Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease von Zagaglia, S, Selch, C, Nisevic, JR, Mei, D, Michalak, Z, Hernandez-Hernandez, L, Krithika, S, Vezyroglou, K, Varadkar, SM, Pepler, A, Biskup, S, Leão, M, Gärtner, J, Merkenschlager, A, Jaksch, M, Møller, RS, Gardella, E, Kristiansen, BS, Hansen, LK, Vari, MS, Helbig, KL, Desai, S, Smith-Hicks, CL, Hino-Fukuyo, N, Talvik, T, Laugesaar, R, Ilves, P, Õunap, K, Körber, I, Hartlieb, T, Kudernatsch, M, Winkler, P, Schimmel, M, Hasse, A, Knuf, M, Heinemeyer, J, Makowski, C, Ghedia, S, Subramanian, GM, Striano, P, Thomas, RH, Micallef, C, Thom, M, Werring, DJ, Kluger, GJ, Cross, JH, Guerrini, R, Balestrini, S, Sisodiya, SM

Volltext bestellen

Perinatal outcome after first‐trimester risk assessment in monochorionic and dichorionic twin pregnancies: a population‐based register study von Kristiansen, MK, Joensen, BS, Ekelund, CK, Petersen, OB, Sandager, P

Volltext

Higher vs lower doses of dexamethasone in patients with COVID‐19 and severe hypoxia (COVID STEROID 2) trial: Protocol and statistical analysis plan von Munch, MW, Granholm, Anders, Myatra, SN, Vijayaraghavan, BKT, Cronhjort, Maria, Wahlin, RR, Jakob, Stephan M., Cioccari, Luca, Kjær, MN, Vesterlund, GK, Meyhoff, TS, Helleberg, Marie, Møller, MH, Benfield, Thomas, Venkatesh, Balasubramanian, Hammond, Naomi, Micallef, Sharon, Bassi, Abhinav, John, Oommen, Jha, Vivekanand, Kristiansen, KT, Ulrik, CS, Jørgensen, VL, Smitt, Margit, Bestle, Morten H., Andreasen, AS, Poulsen, LM, Rasmussen, BS, Brøchner, AC, Strøm, Thomas, Møller, Anders, Khan, MS, Padmanaban, Ajay, Divatia, JV, Saseedharan, Sanjith, Borawake, Kapil, Kapadia, Farhad, Dixit, Subhal, Chawla, Rajesh, Shukla, Urvi, Amin, Pravin, Chew, Michelle S., Gluud, Christian, Lange, Theis, Perner, Anders

Volltext

Incorrect Equivalent Dose and P Values in Figure 3 von Munch, MW, Myatra, SN, Vijayaraghavan, BKT, Saseedharan, S, Benfield, T, Wahlin, RR, Rasmussen, BS, Andreasen, AS, Poulsen, LM, Cioccari, L, Khan, MS, Kapadia, F, Divatia, JV, Brochner, AC, Bestle, MH, Helleberg, M, Michelsen, J, Padmanaban, A, Bose, N, Moller, A, Borawake, K, Kristiansen, KT, Shukla, U, Chew, MS, Dixit, S, Ulrik, CS, Amin, PR, Chawla, R, Wamberg, CA, Shah, MS, Darfelt, IS, Jorgensen, VL, Smitt, M, Granholm, A, Kjaer, MBN, Moller, MH, Meyhoff, TS, Vesterlund, GK, Hammond, NE, Micallef, S, Bassi, A, John, O, Jha, A, Cronhjort, M, Jakob, SM, Gluud, C, Lange, T, Kadam, V, Marcussen, KV, Hollenberg, J, Hedman, A, Nielsen, H, Schjorring, OL, Jensen, MQ, Leistner, JW, Jonassen, TB, Kristensen, CM, Clapp, EC, Hjortso, CJS, Jensen, TS, Halstad, LS, Bak, ERB, Zaabalawi, R, Metcalf-Clausen, M, Abdi, S, Hatley, EV, Aksnes, TS, Gleipner-Andersen, E, Alarcon, AF, Yamin, G, Heymowski, A, Berggren, A, La Cour, K, Weihe, S, Pind, AH, Engstrom, J, Jha, V, Venkatesh, B, Perner, A

Volltext

Toxic trace element reference levels in blood and urine: influence of gender and lifestyle factors von Kristiansen, Jesper, Christensen, Jytte Molin, Iversen, Bent S., Sabbioni, E.

Volltext

Cloning and Characterization of Human Very-Long-Chain Acyl-CoA Dehydrogenase cDNA, Chromosomal Assignment of the Gene and Identification in Four Patients of Nine Different Mutation... von Andresen, Brage Storstein, Bross, Peter, Vianey-Saban, Christine, Divry, Priscille, Zabot, Marie-Thérèse, Roe, Charles R., Nada, Mohamed A., Byskov, Annette, Kruse, Torben A., Neve, Søren, Kristiansen, Karsten, Knudsen, Inga, Corydon, Morten Juhl, Gregersen, Niels

Volltext

Inductively coupled plasma mass spectrometric determination of molybdenum in urine from a Danish population von IVERSEN, B. S, MENNE, C, WHITE, M. A, KRISTIANSEN, J, CHRISTENSEN, J. M, SABBIONI, E

Volltext

Evaluation of a Simple Dosage Scheme for Transition from Phenprocoumon to Warfarin in Oral Anticoagulation von Kristiansen, Charlotte, Lassen, Jens Flensted, Dahler-Eriksen, Bjarne Steen, Dahler-Eriksen, Kathrine, Larsen, Torben Bjerregaard, Brandslund, Ivan

Volltext

A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein von Jensen, H.K, Holst, H, Jensen, L.G, Jørgensen, M.M, Andreasen, P.H, Jensen, T.G, Andresen, B.S, Heath, F, Hansen, P.S, Neve, S, Kristiansen, K, Færgeman, O, Kølvraa, S, Bolund, L, Gregersen, N

Volltext