Zobrazeno 1 - 10
of 619
pro vyhledávání: '"Heickendorff, L."'
Publikováno v:
In Magnetic Resonance Materials in Physics, Biology & Medicine 2001 12(2):153-166
Autor:
Hulshof, M.M., Bavinck, J.N.Bouwes, Bergman, W., Masclee, A.A.M., Heickendorff, L., Breedveld, F.C., Dijkmans, B.A.C.
Publikováno v:
In Journal of the American Academy of Dermatology December 2000 43(6):1017-1023
Autor:
Jensen, P.-D.1, Heickendorff, L.2, Carlson, I.1, Jensen, F. T.3, Christensen, T.3, Ellegaard, J.1
Publikováno v:
Transfusion Medicine. Feb2001, Vol. 11 Issue 1, p21-30. 10p.
Autor:
Christiansen, P *, Steiniche, T, Brixen, K, Hessov, I, Melsen, F, Heickendorff, L, Mosekilde, Le
Publikováno v:
In Bone 1999 25(5):597-602
Autor:
Christiansen, P. *, Steiniche, T., Brixen, K., Hessov, I., Melsen, F., Heickendorff, L., Mosekilde, Le.
Publikováno v:
In Bone 1999 25(5):589-595
Autor:
Christiansen, P *, Steiniche, T, Brixen, K, Hessov, I, Melsen, F, Heickendorff, L, Mosekilde, Le
Publikováno v:
In Bone 1999 25(2):237-244
Autor:
Rasmussen, TB, Nissen, PH, Palmfeldt, J, Gehmlich, K, Dalager, S, Jensen, UB, Kim, WY, Heickendorff, L, Molgaard, H, Jensen, HK, Baandrup, UT, Bross, P, Mogensen, J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ddf75a611847681ce4a5a5f899fdf70
https://ora.ox.ac.uk/objects/uuid:f78c9a78-0ac0-4b16-b35e-3c9351d6958d
https://ora.ox.ac.uk/objects/uuid:f78c9a78-0ac0-4b16-b35e-3c9351d6958d
Autor:
Rasmussen, G. Bloch, Langdahl, B. L., Heickendorff, L., Vestergaard, Peter, Mosekilde, L., Rejnmark, L.
Publikováno v:
Rasmussen, G B, Langdahl, B L, Heickendorff, L, Vestergaard, P, Mosekilde, L & Rejnmark, L 2014, ' Effects of vitamin d supplementation before and during pregnancy : A randomized controlled trial ', PhD day 2014, Aarhus, Denmark, 24/01/2014-24/01/2014 . < http://phd.au.dk/fileadmin/grads.au.dk/HE/PhD_Day_2014/PhD_Day_2014_abstract_book_01.pdf >
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6bbe3a4b0860bbeddddf2d2eb22a1052
https://vbn.aau.dk/da/publications/32a38901-50cc-4efb-9d22-bee331c82029
https://vbn.aau.dk/da/publications/32a38901-50cc-4efb-9d22-bee331c82029
Autor:
Rasmussen, Tb, Hansen, J., Nissen, Ph, Palmfeldt, J., Dalager, S., Jensen, Ub, Kim, Wy, Heickendorff, L., Mølgaard, H., Jensen, Hk, Sørensen, Ke, Baandrup, Ulrik, Bross, P., Mogensen, J.
Publikováno v:
Rasmussen, T, Hansen, J, Nissen, P, Palmfeldt, J, Dalager, S, Jensen, U, Kim, W, Heickendorff, L, Mølgaard, H, Jensen, H, Sørensen, K, Baandrup, U, Bross, P & Mogensen, J 2013, ' Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms ', Clinical Genetics, vol. 84, no. 1, pp. 20-30 . https://doi.org/10.1111/cge.12056
Clinical Genetics
Clinical Genetics; Vol 84
Rasmussen, T B, Hansen, J, Nissen, P H, Palmfeldt, J, Dalager, S, Jensen, U B, Kim, W Y, Heickendorff, L, Mølgaard, H, Jensen, H K, Sørensen, K E, Baandrup, U T, Bross, P & Mogensen, J 2013, ' Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms ', Clinical Genetics, vol. 84, no. 1, pp. 20-30 . https://doi.org/10.1111/cge.12056
Rasmussen, T B, Hansen, J, Nissen, P H, Palmfeldt, J, Dalager, S, Jensen, U B, Kim, W Y, Heickendorff, L, Molgaard, H, Jensen, H K, Sorensen, K E, Baandrup, U T, Bross, P & Mogensen, J 2013, ' Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms ', Clinical Genetics, vol. 84, no. 1, pp. 20-30 . https://doi.org/10.1111/cge.12056
Clinical Genetics
Clinical Genetics; Vol 84
Rasmussen, T B, Hansen, J, Nissen, P H, Palmfeldt, J, Dalager, S, Jensen, U B, Kim, W Y, Heickendorff, L, Mølgaard, H, Jensen, H K, Sørensen, K E, Baandrup, U T, Bross, P & Mogensen, J 2013, ' Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms ', Clinical Genetics, vol. 84, no. 1, pp. 20-30 . https://doi.org/10.1111/cge.12056
Rasmussen, T B, Hansen, J, Nissen, P H, Palmfeldt, J, Dalager, S, Jensen, U B, Kim, W Y, Heickendorff, L, Molgaard, H, Jensen, H K, Sorensen, K E, Baandrup, U T, Bross, P & Mogensen, J 2013, ' Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms ', Clinical Genetics, vol. 84, no. 1, pp. 20-30 . https://doi.org/10.1111/cge.12056
Mutations in the gene for desmoplakin (DSP) may cause arrhythmogenic right ventricular cardiomyopathy (ARVC) and Carvajal syndrome (CS). Desmoplakin is part of all desmosomes, which are abundantly expressed in both myocardial and epidermal tissue and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6491addfa83095bc699a3f1602ecf678
https://vbn.aau.dk/da/publications/4285db2a-40fb-4e5d-91e4-9e50b1d075f3
https://vbn.aau.dk/da/publications/4285db2a-40fb-4e5d-91e4-9e50b1d075f3
Publikováno v:
International Journal of Angiology (Springer Science & Business Media B.V.). Winter2003, Vol. 12 Issue 1, p29-31. 3p.