-
1
-
-
77955094663
-
Neurocritical care for neonates
-
Glass HC, Bonifacio SL, Peloquin S, Shimotake T, Sehring S, Sun Y, et al. Neurocritical care for neonates. Neurocrit Care. 2010;12(3):421-9.
-
(2010)
Neurocrit Care.
, vol.12
, Issue.3
, pp. 421-429
-
-
Glass, H.C.1
Bonifacio, S.L.2
Peloquin, S.3
Shimotake, T.4
Sehring, S.5
Sun, Y.6
-
2
-
-
70349454019
-
Segregated fronto-cerebellar circuits revealed by intrinsic functional connectivity
-
Krienen FM, Buckner RL. Segregated fronto-cerebellar circuits revealed by intrinsic functional connectivity. Cereb Cortex. 2009;19(10):2485-97.
-
(2009)
Cereb Cortex.
, vol.19
, Issue.10
, pp. 2485-2497
-
-
Krienen, F.M.1
Buckner, R.L.2
-
3
-
-
84864680808
-
The cerebellum and cognition: evidence from functional imaging studies
-
Stoodley CJ. The cerebellum and cognition: evidence from functional imaging studies. Cerebellum. 2012;11(2):352-65.
-
(2012)
Cerebellum.
, vol.11
, Issue.2
, pp. 352-365
-
-
Stoodley, C.J.1
-
4
-
-
0031976207
-
The cerebellar cognitive affective syndrome
-
Schmahmann JD, Sherman JC. The cerebellar cognitive affective syndrome. Brain. 1998;121(Pt 4):561-79.
-
(1998)
Brain.
, vol.121
, pp. 561-579
-
-
Schmahmann, J.D.1
Sherman, J.C.2
-
6
-
-
84922465526
-
Congenital abnormalities of the posterior fossa
-
Bosemani T, Orman G, Boltshauser E, Tekes A, Huisman TA, Poretti A. Congenital abnormalities of the posterior fossa. Radiographics. 2015;35(1): 200-20.
-
(2015)
Radiographics.
, vol.35
, Issue.1
, pp. 200-220
-
-
Bosemani, T.1
Orman, G.2
Boltshauser, E.3
Tekes, A.4
Huisman, T.A.5
Poretti, A.6
-
7
-
-
0038823655
-
Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation
-
Boddaert N, Klein O, Ferguson N, Sonigo P, Parisot D, Hertz-Pannier L, et al. Intellectual prognosis of the Dandy-Walker malformation in children: the importance of vermian lobulation. Neuroradiology. 2003;45(5):320-4.
-
(2003)
Neuroradiology.
, vol.45
, Issue.5
, pp. 320-324
-
-
Boddaert, N.1
Klein, O.2
Ferguson, N.3
Sonigo, P.4
Parisot, D.5
Hertz-Pannier, L.6
-
8
-
-
84881544806
-
Joubert syndrome: congenital cerebellar ataxia with the molar tooth
-
Romani M, Micalizzi A, Valente EM. Joubert syndrome: congenital cerebellar ataxia with the molar tooth. Lancet Neurol. 2013;12(9):894-905.
-
(2013)
Lancet Neurol.
, vol.12
, Issue.9
, pp. 894-905
-
-
Romani, M.1
Micalizzi, A.2
Valente, E.M.3
-
9
-
-
84938982200
-
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity
-
Bachmann-Gagescu R, Dempsey JC, Phelps IG, O'Roak BJ, Knutzen DM, Rue TC, et al. Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity. J Med Genet. 2015;52(8):514-22.
-
(2015)
J Med Genet.
, vol.52
, Issue.8
, pp. 514-522
-
-
Bachmann-Gagescu, R.1
Dempsey, J.C.2
Phelps, I.G.3
O'Roak, B.J.4
Knutzen, D.M.5
Rue, T.C.6
-
10
-
-
0032851825
-
Clinical features and revised diagnostic criteria in Joubert syndrome
-
Maria BL, Boltshauser E, Palmer SC, Tran TX. Clinical features and revised diagnostic criteria in Joubert syndrome. J Child Neurol. 1999;14(9):583-90.
-
(1999)
J Child Neurol.
