174 related articles for article (PubMed ID: 33951919)
1. Adult Hereditary White Matter Diseases With Psychiatric Presentation: Clinical Pointers and MRI Algorithm to Guide the Diagnostic Process.
Costei C; Barbarosie M; Bernard G; Brais B; La Piana R
J Neuropsychiatry Clin Neurosci; 2021; 33(3):180-193. PubMed ID: 33951919
[TBL] [Abstract][Full Text] [Related]
2. Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.
Ayrignac X; Carra-Dalliere C; Menjot de Champfleur N; Denier C; Aubourg P; Bellesme C; Castelnovo G; Pelletier J; Audoin B; Kaphan E; de Seze J; Collongues N; Blanc F; Chanson JB; Magnin E; Berger E; Vukusic S; Durand-Dubief F; Camdessanche JP; Cohen M; Lebrun-Frenay C; Brassat D; Clanet M; Vermersch P; Zephir H; Outteryck O; Wiertlewski S; Laplaud DA; Ouallet JC; Brochet B; Goizet C; Debouverie M; Pittion S; Edan G; Deburghgraeve V; Le Page E; Verny C; Amati-Bonneau P; Bonneau D; Hannequin D; Guyant-Maréchal L; Derache N; Defer GL; Moreau T; Giroud M; Guennoc AM; Clavelou P; Taithe F; Mathis S; Neau JP; Magy L; Devoize JL; Bataillard M; Masliah-Planchon J; Dorboz I; Tournier-Lasserve E; Levade T; Boespflug Tanguy O; Labauge P
Brain; 2015 Feb; 138(Pt 2):284-92. PubMed ID: 25527826
[TBL] [Abstract][Full Text] [Related]
3. Inherited leukoencephalopathies with clinical onset in middle and old age.
Nannucci S; Donnini I; Pantoni L
J Neurol Sci; 2014 Dec; 347(1-2):1-13. PubMed ID: 25307983
[TBL] [Abstract][Full Text] [Related]
4. Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.
Kohlschütter A; Bley A; Brockmann K; Gärtner J; Krägeloh-Mann I; Rolfs A; Schöls L
Brain Dev; 2010 Feb; 32(2):82-9. PubMed ID: 19427149
[TBL] [Abstract][Full Text] [Related]
5. Posterior fossa involvement in the diagnosis of adult-onset inherited leukoencephalopathies.
Ayrignac X; Boutiere C; Carra-Dalliere C; Labauge P
J Neurol; 2016 Dec; 263(12):2361-2368. PubMed ID: 27126452
[TBL] [Abstract][Full Text] [Related]
6. Brain Calcifications in Adult-Onset Genetic Leukoencephalopathies: A Review.
Ayrignac X; Nicolas G; Carra-Dallière C; Hannequin D; Labauge P
JAMA Neurol; 2017 Aug; 74(8):1000-1008. PubMed ID: 28628708
[TBL] [Abstract][Full Text] [Related]
7. The spectrum of adult-onset heritable white-matter disorders.
Helman G; Venkateswaran S; Vanderver A
Handb Clin Neurol; 2018; 148():669-692. PubMed ID: 29478607
[TBL] [Abstract][Full Text] [Related]
8. Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era.
Lynch DS; Wade C; Paiva ARB; John N; Kinsella JA; Merwick Á; Ahmed RM; Warren JD; Mummery CJ; Schott JM; Fox NC; Houlden H; Adams ME; Davagnanam I; Murphy E; Chataway J
J Neurol Neurosurg Psychiatry; 2019 May; 90(5):543-554. PubMed ID: 30467211
[TBL] [Abstract][Full Text] [Related]
9. Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study.
Depienne C; Bugiani M; Dupuits C; Galanaud D; Touitou V; Postma N; van Berkel C; Polder E; Tollard E; Darios F; Brice A; de Die-Smulders CE; Vles JS; Vanderver A; Uziel G; Yalcinkaya C; Frints SG; Kalscheuer VM; Klooster J; Kamermans M; Abbink TE; Wolf NI; Sedel F; van der Knaap MS
Lancet Neurol; 2013 Jul; 12(7):659-68. PubMed ID: 23707145
[TBL] [Abstract][Full Text] [Related]
10. Genetic findings in adolescent and adult-onset leukodystrophies with hypomyelinating features.
Macaron G; Samaan S; Cohen JA; Nadjar Y
J Neurol Neurosurg Psychiatry; 2019 Jul; 90(7):836-838. PubMed ID: 30389777
[No Abstract] [Full Text] [Related]
11. Genetic Leukoencephalopathies in Adults.
Vanderver A
Continuum (Minneap Minn); 2016 Jun; 22(3):916-42. PubMed ID: 27261689
[TBL] [Abstract][Full Text] [Related]
12. [Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].
Wu Y; Jiang YW; Qin J; Xiao JX; Wang JM; Yang YL; Zhang YH; Chang XZ; Lin Q; Wu XR
Zhonghua Er Ke Za Zhi; 2007 Feb; 45(2):115-20. PubMed ID: 17456339
[TBL] [Abstract][Full Text] [Related]
13. Epidemiological, clinical, and genetic characteristics of paediatric genetic white matter disorders in Northern Finland.
Knuutinen OA; Oikarainen JH; Suo-Palosaari MH; Kangas SM; Rahikkala EJ; Pokka TM; Moilanen JS; Hinttala RML; Vieira PM; Uusimaa JM
Dev Med Child Neurol; 2021 Sep; 63(9):1066-1074. PubMed ID: 33948933
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?
Bindu PS; Sonam K; Chiplunkar S; Govindaraj P; Nagappa M; Vekhande CC; Aravinda HR; Ponmalar JJ; Mahadevan A; Gayathri N; Bharath MS; Sinha S; Taly AB
Mult Scler Relat Disord; 2018 Feb; 20():84-92. PubMed ID: 29353736
[TBL] [Abstract][Full Text] [Related]
15. Distinctive diffusion-weighted imaging features in late-onset genetic leukoencephalopathies.
De Cocker LJL; Castillo M
Neuroradiology; 2021 Jan; 63(1):153-156. PubMed ID: 32879996
[TBL] [Abstract][Full Text] [Related]
16. Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood.
Zhang J; Liu M; Zhang Z; Zhou L; Kong W; Jiang Y; Wang J; Xiao J; Wu Y
Pediatr Neurol; 2019 May; 94():38-47. PubMed ID: 30770271
[TBL] [Abstract][Full Text] [Related]
17. White matter disorders with autosomal dominant heredity: a review with personal clinical case studies and their MRI findings.
Sundal C; Ekholm S; Andersen O
Acta Neurol Scand; 2010 May; 121(5):328-37. PubMed ID: 19925533
[TBL] [Abstract][Full Text] [Related]
18. The disappearance of white matter in an adult-onset disease: a case report.
Ho CS; Mangelsdorf S; Walterfang M
BMC Psychiatry; 2020 Mar; 20(1):137. PubMed ID: 32220229
[TBL] [Abstract][Full Text] [Related]
19. Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia.
Wei C; Qin Q; Chen F; Zhou A; Wang F; Zuo X; Chen R; Lyu J; Jia J
BMC Neurol; 2019 Aug; 19(1):203. PubMed ID: 31438897
[TBL] [Abstract][Full Text] [Related]
20. White Matter Disease and Psychiatric Dysfunction: Clinical and Neurobiological Insights.
Filley CM
J Neuropsychiatry Clin Neurosci; 2021; 33(3):178-179. PubMed ID: 33951920
[No Abstract] [Full Text] [Related]
[Next] [New Search]