-
1
-
-
0029803683
-
Naming of syndromes and unethical activities: The case of Hallervorden and Spatz
-
Harper P. Naming of syndromes and unethical activities: the case of Hallervorden and Spatz. Lancet 1996; 348: 1224-1225.
-
(1996)
Lancet
, vol.348
, pp. 1224-1225
-
-
Harper, P.1
-
2
-
-
0034839088
-
Julius Hallervorden's wartime activities: Implication for science under dictatorship
-
Shevell MI, Peiffer J. Julius Hallervorden's wartime activities: implication for science under dictatorship. Pediatr Neurol 2001; 25: 162-165.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 162-165
-
-
Shevell, M.I.1
Peiffer, J.2
-
3
-
-
0030583754
-
Naming of syndromes
-
Morrison P. Naming of syndromes. Lancet 1996; 348: 1662.
-
(1996)
Lancet
, vol.348
, pp. 1662
-
-
Morrison, P.1
-
4
-
-
0030583754
-
Naming of syndromes
-
Shevell M. Naming of syndromes. Lancet 1996; 348: 1662.
-
(1996)
Lancet
, vol.348
, pp. 1662
-
-
Shevell, M.1
-
5
-
-
0030583756
-
Naming of syndromes
-
Jacby R, Oppenheimer C. Naming of syndromes. Lancet 1996; 348: 1662.
-
(1996)
Lancet
, vol.348
, pp. 1662
-
-
Jacby, R.1
Oppenheimer, C.2
-
6
-
-
0034996072
-
Four siblings with Hallervorden-Spatz disease
-
Vaher U, Napa A, Nurmiste A et al. Four siblings with Hallervorden-Spatz disease. Brain Dev 2001; 23: 236-239.
-
(2001)
Brain Dev.
, vol.23
, pp. 236-239
-
-
Vaher, U.1
Napa, A.2
Nurmiste, A.3
-
7
-
-
0034935036
-
A novel pantothenate kinase gene is defective in Hallervorden-Spatz syndrome
-
Zhou B, Westaway SK, Levinson B et al. A novel pantothenate kinase gene is defective in Hallervorden-Spatz syndrome. Nature Genet 2001; 28: 345-349.
-
(2001)
Nature Genet.
, vol.28
, pp. 345-349
-
-
Zhou, B.1
Westaway, S.K.2
Levinson, B.3
-
8
-
-
0029434793
-
The nosology of Hallervorden-Spatz disease
-
Halliday W. The nosology of Hallervorden-Spatz disease. J Neurol Sci 1995; 134: 84-91.
-
(1995)
J. Neurol. Sci.
, vol.134
, pp. 84-91
-
-
Halliday, W.1
-
9
-
-
0343776132
-
Hallervorden-Spatz disease: Two new early childhood onset cases
-
Peña JA, Molina O, Cardozo J. Hallervorden-Spatz disease: two new early childhood onset cases. J Child Neurol 2000; 15: 30-32.
-
(2000)
J. Child Neurol.
, vol.15
, pp. 30-32
-
-
Peña, J.A.1
Molina, O.2
Cardozo, J.3
-
11
-
-
0033897338
-
Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome
-
Grimes DA, Lang AE, Bergeron C. Late adult onset chorea with typical pathology of Hallervorden-Spatz syndrome. J Neurol Neurosurg Psychiatry 2000; 69: 392-395.
-
(2000)
J. Neurol. Neurosurg. Psychiatry
, vol.69
, pp. 392-395
-
-
Grimes, D.A.1
Lang, A.E.2
Bergeron, C.3
-
12
-
-
0028333849
-
Complex tics, stereotypes, and compulsive behaviour as clinical presentation of a juvenile progressive dystonia suggestive of Hallervorden-Spatz disease
-
Nardocci N, Rumi, V Angelini L et al. Complex tics, stereotypes, and compulsive behaviour as clinical presentation of a juvenile progressive dystonia suggestive of Hallervorden-Spatz disease. Mov Disord 1994; 9: 369-371.
-
(1994)
Mov. Disord.
, vol.9
, pp. 369-371
-
-
Nardocci, N.1
Rumi, V.2
Angelini, L.3
-
13
-
-
0028153393
-
Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome
-
Casteels I, Spileers W, Swinnen T et al. Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome. Neuropediatrics 1994; 25: 265-267.
