-
1
-
-
2442674046
-
Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF
-
Assmann BE, Robinson RO, Surtees RA et al. Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF. Neurology 2004; 62: 1872-1874
-
(2004)
Neurology
, vol.62
, pp. 1872-1874
-
-
Assmann, B.E.1
Robinson, R.O.2
Surtees, R.A.3
-
2
-
-
0023896470
-
Normal postnatal development of the corpus callosum as demonstrated by MR imaging
-
Barkovich AJ, Kjos BO. Normal postnatal development of the corpus callosum as demonstrated by MR imaging. AJNR Am J Neuroradiol 1988; 9: 487-491
-
(1988)
AJNR Am J Neuroradiol
, vol.9
, pp. 487-491
-
-
Barkovich, A.J.1
Kjos, B.O.2
-
3
-
-
0023848868
-
Normal maturation of the neonatal and infant brain: MR imaging at 15.T
-
Barkovich AJ, Kjos BO, Jackson Jr DE, Norman D. Normal maturation of the neonatal and infant brain: MR imaging at 15.T. Radiology 1988; 166: 173-180
-
(1988)
Radiology
, vol.166
, pp. 173-180
-
-
Barkovich, A.J.1
Kjos, B.O.2
Jackson Jr, D.E.3
Norman, D.4
-
4
-
-
0027503387
-
Magnetic resonance imaging of normal and abnormal brain development
-
Barkovtch AJ, Maroldo TV. Magnetic resonance imaging of normal and abnormal brain development. Top Magn Reson Imaging 1993; 5: 96-122
-
(1993)
Top Magn Reson Imaging
, vol.5
, pp. 96-122
-
-
Barkovtch, A.J.1
Maroldo, T.V.2
-
5
-
-
27144519664
-
Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys
-
Cavicchioni O, Gomes DM, Leroy B et al. Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys. Prenat Diagn 2005; 25: 876-878
-
(2005)
Prenat Diagn
, vol.25
, pp. 876-878
-
-
Cavicchioni, O.1
Gomes, D.M.2
Leroy, B.3
-
6
-
-
37849040731
-
A patient with the syndrome of megalencephaly, mega-corpus callosum and complete lack of motor development
-
Dagli AI, Stalker HJ, Williams CA. A patient with the syndrome of megalencephaly, mega-corpus callosum and complete lack of motor development. Am J Med Genet A 2008; 146: 204-207
-
(2008)
Am J Med Genet A
, vol.146
, pp. 204-207
-
-
Dagli, A.I.1
Stalker, H.J.2
Williams, C.A.3
-
8
-
-
0035143795
-
MR imaging of the corpus callosum in pediatric patients with neurofibromatosis type 1
-
Dubovsky EC, Booth TN, Veztna G et al. MR imaging of the corpus callosum in pediatric patients with neurofibromatosis type 1. AJNR Am J Neuroradiol 2001; 22: 190-195
-
(2001)
AJNR Am J Neuroradiol
, vol.22
, pp. 190-195
-
-
Dubovsky, E.C.1
Booth, T.N.2
Veztna, G.3
-
9
-
-
0033136771
-
Development of the human corpus callosum during childhood and adolescence: A longitudinal MRI study
-
Giedd JN, Blumenthal J, Jeffries NO et al. Development of the human corpus callosum during childhood and adolescence: a longitudinal MRI study. Prog Neuropsychopharmacol Biol Psychiatry 1999; 23: 571-588
-
(1999)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.23
, pp. 571-588
-
-
Giedd, J.N.1
Blumenthal, J.2
Jeffries, N.O.3
-
10
-
-
0031691514
-
Megalencephaly, megacorpus callosum, and complete lack of motor development: A previously undescribed syndrome
-
Gohlich-Ratmann G, Baethmann M, Lorenz P et al. Megalencephaly, megacorpus callosum, and complete lack of motor development: a previously undescribed syndrome. Am J Med Genet 1998; 79: 161-167
-
(1998)
Am J Med Genet
, vol.79
, pp. 161-167
-
-
Gohlich-Ratmann, G.1
Baethmann, M.2
Lorenz, P.3
-
11
-
-
0027156904
-
Cerebrospinal fluid concentrations of pterins and metabolites of serotonin and dopamine in a pediatric reference population
-
Hyland K, Surtees RA, Heales SJ et al. Cerebrospinal fluid concentrations of pterins and metabolites of serotonin and dopamine in a pediatric reference population. Pediatr Res 1993; 34: 10-14
-
(1993)
Pediatr Res
, vol.34
, pp. 10-14
-
-
Hyland, K.1
Surtees, R.A.2
Heales, S.J.3
-
12
-
-
0029855021
-
The normal and abnormal genu of the corpus callosum: An evolutionary, embryologic, anatomic, and MR analysis
-
Kier EL, Truwit CL. The normal and abnormal genu of the corpus callosum: an evolutionary, embryologic, anatomic, and MR analysis. AJNR Am J Neuroradiol 1996; 17: 1631-1641
-
(1996)
AJNR Am J Neuroradiol
, vol.17
, pp. 1631-1641
-
-
Kier, E.L.1
Truwit, C.L.2
-
13
-
-
0032412407
-
MRI of the brain in the Cohen syndrome: A relatively large corpus callosum in patients with mental retardation and microcephaly
-
