Pre- and Postnatal Characterization of Autosomal Recessive KIDINS220-Associated Ventriculomegaly von Brady, Lauren I., DeFrance, Bryon, Tarnopolsky, Mark

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Time from oocyte retrieval to frozen embryo transfer in the natural cycle does not impact reproductive or neonatal outcomes von Bortoletto, Pietro, Romanski, Phillip A., Magaoay, Brady I., Rosenwaks, Zev, Spandorfer, Steven D.

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POLRMT mutations impair mitochondrial transcription causing neurological disease von Oláhová, Monika, Peter, Bradley, Szilagyi, Zsolt, Diaz-Maldonado, Hector, Singh, Meenakshi, Sommerville, Ewen W., Blakely, Emma L., Collier, Jack J., Hoberg, Emily, Stránecký, Viktor, Hartmannová, Hana, Bleyer, Anthony J., McBride, Kim L., Bowden, Sasigarn A., Korandová, Zuzana, Pecinová, Alena, Ropers, Hans-Hilger, Kahrizi, Kimia, Najmabadi, Hossein, Tarnopolsky, Mark A., Brady, Lauren I., Weaver, K. Nicole, Prada, Carlos E., Õunap, Katrin, Wojcik, Monica H., Pajusalu, Sander, Syeda, Safoora B., Pais, Lynn, Estrella, Elicia A., Bruels, Christine C., Kunkel, Louis M., Kang, Peter B., Bonnen, Penelope E., Mráček, Tomáš, Kmoch, Stanislav, Gorman, Gráinne S., Falkenberg, Maria, Gustafsson, Claes M., Taylor, Robert W.

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Joint aspiration and serum markers - do they matter in the diagnosis of native shoulder sepsis? A systematic review von Salazar, Luis M, Gutierrez-Naranjo, Jose M, Meza, Clarissa, Gabig, Andrew, Bois, Aaron J, Brady, Christina I, Dutta, Anil K

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Upper Extremity Stress Fractures von Koslosky, Ezekial J., Heath, David M., Atkison, Cameron L., Dutta, Anil, Brady, Christina I.

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Pedi-R-MAPP | the development, testing, validation, and refinement of a digital nutrition awareness tool von Marino, L.V., Fandinga, C., Barratt, J., Brady, I., Denton, S.A., Fitzgerald, K., Mills, T., Palframan, K., Phillips, S., Rees, L., Scanlan, N., Ashton, J.J., Beattie, R.M.

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In-Hospital Mortality Risk and Discharge Disposition Following Hip Fractures: An Analysis of the Texas Trauma Registry von Martinez, Victor H., Quirarte, Jaime A., Treffalls, Rebecca N., McCormick, Sekinat, Martin, Case W., Brady, Christina I.

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De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy von Hadjinicolaou, Aristides, Ngo, Kathie J., Conway, Daniel Y., Provias, John P., Baker, Steven K., Brady, Lauren I., Bennett, Craig L., La Spada, Albert R., Fogel, Brent L., Yoon, Grace

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End-stage renal disease and survival in people with diabetes: a national database linkage study von Bell, S, Fletcher, E H, Brady, I, Looker, H C, Levin, D, Joss, N, Traynor, J P, Metcalfe, W, Conway, B, Livingstone, S, Leese, G, Philip, S, Wild, S, Halbesma, N, Sattar, N, Lindsay, R S, McKnight, J, Pearson, D, Colhoun, H M

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Socioeconomic status does not change decision-making in the treatment of distal radius fractures at a level 1 trauma center von Verlinsky, Luke, Ulmer, Clinton J., Griffin, Leah P., Brady, Christina I., Rose, Ryan A.

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Males with MECP2 C-terminal related atypical Rett syndromes and their carrier mothers von Ronen, Gabriel M., MD, MSc, Brady, Lauren I., MSc, Tarnopolsky, Mark A., MD PhD

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Olecranon Tendo-Osseous Allograft Reconstruction for Complex Extensor Mechanism and Bone Loss at the Elbow von Koso, Riikka, Gabig, Andrew M., Brady, Christina I., Dutta, Anil K.

