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Author/Creator Bellesme, Céline

1. Acute ischemic stroke in adolescents. (14th January 2020)

Authors:
Rambaud, Thomas; Legris, Nicolas; Bejot, Yannick; Bellesme, Céline; Lapergue, Bertrand; Jouvent, Eric; Pico, Fernando; Smadja, Didier; Zuber, Mathieu; Crozier, Sophie; Lamy, Catherine; Spelle, Laurent; Tuppin, Philippe; Kossorotoff, Manoelle; Denier, Christian
Journal:
Neurology
Issue:
Volume 94:Number 2(2020)
Page Start:
Record Type:
Journal Article
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2. De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy. Issue 8 (25th March 2017)

Authors:
Guey, Stéphanie; Grangeon, Lou; Brunelle, Francis; Bergametti, Françoise; Amiel, Jeanne; Lyonnet, Stanislas; Delaforge, Audrey; Arnould, Minh; Desnous, Béatrice; Bellesme, Céline; Hervé, Dominique; Schwitalla, Jan C; Kraemer, Markus; Tournier-Lasserve, Elisabeth; Kossorotoff, Manoelle
Journal:
Journal of medical genetics
Issue:
Volume 54:Issue 8(2017)
Page Start:
550
Record Type:
Journal Article
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3. Functional classification of ATM variants in ataxia‐telangiectasia patients. Issue 10 (17th May 2019)

Authors:
Fiévet, Alice; Bellanger, Dorine; Rieunier, Guillaume; Dubois d'Enghien, Catherine; Sophie, Julia; Calvas, Patrick; Carriere, Jean‐Paul; Anheim, Mathieu; Castrioto, Anna; Flabeau, Olivier; Degos, Bertrand; Ewenczyk, Claire; Mahlaoui, Nizar; Touzot, Fabien; Suarez, Felipe; Hully, Marie; Roubertie,...
Journal:
Human mutation
Issue:
Volume 40:Issue 10(2019)
Page Start:
1713
Record Type:
Journal Article
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4. Liver transplantation as a rescue therapy for severe neurologic forms of Wilson disease. (26th May 2020)

Authors:
Poujois, Aurélia; Sobesky, Rodolphe; Meissner, Wassilios G.; Brunet, Anne-Sophie; Broussolle, Emmanuel; Laurencin, Chloé; Lion-François, Laurence; Guillaud, Olivier; Lachaux, Alain; Maillot, François; Belin, Jérémie; Salamé, Ephrem; Vanlemmens, Claire; Heyd, Bruno; Bellesme, Céline; Habes, Dalila...
Journal:
Neurology
Issue:
Volume 94:Number 21(2020)
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Record Type:
Journal Article
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5. Mild Encephalitis/Encephalopathy with reversible splenial lesion syndrome: An unusual presentation of anti-GFAP astrocytopathy. (May 2020)

Authors:
Oger, Valentin; Bost, Chloé; Salah, Lucie; Yazbeck, Elise; Maurey, Hélène; Bellesme, Céline; Sevin, Caroline; Adamsbaum, Catherine; Chrétien, Pascale; Benaiteau, Marie; Honnorat, Jérôme; Deiva, Kumaran
Journal:
European journal of paediatric neurology
Issue:
Volume 26(2020)
Page Start:
89
Record Type:
Journal Article
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6. Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita. Issue 6 (5th April 2021)

Authors:
Laquerriere, Annie; Jaber, Dana; Abiusi, Emanuela; Maluenda, Jérome; Mejlachowicz, Dan; Vivanti, Alexandre; Dieterich, Klaus; Stoeva, Radka; Quevarec, Loic; Nolent, Flora; Biancalana, Valerie; Latour, Philippe; Sternberg, Damien; Capri, Yline; Verloes, Alain; Bessieres, Bettina; Loeuillet, Lauren...
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 6(2022)
Page Start:
559
Record Type:
Journal Article
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