A. Michel's Profile

Role	Title	Level	Year	L/R
🐜	GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction 29 auth. G. Lesca, G. Rudolf, N. Bruneau, N. Lozovaya, A. Labalme, N. Boutry‐Kryza, Manal Salmi, T. Tsintsadze, L. Addis, J. Motte, S. Wright, V. Tsintsadze, A. Michel, D. Doummar, K. Lascelles, ... L. Strug, P. Waters, J. Bellescize, P. Vrielynck, Anne de Saint Martin, D. Ville, P. Ryvlin, A. Arzimanoglou, E. Hirsch, A. Vincent, D. Pal, N. Burnashev, D. Sanlaville, P. Szepetowski	8	2013	8 🐜
🐜	Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia. 20 auth. A. Ducros, C. Denier, A. Joutel, K. Vahedi, A. Michel, F. Darcel, M. Madigand, D. Guerouaou, F. Tison, J. Julien, ... E. Hirsch, F. Chédru, C. Bisgård, G. Lucotte, P. Desprès, C. Billard, M. Barthez, G. Ponsot, M. Bousser, E. Tournier-Lasserve	7	1999	7 🐜
🐜	GRIN2A-related disorders: genotype and functional consequence predict phenotype 69 auth. V. Strehlow, H. Heyne, D. R. Vlaskamp, K. Marwick, G. Rudolf, J. de Bellescize, S. Biskup, E. Brilstra, O. Brouwer, P. Callenbach, J. Hentschel, E. Hirsch, P. Kind, C. Mignot, K. Platzer, ... P. Rump, P. Skehel, D. Wyllie, G. Hardingham, C. V. van Ravenswaaij-Arts, G. Lesca, J. Lemke, A. Arzimanoglou, P. Augustijn, P. van Bogaert, Helene Bourry, P. Burfeind, Yoyo W. Y. Chu, B. Chung, D. Doummar, P. Edery, A. Fattal-Valevski, M. Fradin, M. Gérard, C. D. de Geus, B. Gunning, D. Hasaerts, I. Helbig, K. Helbig, R. Jamra, Mélanie Jennesson Lyver, J. K. Wassink-Ruiter, D. Koolen, D. Lederer, R. Lunsing, M. Mathot, H. Maurey, S. Menascu, A. Michel, G. Mirzaa, D. Mitter, H. Muhle, R. Møller, C. Nava, M. O’Brien, E. van Pinxteren-Nagler, A. V. van Riesen, C. Rougeot, D. Sanlaville, J. Schieving, S. Syrbe, H. Veenstra-Knol, N. Verbeek, D. Ville, Y. Vos, P. Vrielynck, Sabrina Wagner, S. Weckhuysen, M. Willemsen	7	2018	7 🐜
🐜	New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. 10 auth. M. Vérin, Y. Rolland, F. Landgraf, H. Chabriat, B. Bompais, A. Michel, ... K. Vahedi, J. Martinet, E. Tournier-Lasserve, M. Lemaitre	7	1995	7 🐜
🐜	G-Protein-Coupled Receptor Gpr17 Expression in Two Multiple Sclerosis Remyelination Models 8 auth. Stella Nyamoya, Patrizia Leopold, Birte Becker, C. Beyer, F. Hustadt, C. Schmitz, ... A. Michel, M. Kipp	5	2018	5 🐜
🐜	Lethal COVID-19: Radiologic-Pathologic Correlation of the Lungs 15 auth. M. Henkel, T. Weikert, Katharina Marston, N. Schwab, G. Sommer, J. Haslbauer, F. Franzeck, C. Anastasopoulos, B. Stieltjes, A. Michel, ... J. Bremerich, T. Menter, K. Mertz, A. Tzankov, A. Sauter	4	2020	4 🐜
🐬	Underdiagnosis of mild congenital disorders of glycosylation type Ia. I. Giurgea, A. Michel, M. le Merrer, N. Seta, P. de Lonlay	4	2005	4 🐬
🐜	Localized hypertrophic neuropathy of the sciatic nerve in children: MRI findings 9 auth. A. Roux, C. Treguier, B. Bruneau, F. Marin, L. Riffaud, P. Violas, ... A. Michel, Y. Gandon, J. Gauvrit	3	2012	3 🐜