-
1
-
-
30144439539
-
Brain stem and cerebellar findings in Joubert syndrome
-
Alorainy IA, Sabir S, Seidahmed MZ, Farooqu HA, Salih MA. Brain stem and cerebellar findings in Joubert syndrome. J Comput Assist Tomogr 2006; 30: 116-121
-
(2006)
J Comput Assist Tomogr
, vol.30
, pp. 116-121
-
-
Alorainy, I.A.1
Sabir, S.2
Seidahmed, M.Z.3
Farooqu, H.A.4
Salih, M.A.5
-
2
-
-
0032231712
-
Neuroimaging manifestations and classification of congenital muscular dystrophies
-
Barkovich AJ. Neuroimaging manifestations and classification of congenital muscular dystrophies. AJNR Am J Neuroradiol 1998; 19: 1389-1396
-
(1998)
AJNR Am J Neuroradiol
, vol.19
, pp. 1389-1396
-
-
Barkovich, A.J.1
-
3
-
-
0004289354
-
-
4th edn, Philadelphia: Lippincott Williams & Wilkins
-
Barkovich AJ. Pediatric neuroimaging. 4th edn., Philadelphia: Lippincott Williams & Wilkins 2005
-
(2005)
Pediatric neuroimaging
-
-
Barkovich, A.J.1
-
4
-
-
16844372994
-
Cerebellar injury in the extremely premature infant: Newly recognized but relatively common outcome
-
Bodensteiner JB, Johnsen SD. Cerebellar injury in the extremely premature infant: newly recognized but relatively common outcome. J Child Neurol 2005; 20: 139-142
-
(2005)
J Child Neurol
, vol.20
, pp. 139-142
-
-
Bodensteiner, J.B.1
Johnsen, S.D.2
-
5
-
-
2142825062
-
Cerebellum-small brain but large confusion: A review of selected cerebellar malformations and disruptions
-
Boltshauser E. Cerebellum-small brain but large confusion: a review of selected cerebellar malformations and disruptions. Am J Med Genet A 2004; 126: 376-385
-
(2004)
Am J Med Genet A
, vol.126
, pp. 376-385
-
-
Boltshauser, E.1
-
6
-
-
0036227971
-
Vanishing cerebellum in myelomeningocoele
-
Boltshauser E, Schneider J, Kollias S, Waibel P, Weissert M. Vanishing cerebellum in myelomeningocoele. Eur J Paediatr Neurol 2002; 6: 109-113
-
(2002)
Eur J Paediatr Neurol
, vol.6
, pp. 109-113
-
-
Boltshauser, E.1
Schneider, J.2
Kollias, S.3
Waibel, P.4
Weissert, M.5
-
8
-
-
0030065606
-
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
-
Brunelli S, Faiella A, Capra V, Nigra V, Simeone A, Cama A et al. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nat Genet 1996; 12: 94-96
-
(1996)
Nat Genet
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
Nigra, V.4
Simeone, A.5
Cama, A.6
-
9
-
-
24344437604
-
Schizencephaly: Heterogeneous etiologies in a population of 4 million California births
-
Curry CJ, Lammer EJ, Nelson V, Show GM. Schizencephaly: heterogeneous etiologies in a population of 4 million California births. Am J Med Genet A 2005; 137: 181-189
-
(2005)
Am J Med Genet A
, vol.137
, pp. 181-189
-
-
Curry, C.J.1
Lammer, E.J.2
Nelson, V.3
Show, G.M.4
-
10
-
-
0036794912
-
Neonatal alloimmune thrombocytopenia: Ante-natal and postnatal imaging findings in the pediatric brain
-
Dale ST, Coleman LT. Neonatal alloimmune thrombocytopenia: ante-natal and postnatal imaging findings in the pediatric brain. AJNR Am J Neuroradiol 2002; 23: 1457-1465
-
(2002)
AJNR Am J Neuroradiol
, vol.23
, pp. 1457-1465
-
-
Dale, S.T.1
Coleman, L.T.2
-
11
-
-
0031896301
-
Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly
-
Debus O, Koch HG, Kurlemann G, Strater R, Vielhaber H, Weber P et al. Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly. Arch Dis Child Fetal Neonatal 1998; 78: F121-124
-
(1998)
Arch Dis Child Fetal Neonatal
