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Publisher: Wiley-Blackwell

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Volume 166, Number 4, 1 April 2012

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Abstracts
pp. e15-e40(26)

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A randomized trial of methotrexate vs. azathioprine for severe atopic eczema: a critical appraisal
pp. 701-703(3)
Authors: Patel, A.N.; Langan, S.M.; Batchelor, J.M.

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Response to a randomized trial of methotrexate vs. azathioprine for severe atopic eczema: a critical appraisal
pp. 704-704(1)
Authors: Schram, M.E.; Roekevisch, E.; Leeflang, M.M.G.; Bos, J.D.; Schmitt, J.; Spuls, P.I.

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Angiokeratoma: decision‐making aid for the diagnosis of Fabry disease
pp. 712-720(9)
Authors: Zampetti, A.; Orteu, C.H.; Antuzzi, D.; Bongiorno, M.R.; Manco, S.; Gnarra, M.; Morrone, A.; Cardinali, G.; Kovacs, D.; Aspite, N.; Linder, D.; Parini, R.; Feliciani, C.; the Interdisciplinary Study Group on Fabry Disease (ISGF)cr14

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Primary cutaneous Ewing sarcoma: a systematic review focused on treatment and outcome
pp. 721-726(6)
Authors: Delaplace, M.; Lhommet, C.; de Pinieux, G.; Vergier, B.; de Muret, A.; Machet, L.

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Melanoma of the hand and foot: epidemiological, prognostic and genetic features. A systematic review
pp. 727-739(13)
Authors: Durbec, F.; Martin, L.; Derancourt, C.; Grange, F.

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Demodex‐associated bacterial proteins induce neutrophil activation
pp. 753-760(8)
Authors: O’Reilly, N.; Bergin, D.; Reeves, E.P.; McElvaney, N.G.; Kavanagh, K.

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Concentration variability of potent allergens of ptert‐butylphenol‐formaldehyde resin (PTBP‐FR) in patch test preparations and commercially available PTBP‐FR
pp. 761-770(10)
Authors: Hamann, C.R.; Zimerson, E.; Hamann, D.; Laugesen, L.; Carlsson, B.; Nathansen, C.; Hamann, C.; Bruze, M.

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Interstitial granulomatous dermatitis: a distinct entity with characteristic histological and clinical pattern
pp. 775-783(9)
Authors: Peroni, A.; Colato, C.; Schena, D.; Gisondi, P.; Girolomoni, G.

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FGFR3, PIK3CA and RAS mutations in benign lichenoid keratosis
pp. 784-788(5)
Authors: Groesser, L.; Herschberger, E.; Landthaler, M.; Hafner, C.

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Peripheral natural killer cells exhibit qualitative and quantitative changes in patients with psoriasis and atopic dermatitis
pp. 789-796(8)
Authors: Luci, C.; Gaudy‐Marqueste, C.; Rouzaire, P.; Audonnet, S.; Cognet, C.; Hennino, A.; Nicolas, J.‐F.; Grob, J.‐J.; Tomasello, E.

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Analysis of three outcome measures in moderate to severe psoriasis: a registry‐based study of 2450 patients
pp. 797-802(6)
Authors: Norlin, J.M.; Steen Carlsson, K.; Persson, U.; Schmitt‐Egenolf, M.

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Psoriasis and risk of nonfatal cardiovascular disease in U.S. women: a cohort study
pp. 811-818(8)
Authors: Li, W.‐Q.; Han, J.‐L.; Manson, J.E.; Rimm, E.B.; Rexrode, K.M.; Curhan, G.C.; Qureshi, A.A.

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A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India
pp. 819-829(11)
Authors: Bashyam, M.D.; Chaudhary, A.K.; Reddy, E.C.; Reddy, V.; Acharya, V.; Nagarajaram, H.A.; Devi, A.R.R.; Bashyam, L.; Dalal, A.B.; Gupta, N.; Kabra, M.; Agarwal, M.; Phadke, S.R.; Tainwala, R.; Kumar, R.; Hariharan, S.V.

