-
1
-
-
0023275907
-
Mendelian etiologies of stroke
-
Natowicz M, Kelley RI: Mendelian etiologies of stroke. Ann Neurol 1987;22:175-192.
-
(1987)
Ann Neurol
, vol.22
, pp. 175-192
-
-
Natowicz, M.1
Kelley, R.I.2
-
3
-
-
0021143782
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
-
Pavlakis SG, Philips PC, DiMauro S, et al: Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome. Ann Neurol 1984;16:481-488.
-
(1984)
Ann Neurol
, vol.16
, pp. 481-488
-
-
Pavlakis, S.G.1
Philips, P.C.2
DiMauro, S.3
-
4
-
-
0028107258
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): Current concepts
-
Hirano M, Pavlakis SG: Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): Current concepts. J Child Neurol 1994;9:4-13.
-
(1994)
J Child Neurol
, vol.9
, pp. 4-13
-
-
Hirano, M.1
Pavlakis, S.G.2
-
6
-
-
0028035427
-
Hereditary and acquired risk factors for childhood stroke
-
Riikonen R, Santavuori P: Hereditary and acquired risk factors for childhood stroke. Neuropediatrics 1994;25:227-233.
-
(1994)
Neuropediatrics
, vol.25
, pp. 227-233
-
-
Riikonen, R.1
Santavuori, P.2
-
8
-
-
0021848721
-
Familial right ventricular dilated cardiomyopathy
-
Ibsen HH, Baandrup U, Simonsen EE: Familial right ventricular dilated cardiomyopathy. Br Heart J 1985;54:156-159.
-
(1985)
Br Heart J
, vol.54
, pp. 156-159
-
-
Ibsen, H.H.1
Baandrup, U.2
Simonsen, E.E.3
-
9
-
-
0020670894
-
Inherited primary disorders of cardiac rhythm and conduction
-
Guntheroth WG, Motulsky AG: Inherited primary disorders of cardiac rhythm and conduction. Prog Med Genet 1983;5:381-402.
-
(1983)
Prog Med Genet
, vol.5
, pp. 381-402
-
-
Guntheroth, W.G.1
Motulsky, A.G.2
-
10
-
-
0016786471
-
Familial atrial myxoma
-
Farah MG: Familial atrial myxoma. Ann Intern Med 1975;83: 358-360.
-
(1975)
Ann Intern Med
, vol.83
, pp. 358-360
-
-
Farah, M.G.1
-
11
-
-
0024556192
-
Strokes in tuberous sclerosis: Are rhabdomyomas a cause?
-
Gomez MR: Strokes in tuberous sclerosis: Are rhabdomyomas a cause? Brain Dev 1989;11:14-19.
-
(1989)
Brain Dev
, vol.11
, pp. 14-19
-
-
Gomez, M.R.1
-
12
-
-
0018676446
-
Gorlin's syndrome and the heart
-
Littler BO: Gorlin's syndrome and the heart. Br J Oral Surg 1979;17:135-146.
-
(1979)
Br J Oral Surg
, vol.17
, pp. 135-146
-
-
Littler, B.O.1
-
13
-
-
0021998698
-
Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease
-
Boers GHJ, Smals AGH, Trijbels FJ, et al: Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease. N Eng J Med 1985;313:709-715.
-
(1985)
N Eng J Med
, vol.313
, pp. 709-715
-
-
Boers, G.H.J.1
Smals, A.G.H.2
Trijbels, F.J.3
-
14
-
-
0029847109
-
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR
-
Goyette P, Christensen B, Rosenblatt DS, Rozen R: Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR. Am J Hum. Genet 1996;59:1268-1275.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1268-1275
-
-
Goyette, P.1
Christensen, B.2
Rosenblatt, D.S.3
Rozen, R.4
-
15
-
-
0030769174
-
Functional methionine synthase deficiency due to cblG disorder: A report of two patients and a review
-
Harding CO, Arnold G, Barness LA, et al: Functional methionine synthase deficiency due to cblG disorder: A report of two patients and a review. Am J Hum Genet 1997;71:384-390.
