The rate of quasiparticle recombination probes the onset of coherence in cuprate superconductors von Hinton, J. P., Thewalt, E., Alpichshev, Z., Mahmood, F., Koralek, J. D., Chan, M. K., Veit, M. J., Dorow, C. J., Barišić, N., Kemper, A. F., Bonn, D. A., Hardy, W. N., Liang, Ruixing, Gedik, N., Greven, M., Lanzara, A., Orenstein, J.

Volltext

Charge order and its connection with Fermi-liquid charge transport in a pristine high-Tc cuprate von Tabis, W., Li, Y., Tacon, M. Le, Braicovich, L., Kreyssig, A., Minola, M., Dellea, G., Weschke, E., Veit, M. J., Ramazanoglu, M., Goldman, A. I., Schmitt, T., Ghiringhelli, G., Barišić, N., Chan, M. K., Dorow, C. J., Yu, G., Zhao, X., Keimer, B., Greven, M.

Volltext

The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome von Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

Volltext

Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation von Barisic, N., Claeys, K. G., Sirotković‐Skerlev, M., Löfgren, A., Nelis, E., De Jonghe, P., Timmerman, V.

Volltext

Single reconstructed Fermi surface pocket in an underdoped single-layer cuprate superconductor von Chan, M. K., Harrison, N., McDonald, R. D., Ramshaw, B. J., Modic, K. A., Barišić, N., Greven, M.

Volltext

Two Ising-like magnetic excitations in a single-layer cuprate superconductor von Li, Yuan, Yu, G., Chan, M. K., Balédent, V., Li, Yangmu, Barišić, N., Zhao, X., Hradil, K., Mole, R. A., Sidis, Y., Steffens, P., Bourges, P., Greven, M.

Volltext

Transport properties and doping evolution of the Fermi surface in cuprates von Klebel-Knobloch, B., Tabiś, W., Gala, M. A., Barišić, O. S., Sunko, D. K., Barišić, N.

Volltext

Low bone mineral density for age/osteoporosis in triple A syndrome—an overlooked symptom of unexplained etiology von Dumic, M., Putarek, N. R., Kusec, V., Barisic, N., Koehler, K., Huebner, A.

Volltext

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients von Kovel, Carolien G.F., Brilstra, Eva H., Kempen, Marjan J.A., Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber

Volltext

Correlation of phenotype and genotype in Croatian patients with Collagen VI (COL6) gene de novo mutations von Barisic, N, Mustapic, M, Lehman, I, Zvonar, V, Topf, A, Lochmuller, H

Volltext

High-T c Cuprates: a Story of Two Electronic Subsystems von Barišić, N, Sunko, D K

Volltext

Evidence for a universal Fermi-liquid scattering rate throughout the phase diagram of the copper-oxide superconductors von Bariši, N, Chan, M K, Veit, M J, Dorow, C J, Ge, Y, Li, Y, Tabis, W, Tang, Y, Yu, G, Zhao, X, Greven, M

Volltext

Unusual behavior of cuprates explained by heterogeneous charge localization von Pelc, D, Popčević, P, Požek, M, Greven, M, Barišić, N

Volltext

Phenotype variability in patients with infantile spinal muscular atrophy: Distal muscle weakness and peripheral neuropathy in compound heterozygotes with SMN1 gene deletions von Barisic, N, Grdjan, P, Lehman, I, Sertic, J, Cvitanovic-Sojat, L.J, Jakovcevic, A, Rudnik-Schöneborn, S

Volltext

Are inherited prothrombotic gene polymorphisms associated with lesion location in pediatric arterial ischemic stroke? von Čeri, A, Coen Herak, D, Lenicek Krleza, J, Radic Antolic, M, Horvat, I, Djuranovic, V, Barisic, N, Zadro, R

Volltext

Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations von Schara, U, Barisic, N, Deschauer, M, Lindberg, C, Straub, V, Strigl-Pill, N, Wendt, M, Abicht, A, Müller, J.S, Lochmüller, H

Volltext

Unusual magnetic order in the pseudogap region of the superconductor HgBa2CuO4+δ von Li, Y., Balédent, V., Barišić, N., Cho, Y., Fauqué, B., Sidis, Y., Yu, G., Zhao, X., Bourges, P., Greven, M.

Volltext

THE EFFECTS OF TRAFFIC-RELATED AIR POLLUTION ON THE FLOWER MORPHOLOGY OF IRIS PUMILA – COMPARISON OF A POLLUTED CITY AREA AND THE UNPOLLUTED DELIBLATO SANDS (NATURE RESERVE) von Vujic, V, Avramov, S, TARASJEV, A, KLISARIC, N BARISIC, Zivkovic, U, Miljkovic, D

Volltext

Hole pocket-driven superconductivity and its universal features in the electron-doped cuprates von Li, Yangmu, Tabis, W, Tang, Y, Yu, G, Jaroszynski, J, Barišić, N, Greven, M

Volltext

Severe Form of Salih Myopathy Caused by Combination of Two Heterozygous TTN Mutations von Milojković, M, Jarić, M, Stojanović, V, Barišić, N, Kavečan, I

Volltext