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Author/Creator Catala, Martin

1. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization. Issue 9 (6th August 2015)

Authors:
Brioude, Frederic; Netchine, Irène; Praz, Francoise; Le Jule, Marilyne; Calmel, Claire; Lacombe, Didier; Edery, Patrick; Catala, Martin; Odent, Sylvie; Isidor, Bertrand; Lyonnet, Stanislas; Sigaudy, Sabine; Leheup, Bruno; Audebert‐Bellanger, Séverine; Burglen, Lydie; Giuliano, Fabienne; Alessandr...
Journal:
Human mutation
Issue:
Volume 36:Issue 9(2015:Sep.)
Page Start:
894
Record Type:
Journal Article
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4. Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study. Issue 2 (27th June 2019)

Authors:
Querin, Giorgia; Bede, Peter; El Mendili, Mohamed Mounir; Li, Menghan; Pélégrini‐Issac, Mélanie; Rinaldi, Daisy; Catala, Martin; Saracino, Dario; Salachas, François; Camuzat, Agnes; Marchand‐Pauvert, Véronique; Cohen‐Adad, Julien; Colliot, Olivier; Le Ber, Isabelle; Pradat, Pierre‐François
Journal:
Annals of neurology
Issue:
Volume 86:Issue 2(2019)
Page Start:
158
Record Type:
Journal Article
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5. Spinal lipoma as a dysembryogenetic anomaly: Four unusual cases of ectopic iliac rib within the spinal lipoma. Issue 7 (18th April 2016)

Authors:
Accogli, Andrea; Pavanello, Marco; Accorsi, Patrizia; De Marco, Patrizia; Merello, Elisa; Pacetti, Mattia; Nozza, Paolo; Fiorillo, Chiara; Pinelli, Lorenzo; Cama, Armando; Rossi, Andrea; Catala, Martin; Capra, Valeria
Journal:
Birth defects research
Issue:
Volume 106:Issue 7(2016)
Page Start:
530
Record Type:
Journal Article
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