Zobrazeno 1 - 10
of 14
pro vyhledávání: '"L H Poulsen"'
Autor:
C. J. Vinther, L. H. Poulsen, P. Nicolaisen, M. L. Obling, T. H. Brix, A. P. Hermann, L. Hegedüs, N. R. Jørgensen, S. Hansen, S. J. Bonnema
Publikováno v:
Journal of Endocrinological Investigation. 46:345-358
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22cbb999c688395fbb5f80de6a84859d
https://doi.org/10.1007/s40618-022-01907-2
https://doi.org/10.1007/s40618-022-01907-2
Publikováno v:
BMC Hematology, Vol 18, Iss 1, Pp 1-4 (2018)
BMC Hematology
Nissen, S K, Laursen, A L, Poulsen, L H & Mogensen, T H 2018, ' Identification of a novel mutation in the factor VIII gene causing severe haemophilia A ', BMC Hematology, vol. 18, pp. 17 . https://doi.org/10.1186/s12878-018-0113-4
BMC Hematology
Nissen, S K, Laursen, A L, Poulsen, L H & Mogensen, T H 2018, ' Identification of a novel mutation in the factor VIII gene causing severe haemophilia A ', BMC Hematology, vol. 18, pp. 17 . https://doi.org/10.1186/s12878-018-0113-4
Background Deficiency in coagulation factor VIII encoded by F8 results in the X-linked recessive bleeding disorder haemophilia A (HEMA). Here we describe the identification of a novel variant in the factor VIII gene, F8, in an adult male patient with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef14e14625b2e3e6b2272a1fea85d01
http://link.springer.com/article/10.1186/s12878-018-0113-4
http://link.springer.com/article/10.1186/s12878-018-0113-4
Clinical evaluation of glycoPEGylated recombinant FVIII: Efficacy and safety in severe haemophilia A
Autor:
A. Tiede, Paul Giangrande, K. Hampton, T. Lambert, Meera Chitlur, L. Alberio, C. Negrier, H. Takedani, Michael Recht, S. Lentz, Woei Tsay, S. Dunkley, Miguel A. Escobar, T. Fujii, P. Kampmann, Christine M. Knoll, M. Shima, T. A. Andreeva, Peter G. Jönsson, Steven R. Lentz, Chris Barnes, L. Nemes, Johannes Oldenburg, K. Fukutake, B. Brand, H. Hanabusa, Elena Santagostino, M. Guerrera, E. Cockrell, Tadashi Matsushita, Jerry S. Powell, Lone Hvitfeldt Poulsen, Ralph A. Gruppo, Laszlo Nemes, J. Morales, C. Rothschild, G. Thomson, P. Chowdary, J. Felgenhauer, S. Zupancic-Salek, J. Sathar, N. Apollonsky, A. Tosetto, Roshni Kulkarni, J. Lazarchick, E. M. Mingot, S. Madoiwa, M. Misgav, V Jiménez Yuste, Z. Boda, K. Meijer, E. Zetterberg, G. K. Guron, M. Castro Ozelo, G. R. Nagasubramanian, S. Kearney, Pratima Chowdary, J. Oldenburg, C. Albayrak, Frank W.G. Leebeek, Silke Ehrenforth, Savita Rangarajan, Tatiana Andreeva, K. Kavakli, H. Eichler, L. H. Poulsen, Faraizah Abdul Karim, A. Kutlar, J. Wright, M. Trossaert, P. Kavasch, M. C. Shen, Chur Woo You, P. A. Holme, E. Santagostino, Wan Hui Ong Clausen, N. Curry, I. Sasmaz, W. Miesbach, A. Shibuya, A. Paroskie-Wheeler, E. Lowe, Clifford M Takemoto, D. Yee, F. Boehlen, S. Brown, F. W. G. Leebeek, J. Lasky, Peter William Collins, T. Sato, Robert Klamroth, K. Dunsmore
Publikováno v:
Thrombosis and Haemostasis, 117(2), 252-261. Georg Thieme Verlag
Giangrande, P, Andreeva, T, Chowdary, P, Ehrenforth, S, Hanabusa, H, Leebeek, F W G, Lentz, S R, Nemes, L, Poulsen, L H, Santagostino, E, You, C W, Clausen, W H O, Jönsson, P G, Oldenburg, J & Pathfinder™2 Investigators 2017, ' Clinical evaluation of glycoPEGylated recombinant FVIII : Efficacy and safety in severe haemophilia A ', Thrombosis and Haemostasis, pp. 252-261 . https://doi.org/10.1160/TH16-06-0444
Giangrande, P, Andreeva, T, Chowdary, P, Ehrenforth, S, Hanabusa, H, Leebeek, F W G, Lentz, S R, Nemes, L, Poulsen, L H, Santagostino, E, You, C W, Clausen, W H O, Jönsson, P G, Oldenburg, J & Pathfinder™2 Investigators 2017, ' Clinical evaluation of glycoPEGylated recombinant FVIII : Efficacy and safety in severe haemophilia A ', Thrombosis and Haemostasis, pp. 252-261 . https://doi.org/10.1160/TH16-06-0444
Turoctocog alfa pegol (N8-GP) is a novel glycoPEGylated extended half-life recombinant factor VIII (FVIII) product developed for prophylaxis and treatment of bleeds in patients with haemophilia A, to enable higher activity levels with less frequent i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deca7c652b62e159aa11378000e7fe8c
https://pure.eur.nl/en/publications/5f120d71-685a-4410-9b98-59e6346a7976
https://pure.eur.nl/en/publications/5f120d71-685a-4410-9b98-59e6346a7976
Autor:
G van Overeem Hansen, Peter Junker, L H Poulsen, Jørgen Holm Petersen, Søren Jacobsen, Halberg P, Ulrik Tarp, J M Rasmussen, Anne Voss, T M Hansen, S Ullman, Jan Pødenphant, B Skaarup