Kivitie-Kallio S, Autti T, Salonen O, Norio R. MRI of the brain in the Cohen syndrome: a relatively large corpus callosum in patients with mental retardation and microcephaly. Neuropediatrics 1998; 29: 298-301
-
(1998)
Neuropediatrics
, vol.29
, pp. 298-301
-
-
Kivitie-Kallio, S.1
Autti, T.2
Salonen, O.3
Norio, R.4
-
14
-
-
0035425580
-
Cohen syndrome: Essential features, natural history, and heterogeneity
-
Kivitie-Kallio S, Norio R. Cohen syndrome: essential features, natural history, and heterogeneity. Am J Med Genet 2001; 102: 125-135
-
(2001)
Am J Med Genet
, vol.102
, pp. 125-135
-
-
Kivitie-Kallio, S.1
Norio, R.2
-
15
-
-
0038353767
-
Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport
-
Kolehmainen J, Black GC, Saarinen A et al. Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport. Am J Hum Genet 2003; 72: 1359-1369
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1359-1369
-
-
Kolehmainen, J.1
Black, G.C.2
Saarinen, A.3
-
16
-
-
0030975769
-
The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes
-
Malinow MR, Nieto FJ, Kruger WD et al. The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes. Arterioscler Thromb Vasc Biol 1997; 17: 1157-1162
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1157-1162
-
-
Malinow, M.R.1
Nieto, F.J.2
Kruger, W.D.3
-
17
-
-
11144322795
-
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: A rare brain malformation syndrome associated with mental retardation and seizures
-
Mirzaa G, Dodge NN, Glass I et al. Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizures. Neuropediatrics 2004; 35: 353-359
-
(2004)
Neuropediatrics
, vol.35
, pp. 353-359
-
-
Mirzaa, G.1
Dodge, N.N.2
Glass, I.3
-
18
-
-
0034326705
-
Spina bifida and other neural tube defects
-
Northrup H, Volcik KA. Spina bifida and other neural tube defects. Curr Probl Pediatr 2000; 30: 313-332
-
(2000)
Curr Probl Pediatr
, vol.30
, pp. 313-332
-
-
Northrup, H.1
Volcik, K.A.2
-
19
-
-
7444222807
-
Hypertrichosis, hyperkeratosis abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females
-
Poyhonen MH, Peippo MM, Valanne LK et al. Hypertrichosis, hyperkeratosis abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females. Clin Dysmorphol 2004; 13: 85-90
-
(2004)
Clin Dysmorphol
, vol.13
, pp. 85-90
-
-
Poyhonen, M.H.1
Peippo, M.M.2
Valanne, L.K.3
-
20
-
-
0014223464
-
Development of the corpus callosum and cavum septi in man
-
Rakic P, Yakovlev PI. Development of the corpus callosum and cavum septi in man. J Comp Neurol 1968; 132: 45-72
-
(1968)
J Comp Neurol
, vol.132
, pp. 45-72
-
-
Rakic, P.1
Yakovlev, P.I.2
-
21
-
-
0033554310
-
Neurofibromin, the neurofibromatosis type 1 Ras-GAP, is required for appropriate P0 expression and myelination
-
Rosenbaum T, Kim HA, Boissy YL, Ling B, Ratner N. Neurofibromin, the neurofibromatosis type 1 Ras-GAP, is required for appropriate P0 expression and myelination. Ann N Y Acad Sci 1999; 883: 203-214
-
(1999)
Ann N Y Acad Sci
, vol.883
, pp. 203-214
-
-
Rosenbaum, T.1
Kim, H.A.2
Boissy, Y.L.3
Ling, B.4
Ratner, N.5
-
22
-
-
0029831546
-
Prenatal MR diagnosis of a thick corpus callosum
-
Rypens F, Sonigo P, Aubry MC et al. Prenatal MR diagnosis of a thick corpus callosum. AJNR Am J Neuroradiol 1996; 17: 1918-1920
-
(1996)
AJNR Am J Neuroradiol
, vol.17
, pp. 1918-1920
-
-
Rypens, F.1
Sonigo, P.2
Aubry, M.C.3
-
23
-
-
0031971515
-
-
Put NM van der, Gabreels F, Stevens EM et al. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet 1998; 62: 1044-1051
-
Put NM van der, Gabreels F, Stevens EM et al. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet 1998; 62: 1044-1051
-
-
-
-
24
-
-
15744396344
-
Neurofibromatosis 1: From lab bench to clinic
-
Ward BA, Gutmann DH. Neurofibromatosis 1: from lab bench to clinic. Pediatr Neurol 2005; 32: 221-228
-
(2005)
Pediatr Neurol
, vol.32
, pp. 221-228
-
-
Ward, B.A.1
Gutmann, D.H.2
-
25
-
-
0029054625
-
MRI in neurofibromatosis type I: Using fluid-attenuated inversion recovery pulse sequences
-
Yamanouchi H, Kato T, Matsuda H et al. MRI in neurofibromatosis type I: using fluid-attenuated inversion recovery pulse sequences. Pediatr Neurol 1995; 12: 286-290
-
(1995)
Pediatr Neurol
, vol.12
, pp. 286-290
-
-
Yamanouchi, H.1
Kato, T.2
Matsuda, H.3
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