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

Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS.

Practical guidelines for managing adults with 22q11.2 deletion syndrome

Genet Med, 2015

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

Andrade DM.

Dravet syndrome, lamotrigine, and personalized medicine

Dev Med Child Neurol, 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

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