Showing 1 - 20 results of 148 for search 'Clement E.', query time: 0.06s
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Exclusion of WWP1 mutations in a cohort of dystroglycanopathy patients by Godfrey, C, Clement, E, Abbs, S, Muntoni, F
Published 2011Journal article -
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Dynamic modulation of mouse thalamocortical visual activity by salient sounds by Clément E. Lemercier, Patrik Krieger, Denise Manahan-Vaughan
Published 2024-04-01
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Dystroglycanopathies: coming into focus by Godfrey, C, Foley, A, Clement, E, Muntoni, F
Published 2011Journal article -
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Effect of venlafaxine on pineal melatonin and noradrenaline in the male rat. by Franklin, M, Clement, E, Campling, G, Cowen, P
Published 1998Journal article -
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Antimelanoma differentiation-associated gene 5 (anti-MDA5) antibody-positive dermatomyositis: clinical features and outcomes in a racially diverse patient cohort by Sai K. Koyoda, Fatema Ezzy, Dawn Wahezi, Anand Kumthekar, Xianhong Xie, Clement E. Tagoe, Bibi Ayesha
Published 2025-01-01
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Adding Size Exclusion Chromatography (SEC) and Light Scattering (LS) Devices to Obtain High-Quality Small Angle X-Ray Scattering (SAXS) Data by Melissa A. Graewert, Stefano Da Vela, Tobias W. Gräwert, Dmitry S. Molodenskiy, Clément E. Blanchet, Dmitri I. Svergun, Cy M. Jeffries
Published 2020-10-01
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Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008 by Clement, E, Feng, L, Mein, R, Sewry, C, Robb, SA, Manzur, A, Mercuri, E, Godfrey, C, Cullup, T, Abbs, S, Muntoni, F
Published 2012Journal article -
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Comparative study between radiofrequency-induced and muscimol-induced inhibition of cultured networks of cortical neuron. by Clément E Lemercier, André Garenne, Florence Poulletier de Gannes, Corinne El Khoueiry, Delia Arnaud-Cormos, Philippe Levêque, Isabelle Lagroye, Yann Percherancier, Noëlle Lewis
Published 2022-01-01
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gene mutations in steroid-responsive limb girdle muscular dystrophy by Godfrey, C, Escolar, D, Brockington, M, Clement, E, Mein, R, Jimenez-Mallebrera, C, Torelli, S, Feng, L, Brown, S, Sewry, C, Rutherford, M, Shapira, Y, Abbs, S, Muntoni, F
Published 2006Journal article -
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Mild POMGnT1 Mutations Underlie a Novel Limb-Girdle Muscular Dystrophy Variant by Clement, E, Godfrey, C, Tan, J, Brockington, M, Torelli, S, Feng, L, Brown, S, Jimenez-Mallebrera, C, Sewry, C, Longman, C, Mein, R, Abbs, S, Vajsar, J, Schachter, H, Muntoni, F
Published 2008Journal article -
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Highly Sensitive Immunoresistive Sensor for Point-Of-Care Screening for COVID-19 by Tianyi Li, Scott D. Soelberg, Zachary Taylor, Vigneshwar Sakthivelpathi, Clement E. Furlong, Jong-Hoon Kim, Sang-gyeun Ahn, Peter D. Han, Lea M. Starita, Jia Zhu, Jae-Hyun Chung
Published 2022-02-01
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Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol by Lewis, C, Buchanan, JR, Clarke, A, Clement, E, Friedrich, B, Hastings-Ward, J, Hill, M, Horn, R, Lucassen, AM, Patch, C, Pickard, A, Roberts, L, Sanderson, SC, Lewell, SL, Vindrola-Padros, C, Lakhanpaul, M
Published 2021Journal article