Résultats de la recherche - Timothy Lotze
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Association of Rituximab Use With Adverse Events in Children, Adolescents, and Young Adults par Casey L. McAtee, Joseph Lubega, Kristen Underbrink, Kristen Curry, Pavlos Msaouel, M.E.H. BARROW, Eyal Muscal, Timothy Lotze, Poyyapakkam Srivaths, Lisa R. Forbes, Carl E. Allen, M. Brooke Bernhardt
Publié 2021Artigo -
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Feasibility and Reproducibility of Echocardiographic Measures in Children with Muscular Dystrophies par Christopher F. Spurney, Francis McCaffrey, Avital Cnaan, Lauren P. Morgenroth, Sunil J. Ghelani, Heather Gordish‐Dressman, A. Arrieta, Anne M. Connolly, Timothy Lotze, Craig M. McDonald, Robert T. Leshner, Paula R. Clemens
Publié 2015Artigo -
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Use of newer disease-modifying therapies in pediatric multiple sclerosis in the US par Kristen M. Krysko, Jennifer Graves, Mary Rensel, Bianca Weinstock‐Guttman, Gregory Aaen, Leslie Benson, Tanuja Chitnis, Mark Gorman, Manu S. Goyal, Lauren Krupp, Timothy Lotze, Soe Mar, Moses Rodriguez, John Rose, Michael Waltz, T. Charles Casper, Emmanuelle Waubant, Kristen M. Krysko, Jennifer Graves, Mary Rensel, Bianca Weinstock‐Guttman, Gregory Aaen, Anita Belman, Leslie Benson, Tanuja Chitnis, Mark Gorman, Manu S. Goyal, Yolanda Harris, Lauren Krupp, Timothy Lotze, Soe Mar, Manikum Moodley, Jayne Ness, Moses Rodriguez, John Rose, Teri Schreiner, Jan‐Mendelt Tillema, Michael Waltz, T. Charles Casper, Emmanuelle Waubant
Publié 2018Artigo -
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Mutations in<i>VRK1</i>Associated With Complex Motor and Sensory Axonal Neuropathy Plus Microcephaly par Claudia Gonzaga‐Jauregui, Timothy Lotze, Leila Jamal, Samantha Penney, Ian M. Campbell, Davut Pehli̇van, Jill V. Hunter, Suzanne L. Woodbury, Gerald V. Raymond, Adekunle M. Adesina, Shalini N. Jhangiani, Jeffrey G. Reid, Donna M. Muzny, Eric Boerwinkle, James R. Lupski, Richard A. Gibbs, Wojciech Wiszniewski
Publié 2013Artigo -
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Improved relapse recovery in paediatric compared to adult multiple sclerosis par Tanuja Chitnis, Greg Aaen, Anita Belman, Leslie Benson, Mark Gorman, Manu S. Goyal, Jennifer Graves, Yolanda Harris, Lauren Krupp, Timothy Lotze, Soe Mar, Jayne Ness, Mary Rensel, Teri Schreiner, Jan‐Mendelt Tillema, Emmanuelle Waubant, Bianca Weinstock‐Guttman, Shelly Roalstad, John Rose, Howard L. Weiner, T. Charles Casper, Moses Rodriguez
Publié 2020Artigo -
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Distinct effects of obesity and puberty on risk and age at onset of pediatric MS par Tanuja Chitnis, Jennifer Graves, Bianca Weinstock‐Guttman, Anita Belman, Cody S. Olsen, Madhusmita Misra, Gregory Aaen, Leslie Benson, Meghan Candee, Mark Gorman, Benjamin Greenberg, Lauren Krupp, Timothy Lotze, Soe Mar, Jayne Ness, John Rose, Jennifer Rubin, Teri Schreiner, Jan Mendelt Tillema, Amy Waldman, Moses Rodriguez, Charlie Casper, Emmanuelle Waubant
Publié 2016Artigo -
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Randomized, blinded trial of weekend vs daily prednisone in Duchenne muscular dystrophy par Diana M. Escolar, Lauren P. Hache, Paula R. Clemens, Avital Cnaan, Craig M. McDonald, Viswanathan Venkataraman, Andrew J. Kornberg, T. E. Bertoríni, Yoram Nevo, Timothy Lotze, Alan Pestronk, Monique M. Ryan, Eugenio Monasterio, John Day, Andrew Zimmerman, A. Arrieta, Erik Henricson, J. Mayhew, Julaine Florence, F. Hu, Anne M. Connolly
Publié 2011Artigo -
