-
1
-
-
0027164261
-
Hereditary spastic paraplegia. A diagnostic reminder
-
Gordon N. Hereditary spastic paraplegia. A diagnostic reminder. Dev Med Child Neurol 1993;35:449-455
-
(1993)
Dev Med Child Neurol
, vol.35
, pp. 449-455
-
-
Gordon, N.1
-
2
-
-
0002882906
-
Familial Spastic Paraplegia
-
Vinken PJ, Bruyn GW. editors. Amsterdam: North Holland
-
Sutherland JM. Familial Spastic Paraplegia. In: Vinken PJ, Bruyn GW. editors. Handbook of clinical neurology, vol 22. System disorders and atrophies, part II. Amsterdam: North Holland, 1975:421-32
-
(1975)
Handbook of Clinical Neurology, Vol 22. System Disorders and Atrophies, Part II
, vol.22
, pp. 421-432
-
-
Sutherland, J.M.1
-
4
-
-
0020641096
-
Classification of the hereditary ataxias and paraplegias
-
Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet 1983;i:1151-4
-
(1983)
Lancet
, vol.1
, pp. 1151-1154
-
-
Harding, A.E.1
-
5
-
-
0021684976
-
Familial spastic ataxia associated with Ehlers Danlos syndrome with platelet dysfunction
-
Chouza C, Caamano JL, De Medina O, Bogacz J, Oehninger C, Vignale R, et al. Familial spastic ataxia associated with Ehlers Danlos syndrome with platelet dysfunction. Can J Neurol Sci 1984;11:541
-
(1984)
Can J Neurol Sci
, vol.11
, pp. 541
-
-
Chouza, C.1
Caamano, J.L.2
De Medina, O.3
Bogacz, J.4
Oehninger, C.5
Vignale, R.6
-
6
-
-
0025077713
-
Familial case of May Hegglin anomaly, associated with familial spastic paraplegia
-
Fujita Y, Fujii T, Nishio A, Tuboi K, Tsuji K, Nakamura M, et al. Familial case of May Hegglin anomaly, associated with familial spastic paraplegia. Am J Hematol 1990;35(3):219-21
-
(1990)
Am J Hematol
, vol.35
, Issue.3
, pp. 219-221
-
-
Fujita, Y.1
Fujii, T.2
Nishio, A.3
Tuboi, K.4
Tsuji, K.5
Nakamura, M.6
-
7
-
-
0021015712
-
Familial spastic paraplegia, mental retardation and precocious puberty
-
Raphaelson M, Stevens J, Elders J, Comite F, Theodore W. Familial spastic paraplegia, mental retardation and precocious puberty. Arch Neurol 1983;40:809-10
-
(1983)
Arch Neurol
, vol.40
, pp. 809-810
-
-
Raphaelson, M.1
Stevens, J.2
Elders, J.3
Comite, F.4
Theodore, W.5
-
8
-
-
0026035171
-
Pure and complicated forms of hereditary spastic paraplegia presenting in childhood
-
Appleton RE, Farrel K, Dunn HG. Pure and complicated forms of hereditary spastic paraplegia presenting in childhood. Dev Med Child Neurol 1991;33:304-12
-
(1991)
Dev Med Child Neurol
, vol.33
, pp. 304-312
-
-
Appleton, R.E.1
Farrel, K.2
Dunn, H.G.3
-
9
-
-
0001544299
-
Acquired haemolytic anaemia: I. The relation of erythrocyte antibody production to activity of the disease. II. The significance of thrombocytopenia and leukopenia
-
Evans RS, Duane RT. Acquired haemolytic anaemia: I. The relation of erythrocyte antibody production to activity of the disease. II. The significance of thrombocytopenia and leukopenia. Blood 1949;4:1196-213
-
(1949)
Blood
, vol.4
, pp. 1196-1213
-
-
Evans, R.S.1
Duane, R.T.2
-
10
-
-
0023754297
-
Evans' syndrome in childhood: Pathophysiology, clinical course, and treatment
-
Wang WC. Evans' syndrome in childhood: pathophysiology, clinical course, and treatment. Am J Ped Hematol Oncol 1988;10(4):330-8
-
(1988)
Am J Ped Hematol Oncol
, vol.10
, Issue.4
, pp. 330-338
-
-
Wang, W.C.1
-
11
-
-
0028145138
-
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity
-
Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustang RM, et al. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Hum Mol Genet 1994;3(8); 1263-7
-
(1994)
Hum Mol Genet
, vol.3
, Issue.8
, pp. 1263-1267
-
-
Hentati, A.1
Pericak-Vance, M.A.2
Hung, W.Y.3
Belal, S.4
Laing, N.5
Boustang, R.M.6
-
12
-
-
0021962868
-
Superior sagittal sinus thrombosis associated with Evans' syndrome of haemolytic anaemia
-
Shiozawa Z, Ueda R, Mano T, Tsujane R, Kageyama N, et al. Superior sagittal sinus thrombosis associated with Evans' syndrome of haemolytic anaemia. J Neurol 1985:280-2
-
(1985)
J Neurol
, pp. 280-282
-
-
Shiozawa, Z.1
Ueda, R.2
Mano, T.3
Tsujane, R.4
Kageyama, N.5
-
13
-
-
0029058623
-
Evans' syndrome associated with venous thrombosis
-
Al-Fiar FZ, Clink HM. Evans' syndrome associated with venous thrombosis. Ann Saudi Med 1995;15(2): 168-70
-
(1995)
Ann Saudi Med
, vol.15
, Issue.2
, pp. 168-170
-
-
Al-Fiar, F.Z.1
Clink, H.M.2
-
14
-
-
0027322957
-
Abnormal thyroid function test results in patients with Fisher-Evans syndrome
-
Lio S, Albin M, Girelli G, Perrone MP, Gandolfo G, Conti L, et al. Abnormal thyroid function test results in patients with Fisher-Evans syndrome. J Endocrinol Invest 1993;16(3): 163-7
-
(1993)
J Endocrinol Invest
, vol.16
, Issue.3
, pp. 163-167
-
-
Lio, S.1
Albin, M.2
Girelli, G.3
Perrone, M.P.4
Gandolfo, G.5
Conti, L.6
-
15
-
-
0021047996
-
Autoimmune pancytopenia of childhood associated with multisystem disease manifestations
-
Miller BA, Beardsley DS. Autoimmune pancytopenia of childhood associated with multisystem disease manifestations. J Pediatr 1983;103:877-81
-
(1983)
J Pediatr
, vol.103
, pp. 877-881
-
-
Miller, B.A.1
Beardsley, D.S.2
|