-
(1994)
Neuropediatrics
, vol.25
, pp. 265-267
-
-
Casteels, I.1
Spileers, W.2
Swinnen, T.3
-
15
-
-
0033544428
-
Hallervorden Spatz disease and acanthocytes
-
Muthane UB, Shetty R, Panda K et al. Hallervorden Spatz disease and acanthocytes. Neurology 1999; 53: 32A.
-
(1999)
Neurology
, vol.53
-
-
Muthane, U.B.1
Shetty, R.2
Panda, K.3
-
16
-
-
0029154352
-
Myopathic involvement in two cases of Hallervorden-Spatz disease
-
Malandrini A, Bonuccelli U, Parrotta E et al. Myopathic involvement in two cases of Hallervorden-Spatz disease. Brain Dev 1995; 17: 286-290.
-
(1995)
Brain Dev.
, vol.17
, pp. 286-290
-
-
Malandrini, A.1
Bonuccelli, U.2
Parrotta, E.3
-
17
-
-
0035174081
-
What's new in neurogenetics? Focus on neurodegenerative disorders
-
Suri M. What's new in neurogenetics? Focus on neurodegenerative disorders. Eur J Paediatr Neurol 2001; 5: 221-224.
-
(2001)
Eur. J. Paediatr. Neurol.
, vol.5
, pp. 221-224
-
-
Suri, M.1
-
18
-
-
0035134162
-
How broad is the phenotype of Hallervorden-Spatz disease?
-
Hickman SJ, Ward NS, Surtees RAH, Stevens JM, Farmer SF. How broad is the phenotype of Hallervorden-Spatz disease? Acta Neurol Scand 2001; 103: 201-203.
-
(2001)
Acta Neurol. Scand.
, vol.103
, pp. 201-203
-
-
Hickman, S.J.1
Ward, N.S.2
Surtees, R.A.H.3
Stevens, J.M.4
Farmer, S.F.5
-
19
-
-
0027513596
-
Syndrome de Hallervorden-Spatz et IRM: 'L'oeil du tigre'
-
Trussart V, Lebouco N, Carlander B, Billiard M, Castan P. Syndrome de Hallervorden-Spatz et IRM: 'l'oeil du tigre'. J Neuroradiol 1993; 20: 70-75.
-
(1993)
J. Neuroradiol.
, vol.20
, pp. 70-75
-
-
Trussart, V.1
Lebouco, N.2
Carlander, B.3
Billiard, M.4
Castan, P.5
-
20
-
-
0033709213
-
The eye-of-the-tiger sign
-
Guillerman RP. The eye-of-the-tiger sign. Radiology 2000; 217: 895-896.
-
(2000)
Radiology
, vol.217
, pp. 895-896
-
-
Guillerman, R.P.1
-
21
-
-
0033897317
-
Constellation of findings on nigrostriatal system in case of Hallervorden-Spatz disease
-
Hermann W, Barthel H, Reuter M, et al. Constellation of findings on nigrostriatal system in case of Hallervorden-Spatz disease. Nervenarzt 2000; 71: 660-665.
-
(2000)
Nervenarzt
, vol.71
, pp. 660-665
-
-
Hermann, W.1
Barthel, H.2
Reuter, M.3
-
22
-
-
0032586053
-
Iron deposits in the subthalamic nuclei in Hallervorden-Spatz disease
-
Müller T, Amoiridis G, Kuhn W, Przuntek H. Iron deposits in the subthalamic nuclei in Hallervorden-Spatz disease. Eur Neurol 1999; 42: 240-241.
-
(1999)
Eur. Neurol.
, vol.42
, pp. 240-241
-
-
Müller, T.1
Amoiridis, G.2
Kuhn, W.3
Przuntek, H.4
-
23
-
-
0034850470
-
Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome
-
Hayflick S, Penzien JM, Michl W et al. Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 166-169.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 166-169
-
-
Hayflick, S.1
Penzien, J.M.2
Michl, W.3
-
24
-
-
0034845760
-
Iron in the Hallervorden-Spatz syndrome
-
Koeppen AH, Dickson AC. Iron in the Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 148-155.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 148-155
-
-
Koeppen, A.H.1
Dickson, A.C.2
-
25
-
-
0033953962
-
Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology
-
Wakabayashi K, Fukushima T, Koide R et al. Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology. Acta Neuropathol 2000; 99: 331-336.
-
(2000)
Acta Neuropathol.
