Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 110

1.

Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy.

Wolf NI, Harting I, Innes AM, Patzer S, Zeitler P, Schneider A, Wolff A, Baier K, Zschocke J, Ebinger F, Boltshauser E, Rating D.

Neuropediatrics. 2007 Apr;38(2):64-70.

PMID:
17712733
2.

Leukoencephalopathy with ataxia, hypodontia, and hypomyelination.

Wolf NI, Harting I, Boltshauser E, Wiegand G, Koch MJ, Schmitt-Mechelke T, Martin E, Zschocke J, Uhlenberg B, Hoffmann GF, Weber L, Ebinger F, Rating D.

Neurology. 2005 Apr 26;64(8):1461-4.

PMID:
15851747
3.

When neuropediatrics meets odontology.

Bloch-Zupan A.

Neuropediatrics. 2007 Apr;38(2):57-8. No abstract available.

PMID:
17712730
4.

New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.

van der Knaap MS, Naidu S, Pouwels PJ, Bonavita S, van Coster R, Lagae L, Sperner J, Surtees R, Schiffmann R, Valk J.

AJNR Am J Neuroradiol. 2002 Oct;23(9):1466-74.

5.

Childhood ataxia with cerebral hypomyelination (CACH) syndrome: a study of three siblings.

Vaidya SR, Desai SB, Khadilkar SV, Mehta NA.

Neurol India. 2004 Sep;52(3):372-4.

6.

Rare dental peculiarities associated with the hypomyelinating leukoencephalopathy 4H syndrome/ADDH.

Wolff A, Koch MJ, Benzinger S, van Waes H, Wolf NI, Boltshauser E, Luder HU.

Pediatr Dent. 2010 Sep-Oct;32(5):386-92.

PMID:
21070704
7.

Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.

van der Knaap MS, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S.

Neurology. 2007 Jul 10;69(2):166-71.

PMID:
17620549
8.

Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorder.

Rossi A, Biancheri R, Zara F, Bruno C, Uziel G, van der Knaap MS, Minetti C, Tortori-Donati P.

AJNR Am J Neuroradiol. 2008 Feb;29(2):301-5. Epub 2007 Nov 1.

9.

Myelinopathia centralis diffusa (vanishing white matter disease) in a four-year-old boy.

Sinzig JK, Seitz A, Brockmann K, König S.

J Neuroradiol. 2004 Mar;31(2):142-4.

10.

Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum.

Sasaki M, Takanashi J, Tada H, Sakuma H, Furushima W, Sato N.

Brain Dev. 2009 Sep;31(8):582-7. doi: 10.1016/j.braindev.2008.09.003. Epub 2008 Oct 11.

PMID:
18851904
11.

Membrane phospholipids and high-energy metabolites in childhood ataxia with CNS hypomyelination.

Blüml S, Philippart M, Schiffmann R, Seymour K, Ross BD.

Neurology. 2003 Sep 9;61(5):648-54.

PMID:
12963756
12.

New case of 4H syndrome and a review of the literature.

Orcesi S, Tonduti D, Uggetti C, Larizza D, Fazzi E, Balottin U.

Pediatr Neurol. 2010 May;42(5):359-64. doi: 10.1016/j.pediatrneurol.2010.01.015. Review.

PMID:
20399393
13.

Unraveling pathology in juvenile Alexander disease: serial quantitative MR imaging and spectroscopy of white matter.

van der Voorn JP, Pouwels PJ, Salomons GS, Barkhof F, van der Knaap MS.

Neuroradiology. 2009 Oct;51(10):669-75. doi: 10.1007/s00234-009-0540-9. Epub 2009 May 30.

14.

Five patients with a recently described novel leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate.

Serkov SV, Pronin IN, Bykova OV, Maslova OI, Arutyunov NV, Muravina TI, Kornienko VN, Fadeeva LM, Marks H, Bönnemann C, Schiffmann R, van der Knaap MS.

Neuropediatrics. 2004 Feb;35(1):1-5.

PMID:
15002045
15.

Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study.

Dreha-Kulaczewski SF, Dechent P, Finsterbusch J, Brockmann K, Gärtner J, Frahm J, Hanefeld FA.

Pediatr Res. 2008 Apr;63(4):444-9. doi: 10.1203/01.pdr.0000304934.90198.25.

PMID:
18356755
16.

Assessment of citrullinated myelin by 1H-MR spectroscopy in early-onset multiple sclerosis.

Oguz KK, Kurne A, Aksu AO, Karabulut E, Serdaroglu A, Teber S, Haspolat S, Senbil N, Kurul S, Anlar B.

AJNR Am J Neuroradiol. 2009 Apr;30(4):716-21. doi: 10.3174/ajnr.A1425. Epub 2009 Jan 15.

17.

Congenital ataxia of parietal origin? Report of two cases.

Steinlin M, Schmitt B, Ferrini B.

Brain Dev. 1998 Jun;20(4):242-4.

PMID:
9661970
18.

Cerebellar leukoencephalopathy: most likely histiocytosis-related.

van der Knaap MS, Arts WF, Garbern JY, Hedlund G, Winkler F, Barbosa C, King MD, Bjørnstad A, Hussain N, Beyer MK, Gomez C, Patterson MC, Grattan-Smith P, Timmons M, van der Valk P.

Neurology. 2008 Oct 21;71(17):1361-7. doi: 10.1212/01.wnl.0000327680.74910.93.

PMID:
18936429
19.

Dominant form of vanishing white matter-like leukoencephalopathy.

Labauge P, Fogli A, Castelnovo G, Le Bayon A, Horzinski L, Nicoli F, Cozzone P, Pagès M, Briere C, Marty-Double C, Delhaume O, Gelot A, Boespflug-Tanguy O, Rodriguez D.

Ann Neurol. 2005 Oct;58(4):634-9.

PMID:
16047349
20.

Dental anomalies in patients with Down syndrome.

de Moraes ME, de Moraes LC, Dotto GN, Dotto PP, dos Santos LR.

Braz Dent J. 2007;18(4):346-50.

Supplemental Content

Support Center