Publikováno v:
Scopus-Elsevier
A multicentre cohort of 513 clinic attenders with systemic lupus erythematosus (SLE) was retrospectively identified, representing 4185 patient-years of follow-up. Expected numbers of death were calculated by means of age- and sex-specific mortality r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3b8a129f4a808759d8e2977fc855713
https://doi.org/10.1080/030097499442522
https://doi.org/10.1080/030097499442522
Autor:
E S S Hansen, Ellen Margrethe Hauge, K Stengaard-Petersen, L H Poulsen, A Blavnsfeldt, H Mølgaard, S Høyer
Publikováno v:
Blavnsfeldt, A-B, Høyer, S, Mølgaard, H, Poulsen, L H, Hansen, E, Stengaard-Pedersen, K & Hauge, E M 2015, ' Severe acute and reversible heart failure shortly after childbirth : systemic lupus erythematosus or peripartum cardiomyopathy? ', Scandinavian Journal of Rheumatology, vol. 44, no. 1, pp. 83-4 . https://doi.org/10.3109/03009742.2014.943805
A 27-year-old gravida 1 para 0 was admitted to the obstetrics ward with suspicion of HELLP syndrome. She had a 2-year history of anti-phospholipid syndrome (APS) after a spontaneous deep venous thr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10dc45f65dbffb3924a810a21480ee8c
https://doi.org/10.3109/03009742.2014.943805
https://doi.org/10.3109/03009742.2014.943805
Autor:
Halberg P, Jørgen Holm Petersen, Anne Voss, Peter Junker, J. Pødenphant, T M Hansen, G van Overeem Hansen, Ulrik Tarp, Ullman S, Søren Jacobsen, L H Poulsen, J M Rasmussen, B Skaarup
Publikováno v:
Jacobsen, S, Petersen, J, Ullman, S, Junker, P, Voss, A, Rasmussen, J M, Tarp, U, Poulsen, L H, van Overeem Hansen, G, Skaarup, B, Hansen, T M, Pødenphant, J & Halberg, P 1998, ' A multicentre study of 513 Danish patients with systemic lupus erythematosus. I. Disease manifestations and analyses of clinical subsets ', Clinical Rheumatology, vol. 17, no. 6, pp. 468-77 . https://doi.org/10.1007/BF01451282
Capital Region of Denmark
Capital Region of Denmark
A Danish multicentre study was undertaken of the manifestations, infections, thrombotic events, survival and predictive factors of survival in 513 Danish patients with systemic lupus erythematosus (SLE) according to the 1982 classification criteria o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a41064e05aab2da8d23cee163cfd1a
https://doi.org/10.1007/bf01451282
https://doi.org/10.1007/bf01451282
Autor:
P Petersen, L H Poulsen, Susanne Helweg-Larsen, Jannick Brennum, Troels S. Jensen, A Andreasen, Asbjørn Mohr Drewes
Publikováno v:
Europe PubMed Central
Objective: To develop a methodology for translating the McGill Pain Questionaire (MPQ) into a Danish version, and to make comparisons to studies of patients speaking other languages. Design: Finding suitable Danish adjectives using the same methodolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4e8090c4136baa0d506895c4fda9ca4
https://doi.org/10.1097/00002508-199306000-00002
https://doi.org/10.1097/00002508-199306000-00002
Publikováno v:
The British journal of dermatology. 164(2)
Peristomal skin problems are common and are treated by a variety of health professionals. Clear and consistent communication among these professionals is therefore particularly important. The Ostomy Skin Tool (OST) is a new assessment instrument for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b835379dd5a08b340dc4464686391119
https://pubmed.ncbi.nlm.nih.gov/20973766
https://pubmed.ncbi.nlm.nih.gov/20973766
Publikováno v:
European journal of haematology. 73(6)
In this study, we present a case of late-puerperal onset of thrombohemorrhagic complications in a 33-yr-old woman with known antiphospholipid syndrome (APS) and heterozygosity for factor V Leiden gene mutation. Antithrombotic prophylaxis with low-mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c999b2a1584484cd10092e4c69e73612
https://pubmed.ncbi.nlm.nih.gov/15522067
https://pubmed.ncbi.nlm.nih.gov/15522067
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 9(4)
In the clinical setting, patients suffering from haemophilia are classified according to the residual level of the deficient coagulation factor. Patients suffering from the severe form of haemophilia (critical factor level0.01 IU mL-1) display some h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7a7733413f650b5b639841b1dd50e007
https://pubmed.ncbi.nlm.nih.gov/12828667
https://pubmed.ncbi.nlm.nih.gov/12828667