Detection of delta-9-tetrahydrocannabinol (THC) in oral fluid, blood and urine following oral consumption of low-content THC hemp oil by Hayley, Amie C., Downey, Luke A., Hansen, Glyn, Dowell, Ashley, Savins, Dale, Buchta, Richard, Catubig, Reinilda, Houlden, Robert, Stough, Con K.K.

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Simultaneous determination of tretinoin and clindamycin phosphate and their degradation products in topical formulations by reverse phase HPLC by Ye, Yuerong Rose, Bektic, Edin, Buchta, Richard, Houlden, Robert, Hunt, Barry

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Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications by Chelban, Viorica, Aksnes, Henriette, Maroofian, Reza, LaMonica, Lauren C., Seabra, Luis, Siggervåg, Anette, Devic, Perrine, Shamseldin, Hanan E., Vandrovcova, Jana, Murphy, David, Richard, Anne-Claire, Quenez, Olivier, Bonnevalle, Antoine, Zanetti, M. Natalia, Kaiyrzhanov, Rauan, Salpietro, Vincenzo, Efthymiou, Stephanie, Schottlaender, Lucia V., Morsy, Heba, Scardamaglia, Annarita, Tariq, Ambreen, Pagnamenta, Alistair T., Pennavaria, Ajia, Krogstad, Liv S., Bekkelund, Åse K., Caiella, Alessia, Glomnes, Nina, Brønstad, Kirsten M., Tury, Sandrine, Moreno De Luca, Andrés, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-François, Anheim, Mathieu, Cretin, Benjamin, Vona, Barbara, Alajlan, Fahad, Abdulwahab, Firdous, Battini, Jean-Luc, İpek, Rojan, Bauer, Peter, Zifarelli, Giovanni, Gungor, Serdal, Kurul, Semra Hiz, Lochmuller, Hanns, Da’as, Sahar I., Fakhro, Khalid A., Gómez-Pascual, Alicia, Botía, Juan A., Wood, Nicholas W., Horvath, Rita, Ernst, Andreas M., Rothman, James E., McEntagart, Meriel, Crow, Yanick J., Alkuraya, Fowzan S., Nicolas, Gaël, Arnesen, Thomas, Houlden, Henry

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Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signaling by Beaufort, Nathalie, Scharrer, Eva, Kremmer, Elisabeth, Lux, Vanda, Ehrmann, Michael, Huber, Robert, Houlden, Henry, Werring, David, Haffner, Christof, Dichgans, Martin

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Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids by Penno, Anke, Reilly, Mary M., Houlden, Henry, Laurá, Matilde, Rentsch, Katharina, Niederkofler, Vera, Stoeckli, Esther T., Nicholson, Garth, Eichler, Florian, Brown, Robert H., von Eckardstein, Arnold, Hornemann, Thorsten

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies by Vallerga, Costanza L, Tan, Manuela, Kia, Demis A, Xue, Angli, Young, Emily, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Botia, Juan A, Martinez, Maria, Jankovic, Joseph, Sutherland, Margaret, Majamaa, Kari, Andreassen, Ole A, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Gratten, Jacob, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Bergareche Yarza, Jesús Alberto, Billingsley, Kimberley, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Bubb, Vivien, Buiza-Rueda, Dolores, Cerdan, Debora, Chelban, Viorica, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Escott-Price, Valentina, Ezquerra, Mario, Fernández, Manel, Fernández-Santiago, Rubén, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Hernandez, Dena G, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Kaiyrzhanov, Rauan, Kia, Demis A, Leonard, Hampton L, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Majamaa, Kari, Manzoni, Claudia, Marti, Maria Jose, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Muñoz, Esteban, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Reed, Xylena, Rezola, Elisabet Mondragon, Rodriguez, Antonio Sanchez, Ruiz-Martínez, Javier, Sadykova, Dinara, Shashkin, Chingiz, Sierra, María, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tolosa, Eduard, van Hilten, Jacobus J, Vargas-González, Laura, Wood, Nicholas W, Zimprich, Alexander, Reich, Stephen, Savitt, Joseph, Bryc, Katarzyna, Hicks, Barry, Jiang, Yunxuan, McCreight, Jennifer C., McIntyre, Matthew H., Noblin, Elizabeth S., Sathirapongsasuti, J. Fah, Tung, Joyce, Anderson, Tim, Bentley, Steven, Kennedy, Martin, Mellick, George, Sidorenko, Julia, Silburn, Peter A., Visscher, Peter M., Yang, Jian

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Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondria by Akman, Gokhan, Desai, Radha, Bailey, Laura J., Yasukawa, Takehiro, Rosa, Ilaria Dalla, Durigon, Romina, Holmes, J. Bradley, Moss, Chloe F., Mennuni, Mara, Houlden, Henry, Crouch, Robert J., Hanna, Michael G., Pitceathly, Robert D. S., Spinazzola, Antonella, Holt, Ian J.