-
(1997)
Am J Hum Genet
, vol.71
, pp. 384-390
-
-
Harding, C.O.1
Arnold, G.2
Barness, L.A.3
-
16
-
-
0025756673
-
Hyperhomocysteinemia: An independent risk factor for vascular disease
-
Clarke R, Daly L, Robinson K, et al: Hyperhomocysteinemia: An independent risk factor for vascular disease. N Eng J Med 1991;324:1149-1155.
-
(1991)
N Eng J Med
, vol.324
, pp. 1149-1155
-
-
Clarke, R.1
Daly, L.2
Robinson, K.3
-
17
-
-
0028052980
-
Stroke in Fabry's disease
-
Grewal RP: Stroke in Fabry's disease. J Neurol 1994;241:153-156.
-
(1994)
J Neurol
, vol.241
, pp. 153-156
-
-
Grewal, R.P.1
-
20
-
-
0020083364
-
Pediatric victims of unexplained stroke and their families: Familial lipid and lipoprotein abnormalities
-
Glueck CJ, Daniels SR, Bates S, et al: Pediatric victims of unexplained stroke and their families: Familial lipid and lipoprotein abnormalities. Pediatrics 1982;69:308-316.
-
(1982)
Pediatrics
, vol.69
, pp. 308-316
-
-
Glueck, C.J.1
Daniels, S.R.2
Bates, S.3
-
21
-
-
0343177630
-
Lipoprotein (a): Its role in thromboembolism
-
Nowak-Gottl U, Debus O, Findeisen M, et al: Lipoprotein (a): Its role in thromboembolism, abstract. Pediatrics 1997;99:865.
-
(1997)
Pediatrics
, vol.99
, pp. 865
-
-
Nowak-Gottl, U.1
Debus, O.2
Findeisen, M.3
-
22
-
-
0000423642
-
Genetic causes of childhood stroke
-
Alberts MJ (ed). New York, Futura Publishing
-
Andrews PI, Ryan MM, Kandt RS: Genetic causes of childhood stroke, in Alberts MJ (ed): Genetics of Cerebrovascular Disease. New York, Futura Publishing, 1999, pp 261-311.
-
(1999)
Genetics of Cerebrovascular Disease
, pp. 261-311
-
-
Andrews, P.I.1
Ryan, M.M.2
Kandt, R.S.3
-
23
-
-
0029083938
-
Multifocal intracranial occlusive vasculopathy resulting in stroke: An unusual manifestation of Williams syndrome
-
Putnam CM, Chaloupka JC, Eklund JE, Fulbright RK: Multifocal intracranial occlusive vasculopathy resulting in stroke: An unusual manifestation of Williams syndrome. AJNR 1995;16:1536-1538.
-
(1995)
AJNR
, vol.16
, pp. 1536-1538
-
-
Putnam, C.M.1
Chaloupka, J.C.2
Eklund, J.E.3
Fulbright, R.K.4
-
25
-
-
85037970603
-
HLA type predicts the risk of stroke in sickle cell disease
-
Hoppe CC, Trachtenberg EA, Klitz W, et al: HLA type predicts the risk of stroke in sickle cell disease. Neurology 1999;52:A103-A104.
-
(1999)
Neurology
, vol.52
-
-
Hoppe, C.C.1
Trachtenberg, E.A.2
Klitz, W.3
-
26
-
-
1842338762
-
Protein C and protein S activity in sickle cell disease and stroke
-
Tam DA: Protein C and protein S activity in sickle cell disease and stroke. J Child Neurol 1997;12:19-21.
