Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Jesper Petersen"'
Autor:
Andreas Glenthøj, Andreas Ørslev Rasmussen, Selma Kofoed Bendtsen, Henrik Hasle, Marianne Hoffmann, Klaus Rieneck, Morten Hanefeld Dziegiel, Lene Dissing Sjö, Henrik Frederiksen, Dennis Lund Hansen, Daniel El Fassi, Mathias Rathe, Peter-Diedrich Matthias Jensen, Anne Winther-Larsen, Christian Nielsen, Marianne Olsen, Nina Toft, Mads Okkels Birk Lorenzen, Lise Heilmann Jensen, Sif Gudbrandsdottir, Jens Helby, Maria Rossing, Richard van Wijk, Jesper Petersen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Hereditary anemias are a group of genetic diseases prevalent worldwide and pose a significant health burden on patients and societies. The clinical phenotype of hereditary anemias varies from compensated hemolysis to life-threaten
Externí odkaz:
https://doaj.org/article/571fe371a8f54ba6b50bfb5757c53faf
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Glucose-6-phosphate isomerase deficiency is a rare genetic disorder causing hereditary nonspherocytic hemolytic anemia. It is the second most common glycolytic enzymopathy in red blood cells. About 90 cases are reported worldwide,
Externí odkaz:
https://doaj.org/article/ae8494b4635f440bb46b234b20e90fbf
Autor:
Niels Vejlstrup, Pierre Fenaux, Jesper Petersen, Eduard J van Beers, Andreas Glenthøj, Kevin H M Kuo, Richard van Wijk, Minke A E Rab, Evelyn Groot, Nina Toft, Selma Kofoed Bendtsen, Jens Helby, Fatiha Chermat
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Introduction Membranopathies encompass haemolytic disorders arising from genetic variants in erythrocyte membrane proteins, including hereditary spherocytosis and stomatocytosis. Congenital dyserythropoietic anaemia type II (CDA II) is associated wit
Externí odkaz:
https://doaj.org/article/6958cd02f6274f47ad7b9e2b612e7a5c
Autor:
Mathis Mottelson, Jens Helby, Børge Grønne Nordestgaard, Christina Ellervik, Thomas Mandrup-Poulsen, Jesper Petersen, Stig Egil Bojesen, Andreas Glenthøj
Publikováno v:
HemaSphere, Vol 7, p e7367624 (2023)
Externí odkaz:
https://doaj.org/article/fa4d9c99c8574fca9d852754b54d2058
Autor:
Esther Gravholt, Jesper Petersen, Mathis Mottelson, Amina Nardo‐marino, Mathias Rathe, Marianne Olsen, Charlotte Holm, Finn Jørgensen, Henrik Birgens, Andreas Glenthøj
Publikováno v:
HemaSphere, Vol 7, p e484735b (2023)
Externí odkaz:
https://doaj.org/article/fde5f42fcb6d453b877b27a34337ef3e
Autor:
Lars Konradsen, Mikael Boesen, Philip Hansen, Michael Kjaer, Peter Magnusson, Michael Krogsgaard, Peter Rasmussen, Jesper Petersen, Rikke Høffner, Anne-Sofie Agergaard, Rene Svensson, Rasmus Mikkelsen
Publikováno v:
BMJ Open Sport & Exercise Medicine, Vol 9, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/f8a1f498dc18430e94bfe70905ce9b9b
Autor:
Andreas Glenthøj, Christian Brieghel, Amina Nardo‐Marino, Richard vanWijk, Henrik Birgens, Jesper Petersen
Publikováno v:
eJHaem, Vol 2, Iss 4, Pp 716-728 (2021)
Abstract The eosin‐5′‐maleimide (EMA) binding test is widely used as diagnostic test for hereditary spherocytosis (HS), one of the most common haemolytic disorders in Caucasian populations. We recently described the advantages of replacing the
Externí odkaz:
https://doaj.org/article/ae1d224784b14e03990957bcb80e71ca
Autor:
Jesper Petersen
Publikováno v:
Tidsskrift for Islamforskning, Vol 16, Iss 2 (2022)
Essays udgivet af Scandinavian Journal of Islamic Studies er ikke fagfællebedømt.
Externí odkaz:
https://doaj.org/article/dd50a550c734405882932c36e1ebb2b5
Autor:
Jesper Petersen
Publikováno v:
Tidsskrift for Islamforskning, Vol 16, Iss 2 (2022)
Denne artikel udgør et pilotstudie, som baseret på fem semi-strukturerede interviews undersøger minoritetsunges sproglige konceptualisering af æresrelaterede konflikter og de følelser, disse giver anledning til. Således har artiklens første de
Externí odkaz:
https://doaj.org/article/469bc5a7bd684ed08fecdf84c4e45500
Autor:
Nanna Brøns, Carlo Zaninetti, Sisse Rye Ostrowski, Jesper Petersen, Andreas Greinacher, Maria Rossing, Eva Leinøe
Publikováno v:
Platelets, Vol 32, Iss 5, Pp 701-704 (2021)
Genetic variants in growth factor-independent 1B (GFI1B), encoding transcription factor GFI1B, are causative of platelet-type bleeding disorder-17. Presently, 53 cases of GFI1B associated inherited thrombocytopenia (IT) have been published, however o
Externí odkaz:
https://doaj.org/article/d41c21d71e054f66afbe48257970edb5