Claude Besmond

Years Active: 2019-2021
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Anne Schänzer, Melanie T Achleitner, Dietrich Trümbach, Laurence Hubert, Arnold Munnich, Barbara Ahlemeyer, Maha M AlAbdulrahim, Philipp A Greif, Sebastian Vosberg, Blake Hummer, René Günther Feichtinger, Johannes A Mayr, Saskia B Wortmann, Heidi Aichner, Sabine Rudnik-Schöneborn, Anna Ruiz, Elisabeth Gabau, Jacobo Pérez Sánchez, Sian Ellard, Tessa Homfray, Karen L Stals, Wolfgang Wurst, Bernd A Neubauer, Till Acker, Stefan K Bohlander, Cédric Asensio, Claude Besmond, Fowzan Sami Alkuraya, Moenaldeen D AlSayed, Andreas Hahn, Axel Weber
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism. Annals of neurology 90 (1) (2021)
Alessandra Pennisi, Agnès Rötig, Charles-Joris Roux, Raphaël Lévy, Marco Henneke, Jutta Gärtner, Pelin Teke Kisa, Fatma Ceren Sarioglu, Uluç Yiş, Laura L Konczal, Deepika D Burkardt, Sulin Wu, Pauline Gaignard, Claude Besmond, Laurence Hubert, Marlène Rio, Giulia Barcia, Arnold Munnich, Nathalie Boddaert, Manuel Schiff
Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both? Journal of medical genetics (2020)
Laurence Hubert, Magda Cannata Serio, Laure Villoing-Gaudé, Nathalie Boddaert, Anna Kaminska, Marlène Rio, Stanislas Lyonnet, Arnold Munnich, Karine Poirier, Matias Simons, Claude Besmond
De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures. Journal of medical genetics 57 (2) (2019)

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