Publications and scholarly work
Ensina LF, Valle SO, Juliani AP, Galeane M, Vieira dos Santos R, Arruda LK, Melo JM, de Souza PK, Serpa FS, de Andrade DM, França AT, Campos RA, Camelo-Nunes I, Solé D.
Omalizumab in Chronic Spontaneous Urticaria: A Brazilian Real-Life Experience
Int Arch Allergy Immunol, 2016
Steshenko O, Andrade DM, Honigmann A, Mueller V, Schneider F, Sezgin E, Hell SW, Simons M, Eggeling C.
Reorganization of Lipid Diffusion by Myelin Basic Protein as Revealed by STED Nanoscopy
Biophys J, 2016
Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS.
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
Genet Med, 2015
Butcher NJ, Fung WL, Fitzpatrick L, Guna A, Andrade DM, Lang AE, Chow EW, Bassett AS.
Response to clozapine in a clinically identifiable subtype of schizophrenia
Br J Psychiatry, 2015
Muona M, Berkovic SF, Dibbens LM, Oliver KL, Maljevic S, Bayly MA, Joensuu T, Canafoglia L, Franceschetti S, Michelucci R, Markkinen S, Heron SE, Hildebrand MS, Andermann E, Andermann F, Gambardella A, Tinuper P, Licchetta L, Scheffer IE, Criscuolo C, Filla A, Ferlazzo E, Ahmad J, Ahmad A, Baykan B, Said E, Topcu M, Riguzzi P, King MD, Ozkara C, Andrade DM, Engelsen BA, Crespel A, Lindenau M, Lohmann E, Saletti V, Massano J, Privitera M, Espay AJ, Kauffmann B, Duchowny M, Møller RS, Straussberg R, Afawi Z, Ben-Zeev B, Samocha KE, Daly MJ, Petrou S, Lerche H, Palotie A, Lehesjoki AE.
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Nat Genet, 2015