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MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy by Bugiardini, Enrico, Mitchell, Alice L, Rosa, Ilaria Dalla, Horning-Do, Hue-Tran, Pitmann, Alan M, Poole, Olivia V, Holton, Janice L, Shah, Sachit, Woodward, Cathy, Hargreaves, Iain, Quinlivan, Rosaline, Amunts, Alexey, Wiesner, Rudolf J, Houlden, Henry, Holt, Ian J, Hanna, Michael G, Pitceathly, Robert D S, Spinazzola, Antonella

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Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 by FOLEY, A. Reghan, MENEZES, Manoj P, HUGHES, Imelda, MCCULLAGH, B. Gary, JUNGBLUTH, Heinz, LIM, Ming J, LIN, Jean-Pierre, MEGARBANE, Andre, ANDONI URTIZBEREA, J, SHAH, Ayaz H, ANTONY, Jayne, WEBSTER, Richard, PANDRAUD, Amelie, BROOMFIELD, Alexander, NG, Joanne, MATHEW, Ann A, O'BYRNE, James J, FORMAN, Eva, SCOTO, Mariacristina, PRASAD, Manish, O'BRIEN, Katherine, OLPIN, Simon, OPPENHEIM, Marcus, GONZALEZ, Michael A, HARGREAVES, Iain, LAND, John M, WANG, Min X, CARPENTER, Kevin, HORVATH, Rita, STRAUB, Volker, LEK, Monkol, GOLD, Wendy, FARRELL, Michael O, BRANDNER, Sebastian, AL-ODAIB, Ahmad, PHADKE, Rahul, MATSUBARA, Kazuo, McCGARVEY, Michael L, SCHERER, Steven S, BAXTER, Peter S, KING, Mary D, CLAYTON, Peter, RAHMAN, Shamima, REILLY, Mary M, OUVRIER, Robert A, ABRAMS, Alexander J, CHRISTODOULOU, John, ZÜCHNER, Stephan, MUNTONI, Francesco, HOULDEN, Henry, SUGANO, Kumiko, YONEZAWA, Atsushi, MANZUR, Adnan Y, BURNS, Joshua

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Continuous glucose monitoring in pregnant women with type 1 diabetes (CONCEPTT): a multicentre international randomised controlled trial by Feig, Denice S, Donovan, Lois E, Corcoy, Rosa, Amiel, Stephanie A, Hunt, Katharine F, Asztalos, Elizabeth, Barrett, Jon F R, de Leiva, Alberto, Hod, Moshe, Jovanovic, Lois, Keely, Erin, McManus, Ruth, Hutton, Eileen K, Stewart, Zoe A, Wysocki, Tim, O'Brien, Robert, Kollman, Craig, Tomlinson, George, Murphy, Helen R, Grisoni, Jeannie, Byrne, Carolyn, Davenport, Katy, Neoh, Sandra, Gougeon, Claire, Oldford, Carolyn, Young, Catherine, Green, Louisa, Rossi, Benedetta, Rogers, Helen, Cleave, Barbara, Strom, Michelle, Adelantado, Juan María, Tundidor, Diana, Henry, Kathy, Morris, Damian, Rayman, Gerry, Fowler, Duncan, Mitchell, Susan, Rosier, Josephine, Temple, Rosemary, Turner, Jeremy, Hewapathirana, Niranjala, Piper, Leanne, Kudirka, Anne, Watson, Margaret, Bonomo, Matteo, Pintaudi, Basilio, Bertuzzi, Federico, Daniela, Giuseppina, Mion, Elena, Lowe, Julia, Halperin, Ilana, Rogowsky, Anna, Adib, Sapida, Carty, David, Crawford, Isobel, Mackenzie, Fiona, McInnes, Natalia, Smith, Ada, Stanton, Irene, Tazzeo, Tracy, Weisnagel, John, Jones, Nia, MacDougall, Malcolm, Chilton, Sharon, Scott, Eleanor, Endersby, Del, Novodorsky, Peter, Hudson, Sue, Nisbet, Chloe, Coolen, Jill, Baxendale, Darlene, Holt, Richard, Forbes, Jane, Martin, Nicki, Conway, Sharon, Egan, Aoife, Kirwin, Collette, Maresh, Michael, Kearney, Gretta, Quinn, Susan, Bilous, Rudy, Godbout, Ariane, Lubina, Alexandra, Jackson, Margaret, Paul, Emma, Taylor, Julie, Houlden, Robyn, Breen, Adriana, Banerjee, Anita, Reid, Anna, Singh, Claire, Newstead-Angel, Jill, Baxter, Janet, Philip, Sam, Murray, Lynne, Castorino, Kristin, Frase, Donna, Lou, Olivia, Pragnell, Marlon

