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Items: 9

1.

ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.

Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA.

Neurol Genet. 2018 Mar 21;4(2):e223. doi: 10.1212/NXG.0000000000000223. eCollection 2018 Apr.

2.

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.

de Vrij FM, Bouwkamp CG, Gunhanlar N, Shpak G, Lendemeijer B, Baghdadi M, Gopalakrishna S, Ghazvini M, Li TM, Quadri M, Olgiati S, Breedveld GJ, Coesmans M, Mientjes E, de Wit T, Verheijen FW, Beverloo HB, Cohen D, Kok RM, Bakker PR, Nijburg A, Spijker AT, Haffmans PMJ, Hoencamp E, Bergink V; GROUP Study Consortium, Vorstman JA, Wu T, Olde Loohuis LM, Amin N, Langen CD, Hofman A, Hoogendijk WJ, van Duijn CM, Ikram MA, Vernooij MW, Tiemeier H, Uitterlinden AG, Elgersma Y, Distel B, Gribnau J, White T, Bonifati V, Kushner SA.

Mol Psychiatry. 2018 Jan 4. doi: 10.1038/s41380-017-0004-2. [Epub ahead of print]

PMID:
29302076
3.

Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in Psychiatry.

Bouwkamp CG, Kievit AJA, Markx S, Friedman JI, van Zutven L, van Minkelen R, Vrijenhoek T, Xu B, Sterrenburg-van de Nieuwegiessen I, Veltman JA, Bonifati V, Kushner SA.

Am J Psychiatry. 2017 Nov 1;174(11):1036-1050. doi: 10.1176/appi.ajp.2017.16080946. No abstract available.

PMID:
29088930
4.

[Psychodynamic consequences of a family history with psychiatric disorders].

Bouwkamp CG, den Berg MPL, Kievit AJA, Kushner SA.

Tijdschr Psychiatr. 2017;59(8):474-481. Dutch.

5.

The levonorgestrel-releasing intrauterine device potentiates stress reactivity.

Aleknaviciute J, Tulen JHM, De Rijke YB, Bouwkamp CG, van der Kroeg M, Timmermans M, Wester VL, Bergink V, Hoogendijk WJG, Tiemeier H, van Rossum EFC, Kooiman CG, Kushner SA.

Psychoneuroendocrinology. 2017 Jun;80:39-45. doi: 10.1016/j.psyneuen.2017.02.025. Epub 2017 Feb 28.

PMID:
28315609
6.

A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion.

Kolaitis G, Bouwkamp CG, Papakonstantinou A, Otheiti I, Belivanaki M, Haritaki S, Korpa T, Albani Z, Terzioglou E, Apostola P, Skamnaki A, Xaidara A, Kosma K, Kitsiou-Tzeli S, Tzetis M.

Child Adolesc Psychiatry Ment Health. 2016 Sep 15;10:33. doi: 10.1186/s13034-016-0121-8. eCollection 2016.

7.

A balanced translocation disrupting BCL2L10 and PNLDC1 segregates with affective psychosis.

Bouwkamp CG, Kievit AJ, Olgiati S, Breedveld GJ, Coesmans M, Bonifati V, Kushner SA.

Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):214-219. doi: 10.1002/ajmg.b.32465. Epub 2016 Jun 3.

8.

DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease.

Olgiati S, Quadri M, Fang M, Rood JP, Saute JA, Chien HF, Bouwkamp CG, Graafland J, Minneboo M, Breedveld GJ, Zhang J; International Parkinsonism Genetics Network, Verheijen FW, Boon AJ, Kievit AJ, Jardim LB, Mandemakers W, Barbosa ER, Rieder CR, Leenders KL, Wang J, Bonifati V.

Ann Neurol. 2016 Feb;79(2):244-56. doi: 10.1002/ana.24553. Epub 2016 Jan 14.

PMID:
26528954
9.

Interpersonal and social rhythm group therapy for patients with bipolar disorder.

Bouwkamp CG, de Kruiff ME, van Troost TM, Snippe D, Blom MJ, de Winter RF, Judith Haffmans PM.

Int J Group Psychother. 2013 Jan;63(1):97-115. doi: 10.1521/ijgp.2013.63.1.97.

PMID:
23252817

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