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Search Results - Ghijsels, Jody
Search Results - Ghijsels, Jody
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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
by
Schuermans, Nika
,
Hemelsoet, Dimitri
,
Terryn, Wim
,
Steyaert, Sanne
,
Van Coster, Rudy
,
Coucke, Paul J
,
Steyaert, Wouter
,
Callewaert, Bert
,
Bogaert, Elke
,
Verloo, Patrick
,
Vanlander, Arnaud V
,
Debackere, Elke
,
Ghijsels, Jody
,
LeBlanc, Pontus
,
Verdin, Hannah
,
Naesens, Leslie
,
Haerynck, Filomeen
,
Callens, Steven
,
Dermaut, Bart
,
Poppe, Bruce
Published in
Orphanet journal of rare diseases
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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)
by
Van den Broecke, Astrid
,
Decruyenaere, Alexander
,
Schuermans, Nika
,
Verdin, Hannah
,
Ghijsels, Jody
,
Sieben, Anne
,
Dermaut, Bart
,
Hemelsoet, Dimitri
Published in
Journal of neurology
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Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders
by
Schuermans, Nika
,
Verdin, Hannah
,
Ghijsels, Jody
,
Hellemans, Madeleine
,
Debackere, Elke
,
Bogaert, Elke
,
Symoens, Sofie
,
Naesens, Leslie
,
Lecomte, Elien
,
Crosiers, David
,
Bergmans, Bruno
,
Verhoeven, Kristof
,
Poppe, Bruce
,
Laureys, Guy
,
Herdewyn, Sarah
,
Van Langenhove, Tim
,
Santens, Patrick
,
De Bleecker, Jan L
,
Hemelsoet, Dimitri
,
Dermaut, Bart
Published in
Neurology. Genetics
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Journal Of Neurology
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Neurology. Genetics
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Orphanet Journal Of Rare Diseases
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Creutzfeldt-Jakob Syndrome
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Gerstmann–Sträussler–Scheinker Syndrome
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