Search Results - "Di Zenzo, G"

A sensitive and specific assay for the serological diagnosis of antilaminin 332 mucous membrane pemphigoid by Goletz, S., Probst, C., Komorowski, L., Schlumberger, W., Fechner, K., van Beek, N., Holtsche, M.M., Recke, A., Yancey, K.B., Hashimoto, T., Antonicelli, F., Di Zenzo, G., Zillikens, D., Stöcker, W., Schmidt, E.

“…Summary Background Antilaminin 332 mucous membrane pemphigoid (MMP) is an autoimmune subepidermal blistering disease with predominant mucosal involvement and…”
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IgE autoantibodies in serum and skin of non‐bullous and bullous pemphigoid patients by Lamberts, A., Kotnik, N., Diercks, G.F.H., Meijer, J.M., Di Zenzo, G., Pas, H.H., Jonkman, M.F., Gibbs, B.F., Raap, U., Horváth, B.

“…Background Non‐bullous pemphigoid (NBP) is a pemphigoid variant which frequently resembles other pruritic skin diseases. In contrast with bullous pemphigoid…”
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A new clinical variant of acquired reactive perforating dermatosis‐like bullous pemphigoid by Schauer, F., Kern, J.S., Virtic, O., Technau‐Hafsi, K., Meiss, F., Thoma, K., Athanasiou, I., Sitaru, C., Di Zenzo, G., Izumi, K., Nishie, W., Shimizu, H., Bruckner‐Tuderman, L., Kiritsi, D.

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Lack of K140 immunoreactivity in junctional epidermolysis bullosa skin and keratinocytes associates with misfolded laminin epidermal growth factor‐like motif 2 of the β3 short arm by Condorelli, A.G., Fortugno, P., Cianfarani, F., Proto, V., Di Zenzo, G., Didona, B., Zambruno, G., Castiglia, D.

“…Summary Recessive mutations in the LAMA3, LAMB3 and LAMC2 genes that encode laminin‐332 (LM332) (α3a, β3 and γ2 chains, respectively) cause different…”
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Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis by Schmidt, T., Hoch, M., Lotfi Jad, S.S., Solimani, F., Di Zenzo, G., Marzano, A.V., Goebeler, M., Cozzani, E., Kern, J.S., Sitaru, C., Lakoš Jukić, I., Sárdy, M., Uzun, S., Jedlickova, H., Gläser, R., Kaneda, M., Eming, R., Göpel, G., Ishii, N., Greene, B., Hashimoto, T., Hertl, M.

“…Summary Background Epidermolysis bullosa acquisita (EBA) is a rare, potentially devastating autoimmune disease of the skin. IgG autoantibodies directed against…”
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Inter‐rater reliability of the BIOCHIP indirect immunofluorescence dermatology mosaic in bullous pemphigoid and pemphigus patients by Yang, A., Xuan, R.R., Melbourne, W., Hashimoto, T., Uzun, S., Daneshpazhooh, M., Yamagami, J., Di Zenzo, G., Mascaro, J.M., Mahmoudi, H., Patsatsi, A., Drenovska, K., Vassileva, S., Murrell, D.F.

“…Background The BIOCHIP (Dermatology Mosaic 7; EUROIMMUN, Lubeck, Germany) is a novel multiplex indirect immunofluorescence (IIF) technique used in the…”
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Urban legend series: mucous membrane pemphigoid by Di Zenzo, G, Carrozzo, M, Chan, LS

“…Mucous membrane pemphigoid (MMP) is a heterogeneous group of autoimmune subepithelial blistering diseases affecting primarily mucous membranes showing marked…”
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Induction of senescence pathways in Kindler syndrome primary keratinocytes by Piccinni, E., Di Zenzo, G., Maurelli, R., Dellambra, E., Teson, M., Has, C., Zambruno, G., Castiglia, D.

“…Summary Background  Individuals with Kindler syndrome (KS) have loss‐of‐function mutations in the FERMT1 gene that encodes the focal adhesion component…”
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Detection of IgG and IgE reactivity to BP180 using the ISAC® microarray system by Pomponi, D., Di Zenzo, G., Zennaro, D., Calabresi, V., Eming, R., Zuzzi, S., Bernardi, M.L., Scala, E., Mari, A.

“…Summary Background  Bullous pemphigoid (BP) is an autoimmune skin disease in which patient autoantibodies react with BP180 and BP230 proteins. In addition to…”
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Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV) by Borradori, L., Van Beek, N., Feliciani, C., Tedbirt, B., Antiga, E., Bergman, R., Böckle, B. C., Caproni, M., Caux, F., Chandran, N.S., Cianchini, G., Daneshpazhooh, M., De, D., Didona, D., Di Zenzo, G. M., Dmochowski, M., Drenovska, K., Ehrchen, J., Goebeler, M., Groves, R., Günther, C., Horvath, B., Hertl, M., Hofmann, S., Ioannides, D., Itzlinger‐Monshi, B., Jedličková, J., Kowalewski, C., Kridin, K., Lim, Y. L., Marinovic, B., Marzano, A. V., Mascaro, J.‐M., Meijer, J.M., Murrell, D., Patsatsi, K., Pincelli, C., Prost, C., Rappersberger, K., Sárdy, M., Setterfield, J., Shahid, M., Sprecher, E., Tasanen, K., Uzun, S., Vassileva, S., Vestergaard, K., Vorobyev, A., Vujic, I., Wang, G., Wozniak, K., Yayli, S., Zambruno, G., Zillikens, D., Schmidt, E., Joly, P.

