Bartnik, S. Cucinotta, A. Pokrywka, M.L. Irmer, J. Triebus, E. Witte-H?ndel, G. Salinas, T. Leeuw, H.-D. Volk, K. Ghoreschi, R. Sabat
doi : 10.1111/bjd.19795
Volume185, Issue1,Pages 164-176
L.M. Prens, K. Bouwman, P. Aarts, S. Arends, K.R. van Straalen, K. Dudink, B. Horv?th, E.P. Prens
doi : 10.1111/bjd.19863
Volume185, Issue1,Pages 177-184
J.I. Silverberg, E.M. Warshaw, H.I. Maibach, J.G. DeKoven, J.S. Taylor, A.R. Atwater, D. Sasseville, K.A. Zug, M.J. Reeder, J.F. Fowler Jr., M.D. Pratt, A.F. Fransway, M.J. Zirwas, D.V. Belsito, J.G. Marks Jr, V.A. DeLeo
doi : 10.1111/bjd.19818
Volume185, Issue1,Pages 185-194
C. Bergqvist, R.S. Stern, O. Chosidow
doi : 10.1111/bjd.19715
Volume185, Issue1,Pages 195-197
U.K. Okoji, S.C. Taylor, J.B. Lipoff
doi : 10.1111/bjd.19932
Volume185, Issue1,Pages 198-199
M.T. Taylor, M.H. Noe, D.B. Horton, J.S. Barbieri
doi : 10.1111/bjd.19865
Volume185, Issue1,Pages 200-201
H. A. B. Vermeer, H. Rashid, M. D. Esajas, J. M. Oldhoff, B. Horv?th
doi : 10.1111/bjd.19870
Volume185, Issue1,Pages 201-203
K. Abuabara, S.G. Nicholls, S.M. Langan, E. Guttman-Yassky, N.J. Reynolds, A.S. Paller, S.J. Brown, the International Eczema Council Priority Research Group
doi : 10.1111/bjd.19874
Volume185, Issue1,Pages 203-205
T. Omodaka, A. Minagawa, R. Okuyama
doi : 10.1111/bjd.19875
Volume185, Issue1,Pages 205-207
W.T. Hodges, T. Bhat, N.S. Raval, C. Herbosa, P. Ugwu-Dike, S.G. Kwatra, A. Musiek, C. Mann, Y.R. Semenov
doi : 10.1111/bjd.19876
Volume185, Issue1,Pages 207-209
E. Sotiriou, K. Bakirtzi, I. Papadimitriou, E. Paschou, E. Vakirlis, A. Lallas, D. Ioannides
doi : 10.1111/bjd.19882
Volume185, Issue1,Pages 209-210
D. S. Yoo, J. H. Lee, S. -C. Kim, J. H. Kim
doi : 10.1111/bjd.19890
Volume185, Issue1,Pages 210-212
D.E. McMahon, L. Oyesiku, E. Amerson, H. Beltraminelli, A.Y. Chang, A. Forrestel, R. Hay, A. Knapp, C. Kovarik, T. Maurer, S.A. Norton, W. Rehmus, C. Van Hees, K.A. Wanat, V.L. Williams, L.C. Fuller, E.E. Freeman
doi : 10.1111/bjd.19889
Volume185, Issue1,Pages 212-214
E.E. Freeman, D.E. McMahon, J.B. Lipoff, M. Rosenbach, S.R. Desai, M. Fassett, L.E. French, H.W. Lim, G.J. Hruza, L.P. Fox
doi : 10.1111/bjd.19894
Volume185, Issue1,Pages 214-216
V. Bettoli, G. Toni, G. Odorici, R. Forconi, M. Corazza
doi : 10.1111/bjd.19867
Volume185, Issue1,Pages 216-217
A. Campanati, M. Di Vincenzo, G. Radi, G. Rizzetto, G. Carnevale, S. Marchi, M. Orciani, A. Offidani
doi : 10.1111/bjd.19892
Volume185, Issue1,Pages 217-219
K.X. Liu, V. Huang, C.A. Chen, C.P. Elco, S.T. Chen, R.S. Stern, P.A. Wu
doi : 10.1111/bjd.19871
Volume185, Issue1,Pages 219-221
Z.J. Wolner, N.I. Flowers, M.L. Yushak, S.C. Chen, H. Yeung
doi : 10.1111/bjd.19868
Volume185, Issue1,Pages 221-223
L.F. Soriano, M.M.U. Chowdhury, S.M. Cooper, P. Cousen, S. Dawe, A. Havelin, C.R. Holden, G.A. Johnston, D.I. Orton, A. Ramoutar, N.M. Stone, D.A. Thompson, D.A. Buckley
doi : 10.1111/bjd.19898
Volume185, Issue1,Pages 223-225
A.M. Thompson, J.M. Fernandez, J. Rick, A.J. Hendricks, M. Maarouf, E.M. Mata, E.K. Collier, T.R. Grogan, J.L. Hsiao, V.Y. Shi
doi : 10.1111/bjd.19926
Volume185, Issue1,Pages 225-226