, vol.78
-
-
Debus, O.1
Koch, H.G.2
Kurlemann, G.3
Strater, R.4
Vielhaber, H.5
Weber, P.6
-
12
-
-
0036939526
-
Abnormalities of cerebellar foliation and fissuration: Classification, neurogenetics and clinicoradiological correlations
-
Demaerel P. Abnormalities of cerebellar foliation and fissuration: classification, neurogenetics and clinicoradiological correlations. Neuro-radiology 2002: 44: 639-646
-
(2002)
Neuro-radiology
, vol.44
, pp. 639-646
-
-
Demaerel, P.1
-
15
-
-
0035039432
-
Cerebellar defect associated with Schimke immuno-osseous dysplasia
-
Dhillon AS, Chapman S, Milford DV. Cerebellar defect associated with Schimke immuno-osseous dysplasia. Eur J Pediatr 2001; 160: 372-374
-
(2001)
Eur J Pediatr
, vol.160
, pp. 372-374
-
-
Dhillon, A.S.1
Chapman, S.2
Milford, D.V.3
-
16
-
-
33748437717
-
Natural history of brain lesions in extremely preterm infants studied with serial magnetic resonance imaging from birth and neurodevelopmental assessment
-
Dyet LE, Kennea N, Counsell SJ, Maalouf EF, Ajayi-Obe M, Duggan PJ et al. Natural history of brain lesions in extremely preterm infants studied with serial magnetic resonance imaging from birth and neurodevelopmental assessment. Pediatrics 2006; 118: 536-548
-
(2006)
Pediatrics
, vol.118
, pp. 536-548
-
-
Dyet, L.E.1
Kennea, N.2
Counsell, S.J.3
Maalouf, E.F.4
Ajayi-Obe, M.5
Duggan, P.J.6
-
17
-
-
10744229593
-
Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes
-
Gleeson JG, Keeler LC, Parisi MA, Marsh SE, Chance PF, Glass IA et al. Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes. Am J Med Genet A 2004; 125: 125-134
-
(2004)
Am J Med Genet A
, vol.125
, pp. 125-134
-
-
Gleeson, J.G.1
Keeler, L.C.2
Parisi, M.A.3
Marsh, S.E.4
Chance, P.F.5
Glass, I.A.6
-
18
-
-
31144439283
-
Fetal magnetic resonance imaging in the prenatal diagnosis of cerebellar hemorrhage
-
Gorincour G, Rypens F, Lapierre C, Costa T, Audibert F, Robitaille Y. Fetal magnetic resonance imaging in the prenatal diagnosis of cerebellar hemorrhage. Ultrasound Obstet Gynecol 2006; 27: 78-80
-
(2006)
Ultrasound Obstet Gynecol
, vol.27
, pp. 78-80
-
-
Gorincour, G.1
Rypens, F.2
Lapierre, C.3
Costa, T.4
Audibert, F.5
Robitaille, Y.6
-
19
-
-
0030975567
-
Familial schizencephaly associated with EMX2 mutation
-
Granata T, Farina L, Faiella A, Cardini R, D'Incerti L, Boncinelli E et al. Familial schizencephaly associated with EMX2 mutation. Neurology 1997; 48: 1403-1406
-
(1997)
Neurology
, vol.48
, pp. 1403-1406
-
-
Granata, T.1
Farina, L.2
Faiella, A.3
Cardini, R.4
D'Incerti, L.5
Boncinelli, E.6
-
20
-
-
15444370322
-
Frequency and nature of cerebellar injury in the extremely premature survivor with cerebral palsy
-
Johnsen SD, Bodensteiner JB, Lotze TE. Frequency and nature of cerebellar injury in the extremely premature survivor with cerebral palsy. J Child Neurol 2005; 20: 60-64
-
(2005)
J Child Neurol
, vol.20
, pp. 60-64
-
-
Johnsen, S.D.1
Bodensteiner, J.B.2
Lotze, T.E.3
-
21
-
-
0141743551
-
Dandy-Walker malformation: Prenatal diagnosis and prognosis
-
Klein O, Pierre-Kahn A, Boddaert N, Parisot D, Brunelle F. Dandy-Walker malformation: prenatal diagnosis and prognosis. Childs Nerv Syst 2003; 19: 484-489
-
(2003)
Childs Nerv Syst
, vol.19
, pp. 484-489
-
-
Klein, O.1
Pierre-Kahn, A.2
Boddaert, N.3
Parisot, D.4
Brunelle, F.5
-
22
-
-
33845894667
-