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Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons by Pappas, Samuel S, Darr, Katherine, Holley, Sandra M, Cepeda, Carlos, Mabrouk, Omar S, Wong, Jenny-Marie T, LeWitt, Tessa M, Paudel, Reema, Houlden, Henry, Kennedy, Robert T, Levine, Michael S, Dauer, William T

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Alzheimer's disease and vascular dementia in developing countries: prevalence, management, and risk factors by Kalaria, Raj N, FRCPath, Maestre, Gladys E, MD, Arizaga, Raul, MD, Friedland, Robert P, MD, Galasko, Doug, MD, Hall, Kathleen, PhD, Luchsinger, José A, MD, Ogunniyi, Adesola, MBBS, Perry, Elaine K, FMedSci, Potocnik, Felix, MD, Prince, Martin, MRCPsych, Stewart, Robert, MRCPsych, Wimo, Anders, MD, Zhang, Zhen-Xin, MD, Antuono, Piero, MD

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NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease by Pitceathly, Robert D.S., Rahman, Shamima, Wedatilake, Yehani, Polke, James M., Cirak, Sebahattin, Foley, A. Reghan, Sailer, Anna, Hurles, Matthew E., Stalker, Jim, Hargreaves, Iain, Woodward, Cathy E., Sweeney, Mary G., Muntoni, Francesco, Houlden, Henry, Taanman, Jan-Willem, Hanna, Michael G.

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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis by Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M, Brady, Stefen, Holton, Janice L, Pittman, Alan M, Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David, Shieh, Perry B, Needham, Merrilee, Liang, Christina, Zanoteli, Edmar, de Camargo, Leonardo Valente, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J, Dimachkie, Mazen M, Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Singleton, Andrew B, Hanna, Michael G, Houlden, Henry

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Aggregation-resistant alpha-synuclein tetramers are reduced in the blood of Parkinson’s patients by de Boni, Laura, Wallis, Amber, Hays Watson, Aurelia, Ruiz-Riquelme, Alejandro, Leyland, Louise-Ann, Bourinaris, Thomas, Hannaway, Naomi, Wüllner, Ullrich, Peters, Oliver, Priller, Josef, Falkenburger, Björn H, Wiltfang, Jens, Bähr, Mathias, Zerr, Inga, Bürger, Katharina, Perneczky, Robert, Teipel, Stefan, Löhle, Matthias, Hermann, Wiebke, Schott, Björn-Hendrik, Brockmann, Kathrin, Spottke, Annika, Haustein, Katrin, Breuer, Peter, Houlden, Henry, Weil, Rimona S, Bartels, Tim

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Effects of dapagliflozin on mortality in patients with chronic kidney disease: a pre-specified analysis from the DAPA-CKD randomized controlled trial by Heerspink, Hiddo J L, Sjöström, C David, Jongs, Niels, Chertow, Glenn M, Kosiborod, Mikhail, Hou, Fan Fan, McMurray, John J V, Rossing, Peter, Correa-Rotter, Ricardo, Kurlyandskaya, Raisa, Stefansson, Bergur V, Toto, Robert D, Langkilde, Anna Maria, Wheeler, David C