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Acquisition of Early Developmental Milestones and Need for Special Education Services in Pediatric Multiple Sclerosis par Aaen, Gregory, Waltz, Michael, Vargas, Wendy, Makhani, Naila, Ness, Jayne, Harris, Yolanda, Casper, T. Charles, Benson, Leslie, Candee, Meghan, Chitnis, Tanuja, Gorman, Mark, Graves, Jennifer, Greenberg, Benjamin, MD, Timothy Lotze, Mar, Soe, Tillema, Jan-Mendelt, Rensel, Mary, Rodriguez, Moses, Rose, John, Rubin, Jennifer, Schreiner, Teri, Waldman, Amy, Weinstock-Guttman, Bianca, Belman, Anita, Waubant, Emmanuelle, Krupp, Lauren
Publié 2018Texte -
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Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially par Xi Luo, Jill A. Rosenfeld, Shinya Yamamoto, Tamar Harel, Zhongyuan Zuo, Melissa Hall, Klaas J. Wierenga, Matthew Pastore, Dennis Bartholomew, Mauricio R. Delgado, Joshua Rotenberg, Richard A. Lewis, Lisa Emrick, Carlos A. Bacino, Mohammad K. Eldomery, Zeynep Coban‐Akdemir, Fan Xia, Yaping Yang, Seema R. Lalani, Timothy Lotze, James R. Lupski, Brendan Lee, Hugo J. Bellen, Michael F. Wangler
Publié 2017Artigo -
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Routine Neuroimaging of the Preterm Brain par Ivan Hand, Renée A. Shellhaas, Sarah Sarvis Milla, James J. Cummings, Ira Adams‐Chapman, Susan W. Aucott, Jay P. Goldsmith, David A. Kaufman, Camilia R. Martin, Karen M. Puopolo, Adam L. Hartman, Joshua L. Bonkowsky, Jamie K. Capal, Timothy Lotze, David K. Urion, Adina Alazraki, Aparna Annam, Ellen Benya, Brandon P. Brown, Hansel J. Otero, Edward Richer
Publié 2020Artigo -
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A case-control study of dietary salt intake in pediatric-onset multiple sclerosis par Jamie McDonald, Jennifer Graves, Amy Waldman, Timothy Lotze, Teri Schreiner, Anita Belman, Benjamin Greenberg, Bianca Weinstock‐Guttman, Gregory Aaen, Jan‐Mendelt Tillema, Janace Hart, Sabeen Lulu, Jayne Ness, Yolanda Harris, Jennifer Rubin, Meghan Candee, Lauren Krupp, Mark Gorman, Lina Benson, Moses Rodriguez, Tanuja Chitnis, Soe Mar, Lisa F. Barcellos, Barbara Laraia, John Rose, Shelly Roalstad, Timothy Simmons, T. Charles Casper, Emmanuelle Waubant
Publié 2016Artigo -
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Multiple Sclerosis and Related Disorders par Jamie McDonald, Jennifer Graves, Amy Waldman, Timothy Lotze, Teri Schreiner, Anita Belman, Benjamin Greenberg, Bianca Weinstock‐Guttman, Gregory Aaen, Jan‐Mendelt Tillema, Janace Hart, Sabeen Lulu, Jayne Ness, Yolanda Harris, Jennifer Rubin, Meghan Candee, Lauren Krupp, Mark Gorman, Lina Benson, Moses Rodriguez, Tanuja Chitnis, Lisa F. Barcellos, Barbara Laraia, John Rose, Shelly Roalstad, Timothy Simmons, T. J. Charles, Emmanuelle Waubant
Publié 2016Artigo -
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<i>DMD</i> genotypes and loss of ambulation in the CINRG Duchenne Natural History Study par Luca Bello, Lauren P. Morgenroth, Heather Gordish‐Dressman, Eric P. Hoffman, Craig M. McDonald, Sebahattin Çirak, Avital Cnaan, Mathula Thangarajh, Richard T. Abresch, Erik Henricson, Venkatarman Viswanathan, Laura McAdam, Jean K. Mah, M. Tulinius, Monique M. Ryan, Yoram Nevo, Alberto Dubrovsky, Paula R. Clemens, Anne M. Connolly, Jean Teasley, T. E. Bertoríni, Richard Webster, Hanna Kolski, K. Gorni, Timothy Lotze, Peter Karachunski, John B. Bodensteiner, James J. Carlo
Publié 2016Artigo -
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Clinical characterization of Collagen <scp>XII</scp>‐related disease caused by biallelic <i>COL12A1</i> variants par Riley M. McCarty, Dimah Saade, Pinki Munot, Chamindra G. Laverty, Hailey Pinz, Yaqun Zou, Meghan McAnally, Pomi Yun, Cuixia Tian, Ying Hu, Lucy Feng, Rahul Phadke, Sophia Ceulemans, Pilar Magoulas, Andrew J. Skalsky, Jennifer Friedman, Stephen R. Braddock, Sarah Neuhaus, Denise Malicki, Matthew N. Bainbridge, Shareef Nahas, David Dimmock, Stephen F. Kingsmore, Timothy Lotze, A. Reghan Foley, Francesco Muntoni, Volker Straub, Sandra Donkervoort, Carsten G. Bönnemann
Publié 2025Artigo -
