Pressure Ulcers and Nutrition: A New European Guideline von Schols, Joseph, Clark, Michael, Benati, Giuseppe, Jackson, Pam, Engfer, Meike, Langer, Gero, Kerry, Bernadette, Colin, Denis

Volltext

COVID-19 pandemic and mortality in nursing homes across USA and Europe up to October 2021 von Aalto, Ulla L., Pitkälä, Kaisu H., Andersen-Ranberg, Karen, Bonin-Guillaume, Sylvie, Cruz-Jentoft, Alfonso Jose, Eriksdotter, Maria, Gordon, Adam L., Gosch, Markus, Holmerova, Iva, Kautiainen, Hannu, Kivipelto, Miia, Macijauskiene, Jurate, O’Neill, Desmond, van den Noortgate, Nele, Ranhoff, Anette H., Schols, Jos M. G. A., Singler, Katrin, Stankunas, Mindaugas, Ouslander, Joseph G.

Volltext

Investigation of griffithsin's interactions with human cells confirms its outstanding safety and efficacy profile as a microbicide candidate von Kouokam, Joseph Calvin, Huskens, Dana, Schols, Dominique, Johannemann, Andrew, Riedell, Shonna K, Walter, Wendye, Walker, Janice M, Matoba, Nobuyuki, O'Keefe, Barry R, Palmer, Kenneth E

Volltext

CXCR4-targeting nanobodies differentially inhibit CXCR4 function and HIV entry von Van Hout, Anneleen, Klarenbeek, Alex, Bobkov, Vladimir, Doijen, Jordi, Arimont, Marta, Zhao, Chunxia, Heukers, Raimond, Rimkunas, Rebecca, de Graaf, Chris, Verrips, Theo, van der Woning, Bas, de Haard, Hans, Rucker, Joseph B., Vermeire, Kurt, Handel, Tracy, Van Loy, Tom, Smit, Martine J., Schols, Dominique

Volltext

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia von Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni

Volltext

Treatable inherited rare movement disorders von Jinnah, H. A., Albanese, Alberto, Bhatia, Kailash P., Cardoso, Francisco, Da Prat, Gustavo, de Koning, Tom J., Espay, Alberto J., Fung, Victor, Garcia‐Ruiz, Pedro J., Gershanik, Oscar, Jankovic, Joseph, Kaji, Ryuji, Kotschet, Katya, Marras, Connie, Miyasaki, Janis M., Morgante, Francesca, Munchau, Alexander, Pal, Pramod Kumar, Rodriguez Oroz, Maria C., Rodríguez‐Violante, Mayela, Schöls, Ludger, Stamelou, Maria, Tijssen, Marina, Uribe Roca, Claudia, de la Cerda, Andres, Gatto, Emilia M.

Volltext

Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3 von Raposo, Mafalda, Hübener-Schmid, Jeannette, Ferreira, Ana F, Vieira Melo, Ana Rosa, Vasconcelos, João, Pires, Paula, Kay, Teresa, Garcia-Moreno, Hector, Giunti, Paola, Santana, Magda M, Pereira de Almeida, Luis, Infante, Jon, van de Warrenburg, Bart P, de Vries, Jeroen J, Faber, Jennifer, Klockgether, Thomas, Casadei, Nicolas, Admard, Jakob, Schöls, Ludger, Riess, Olaf, Lima, Manuela

