-
1
-
-
0021336060
-
A progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis
-
Aicardi, J., Goutières F. A progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis. Ann. Neurol. 15, 49-54 (1984).
-
(1984)
Ann. Neurol.
, vol.15
, pp. 49-54
-
-
Aicardi, J.1
Goutières, F.2
-
2
-
-
0024556451
-
Encephalopathy with calcification of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new cases
-
Billard, C., Dulac, O., Bouloche, J., Echenne; B., Lebon, P., Robain, O., Santini, J. J. Encephalopathy with calcification of the basal ganglia in children. A reappraisal of Fahr's syndrome with respect to 14 new cases. Neuropediatrics 20, 12-19 (1989).
-
(1989)
Neuropediatrics
, vol.20
, pp. 12-19
-
-
Billard, C.1
Dulac, O.2
Bouloche, J.3
Echenne, B.4
Lebon, P.5
Robain, O.6
Santini, J.J.7
-
3
-
-
0025900653
-
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly and retinal degeneration. Two siblings confirming a probable distinct entity
-
Bönnemann, C. G., Meinecke, P., Reich, H. Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly and retinal degeneration. Two siblings confirming a probable distinct entity. J. Med. Genet. 28, 708-711 (1991).
-
(1991)
J. Med. Genet.
, vol.28
, pp. 708-711
-
-
Bönnemann, C.G.1
Meinecke, P.2
Reich, H.3
-
4
-
-
0026636362
-
Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis - Another case of the Aicardi-Goutières syndrome
-
Bönnemann, C. G., Meinecke, P. Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis - another case of the Aicardi-Goutières syndrome. Neuropediatrics 23, 157-161 (1992).
-
(1992)
Neuropediatrics
, vol.23
, pp. 157-161
-
-
Bönnemann, C.G.1
Meinecke, P.2
-
5
-
-
0025978312
-
Magnetic resonance imaging in infantile encephalopathy with cerebral calcification and leukodystrophy
-
Boltshauser, E., Steinlein, M., Boesch, C., Martin, E., Schubiger, G. Magnetic resonance imaging in infantile encephalopathy with cerebral calcification and leukodystrophy. Neuropediatrics 22, 33-35 (1991).
-
(1991)
Neuropediatrics
, vol.22
, pp. 33-35
-
-
Boltshauser, E.1
Steinlein, M.2
Boesch, C.3
Martin, E.4
Schubiger, G.5
-
6
-
-
0022875811
-
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection
-
Burns, J., Wickramasinghe, H. T., Harding, B., Barister, M. A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection. Clin. Genet. 30, 112-116 (1986).
-
(1986)
Clin. Genet.
, vol.30
, pp. 112-116
-
-
Burns, J.1
Wickramasinghe, H.T.2
Harding, B.3
Barister, M.4
-
7
-
-
0022735679
-
Sindrome de calcificacoes de gânglios da base, leucodistrofia e pleocitose linfomonocitária crônica do liquido celalorraqueano
-
Diament, A. J., Machado, L. R., Cypel, S., Ramos, J. L. A. Sindrome de calcificacoes de gânglios da base, leucodistrofia e pleocitose linfomonocitária crônica do liquido celalorraqueano. Arg. Neuropsiquitar. 44, 185-190 (1986).
-
(1986)
Arg. Neuropsiquitar.
, vol.44
, pp. 185-190
-
-
Diament, A.J.1
Machado, L.R.2
Cypel, S.3
Ramos, J.L.A.4
-
8
-
-
0022511264
-
A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic spinal fluid lymphocytosis
-
Giroud, M., Gouyon, J. B., Chaumet, F., Cinguin, A. M., Chevalier-Nievelon, A., Alison, M., Dumas, R. A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic spinal fluid lymphocytosis. Child's Nerv. Syst. 2, 47-48 (1986).
-
(1986)
Child's Nerv. Syst.
, vol.2
, pp. 47-48
-
-
Giroud, M.1
Gouyon, J.B.2
Chaumet, F.3
Cinguin, A.M.4
Chevalier-Nievelon, A.5
Alison, M.6
Dumas, R.7
-
9
-
-
0023873028
-
Intrathecal synthesis of interferon-alpha in patients with progressive familial encephalopathy
-
Lebon, P., Badoual, J., Ponsot, G., Goutières, F., Hèmeury-Cukier, F., Aicardi, J. Intrathecal synthesis of interferon-alpha in patients with progressive familial encephalopathy. J. Neurol. Sci. 84, 201-208 (1988).
-
(1988)
J. Neurol. Sci.
, vol.84
, pp. 201-208
-
-
Lebon, P.1
Badoual, J.2
Ponsot, G.3
Goutières, F.4
Hèmeury-Cukier, F.5
Aicardi, J.6
-
10
-
-
0022579384
-
Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis
-
Metha, L., Trounce, J. Q., Moore, J. R., Young, I. D. Familial calcification of the basal ganglia with cerebrospinal fluid pleocytosis. J. Med. Genet 23, 157-160 (1986).
-
(1986)
J. Med. Genet
, vol.23
, pp. 157-160
-
-
Metha, L.1
Trounce, J.Q.2
Moore, J.R.3
Young, I.D.4
-
11
-
-
0023950603
-
Infantile familial encephalopathy with cerebral calcifications and leukodystrophy
-
Razavi-Encha, F., Larroche, J. C., Gaillard, D. Infantile familial encephalopathy with cerebral calcifications and leukodystrophy. Neuropediatrics 19, 72-79 (1988).
-
(1988)
Neuropediatrics
, vol.19
, pp. 72-79
-
-
Razavi-Encha, F.1
Larroche, J.C.2
Gaillard, D.3
-
12
-
-
0028017854
-
Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcifications, and CNS disease
-
Reardon, W., Hockey, A., Silberstein, P., Kendall, B., Farag, T. I., Swash, M., Stevenson, R., Baraitser, M. Autosomal recessive congenital intrauterine infection-like syndrome of microcephaly, intracranial calcifications, and CNS disease. Am. J. Med. Genet. 52, 58-65 (1994).
-
(1994)
Am. J. Med. Genet.
, vol.52
, pp. 58-65
-
-
Reardon, W.1
Hockey, A.2
Silberstein, P.3
Kendall, B.4
Farag, T.I.5
Swash, M.6
Stevenson, R.7
Baraitser, M.8
-
13
-
-
0028972864
-
The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)
-
Tolmie, J. L., Shillito, P., Hughes-Benzie, R., Stephenson, J. B. P. The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis). J. Med. Genet. 32, 881-884 (1995).
-
(1995)
J. Med. Genet.
, vol.32
, pp. 881-884
-
-
Tolmie, J.L.1
Shillito, P.2
Hughes-Benzie, R.3
Stephenson, J.B.P.4
-
14
-
-
0030611282
-
The Aicardi-Goutières syndrome: Variable clinical expression in two siblings
-
Verrips, A., Hiel, J. A. P., Grabreëls, F. J. M., Wesseling, P., Rotteveel, J. J. The Aicardi-Goutières syndrome: Variable clinical expression in two siblings. Pediatr. Neurol. 16, 323-325 (1997).
-
(1997)
Pediatr. Neurol.
, vol.16
, pp. 323-325
-
-
Verrips, A.1
Hiel, J.A.P.2
Grabreëls, F.J.M.3
Wesseling, P.4
Rotteveel, J.J.5
|