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Items: 1 to 50 of 274

1.

Comparison of 3 instruments to measure muscle strength in children: A prospective study.

Van den Beld WA, Van der Sanden GA, Janssen AJ, Sengers RC, Verbeek AL, Gabreëls FJ.

Eur J Paediatr Neurol. 2011 Nov;15(6):512-8. doi: 10.1016/j.ejpn.2011.05.006. Epub 2011 Jul 1.

PMID:
21723758
2.

Antihypertensive treatment during pregnancy and functional development at primary school age in a historical cohort study.

Pasker-de Jong PC, Zielhuis GA, van Gelder MM, Pellegrino A, Gabreëls FJ, Eskes TK.

BJOG. 2010 Aug;117(9):1080-6. doi: 10.1111/j.1471-0528.2010.02568.x. Epub 2010 May 19.

3.

Muscle reflexes and synergies triggered by an unexpected support surface height during walking.

van der Linden MH, Marigold DS, Gabreëls FJ, Duysens J.

J Neurophysiol. 2007 May;97(5):3639-50. Epub 2007 Mar 28.

4.

Validity and reproducibility of the Jamar dynamometer in children aged 4-11 years.

van den Beld WA, van der Sanden GA, Sengers RC, Verbeek AL, Gabreëls FJ.

Disabil Rehabil. 2006 Nov 15;28(21):1303-9.

PMID:
17023377
5.

A new motor performance test in a prospective study on children with suspected myopathy.

van den Beld WA, van der Sanden GA, Feuth T, Janssen AJ, Sengers RC, Verbeek AL, Gabreëls FJ.

Dev Med Child Neurol. 2006 Sep;48(9):739-43.

6.

Fragmented visuospatial processing in children with pervasive developmental disorder.

Schlooz WA, Hulstijn W, van den Broek PJ, van der Pijll AC, Gabreëls F, van der Gaag RJ, Rotteveel JJ.

J Autism Dev Disord. 2006 Nov;36(8):1025-37.

PMID:
16897391
7.

Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia.

Hiel JA, van Engelen BG, Weemaes CM, Broeks A, Verrips A, ter Laak H, Vingerhoets HM, van den Heuvel LP, Lammens M, Gabreëls FJ, Last JI, Taylor AM.

Neurology. 2006 Jul 25;67(2):346-9.

PMID:
16864838
8.

Validity and reproducibility of hand-held dynamometry in children aged 4-11 years.

van den Beld WA, van der Sanden GA, Sengers RC, Verbeek AL, Gabreëls FJ.

J Rehabil Med. 2006 Jan;38(1):57-64.

9.

Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy.

van den Beld WA, van der Sanden GA, Sengers RC, Verbeek AL, Gabreëls FJ.

Dev Med Child Neurol. 2006 Jan;48(1):20-7.

10.

Histology of hereditary neuralgic amyotrophy.

van Alfen N, Gabreëls-Festen AA, Ter Laak HJ, Arts WF, Gabreëls FJ, van Engelen BG.

J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):445-7.

11.

Botulinum toxin effect on salivary flow rate in children with cerebral palsy.

Jongerius PH, Rotteveel JJ, van Limbeek J, Gabreëls FJ, van Hulst K, van den Hoogen FJ.

Neurology. 2004 Oct 26;63(8):1371-5.

PMID:
15505151
12.

Effect of botulinum toxin in the treatment of drooling: a controlled clinical trial.

Jongerius PH, van den Hoogen FJ, van Limbeek J, Gabreëls FJ, van Hulst K, Rotteveel JJ.

Pediatrics. 2004 Sep;114(3):620-7.

PMID:
15342830
13.

MR imaging and proton MR spectroscopic studies in Sjögren-Larsson syndrome: characterization of the leukoencephalopathy.

Willemsen MA, Van Der Graaf M, Van Der Knaap MS, Heerschap A, Van Domburg PH, Gabreëls FJ, Rotteveel JJ.

AJNR Am J Neuroradiol. 2004 Apr;25(4):649-57.

14.

A systematic review for evidence of efficacy of anticholinergic drugs to treat drooling.

Jongerius PH, van Tiel P, van Limbeek J, Gabreëls FJ, Rotteveel JJ.

Arch Dis Child. 2003 Oct;88(10):911-4. Review.

15.

Nijmegen breakage syndrome: a neuropathological study.

Lammens M, Hiel JA, Gabreëls FJ, van Engelen BG, van den Heuvel LP, Weemaes CM.

Neuropediatrics. 2003 Aug;34(4):189-93.

PMID:
12973659
16.

Planning of syllables in children with developmental apraxia of speech.

Nijland L, Maassen B, Van Der Meulen S, Gabreëls F, Kraaimaat FW, Schreuder R.

Clin Linguist Phon. 2003 Jan-Feb;17(1):1-24.