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A geroscience approach for Parkinson’s disease: Conceptual framework and design of PROPAG-AGEING project by Pirazzini, Chiara, Azevedo, Tiago, Baldelli, Luca, Bartoletti-Stella, Anna, Calandra-Buonaura, Giovanna, Gómez-Garre, Pilar, Hägg, Sara, Hällqvist, Jenny, Halsband, Claire, Jesús, Silvia, Jylhävä, Juulia, Kwiatkowska, Katarzyna Malgorzata, Licari, Cristina, Milazzo, Maddalena, Ravaioli, Francesco, Sala, Claudia, Schade, Sebastian, Schreglmann, Sebastian, Spasov, Simeon, Tenori, Leonardo, Williams, Dylan, Xumerle, Luciano, Zago, Elisa, Bhatia, Kailash P., Capellari, Sabina, Cortelli, Pietro, Garagnani, Paolo, Liò, Pietro, Luchinat, Claudio, Mills, Kevin, Mir, Pablo, Mollenhauer, Brit, Nardini, Christine, Pedersen, Nancy L., Turano, Paola, Bacalini, Maria Giulia, Adarmes-Gómez, Astrid, Azevedo, Tiago, Baldelli, Luca, Bartoletti-Stella, Anna, Bhatia, Kailash P., Bonilla-Toribio, Marta, Boninsegna, Claudia, Broli, Marcella, Buiza-Rueda, Dolores, Calandra-Buonaura, Giovanna, Carrión-Claro, Mario, Clayton, Robert, Cortelli, Pietro, De Luca, Silvia, Dimitri, Giovanna Maria, Doykov, Ivan, Escuela-Martin, Rocio, Fabbri, Giovanni, Franceschi, Claudio, Gabellini, Anna, Garagnani, Paolo, Giuliani, Cristina, Gómez-Garre, Pilar, Guaraldi, Pietro, Hägg, Sara, Hällqvist, Jenny, Halsband, Claire, Houlden, Henry, Huertas, Ismae, Jesús, Silvia, Jylhävä, Juulia, Labrador-Espinosa, Miguel A., Licari, Cristina, Liò, Pietro, Luchinat, Claudio, Macias, Daniel, Macrì, Stefania, Magrinelli, Francesca, Rodríguez, Juan Francisco Martín, Delledonne, Massimo, Maturo, Maria Giovanna, Mengozzi, Giacomo, Meoni, Gaia, Mignani, Francesco, Milazzo, Maddalena, Mir, Pablo, Nardini, Christine, Nassetti, Stefania Alessandra, Pedersen, Nancy L., Pirazzini, Chiara, Provini, Federica, Ravaioli, Francesco, Sala, Claudia, Scaglione, Cesa Lorella Maria, Schade, Sebastian, Schreglmann, Sebastian, Spasov, Simeon, Strom, Stephen, Tenori, Leonardo, Trenkwalder, Claudia, Turano, Paola, Valzania, Franco, Ortega, Rosario Vigo, Zago, Elisa

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Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study by Schon, Katherine R, Horvath, Rita, Wei, Wei, Calabrese, Claudia, Tucci, Arianna, Ibañez, Kristina, Ratnaike, Thiloka, Pitceathly, Robert D S, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G, Clement, Emma, Ashton, Emma, Sayer, John A, Brennan, Paul, Josifova, Dragana, Izatt, Louise, Fratter, Carl, Nesbitt, Victoria, Barrett, Timothy, McMullen, Dominic J, Smith, Audrey, Deshpande, Charulata, Smithson, Sarah F, Festenstein, Richard, Canham, Natalie, Caulfield, Mark, Houlden, Henry, Rahman, Shamima, Chinnery, Patrick F, Ambrose, John C, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R, Brittain, Helen, Caulfield, Mark J, Chan, Georgia C, Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J P, Jackson, Rob, Jones, Louise J, Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E A, Leong, Ivonne U S, Lopez, Javier F, Maleady-Crowe, Fiona, McEntegart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C, O’Donovan, Peter, Odhams, Chris A, Patch, Christine, Buonerimo Pereira, Mariana, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C, Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R A, Thompson, Simon R, Tucci, Arianna, Welland, Matthew J, Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M

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Rhabdomyolysis: a genetic perspective by Scalco, Renata Siciliani, Gardiner, Alice R, Pitceathly, Robert Ds, Zanoteli, Edmar, Becker, Jefferson, Holton, Janice L, Houlden, Henry, Jungbluth, Heinz, Quinlivan, Ros

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Introducing The International Centre for Genomic Medicine in Neuromuscular Diseases (ICGNMD) by Macken, William, Vandrovcova, Jana, Wilson, Lindsay, Morsy, Heba, Record, Christopher, Pitceathly, Robert, Houlden, Henry, Reilly, Mary, Hanna, Michael

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