All papers authored by Esther de Graaff
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Roderick P. Tas,
Sybren Portegies,
Bastiaan J. Viergever ,
Esther de Graaff ,
Casper C. Hoogenraad ,
Eelco J. P. de Koning,
Françoise Carlotti,
Lukas C. Kapitein ,
Anna Akhmanova
Organization and dynamics of the cortical complexes controlling insulin secretion in β-cells
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Marco W. J. Schreurs,
Jeroen A. A. Demmers,
Melanie Ramberger,
Esther S. P. Hulsenboom,
Mariska M. P. Nagtzaam,
Sanae Boukhrissi,
Jan H. Veldink,
Jan J. G. M. Verschuuren,
Casper C. Hoogenraad,
Peter A. E. Sillevis Smitt,
Maarten J. Titulaer,
Danielle A. E. M. Bastiaansen
and 1 other authors
The expanded clinical spectrum of anti-GABABR encephalitis and added value of KCTD16 autoantibodies
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Peter A. E. Sillevis Smitt,
Casper C. Hoogenraad
Antibodies to TRIM46 are associated with paraneoplastic neurological syndromes
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Maarten Titulaer ,
Annemieke J. Rozemuller,
Peter Sillevis Smitt
Pathologically confirmed autoimmune encephalitis in suspected Creutzfeldt-Jakob disease
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Marleen van Coevorden-Hameete,
Veronique Rogemond,
Jerome Honnorat,
Lidia Sabeter,
Francesc Graus,
Sven Jarius,
Raymond Voltz,
Brigitte Wildemann,
Diego Franciotta,
Inga M. Blöcker,
Wolfgang Schlumberger,
Winfried Stöcker
and 1 other authors
Standardized test for anti-Tr/DNER in patients with paraneoplastic cerebellar degeneration
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Hein A. Lith,
Ewart Bruijn,
Sophietje Sonnaville,
Nienke E. Verbeek,
Dick Lindhout ,
Carolien G. F. Kovel,
Bobby P. C. Koeleman,
Marjan Kempen,
Eva Brilstra,
Edwin Cuppen
and 19 other authors
Identification ofSrp9as a febrile seizure susceptibility gene
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Peter Maat,
Esther Hulsenboom,
Robert van den Berg ,
Martin van den Bent,
Jeroen Demmers,
Pieternella J. Lugtenburg,
Casper C. Hoogenraad,
Peter Sillevis Smitt
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Nico M. van Beveren,
Esther Hulsenboom,
Kathelijne Koorengevel,
Robert M. Verdijk ,
Martijn van Duijn,
Herbert Hooijkaas,
Casper Hoogenraad,
Peter A. Sillevis Smitt
Psychiatric phenomena as initial manifestation of encephalitis by anti-NMDAR antibodies
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Esther de Graaff,
Alice S. Brooks,
Marco Metzger,
Ulrich L. M. Eisel,
Iain Shepherd,
Bart J. L. Eggen,
Robert M. W. Hofstra
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M. C. J. Dekker,
P. Montagna,
A. Baruzzi,
E. H. Yonova,
L. Correia Guedes,
L. Correia Guedes,
A. Szczerbinska,
T. Zhao,
L. O. M. Dubbel-Hulsman,
C. H. Wouters,
E. de Graaff ,
E. de Graaff,
W. J. G. Oyen,
E. J. Simons
and 4 other authors
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome.
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