Septic shock with disseminated microfoci in multiple organs in humans by TALVIK, R, LIIGANT, A, TAPFER, H, TAMME, K, METSVAHT, T

Get full text

Bacterial Dissemination and the Value of Blood Cultures in Patients Who Die of Septic Shock by Tamme, K, Liigant, A, Tapfer, H, Talvik, R

Request full text

Dissemination of Bacteria in Multiple Organs Associated with Apoptosis and Macrophage Activity in Different Stages of Experimental Sepsis by Tapfer, H., Liigant, A., Simovart, H. E., Põldoja, E., Kokk, K., Naaber, P., Talvik, R.

Request full text

Changes in Doppler ultrasonography in asphyxiated term infants with hypoxic-ischaemic encephalopathy by Ilves, P, Talvik, R, Talvik, T

Get full text

Out-of-hospital resuscitation in Tartu: Effect of reorganization of Estonian EMS system by Sipria, Aleksander, Talvik, Raul, Kõrgvee, Ago, Sarapuu, Silver, Ööpik, Aare

Get full text

The evidence of oxidative stress in cardiac surgery and septic patients: A comparative study by Starkopf, Joel, Tamme, Kadri, Zilmer, Mihkel, Talvik, Raul, Samarütel, Jüri

Get full text

Possible oxidative stress in healthy term newborns by Metsvaht, T, Ilves, P, Talvik, T, Zilmer, K, Zilmer, M, Talvik, R

Get full text

Changes in endogenous anti-endotoxin core antibodies and TNF-α in septic patients with MOF.: 92 by Sipria, A., Kokk, K., Talvik, R., Uibo, R.

Get full text

Changes in endogenous anti-endotoxin core antibodies and TNF-α in septic patients with MOF: 92 by Sipria, A., Kokk, K., Talvik, R., Uibo, R.

Get full text

Respiratory failure in acute pancreatitis by Talvik, R, Liigant, A, Sissak, H M, O'Konnel-Bronina, N

Get full text

Trauma by Ruiz-Lopez, M. J., Serrano-Gonzalez, A., Ruíz-Beltran, A., Garcia-Perez, J., Casado-Flores, J., da Costa, R. B. Carrington, Pimentel, J., Rebelo, A., Costa, J. J., Sousa, J. P. A., Femandes, V., Simões, A., Robalo-Cordeiro, C., Mesqulta, L., Berrarda, R. Azevedo, Beretta, L., Citerio, G., Dell’Acqua, A., Napolitano, L., Frascoli, C., Cenzato, M., Anzalone, N., Charpentier, C., Audibert, G., Garric, J., Welfringer, P., Laxenaire, M. C., Mata, G. Vazquez, Aragon, A. Perez, Fernandez, R. Rivera, Navarro, P. Navarrete, Mondejar, E. Fernandez, Ferrón, F. Ruiz, Barth, J., Hochhaus, G., Möllmann, H. W., Schumann, F., Bötel, U., Winden, E. v., Derendorf, H., Velasco, P., Domingo, C., Rincón, R., Tomás, R., Esquirol, J., Armengol, S., Gener, J., Djordjević, Ž., Antunović, V., Nestorović, B., Djurović, B., Jovanović, I., Talvik, R., O’Konnel-Bronina, N., Huping, Zhou, Zhongmin, Hou, Quesada, A., Teja, J. L., Serrano, J., Rabanal, J. M., Espadas, F. L., Herrera, S. G., Regañon, G. D., Garrido, C., Kremžar, B., Špec-Marn, A., Burja, H., Toš, L., Ciaglia, P., Barron, J., Graniero, K., Marx, W., Tran, D. D., Cuesta, M. A., van Leeuwen, P. A. M., Wesdorp, R. I. C., Mavrocordatos, P., Chiolero, R., Revelly, J. -P., Cayeux, C., Livio, J. -J., Bui-Xuan, B., Godard, Guillaume, C., Vedrinne, J. M., Bachmann, P., Allaouchiche, B., Reverdy, M. E.

