Sfoglia per AUTORE
LEVY M
Collezione AOU San Luigi di Orbassano

  

Items : 3

Identification of the DNA methylation signature of Mowat-Wilson syndrome. in European journal of human genetics : EJHG / Eur J Hum Genet. 2024 Jun;32(6):619-629. doi: 10.1038/s41431-024-01548-4. Epub 2024 Feb 13.
2024
AOU San Luigi di Orbassano
AOU Città della Salute di Torino

Trajkova S; Zuntini R; Relator R; Haghshenas S; Levy MA; Garavelli L; Sadikovic B; Ferrero GB; Tartaglia M; McConkey H; Zollino M; Pullano V; Brusco A; Pavinato L; Ivanovski I; Fetta A; Sukarova E; Lauzon C; Cordelli DM; Mandrile G; Baldo C; Rooney K; Caraffi SG; van der Laan L;

Treatment of MOG-IgG-associated disorder with rituximab: An international study of 121 patients. in Multiple sclerosis and related disorders / Mult Scler Relat Disord. 2020 Sep;44:102251. doi: 10.1016/j.msard.2020.102251. Epub 2020 Jun 2.
2020
AOU San Luigi di Orbassano

Whittam DH; Cobo-Calvo A; Lopez-Chiriboga AS; Pardo S; Gornall M; Cicconi S; Brandt A; Berek K; Berger T; Jelcic I; Gombolay G; Oliveira LM; Callegaro D; Kaneko K; Misu T; Capobianco M; Gibbons E; Karthikeayan V; Brochet B; Audoin B; Mathey G; Laplaud D; Thouvenot E; Cohen M; Tourbah A; Maillart E; Ciron J; Deschamps R; Biotti D; et alii...

Treatment of MOG antibody associated disorders: results of an international survey. in Journal of neurology / J Neurol. 2020 Dec;267(12):3565-3577. doi: 10.1007/s00415-020-10026-y. Epub 2020 Jul 4.
2020
AOU San Luigi di Orbassano

Whittam DH; Karthikeayan V; Gibbons E; Kneen R; Chandratre S; Ciccarelli O; Hacohen Y; de Seze J; Deiva K; Hintzen RQ; Wildemann B; Jarius S; Kleiter I; Rostasy K; Huppke P; Hemmer B; Paul F; Aktas O; Pröbstel AK; Arrambide G; Tintore M; Amato MP; Nosadini M; Mancardi MM; Capobianco M; Illes Z; Siva A; Altintas A; Akman-Demir G; et alii...