Volltext

Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project von Stenton, Sarah L, O'Leary, Melanie C, Lemire, Gabrielle, VanNoy, Grace E, DiTroia, Stephanie, Ganesh, Vijay S, Groopman, Emily, O'Heir, Emily, Mangilog, Brian, Osei-Owusu, Ikeoluwa, Pais, Lynn S, Serrano, Jillian, Singer-Berk, Moriel, Weisburd, Ben, Wilson, Michael W, Austin-Tse, Christina, Abdelhakim, Marwa, Althagafi, Azza, Babbi, Giulia, Bellazzi, Riccardo, Bovo, Samuele, Carta, Maria Giulia, Casadio, Rita, Coenen, Pieter-Jan, De Paoli, Federica, Floris, Matteo, Gajapathy, Manavalan, Hoehndorf, Robert, Jacobsen, Julius O B, Joseph, Thomas, Kamandula, Akash, Katsonis, Panagiotis, Kint, Cyrielle, Lichtarge, Olivier, Limongelli, Ivan, Lu, Yulan, Magni, Paolo, Mamidi, Tarun Karthik Kumar, Martelli, Pier Luigi, Mulargia, Marta, Nicora, Giovanna, Nykamp, Keith, Pejaver, Vikas, Peng, Yisu, Pham, Thi Hong Cam, Podda, Maurizio S, Rao, Aditya, Rizzo, Ettore, Saipradeep, Vangala G, Savojardo, Castrense, Schols, Peter, Shen, Yang, Sivadasan, Naveen, Smedley, Damian, Soru, Dorian, Srinivasan, Rajgopal, Sun, Yuanfei, Sunderam, Uma, Tan, Wuwei, Tiwari, Naina, Wang, Xiao, Wang, Yaqiong, Williams, Amanda, Worthey, Elizabeth A, Yin, Rujie, You, Yuning, Zeiberg, Daniel, Zucca, Susanna, Bakolitsa, Constantina, Brenner, Steven E, Fullerton, Stephanie M, Radivojac, Predrag, Rehm, Heidi L, O'Donnell-Luria, Anne

Volltext

CXCR4-targeting nanobodies differentially inhibit CXCR4 function and HIV entry von Van Hout, Anneleen, Klarenbeek, Alex, Bobkov, Vladimir, Doijen, Jordi, Arimont, Marta, Zhao, Chunxia, Heukers, Raimond, Rimkunas, Rebecca, de Graaf, Chris, Verrips, Theo, van der Woning, Bas, de Haard, Hans, Rucker, Joseph B, Vermeire, Kurt, Handel, Tracy, Van Loy, Tom, Smit, Martine J, Schols, Dominique

Volltext

COVID-19 pandemic and mortality in nursing homes across USA and Europe up to October 2021 von Aalto, Ulla L., Pitkala, Kaisu H, Andersen-Ranberg, Karen, Bonin-Guillaume, Sylvie, Cruz-Jentoft, Alfonso J., Eriksdotter, Maria, Gordon, Adam, Gosch, Markus, Holmerova, Iva, Kautiainen, Hannu, Kivipelto, Miia, Macijauskiene, Jurate, O’Neill, Desmond, Van Den Noortgate, Nele, Ranhoff, Anette Hylen, Schols, Jos M. G. A., Singler, Katrin, Stankunas, Mindaugas, Ouslander, Joseph G.

Volltext

COVID-19 pandemic and mortality in nursing homes across USA and Europe up to October 2021 von Aalto, Ulla L, Pitkälä, Kaisu H, Andersen-Ranberg, Karen, Bonin-Guillaume, Sylvie, Cruz-Jentoft, Alfonso Jose, Eriksdotter, Maria, Gordon, Adam L, Gosch, Markus, Holmerova, Iva, Kautiainen, Hannu, Kivipelto, Miia, Macijauskiene, Jurate, O’Neill, Desmond, Van Den Noortgate, Nele, Ranhoff, Anette H, Schols, Jos M. G. A, Singler, Katrin, Stankunas, Mindaugas, Ouslander, Joseph G

Volltext

The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors von Hengel, Holger, Martus, Peter, Faber, Jennifer, Giunit, Paola, Garcia-Moreno, Hector, Solanky, Nita, Klockgether, Thomas, Reetz, Kathrin, van de Warrenburg, Bart P., Santana, Magda M., Silva, Patrick, Cunha, Inês, de Almeida, Luís Pereira, Timmann, Dagmar, Infante, Jon, de Vries, Jeroen, Lima, Manuela, Pires, Paula, Bushara, Khalaf, Jacobi, Heike, Onyike, Chiadi, Schmahmann, Jeremy D., Hübener-Schmid, Jeannette, Synofzik, Matthis, Schöls, Ludger

