Muscle Biopsy and Electromyography Correlation

por Naddaf, Elie, Milone, Margherita, Mauermann, Michelle L., Mandrekar, Jayawant, Litchy, William J.
Publicado 2018

Intramuscular Pressure of Human Tibialis Anterior Muscle Reflects in vivo Muscular Activity

por Ateş, Filiz, Davies, Brenda L., Chopra, Swati, Coleman-Wood, Krista, Litchy, William, Kaufman, Kenton R.
Publicado 2019

Peripheral Nervous, Hepatic, and Gastrointestinal Endpoints for AL Amyloidosis Clinical Trials: Report from the Amyloidosis Forum Multi-organ System Working Group

por Mauermann, Michelle L., Clarke, John O., Litchy, William J., Obici, Laura, Lousada, Isabelle, Gertz, Morie A.
Publicado 2023

Intramuscular Pressure of Tibialis Anterior Reflects Ankle Torque but Does Not Follow Joint Angle-Torque Relationship

por Ateş, Filiz, Davies, Brenda L., Chopra, Swati, Coleman-Wood, Krista, Litchy, William J., Kaufman, Kenton R.
Publicado 2018

A tropomyosin-receptor kinase-fused gene mutation associates with vacuolar myopathy

por Madigan, Nicolas N., Tracy, Jennifer A., Litchy, William J., Niu, Zhiyv, Chen, Chunhua, Ling, Kun, Milone, Margherita
Publicado 2018

Procedures for obtaining muscle physiology parameters during a gracilis free-functioning muscle transfer in adult patients with brachial plexus injury

por Persad, Lomas S., Ates, Filiz, Evertz, Loribeth Q., Litchy, William J., Lieber, Richard L., Kaufman, Kenton R., Shin, Alexander Y.
Publicado 2022

Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy

por Adams, David, Suhr, Ole B., Dyck, Peter J., Litchy, William J., Leahy, Raina G., Chen, Jihong, Gollob, Jared, Coelho, Teresa
Publicado 2017

Efficacy and Safety of Antioxidant Treatment With α-Lipoic Acid Over 4 Years in Diabetic Polyneuropathy: The NATHAN 1 trial

por Ziegler, Dan, Low, Phillip A., Litchy, William J., Boulton, Andrew J.M., Vinik, Aaron I., Freeman, Roy, Samigullin, Rustem, Tritschler, Hans, Munzel, Ullrich, Maus, Joachim, Schütte, Klemens, Dyck, Peter J.
Publicado 2011

mNIS+7 and lower limb function in inotersen treatment of hereditary transthyretin‐mediated amyloidosis

por Dyck, P. James B., Kincaid, John C., Wiesman, Janice F., Polydefkis, Michael, Litchy, William J., Mauermann, Michelle L., Ackermann, Elizabeth J., Guthrie, Spencer, Pollock, Michael, Jung, Shiangtung W., Baker, Brenda F., Dyck, Peter J.
Publicado 2020

Impaired Glycemia and Diabetic Polyneuropathy: The OC IG Survey

por Dyck, Peter J., Clark, Vicki M., Overland, Carol J., Davies, Jenny L., Pach, John M., Dyck, P. James B., Klein, Christopher J., Rizza, Robert A., Melton, L. Joseph, Carter, Rickey E., Klein, Ronald, Litchy, William J.
Publicado 2012

Identification of Caveolae-Associated Protein 4 Autoantibodies as a Biomarker of Immune-Mediated Rippling Muscle Disease in Adults

por Dubey, Divyanshu, Beecher, Grayson, Hammami, M. Bakri, Knight, Andrew M., Liewluck, Teerin, Triplett, James, Datta, Abhigyan, Dasari, Surendra, Zhang, Youwen, Roforth, Matthew M., Jerde, Calvin R., Murphy, Stephen J., Litchy, William J., Amato, Anthony, Lennon, Vanda A., McKeon, Andrew, Mills, John R., Pittock, Sean J., Milone, Margherita
Publicado 2022

Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosis

por Dyck, P. James B., Coelho, Teresa, Waddington Cruz, Marcia, Brannagan, Thomas H., Khella, Sami, Karam, Chafic, Berk, John L., Polydefkis, Michael J., Kincaid, John C., Wiesman, Janice F., Litchy, William J., Mauermann, Michelle L., Ackermann, Elizabeth J., Baker, Brenda F., Jung, Shiangtung W., Guthrie, Spencer, Pollock, Michael, Dyck, Peter J.
Publicado 2020

Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-L(Rx) (ION-682884-CS3) in Hereditary Transthyretin-Mediated Amyloid Polyneu...

por Coelho, Teresa, Ando, Yukio, Benson, Merrill D., Berk, John L., Waddington-Cruz, Márcia, Dyck, Peter J., Gillmore, Julian D., Khella, Sami L., Litchy, William J., Obici, Laura, Monteiro, Cecilia, Tai, Li-Jung, Viney, Nicholas J., Buchele, Gustavo, Brambatti, Michela, Jung, Shiangtung W., St. L. O’Dea, Louis, Tsimikas, Sotirios, Schneider, Eugene, Geary, Richard S., Monia, Brett P., Gertz, Morie
Publicado 2021

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

por Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I., Dyck, Peter J.
Publicado 2011