Výsledky vyhledávání - "G. Pohla‐Gubo"

Low rate of new‐onset primary biliary cholangitis in a cohort of anti‐mitochondrial antibody‐positive subjects over six years of follow‐up

Autor: G. Pohla‐Gubo, Bernhard Paulweber, Elmar Aigner, Ursula Huber-Schönauer, Christian Datz, Thomas K. Felder, Stephan Zandanell, Julia Tevini, Alexandra Feldman, G. Strebinger, Michael Strasser, S. Ruhaltinger, David Niederseer

Publikováno v: Journal of Internal Medicine

Background and Aims Anti‐mitochondrial antibodies (AMA) are closely linked to primary biliary cholangitis (PBC). The prevalence of AMA in the general population is low, and AMA positivity may precede PBC. We aimed to determine the natural history o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1acc9e549190f3d840fd2003618135a
https://doi.org/10.1111/joim.13005

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Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa

Autor: Maria C. Bolling, K. Wertheim‐Tysarowska, P. C. van den Akker, G. Pohla-Gubo, M. El Hachem, Giovanna Zambruno, S. Büchel, Cristina Has, R. Hiremagalore, María José Escámez, Ignacia Fuentes, A. Charlesworth, Lin Liu

Publikováno v: BRITISH JOURNAL OF DERMATOLOGY, 182(3), 574-592. Wiley

This guideline were initiated by DEBRA International; financial support was provided by DEBRA Austria. The generous assistance of Rebecca Bodan, Lisa Brains, Sharon Cassidy and Kelsey Townsend-Miller is gratefully acknowledged in providing patient or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae58ebd11febeaaeadad241a9fb10ee0
https://pubmed.ncbi.nlm.nih.gov/31436321

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Mapeo por inmunofluorescencia para el diagnóstico de epidermólisis ampollosa congénita

Autor: Rodrigo Cepeda-Valdes, J. Ancer-Rodríguez, José R. Borbolla-Escoboza, Oralia Barboza-Quintana, G. Pohla-Gubo, H. Hintner, J.C. Salas-Alanis

Publikováno v: Actas Dermo-Sifiliográficas. 101:673-682

The tools for diagnosis of epidermolysis bullosa have advanced greatly since Hintner's group introduced antigen mapping as a diagnostic test for this family of genodermatoses. Monoclonal or polyclonal antibodies raised against some of the specific pr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc457b4d531f245db548abddec60f3d7
https://doi.org/10.1016/j.ad.2010.06.003

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Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis Bullosa

Autor: J. Ancer-Rodríguez, José R. Borbolla-Escoboza, J.C. Salas-Alanisa, Rodrigo Cepeda-Valdes, H. Hintner, G. Pohla-Gubo, Oralia Barboza-Quintana

Publikováno v: Actas Dermo-Sifiliográficas (English Edition). 101:673-682

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::069b451eecc376a26fd1b578b5dda269
https://doi.org/10.1016/s1578-2190(10)70697-1

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Epidermolysis bullosa hereditaria

Autor: E. Nischler, Johann W. Bauer, C. M. Lanschützer, Martin Laimer, H. Hintner, G. Pohla-Gubo, A. Diem, Alfred Klausegger

Publikováno v: Monatsschrift Kinderheilkunde. 156:110-121

Epidermolysis bullosa (EB) steht fur eine heterogene Gruppe seltener, erblicher Krankheiten, deren Hauptcharakteristikum die ausgepragte Fragilitat der Haut und Schleimhaute bei geringster mechanischer Belastung ist. In den letzten Jahren wurden bede

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9d8e6d7d1d23bb6a1331ab1b1d1f9f7d
https://doi.org/10.1007/s00112-007-1663-x

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Zahnveranderung bei junktionaler Epidermolysis bullosa - Bericht uber eine Patientin mit einer Mutation im LAMB3-Gen. Dental alterations in junctional epidermolysis bullosa - report of a patient with a mutation in the LAMB3-gene

Autor: Martin Laimer, Johannes Hachleitner, G. Pohla-Gubo, Elke Sadler, Rudolf J. Stadlhuber, Wolfgang Muss, Alfred Klausegger, Helmut Hintner, Johann W. Bauer, Anja Diem

Publikováno v: Journal der Deutschen Dermatologischen Gesellschaft. 3:359-363

During early odontogenesis the basement membrane is known to be important in epithelio-mesenchymal interactions. Mutations in the gene of one of the major structural proteins of the basement membrane such as laminin 5 might therefore be expected eith

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d300eec267af4ba8c2551cac68f86d1e
https://doi.org/10.1111/j.1610-0387.2005.05703.x

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Telepathology using immunofluorescence/immunoperoxidase microscopy

Autor: G Pohla-Gubo, Takashi Hashimoto, B. Schafleitner, J W Bauer, CM Lanschuetzer, H Hintner, R Hametner, Wolfgang Salmhofer

Publikováno v: Journal of Telemedicine and Telecare. 10:39-43

We evaluated low-cost, store-and-forward telepathology interpretation of digital images of skin sections stained immunohistochemically, using immunofluorescence (IF) and immunoperoxidase (IP). The sample comprised 17 patients with skin diseases chara

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd3af1cab106e743ccda9016ac606cf
https://doi.org/10.1258/135763304322764185

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Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Autor: W. H. Muss, G. Pohla-Gubo, CM Lanschuetzer, Michael Emberger, J W Bauer, H Hintner, A. Klausegger

Publikováno v: Journal of Cutaneous Pathology. 30:553-560

Background: Kindler's syndrome is a rare genodermatosis mainly characterized by the onset of skin blistering in early childhood, web formation of fingers and toes, photosensitivity, and progressive poikiloderma. There is still debate whether this dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::83924f9bcd0134650d2ddd09943946b6
https://doi.org/10.1034/j.1600-0560.2003.00119.x

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