Volltext

Rhamnogalacturonan alpha-L-rhamnopyranohydrolase: a novel enzyme specific for the terminal nonreducing rhamnosyl unit in rhamnogalacturonan regions of pectin von Mutter, M, Beldman, G, Schols, H A, Voragen, A G

Volltext

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease von Raposo, Mafalda, Hübener-Schmid, Jeannette, Tagett, Rebecca, Ferreira, Ana F., Vieira Melo, Ana Rosa, Vasconcelos, João, Pires, Paula, Kay, Teresa, Garcia-Moreno, Hector, Giunti, Paola, Santana, Magda M., Pereira de Almeida, Luis, Infante, Jon, van de Warrenburg, Bart P., de Vries, Jeroen J., Faber, Jennifer, Klockgether, Thomas, Casadei, Nicolas, Admard, Jakob, Schöls, Ludger, Riess, Olaf, Costa, Maria do Carmo, Lima, Manuela

Volltext

Investigation of Griffithsin's interactions with human cells confirms Its outstanding safety and efficacy profile as a microbicide candidate von Kouokam, Joseph Calvin, Huskens, Dana, Schols, Dominique, Johannemann, Andrew, Riedell, Shonna K, Walter, Wendye, Walker, Janice M, Matoba, Nobuyuki, O'Keefe, Barry R, Palmer, Kenneth E

Volltext

Polyglutamine‐Expanded Ataxin‐3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood von Hübener‐Schmid, Jeannette, Kuhlbrodt, Kirsten, Peladan, Julien, Faber, Jennifer, Santana, Magda M., Hengel, Holger, Jacobi, Heike, Reetz, Kathrin, Garcia‐Moreno, Hector, Raposo, Mafalda, Gaalen, Judith, Infante, Jon, Steiner, Katharina M., Vries, Jeroen, Verbeek, Marcel M., Giunti, Paola, Pereira de Almeida, Luis, Lima, Manuela, Warrenburg, Bart, Schöls, Ludger, Klockgether, Thomas, Synofzik, Matthis, Riess, Olaf

Volltext

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy von Hengel, Holger, Bosso-Lefèvre, Célia, Grady, George, Szenker-Ravi, Emmanuelle, Li, Hankun, Pierce, Sarah, Lebigot, Élise, Tan, Thong-Teck, Eio, Michelle Y., Narayanan, Gunaseelan, Utami, Kagistia Hana, Yau, Monica, Handal, Nader, Deigendesch, Werner, Keimer, Reinhard, Marzouqa, Hiyam M., Gunay-Aygun, Meral, Muriello, Michael J., Verhelst, Helene, Weckhuysen, Sarah, Mahida, Sonal, Naidu, Sakkubai, Thomas, Terrence G., Lim, Jiin Ying, Tan, Ee Shien, Haye, Damien, Willemsen, Michèl A. A. P., Oegema, Renske, Mitchell, Wendy G., Pierson, Tyler Mark, Andrews, Marisa V., Willing, Marcia C., Rodan, Lance H., Barakat, Tahsin Stefan, van Slegtenhorst, Marjon, Gavrilova, Ralitza H., Martinelli, Diego, Gilboa, Tal, Tamim, Abdullah M., Hashem, Mais O., AlSayed, Moeenaldeen D., Abdulrahim, Maha M., Al-Owain, Mohammed, Awaji, Ali, Mahmoud, Adel A. H., Faqeih, Eissa A., Asmari, Ali Al, Algain, Sulwan M., Jad, Lamyaa A., Aldhalaan, Hesham M., Helbig, Ingo, Koolen, David A., Riess, Angelika, Kraegeloh-Mann, Ingeborg, Bauer, Peter, Gulsuner, Suleyman, Stamberger, Hannah, Ng, Alvin Yu Jin, Tang, Sha, Tohari, Sumanty, Keren, Boris, Schultz-Rogers, Laura E., Klee, Eric W., Barresi, Sabina, Tartaglia, Marco, Mor-Shaked, Hagar, Maddirevula, Sateesh, Begtrup, Amber, Telegrafi, Aida, Pfundt, Rolph, Schüle, Rebecca, Ciruna, Brian, Bonnard, Carine, Pouladi, Mahmoud A., Stewart, James C., Claridge-Chang, Adam, Lefeber, Dirk J., Alkuraya, Fowzan S., Mathuru, Ajay S., Venkatesh, Byrappa, Barycki, Joseph J., Simpson, Melanie A., Jamuar, Saumya S., Schöls, Ludger, Reversade, Bruno

