Catsman-Berrevoets C - Search Results

1

Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.

Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group. Wolf NI, et al. Neurology. 2014 Nov 18;83(21):1898-905. doi: 10.1212/WNL.0000000000001002. Epub 2014 Oct 22. Neurology. 2014. PMID: 25339210 Free PMC article.

2

Development of the anterior cingulate syndrome in a child due to delayed necrotising methotrexate leukoencephalopathy.

Catsman-Berrevoets CE, van Dongen HR, Kros JM. Catsman-Berrevoets CE, et al. J Neurol Neurosurg Psychiatry. 1997 Mar;62(3):301-2. doi: 10.1136/jnnp.62.3.301. J Neurol Neurosurg Psychiatry. 1997. PMID: 9069504 Free PMC article. No abstract available.

3

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.

van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J. van der Knaap MS, et al. Ann Neurol. 1997 Jul;42(1):50-9. doi: 10.1002/ana.410420110. Ann Neurol. 1997. PMID: 9225685

4

A mitochondrial tRNA(Val) gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes.

de Coo IF, Sistermans EA, de Wijs IJ, Catsman-Berrevoets C, Busch HF, Scholte HR, de Klerk JB, van Oost BA, Smeets HJ. de Coo IF, et al. Neurology. 1998 Jan;50(1):293-5. doi: 10.1212/wnl.50.1.293. Neurology. 1998. PMID: 9443499

5

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?

van der Knaap MS, Jakobs C, Hoffmann GF, Nyhan WL, Renier WO, Smeitink JA, Catsman-Berrevoets CE, Hjalmarson O, Vallance H, Sugita K, Bowe CM, Herrin JT, Craigen WJ, Buist NR, Brookfield DS, Chalmers RA. van der Knaap MS, et al. Ann Neurol. 1999 Jan;45(1):111-9. doi: 10.1002/1531-8249(199901)45:1<111::aid-art17>3.0.co;2-n. Ann Neurol. 1999. PMID: 9894884

6

Long-term sequelae in children after cerebellar astrocytoma surgery.

Aarsen FK, Van Dongen HR, Paquier PF, Van Mourik M, Catsman-Berrevoets CE. Aarsen FK, et al. Neurology. 2004 Apr 27;62(8):1311-6. doi: 10.1212/01.wnl.0000120549.77188.36. Neurology. 2004. PMID: 15111667

7

Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families.

Mancini GM, Catsman-Berrevoets CE, de Coo IF, Aarsen FK, Kamphoven JH, Huijmans JG, Duran M, van der Knaap MS, Jakobs C, Salomons GS. Mancini GM, et al. Am J Med Genet A. 2005 Jan 30;132A(3):288-95. doi: 10.1002/ajmg.a.30473. Am J Med Genet A. 2005. PMID: 15690373

8

Effect of topiramate on cognition in obese children.

Aarsen FK, van den Akker EL, Drop SL, Catsman-Berrevoets CE. Aarsen FK, et al. Neurology. 2006 Oct 10;67(7):1307-8. doi: 10.1212/01.wnl.0000238099.36998.6b. Neurology. 2006. PMID: 17030778 Clinical Trial. No abstract available.

9

Prognostic factors after a first attack of inflammatory CNS demyelination in children.

Neuteboom RF, Boon M, Catsman Berrevoets CE, Vles JS, Gooskens RH, Stroink H, Vermeulen RJ, Rotteveel JJ, Ketelslegers IA, Peeters E, Poll-The BT, De Rijk-Van Andel JF, Verrips A, Hintzen RQ. Neuteboom RF, et al. Neurology. 2008 Sep 23;71(13):967-73. doi: 10.1212/01.wnl.0000316193.89691.e1. Epub 2008 Jul 30. Neurology. 2008. PMID: 18672475

10

Barkhof magnetic resonance imaging criteria predict early relapse in pediatric multiple sclerosis.

Neuteboom RF, Ketelslegers IA, Boon M, Catsman-Berrevoets CE, Hintzen RQ; Dutch Study Group on Childhood Multiple Sclerosis and Acute Disseminated Encephalomyelitis. Neuteboom RF, et al. Pediatr Neurol. 2010 Jan;42(1):53-5. doi: 10.1016/j.pediatrneurol.2009.07.013. Pediatr Neurol. 2010. PMID: 20004863

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