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Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry par Calvin Chi, Xiaorong Shao, Brooke Rhead, Edlin Gonzales, Jessica B. Smith, Anny H. Xiang, Jennifer Graves, Amy Waldman, Timothy Lotze, Teri Schreiner, Bianca Weinstock‐Guttman, Gregory Aaen, Jan-Mendelt Tillema, Jayne Ness, Meghan Candee, Lauren Krupp, Mark Gorman, Lina Benson, Tanuja Chitnis, Soe Mar, Anita Belman, T. Charles Casper, John Rose, Manikum Moodley, Mary Rensel, Moses Rodriguez, Benjamin Greenberg, Llana Kahn, Jennifer Rubin, Catherine Schaefer, Emmanuelle Waubant, Annette Langer‐Gould, Lisa F. Barcellos
Publié 2019Artigo -
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Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy par Joel A. Morales‐Rosado, Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van, Sandra Donkervoort, Jill A. Rosenfeld, Grace E. Boyum, Ying Hu, Anh Cong, Timothy Lotze, Carrie Mohila, Dimah Saade, Diana Bharucha‐Goebel, Katherine R. Chao, Christopher Grunseich, Christine C. Bruels, Hannah R. Littel, Elicia Estrella, Lynn Pais, Peter B. Kang, Michael T. Zimmermann, James R. Lupski, Brendan Lee, Matthew J. Schellenberg, Karl J. Clark, Klaas J. Wierenga, Carsten G. Bönnemann, Eric W. Klee
Publié 2023Artigo -
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Genetic risk factors for pediatric-onset multiple sclerosis par Milena Gianfrancesco, Pernilla Stridh, Xiaorong Shao, Brooke Rhead, Jennifer Graves, Tanuja Chitnis, Amy Waldman, Timothy Lotze, Teri Schreiner, Anita Belman, Benjamin Greenberg, Bianca Weinstock–Guttman, Gregory Aaen, Jan Mendelt Tillema, Janace Hart, Stacy J. Caillier, Jayne Ness, Yolanda Harris, Jennifer Rubin, Meghan Candee, Lauren Krupp, Mark Gorman, Lina Benson, Moses Rodriguez, Soe Mar, Ilana Kahn, John Rose, Shelly Roalstad, T. Charles Casper, Ling Shen, Hong Quach, Diana Quach, Jan Hillert, Anna Karin Hedström, Tomas Olsson, Ingrid Kockum, Lars Alfredsson, Catherine Schaefer, Lisa F. Barcellos, Emmanuelle Waubant
Publié 2017Artigo -
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Mutations in PURA Cause Profound Neonatal Hypotonia, Seizures, and Encephalopathy in 5q31.3 Microdeletion Syndrome par Seema R. Lalani, Jing Zhang, Christian P. Schaaf, Chester Brown, Pilar Magoulas, Anne Chun‐Hui Tsai, Areeg El‐Gharbawy, Klaas J. Wierenga, Dennis Bartholomew, Chin-To Fong, Tina Barbaro‐Dieber, Mary K. Kukolich, Lindsay C. Burrage, Elise G. Austin, Kory Keller, Matthew Pastore, Fabio Fernandez, Timothy Lotze, Angus A. Wilfong, Gabriela Purcarin, Wenmiao Zhu, William J. Craigen, Marianne McGuire, Mahim Jain, Erin Cooney, Mahshid S. Azamian, Matthew N. Bainbridge, Donna M. Muzny, Eric Boerwinkle, Richard Person, Zhiyv Niu, Christine M. Eng, James R. Lupski, Richard A. Gibbs, Arthur L. Beaudet, Yaping Yang, Meng C. Wang, Fan Xia
Publié 2014Artigo -
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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities par Nicola Brunetti‐Pierri, Jonathan S. Berg, Fernando Scaglia, John W. Belmont, Carlos A. Bacino, Trilochan Sahoo, Seema R. Lalani, Brett H. Graham, Brendan Lee, Marwan Shinawi, Joseph Shen, Sung-Hae L. Kang, Amber N. Pursley, Timothy Lotze, Gail Kennedy, Susan Lansky-Shafer, Christine A. Weaver, Elizabeth Roeder, Theresa A. Grebe, Georgianne L. Arnold, Terry Hutchison, Tyler Reimschisel, Stephen Amato, Michael T Geragthy, Jeffrey W. Innis, Ewa Obersztyn, Beata Nowakowska, Sally Rosengren, Patricia I. Bader, Dorothy K. Grange, Sayed Naqvi, Adolfo D. Garnica, Saunder Bernes, Chin-To Fong, Anne Summers, William D. Walters, James R. Lupski, Paweł Stankiewicz, Sau Wai Cheung, Ankita Patel
Publié 2008Artigo
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Medicine
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Duchenne muscular dystrophy
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