Are Repeated Single-Limb Heel Raises and Manual Muscle Testing Associated With Peak Plantar-Flexor Force in People With Inclusion Body Myositis?

Por Harris-Love, Michael O., Shrader, Joseph A., Davenport, Todd E., Joe, Galen, Rakocevic, Goran, McElroy, Beverly, Dalakas, Marinos
Publicado em 2014

Acquired Hemophilia A after Stem Cell Transplant for Sickle Cell Disease: Treatment with Recombinant Porcine Factor VIII (OBI-1) and Tolerance Induction with Rituximab/Prednisone

Por Lozier, Jay N., Nghiem, Khanh, Lee, Martin, Hodsdon, Bonnie, Joe, Galen, Weitzel, R. Patrick, Tisdale, John F., Hsieh, Matthew
Publicado no Haemophilia (2014)

Prevalence of isolated joint involvement in chronic graft-versus-chronic disease Comment on Inamoto et al

Por Kuzmina, Zoya, Joe, Galen O., Baird, Kristin, Cowen, Edward W., Naik, Haley B., Steinberg, Seth M., Curtis, Lauren, Comis, Leora E, Pavletic, Steven Z.
Publicado em 2014

Reliability of the Adult Myopathy Assessment Tool in Individuals with Myositis

Por Harris-Love, Michael O., Joe, Galen, Davenport, Todd E., Koziol, Deloris, Rose, Kristen Abbett, Shrader, Joseph A., Vasconcelos, Olavo M., McElroy, Beverly, Dalakas, Marinos C.
Publicado no Arthritis Care Res (Hoboken) (2015)

Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study

Por Dorward Heidi, Ciccone Carla, Sonies Barbara, Harris-Love Michael, Shrader Joseph, Manoli Irini, Joe Galen, Rakocevic Goran, Sparks Susan, Krasnewich Donna, Huizing Marjan, Dalakas Marinos C, Gahl William A
Publicado em 2007-01-01

Intravenous immune globulin in hereditary inclusion body myopathy: a pilot study

Por Sparks, Susan, Rakocevic, Goran, Joe, Galen, Manoli, Irini, Shrader, Joseph, Harris-Love, Michael, Sonies, Barbara, Ciccone, Carla, Dorward, Heidi, Krasnewich, Donna, Huizing, Marjan, Dalakas, Marinos C, Gahl, William A
Publicado em 2007

Low Dose Once Daily, Intraclot Injections of Alteplase for Treatment of Acute Deep Venous Thrombosis

Por Chang, Richard, Horne, Mc Donald K., Shawker, Thomas H., Kam, Anthony W., Chen, Enn Alexandria, Joe, Galen O., Ching, Willie L., Mao, Edie, Wyrick, David A., Lozier, Jay N.
Publicado em 2011

Sclerotic-type chronic GVHD of the skin: clinical risk factors, laboratory markers, and burden of disease

Por Martires, Kathryn J., Baird, Kristin, Steinberg, Seth M., Grkovic, Lana, Joe, Galen O., Williams, Kirsten M., Mitchell, Sandra A., Datiles, Manuel, Hakim, Fran T., Pavletic, Steven Z., Cowen, Edward W.
Publicado em 2011

Assessing Function and Endurance in Adults with Spinal and Bulbar Muscular Atrophy: Validity of the Adult Myopathy Assessment Tool

Por Harris-Love, Michael O., Fernandez-Rhodes, Lindsay, Joe, Galen, Shrader, Joseph A., Kokkinis, Angela, La Pean Kirschner, Alison, Auh, Sungyoung, Chen, Cheunju, Li, Li, Levy, Ellen, Davenport, Todd E., Di Prospero, Nicholas A., Fischbeck, Kenneth H.
Publicado em 2014

Imatinib mesylate for the treatment of steroid-refractory sclerotic-type cutaneous chronic graft-versus-host disease

Por Baird, Kristin, Comis, Leora E., Joe, Galen O., Steinberg, Seth M., Hakim, Fran T., Rose, Jeremy J., Mitchell, Sandra A., Pavletic, Steven Z., Figg, William D., Yao, Lawrence, Flanders, Kathleen C., Takebe, Naoko, Sarantopoulos, Stefanie, Booher, Susan, Cowen, Edward W.
Publicado no Biol Blood Marrow Transplant (2015)

A randomized controlled trial of exercise in spinal and bulbar muscular atrophy

Por Shrader, Joseph A, Kats, Ilona, Kokkinis, Angela, Zampieri, Cris, Levy, Ellen, Joe, Galen O, Woolstenhulme, Joshua G, Drinkard, Bart E, Smith, Michaele R, Ching, Willie, Ghosh, Laboni, Fox, Derrick, Auh, Sungyoung, Schindler, Alice B, Fischbeck, Kenneth H, Grunseich, Christopher
Publicado no Ann Clin Transl Neurol (2015)

Atypical presentation of GNE myopathy with asymmetric hand weakness

Por de Dios, John Karl L., Shrader, Joseph A., Joe, Galen O., McClean, Jeffrey C., Williams, Kayla, Evers, Robert, Malicdan, May Christine V., Ciccone, Carla, Mankodi, Ami, Huizing, Marjan, McKew, John C., Bluemke, David A., Gahl, William A., Carrillo-Carrasco, Nuria
Publicado no Neuromuscul Disord (2014)

Identification of an Alu element‐mediated deletion in the promoter region of GNE in siblings with GNE myopathy

Por Garland, Jennifer, Stephen, Joshi, Class, Bradley, Gruber, Angela, Ciccone, Carla, Poliak, Aaron, Hayes, Christina P., Singhal, Vandana, Slota, Christina, Perreault, John, Gavrilova, Ralitza, Shrader, Joseph A., Chittiboina, Prashant, Joe, Galen, Heiss, John, Gahl, William A., Huizing, Marjan, Carrillo, Nuria, Malicdan, May Christine V.
Publicado no Mol Genet Genomic Med (2017)