Get full text

Infections I by Schneider, F., Lutun, Ph, Runge, I., Launoy, A., Hasselmann, M., Tempé, J. D., Sipria, A., Talvik, R., Mancebo, J., Domingo, P., Coll, P., Net, A., Ibarz, M., Sancho, J., Sitges-Serra, A., Woittiez, A. J. J., Kaan, J., Goldhoorn, P., Almirall, J., Mesalles, E., Klanturg, J., Armengol, S., Agudo, A., González, C. A., Tomasa, A., Santré, C., Leroy, O., Beuscart, C., Guéry, B., Georges, H., Beaucaire, G., Salord, F., Grando, J., Verges, M., Desgaches, C., Chacornac, R., Maravi, E., García-Jalón, J., Sánchez-Nicolay, I., Saenz, JJ, Maynar, J., Fonseca, F., Jiménez, I., Eami, V., Mencherini, S., Barzaghi, N., Marone, P., Gallini, G. Sala, Olivei, M., Eraschi, A., Nouira, S., Elatrous, S., Abroug, F., Jaafoura, M., Bouchoucha, S., Thabet, H., Rauss, A., Brun-Buisson, C., Sproat, Lu, Inglis, T. J. J., Elkharrat, D., Mauboussin, Ph, Bodossian, P., Porché, M., Pénicaud, M., Le Corre, A., Caulin, C., Leleu, G., Le Junter, J., Villiers, S., Garrouste, M. T., Rabbat, A., Schremmer, B., Le Gall, J. R., Morinet, F., Schlemmer, B., Ribeiro, C., Moreira, J., Costa, D., Costa, M., Pina, E., Salgado, M. J., Gasanovic-Popovic, D., Ratkovic, R., Bura-Nikolic, G., Stosic, M., Kaludjerovic, M., Grujicic, D., Santré, Ch, Simon, M., Konrad, F., Wagner, R., Kilian, J., Georgieff, M., Zhongmin, Hou, Huping, Zhou, Sarmiento, X., Tonig, R., Hosallos, E., Torres, A.

Get full text

De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies by Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Singh, Rani, Smith, Michael C., Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Marson, Anthony G., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K.

Get full text

Diagnostic implications of genetic copy number variation in epilepsy plus by Coppola, Antonietta, Cellini, Elena, Stamberger, Hannah, Saarentaus, Elmo, Cetica, Valentina, Lal, Dennis, Djémié, Tania, Bartnik‐Glaska, Magdalena, Ceulemans, Berten, Helen Cross, J., Deconinck, Tine, Masi, Salvatore De, Dorn, Thomas, Guerrini, Renzo, Hoffman‐Zacharska, Dorotha, Kooy, Frank, Lagae, Lieven, Lench, Nicholas, Lemke, Johannes R., Lucenteforte, Ersilia, Madia, Francesca, Mefford, Heather C., Morrogh, Deborah, Nuernberg, Peter, Palotie, Aarno, Schoonjans, An‐Sofie, Striano, Pasquale, Szczepanik, Elzbieta, Tostevin, Anna, Vermeesch, Joris R., Van Esch, Hilde, Van Paesschen, Wim, Waters, Jonathan J, Weckhuysen, Sarah, Zara, Federico, De Jonghe, Peter, Sisodiya, Sanjay M., Marini, Carla, Lehesjioki, Anna‐Elina, Craiu, Dana, Talvik, Tiina, Caglayan, Hande, Serratosa, Jose, Sterbova, Katalin, Møller, Rikke S., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne, Helbig, Ingo, Spiczak, Sarah, Barba, Carmen, Bogaerts, Anneleen, Boni, Antonella, Galizia, Elisabeth Caruana, Chiari, Sara, Gacomo, Gianpiero, Ferrari, Annarita, Guarducci, Silvia, Giglio, Sabrina, Holmgren, Philip, Leu, Costin, Melani, Federico, Novara, Francesca, Pantaleo, Marilena, Peeters, Elke, Pisano, Tiziana, Rosati, Anna, Sander, Josemir, Schoeler, Natasha, Stankiewicz, Pawel, Striano, Salvatore, Suls, Arvid, Traverso, Monica, Vandeweyer, Geert, Dijck, Anke, Zuffardi, Orsetta

