Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kristin Kernland Lang"'
Autor:
Susanne von der Heydt, Regula Waelchli, Alexandra Smith, Martin Theiler, Ralph Gnannt, Lisa Weibel, Sarah F. Schoch, Kathrin Neuhaus, Isabelle Luchsinger, Malcolm Kohler, Agnes Schwieger-Briel, Salome Kurth, Nicole Knöpfel, Kristin Kernland-Lang
Publikováno v:
European Journal of Pediatrics
Sleep problems are frequently reported in infants treated with propranolol for infantile hemangiomas, possibly serving as a marker for a negative impact on central nervous system function. In this cohort study, we objectively investigate the sleep be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4070002594626cedca708f3bf6fee37d
https://doi.org/10.1007/s00431-021-04147-3
https://doi.org/10.1007/s00431-021-04147-3
Autor:
Martin Theiler, Regula Wälchli, Kristin Kernland-Lang, Lisa Weibel, Nicole Knöpfel, Katharina Steindl
Publikováno v:
Pediatric Dermatology. 37:740-741
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef5724cdaa8c207c336106658ee56fc6
https://doi.org/10.1111/pde.14223
https://doi.org/10.1111/pde.14223
Autor:
Kristin Kernland Lang, Miranda Nijenhuis, Katarzyna B. Gostynska, Marcel F. Jonkman, Maria J. Castañón, Hendrikus Pas, Gerhard Wiche, Henny H. Lemmink, Anna M.G. Pasmooij
Publikováno v:
Human Molecular Genetics, 24(11), 3155-3162. Oxford University Press
Gostyńska, Katarzyna B.; Nijenhuis, Miranda; Lemmink, Henny; Pas, Hendri H.; Pasmooij, Anna M.G.; Kernland Lang, Kristin; Castañón, Maria J.; Wiche, Gerhard; Jonkman, Marcel F. (2015). Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. Human molecular genetics, 24(11), pp. 3155-3162. Oxford University Press 10.1093/hmg/ddv066
Gostyńska, Katarzyna B.; Nijenhuis, Miranda; Lemmink, Henny; Pas, Hendri H.; Pasmooij, Anna M.G.; Kernland Lang, Kristin; Castañón, Maria J.; Wiche, Gerhard; Jonkman, Marcel F. (2015). Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. Human molecular genetics, 24(11), pp. 3155-3162. Oxford University Press 10.1093/hmg/ddv066
PLEC, the gene encoding the cytolinker protein plectin, has eight tissue-specific isoforms in humans, arising by alternate splicing of the first exon. To date, all PLEC mutations that cause epidermolysis bullosa simplex (EBS) were found in exons comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd8f6645de9a7513236b8fa45cd826c
http://doc.rero.ch/record/299576/files/ddv066.pdf
http://doc.rero.ch/record/299576/files/ddv066.pdf
Publikováno v:
Lemke, Johannes R.; Kernland Lang, Kristin Helene; Hörtnagel, Konstanze; Itin, Peter (2014). Monogenic Human Skin Disorders. Dermatology, 229(2), pp. 55-64. Karger 10.1159/000362200
Human genodermatoses represent a broad and partly confusing spectrum of countless rare diseases with confluent and overlapping phenotypes often impeding a precise diagnosis in an affected individual. High-throughput sequencing techniques have expedit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a55a1a8ed5f2416681dc5b8663e7c535
https://doi.org/10.1159/000362200
https://doi.org/10.1159/000362200
Autor:
Carrie J. Markowski, Lasse R. Braathen, Gustav Gaudernack, Kristin Kernland Lang, Mona Møller, Anne Marie Rasmussen, Jon Alm Eriksen, Sissel Trachsel, Robert E. Hunger
Publikováno v:
Hunger, Robert E; Kernland Lang, Kristin; Markowski, Carrie J; Trachsel, Sissel; Møller, Mona; Eriksen, Jon A; Rasmussen, Anne-Marie; Braathen, Lasse R; Gaudernack, Gustav (2011). Vaccination of patients with cutaneous melanoma with telomerase-specific peptides. Cancer immunology, immunotherapy, 60(11), pp. 1553-64. Heidelberg: Springer-Verlag 10.1007/s00262-011-1061-z
Purpose: A phase I study was conducted to investigate the safety, tolerability, and immunological responses to vaccination with a combination of telomerase-derived peptides GV1001 (hTERT: 611-626) and p540 (hTERT: 540-548) using granulocyte-macrophag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf4bd877c95f973de2d6b583a5c3252
https://doi.org/10.1007/s00262-011-1061-z
https://doi.org/10.1007/s00262-011-1061-z
Autor:
John A. McGrath, Wataru Fujimoto, Iliana Tantcheva-Poor, Cristina Has, Emma Wedgeworth, Kristin Kernland-Lang, Jemima E. Mellerio, Leena Bruckner-Tuderman, Peter Itin, Michael A. Simpson, Dimitra Kiritsi, Claus-Werner Franzke, Patricia J.C. Dopping-Hepenstal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14c82d8c31810ec44d9c1dc4ddaaef7f
Autor:
Roland A. Ammann, Kurt Leibundgut, Christoph Aebi, Kristin Kernland Lang, Miriam Diepold, Sara Bernhard, Sonja Lüer
Publikováno v:
The Pediatric infectious disease journal. 31(7)
Voriconazole is used in antifungal prophylaxis. We performed a retrospective review of immunocompromised children receiving prophylaxis with voriconazole during major hospital renovation, who developed phototoxic skin reactions. The overall incidence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6902985e05e8553628201f716b2b2997
https://pubmed.ncbi.nlm.nih.gov/22517339
https://pubmed.ncbi.nlm.nih.gov/22517339
Autor:
Kristin Kernland Lang, Dagmar Simon
Publikováno v:
Current opinion in pediatrics. 23(6)
Recent published work on atopic dermatitis focusing on the pathogenesis and epidemiology, which have a direct effect on treatment, is presented.Worldwide, the incidence of atopic dermatitis is still increasing, although a plateau seems to be reached
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8f9d020dc6c7c06f2564a89ffcfa09f
https://pubmed.ncbi.nlm.nih.gov/21970829
https://pubmed.ncbi.nlm.nih.gov/21970829
Publikováno v:
Journal of the American Academy of Dermatology. 50:P136
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4511b7f138851047af1c93d3f171f4ac
https://doi.org/10.1016/j.jaad.2003.10.471
https://doi.org/10.1016/j.jaad.2003.10.471
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