A Patient with Moderate Intellectual Disability and 49, XXXYY Karyotype von Verhoeven, Willem M A, Egger, Jos I M, Mergler, Sandra, Meijer, Ton A A, Pfundt, Rolph, Willemsen, Marjolein H

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Beta-propeller protein-associated neurodegeneration (BPAN), a rare form of NBIA: Novel mutations and neuropsychiatric phenotype in three adult patients von Verhoeven, Willem M.A, Egger, Jos I.M, Koolen, David A, Yntema, Helger, Olgiati, Simone, Breedveld, Guido J, Bonifati, Vincenzo, van de Warrenburg, Bart P.C

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Neurosyphilis in the mixed urban–rural community of the Netherlands von Daey Ouwens, Ingrid M., Koedijk, Femke D.H., Fiolet, Aernoud T.L., van Veen, Maaike G., van den Wijngaard, Kees C., Verhoeven, Willem M.A., Egger, Jos I.M., van der Sande, Marianne A.B.

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Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype? von Verhoeven, Willem Ma, Egger, Jos Im, Willemsen, Marjolein H, de Leijer, Gert Jm, Kleefstra, Tjitske

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Cycloid psychoses in the psychosis spectrum: evidence for biochemical differences with schizophrenia von van de Kerkhof, Nora Wa, Fekkes, Durk, van der Heijden, Frank Mma, Hoogendijk, Witte Jg, Stöber, Gerald, Egger, Jos Im, Verhoeven, Willem Ma

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Neuropsychological phenotype of a patient with a de novo 970 kb interstitial deletion in the distal 16p11.2 region von Egger, Jos I M, Verhoeven, Willem M A, Verbeeck, Wim, de Leeuw, Nicole

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A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy von Verhoeven, Willem M.A, Egger, Jos I.M, Feenstra, Ilse, de Leeuw, Nicole

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Behavioural phenotype of a patient with a de novo 1.2 Mb chromosome 4q25 microdeletion von Verhoeven, Willem M.A, Egger, Jos I.M, Goffin, Luc, van Zutven, Laura J.C.M, Mancini, Grazia M.S

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A longitudinal perspective on the pharmacotherapy of 24 adult patients with Phelan McDermid syndrome von Verhoeven, Willem M.A., Egger, Jos I.M., de Leeuw, Nicole

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Genetic disorders and the autism spectrum von Verhoeven, Willem M.A, Egger, Jos I.M, Feenstra, Ilse

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Copy number variants in a sample of patients with psychotic disorders: is standard screening relevant for actual clinical practice? von Van de Kerkhof, Noortje Wa, Feenstra, Ilse, van der Heijden, Frank Mma, de Leeuw, Nicole, Pfundt, Rolph, Stöber, Gerald, Egger, Jos Im, Verhoeven, Willem Ma

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Metabolic syndrome in relation to psychotropic polypharmacy von Steylen, Pauline M.J, van der Heijden, Frank M.M.A, Kok, Hans D.H, Sijben, No A.S, Verhoeven, Willem M.A

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Phelan-McDermid syndrome due to SHANK3 mutation in an intellectually disabled adult male: successful treatment with lithium von Egger, Jos I M, Verhoeven, Willem M A, Groenendijk-Reijenga, Renske, Kant, Sarina G

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Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene von Verhoeven, Willem M A, Egger, Jos I M, Janssen, Paddy K C, van Haeringen, Arie

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Neuropsychiatric Adverse Events of Varenicline: A Systematic Review of Published Reports von AHMED, Amir I. A, ALI, Abdullah N. A, KRAMERS, Cees, HÄRMARK, Linda V. D, BURGER, David M, VERHOEVEN, Willem M. A

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Kleefstra syndrome in three adult patients: Further delineation of the behavioral and neurological phenotype shows aspects of a neurodegenerative course von Verhoeven, Willem M.A., Egger, Jos I.M., Vermeulen, Karlijn, van de Warrenburg, Bart P.C., Kleefstra, Tjitske

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Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2 von Verhoeven, Willem Ma, Egger, Jos Im, Knegt, Alida C, Zuydam, José, Kleefstra, Tjitske

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The neurocognition of alexithymia: evidence from neuropsychological and neuroimaging studies von Wingbermühle, Ellen, Theunissen, Hanneke, Verhoeven, Willem M. A., Kessels, Roy P. C., Egger, Jos I. M.

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Malaria Fever Therapy for General Paralysis of the Insane: A Historical Cohort Study von Daey Ouwens, Ingrid M., Lens, C. Elisabeth, Fiolet, Aernoud T.L., Ott, Alewijn, Koehler, Peter J., Kager, Piet A., Verhoeven, Willem M.A.

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A de novo CTNNB1 Novel Splice Variant in an Adult Female with Severe Intellectual Disability von Verhoeven, Willem MA, Egger, Jos IM, Jongbloed, Rob E, Meijer van Putten, Marloes, de Bruijn-van Zandwijk, Marieke, Zwemer, Anne-Suus, Pfundt, Rolph, Willemsen, Marjolein H

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