Sonographic detection of fetal cerebellar cavernous hemangioma with inutero hemorrhage leading to cerebellar hemihypoplasia
-
Lerner A, Gilboa Y, Gerad L, Malinger G, Kidron D, Achiron R. Sonographic detection of fetal cerebellar cavernous hemangioma with inutero hemorrhage leading to cerebellar hemihypoplasia. Ultrasound Obstet Gynecol 2006; 28: 968-971
-
(2006)
Ultrasound Obstet Gynecol
, vol.28
, pp. 968-971
-
-
Lerner, A.1
Gilboa, Y.2
Gerad, L.3
Malinger, G.4
Kidron, D.5
Achiron, R.6
-
23
-
-
33644619824
-
Cerebellar hemorrhage in the preterm infant: Ultrasonographic findings and risk factors
-
Limperopoulos C, Benson CB, Bassan H, Disalvo DN, Kinnamon DD, Moore M et al. Cerebellar hemorrhage in the preterm infant: ultrasonographic findings and risk factors. Pediatrics 2005; 116: 717-724
-
(2005)
Pediatrics
, vol.116
, pp. 717-724
-
-
Limperopoulos, C.1
Benson, C.B.2
Bassan, H.3
Disalvo, D.N.4
Kinnamon, D.D.5
Moore, M.6
-
24
-
-
33646196918
-
Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosis
-
Malinger G, Zahalka N, Kidron D, Ben-Sira L, Lev D, Lerman-Sagie T. Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosis. Eur J Paediatr Neurol 2006; 10: 93-96
-
(2006)
Eur J Paediatr Neurol
, vol.10
, pp. 93-96
-
-
Malinger, G.1
Zahalka, N.2
Kidron, D.3
Ben-Sira, L.4
Lev, D.5
Lerman-Sagie, T.6
-
25
-
-
0032325428
-
A new pattern of cerebellar hemorrhages in preterm infants
-
Merrill JD, Piecuch RE, Fell SC, Barkovich AJ, Goldstein RB. A new pattern of cerebellar hemorrhages in preterm infants. Pediatrics 1998; 102: E62
-
(1998)
Pediatrics
, vol.102
-
-
Merrill, J.D.1
Piecuch, R.E.2
Fell, S.C.3
Barkovich, A.J.4
Goldstein, R.B.5
-
26
-
-
24344485189
-
Disruption of cerebellar development: Potential complication of extreme prematurity
-
Messerschmidt A, Brugger PC, Boltshauser E, Zoder G, Sterniste W, Birnbacher R et al. Disruption of cerebellar development: potential complication of extreme prematurity. AJNR Am J Neuroradiol 2005; 26: 1659-1667
-
(2005)
AJNR Am J Neuroradiol
, vol.26
, pp. 1659-1667
-
-
Messerschmidt, A.1
Brugger, P.C.2
Boltshauser, E.3
Zoder, G.4
Sterniste, W.5
Birnbacher, R.6
-
27
-
-
4544364988
-
A different approach to cysts of the posterior fossa
-
Nelson Jr MD, Maher K, Gilles FH. A different approach to cysts of the posterior fossa. Pediatr Radiol 2004; 34: 720-732
-
(2004)
Pediatr Radiol
, vol.34
, pp. 720-732
-
-
Nelson Jr, M.D.1
Maher, K.2
Gilles, F.H.3
-
28
-
-
1942532075
-
Severe fetal cytomegalovirus infection associated with cerebellar hemorrhage
-
Ortiz JU, Ostermayer E, Fischer T, Kuschel B, Rudelius M, Schneider KT. Severe fetal cytomegalovirus infection associated with cerebellar hemorrhage. Ultrasound Obstet Gynecol 2004; 23: 402-406
-
(2004)
Ultrasound Obstet Gynecol
, vol.23
, pp. 402-406
-
-
Ortiz, J.U.1
Ostermayer, E.2
Fischer, T.3
Kuschel, B.4
Rudelius, M.5
Schneider, K.T.6
-
30
-
-
0003657556
-
-
1st edn, San Diego: Academic Press
-
Schmahmann JD, Doyon J, Toga AW, Petrides M, Evans AC. MRI Atlas of the Human Cerebellum. 1st edn., San Diego: Academic Press 2000
-
(2000)
MRI Atlas of the Human Cerebellum
-
-
Schmahmann, J.D.1
Doyon, J.2
Toga, A.W.3
Petrides, M.4
Evans, A.C.5
-
31
-
-
0029410595
-
Cerebellar agenesis versus vanishing cerebellum in Chiari II malformation
-
Sener RN. Cerebellar agenesis versus vanishing cerebellum in Chiari II malformation. Comput Med Imaging Graph 1995; 19: 491-494