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Clinical, molecular and biochemical characterization of nine Spanish families with Conradi–Hünermann–Happle syndrome: new insights into X‐linked dominant chondrodysplasia punctata with a comprehensive review of the literature
pp. 830-838(9)
Authors: Cañueto, J.; Girós, M.; Ciria, S.; Pi‐Castán, G.; Artigas, M.; García‐Dorado, J.; García‐Patos, V.; Virós, A.; Vendrell, T.; Torrelo, A.; Hernández‐Martín, Á.; Martín‐Hernández, E.; Garcia‐Silva, M.T.; Fernández‐Burriel, M.; Rosell, J.; Tejedor, M.; Martínez, F.; Valero, J.; García, J.L.; Sánchez‐Tapia, E.M.; Unamuno, P.; González‐Sarmiento, R.

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Markers of oxidative stress are increased in exhaled breath condensates of children with atopic dermatitis
pp. 839-843(5)
Authors: Peroni, D.G.; Bodini, A.; Corradi, M.; Coghi, A.; Boner, A.L.; Piacentini, G.L.

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Combined treatment with immunoadsorption and rituximab leads to fast and prolonged clinical remission in difficult‐to‐treat pemphigus vulgaris
pp. 844-852(9)
Authors: Behzad, M.; Möbs, C.; Kneisel, A.; Möller, M.; Hoyer, J.; Hertl, M.; Eming, R.

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Efficacy and safety of topical WBI‐1001 in patients with mild to severe atopic dermatitis: results from a 12‐week, multicentre, randomized, placebo‐controlled double‐blind trial
pp. 853-860(8)
Authors: Bissonnette, R.; Poulin, Y.; Zhou, Y.; Tan, J.; Hong, H.C.; Webster, J.; Ip, W.; Tang, L.; Lyle, M.

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Long‐term efficacy of ustekinumab in patients with moderate‐to‐severe psoriasis: results from the PHOENIX 1 trial through up to 3 years
pp. 861-872(12)
Authors: Kimball, A.B.; Gordon, K.B.; Fakharzadeh, S.; Yeilding, N.; Szapary, P.O.; Schenkel, B.; Guzzo, C.; Li, S.; Papp, K.A.

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Erythrocyte sedimentation rate as an independent prognostic factor in mycosis fungoides
pp. 873-874(2)
Authors: Hallermann, C.; Niermann, C.; Fischer, R.‐J.; Schulze, H.‐J.

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Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16
pp. 875-878(4)
Authors: Spaunhurst, K.M.; Hogendorf, A.M.; Smith, F.J.D.; Lingala, B.; Schwartz, M.E.; Cywinska‐Bernas, A.; Zeman, K.J.; Tang, J.Y.

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Bacteriology of hidradenitis suppurativa exacerbations and deep tissue cultures obtained during carbon dioxide laser treatment
pp. 879-883(5)
Authors: Sartorius, K.; Killasli, H.; Oprica, C.; Sullivan, A.; Lapins, J.

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Compound heterozygous mutations in desmoplakin cause skin fragility and woolly hair
pp. 894-896(3)
Authors: Smith, F.J.D.; Wilson, N.J.; Moss, C.; Dopping‐Hepenstal, P.; McGrath, J.

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Genotype analysis in a patient with oculocutaneous albinism 1 minimal pigment type
pp. 896-898(3)
Authors: Kono, M.; Kondo, T.; Ito, S.; Suzuki, T.; Wakamatsu, K.; Ito, S.; Tomita, Y.

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Buschke–Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation
pp. 900-903(4)
Authors: Korekawa, A.; Nakano, H.; Toyomaki, Y.; Takiyoshi, N.; Rokunohe, D.; Akasaka, E.; Nakajima, K.; Sawamura, D.

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Possible modifier effects of keratin 17 gene mutation on keratitis–ichthyosis–deafness syndrome
pp. 903-905(3)
Authors: Natsuga, K.; Shinkuma, S.; Kanda, M.; Suzuki, Y.; Chosa, N.; Narita, Y.; Setoyama, M.; Nishie, W.; Akiyama, M.; Shimizu, H.

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Clinically manifest X‐linked recessive ichthyosis in a female due to a homozygous interstitial 1·6‐Mb deletion of Xp22.31
pp. 905-907(3)
Authors: Nagtzaam, I.F.; Stegmann, A.P.A.; Steijlen, P.M.; Herbergs, J.; Van Lent‐Albrechts, J.A.; Van Geel, M.; Van Steensel, M.A.M.

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News and Notices
pp. 909-910(2)

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