These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
246 related articles for article (PubMed ID: 15851747)
21. MR spectroscopy in 18q(-) syndrome suggesting other than hypomyelination. Tada H; Takanashi J Brain Dev; 2014 Jan; 36(1):57-60. PubMed ID: 23332863 [TBL] [Abstract][Full Text] [Related]
22. Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation. Hamilton EM; Polder E; Vanderver A; Naidu S; Schiffmann R; Fisher K; Raguž AB; Blumkin L; ; van Berkel CG; Waisfisz Q; Simons C; Taft RJ; Abbink TE; Wolf NI; van der Knaap MS Brain; 2014 Jul; 137(Pt 7):1921-30. PubMed ID: 24785942 [TBL] [Abstract][Full Text] [Related]
23. Tourettism in multiple sclerosis: a case report. Nociti V; Fasano A; Bentivoglio AR; Frisullo G; Tartaglione T; Tonali PA; Batocchi AP J Neurol Sci; 2009 Dec; 287(1-2):288-90. PubMed ID: 19695578 [TBL] [Abstract][Full Text] [Related]
24. Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17). Lasek K; Lencer R; Gaser C; Hagenah J; Walter U; Wolters A; Kock N; Steinlechner S; Nagel M; Zühlke C; Nitschke MF; Brockmann K; Klein C; Rolfs A; Binkofski F Brain; 2006 Sep; 129(Pt 9):2341-52. PubMed ID: 16760196 [TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 12372733 [TBL] [Abstract][Full Text] [Related]
26. Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families. Passemard S; Gelot A; Fogli A; N'Guyen S; Barnerias C; Niel F; Doummar D; Arbues AS; Mignot C; de Villemeur TB; Ponsot G; Boespflug-Tanguy O; Rodriguez D Neurology; 2007 Jul; 69(4):400-2. PubMed ID: 17646634 [No Abstract] [Full Text] [Related]
27. Grey matter pathology in clinically early multiple sclerosis: evidence from magnetic resonance imaging. Chard D; Miller D J Neurol Sci; 2009 Jul; 282(1-2):5-11. PubMed ID: 19201002 [TBL] [Abstract][Full Text] [Related]
28. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature. Bhidayasiri R; Perlman SL; Pulst SM; Geschwind DH Arch Neurol; 2005 Dec; 62(12):1865-9. PubMed ID: 16344344 [TBL] [Abstract][Full Text] [Related]
29. Brain atrophy and lesion load in a large population of patients with multiple sclerosis. Tedeschi G; Lavorgna L; Russo P; Prinster A; Dinacci D; Savettieri G; Quattrone A; Livrea P; Messina C; Reggio A; Bresciamorra V; Orefice G; Paciello M; Brunetti A; Coniglio G; Bonavita S; Di Costanzo A; Bellacosa A; Valentino P; Quarantelli M; Patti F; Salemi G; Cammarata E; Simone IL; Salvatore M; Bonavita V; Alfano B Neurology; 2005 Jul; 65(2):280-5. PubMed ID: 16043800 [TBL] [Abstract][Full Text] [Related]
30. Neurological manifestations of the oculodentodigital dysplasia syndrome. Loddenkemper T; Grote K; Evers S; Oelerich M; Stögbauer F J Neurol; 2002 May; 249(5):584-95. PubMed ID: 12021949 [TBL] [Abstract][Full Text] [Related]
31. A Japanese family with early-onset ataxia with motor and sensory neuropathy. Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771 [TBL] [Abstract][Full Text] [Related]
32. Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children. van der Knaap MS; Barth PG; Stroink H; van Nieuwenhuizen O; Arts WF; Hoogenraad F; Valk J Ann Neurol; 1995 Mar; 37(3):324-34. PubMed ID: 7695231 [TBL] [Abstract][Full Text] [Related]
33. White matter proton MR spectroscopy in children with isolated developmental delay: does it mean delayed myelination? Fayed N; Morales H; Modrego PJ; Muñoz-Mingarro J Acad Radiol; 2006 Feb; 13(2):229-35. PubMed ID: 16428059 [TBL] [Abstract][Full Text] [Related]
34. Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). Report of a new case. Mercimek-Mahmutoglu S; van der Knaap MS; Baric I; Prayer D; Stoeckler-Ipsiroglu S Neuropediatrics; 2005 Jun; 36(3):223-6. PubMed ID: 15944912 [TBL] [Abstract][Full Text] [Related]
35. New pattern of brain MRI lesions in isolated complex I deficiency. Wolf NI; Seitz A; Harting I; Smeitink JA; Trijbels F; van den Heuvel LP; Schlemmer H; Ebinger F; Evert W; Rating D Neuropediatrics; 2003 Jun; 34(3):156-9. PubMed ID: 12910441 [TBL] [Abstract][Full Text] [Related]
36. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease. Meissner B; Kallenberg K; Sanchez-Juan P; Collie D; Summers DM; Almonti S; Collins SJ; Smith P; Cras P; Jansen GH; Brandel JP; Coulthart MB; Roberts H; Van Everbroeck B; Galanaud D; Mellina V; Will RG; Zerr I Neurology; 2009 Jun; 72(23):1994-2001. PubMed ID: 19506221 [TBL] [Abstract][Full Text] [Related]
38. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia. Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408 [TBL] [Abstract][Full Text] [Related]
39. Progression of the olivopontocerebellar form of adrenoleukodystrophy as shown by MRI. Suda S; Komaba Y; Kumagai T; Yamazaki M; Katsumata T; Kamiya T; Katayama Y Neurology; 2006 Jan; 66(1):144-5. PubMed ID: 16401870 [No Abstract] [Full Text] [Related]
40. 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. PubMed ID: 16047349 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]