Verrips A - Search Results

1

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. Verrips A, et al. Neuromuscul Disord. 2000 Aug;10(6):407-14. doi: 10.1016/s0960-8966(00)00112-7. Neuromuscul Disord. 2000. PMID: 10899446 Clinical Trial.

2

A comparison of MRI criteria for diagnosing pediatric ADEM and MS.

Ketelslegers IA, Neuteboom RF, Boon M, Catsman-Berrevoets CE, Hintzen RQ; Dutch Pediatric MS Study Group. Ketelslegers IA, et al. Neurology. 2010 May 4;74(18):1412-5. doi: 10.1212/WNL.0b013e3181dc138b. Epub 2010 Mar 24. Neurology. 2010. PMID: 20335562

3

Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis.

de Bruijn MAAM, Aarsen FK, van Oosterhout MP, van der Knoop MM, Catsman-Berrevoets CE, Schreurs MWJ, Bastiaansen DEM, Sillevis Smitt PAE, Neuteboom RF, Titulaer MJ; CHANCE Study Group. de Bruijn MAAM, et al. Neurology. 2018 May 29;90(22):e1997-e2005. doi: 10.1212/WNL.0000000000005605. Epub 2018 Apr 27. Neurology. 2018. PMID: 29703768 Free PMC article.

4

Cerebrospinal fluid homocysteine and the cobalamin status of the brain.

Blom HJ, Wevers RA, Verrips A, TePoele-Pothoff MT, Trijbels JM. Blom HJ, et al. Among authors: verrips a. J Inherit Metab Dis. 1993;16(3):517-9. doi: 10.1007/BF00711669. J Inherit Metab Dis. 1993. PMID: 7609440 No abstract available.

5

Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis.

Verrips A, Steenbergen-Spanjers GC, Luyten JA, van den Heuvel LP, Keyser A, Gabreëls FJ, Wevers RA. Verrips A, et al. Hum Genet. 1996 Dec;98(6):735-7. doi: 10.1007/s004390050294. Hum Genet. 1996. PMID: 8931710

6

Pulmonary lymphangioleiomyomatosis and cerebrotendinous xanthomatosis: is there a link?

Dormans TP, Verrips A, Bulten J, Cox N. Dormans TP, et al. Among authors: verrips a. Chest. 1997 Jul;112(1):273-4. doi: 10.1378/chest.112.1.273. Chest. 1997. PMID: 9228390

7

Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis.

Verrips A, Steenbergen-Spanjers GC, Luyten JA, Wevers RA, Wokke JH, Gabreëls FJ, Wolthers BG, van den Heuvel LP. Verrips A, et al. Hum Genet. 1997 Aug;100(2):284-6. doi: 10.1007/s004390050506. Hum Genet. 1997. PMID: 9254865

8

The Aircardi-Goutières syndrome: variable clinical expression in two siblings.

Verrips A, Hiel JA, Gabreëls FJ, Wesseling P, Rotteveel JJ. Verrips A, et al. Pediatr Neurol. 1997 May;16(4):323-5. doi: 10.1016/s0887-8994(97)00028-3. Pediatr Neurol. 1997. PMID: 9258967

9

Treatment and follow-up of children with cerebrotendinous xanthomatosis.

van Heijst AF, Verrips A, Wevers RA, Cruysberg JR, Renier WO, Tolboom JJ. van Heijst AF, et al. Among authors: verrips a. Eur J Pediatr. 1998 Apr;157(4):313-6. doi: 10.1007/s004310050818. Eur J Pediatr. 1998. PMID: 9578968

10

Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes.

Hiel JA, Verrips A, Keyser A, Jansen TL, Wesseling P, de Coo R, Gabreëls FJ. Hiel JA, et al. Among authors: verrips a. Neth J Med. 1998 Jul;53(1):27-31. doi: 10.1016/s0300-2977(98)00018-7. Neth J Med. 1998. PMID: 9718939

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