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Items: 22

1.

Low maternal melatonin level increases autism spectrum disorder risk in children.

Braam W, Ehrhart F, Maas APHM, Smits MG, Curfs L.

Res Dev Disabil. 2018 Nov;82:79-89. doi: 10.1016/j.ridd.2018.02.017. Epub 2018 Mar 1.

PMID:
29501372
2.

Exploration of differences in types of sleep disturbance and severity of sleep problems between individuals with Cri du Chat syndrome, Down's syndrome, and Jacobsen syndrome: a case control study.

Maas AP, Didden R, Korzilius H, Curfs LM.

Res Dev Disabil. 2012 Nov-Dec;33(6):1773-9. doi: 10.1016/j.ridd.2012.04.017. Epub 2012 Jun 13.

PMID:
22699250
3.

Psychometric properties of a sleep questionnaire for use in individuals with intellectual disabilities.

Maas AP, Didden R, Korzilius H, Braam W, Collin P, Smits MG, Curfs LM.

Res Dev Disabil. 2011 Nov-Dec;32(6):2467-79. doi: 10.1016/j.ridd.2011.07.013. Epub 2011 Aug 12.

PMID:
21840166
4.

Hereditary thrombocytosis not as innocent as thought? Development into acute leukemia and myelofibrosis.

Posthuma HL, Skoda RC, Jacob FA, van der Maas AP, Valk PJ, Posthuma EF.

Blood. 2010 Oct 28;116(17):3375-6. doi: 10.1182/blood-2010-06-290718. No abstract available.

PMID:
21030572
5.

Sleep disturbances and behavioural problems in adults with Prader-Willi syndrome.

Maas AP, Sinnema M, Didden R, Maaskant MA, Smits MG, Schrander-Stumpel CT, Curfs LM.

J Intellect Disabil Res. 2010 Oct;54(10):906-17. doi: 10.1111/j.1365-2788.2010.01306.x. Epub 2010 Jul 15.

PMID:
20636465
6.

Melatonin decreases daytime challenging behaviour in persons with intellectual disability and chronic insomnia.

Braam W, Didden R, Maas AP, Korzilius H, Smits MG, Curfs LM.

J Intellect Disabil Res. 2010 Jan 1;54(1):52-9. doi: 10.1111/j.1365-2788.2009.01223.x. Epub 2009 Nov 2.

PMID:
19888921
7.

Sleep in individuals with Cri du Chat syndrome: a comparative study.

Maas AP, Didden R, Korzilius H, Braam W, Smits MG, Curfs LM.

J Intellect Disabil Res. 2009 Aug;53(8):704-15. doi: 10.1111/j.1365-2788.2009.01184.x. Epub 2009 Jun 8.

PMID:
19508289
8.

Scatter plot analysis of excessive daytime sleepiness and severe disruptive behavior in adults with Prader-Willi syndrome: a pilot study.

Maas AP, Didden R, Bouts L, Smits MG, Curfs LM.

Res Dev Disabil. 2009 May-Jun;30(3):529-37. doi: 10.1016/j.ridd.2008.08.001. Epub 2008 Sep 14.

PMID:
18790602
9.

Sleep problems in individuals with 11q terminal deletion disorder (Jacobsen syndrome).

Maas AP, Grossfeld PD, Didden R, Korzilius H, Braam WJ, Smits MG, Curfs LM.

Genet Couns. 2008;19(2):225-35.

PMID:
18618998
10.

A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family.

Liu K, Kralovics R, Rudzki Z, Grabowska B, Buser AS, Olcaydu D, Gisslinger H, Tiedt R, Frank P, OkoƱ K, van der Maas AP, Skoda RC.

Haematologica. 2008 May;93(5):706-14. doi: 10.3324/haematol.11801. Epub 2008 Mar 26.

11.

Comparison of molecular markers in a cohort of patients with chronic myeloproliferative disorders.

Kralovics R, Buser AS, Teo SS, Coers J, Tichelli A, van der Maas AP, Skoda RC.

Blood. 2003 Sep 1;102(5):1869-71. Epub 2003 May 1.

PMID:
12730106
12.

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

Wiestner A, Schlemper RJ, van der Maas AP, Skoda RC.

Nat Genet. 1998 Jan;18(1):49-52.

PMID:
9425899
13.

H reflexes as a measure for uremic polyneuropathy. A longitudinal study in patients treated with dialysis or renal transplantation.

De Weerd AW, Nihom J, Rozeman CA, Poortvliet DC, Jonkman EJ, Van der Maas AP, Tjandra YI.

Electroencephalogr Clin Neurophysiol. 1994 Aug;93(4):276-80.

PMID:
7521287
14.

Familial essential thrombocythemia: clinical characteristics of 11 cases in one family.

Schlemper RJ, van der Maas AP, Eikenboom JC.

Ann Hematol. 1994 Mar;68(3):153-8.

PMID:
8167182
15.
16.

Encephalopathy in patients on continuous ambulatory peritoneal dialysis and patients on chronic haemodialysis.

Rozeman CA, Jonkman EJ, Poortvliet DC, Emmen HH, de Weerd AW, van der Maas AP, Tjandra YI, Beermann EM.

Nephrol Dial Transplant. 1992;7(12):1213-8.

PMID:
1337162
17.

[Polyarteritis nodosa with hepatitis and pancreatitis].

Brumsen C, de Man RA, van der Maas AP, Swart GR.

Ned Tijdschr Geneeskd. 1991 Apr 27;135(17):763-6. Dutch.

PMID:
1675434
18.

The use of the fibrinogen turnover and the isotope scanning of the legs for the diagnosis of venous thrombosis in non surgical patients.

Ottolander GJ, van der Maas AP, Schopmen W.

Thromb Diath Haemorrh. 1974 Dec 31;32(2-3):277-83. No abstract available.

PMID:
4450186
19.

[The use of I-131-fibrinogen in the diagnosis of venous thrombosis and in the evaluation of the effect of anticoagulant treatment].

van der Maas AP, Teulings FA, Schopman W, den Ottolander GJ.

Ned Tijdschr Geneeskd. 1973 Sep 15;117(37):1388-96. Dutch. No abstract available.

PMID:
4787074
20.

The influence of acenocumarole on the fibrinogen-turnover in normal subjects, venous thrombosis and congestive heart failure.

van der Maas AP, Teulings FA, Schopman W, den Ottolander GJ.

Thromb Diath Haemorrh. 1972 Dec 31;28(3):496-508. No abstract available.

PMID:
4649280
21.

The use of labelled fibrinogen in the diagnosis of venous thrombosis.

van der Maas AP, Teulings FA, den Ottolander GJ.

Thromb Diath Haemorrh. 1971 Aug 31;26(1):1-8. No abstract available.

PMID:
4939436
22.

[Use of radioisotopes in the diagnosis of venous thrombosis and lung embolies].

den Ottolander GJ, van der Maas AP, Schopman W, Teulings FA.

Ned Tijdschr Geneeskd. 1971 Feb 6;115(6):251-3. Dutch. No abstract available.

PMID:
5542585

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