-
1
-
-
0344421146
-
Pathology of the nervous system
-
Kissane JM, editor. 9th ed. St. Louis: The C.V. Mosby Company
-
Nelson JS. Pathology of the nervous system. In: Kissane JM, editor. Anderson's pathology, Vol. Two, 9th ed. St. Louis: The C.V. Mosby Company, 1990;2179-80.
-
(1990)
Anderson's Pathology
, vol.2
, pp. 2179-2180
-
-
Nelson, J.S.1
-
2
-
-
15444356267
-
Nervous system
-
9th ed. Philadelphia: Lea & Febiger
-
Ritchie AC. Nervous system. Boyd's textbook of pathology, Vol. Two, 9th ed. Philadelphia: Lea & Febiger, 1990;1775-7.
-
(1990)
Boyd's Textbook of Pathology
, vol.2
, pp. 1775-1777
-
-
Ritchie, A.C.1
-
3
-
-
15444351939
-
Progressive genetic-metabolic diseases of the central nervous system
-
Rudolph AM, editor. New York: Appleton-Century-Crofts
-
Rapin I. Progressive genetic-metabolic diseases of the central nervous system. In: Rudolph AM, editor. Pediatrics, 16th ed. New York: Appleton-Century-Crofts, 1977;1915-21.
-
(1977)
Pediatrics, 16th Ed.
, pp. 1915-1921
-
-
Rapin, I.1
-
4
-
-
15444346589
-
The nervous system
-
Robbins SL, Cotran RS. Philadelphia: W.B. Saunders Company
-
Schoene WC. The nervous system. In: Robbins SL, Cotran RS. Pathologic basis of disease, 2nd ed. Philadelphia: W.B. Saunders Company, 1979;1592-4.
-
(1979)
Pathologic Basis of Disease, 2nd Ed.
, pp. 1592-1594
-
-
Schoene, W.C.1
-
5
-
-
15444342906
-
Leukodystrophies
-
Rudolph AM, editor. Norwalk: Appleton & Lange
-
Johnson WG. Leukodystrophies. In: Rudolph AM, editor. Rudolph's pediatrics, 19th ed. Norwalk: Appleton & Lange, 1991; 1857-63.
-
(1991)
Rudolph's Pediatrics, 19th Ed.
, pp. 1857-1863
-
-
Johnson, W.G.1
-
6
-
-
0026733382
-
Alexander's disease in infancy and childhood: A report of two cases
-
Neal JW, Cave EM, Singhrao SK, Cole G, Wallace SJ. Alexander's disease in infancy and childhood: a report of two cases. Acta Neuropathologica 1992;84:322-7.
-
(1992)
Acta Neuropathologica
, vol.84
, pp. 322-327
-
-
Neal, J.W.1
Cave, E.M.2
Singhrao, S.K.3
Cole, G.4
Wallace, S.J.5
-
7
-
-
0029400350
-
Degenerative central nervous system disease
-
Vadasz AG, Epstein LG. Degenerative central nervous system disease. Pediatrics in Review 1995;16:426-31.
-
(1995)
Pediatrics in Review
, vol.16
, pp. 426-431
-
-
Vadasz, A.G.1
Epstein, L.G.2
-
9
-
-
0027276701
-
Alexander's disease: Clues to diagnosis
-
Pridmore CL, Baraitser M, Harding B, Boyd SG, Kendall B, Brett EM. Alexander's disease: clues to diagnosis. J Child Neurol 1993; 8:134-44.
-
(1993)
J Child Neurol
, vol.8
, pp. 134-144
-
-
Pridmore, C.L.1
Baraitser, M.2
Harding, B.3
Boyd, S.G.4
Kendall, B.5
Brett, E.M.6
-
10
-
-
0021775984
-
Alexander's disease
-
Townsend JJ, Wilson JF, Harris T, Coulter D; Fife R. Alexander's disease. Acta Neuropath 1985;67:163-6.
-
(1985)
Acta Neuropath
, vol.67
, pp. 163-166
-
-
Townsend, J.J.1
Wilson, J.F.2
Harris, T.3
Coulter, D.4
Fife, R.5
-
11
-
-
0021826540
-
Alexander's disease: A disease of astrocytes
-
Borrett D, Becker LE. Alexander's disease: a disease of astrocytes. Brain 1985;108:367-85.
-
(1985)
Brain
, vol.108
, pp. 367-385
-
-
Borrett, D.1
Becker, L.E.2
-
12
-
-
0017074881
-
Alexander's disease: A report and reappraisal
-
Russo Jr, LS, Aron A, Anderson PJ. Alexander's disease: a report and reappraisal. Neurology 1976;26:607-14.