, vol.99
, pp. 331-336
-
-
Wakabayashi, K.1
Fukushima, T.2
Koide, R.3
-
26
-
-
0027489477
-
A case of Hallervorden-Spatz syndrome with marked atrophy of the brainstem and cerebellum
-
Sodeyama N, Arai M, Sanjoh N, Orimo S, Tamaki M. A case of Hallervorden-Spatz syndrome with marked atrophy of the brainstem and cerebellum. Rinsho Shinkeigaku 1993; 33: 525-529.
-
(1993)
Rinsho Shinkeigaku
, vol.33
, pp. 525-529
-
-
Sodeyama, N.1
Arai, M.2
Sanjoh, N.3
Orimo, S.4
Tamaki, M.5
-
27
-
-
0013421634
-
Hallervorden-Spatz syndrome in four children
-
Schwerin A, Peak D, Green SH, Chapman S. Hallervorden-Spatz syndrome in four children. Dev Med Child Neurol 2001; 43 (Suppl 90): 19.
-
(2001)
Dev. Med. Child Neurol.
, vol.43
, Issue.SUPPL. 90
, pp. 19
-
-
Schwerin, A.1
Peak, D.2
Green, S.H.3
Chapman, S.4
-
28
-
-
16144365391
-
Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p 12.3-p13
-
Taylor TD, Litt M, Kramer P et al. Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p 12.3-p13. Nature Genet 1996; 14: 479-481.
-
(1996)
Nature Genet.
, vol.14
, pp. 479-481
-
-
Taylor, T.D.1
Litt, M.2
Kramer, P.3
-
29
-
-
1642555537
-
Iron involvement in neural danage and microgliosis in models of neurodegenerative diseases
-
Shoham S, Youdim MBH. Iron involvement in neural danage and microgliosis in models of neurodegenerative diseases. Cell Mol Biol 2000; 46: 743-760.
-
(2000)
Cell Mol. Biol.
, vol.46
, pp. 743-760
-
-
Shoham, S.1
Youdim, M.B.H.2
-
30
-
-
0034851607
-
First scientific workshop on Hallervorden-Spatz syndrome: Executive summary
-
Hayflick SJ. First scientific workshop on Hallervorden-Spatz syndrome: Executive summary. Pediatr Neurol 2001; 25: 99-101.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 99-101
-
-
Hayflick, S.J.1
-
31
-
-
0033709847
-
Friedreich's ataxia and iron metabolism
-
Gordon N. Friedreich's ataxia and iron metabolism. Brain Dev 2000; 22: 465-468.
-
(2000)
Brain Dev.
, vol.22
, pp. 465-468
-
-
Gordon, N.1
-
32
-
-
0035112680
-
Hereditary vitamin-E deficiency
-
Gordon N. Hereditary vitamin-E deficiency. Dev Med Child Neurol 2001; 43: 133-135.
-
(2001)
Dev. Med. Child Neurol.
, vol.43
, pp. 133-135
-
-
Gordon, N.1
-
33
-
-
0033817296
-
α-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formally Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies
-
Neumann M, Adler S, Schlüter O et al. α-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formally Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies. Acta Neuropathol 2000; 100: 568-574.
-
(2000)
Acta Neuropathol.
, vol.100
, pp. 568-574
-
-
Neumann, M.1
Adler, S.2
Schlüter, O.3
-
34
-
-
0033897735
-
Neurodegeneration with brain iron accumulation, type 1 is characterized by α- β-and γ-synuclein neuropathology
-
Galvin JE, Giasson B, Hurtig HI, Lee MV-Y, Trojanowski JQ. Neurodegeneration with brain iron accumulation, type 1 is characterized by α- β-and γ-synuclein neuropathology. Am J Pathol 2000; 157: 361-368.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 361-368
-
-
Galvin, J.E.1
Giasson, B.2
Hurtig, H.I.3
Lee, M.V.-Y.4
Trojanowski, J.Q.5
-
35
-
-
0029039795
-
Time-dependent changes in iron levels and associated neuronal loss within the substantia nigra following lesions within the neostriatum/globus pallidus complex
-
Sastry S, Arendash GW. Time-dependent changes in iron levels and associated neuronal loss within the substantia nigra following lesions within the neostriatum/globus pallidus complex. Neuroscience 1995; 67: 649-666.