-
(1997)
J Child Neurol
, vol.12
, pp. 19-21
-
-
Tam, D.A.1
-
27
-
-
0028231790
-
Alpha thalassemia and stroke risk in sickle cell anemia
-
Adams RJ, Kutlar A, McKie V, et al: Alpha thalassemia and stroke risk in sickle cell anemia. Am J Hematol 1994;45:279-282.
-
(1994)
Am J Hematol
, vol.45
, pp. 279-282
-
-
Adams, R.J.1
Kutlar, A.2
McKie, V.3
-
28
-
-
0032912719
-
Hypertensive encephalopathy, reversible occipitoparietal encephalopathy, or reversible posterior encephalopathy: Three names for an old syndrome
-
Pavlakis SG, Frank Y, Chusid R: Hypertensive encephalopathy, reversible occipitoparietal encephalopathy, or reversible posterior encephalopathy: Three names for an old syndrome. J Child Neurol 1999;14:277-281.
-
(1999)
J Child Neurol
, vol.14
, pp. 277-281
-
-
Pavlakis, S.G.1
Frank, Y.2
Chusid, R.3
-
30
-
-
0029801189
-
Ischaemic stroke in infancy and childhood: Role of the Arg506 to Gln mutation in the factor V gene
-
Nowak-Gottl U, Strater R, Dubbers A, et al: Ischaemic stroke in infancy and childhood: Role of the Arg506 to Gln mutation in the factor V gene. Blood Coagul Fibrinolysis 1996;7:684-688.
-
(1996)
Blood Coagul Fibrinolysis
, vol.7
, pp. 684-688
-
-
Nowak-Gottl, U.1
Strater, R.2
Dubbers, A.3
-
31
-
-
0031674638
-
Prothrombotic disorders in infants and children with cerebral thromboembolism
-
deVeher G, Monagle P, Chan A, et al: Prothrombotic disorders in infants and children with cerebral thromboembolism. Arch Neurol 1998;55:1539-1543.
-
(1998)
Arch Neurol
, vol.55
, pp. 1539-1543
-
-
DeVeher, G.1
Monagle, P.2
Chan, A.3
-
32
-
-
0032818962
-
Prethrombotic disorders in children with arterial ischemic stroke and sinovenous thrombosis
-
Bonduel M, Sciuccati G, Hepner M, et al: Prethrombotic disorders in children with arterial ischemic stroke and sinovenous thrombosis. Arch Neurol 1999;56:967-971.
-
(1999)
Arch Neurol
, vol.56
, pp. 967-971
-
-
Bonduel, M.1
Sciuccati, G.2
Hepner, M.3
-
33
-
-
33747149870
-
DNA typing of HLA in the patients with moyamoya disease
-
Inoue TK, Ikezaki K, Sasazuki T, et al: DNA typing of HLA in the patients with moyamoya disease. Jpn J Hum Genet 1997;42: 507-515.
-
(1997)
Jpn J Hum Genet
, vol.42
, pp. 507-515
-
-
Inoue, T.K.1
Ikezaki, K.2
Sasazuki, T.3
-
34
-
-
0030722062
-
Epidemiological features of moyamoya disease in Japan: Findings from a nationwide survey
-
Wakai K, Tamakoshi A, Ikezaki K, et al: Epidemiological features of moyamoya disease in Japan: Findings from a nationwide survey. Clin Neurol Neurosurg 1997;99(Suppl 2):S1-S5.
-
(1997)
Clin Neurol Neurosurg
, vol.99
, Issue.SUPPL. 2
-
-
Wakai, K.1
Tamakoshi, A.2
Ikezaki, K.3
-
35
-
-
0029042362
-
Fanconi anemia and moyamoya: Evidence for an association
-
Pavlakis SG, Verlander PC, Gould RJ, et al: Fanconi anemia and moyamoya: Evidence for an association. Neurology 1995;45: 998-1000.