, vol.14
, Issue.9
, pp. 583-590
-
-
Maria, B.L.1
Boltshauser, E.2
Palmer, S.C.3
Tran, T.X.4
-
11
-
-
84908381441
-
Horizontal head titubation in infants with Joubert syndrome: a new finding
-
Poretti A, Christen HJ, Elton LE, Baumgartner M, Korenke GC, Sukhudyan B, et al. Horizontal head titubation in infants with Joubert syndrome: a new finding. Dev Med Child Neurol. 2014;56(10):1016-20.
-
(2014)
Dev Med Child Neurol.
, vol.56
, Issue.10
, pp. 1016-1020
-
-
Poretti, A.1
Christen, H.J.2
Elton, L.E.3
Baumgartner, M.4
Korenke, G.C.5
Sukhudyan, B.6
-
12
-
-
80052882184
-
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
-
Poretti A, Huisman TA, Scheer I, Boltshauser E. Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients. AJNR Am J Neuroradiol. 2011;32(8):1459-63.
-
(2011)
AJNR Am J Neuroradiol.
, vol.32
, Issue.8
, pp. 1459-1463
-
-
Poretti, A.1
Huisman, T.A.2
Scheer, I.3
Boltshauser, E.4
-
13
-
-
57449115433
-
Cognitive outcome in children with rhombencephalosynapsis
-
Poretti A, Alber FD, Burki S, Toelle SP, Boltshauser E. Cognitive outcome in children with rhombencephalosynapsis. Eur J Paediatr Neurol. 2009;13(1): 28-33.
-
(2009)
Eur J Paediatr Neurol.
, vol.13
, Issue.1
, pp. 28-33
-
-
Poretti, A.1
Alber, F.D.2
Burki, S.3
Toelle, S.P.4
Boltshauser, E.5
-
14
-
-
78649326710
-
Gomez-Lopez-Hernandez syndrome: reappraisal of the diagnostic criteria
-
Sukhudyan B, Jaladyan V, Melikyan G, Schlump JU, Boltshauser E, Poretti A. Gomez-Lopez-Hernandez syndrome: reappraisal of the diagnostic criteria. Eur J Pediatr. 2010;169(12):1523-8.
-
(2010)
Eur J Pediatr.
, vol.169
, Issue.12
, pp. 1523-1528
-
-
Sukhudyan, B.1
Jaladyan, V.2
Melikyan, G.3
Schlump, J.U.4
Boltshauser, E.5
Poretti, A.6
-
15
-
-
84860603464
-
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity
-
Ishak GE, Dempsey JC, Shaw DW, Tully H, Adam MP, Sanchez-Lara PA, et al. Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity. Brain. 2012;135(Pt 5):1370-86.
-
(2012)
Brain.
, vol.135
, pp. 1370-1386
-
-
Ishak, G.E.1
Dempsey, J.C.2
Shaw, D.W.3
Tully, H.4
Adam, M.P.5
Sanchez-Lara, P.A.6
-
16
-
-
79960175586
-
Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia
-
Namavar Y, Barth PG, Poll-The BT, Baas F. Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia. Orphanet J Rare Dis. 2011;6:50.
-
(2011)
Orphanet J Rare Dis
, vol.6
, pp. 50
-
-
Namavar, Y.1
Barth, P.G.2
Poll-The, B.T.3
Baas, F.4
-
17
-
-
0027771377
-
Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset.
-
Barth PG. Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset. Brain Dev. 1993;15(6):411-22.
-
(1993)
Brain Dev.
, vol.15
, Issue.6
, pp. 411-422
-
-
Barth, P.G.1
-
18
-
-
0027419104
-
Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly Report of three siblings.
-
Albrecht S, Schneider MC, Belmont J, Armstrong DL. Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings. Acta Neuropathol. 1993;85(4):394-9.
-
(1993)
Acta Neuropathol.
, vol.85
, Issue.4
, pp. 394-399
-
-
Albrecht, S.1
Schneider, M.C.2
Belmont, J.3
Armstrong, D.L.4
-
19
-
-
35348983348
-
Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia
-
Edvardson S, Shaag A, Kolesnikova O, Gomori JM, Tarassov I, Einbinder T, et al. Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia. Am J Hum Genet. 2007;81(4):857-62.
-
(2007)
Am J Hum Genet.
