Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia von Weihl, Conrad C, Pestronk, Alan, Kimonis, Virginia E

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Rapamycin and chloroquine: the in vitro and in vivo effects of autophagy-modifying drugs show promising results in valosin containing protein multisystem proteinopathy von Nalbandian, Angèle, Llewellyn, Katrina J, Nguyen, Christopher, Yazdi, Puya G, Kimonis, Virginia E

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Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome von Montes, Andrea S, Osann, Kathryn E, Gold, June Anne, Tamura, Roy N, Driscoll, Daniel J, Butler, Merlin G, Kimonis, Virginia E

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Mothers, Fathers, and Parental Systems: A Conceptual Model of Parental Engagement in Programmes for Child Mental Health—Connect, Attend, Participate, Enact (CAPE) von Piotrowska, Patrycja J., Tully, L. A., Lenroot, R., Kimonis, E., Hawes, D., Moul, C., Frick, P. J., Anderson, V., Dadds, M. R.

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein von Watts, Giles D J, Wymer, Jill, Kovach, Margaret J, Mehta, Sarju G, Mumm, Steven, Darvish, Daniel, Pestronk, Alan, Whyte, Michael P, Kimonis, Virginia E

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VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease von Badadani, Mallikarjun, Nalbandian, Angèle, Watts, Giles D, Vesa, Jouni, Kitazawa, Masashi, Su, Hailing, Tanaja, Jasmin, Dec, Eric, Wallace, Douglas C, Mukherjee, Jogeshwar, Caiozzo, Vincent, Warman, Matthew, Kimonis, Virginia E

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Contributing factors of mortality in Prader–Willi syndrome von Proffitt, Jennifer, Osann, Kathryn, McManus, Barbara, Kimonis, Virginia E., Heinemann, Janalee, Butler, Merlin G., Stevenson, David A., Gold, June‐Anne

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Development of an Empathy Rating Scale for Young Children von Kimonis, Eva R., Jain, Natasha, Neo, Bryan, Fleming, Georgette E., Briggs, Nancy

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Assessing Callous-Unemotional Traits in Adolescents: Validity of the Inventory of Callous-Unemotional Traits Across Gender, Age, and Community/Institutionalized Status von Pihet, S., Etter, S., Schmid, M., Kimonis, E. R.

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Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia von Mehta, SG, Khare, M, Ramani, R, Watts, GDJ, Simon, M, Osann, KE, Donkervoort, S, Dec, E, Nalbandian, A, Platt, J, Pasquali, M, Wang, A, Mozaffar, T, Smith, CD, Kimonis, VE

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Administration of CoQ10 analogue ameliorates dysfunction of the mitochondrial respiratory chain in a mouse model of Angelman syndrome von Llewellyn, Katrina J, Nalbandian, Angèle, Gomez, Arianna, Wei, Don, Walker, Naomi, Kimonis, Virginia E

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Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia von Kimonis, Virginia. E., Mehta, Sarju G., Fulchiero, Erin C., Thomasova, Dana, Pasquali, Marzia, Boycott, Kym, Neilan, Edward G., Kartashov, Alex, Forman, Mark S., Tucker, Stuart, Kimonis, Katerina, Mumm, Steven, Whyte, Michael P., Smith, Charles D., Watts, Giles D. J.

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Myogenic differentiation of VCP disease-induced pluripotent stem cells: A novel platform for drug discovery von Llewellyn, Katrina J, Nalbandian, Angèle, Weiss, Lan N, Chang, Isabela, Yu, Howard, Khatib, Bibo, Tan, Baichang, Scarfone, Vanessa, Kimonis, Virginia E

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TDP-43 in the Ubiquitin Pathology of Frontotemporal Dementia With VCP Gene Mutations von Neumann, Manuela, Mackenzie, Ian R, Cairns, Nigel J, Boyer, Philip J, Markesbery, William R, Smith, Charles D, Taylor, J Paul, Kretzschmar, Hans A, Kimonis, Virginia E, Forman, Mark S

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Multisystem proteinopathy: Where myopathy and motor neuron disease converge von Korb, Manisha K., Kimonis, Virginia E., Mozaffar, Tahseen

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Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia von Watts, GDJ, Thomasova, D, Ramdeen, SK, Fulchiero, EC, Mehta, SG, Drachman, DA, Weihl, CC, Jamrozik, Z, Kwiecinski, H, Kaminska, A, Kimonis, VE

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Early Diagnosis in Prader-Willi Syndrome Reduces Obesity and Associated Co-Morbidities von Kimonis, Virginia E, Tamura, Roy, Gold, June-Anne, Patel, Nidhi, Surampalli, Abhilasha, Manazir, Javeria, Miller, Jennifer L, Roof, Elizabeth, Dykens, Elisabeth, Butler, Merlin G, Driscoll, Daniel J

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The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology von Nalbandian, Angèle, Llewellyn, Katrina J, Kitazawa, Masashi, Yin, Hong Z, Badadani, Mallikarjun, Khanlou, Negar, Edwards, Robert, Nguyen, Christopher, Mukherjee, Jogeshwar, Mozaffar, Tahseen, Watts, Giles, Weiss, John, Kimonis, Virginia E

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Exercise training reverses skeletal muscle atrophy in an experimental model of VCP disease von Nalbandian, Angèle, Nguyen, Christopher, Katheria, Veeral, Llewellyn, Katrina J, Badadani, Mallikarjun, Caiozzo, Vincent, Kimonis, Virginia E

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Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review von El-Hattab, Ayman W, Schaaf, Christian P, Fang, Ping, Roeder, Elizabeth, Kimonis, Virginia E, Church, Joseph A, Patel, Ankita, Cheung, Sau Wai

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