254 related articles for article (PubMed ID: 7692130)
1. The inherited leukodystrophies: a clinical overview.
Aicardi J
J Inherit Metab Dis; 1993; 16(4):733-43. PubMed ID: 7692130
[TBL] [Abstract][Full Text] [Related]
2. Leukodystrophies.
Perlman SJ; Mar S
Adv Exp Med Biol; 2012; 724():154-71. PubMed ID: 22411242
[TBL] [Abstract][Full Text] [Related]
3. Pelizaeus-Merzbacher disease: an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.
Gencic S; Abuelo D; Ambler M; Hudson LD
Am J Hum Genet; 1989 Sep; 45(3):435-42. PubMed ID: 2773936
[TBL] [Abstract][Full Text] [Related]
4. [Pathogenesis and pathomorphology of human leukodystrophies].
Zhabotinskiĭ IuM; Shefer VF
Arkh Patol; 1981; 43(11):86-92. PubMed ID: 7032481
[TBL] [Abstract][Full Text] [Related]
5. Molecular diagnostics for myelin proteolipid protein gene mutations in Pelizaeus-Merzbacher disease.
Doll R; Natowicz MR; Schiffmann R; Smith FI
Am J Hum Genet; 1992 Jul; 51(1):161-9. PubMed ID: 1376966
[TBL] [Abstract][Full Text] [Related]
6. [Leukodystrophies: clinical aspects and findings with computerized tomography and magnetic resonance imaging].
Magnaldi S
Radiol Med; 1991; 82(1-2):13-26. PubMed ID: 1896564
[TBL] [Abstract][Full Text] [Related]
7. Leukodystrophy Imaging: Insights for Diagnostic Dilemmas.
Thakkar RN; Patel D; Kioutchoukova IP; Al-Bahou R; Reddy P; Foster DT; Lucke-Wold B
Med Sci (Basel); 2024 Jan; 12(1):. PubMed ID: 38390857
[TBL] [Abstract][Full Text] [Related]
8. Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients.
Müller vom Hagen J; Karle KN; Schüle R; Krägeloh-Mann I; Schöls L
Eur J Neurol; 2014 Jul; 21(7):983-8. PubMed ID: 24698313
[TBL] [Abstract][Full Text] [Related]
9. An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Ashrafi MR; Amanat M; Garshasbi M; Kameli R; Nilipour Y; Heidari M; Rezaei Z; Tavasoli AR
Expert Rev Neurother; 2020 Jan; 20(1):65-84. PubMed ID: 31829048
[No Abstract] [Full Text] [Related]
10. Epilepsy in children with leukodystrophies.
Zhang J; Ban T; Zhou L; Ji H; Yan H; Shi Z; Cao B; Jiang Y; Wang J; Wu Y
J Neurol; 2020 Sep; 267(9):2612-2618. PubMed ID: 32388833
[TBL] [Abstract][Full Text] [Related]
11. Some thoughts on the neurobiology of the leukodystrophies.
Norton WT
Neuropediatrics; 1984 Sep; 15 Suppl():28-31. PubMed ID: 6100796
[TBL] [Abstract][Full Text] [Related]
12. Structural manifestations of leukodystrophies.
Seitelberger F
Neuropediatrics; 1984 Sep; 15 Suppl():53-61. PubMed ID: 6152813
[TBL] [Abstract][Full Text] [Related]
13. Immunocytochemical investigations of some human leukodystrophies.
Ulrich J; Kohler R; Heitz PU; Probst A
Acta Neuropathol; 1983; 60(3-4):199-206. PubMed ID: 6193676
[TBL] [Abstract][Full Text] [Related]
14. Selected leukodystrophies.
Powers JM; Rubio A
Semin Pediatr Neurol; 1995 Sep; 2(3):200-10. PubMed ID: 9422247
[TBL] [Abstract][Full Text] [Related]
15. Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants.
Mahdieh N; Soveizi M; Tavasoli AR; Rabbani A; Ashrafi MR; Kohlschütter A; Rabbani B
Sci Rep; 2021 Feb; 11(1):3231. PubMed ID: 33547378
[TBL] [Abstract][Full Text] [Related]
16. Duplication of proteolipid protein gene: a possible major cause of Pelizaeus-Merzbacher disease.
Wang PJ; Hwu WL; Lee WT; Wang TR; Shen YZ
Pediatr Neurol; 1997 Sep; 17(2):125-8. PubMed ID: 9367291
[TBL] [Abstract][Full Text] [Related]
17. Biochemical pathogenesis of genetic leukodystrophies: comparison of metachromatic leukodystrophy and globoid cell leukodystrophy (Krabbe's disease).
Suzuki K
Neuropediatrics; 1984 Sep; 15 Suppl():32-6. PubMed ID: 6152811
[TBL] [Abstract][Full Text] [Related]
18. A correlative synopsis of the leukodystrophies.
Morell P
Neuropediatrics; 1984 Sep; 15 Suppl():62-5. PubMed ID: 6546165
[TBL] [Abstract][Full Text] [Related]
19. Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease.
Koeppen AH; Ronca NA; Greenfield EA; Hans MB
Ann Neurol; 1987 Feb; 21(2):159-70. PubMed ID: 3827224
[TBL] [Abstract][Full Text] [Related]
20. A case of Pelizaeus-Merzbacher disease showing increased dosage of the proteolipid protein gene.
Harding B; Ellis D; Malcolm S
Neuropathol Appl Neurobiol; 1995 Apr; 21(2):111-5. PubMed ID: 7541900
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]