, vol.81
, Issue.4
, pp. 857-862
-
-
Edvardson, S.1
Shaag, A.2
Kolesnikova, O.3
Gomori, J.M.4
Tarassov, I.5
Einbinder, T.6
-
20
-
-
78650693958
-
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia
-
Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, et al. Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia. Brain. 2011;134(Pt 1):143-56.
-
(2011)
Brain.
, vol.134
, pp. 143-156
-
-
Namavar, Y.1
Barth, P.G.2
Kasher, P.R.3
van Ruissen, F.4
Brockmann, K.5
Bernert, G.6
-
21
-
-
84895794868
-
Diagnostic approach to the congenital muscular dystrophies
-
Bonnemann CG, Wang CH, Quijano-Roy S, Deconinck N, Bertini E, Ferreiro A, et al. Diagnostic approach to the congenital muscular dystrophies. Neuromuscul Disord. 2014;24(4):289-311.
-
(2014)
Neuromuscul Disord.
, vol.24
, Issue.4
, pp. 289-311
-
-
Bonnemann, C.G.1
Wang, C.H.2
Quijano-Roy, S.3
Deconinck, N.4
Bertini, E.5
Ferreiro, A.6
-
22
-
-
57749100373
-
Brain involvement in muscular dystrophies with defective dystroglycan glycosylation
-
Clement E, Mercuri E, Godfrey C, Smith J, Robb S, Kinali M, et al. Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Ann Neurol. 2008;64(5):573-82.
-
(2008)
Ann Neurol.
, vol.64
, Issue.5
, pp. 573-582
-
-
Clement, E.1
Mercuri, E.2
Godfrey, C.3
Smith, J.4
Robb, S.5
Kinali, M.6
-
23
-
-
34848837334
-
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
-
Godfrey C, Clement E, Mein R, Brockington M, Smith J, Talim B, et al. Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. Brain. 2007;130(Pt 10):2725-35.
-
(2007)
Brain.
, vol.130
, pp. 2725-2735
-
-
Godfrey, C.1
Clement, E.2
Mein, R.3
Brockington, M.4
Smith, J.5
Talim, B.6
-
24
-
-
84929711618
-
Cerebellar cysts in children: a pattern recognition approach
-
Boltshauser E, Scheer I, Huisman TA, Poretti A. Cerebellar cysts in children: a pattern recognition approach. Cerebellum. 2015;14(3):308-16.
-
(2015)
Cerebellum.
, vol.14
, Issue.3
, pp. 308-316
-
-
Boltshauser, E.1
Scheer, I.2
Huisman, T.A.3
Poretti, A.4
-
25
-
-
34548227899
-
Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance
-
Barth PG, Majoie CB, Caan MW, Weterman MA, Kyllerman M, Smit LM, et al. Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance. Brain. 2007;130(Pt 9):2258-66.
-
(2007)
Brain.
, vol.130
, pp. 2258-2266
-
-
Barth, P.G.1
Majoie, C.B.2
Caan, M.W.3
Weterman, M.A.4
Kyllerman, M.5
Smit, L.M.6
-
26
-
-
70349910567
-
Pontine tegmental cap dysplasia: the severe end of the clinical spectrum
-
Rauscher C, Poretti A, Neuhann TM, Forstner R, Hahn G, Koch J, et al. Pontine tegmental cap dysplasia: the severe end of the clinical spectrum. Neuropediatrics. 2009;40(1):43-6.
-
(2009)
Neuropediatrics.
, vol.40
, Issue.1
, pp. 43-46
-
-
Rauscher, C.1
Poretti, A.2
Neuhann, T.M.3
Forstner, R.4
Hahn, G.5
Koch, J.6
-
27
-
-
84964303783
-
Brainstem disconnection: two additional patients and expansion of the phenotype
-
Poretti A, Denecke J, Miller DC, Schiffmann H, Buhk JH, Grange DK, et al. Brainstem disconnection: two additional patients and expansion of the phenotype. Neuropediatrics. 2015;46(2):139-44.
-
(2015)
Neuropediatrics.