“…Background Bullous pemphigoid (BP) is the most common autoimmune subepidermal blistering disease of the skin and mucous membranes. This disease typically…”
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European Guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology – Part II by Schmidt, E., Rashid, H., Marzano, A.V., Lamberts, A., Di Zenzo, G., Diercks, G.F.H., Alberti‐Violetti, S., Barry, R.J., Borradori, L., Caproni, M., Carey, B., Carrozzo, M., Cianchini, G., Corrà, A., Dikkers, F.G., Feliciani, C., Geerling, G., Genovese, G., Hertl, M., Joly, P., Meijer, J.M., Mercadante, V., Murrell, D.F., Ormond, M., Pas, H.H., Patsatsi, A., Rauz, S., Rhijn, B.D., Roth, M., Setterfield, J., Zillikens, D., C.Prost, Zambruno, G., Horváth, B., Caux, F.

“…This guideline has been initiated by the task force Autoimmune Blistering Diseases of the European Academy of Dermatology and Venereology, including physicians…”
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European guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology – Part I by Rashid, H., Lamberts, A., Borradori, L., Alberti‐Violetti, S., Barry, R.J., Caproni, M., Carey, B., Carrozzo, M., Caux, F., Cianchini, G., Corrà, A., Diercks, G.F.H., Dikkers, F.G., Di Zenzo, G., Feliciani, C., Geerling, G., Genovese, G., Hertl, M., Joly, P., Marzano, A.V., Meijer, J.M., Mercadante, V., Murrell, D.F., Ormond, M., Pas, H.H., Patsatsi, A., Prost, C., Rauz, S., Rhijn, B.D., Roth, M., Schmidt, E., Setterfield, J., Zambruno, G., Zillikens, D., Horváth, B.

“…This guideline on mucous membrane pemphigoid (MMP) has been elaborated by the Task Force for Autoimmune Blistering Diseases of the European Academy of…”
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Commentary on ‘Changing prevalence of diabetes mellitus in bullous pemphigoid: it is the dipeptidyl peptidase‐4 inhibitors’ by Fania, L., Di Zenzo, G., Mazzanti, C., Abeni, D.

“…Linked article: This article is commented on by A. Gravani et al., pp. e438–e439 in this issue. To view this article visit https://doi.org/10.1111/jdv.14957…”
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Increased prevalence of diabetes mellitus in bullous pemphigoid patients during the last decade by Fania, L., Di Zenzo, G., Didona, B., Pilla, M. A., Sobrino, L., Panebianco, A., Mazzanti, C., Abeni, D.

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Mortality and prognostic factors in patients with bullous pemphigoid: a retrospective multicenter Italian study by Bardazzi, F., Filippi, F., Chessa, M.A., Iommi, M., Loi, C., Campanati, A., Rizzetto, G., Tagliati, C., Atzori, L., Muratori, S., Genovese, G., Gisondi, P., Schena, D., Balestri, R., Rech, G., Feliciani, C., Lasagni, C., Bigi, L., De Simone, C., Di Zenzo, G., Moro, F., Borghi, A., Di Lernia, V., D'Arrigo, G., Tripepi, G., Gori, M., Pitino, A.

“…Introduction Bullous pemphigoid is the most common autoimmune bullous dermatosis. In recent years several studies have tried to identify the main factors of…”
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Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areata by Guerra, L., Pacifico, V., Calabresi, V., De Luca, N., Castiglia, D., Angelo, C., Zambruno, G., Di Zenzo, G.

“…Summary Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal blistering disease associated with autoantibodies against type VII collagen…”
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Development of bullous pemphigoid in junctional epidermolysis bullosa by Fania, L., Provini, A., Salemme, A., Sinagra, J.L., Guerra, L., Mazzanti, C., Didona, B., Castiglia, D., Di Zenzo, G.

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IgA tracheobronchial deposits underlie respiratory compromise in neonatal linear IgA bullous dermatosis by Diociaiuti, A., Zambruno, G., Diomedi Camassei, F., Di Zenzo, G., Capolupo, I., Stoppa, F., Forziati, V., El Hachem, M.

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New versatile monoclonal antibodies against type XVII collagen endodomain for diagnosis and subtyping COL17A1-associated junctional epidermolysis bullosa by Yuen, W.Y., Di Zenzo, G., Jonkman, M.F., Pas, H.H.

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A truncating mutation in the laminin-332α chain highlights the role of the LG45 proteolytic domain in regulating keratinocyte adhesion and migration by Di Zenzo, G., El Hachem, M., Diociaiuti, A., Boldrini, R., Calabresi, V., Cianfarani, F., Fortugno, P., Piccinni, E., Zambruno, G., Castiglia, D.

“…Summary Background Altered function of laminin‐332 (α3β3γ2) consequent to mutations in the LAMA3, LAMB3 and LAMC2 genes causes junctional epidermolysis bullosa…”
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