1. Granular and particle-laden flows: from laboratory experiments to field observations. (5th January 2017) Authors: Delannay, R; Valance, A; Mangeney, A; Roche, O; Richard, P Journal: Journal of physics Issue: Volume 50:Number 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Maintaining and disseminating the kilogram following its redefinition. (25th October 2017) Authors: Stock, M; Davidson, S; Fang, H; Milton, M; de Mirandés, E; Richard, P; Sutton, C Journal: Metrologia Issue: Volume 54:Number 6(2017:Dec.) Page Start: S99 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. P6192Pediatric cardiomyopathies: assessment of genetic causes by next generation sequencing of cardiomyopathy genes and genotype-phenotype correlation. (28th August 2018) Authors: Ader, F; Khraiche, D; Kuster, A; Troadec, Y; Rooryck-Thambo, C; Rambaud, C; Bendrik, N; Bordet, C; Bonnet, D; Charron, P; Richard, P Journal: European heart journal Issue: Volume 39(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. P2249Targeted panel sequencing and allelic spectrum in 95 unrelated adults with left ventricular non-compaction. (28th August 2018) Authors: Richard, P; Ader, F; Roux, M; Donal, E; Eicher, J C; Huttin, O; Coisne, D; Jondeau, G; Damy, T; Mansencal, N; Nguyen, K; Lavoute, C; Tregouet, D A; Habib, G; Charron, P Journal: European heart journal Issue: Volume 39(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Significance of deep T-wave inversions in asymptomatic athletes with normal cardiovascular examinations: practical solutions for managing the diagnostic conundrum. (24th October 2012) Authors: Wilson, M G; Sharma, S; Carré, F; Charron, P; Richard, P; O'Hanlon, R; Prasad, S K; Heidbuchel, H; Brugada, J; Salah, O; Sheppard, M; George, K P; Whyte, G; Hamilton, B; Chalabi, H Journal: British journal of sports medicine Issue: Volume 46(2012)Supplement 1 Page Start: i51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution. Issue 12 (22nd December 2014) Authors: Deconinck, N; Richard, P; Allamand, V; Behin, A; Lafôret, P; Ferreiro, A; de Becdelievre, A; Ledeuil, C; Gartioux, C; Nelson, I; Carlier, R Y; Carlier, P; Wahbi, K; Romero, N; Zabot, M T; Bouhour, F; Tiffreau, V; Lacour, A; Eymard, B; Stojkovic, T Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 86:Issue 12(2015) Page Start: 1337 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. Issue 3 (March 1998) Authors: Guicheney, P; Vignier, N; Zhang, X; He, Y; Cruaud, C; Frey, V; Helbling-Leclerc, A; Richard, P; Estournet, B; Merlini, L; Topaloglu, H; Mora, M; Harpey, J P; Haenggeli, C A; Barois, A; Hainque, B; Schwartz, K; Tomé, F M; Fardeau, M; Tryggvason, K Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients. Issue 12 (16th November 2009) Authors: Bourteel, H; Vermersch, P; Cuisset, J-M; Maurage, C-A; Laforet, P; Richard, P; Stojkovic, T Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 80:Issue 12(2009) Page Start: 1405 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey. Issue 10 (1st October 2004) Authors: Charron, P; Villard, E; Sébillon, P; Laforêt, P; Maisonobe, T; Duboscq-Bidot, L; Romero, N; Drouin-Garraud, V; Frébourg, T; Richard, P; Eymard, B; Komajda, M Journal: Journal of medical genetics Issue: Volume 41:Issue 10(2004) Page Start: 751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel ϵ subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome. Issue 4 (16th March 2009) Authors: Outteryck, O; Richard, P; Lacour, A; Fournier, E; Zéphir, H; Gaudon, K; Eymard, B; Hantaï, D; Vermersch, P; Stojkovic, T Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 80:Issue 4(2009) Page Start: 450 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