, vol.46
, Issue.2
, pp. 139-144
-
-
Poretti, A.1
Denecke, J.2
Miller, D.C.3
Schiffmann, H.4
Buhk, J.H.5
Grange, D.K.6
-
28
-
-
0141855200
-
The Chiari II malformation: cause and impact
-
McLone DG, Dias MS. The Chiari II malformation: cause and impact. Childs Nerv Syst. 2003;19(7-8):540-50.
-
(2003)
Childs Nerv Syst.
, vol.19
, Issue.7-8
, pp. 540-550
-
-
McLone, D.G.1
Dias, M.S.2
-
29
-
-
84856746278
-
Stridor at birth predicts poor outcome in neonates with myelomeningocele
-
Ocal E, Irwin B, Cochrane D, Singhal A, Steinbok P. Stridor at birth predicts poor outcome in neonates with myelomeningocele. Childs Nerv Syst. 2012; 28(2):265-71.
-
(2012)
Childs Nerv Syst.
, vol.28
, Issue.2
, pp. 265-271
-
-
Ocal, E.1
Irwin, B.2
Cochrane, D.3
Singhal, A.4
Steinbok, P.5
-
30
-
-
42449161550
-
The old and the new: supratentorial MR findings in Chiari II malformation
-
Miller E, Widjaja E, Blaser S, Dennis M, Raybaud C. The old and the new: supratentorial MR findings in Chiari II malformation. Childs Nerv Syst. 2008; 24(5):563-75.
-
(2008)
Childs Nerv Syst.
, vol.24
, Issue.5
, pp. 563-575
-
-
Miller, E.1
Widjaja, E.2
Blaser, S.3
Dennis, M.4
Raybaud, C.5
-
31
-
-
79952810327
-
A randomized trial of prenatal versus postnatal repair of myelomeningocele
-
Adzick NS, Thom EA, Spong CY, Brock 3rd JW, Burrows PK, Johnson MP, et al. A randomized trial of prenatal versus postnatal repair of myelomeningocele. N Engl J Med. 2011;364(11):993-1004.
-
(2011)
N Engl J Med.
, vol.364
, Issue.11
, pp. 993-1004
-
-
Adzick, N.S.1
Thom, E.A.2
Spong, C.Y.3
Brock, J.W.4
Burrows, P.K.5
Johnson, M.P.6
-
32
-
-
83855163426
-
Fetal endoscopic myelomeningocele closure preserves segmental neurological function
-
Verbeek RJ, Heep A, Maurits NM, Cremer R, Hoving EW, Brouwer OF, et al. Fetal endoscopic myelomeningocele closure preserves segmental neurological function. Dev Med Child Neurol. 2012;54(1):15-22.
-
(2012)
Dev Med Child Neurol
, vol.54
, Issue.1
, pp. 15-22
-
-
Verbeek, R.J.1
Heep, A.2
Maurits, N.M.3
Cremer, R.4
Hoving, E.W.5
Brouwer, O.F.6
-
33
-
-
84893734160
-
Solving glycosylation disorders: fundamental approaches reveal complicated pathways
-
Freeze HH, Chong JX, Bamshad MJ, Ng BG. Solving glycosylation disorders: fundamental approaches reveal complicated pathways. Am J Hum Genet. 2014;94(2):161-75.
-
(2014)
Am J Hum Genet
, vol.94
, Issue.2
, pp. 161-175
-
-
Freeze, H.H.1
Chong, J.X.2
Bamshad, M.J.3
Ng, B.G.4
-
34
-
-
84871749391
-
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a
-
Feraco P, Mirabelli-Badenier M, Severino M, Alpigiani MG, Di Rocco M, Biancheri R, et al. The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a. AJNR Am J Neuroradiol. 2012;33(11):2062-7.
-
(2012)
AJNR Am J Neuroradiol.
, vol.33
, Issue.11
, pp. 2062-2067
-
-
Feraco, P.1
Mirabelli-Badenier, M.2
Severino, M.3
Alpigiani, M.G.4
Di Rocco, M.5
Biancheri, R.6
-
35
-
-
0034097540
-
The Smith-Lemli-Opitz syndrome
-
Kelley RI, Hennekam RC. The Smith-Lemli-Opitz syndrome. J Med Genet. 2000;37(5):321-35.
-
(2000)
J Med Genet.
