Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family von Kullar, Peter J, Gomez-Duran, Aurora, Gammage, Payam A, Garone, Caterina, Minczuk, Michal, Golder, Zoe, Wilson, Janet, Montoya, Julio, Häkli, Sanna, Kärppä, Mikko, Horvath, Rita, Majamaa, Kari, Chinnery, Patrick F

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Case report: The management of advanced oral cancer in a Jehovah's Witness using the Ultracision Harmonic Scalpel von Kullar, Peter J, Sorenson, Kristian, Weerakkody, Ruwan, Adams, James

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Frequency and signature of somatic variants in 1461 human brain exomes von Wei, Wei, Keogh, Michael J., Aryaman, Juvid, Golder, Zoe, Kullar, Peter J., Wilson, Ian, Talbot, Kevin, Turner, Martin R., McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Sarraj, Safa Al, Morris, Chris M., Ansorge, Olaf, Jones, Nick S., Ironside, James W., Chinnery, Patrick F.

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Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction von Kullar, Peter J, Quail, Jenna, Lindsey, Phillip, Wilson, Janet A, Horvath, Rita, Yu-Wai-Man, Patrick, Gorman, Grainne S, Taylor, Robert W, Ng, Yi, McFarland, Robert, Moore, Brian C J, Chinnery, Patrick F

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Emergency endovascular management of peripheral artery aneurysms and pseudoaneurysms - a review von Sadat, Umar, Kullar, Peter J, Noorani, Ayesha, Gillard, Jonathan H, Cooper, David G, Boyle, Jonathan R

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Frequency and signature of somatic variants in 1461 human brain exomes von Wei, Wei, Keogh, Michael J, Aryaman, Juvid, Golder, Zoe, Kullar, Peter J, Wilson, Ian, Talbot, Kevin, Turner, Martin R, McKenzie, Chris-Anne, Troakes, Claire, Attems, Johannes, Smith, Colin, Sarraj, Safa Al, Morris, Chris M, Ansorge, Olaf, Jones, Nick S, Ironside, James W, Chinnery, Patrick F

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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family von Kullar, Peter J, Gomez-Duran, Aurora, Gammage, Payam A, Garone, Caterina, Minczuk, Michal, Golder, Zoe, Wilson, Janet, Montoya, Julio, Häkli, Sanna, Kärppä, Mikko, Horvath, Rita, Majamaa, Kari, Chinnery, Patrick F

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Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction von Kullar, Peter J, Quail, Jenna, Lindsey, Phillip, Wilson, Janet A, Horvath, Rita, Yu-Wai-Man, Patrick, Gorman, Grainne S, Taylor, Robert W, Ng, Yi, McFarland, Robert, Moore, Brian CJ, Chinnery, Patrick F

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Emergency endovascular management of peripheral artery aneurysms and pseudoaneurysms - a review von Sadat, Umar, Kullar, Peter J, Noorani, Ayesha, Gillard, Jonathan H, Cooper, David G, Boyle, Jonathan R

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Soluble fms-Like tyrosine kinase 1 (sFlt1), endoglin and placental growth factor (PlGF) in preeclampsia among high risk pregnancies von Powers, Robert W, Jeyabalan, Arun, Clifton, Rebecca G, Van Dorsten, Peter, Hauth, John C, Klebanoff, Mark A, Lindheimer, Marshall D, Sibai, Baha, Landon, Mark, Miodovnik, Menachem

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