-
(1995)
Neuroscience
, vol.67
, pp. 649-666
-
-
Sastry, S.1
Arendash, G.W.2
-
36
-
-
0348050366
-
Superoxide dismutase-like immunoreactivity in spheroids in Hallervorden-Spatz disease
-
Nishiyama K, Murayama S, Nishimura Y, Asayama K, Kanazawa I. Superoxide dismutase-like immunoreactivity in spheroids in Hallervorden-Spatz disease. Acta Neuropathol 1997; 93: 19-23.
-
(1997)
Acta Neuropathol.
, vol.93
, pp. 19-23
-
-
Nishiyama, K.1
Murayama, S.2
Nishimura, Y.3
Asayama, K.4
Kanazawa, I.5
-
38
-
-
0029589683
-
Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy
-
Malandrini A, Cavallaro T, Fabrizi GM et al. Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Virchows Arch 1995; 427: 415-421.
-
(1995)
Virchows Arch.
, vol.427
, pp. 415-421
-
-
Malandrini, A.1
Cavallaro, T.2
Fabrizi, G.M.3
-
39
-
-
0035964047
-
New genes reveal major role for iron in neurodegeneration
-
Senior K. New genes reveal major role for iron in neurodegeneration. Lancet 2001; 358: 302.
-
(2001)
Lancet
, vol.358
, pp. 302
-
-
Senior, K.1
-
40
-
-
0030908572
-
Hallervorden-Spatz disease: Late infantile type
-
Singhi P,Mitra S. Hallervorden-Spatz disease: late infantile type. J Child Neurol 1997; 12: 280-282.
-
(1997)
J. Child Neurol.
, vol.12
, pp. 280-282
-
-
Singhi, P.1
Mitra, S.2
-
41
-
-
0029939071
-
Continuous intrathecal baclofen infusion for symptomatic generalized dystonia
-
Albright AL, Barry MJ, Fasick P, Barron W, Shultz B. Continuous intrathecal baclofen infusion for symptomatic generalized dystonia. Neurosurgery 1996; 38: 934-939.
-
(1996)
Neurosurgery
, vol.38
, pp. 934-939
-
-
Albright, A.L.1
Barry, M.J.2
Fasick, P.3
Barron, W.4
Shultz, B.5
-
42
-
-
0031241013
-
Enfermedad de Hallervorden-Spatz y toxina botulinica
-
Diego MR, Garcia JN. Enfermedad de Hallervorden-Spatz y toxina botulinica. An Esp Pediatr 1997; 47: 443-444.
-
(1997)
An. Esp. Pediatr.
, vol.47
, pp. 443-444
-
-
Diego, M.R.1
Garcia, J.N.2
-
44
-
-
0034125558
-
Anesthetic management for two-stage computer-assisted, stereotactic thalamotomy in a child with Hallervorden-Spatz disease
-
Keegan MT, Flick RP, Matsumoto JY, Davis DH, Lanier WL. Anesthetic management for two-stage computer-assisted, stereotactic thalamotomy in a child with Hallervorden-Spatz disease. J Neurosurg Anesthesiol 2000; 12: 107-111.
-
(2000)
J. Neurosurg. Anesthesiol.
, vol.12
, pp. 107-111
-
-
Keegan, M.T.1
Flick, R.P.2
Matsumoto, J.Y.3
Davis, D.H.4
Lanier, W.L.5
-
45
-
-
0035016293
-
Botulinium toxin for treatment of jaw opening dystonia in Hallervorden-Spatz syndrome
-
Dressler D, Wittstock M, Benecke R. Botulinium toxin for treatment of jaw opening dystonia in Hallervorden-Spatz syndrome. Eur Neurol 2001; 45: 287-288.
-
(2001)
Eur. Neurol.
, vol.45
, pp. 287-288
-
-
Dressler, D.1
Wittstock, M.2
Benecke, R.3
-
46
-
-
0034838767
-
Hallervorden-Spatz syndrome
-
Swaiman KF. Hallervorden-Spatz syndrome. Pediatr Neurol 2001; 25: 102-108.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 102-108
-
-
Swaiman, K.F.1
-
48
-
-
0034851578
-
Iron overload, oxidative stress, and axonal dystrophy in brain disorders
-
Chiuch CC. Iron overload, oxidative stress, and axonal dystrophy in brain disorders. Pediatr Neurol 2001; 25: 138-147.
-
(2001)
Pediatr. Neurol.
, vol.25
, pp. 138-147
-
-
Chiuch, C.C.1
|