, vol.37
, Issue.5
, pp. 321-335
-
-
Kelley, R.I.1
Hennekam, R.C.2
-
36
-
-
84872893693
-
Neonatal neuroimaging findings in inborn errors of metabolism
-
Poretti A, Blaser SI, Lequin MH, Fatemi A, Meoded A, Northington FJ, et al. Neonatal neuroimaging findings in inborn errors of metabolism. J Magn Reson Imaging. 2013;37(2):294-312.
-
(2013)
J Magn Reson Imaging.
, vol.37
, Issue.2
, pp. 294-312
-
-
Poretti, A.1
Blaser, S.I.2
Lequin, M.H.3
Fatemi, A.4
Meoded, A.5
Northington, F.J.6
-
37
-
-
8844270815
-
Natural history of nonketotic hyperglycinemia in 65 patients
-
Hoover-Fong JE, Shah S, Van Hove JL, Applegarth D, Toone J, Hamosh A. Natural history of nonketotic hyperglycinemia in 65 patients. Neurology. 2004;63(10):1847-53.
-
(2004)
Neurology.
, vol.63
, Issue.10
, pp. 1847-1853
-
-
Hoover-Fong, J.E.1
Shah, S.2
Van Hove, J.L.3
Applegarth, D.4
Toone, J.5
Hamosh, A.6
-
38
-
-
0036264313
-
Diagnosis and treatment of maple syrup disease: a study of 36 patients
-
Morton DH, Strauss KA, Robinson DL, Puffenberger EG, Kelley RI. Diagnosis and treatment of maple syrup disease: a study of 36 patients. Pediatrics. 2002;109(6):999-1008.
-
(2002)
Pediatrics.
, vol.109
, Issue.6
, pp. 999-1008
-
-
Morton, D.H.1
Strauss, K.A.2
Robinson, D.L.3
Puffenberger, E.G.4
Kelley, R.I.5
-
39
-
-
0025910020
-
Cerebral edema causing death in children with maple syrup urine disease
-
Riviello Jr JJ, Rezvani I, DiGeorge AM, Foley CM. Cerebral edema causing death in children with maple syrup urine disease. J Pediatr. 1991;119(1 Pt 1):42-5.
-
(1991)
J Pediatr.
, vol.119
, Issue.1
, pp. 42-45
-
-
Riviello, J.J.1
Rezvani, I.2
DiGeorge, A.M.3
Foley, C.M.4
-
40
-
-
33746865225
-
Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease
-
Simon E, Fingerhut R, Baumkotter J, Konstantopoulou V, Ratschmann R, Wendel U. Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease. J Inherit Metab Dis. 2006;29(4):532-7.
-
(2006)
J Inherit Metab Dis.
, vol.29
, Issue.4
, pp. 532-537
-
-
Simon, E.1
Fingerhut, R.2
Baumkotter, J.3
Konstantopoulou, V.4
Ratschmann, R.5
Wendel, U.6
-
41
-
-
75349092696
-
Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis
-
Barnerias C, Saudubray JM, Touati G, De Lonlay P, Dulac O, Ponsot G, et al. Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis. Dev Med Child Neurol. 2010;52(2):e1-9.
-
(2010)
Dev Med Child Neurol.
, vol.52
, Issue.2
-
-
Barnerias, C.1
Saudubray, J.M.2
Touati, G.3
De Lonlay, P.4
Dulac, O.5
Ponsot, G.6
-
42
-
-
84872119988
-
Molybdenum cofactor deficiency: review of 12 cases (MoCD and review)
-
Bayram E, Topcu Y, Karakaya P, Yis U, Cakmakci H, Ichida K, et al. Molybdenum cofactor deficiency: review of 12 cases (MoCD and review). Eur J Paediatr Neurol. 2013;17(1):1-6.
-
(2013)
Eur J Paediatr Neurol.
, vol.17
, Issue.1
, pp. 1-6
-
-
Bayram, E.1
Topcu, Y.2
Karakaya, P.3
Yis, U.4
Cakmakci, H.5
Ichida, K.6
-
43
-
-
79960691564
-
Clinical and imaging observations in isolated sulfite oxidase deficiency
-
Bindu PS, Christopher R, Mahadevan A, Bharath RD. Clinical and imaging observations in isolated sulfite oxidase deficiency. J Child Neurol. 2011;26(8): 1036-40.
