Search Results - "Wiedau‐Pazos, Martina"

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    Assessment of feasibility and utility of universal referral to specialty palliative care in a multidisciplinary amyotrophic lateral sclerosis clinic: A cohort study by Hafer, Julia, Jensen, Sarah, WiedauPazos, Martina, Mehta, Ambereen K.

    Published in Muscle & nerve (01-06-2021)
    “…Introduction Although the value of palliative care integration in multidisciplinary amyotrophic lateral sclerosis (ALS) clinics has been increasingly…”
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    Long‐term edaravone efficacy in amyotrophic lateral sclerosis: Post‐hoc analyses of Study 19 (MCI186‐19) by Shefner, Jeremy, Heiman‐Patterson, Terry, Pioro, Erik P., WiedauPazos, Martina, Liu, Shawn, Zhang, Jeffrey, Agnese, Wendy, Apple, Stephen

    Published in Muscle & nerve (01-02-2020)
    “…Background In a Phase 3 study, amyotrophic lateral sclerosis (ALS) patients experienced significantly less physical functional decline with 24‐week edaravone…”
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    Mexiletine for muscle cramps in amyotrophic lateral sclerosis: A randomized, double‐blind crossover trial by Oskarsson, Björn, Moore, Dan, Mozaffar, Tahseen, Ravits, John, WiedauPazos, Martina, Parziale, Nicholas, Joyce, Nanette C., Mandeville, Ross, Goyal, Namita, Cudkowicz, Merit E., Weiss, Michael, Miller, Robert G., McDonald, Craig M.

    Published in Muscle & nerve (01-07-2018)
    “…ABSTRACT Introduction: More than 90% of amyotrophic lateral sclerosis (ALS) patients have muscle cramps, but evidence‐based treatments have not been available…”
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    Induction of Nrf2 and xCT are involved in the action of the neuroprotective antibiotic ceftriaxone in vitro by Lewerenz, Jan, Albrecht, Philipp, Tien, Mai-Ly Tran, Henke, Nadine, Karumbayaram, Saravanan, Kornblum, Harley I, Wiedau-Pazos, Martina, Schubert, Dave, Maher, Pamela, Methner, Axel

    Published in Journal of neurochemistry (01-10-2009)
    “…In amyotrophic lateral sclerosis, down-regulation of the astrocyte-specific glutamate excitatory amino acid transporter 2 is hypothesized to increase…”
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    Edaravone efficacy in amyotrophic lateral sclerosis with reduced forced vital capacity: Post-hoc analysis of Study 19 (MCI186-19) [clinical trial NCT01492686] by Brooks, Benjamin Rix, Heiman-Patterson, Terry, Wiedau-Pazos, Martina, Liu, Shawn, Zhang, Jeffrey, Apple, Stephen

    Published in PloS one (14-06-2022)
    “…Edaravone slowed the rate of functional decline in subjects with amyotrophic lateral sclerosis (ALS) in phase 3 study MCI186-19 (Study 19). One of the Study 19…”
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    Resurgent Na+ Current Offers Noise Modulation in Bursting Neurons by Venugopal, Sharmila, Seki, Soju, Terman, David H, Pantazis, Antonios, Olcese, Riccardo, Wiedau-Pazos, Martina, Chandler, Scott H

    Published in PLoS computational biology (01-06-2019)
    “…Neurons utilize bursts of action potentials as an efficient and reliable way to encode information. It is likely that the intrinsic membrane properties of…”
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    Integrative gene–tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis by Kudo, Lili C., Parfenova, Liubov, Vi, Nancy, Lau, Kimbley, Pomakian, Justine, Valdmanis, Paul, Rouleau, Guy A., Vinters, Harry V., Wiedau-Pazos, Martina, Karsten, Stanislav L.

    Published in Human molecular genetics (15-08-2010)
    “…Advances in genomics and proteomics permit rapid identification of disease-relevant genes and proteins. Challenges include biological differences between…”
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    Wnt-pathway activation during the early stage of neurodegeneration in FTDP-17 mice by Wiedau-Pazos, Martina, Wong, Eugene, Solomon, Esther, Alarcon, Maricela, Geschwind, Daniel H

    Published in Neurobiology of aging (01-01-2009)
    “…Abstract Glycogen synthase kinase-3beta (GSK-3β), a key component of the Wnt signaling pathway, has been recognized as an important tau kinase with a potential…”
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    Altered Reactivity of Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis by Wiedau-Pazos, Martina, Goto, Joy J., Rabizadeh, Shahrooz, Gralla, Edith B., Roe, James A., Lee, Michael K., Valentine, Joan S., Bredesen, Dale E.

    “…A subset of individuals with familial amyotrophic lateral sclerosis (FALS) possesses dominantly inherited mutations in the gene that encodes copper-zinc…”
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    Human embryonic stem cell-derived motor neurons expressing SOD1 mutants exhibit typical signs of motor neuron degeneration linked to ALS by Karumbayaram, Saravanan, Kelly, Theresa K, Paucar, Andres A, Roe, Anne J T, Umbach, Joy A, Charles, Andrew, Goldman, Steven A, Kornblum, Harley I, Wiedau-Pazos, Martina

    Published in Disease models & mechanisms (01-03-2009)
    “…Human embryonic stem cell (hESC)-derived neurons have the potential to model neurodegenerative disorders. Here, we demonstrate the expression of a mutant gene,…”
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    Circuit-Specific Early Impairment of Proprioceptive Sensory Neurons in the SOD1(G93A) Mouse Model for ALS by Seki, Soju, Yamamoto, Toru, Quinn, Kiara, Spigelman, Igor, Pantazis, Antonios, Olcese, Riccardo, Wiedau-Pazos, Martina, Chandler, Scott H., Venugopal, Sharmila

    Published in The Journal of neuroscience (30-10-2019)
    “…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease in which motor neurons degenerate, resulting in muscle atrophy, paralysis, and fatality…”
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    Circuit-Specific Early Impairment of Proprioceptive Sensory Neurons in the SOD1G93A Mouse Model for ALS by Seki, Soju, Yamamoto, Toru, Quinn, Kiara, Spigelman, Igor, Pantazis, Antonios, Olcese, Riccardo, Wiedau-Pazos, Martina, Chandler, Scott H, Venugopal, Sharmila

    Published in The Journal of neuroscience (30-10-2019)
    “…Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease in which motor neurons degenerate, resulting in muscle atrophy, paralysis, and fatality…”
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    Palliative Care Consults in an Inpatient Setting for Patients With Amyotrophic Lateral Sclerosis by Mehta, Ambereen K., Jackson, Nicholas J., Wiedau-Pazos, Martina

    “…Background: Limited data about the frequency and outcomes of palliative care (PC) specialty consultations for patients with amyotrophic lateral sclerosis (ALS)…”
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