-
(1995)
Comput Med Imaging Graph
, vol.19
, pp. 491-494
-
-
Sener, R.N.1
-
32
-
-
0032710736
-
Prenatal diagnosis of fetal cerebellar lesions: A case report and review of the literature
-
Sharony R, Kidron D, Aviram R, Beyth Y, Tepper R. Prenatal diagnosis of fetal cerebellar lesions: a case report and review of the literature. Prenat Diagn 1999; 19: 1077-1080
-
(1999)
Prenat Diagn
, vol.19
, pp. 1077-1080
-
-
Sharony, R.1
Kidron, D.2
Aviram, R.3
Beyth, Y.4
Tepper, R.5
-
33
-
-
0033827918
-
Cerebellar cortical dysplasia: MR findings in a complex entity
-
Soto-Ares G, Delmaire C, Deries B, Vallee L, Pruvo JP. Cerebellar cortical dysplasia: MR findings in a complex entity. AJNR Am J Neuroradiol 2000; 21: 1511-1519 2000
-
(2000)
AJNR Am J Neuroradiol 2000
, vol.21
, pp. 1511-1519
-
-
Soto-Ares, G.1
Delmaire, C.2
Deries, B.3
Vallee, L.4
Pruvo, J.P.5
-
34
-
-
0036677272
-
Neuropathologic and MR imaging correlation in a neonatal case of cerebellar cortical dysplasia
-
Soto-Ares G, Devisme L, Jorriot S, Deries B, Pruvo JP, Ruchoux MM. Neuropathologic and MR imaging correlation in a neonatal case of cerebellar cortical dysplasia. AJNR Am J Neuroradiol 2002; 23: 1101-1104
-
(2002)
AJNR Am J Neuroradiol
, vol.23
, pp. 1101-1104
-
-
Soto-Ares, G.1
Devisme, L.2
Jorriot, S.3
Deries, B.4
Pruvo, J.P.5
Ruchoux, M.M.6
-
35
-
-
0032706114
-
Experimental schizencephaly induced by Kilham strain of mumps virus: Pathogenesis of cleft formation
-
Takano T, Takikita S, Shimada M. Experimental schizencephaly induced by Kilham strain of mumps virus: pathogenesis of cleft formation. Neuroreport 1999; 10: 3149-3154
-
(1999)
Neuroreport
, vol.10
, pp. 3149-3154
-
-
Takano, T.1
Takikita, S.2
Shimada, M.3
-
36
-
-
20044385426
-
EMX2-independent familial schizencephaly: Clinical and genetic analyses
-
Tietjen I, Erdogan F, Currier S, Apse K, Chang BS, Hill RS et al. EMX2-independent familial schizencephaly: clinical and genetic analyses. Am J Med Genet A 2005; 135: 166-170
-
(2005)
Am J Med Genet A
, vol.135
, pp. 166-170
-
-
Tietjen, I.1
Erdogan, F.2
Currier, S.3
Apse, K.4
Chang, B.S.5
Hill, R.S.6
-
37
-
-
33747593324
-
Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome
-
Titomanlio L, Brasi D De, Romano A, Genesio R, Diano AA, Del Giudice E. Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome. Acta Paediatr 2006; 95: 861-863
-
(2006)
Acta Paediatr
, vol.95
, pp. 861-863
-
-
Titomanlio, L.1
Brasi, D.D.2
Romano, A.3
Genesio, R.4
Diano, A.A.5
Del Giudice, E.6
-
38
-
-
18544387322
-
Rhombencephalosynapsis: Clinical findings and neuroimaging in 9 children
-
Toelle SP, Yalcinkaya C, Kocer N, Deonna T, Overweg-Plandsoen WC, Bast T et al. Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children. Neuropediatrics 2002; 33: 209-214
-
(2002)
Neuropediatrics
, vol.33
, pp. 209-214
-
-
Toelle, S.P.1
Yalcinkaya, C.2
Kocer, N.3
Deonna, T.4
Overweg-Plandsoen, W.C.5
Bast, T.6
-
39
-
-
0041742190
-
Fetal cerebellar hemorrhage in a severely growth-restricted fetus: Natural history and differential diagnosis from Dandy-Walker malformation
-
Yuksel A, Batukan C. Fetal cerebellar hemorrhage in a severely growth-restricted fetus: natural history and differential diagnosis from Dandy-Walker malformation. Ultrasound Obstet Gynecol 2003; 22: 178-181
-
(2003)
Ultrasound Obstet Gynecol
, vol.22
, pp. 178-181
-
-
Yuksel, A.1
Batukan, C.2
|