Human pathology in NCL
Anderson, Glenn W., Goebel, Hans H., Simonati, Alessandro
Published in Biochimica et biophysica acta (01.11.2013)
Published in Biochimica et biophysica acta (01.11.2013)
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Journal Article
Current Threat of Triclabendazole Resistance in Fasciola hepatica
Kelley, Jane M, Elliott, Timothy P, Beddoe, Travis, Anderson, Glenn, Skuce, Philip, Spithill, Terry W
Published in Trends in parasitology (01.06.2016)
Published in Trends in parasitology (01.06.2016)
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A Commentary on 'Racism Within the Deaf Community'
Anderson, Glenn B, Dunn, Lindsay Moeletsi
Published in American annals of the deaf (Washington, D.C. 1886) (01.01.2023)
Published in American annals of the deaf (Washington, D.C. 1886) (01.01.2023)
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Journal Article
Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis
Mole, Sara E, Anderson, Glenn, Band, Heather A, Berkovic, Samuel F, Cooper, Jonathan D, Kleine Holthaus, Sophia-Martha, McKay, Tristan R, Medina, Diego L, Rahim, Ahad A, Schulz, Angela, Smith, Alexander J
Published in Lancet neurology (01.01.2019)
Published in Lancet neurology (01.01.2019)
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Astrovirus VA1/HMO-C: An Increasingly Recognized Neurotropic Pathogen in Immunocompromised Patients
Brown, Julianne R., Morfopoulou, Sofia, Hubb, Jonathan, Emmett, Warren A., Ip, Winnie, Shah, Divya, Brooks, Tony, Paine, Simon M. L., Anderson, Glenn, Virasami, Alex, Tong, C. Y. William, Clark, Duncan A., Plagnol, Vincent, Jacques, Thomas S., Qasim, Waseem, Hubank, Mike, Breuer, Judith
Published in Clinical infectious diseases (15.03.2015)
Published in Clinical infectious diseases (15.03.2015)
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Journal Article
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans
Buonocore, Federica, Kühnen, Peter, Suntharalingham, Jenifer P, Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F, Blankenstein, Oliver, Procter, Annie M, Dimitri, Paul, Wales, Jerry K H, Ghirri, Paolo, Knöbl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W, Chen, Wei, Kokai, George K, Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A, McKee, Shane A, Niemeyer, Charlotte M, Grüters, Annette, Achermann, John C
Published in The Journal of clinical investigation (01.05.2017)
Published in The Journal of clinical investigation (01.05.2017)
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Journal Article
The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells
Hughes, Sean David, Kanabus, Marta, Anderson, Glenn, Hargreaves, Iain P., Rutherford, Tricia, Donnell, Maura O’, Cross, J. Helen, Rahman, Shamima, Eaton, Simon, Heales, Simon J. R.
Published in Journal of neurochemistry (01.05.2014)
Published in Journal of neurochemistry (01.05.2014)
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Journal Article
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration
Ku, Cristy A, Hull, Sarah, Arno, Gavin, Vincent, Ajoy, Carss, Keren, Kayton, Robert, Weeks, Douglas, Anderson, Glenn W, Geraets, Ryan, Parker, Camille, Pearce, David A, Michaelides, Michel, MacLaren, Robert E, Robson, Anthony G, Holder, Graham E, Heon, Elise, Raymond, F Lucy, Moore, Anthony T, Webster, Andrew R, Pennesi, Mark E
Published in JAMA ophthalmology (01.07.2017)
Published in JAMA ophthalmology (01.07.2017)
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Journal Article
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20
Bryant, Dale, Liu, Yang, Datta, Sanchari, Hariri, Hanaa, Seda, Marian, Anderson, Glenn, Peskett, Emma, Demetriou, Charalambos, Sousa, Sergio, Jenkins, Dagan, Clayton, Peter, Bitner-Glindzicz, Maria, Moore, Gudrun E, Henne, W Mike, Stanier, Philip
Published in Human molecular genetics (01.06.2018)
Published in Human molecular genetics (01.06.2018)