S. Maanaoui, F. Salez, O. Carpentier
doi : 10.1111/bjd.20070
Volume185, Issue1,Pages 227-228
U. Wehkamp, C. Mitteldorf, S. Stendel, R. Stranzenbach, J.P. Nicolay, M. Wobser, M. Weichenthal, R. Schneiderbauer, C.-D. Klemke, U. Hillen, W. Kempf, C. Assaf
doi : 10.1111/bjd.19823
Volume185, Issue1,Pages 228-230
J.L. Jia, V.J. Hua, D.E. Mills, K.Y. Sarin
doi : 10.1111/bjd.20065
Volume185, Issue1,Pages 230-232
C. Wang
doi : 10.1111/bjd.19881
Volume185, Issue1,Pages 233-233
T. Kogame, N. Kambe, R. Takimoto-Ito, T. Nomura, K. Kabashima
doi : 10.1111/bjd.19884
Volume185, Issue1,Pages 233-234
G. Quinn, C. MacEochagain, J. Mac Mahon, L. Killion, N. Ralph, P. Lenane, A. Murad, I. McDonald, F.J. Moloney
doi : 10.1111/bjd.19869
Volume185, Issue1,Pages 234-235
B. Duarte, M.J. Paiva Lopes
doi : 10.1111/bjd.20061
Volume185, Issue1,Pages 235-236
C.E.M. Griffiths
doi : 10.1111/bjd.20075
Volume185, Issue1,Pages 237-238
Y.H. Wang, W.T. Chen
doi : 10.1111/bjd.20056
Volume185, Issue1,Pages e1-e1
H. Mahmoudi, A. Nili, A. Salehi Farid, S. Tavakolpour, M. Daneshpazhooh
doi : 10.1111/bjd.20054
Volume185, Issue1,Pages e2-e2
A. Pileri, A. Guglielmo, B. Raone, A. Patrizi
doi : 10.1111/bjd.20060
Volume185, Issue1,Pages e3-e3
doi : 10.1111/bjd.20442
Volume185, Issue1,Pages e4-e4
doi : 10.1111/bjd.20443
Volume185, Issue1,Pages e5-e5
Zoster (shingles) is a painful skin disease caused by the same virus that is responsible for chickenpox (varicella). After chickenpox infection, the virus rests in the nerves of the body; but later in life it may become activated and then zoster develops. This occurs in roughly one-third of the population during their lifetime and it can be triggered by a weakened immune system. Because psychological stress can have a negative impact on the immune system, it has been suggested that it can lead to zoster.
doi : 10.1111/bjd.20444
Volume185, Issue1,Pages e6-e6
Acne is a common skin disease that causes a lot of burden and distress. Acne can be treated with medication applied to the skin (e.g. creams) and with oral medication (e.g. tablets). It is important to know how satisfied people with acne actually are with their treatment. So this should be measured in studies that evaluate acne treatments.
doi : 10.1111/bjd.20445
Volume185, Issue1,Pages e7-e7
Psoriasis is an inflammatory skin disease that can begin during childhood. In Germany, psoriasis affects seven out of 1000 children and adolescents. The condition in these young people is challenging to treat because many drugs are only approved for adults. Tablets containing fumaric acid esters are successfully used to treat adults with psoriasis. This study from Germany aimed to find out if fumaric acid esters can also improve psoriasis in children and adolescents.
doi : 10.1111/bjd.20446
Volume185, Issue1,Pages e8-e8
As a background to this study it is known that children with atopic dermatitis (AD) have an increased risk of developing skin infections caused by bacteria such as Staphylococcus aureus as well as viruses including herpes simplex. This then raises the question as to whether children with AD are, in addition, at greater risk from internal infections.