PMID:
12737052
17.

The treatment of drooling by ultrasound-guided intraglandular injections of botulinum toxin type A into the salivary glands.

Jongerius PH, Joosten F, Hoogen FJ, Gabreels FJ, Rotteveel JJ.

Laryngoscope. 2003 Jan;113(1):107-11.

PMID:
12514392
18.

Coarticulation patterns in children with developmental apraxia of speech.

Nijland L, Maassen B, Van der Meulen S, Gabreels F, Kraaimaat FW, Schreuder R.

Clin Linguist Phon. 2002 Sep;16(6):461-83.

PMID:
12469451
19.

Diagnosis and differential diagnosis of muscle cramps: a clinical approach.

Jansen PH, Gabreëls FJ, van Engelen BG.

J Clin Neuromuscul Dis. 2002 Dec;4(2):89-94.

PMID:
19078696
20.

Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene.

van de Wetering RA, Gabreëls-Festen AA, Timmerman V, Padberg GM, Gabreëls FJ, Mariman EC.

Neuromuscul Disord. 2002 Oct;12(7-8):651-5.

PMID:
12207933
21.

MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings.

Geerdink N, Rotteveel JJ, Lammens M, Sistermans EA, Heikens GT, Gabreëls FJ, Mullaart RA, Hamel BC.

Neuropediatrics. 2002 Feb;33(1):33-6.

PMID:
11930274
22.

Nonmuscular involvement in merosin-negative congenital muscular dystrophy.

Gilhuis HJ, ten Donkelaar HJ, Tanke RB, Vingerhoets DM, Zwarts MJ, Verrips A, Gabreëls FJ.

Pediatr Neurol. 2002 Jan;26(1):30-6.

PMID:
11814732
23.

Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defect.

van Engelen BG, Hiel JA, Gabreëls FJ, van den Heuvel LP, van Gent DC, Weemaes CM.

Hum Immunol. 2001 Dec;62(12):1324-7.

PMID:
11756000
24.

Botulinum toxin A: a new option for treatment of drooling in children with cerebral palsy. Presentation of a case series.

Jongerius PH, Rotteveel JJ, van den Hoogen F, Joosten F, van Hulst K, Gabreëls FJ.

Eur J Pediatr. 2001 Aug;160(8):509-12.

PMID:
11548191
25.

Idiopathic neuralgic amyotrophy in children. A distinct phenotype compared to the adult form.

van Alfen N, Schuuring J, van Engelen BG, Rotteveel JJ, Gabreëls FJ.

Neuropediatrics. 2000 Dec;31(6):328-32. Review.

PMID:
11508556
26.

Recurrent alternating facial paralysis and malignant hypertension.

Harms MM, Rotteveel JJ, Kar NC, Gabreëls FJ.

Neuropediatrics. 2000 Dec;31(6):318-20.

PMID:
11508553
27.

Scheie syndrome presenting as myopathy.

Verrips A, van Engelen BG, ter Laak H, Wesseling P, de Jong J, Gabreëls FJ.

Neuropediatrics. 2001 Apr;32(2):93-6.

PMID:
11414650
28.

Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndrome.

Willemsen MA, IJlst L, Steijlen PM, Rotteveel JJ, de Jong JG, van Domburg PH, Mayatepek E, Gabreëls FJ, Wanders RJ.

Brain. 2001 Jul;124(Pt 7):1426-37. Review.

PMID:
11408337
29.

Nijmegen breakage syndrome in a Dutch patient not resulting from a defect in NBS1.

Hiel JA, Weemaes CM, van Engelen BG, Smeets D, Ligtenberg M, van Der Burgt I, van Den Heuvel LP, Cerosaletti KM, Gabreëls FJ, Concannon P.

J Med Genet. 2001 Jun;38(6):E19. No abstract available.

30.

[Development and developmental disorders of the human brain. III. Neuronal migration disorders of the cerebrum].

ten Donkelaar HJ, Lammens M, Wesseling P, Thijssen HO, Renier WO, Gabreëls FJ.

Ned Tijdschr Geneeskd. 2001 Mar 10;145(10):466-74. Review. Dutch.

PMID:
11268908
31.

[Development and developmental disorders of the human brain. II. Development of the cerebral cortex and major tract systems].

ten Donkelaar HJ, Wesseling P, Lammens M, Thijssen HO, Renier WO, Gabreëls FJ.

Ned Tijdschr Geneeskd. 2001 Mar 3;145(9):401-10. Review. Dutch.

PMID:
11253494
32.

L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiency.

de Rijk-Van Andel JF, Gabreëls FJ, Geurtz B, Steenbergen-Spanjers GC, van Den Heuvel LP, Smeitink JA, Wevers RA.

Neurology. 2000 Dec 26;55(12):1926-8.

PMID:
11134401
33.

Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings.

Barkhof F, Verrips A, Wesseling P, van Der Knaap MS, van Engelen BG, Gabreëls FJ, Keyser A, Wevers RA, Valk J.

Radiology. 2000 Dec;217(3):869-76.

PMID:
11110956
34.

Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients.

Verrips A, van Engelen BG, ter Laak H, Gabreëls-Festen A, Janssen A, Zwarts M, Wevers RA, Gabreëls FJ.

Neuromuscul Disord. 2000 Aug;10(6):407-14.

PMID:
10899446
35.

A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome.

Tranebjaerg L, Hamel BC, Gabreels FJ, Renier WO, Van Ghelue M.

Eur J Hum Genet. 2000 Jun;8(6):464-7.

36.

Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease.

McNeill PM, Verrips A, Mullaart R, Gabreëls FJ, Gabreëls-Festen AW, Knibbeler JG.

J Neurol Neurosurg Psychiatry. 2000 Jun;68(6):797. No abstract available.

37.

Congenital fibre type disproportion a time-locked diagnosis: a clinical and morphological follow-up study.

Bartholomeus MG, Gabreëls FJ, ter Laak HJ, van Engelen BG.

Clin Neurol Neurosurg. 2000 Jun;102(2):97-101. Review.

PMID:
10817896
38.

Abeta fibers mediate cutaneous reflexes during human walking.

van Wezel BM, van Engelen BG, Gabreëls FJ, Gabreëls-Festen AA, Duysens J.

J Neurophysiol. 2000 May;83(5):2980-6.

39.

Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis.

Verrips A, Hoefsloot LH, Steenbergen GC, Theelen JP, Wevers RA, Gabreëls FJ, van Engelen BG, van den Heuvel LP.

Brain. 2000 May;123 ( Pt 5):908-19.

PMID:
10775536
40.

Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis.

Verrips A, van Engelen BG, Wevers RA, van Geel BM, Cruysberg JR, van den Heuvel LP, Keyser A, Gabreëls FJ.

Arch Neurol. 2000 Apr;57(4):520-4. Review.

PMID:
10768627
41.

The natural history of hereditary neuralgic amyotrophy in the Dutch population: two distinct types?

van Alfen N, van Engelen BG, Reinders JW, Kremer H, Gabreëls FJ.

Brain. 2000 Apr;123 ( Pt 4):718-23.

PMID:
10734003
42.

Preterm birth in Sjögren-Larsson syndrome.

Willemsen MA, Rotteveel JJ, van Domburg PH, Gabreëls FJ, Mayatepek E, Sengers RC.

Neuropediatrics. 1999 Dec;30(6):325-7.

PMID:
10706028
43.

Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy.

Strijks E, Poort SR, Renier WO, Gabreëls FJ, Bertina RM.

Neuropediatrics. 1999 Dec;30(6):320-4. Review. Erratum in: Neuropediatrics 2000 Aug;31(4):223.

PMID:
10706027
44.

Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.

Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.

Eur J Paediatr Neurol. 2000;4(1):39-43. Review.

PMID:
10701104
45.

Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.

van der Knaap MS, Wevers RA, Kure S, Gabreëls FJ, Verhoeven NM, van Raaij-Selten B, Jaeken J.

J Child Neurol. 1999 Nov;14(11):728-31.

PMID:
10593550
46.

Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression.

van der Burgt I, Thoonen G, Roosenboom N, Assman-Hulsmans C, Gabreels F, Otten B, Brunner HG.

J Pediatr. 1999 Dec;135(6):707-13.

PMID:
10586173
47.

Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis.

Verrips A, Nijeholt GJ, Barkhof F, Van Engelen BG, Wesseling P, Luyten JA, Wevers RA, Stam J, Wokke JH, van den Heuvel LP, Keyser A, Gabreëls FJ.

Brain. 1999 Aug;122 ( Pt 8):1589-95.

PMID:
10430841
48.

A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).

Wevers RA, de Rijk-van Andel JF, Bräutigam C, Geurtz B, van den Heuvel LP, Steenbergen-Spanjers GC, Smeitink JA, Hoffmann GF, Gabreëls FJ.

J Inherit Metab Dis. 1999 Jun;22(4):364-73. Review.

PMID:
10407773
49.

Molecular genetic analysis of human folate receptors in neural tube defects.

Heil SG, van der Put NM, Trijbels FJ, Gabreëls FJ, Blom HJ.

Eur J Hum Genet. 1999 Apr;7(3):393-6.

50.

Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patients.

van Domburg PH, Willemsen MA, Rotteveel JJ, de Jong JG, Thijssen HO, Heerschap A, Cruysberg JR, Wanders RJ, Gabreëls FJ, Steijlen PM.

Neurology. 1999 Apr 22;52(7):1345-52.

PMID:
10227616

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