-
(1995)
Neurology
, vol.45
, pp. 998-1000
-
-
Pavlakis, S.G.1
Verlander, P.C.2
Gould, R.J.3
-
36
-
-
0030774847
-
Metabolic stroke in carbamyl phosphate synthetase deficiency
-
Sperl W, Felber S, Skladal D, Wermuth B: Metabolic stroke in carbamyl phosphate synthetase deficiency. Neuropediatrics 1997;28: 229-234.
-
(1997)
Neuropediatrics
, vol.28
, pp. 229-234
-
-
Sperl, W.1
Felber, S.2
Skladal, D.3
Wermuth, B.4
-
37
-
-
0021719616
-
Cerebellar hemorrhage complicating methylmalonic and propionic acidemia
-
Dave P, Curless RG, Steimnan L: Cerebellar hemorrhage complicating methylmalonic and propionic acidemia. Arch Neurol 1984; 41:1293-1296.
-
(1984)
Arch Neurol
, vol.41
, pp. 1293-1296
-
-
Dave, P.1
Curless, R.G.2
Steimnan, L.3
-
38
-
-
0019511941
-
Cerebellar hemorrhage complicating isovaleric acidemia: A case report
-
Fischer AQ, Challa VR, Burton BK, McLean WT: Cerebellar hemorrhage complicating isovaleric acidemia: A case report. Neurology 1981;31:746-748.
-
(1981)
Neurology
, vol.31
, pp. 746-748
-
-
Fischer, A.Q.1
Challa, V.R.2
Burton, B.K.3
McLean, W.T.4
-
39
-
-
0024246645
-
Acute extrapyramidal syndrome in methylmalonic acidemia: "Metabolic stroke" involving the globus pallidus
-
Heidenreich R, Natowicz M, Hainline BE, et al: Acute extrapyramidal syndrome in methylmalonic acidemia: "Metabolic stroke" involving the globus pallidus. J Pediatr 1988;113:1022-1027.
-
(1988)
J Pediatr
, vol.113
, pp. 1022-1027
-
-
Heidenreich, R.1
Natowicz, M.2
Hainline, B.E.3
-
43
-
-
0028024334
-
Stroke, hemiparesis, and deficient mitochondrial beta-oxidation
-
Vallee L, Fontaine M, Nuyts JP, et al: Stroke, hemiparesis, and deficient mitochondrial beta-oxidation. Eur J Pediatr 1994;153: 598-603.
-
(1994)
Eur J Pediatr
, vol.153
, pp. 598-603
-
-
Vallee, L.1
Fontaine, M.2
Nuyts, J.P.3
-
44
-
-
0022550067
-
A typical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
-
Zoghbi HY, Spence JE, Beaudet AL, et al: A typical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. Ann Neurol 1986;20:367-369.
-
(1986)
Ann Neurol
, vol.20
, pp. 367-369
-
-
Zoghbi, H.Y.1
Spence, J.E.2
Beaudet, A.L.3
-
45
-
-
0031662268
-
Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
-
Huemer M, Muehl A, Wandl-Vergesslich K, et al: Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. Eur J Pediatr 1998;157:743-746.
-
(1998)
Eur J Pediatr
, vol.157
, pp. 743-746
-
-
Huemer, M.1
Muehl, A.2
Wandl-Vergesslich, K.3
-
46
-
-
85036489772
-
Acute late-infantile manifestation with stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency
-
Toledo SSIEM
-
Steen C, Baumgarten R, Pegel M, et al: Acute late-infantile manifestation with stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency, abstract. 33rd Annual Symposium, Toledo SSIEM 1995;74.
-
(1995)
33rd Annual Symposium
, vol.74
-
-
Steen, C.1
Baumgarten, R.2
Pegel, M.3
-
47
-
-
0024990933
-
Acute hemiparesis as a presenting sign in a heterozygote for ornithine transcarbamylase deficiency
-
deGrauw TJ, Smit LM, Brockstedt M, et al: Acute hemiparesis as a presenting sign in a heterozygote for ornithine transcarbamylase deficiency. Neuropediatrics 1990;21:133-135.