-
(1976)
Neurology
, vol.26
, pp. 607-614
-
-
Russo Jr., L.S.1
Aron, A.2
Anderson, P.J.3
-
14
-
-
0000879584
-
Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant
-
Alexander WS. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. Brain 1949;72:373-81.
-
(1949)
Brain
, vol.72
, pp. 373-381
-
-
Alexander, W.S.1
-
15
-
-
0344673261
-
Alexander's disease
-
Duckett S. editor. Baltimore: Williams & Wilkins
-
Duckett S, Goldman JE. Alexander's disease. In: Duckett S. editor. Pediatric neuropathology. Baltimore: Williams & Wilkins, 1995; 555-60, 620-4.
-
(1995)
Pediatric Neuropathology
, pp. 555-560
-
-
Duckett, S.1
Goldman, J.E.2
-
16
-
-
0028111545
-
Molecular genetics of metachromatic leukodystrophy
-
Gieselmann V, Polten A, Kreysing J, von Figura, K. Molecular genetics of metachromatic leukodystrophy. J Inner Metab Dis 1994; 17:500-9.
-
(1994)
J Inner Metab Dis
, vol.17
, pp. 500-509
-
-
Gieselmann, V.1
Polten, A.2
Kreysing, J.3
Von Figura, K.4
-
17
-
-
0027754255
-
Research update on lysosomal disorders with special emphasis on metachromatic leukodystrophy and Krabbe disease
-
Wenger DA. Research update on lysosomal disorders with special emphasis on metachromatic leukodystrophy and Krabbe disease. APMIS Supplementum 40 1993;101:81-7.
-
(1993)
APMIS Supplementum 40
, vol.101
, pp. 81-87
-
-
Wenger, D.A.1
-
18
-
-
0027375158
-
Metachromatic leukodystrophy: Two sides of a coin
-
Jeffery R, Jeffery A. Metachromatic leukodystrophy: two sides of a coin. BMJ 1993;307:1631-2.
-
(1993)
BMJ
, vol.307
, pp. 1631-1632
-
-
Jeffery, R.1
Jeffery, A.2
-
19
-
-
0001775305
-
A new familial, infantile form of diffuse brain sclerosis
-
Krabbe K. A new familial, infantile form of diffuse brain sclerosis. Brain 1916;39:74-114.
-
(1916)
Brain
, vol.39
, pp. 74-114
-
-
Krabbe, K.1
-
20
-
-
0028820221
-
Pathological case of the month: Globoid cell leukodystrophy (Krabbe's disease)
-
Rueca RE, Taxy JB, Wollmann RL. Pathological case of the month: globoid cell leukodystrophy (Krabbe's disease). Arch Ped and Adol Med 1995;149:1173-4.
-
(1995)
Arch Ped and Adol Med
, vol.149
, pp. 1173-1174
-
-
Rueca, R.E.1
Taxy, J.B.2
Wollmann, R.L.3
-
22
-
-
0030751530
-
X linked adrenoleukodystrophy: Clinical presentation, diagnosis, and therapy
-
van Geel BM, Assies J, Wanders RJ, Barth PG. X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy. J Neurol Neurosurg & Psych 1997;63:4-14.
-
(1997)
J Neurol Neurosurg & Psych
, vol.63
, pp. 4-14
-
-
Van Geel, B.M.1
Assies, J.2
Wanders, R.J.3
Barth, P.G.4
-
24
-
-
0028842858
-
Canavan disease: From spongy degeneration to molecular analysis
-
Matalon R, Michals K, Kaul R. Canavan disease: from spongy degeneration to molecular analysis. J Pediat 1995;127:511-7.
-
(1995)
J Pediat
, vol.127
, pp. 511-517
-
-
Matalon, R.1
Michals, K.2
Kaul, R.3
-
25
-
-
0027302007
-
Canavan disease: Biochemical and molecular studies
-
Matalon R, Kaul R, Michals K. Canavan disease: biochemical and molecular studies. J Inherit Metabol Dis 1993; 16:744-52.
-
(1993)
J Inherit Metabol Dis
, vol.16
, pp. 744-752
-
-
Matalon, R.1
Kaul, R.2
Michals, K.3
-
26
-
-
0141872257
-
Schilder's encephalitis periaxialis diffusa
-
Canavan MM. Schilder's encephalitis periaxialis diffusa. Arch Neurol & Psych 1931;25:299-308.
-
(1931)
Arch Neurol & Psych
, vol.25
, pp. 299-308
-
-
Canavan, M.M.1
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