The role of D-serine and glycine as co-agonists of NMDA receptors in motor neuron degeneration and amyotrophic lateral sclerosis (ALS)

Autor Paul, Praveen, de Belleroche, Jackie
Vydáno 2014

Hepatic Glycogenoses Among Children—Clinical and Biochemical Characterization: Single-Center Study

Autor Korula, Sophy, Danda, Sumita, Paul, Praveen G., Mathai, Sarah, Simon, Anna
Vydáno v J Clin Exp Hepatol (2020)

Tissue‐selective regulation of protein homeostasis and unfolded protein response signalling in sporadic ALS

Autor Montibeller, Luigi, Tan, Li Yi, Kim, Joo Kyung, Paul, Praveen, de Belleroche, Jacqueline
Vydáno v J Cell Mol Med (2020)

Characterisation of the pathogenic effects of the in vivo expression of an ALS-linked mutation in D-amino acid oxidase: Phenotype and loss of spinal cord motor neurons

Autor Kondori, Nazanin Rahmani, Paul, Praveen, Robbins, Jacqueline P., Liu, Ke, Hildyard, John C. W., Wells, Dominic J., de Belleroche, Jacqueline S.
Vydáno v PLoS One (2017)

Focus on the Role of D-serine and D-amino Acid Oxidase in Amyotrophic Lateral Sclerosis/Motor Neuron Disease (ALS)

Autor Kondori, Nazanin R., Paul, Praveen, Robbins, Jacqueline P., Liu, Ke, Hildyard, John C. W., Wells, Dominic J., de Belleroche, Jacqueline S.
Vydáno v Front Mol Biosci (2018)

Cloning of the first sn1-DAG lipases points to the spatial and temporal regulation of endocannabinoid signaling in the brain

Autor Bisogno, Tiziana, Howell, Fiona, Williams, Gareth, Minassi, Alberto, Cascio, Maria Grazia, Ligresti, Alessia, Matias, Isabel, Schiano-Moriello, Aniello, Paul, Praveen, Williams, Emma-Jane, Gangadharan, Uma, Hobbs, Carl, Di Marzo, Vincenzo, Doherty, Patrick
Vydáno 2003

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

Autor Mitchell, John, Paul, Praveen, Chen, Han-Jou, Morris, Alex, Payling, Miles, Falchi, Mario, Habgood, James, Panoutsou, Stefania, Winkler, Sabine, Tisato, Veronica, Hajitou, Amin, Smith, Bradley, Vance, Caroline, Shaw, Christopher, Mazarakis, Nicholas D., de Belleroche, Jacqueline
Vydáno 2010

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Autor Groeneweg, Stefan, van Geest, Ferdy S, Abaci, Ayhan, Alcantud, Alberto, Ambegaonkar, Gautem, Armour, Christine, Bakhtiani, Priyanka, Barca, Diana, Bertini, Enrico S, van Beynum, Ingrid M, Brunetti-Pierri, Nicola, Bugiani, Marianna, Cappa, Marco, Cappuccio, Gerarda, Castaglioni, Claudia, Castellotti, Barbara, Chatterjee, Krishna, de Coo, Irenaeus FM, Coutant, Régis, Craiu, Dana, Crock, Patricia, DeGoede, Christian, Demir, Korcan, Dica, Alice, Dimitri, Paul, Dolcetta-Capuzzo, Anna, Dremmen, Marjolein HG, Dubey, Rachana, Enderli, Anina, Fairchild, Jan, Lorea, Cláudia Fernandes, Gallichan, Jonathan, George, Belinda, Gevers, Evelien F, Hackenberg, Annette, Heinrich, Bianka, Huynh, Tony, Kłosowska, Anna, van der Knaap, Marjo S, van der Knoop, Marieke M, Koolen, David, Konrad, Daniel, Krude, Heiko, Lawson–Yuen, Amy, Lebl, Jan, Linder-Lucht, Michaela, Lunsing, Roelineke J, Lyons, Greta, Malikova, Jana, Mancilla, Edna E, Lourenço, Charles Marques, McGowan, Anne, Mericq, Veronica, Lora, Felipe Monti, Moran, Carla, Müller, Katalin E, de Oliveira Poswar, Fabiano, Oliver-Petit, Isabelle, Paone, Laura, Paul, Praveen G, Polak, Michel, Porta, Francesco, Reinauer, Christina, Rozenkova, Klara, Menevse, Tuba Seven, Simm, Peter, Simon, Anna, Singh, Yogen, Spada, Marco, van der Spek, Jet, Stals, Milou AM, Stoupa, Athanasia, Subramanian, Gopinath M, Tonduti, Davide, Turan, Serap, den Uil, Corstiaan A, Vanderniet, Joel, van der Walt, Adri, Wémeau, Jean-Louis, Wierzba, Jolante, de Wit, Marie-Claire Y, Wolf, Nicole I, Wurm, Michael, Zibordi, Federica, Zung, Amnon, Zwaveling-Soonawala, Nitash, Visser, W Edward
Vydáno v Lancet Diabetes Endocrinol (2020)