doi : 10.1111/bjd.20447
Volume185, Issue1,Pages e9-e9
A lymphoma is a cancer of lymphocytes, cells that form part of the immune system. One type of lymphocyte that can become cancerous is the T-lymphocyte, or ‘T-cell’. Cutaneous T-cell lymphoma (CTCL) is a form of lymphoma that originates in the skin, and the two subtypes we know most about are mycosis fungoides (MF) and Sézary syndrome (SS). MF is the commonest sub-type whereas SS is much rarer. One criterion for diagnosing SS is finding significant numbers of abnormal lymphocytes in the bloodstream, as in leukaemia. Most patients with MF do not have this finding, but the outlook is worse if they do.
doi : 10.1111/bjd.20448
Volume185, Issue1,Pages e10-e10
Immobility is one of the factors contributing to why patients develop pressure-related wounds. Even though hospitals use strategies such as turning patients every 2–4 h, some patients still get these ulcers (also known as pressure sores), which can be painful and expensive to treat. A recent summary of studies showed that on average, 13 out of 100 patients develop pressure ulcers and 50% of these wounds are on the buttock area.
doi : 10.1111/bjd.20449
Volume185, Issue1,Pages e11-e11
The Harmonising Outcome Measures for Eczema (HOME) initiative is an international collaboration involving people with eczema, health professionals, researchers, regulators and industry representatives. The collaboration is working globally to agree a defined list of aspects of eczema that should be measured in all future eczema clinical trials and systematic reviews.
doi : 10.1111/bjd.20450
Volume185, Issue1,Pages e12-e12
Skin melanoma usually arises on healthy-looking skin and this is called de novo melanoma (70% of melanoma). When melanoma arises on a pre-existing naevus (skin mole) it is called naevus-associated melanoma (NAM, 30% of melanoma). The differences between de novo and NAM are not clear because de novo melanoma are thicker tumours and there may have been a naevus component that was later replaced by tumour growth.
doi : 10.1111/bjd.20451
Volume185, Issue1,Pages e13-e13
Atopic dermatitis (AD) is a very common skin condition, affecting around 15% of children. Symptoms, often beginning in early childhood, include itch and interrupted sleep. Children with AD have a higher risk of social isolation and reduced quality of life. Studies from adult patients have shown that depression and anxiety are related to AD. However, in children with AD, besides a connection to attention deficit hyperactivity disorder (ADHD), the occurrence of psychiatric disorders has not been thoroughly investigated.
doi : 10.1111/bjd.20452
Volume185, Issue1,Pages e14-e14
A surprising amount of information about the skin can be obtained by studying the components of its outermost layer, the stratum corneum. For example, resident skin bacteria, proteins expressed in skin diseases such as eczema and even those associated with skin cancer can be investigated in this way.
doi : 10.1111/bjd.20453
Volume185, Issue1,Pages e15-e15
Public health measures such as social/physical distancing were introduced early in the pandemic to limit the spread of COVID-19. Stricter measures referred to as ‘shielding’ (not leaving home and minimizing all face-to-face contact) were recommended in groups of people at higher risk of severe infection. Many people taking drugs that affect the immune system to treat psoriasis or a joint condition (e.g. rheumatoid arthritis) were advised to reduce their risk of developing COVID-19 by shielding. We wanted to find out what factors influenced how much (or strictly) this advice was followed.
doi : 10.1111/bjd.20454
Volume185, Issue1,Pages e16-e16
Hand eczema (HE) is often triggered by something in contact with the skin, either an irritant (such as detergent) or a substance to which the person is allergic. Allergic contact dermatitis (ACD) is diagnosed by patch testing: substances that commonly cause allergy (allergens), placed in small chambers mounted on tape, are stuck on the upper back; after 48 hours the tape is removed and a patch of eczema at the site of a particular allergen reveals the culprit. Most research into ACD has been on adults and the cause is usually related to their work. Children are exposed to different substances so they might need to be patch tested with different allergens.