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GRIN2B encephalopathy: Novel findings on phenotype, variant clustering, functional consequences and treatment aspects von Platzer, Konrad, Yuan, Hongjie, Schütz, Hannah, Winschel, Alexander, Chen, Wenjuan, Hu, Chun, Kusumoto, Hirofumi, Heyne, Henrike O, Helbig, Katherine L, Tang, Sha, Willing, Marcia C, Tinkle, Brad T, Adams, Darius J, Depienne, Christel, Keren, Boris, Mignot, Cyril, Frengen, Eirik, Strømme, Petter, Biskup, Saskia, Docker, Dennis, Strom, Tim M, Mefford, Heather C, Myers, Candace T, Muir, Alison M, LaCroix, Amy, Sadleir, Lynette, Scheffer, Ingrid E, Brilstra, Eva, van Haelst, Mieke M, van der Smagt, Jasper J, Bok, Levinus A, Møller, Rikke S, Jensen, Uffe B, Millichap, John J, Berg, Anne T, Goldberg, Ethan M, De Bie, Isabelle, Fox, Stephanie, Major, Philippe, Jones, Julie R, Zackai, Elaine H, Abou Jamra, Rami, Rolfs, Arndt, Leventer, Richard J, Lawson, John A, Roscioli, Tony, Jansen, Floor E, Ranza, Emmanuelle, Korff, Christian M, Lehesjoki, Anna-Elina, Courage, Carolina, Linnankivi, Tarja, Smith, Douglas R, Stanley, Christine, Mintz, Mark, McKnight, Dianalee, Decker, Amy, Tan, Wen-Hann, Tarnopolsky, Mark A, Brady, Lauren I, Wolff, Markus, Dondit, Lutz, Pedro, Helio F, Parisotto, Sarah E, Jones, Kelly L, Patel, Anup D, Franz, David N, Vanzo, Rena, Marco, Elysa, Ranells, Judith D, Di Donato, Nataliya, Dobyns, William B, Laube, Bodo, Traynelis, Stephen F, Lemke, Johannes R

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Providing Orthopaedic Care to Vulnerably Underserved Patients: AOA Critical Issues von Handcox, Jordan E., Saucedo, James M., Rose, Ryan A., Corley, Fred G., Brady, Christina I.

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Glycogen synthase kinase 3 phosphorylates kinesin light chains and negatively regulates kinesin-based motility von Morfini, Gerardo, Szebenyi, Györgyi, Elluru, Ravindhra, Ratner, Nancy, Brady, Scott T.

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Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy von Fry, Andrew E., Marra, Christopher, Derrick, Anna V., Pickrell, William O., Higgins, Adam T., te Water Naude, Johann, McClatchey, Martin A., Davies, Sally J., Metcalfe, Kay A., Tan, Hui Jeen, Mohanraj, Rajiv, Avula, Shivaram, Williams, Denise, Brady, Lauren I., Mesterman, Ronit, Tarnopolsky, Mark A., Zhang, Yuehua, Yang, Ying, Wang, Xiaodong, Rees, Mark I., Goldfarb, Mitchell, Chung, Seo-Kyung

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Revisiting Amputation Rates in High-Pressure Injection Injuries von Jakkaraju, Sohan Kumar, Sager, Brian W., Brady, Christina I.

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A mitochondrial disorder with ptosis and exercise intolerance without ophthalmoparesis secondary to m.5865 T > C variant von Al-shahoumi, Rashid, Brady, Lauren I., Tarnopolsky, Mark A.

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Clinical and demographic features of chronic progressive external ophthalmoplegia in a large adult-onset cohort von Heighton, Julia N, Brady, Lauren I, Newman, Matthew C, Tarnopolsky, Mark A

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Two cases of congenital myasthenic syndrome with vocal cord paralysis von Al-Shahoumi, Rashid, Brady, Lauren I, Schwartzentruber, Jeremy, Tarnopolsky, Mark A

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