Volltext

Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factors von Hengel, Holger, Martus, Peter, Faber, Jennifer, Giunti, Paola, Garcia-Moreno, Hector, Solanky, Nita, Klockgether, Thomas, Reetz, Kathrin, van de Warrenburg, Bart P., Santana, Magda M., Silva, Patrick, Cunha, Inês, de Almeida, Luís Pereira, Timmann, Dagmar, Infante, Jon, de Vries, Jeroen, Lima, Manuela, Pires, Paula, Bushara, Khalaf, Jacobi, Heike, Onyike, Chiadi, Schmahmann, Jeremy D., Hübener-Schmid, Jeannette, Synofzik, Matthis, Schöls, Ludger

Volltext

Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder von Hengel, Holger, Hannan, Shabab B., Dyack, Sarah, MacKay, Sara B., Schatz, Ulrich, Fleger, Martin, Kurringer, Andreas, Balousha, Ghassan, Ghanim, Zaid, Alkuraya, Fowzan S., Alzaidan, Hamad, Alsaif, Hessa S., Mitani, Tadahiro, Bozdogan, Sevcan, Pehlivan, Davut, Lupski, James R., Gleeson, Joseph J., Dehghani, Mohammadreza, Mehrjardi, Mohammad Y.V., Sherr, Elliott H., Parks, Kendall C., Argilli, Emanuela, Begtrup, Amber, Galehdari, Hamid, Balousha, Osama, Shariati, Gholamreza, Mazaheri, Neda, Malamiri, Reza A., Pagnamenta, Alistair T., Kingston, Helen, Banka, Siddharth, Jackson, Adam, Osmond, Mathew, Rieß, Angelika, Haack, Tobias B., Nägele, Thomas, Schuster, Stefanie, Hauser, Stefan, Admard, Jakob, Casadei, Nicolas, Velic, Ana, Macek, Boris, Ossowski, Stephan, Houlden, Henry, Maroofian, Reza, Schöls, Ludger

Volltext

A standardised protocol for blood and cerebrospinal fluid collection and processing for biomarker research in ataxia von Santana, Magda M., Gaspar, Laetitia S., Pinto, Maria M., Silva, Patrick, Adão, Diana, Pereira, Dina, Ribeiro, Joana Afonso, Cunha, Inês, Huebener‐Schmid, Jeannette, Raposo, Mafalda, Ferreira, Ana F., Faber, Jennifer, Kuhs, Sandra, Garcia‐Moreno, Hector, Reetz, Kathrin, Thieme, Andreas, Infante, Jon, Warrenburg, Bart P. C., Giunti, Paola, Riess, Olaf, Schöls, Ludger, Lima, Manuela, Klockgether, Thomas, Januário, Cristina, Almeida, Luís Pereira, Krahe, Janna, Gaalen, Judith, Gonzalez‐Robles, Cristina, Fleszar, Zofia, Pelayo‐Negro, Ana Lara, Manrique, Leire, Timmann, Dagmar, Steiner, Katharina M., Melo, Ana Rosa Vieira

Volltext