Get full text

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy by Helbig, Ingo, Lopez-Hernandez, Tania, Shor, Oded, Galer, Peter, Ganesan, Shiva, Pendziwiat, Manuela, Rademacher, Annika, Ellis, Colin A., Hümpfer, Nadja, Schwarz, Niklas, Seiffert, Simone, Peeden, Joseph, Shen, Joseph, Štěrbová, Katalin, Hammer, Trine Bjørg, Møller, Rikke S., Shinde, Deepali N., Tang, Sha, Smith, Lacey, Poduri, Annapurna, Krause, Roland, Benninger, Felix, Helbig, Katherine L., Haucke, Volker, Weber, Yvonne G., Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby P.C., Komarek, Vladimir, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Muhle, Hiltrud, Pal, Deb K., Palotie, Aarno, Rosenow, Felix, Schubert-Bast, Susanne, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Zara, Federico, Avillach, Paul, Bartels, Anna, Biswas, Sawona, Bourgeois, Florence, Devkota, Batsal, Glauser, Tracy, Hallinan, Barbara, Heath, Allison, Hirschhorn, Joel, Kilbourn, Judson, Kong, Sek Won, Krantz, Ian, Lee, In-Hee, Mandl, Kenneth D., Marsh, Eric, Sund, Kristen, Taylor, Deanne, White, Peter

Get full text

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome by Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M., Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S., Giraldez, Beatriz G., Serratosa, José, Lemke, Johannes R., Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S., Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D., Lehesjoki, Anna-Elina, de Witte, Peter A.M., Palotie, Aarno, Lerche, Holger, Esguerra, Camila V., De Jonghe, Peter, Helbig, Ingo, Hendrickx, Rik, Holmgren, Philip, Stephani, Ulrich, Muhle, Hiltrud, Pendiziwiat, Manuela, Appenzeller, Silke, Selmer, Kaja, Brilstra, Eva, Koeleman, Bobby, Rosenow, Felix, Leguern, Eric, Sterbova, Katalin, Magdalena, Budisteanu, Rodica, Gherghiceanu, Arsene, Oana Tarta, Diana, Barca, Guerrero-Lopez, Rosa, Ortega, Laura, Todorova, Albena P., Kirov, Andrey V., Robbiano, Angela, Arslan, Mutluay, Yiş, Uluç, Ivanović, Vanja

Get full text

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders by Lal, Dennis, May, Patrick, Perez-Palma, Eduardo, Samocha, Kaitlin E, Kosmicki, Jack A, Robinson, Elise B, Møller, Rikke S, Krause, Roland, Nürnberg, Peter, Weckhuysen, Sarah, De Jonghe, Peter, Guerrini, Renzo, Niestroj, Lisa M, Du, Juliana, Marini, Carla, Ware, James S, Kurki, Mitja, Gormley, Padhraig, Tang, Sha, Wu, Sitao, Biskup, Saskia, Poduri, Annapurna, Neubauer, Bernd A, Koeleman, Bobby P C, Helbig, Katherine L, Weber, Yvonne G, Helbig, Ingo, Majithia, Amit R, Palotie, Aarno, Daly, Mark J

Get full text

Factor V Leiden and prothrombin 21210G>A mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses by Laugesaar, R, Kahre, T, Kolk, A, Uustalu, Ü, Kool, P, Talvik, T

Get full text

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients by 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

Get full text

The screening of SLC6A8 deficiency among Estonian families with X-linked mental retardation by Puusepp, H., Kall, K., Salomons, G. S., Talvik, I., Männamaa, M., Rein, R., Jakobs, C., Õunap, K.

Get full text