Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype? by Hutchinson, S, Furger, A, Halliday, D, Judge, D, Jefferson, A, Dietz, H, Firth, H, Handford, P

System architecture for "Support through Mobile Messaging and Digital Health Technology for Diabetes" (SuMMiT-D): Design and performance in pilot and randomized controlled feasibil... by Chi, Y, Velardo, C, Allen, J, Robinson, S, Riga, E, Judge, D, Tarassenko, L, Farmer, AJ

Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype? by Hutchinson, S, Furger, A, Halliday, D, Judge, D, Jefferson, A, Dietz, H, Firth, H, Handford, P

Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome. by Loeys, B, Gerber, E, Riegert-Johnson, D, Iqbal, S, Whiteman, P, McConnell, V, Chillakuri, C, Macaya, D, Coucke, P, De Paepe, A, Judge, D, Wigley, F, Davis, E, Mardon, H, Handford, P, Keene, DR, Sakai, L, Dietz, H

Extreme Ultraviolet Variability Experiment (EVE) on the Solar Dynamics Observatory (SDO): Overview of Science Objectives, Instrument Design, Data Products, and Model Developments... by Hock, R., Woodraska, D., Judge, D., Didkovsky, L., Lean, J., Mariska, J., Warren, H., McMullin, D., Chamberlin, P., Bailey, S., Fuller-Rowell, T., Sojka, J., Viereck, R., Woods, T. N., Eparvier, F. G., Jones, A. R., Tobiska, W. K., Berthiaume, Gregory D

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The molecular genetics of Marfan syndrome and related disorders. by Robinson, P, Arteaga-Solis, E, Baldock, C, Collod-Béroud, G, Booms, P, De Paepe, A, Dietz, H, Guo, G, Handford, P, Judge, D, Kielty, C, Loeys, B, Milewicz, D, Ney, A, Ramirez, F, Reinhardt, D, Tiedemann, K, Whiteman, P, Godfrey, M

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhyt... by Ackerman, M, Priori, S, Willems, S, Berul, C, Brugada, R, Calkins, H, Camm, A, Ellinor, P, Gollob, M, Hamilton, R, Hershberger, R, Judge, D, Le Marec, H, McKenna, W, Schulze-Bahr, E, Semsarian, C, Towbin, J, Watkins, H, Wilde, A, Wolpert, C, Zipes, D

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: This document was developed as a partnership between the Heart Rhy... by Ackerman, M, Priori, S, Willems, S, Berul, C, Brugada, R, Calkins, H, Camm, A, Ellinor, P, Gollob, M, Hamilton, R, Hershberger, R, Judge, D, Le Marec, H, McKenna, W, Schulze-Bahr, E, Semsarian, C, Towbin, J, Watkins, H, Wilde, A, Wolpert, C, Zipes, D

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhy... by Ackerman, M, Priori, S, Willems, S, Berul, C, Brugada, R, Calkins, H, Camm, A, Ellinor, P, Gollob, M, Hamilton, R, Hershberger, R, Judge, D, Le Marec, H, McKenna, W, Schulze-Bahr, E, Semsarian, C, Towbin, J, Watkins, H, Wilde, A, Wolpert, C, Zipes, D

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies by Ackerman, M, Priori, S, Willems, S, Berul, C, Brugada, R, Calkins, H, Camm, A, Ellinor, P, Gollob, M, Hamilton, R, Hershberger, R, Judge, D, Le Marec, H, McKenna, W, Schulze-Bahr, E, Semsarian, C, Towbin, J, Watkins, H, Wilde, A, Wolpert, C, Zipes, D, Olson, S

Platform Randomised trial of INterventions against COVID-19 In older peoPLE (PRINCIPLE): protocol for a randomised, controlled, open-label, adaptive platform, trial of community tr... by Hayward, G, Butler, CC, Yu, L-M, Saville, BR, Berry, N, Dorward, J, Gbinigie, O, van Hecke, O, Ogburn, E, Swayze, H, Bongard, E, Allen, J, Tonner, S, Rutter, H, Tonkin-Crine, S, Borek, A, Judge, D, Grabey, J, de Lusignan, S, Thomas, NPB, Evans, PH, Andersson, MI, Llewelyn, M, Patel, M, Hopkins, S, Hobbs, FDR