Using Landsat satellite data to support pesticide exposure assessment in California

por Maxwell, Susan K, Airola, Matthew, Nuckols, John R
Publicado 2010

Assisted Reproductive Technology Outcomes in Women With Heart Disease

por Quien, Mary M., Hausvater, Anaïs, Maxwell, Susan M., Weinberg, Catherine R.
Publicado 2022

Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1

por Basiri, Keivan, Belaya, Katsiaryna, Liu, Wei Wei, Maxwell, Susan, Sedghi, Maryam, Beeson, David
Publicado 2013

Rapsyn facilitates recovery from desensitization in fetal and adult acetylcholine receptors expressed in a muscle cell line

por Cetin, Hakan, Liu, Wei, Cheung, Jonathan, Cossins, Judith, Vanhaesebrouck, An, Maxwell, Susan, Vincent, Angela, Beeson, David, Webster, Richard
Publicado 2019

IgG1-3 MuSK Antibodies Inhibit AChR Cluster Formation, Restored by SHP2 Inhibitor, Despite Normal MuSK, DOK7, or AChR Subunit Phosphorylation

por Cao, Michelangelo, Liu, Wei-Wei, Maxwell, Susan, Huda, Saif, Webster, Richard, Evoli, Amelia, Beeson, David, Cossins, Judith A., Vincent, Angela
Publicado 2023

Myasthenia gravis AChR antibodies inhibit function of rapsyn-clustered AChRs

por Cetin, Hakan, Webster, Richard, Liu, Wei Wei, Nagaishi, Akiko, Koneczny, Inga, Zimprich, Fritz, Maxwell, Susan, Cossins, Judith, Beeson, David, Vincent, Angela
Publicado 2020

Effect of salbutamol on neuromuscular junction function and structure in a mouse model of DOK7 congenital myasthenia

por Webster, Richard G, Vanhaesebrouck, An E, Maxwell, Susan E, Cossins, Judith A, Liu, Weiwei, Ueta, Ryo, Yamanashi, Yuji, Beeson, David M W
Publicado 2020

Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission

por Cossins, Judith, Webster, Richard, Maxwell, Susan, Rodríguez Cruz, Pedro M, Knight, Ravi, Llewelyn, John Gareth, Shin, Ji-Yeon, Palace, Jacqueline, Beeson, David
Publicado 2020

Congenital myasthenic syndrome due to mutations in MUSK suggests that the level of MuSK phosphorylation is crucial for governing synaptic structure

por Rodríguez Cruz, Pedro M., Cossins, Judith, Cheung, Jonathan, Maxwell, Susan, Jayawant, Sandeep, Herbst, Ruth, Waithe, Dominic, Kornev, Alexandr P., Palace, Jacqueline, Beeson, David
Publicado 2019

Muscle acetylcholine receptor conversion into chloride conductance at positive potentials by a single mutation

por Cetin, Hakan, Epstein, Max, Liu, Wei W., Maxwell, Susan, Rodriguez Cruz, Pedro M., Cossins, Judith, Vincent, Angela, Webster, Richard, Biggin, Philip C., Beeson, David
Publicado 2019

β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structure

por Vanhaesebrouck, An E, Webster, Richard, Maxwell, Susan, Rodriguez Cruz, Pedro M, Cossins, Judith, Wickens, James, Liu, Wei-wei, Cetin, Hakan, Cheung, Jonathan, Ramjattan, Hayley, Palace, Jacqueline, Beeson, David
Publicado 2019

N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes

por Irani, Sarosh R., Bera, Katarzyna, Waters, Patrick, Zuliani, Luigi, Maxwell, Susan, Zandi, Michael S., Friese, Manuel A., Galea, Ian, Kullmann, Dimitri M., Beeson, David, Lang, Bethan, Bien, Christian G., Vincent, Angela
Publicado 2010

Antibodies to GABA(A) receptor α1 and γ2 subunits: Clinical and serologic characterization

por Pettingill, Philippa, Kramer, Holger B., Coebergh, Jan Adriaan, Pettingill, Rosie, Maxwell, Susan, Nibber, Anjan, Malaspina, Andrea, Jacob, Anu, Irani, Sarosh R., Buckley, Camilla, Beeson, David, Lang, Bethan, Waters, Patrick, Vincent, Angela
Publicado 2015

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

por Cossins, Judith, Belaya, Katsiaryna, Hicks, Debbie, Salih, Mustafa A., Finlayson, Sarah, Carboni, Nicola, Liu, Wei Wei, Maxwell, Susan, Zoltowska, Katarzyna, Farsani, Golara Torabi, Laval, Steven, Seidhamed, Mohammed Zain, Donnelly, Peter, Bentley, David, McGowan, Simon J., Müller, Juliane, Palace, Jacqueline, Lochmüller, Hanns, Beeson, David
Publicado 2013

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

por Logan, Clare V., Cossins, Judith, Rodríguez Cruz, Pedro M., Parry, David A., Maxwell, Susan, Martínez-Martínez, Pilar, Riepsaame, Joey, Abdelhamed, Zakia A., Lake, Alice V.R., Moran, Maria, Robb, Stephanie, Chow, Gabriel, Sewry, Caroline, Hopkins, Philip M., Sheridan, Eamonn, Jayawant, Sandeep, Palace, Jacqueline, Johnson, Colin A., Beeson, David
Publicado 2015

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

por Belaya, Katsiaryna, Rodríguez Cruz, Pedro M., Liu, Wei Wei, Maxwell, Susan, McGowan, Simon, Farrugia, Maria E., Petty, Richard, Walls, Timothy J., Sedghi, Maryam, Basiri, Keivan, Yue, Wyatt W., Sarkozy, Anna, Bertoli, Marta, Pitt, Matthew, Kennett, Robin, Schaefer, Andrew, Bushby, Kate, Parton, Matt, Lochmüller, Hanns, Palace, Jacqueline, Muntoni, Francesco, Beeson, David
Publicado 2015

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

por Todd, Emily J., Yau, Kyle S., Ong, Royston, Slee, Jennie, McGillivray, George, Barnett, Christopher P., Haliloglu, Goknur, Talim, Beril, Akcoren, Zuhal, Kariminejad, Ariana, Cairns, Anita, Clarke, Nigel F., Freckmann, Mary-Louise, Romero, Norma B., Williams, Denise, Sewry, Caroline A, Colley, Alison, Ryan, Monique M., Kiraly-Borri, Cathy, Sivadorai, Padma, Allcock, Richard J.N., Beeson, David, Maxwell, Susan, Davis, Mark R., Laing, Nigel G., Ravenscroft, Gianina
Publicado 2015