Reinventing Medicine von Pfeffer, Gerald

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Diagnosis and treatment of mitochondrial myopathies von Pfeffer, Gerald, Chinnery, Patrick F.

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The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update von Sangha, Amarpreet, Quon, Michaela, Pfeffer, Gerald, Orton, Sarah-Michelle

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Valosin-Containing Protein (VCP): A Review of Its Diverse Molecular Functions and Clinical Phenotypes von Pontifex, Carly S, Zaman, Mashiat, Fanganiello, Roberto D, Shutt, Timothy E, Pfeffer, Gerald

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A new automated tool to quantify nucleoid distribution within mitochondrial networks von Ilamathi, Hema Saranya, Ouellet, Mathieu, Sabouny, Rasha, Desrochers-Goyette, Justine, Lines, Matthew A., Pfeffer, Gerald, Shutt, Timothy E., Germain, Marc

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Neuromuscular Complications of SARS-CoV-2 and Other Viral Infections von Jacob, Sarah, Kapadia, Ronak, Soule, Tyler, Luo, Honglin, Schellenberg, Kerri L, Douville, Renée N, Pfeffer, Gerald

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Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy von Korb, Manisha, Peck, Allison, Alfano, Lindsay N, Berger, Kenneth I, James, Meredith K, Ghoshal, Nupur, Healzer, Elise, Henchcliffe, Claire, Khan, Shaida, Mammen, Pradeep P A, Patel, Sujata, Pfeffer, Gerald, Ralston, Stuart H, Roy, Bhaskar, Seeley, William W, Swenson, Andrea, Mozaffar, Tahseen, Weihl, Conrad, Kimonis, Virginia

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Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics von Sharma, Govinda, Pfeffer, Gerald, Shutt, Timothy E

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Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson’s disease using machine learning von Ramezani, Mehrafarin, Mouches, Pauline, Yoon, Eunjin, Rajashekar, Deepthi, Ruskey, Jennifer A., Leveille, Etienne, Martens, Kristina, Kibreab, Mekale, Hammer, Tracy, Kathol, Iris, Maarouf, Nadia, Sarna, Justyna, Martino, Davide, Pfeffer, Gerald, Gan-Or, Ziv, Forkert, Nils D., Monchi, Oury

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Colchicine Myopathy: A Case Series Including Muscle MRI and ABCB1 Polymorphism Data von Gupta, Mehul, Nikolic, Ana, Ng, Denise, Martens, Kristina, Ebadi, Hamid, Chhibber, Sameer, Pfeffer, Gerald

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Skeletal Phenotypes Due to Abnormalities in Mitochondrial Protein Homeostasis and Import von Zhao, Tian, Goedhart, Caitlin, Pfeffer, Gerald, Greenway, Steven C, Lines, Matthew, Khan, Aneal, Innes, A Micheil, Shutt, Timothy E

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Fibroblast Growth Factor (FGF) 18 Signals through FGF Receptor 3 to Promote Chondrogenesis von Davidson, David, Blanc, Antoine, Filion, Dominic, Wang, Huifen, Plut, Paul, Pfeffer, Gerald, Buschmann, Michael D., Henderson, Janet E.

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Prognostic Utility of Cardiovascular Magnetic Resonance-Based Phenotyping in Patients With Muscular Dystrophy von Kashyap, Niharika, Nikhanj, Anish, Labib, Dina, Prosia, Easter, Rivest, Sandra, Flewitt, Jacqueline, Pfeffer, Gerald, Bakal, Jeffrey A, Siddiqi, Zaeem A, Coulden, Richard A, Thompson, Richard, White, James A, Oudit, Gavin Y

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Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy von Quadir, Asfia, Pontifex, Carly Sabine, Lee Robertson, Helen, Labos, Christopher, Pfeffer, Gerald

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Case Report: Biallelic Loss of Function ATM due to Pathogenic Synonymous and Novel Deep Intronic Variant c.1803-270T > G Identified by Genome Sequencing in a Child With Ataxia-Tela... von Maroilley, Tatiana, Wright, Nicola A M, Diao, Catherine, MacLaren, Linda, Pfeffer, Gerald, Sarna, Justyna R, Billie Au, Ping Yee, Tarailo-Graovac, Maja

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Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue Types von Martens, Kristina, Leckie, Jamie, Fok, Daniel, Wells, Robyn A, Chhibber, Sameer, Pfeffer, Gerald

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Expression of risk genes linked to vitamin D receptor super-enhancer regions and their association with phenotype severity in multiple sclerosis von Orton, Sarah M, Sangha, Amarpreet, Gupta, Mehul, Martens, Kristina, Metz, Luanne M, de Koning, A P J, Pfeffer, Gerald

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Methodology for clinical genotyping of CYP2D6 and CYP2C19 von Carvalho Henriques, Beatriz, Buchner, Avery, Hu, Xiuying, Wang, Yabing, Yavorskyy, Vasyl, Wallace, Keanna, Dong, Rachael, Martens, Kristina, Carr, Michael S., Behroozi Asl, Bahareh, Hague, Joshua, Sivapalan, Sudhakar, Maier, Wolfgang, Dernovsek, Mojca Z., Henigsberg, Neven, Hauser, Joanna, Souery, Daniel, Cattaneo, Annamaria, Mors, Ole, Rietschel, Marcella, Pfeffer, Gerald, Hume, Stacey, Aitchison, Katherine J.

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Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease von Ramezani, Mehrafarin, Ruskey, Jennifer A, Martens, Kristina, Kibreab, Mekale, Javer, Zainul, Kathol, Iris, Hammer, Tracy, Cheetham, Jenelle, Leveille, Etienne, Martino, Davide, Sarna, Justyna R, Gan-Or, Ziv, Pfeffer, Gerald, Ismail, Zahinoor, Monchi, Oury

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GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle Atrophy von Soule, Tyler, Phan, Cecile, White, Chris, Resch, Lothar, Lacson, Atilano, Martens, Kristina, Pfeffer, Gerald

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