-
(2011)
J Child Neurol.
, vol.26
, Issue.8
, pp. 1036-1040
-
-
Bindu, P.S.1
Christopher, R.2
Mahadevan, A.3
Bharath, R.D.4
-
44
-
-
26944447862
-
Isolated sulphite oxidase deficiency mimics the features of hypoxic ischaemic encephalopathy
-
Hobson EE, Thomas S, Crofton PM, Murray AD, Dean JC, Lloyd D. Isolated sulphite oxidase deficiency mimics the features of hypoxic ischaemic encephalopathy. Eur J Pediatr. 2005;164(11):655-9.
-
(2005)
Eur J Pediatr.
, vol.164
, Issue.11
, pp. 655-659
-
-
Hobson, E.E.1
Thomas, S.2
Crofton, P.M.3
Murray, A.D.4
Dean, J.C.5
Lloyd, D.6
-
45
-
-
84867168772
-
Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMP
-
Hitzert MM, Bos AF, Bergman KA, Veldman A, Schwarz G, Santamaria-Araujo JA, et al. Favorable outcome in a newborn with molybdenum cofactor type A deficiency treated with cPMP. Pediatrics. 2012;130(4):e1005-10.
-
(2012)
Pediatrics.
, vol.130
, Issue.4
-
-
Hitzert, M.M.1
Bos, A.F.2
Bergman, K.A.3
Veldman, A.4
Schwarz, G.5
Santamaria-Araujo, J.A.6
-
46
-
-
67649432567
-
Pathogenesis of leukodystrophy for Krabbe disease: molecular mechanism and clinical treatment
-
Sakai N. Pathogenesis of leukodystrophy for Krabbe disease: molecular mechanism and clinical treatment. Brain Dev. 2009;31(7):485-7.
-
(2009)
Brain Dev.
, vol.31
, Issue.7
, pp. 485-487
-
-
Sakai, N.1
-
47
-
-
31144452232
-
Krabbe disease: severe neonatal presentation with a family history of multiple sclerosis
-
Sahai I, Baris H, Kimonis V, Levy HL. Krabbe disease: severe neonatal presentation with a family history of multiple sclerosis. J Child Neurol. 2005;20(10):826-8.
-
(2005)
J Child Neurol.
, vol.20
, Issue.10
, pp. 826-828
-
-
Sahai, I.1
Baris, H.2
Kimonis, V.3
Levy, H.L.4
-
48
-
-
44449119994
-
Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6
-
Falik-Zaccai TC, Laskar M, Kfir N, Nasser W, Slor H, Khayat M. Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6. Am J Med Genet A. 2008;146A(11):1423-9.
-
(2008)
Am J Med Genet A.
, vol.146
, Issue.11
, pp. 1423-1429
-
-
Falik-Zaccai, T.C.1
Laskar, M.2
Kfir, N.3
Nasser, W.4
Slor, H.5
Khayat, M.6
-
49
-
-
84858146268
-
Pelizaeus-Merzbacher disease, Pelizaeus-Merzbacher-like disease 1, and related hypomyelinating disorders
-
Hobson GM, Garbern JY. Pelizaeus-Merzbacher disease, Pelizaeus-Merzbacher-like disease 1, and related hypomyelinating disorders. Semin Neurol. 2012;32(1):62-7.
-
(2012)
Semin Neurol.
, vol.32
, Issue.1
, pp. 62-67
-
-
Hobson, G.M.1
Garbern, J.Y.2
-
50
-
-
71449108906
-
Aicardi-Goutieres syndrome: neuroradiologic findings and follow-up
-
Uggetti C, La Piana R, Orcesi S, Egitto MG, Crow YJ, Fazzi E. Aicardi-Goutieres syndrome: neuroradiologic findings and follow-up. AJNR Am J Neuroradiol. 2009;30(10):1971-6.
-
(2009)
AJNR Am J Neuroradiol.
, vol.30
, Issue.10
, pp. 1971-1976
-
-
Uggetti, C.1
La Piana, R.2
Orcesi, S.3
Egitto, M.G.4
Crow, Y.J.5
Fazzi, E.6
-
51
-
-
33745079623
-
Cathepsin D deficiency underlies congenital human neuronal ceroidlipofuscinosis
-
Siintola E, Partanen S, Stromme P, Haapanen A, Haltia M, Maehlen J, et al. Cathepsin D deficiency underlies congenital human neuronal ceroidlipofuscinosis. Brain. 2006;129(Pt 6):1438-45.