doi : 10.1111/bjd.20455
Volume185, Issue1,Pages e17-e17
Hidradenitis suppurativa is a chronic skin disease in which persistent, painful, boil-like lesions develop especially in the armpits and groin. Treatment is often difficult, and patients with severe disease are eligible for so-called biologic therapy. The only registered biologic agent is adalimumab, a monoclonal antibody to the inflammatory mediator called tumour necrosis factor-? (TNF-?), although other biologic agents such as infliximab (another TNF-? antagonist) have been used. Unfortunately, these agents may lose their effect with time, sometimes because the patient develops antibodies to the drug, or side-effects may develop. Little is known about the long-term results of using these treatments in patients with hidradenitis suppurativa.
doi : 10.1111/bjd.20456
Volume185, Issue1,Pages e18-e18
Hidradenitis suppurativa (HS) is a quite common, chronic skin disease that greatly impairs quality of life. Typically, the disease starts during early adulthood. Patients develop painful, tissue-destructive skin inflammation with abscesses and tunnels in body folds such as the armpit and groin.
doi : 10.1111/bjd.20457
Volume185, Issue1,Pages e19-e19
????????? (CERKL) ???????????????????, ?????????????, ??????????????; CERKL ?? (??) ?????????????????????, ??????????
doi : 10.1111/bjd.20458
Volume185, Issue1,Pages e20-e20
???? (???) ???????? (??) ??????????????????, ???????????; ????????, ????????, ?????????????????????????????, ???????????????????????????????, ??????????????
doi : 10.1111/bjd.20459
Volume185, Issue1,Pages e21-e21
???????????, ???????????????????? (???) ????? (???) ?????????????????????????????, ??????????????????
doi : 10.1111/bjd.20460
Volume185, Issue1,Pages e22-e22
???????????, ???????????, ?????????????? 7/1000?????????????, ???????????????????????????????????????????????????????????????????????
doi : 10.1111/bjd.20461
Volume185, Issue1,Pages e23-e23
????????, ????????? (AD) ?????????????????????????????????????????????, ? AD ????????????????
doi : 10.1111/bjd.20462
Volume185, Issue1,Pages e24-e24
???????????, ?????????????????????????????? T ????, ?“T ??”??? T ????? (CTCL) ????????????, ???????????????? (MF) ? Sézary ??? (SS)?MF ???????, ? SS ???????? SS ????????????????????, ???????? MF ????????, ????, ??????
doi : 10.1111/bjd.20463
Volume185, Issue1,Pages e25-e25
?????????????????????????????????, ??? 2-4 ?????????, ????????????? (?????) , ?????????????????????????, ????, ? 100 ????? 13 ?????????, ?? 50% ????????
doi : 10.1111/bjd.20464
Volume185, Issue1,Pages e26-e26
?????????? (HOME) ?????????, ?????????????????????????????????????????, ????????????????????????????????????
doi : 10.1111/bjd.20465
Volume185, Issue1,Pages e27-e27
??????????????????, ???????? (70% ????) ??????? (???) ??????, ?????????? (NAM,30% ????) ??????? NAM ?????????, ?????????????, ??????????????????
doi : 10.1111/bjd.20466
Volume185, Issue1,Pages e28-e28
????? (AD) ???????????, ?? 15% ?????????????????, ??????????AD ?????????????????????????????, ?????? AD ????? AD ???, ??????????? (ADHD) ???, ?????????????????
doi : 10.1111/bjd.20467
Volume185, Issue1,Pages e29-e29
?????????????, ????????????????, ??????????????????????????????, ????????????
doi : 10.1111/bjd.20468
Volume185, Issue1,Pages e30-e30
???????????/???????????, ??? COVID-19 ??????????????????, ??????“??” (???, ???????????) ?????????????????????????????????? (?????????) ??, ?????????? COVID-19 ?????????????????? (?????) ???????
doi : 10.1111/bjd.20469
Volume185, Issue1,Pages e31-e31
??? (HE) ???????????????, ?????????? (????) , ???????????????????? (ACD) ????????: ?????????? (???) ????????????, ?????????; 48 ???????, ??????????????????? ACD ??????????????, ???????????????????????, ??????????????????????
doi : 10.1111/bjd.20470
Volume185, Issue1,Pages e32-e32
??????????????, ??????????????????, ??????????????????, ?????????????????????????????????, ????????????? a (TNF-?) ??????????, ????????????, ??????? (??? TNF-a ???) ?????, ???????????????????, ????????????, ???????????????????????????????????
doi : 10.1111/bjd.20471
Volume185, Issue1,Pages e33-e33
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