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Journal Article
Racism Within the Deaf Community
Anderson, Glenn B, Bowe, Frank G
Published in American annals of the deaf (Washington, D.C. 1886) (01.01.2022)
Published in American annals of the deaf (Washington, D.C. 1886) (01.01.2022)
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Journal Article
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
Metz, Kyle A., Teng, Xinchen, Coppens, Isabelle, Lamb, Heather M., Wagner, Bart E., Rosenfeld, Jill A., Chen, Xianghui, Zhang, Yu, Kim, Hee Jong, Meadow, Michael E., Wang, Tim Sen, Haberlandt, Edda D., Anderson, Glenn W., Leshinsky‐Silver, Esther, Bi, Weimin, Markello, Thomas C., Pratt, Marsha, Makhseed, Nawal, Garnica, Adolfo, Danylchuk, Noelle R., Burrow, Thomas A., Jayakar, Parul, McKnight, Dianalee, Agadi, Satish, Gbedawo, Hatha, Stanley, Christine, Alber, Michael, Prehl, Isabelle, Peariso, Katrina, Ong, Min Tsui, Mordekar, Santosh R., Parker, Michael J., Crooks, Daniel, Agrawal, Pankaj B., Berry, Gerard T., Loddenkemper, Tobias, Yang, Yaping, Maegawa, Gustavo H. B., Aouacheria, Abdel, Markle, Janet G., Wohlschlegel, James A., Hartman, Adam L., Hardwick, J. Marie
Published in Annals of neurology (01.11.2018)
Published in Annals of neurology (01.11.2018)
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Journal Article
mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis
Yasin, Shireena A., Ali, Abu M., Tata, Mathew, Picker, Simon R., Anderson, Glenn W., Latimer-Bowman, Elizabeth, Nicholson, Sarah L., Harkness, William, Cross, J. Helen, Paine, Simon M. L., Jacques, Thomas S.
Published in Acta neuropathologica (01.08.2013)
Published in Acta neuropathologica (01.08.2013)
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Journal Article
The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease?
Faller, Kiterie M.E., Bras, Jose, Sharpe, Samuel J., Anderson, Glenn W., Darwent, Lee, Kun-Rodrigues, Celia, Alroy, Joseph, Penderis, Jacques, Mole, Sara E., Gutierrez-Quintana, Rodrigo, Guerreiro, Rita J.
Published in Journal of neuroscience research (01.04.2016)
Published in Journal of neuroscience research (01.04.2016)
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Journal Article
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
Thomas, Anna C., Williams, Hywel, Setó-Salvia, Núria, Bacchelli, Chiara, Jenkins, Dagan, O’Sullivan, Mary, Mengrelis, Konstantinos, Ishida, Miho, Ocaka, Louise, Chanudet, Estelle, James, Chela, Lescai, Francesco, Anderson, Glenn, Morrogh, Deborah, Ryten, Mina, Duncan, Andrew J., Pai, Yun Jin, Saraiva, Jorge M., Ramos, Fabiana, Farren, Bernadette, Saunders, Dawn, Vernay, Bertrand, Gissen, Paul, Straatmaan-Iwanowska, Anna, Baas, Frank, Wood, Nicholas W., Hersheson, Joshua, Houlden, Henry, Hurst, Jane, Scott, Richard, Bitner-Glindzicz, Maria, Moore, Gudrun E., Sousa, Sérgio B., Stanier, Philip
Published in American journal of human genetics (06.11.2014)
Published in American journal of human genetics (06.11.2014)
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Journal Article
Investigating ultrastructural morphology in MIRAGE syndrome-derived fibroblasts using transmission electron microscopy. [version 2; peer review: 3 approved with reservations]
Buonocore, Federica, Balys, Monika, Anderson, Glenn, Achermann, John C.
Published in F1000 research (2023)
Published in F1000 research (2023)
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Journal Article
Confirmation of Fasciola hepatica resistant to triclabendazole in naturally infected Australian beef and dairy cattle
Brockwell, Yvette M., Elliott, Timothy P., Anderson, Glenn R., Stanton, Rex, Spithill, Terry W., Sangster, Nicholas C.
Published in International journal for parasitology -- drugs and drug resistance (01.04.2014)
Published in International journal for parasitology -- drugs and drug resistance (01.04.2014)
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