154 related articles for article (PubMed ID: 10073435)
1. Clinical, pathologic, and neurochemical studies of an unusual case of neuronal storage disease with lamellar cytoplasmic inclusions: a new genetic disorder?
Rose AL; Farmer PM; Mitra N; Wisniewski KE; Pullarkat RK
J Child Neurol; 1999 Feb; 14(2):123-9. PubMed ID: 10073435
[TBL] [Abstract][Full Text] [Related]
2. Dysmyelinogenesis in animal model of GM1 gangliosidosis.
Kaye EM; Alroy J; Raghavan SS; Schwarting GA; Adelman LS; Runge V; Gelblum D; Thalhammer JG; Zuniga G
Pediatr Neurol; 1992; 8(4):255-61. PubMed ID: 1388413
[TBL] [Abstract][Full Text] [Related]
3. The AB-variant of GM2-gangliosidosis. Clinical, biochemical, and pathological studies of two patients.
Goldman JE; Yamanaka T; Rapin I; Adachi M; Suzuki K; Suzuki K
Acta Neuropathol; 1980; 52(3):189-202. PubMed ID: 6255724
[TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.
MacDermot KD; Walker RW
J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1342-7. PubMed ID: 3479531
[TBL] [Abstract][Full Text] [Related]
5. Lipid changes in Niemann-Pick disease type C brain: personal experience and review of the literature.
Vanier MT
Neurochem Res; 1999 Apr; 24(4):481-9. PubMed ID: 10227680
[TBL] [Abstract][Full Text] [Related]
6. The fine structure of cytoplasmic inclusions in brain and other visceral organs in Sandhoff disease.
Itoh H; Tanaka J; Morihana Y; Tamaki T
Brain Dev; 1984; 6(5):467-74. PubMed ID: 6097133
[TBL] [Abstract][Full Text] [Related]
7. Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease.
Walkley SU; Thrall MA; Haskins ME; Mitchell TW; Wenger DA; Brown DE; Dial S; Seim H
Neuropathol Appl Neurobiol; 2005 Oct; 31(5):536-44. PubMed ID: 16150124
[TBL] [Abstract][Full Text] [Related]
8. Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathy.
Sone J; Hishikawa N; Koike H; Hattori N; Hirayama M; Nagamatsu M; Yamamoto M; Tanaka F; Yoshida M; Hashizume Y; Imamura H; Yamada E; Sobue G
Neurology; 2005 Nov; 65(10):1538-43. PubMed ID: 16301479
[TBL] [Abstract][Full Text] [Related]
9. Sialidosis type I carrying V217M/G243R mutations in lysosomal sialidase: an autopsy study demonstrating terminal sialic acid in lysosomal lamellar inclusions and cerebellar dysplasia.
Uchihara T; Ohashi K; Kitagawa M; Kurata M; Nakamura A; Hirokawa K; Kasuga T; Kobayashi T
Acta Neuropathol; 2010 Jan; 119(1):135-45. PubMed ID: 19415310
[TBL] [Abstract][Full Text] [Related]
10. Spinal ganglia and peripheral nerves from a patent with Tay-Sachs disease. Morphological and ganglioside studies.
Abe T; Ogawa K; Fuziwara H; Urayama K; Nagashima K
Acta Neuropathol; 1985; 66(3):239-44. PubMed ID: 2990149
[TBL] [Abstract][Full Text] [Related]
11. [Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue].
Pilz H; Heipertz R
Fortschr Neurol Psychiatr Grenzgeb; 1975 Nov; 43(11):602-17. PubMed ID: 53174
[TBL] [Abstract][Full Text] [Related]
12. Adult GM2 gangliosidosis masquerading as slowly progressive muscular atrophy: motor neuron disease phenotype.
Jellinger K; Anzil AP; Seemann D; Bernheimer H
Clin Neuropathol; 1982; 1(1):31-44. PubMed ID: 7166018
[TBL] [Abstract][Full Text] [Related]
13. Progressive white matter pathology in the spinal cord of transgenic mice expressing mutant (P301L) human tau.
Lin WL; Zehr C; Lewis J; Hutton M; Yen SH; Dickson DW
J Neurocytol; 2005 Dec; 34(6):397-410. PubMed ID: 16902761
[TBL] [Abstract][Full Text] [Related]
14. Pathology and pathogenesis of sensory neuropathy in Friedreich's ataxia.
Morral JA; Davis AN; Qian J; Gelman BB; Koeppen AH
Acta Neuropathol; 2010 Jul; 120(1):97-108. PubMed ID: 20339857
[TBL] [Abstract][Full Text] [Related]
15. Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studies.
Alroy J; Schelling SH; Thalhammer JG; Raghavan SS; Natowicz MR; Prence EM; Orgad U
Acta Neuropathol; 1992; 84(6):658-63. PubMed ID: 1471473
[TBL] [Abstract][Full Text] [Related]
16. Neuronal ceroid lipofuscinosis: a clinicopathological study.
Sinha S; Satishchandra P; Santosh V; Gayatri N; Shankar SK
Seizure; 2004 Jun; 13(4):235-40. PubMed ID: 15121131
[TBL] [Abstract][Full Text] [Related]
17. Prominent white matter cavitation in an infant with Alexander's disease.
Klein EA; Anzil AP
Clin Neuropathol; 1994; 13(1):31-8. PubMed ID: 8033460
[TBL] [Abstract][Full Text] [Related]
18. Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome.
Bertini E; Sabatelli M; Di Capua M; Cilio MR; Mignogna T; Federico A; Tonali P
Eur J Paediatr Neurol; 1998; 2(5):245-54. PubMed ID: 10726827
[TBL] [Abstract][Full Text] [Related]
19. Mucolipidosis IV. Clinical, ultrastructural, histochemical, and chemical studies of a case, including a brain biopsy.
Tellez-Nagel I; Rapin I; Iwamoto T; Johnson AB; Norton WT; Nitowsky H
Arch Neurol; 1976 Dec; 33(12):828-35. PubMed ID: 187156
[TBL] [Abstract][Full Text] [Related]
20. Adult type neuronal storage disease with neuraminidase deficiency.
Miyatake T; Atsumi T; Obayashi T; Mizuno Y; Ando S; Ariga T; Matsui-Nakamura K; Yamada T
Ann Neurol; 1979 Sep; 6(3):232-44. PubMed ID: 534422
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]