-
(1990)
Neuropediatrics
, vol.21
, pp. 133-135
-
-
DeGrauw, T.J.1
Smit, L.M.2
Brockstedt, M.3
-
49
-
-
0031750421
-
Magnetic resonance spectroscopy: Use in monitoring MELAS treatment
-
Pavlakis SG, Kingsley PB, Kaplan GP, et al: Magnetic resonance spectroscopy: Use in monitoring MELAS treatment. Arch Neurol 1998;55:849-852.
-
(1998)
Arch Neurol
, vol.55
, pp. 849-852
-
-
Pavlakis, S.G.1
Kingsley, P.B.2
Kaplan, G.P.3
-
50
-
-
0033027623
-
Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency
-
Morin C, Dube J, Robinson BH, et al: Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency. Ann Neurol 1999;45:389-392.
-
(1999)
Ann Neurol
, vol.45
, pp. 389-392
-
-
Morin, C.1
Dube, J.2
Robinson, B.H.3
-
51
-
-
0031934540
-
Mitochondrial DNA in stroke and migraine with aura
-
Qjaimi J, Katsabanis S, Bower S, et al: Mitochondrial DNA in stroke and migraine with aura. Cerebrovasc Dis 1998;8:102-106.
-
(1998)
Cerebrovasc Dis
, vol.8
, pp. 102-106
-
-
Qjaimi, J.1
Katsabanis, S.2
Bower, S.3
-
52
-
-
0028123180
-
Hemiparesis in a girl with cystinosis and renal transplant
-
Van Lierde A, Colombo D, Rossi LN, et al: Hemiparesis in a girl with cystinosis and renal transplant. Eur J Pediatr 1994;153: 702-703.
-
(1994)
Eur J Pediatr
, vol.153
, pp. 702-703
-
-
Van Lierde, A.1
Colombo, D.2
Rossi, L.N.3
-
53
-
-
0017732442
-
Sulfite oxidase deficiency: Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism
-
Shih VE, Abroms IF, Johnson JL, et al: Sulfite oxidase deficiency: Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism. N Engl J Med 1977;297:1022-1028.
-
(1977)
N Engl J Med
, vol.297
, pp. 1022-1028
-
-
Shih, V.E.1
Abroms, I.F.2
Johnson, J.L.3
-
54
-
-
0029112185
-
Defective molybdopterin biosynthesis: Clinical heterogeneity associated with molybdenum cofactor deficiency
-
Mize C, Johnson JL, Rajagopalan KV: Defective molybdopterin biosynthesis: Clinical heterogeneity associated with molybdenum cofactor deficiency. J Inherit Metab Dis 1995;18:283-290.
-
(1995)
J Inherit Metab Dis
, vol.18
, pp. 283-290
-
-
Mize, C.1
Johnson, J.L.2
Rajagopalan, K.V.3
-
55
-
-
0027222950
-
A unique pattern of coagulation abnormalities in carbohydrate-deficient glycoprotein syndrome
-
van Geet C, Jaeken J: A unique pattern of coagulation abnormalities in carbohydrate-deficient glycoprotein syndrome. Pediatr Res 1993;33:540-541.
-
(1993)
Pediatr Res
, vol.33
, pp. 540-541
-
-
Van Geet, C.1
Jaeken, J.2
-
56
-
-
0025745095
-
Neurological findings in the carbohydrate-deficient glycoprotein syndrome
-
Blennow G, Jaeken J, Wiklund LM: Neurological findings in the carbohydrate-deficient glycoprotein syndrome. Acta Paediatr Scand Suppl 1991;375:14-20.
-
(1991)
Acta Paediatr Scand Suppl
, vol.375
, pp. 14-20
-
-
Blennow, G.1
Jaeken, J.2
Wiklund, L.M.3
-
57
-
-
0032889255
-
Coagulation abnormalities in the carbohydrate-deficient glycoprotein syndrome: Case report and review of the literature
-
Young G, Driscoll MC: Coagulation abnormalities in the carbohydrate-deficient glycoprotein syndrome: Case report and review of the literature. Am J Hematol 1999;60:66-69.
-
(1999)
Am J Hematol
, vol.60
, pp. 66-69
-
-
Young, G.1
Driscoll, M.C.2
-
58
-
-
0029818054
-
MR in children with L-carnitine deficiency
-
Thompson JE, Smith M, Castillo M, et al: MR in children with L-carnitine deficiency. AJNR 1996;17:1585-1588.
-
(1996)
AJNR
, vol.17
, pp. 1585-1588
-
-
Thompson, J.E.1
Smith, M.2
Castillo, M.3
-
59
-
-
0028958702
-
Stroke in purine nucleoside phosphorylase deficiency
-
Tam DA, Leshner RT: Stroke in purine nucleoside phosphorylase deficiency. Pediatr Neurol 1995;12:146-148.
-
(1995)
Pediatr Neurol
, vol.12
, pp. 146-148
-
-
Tam, D.A.1
Leshner, R.T.2
-
61
-
-
0028240332
-
Alternating hemiplegia in childhood: A cross sectional study
-
Nevsimalova S, Dittrich J, Havlova M, et al: Alternating hemiplegia in childhood: A cross sectional study. Brain Dev 1994;16: 189-194.
-
(1994)
Brain Dev
, vol.16
, pp. 189-194
-
-
Nevsimalova, S.1
Dittrich, J.2
Havlova, M.3
-
62
-
-
0031975917
-
Livedo reticularis, developmental delay and stroke-like episodes in a 7-year-old male
-
Wheeler PG, Medina S, Dusick A, et al: Livedo reticularis, developmental delay and stroke-like episodes in a 7-year-old male. Clin Dysmorphol 1998;7:69-74.
-
(1998)
Clin Dysmorphol
, vol.7
, pp. 69-74
-
-
Wheeler, P.G.1
Medina, S.2
Dusick, A.3
-
64
-
-
0032471372
-
Neuroradiologic findings in children with mitochondrial disorders
-
Valanne L, Ketonen L, Majander A, et al: Neuroradiologic findings in children with mitochondrial disorders. AJNR 1998;19:369-377.
-
(1998)
AJNR
, vol.19
, pp. 369-377
-
-
Valanne, L.1
Ketonen, L.2
Majander, A.3
-
65
-
-
0343177592
-
Localized proton spectroscopy of neurodegenerative disease and tumor
-
Faerber E (ed). Cambridge, MacKeith Press
-
Tzika AA: Localized proton spectroscopy of neurodegenerative disease and tumor, in Faerber E (ed): CNS Magnetic Resonance Imaging in Infants and Children. Cambridge, MacKeith Press, 1995, pp 279-306.
-
(1995)
CNS Magnetic Resonance Imaging in Infants and Children
, pp. 279-306
-
-
Tzika, A.A.1
-
66
-
-
0032501990
-
Preventing coronary heart disease: B vitamins and homocysteine
-
Omenn GS, Beresford SAA, Motulsky AG: Preventing coronary heart disease: B vitamins and homocysteine. Circulation 1998;97:421-424.
-
(1998)
Circulation
, vol.97
, pp. 421-424
-
-
Omenn, G.S.1
Beresford, S.A.A.2
Motulsky, A.G.3
-
67
-
-
0030874635
-
Homocysteine in sickle cell disease: Relationship to stroke
-
Houston PE, Rana S, Sekhsaria S, et al: Homocysteine in sickle cell disease: Relationship to stroke. Am J Med 1997;103:192-196.
-
(1997)
Am J Med
, vol.103
, pp. 192-196
-
-
Houston, P.E.1
Rana, S.2
Sekhsaria, S.3
|