-
(2006)
Brain.
, vol.129
, pp. 1438-1445
-
-
Siintola, E.1
Partanen, S.2
Stromme, P.3
Haapanen, A.4
Haltia, M.5
Maehlen, J.6
-
52
-
-
84870464151
-
The ever expanding spinocerebellar ataxias
-
Matilla-Duenas A. The ever expanding spinocerebellar ataxias. Editorial Cerebellum. 2012;11(4):821-7.
-
(2012)
Editorial Cerebellum.
, vol.11
, Issue.4
, pp. 821-827
-
-
Matilla-Duenas, A.1
-
53
-
-
77950593139
-
Paediatric and adult autosomal dominant ataxias (update 6)
-
Morrison PJ. Paediatric and adult autosomal dominant ataxias (update 6). Eur J Paediatr Neurol. 2010;14(3):261-3.
-
(2010)
Eur J Paediatr Neurol.
, vol.14
, Issue.3
, pp. 261-263
-
-
Morrison, P.J.1
-
54
-
-
80155141553
-
Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms
-
Paciorkowski AR, Shafrir Y, Hrivnak J, Patterson MC, Tennison MB, Clark HB, et al. Massive expansion of SCA2 with autonomic dysfunction, retinitis pigmentosa, and infantile spasms. Neurology. 2011;77(11):1055-60.
-
(2011)
Neurology.
, vol.77
, Issue.11
, pp. 1055-1060
-
-
Paciorkowski, A.R.1
Shafrir, Y.2
Hrivnak, J.3
Patterson, M.C.4
Tennison, M.B.5
Clark, H.B.6
-
55
-
-
0032511743
-
Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion
-
Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. Am J Med Genet. 1998;79(5):383-7.
-
(1998)
Am J Med Genet.
, vol.79
, Issue.5
, pp. 383-387
-
-
Babovic-Vuksanovic, D.1
Snow, K.2
Patterson, M.C.3
Michels, V.V.4
-
56
-
-
18444411305
-
Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7
-
Mao R, Aylsworth AS, Potter N, Wilson WG, Breningstall G, Wick MJ, et al. Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7. Am J Med Genet. 2002;110(4):338-45.
-
(2002)
Am J Med Genet.
, vol.110
, Issue.4
, pp. 338-345
-
-
Mao, R.1
Aylsworth, A.S.2
Potter, N.3
Wilson, W.G.4
Breningstall, G.5
Wick, M.J.6
-
57
-
-
0031714729
-
Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype
-
Benton CS, de Silva R, Rutledge SL, Bohlega S, Ashizawa T, Zoghbi HY. Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype. Neurology. 1998;51(4):1081-6.
-
(1998)
Neurology.
, vol.51
, Issue.4
, pp. 1081-1086
-
-
Benton, C.S.1
de Silva, R.2
Rutledge, S.L.3
Bohlega, S.4
Ashizawa, T.5
Zoghbi, H.Y.6
-
58
-
-
0034798064
-
Striking anticipation in spinocerebellar ataxia type 7: the infantile phenotype
-
van de Warrenburg BP, Frenken CW, Ausems MG, Kleefstra T, Sinke RJ, Knoers NV, et al. Striking anticipation in spinocerebellar ataxia type 7: the infantile phenotype. J Neurol. 2001;248(10):911-4.
-
(2001)
J Neurol.
, vol.248
, Issue.10
, pp. 911-914
-
-
van de Warrenburg, B.P.1
Frenken, C.W.2
Ausems, M.G.3
Kleefstra, T.4
Sinke, R.J.5
Knoers, N.V.6
-
59
-
-
70349272701
-
Cerebellum of the premature infant: rapidly developing, vulnerable, clinically important
-
Volpe JJ. Cerebellum of the premature infant: rapidly developing, vulnerable, clinically important. J Child Neurol. 2009;24(9):1085-104.
-
(2009)
J Child Neurol.
, vol.24
, Issue.9
, pp. 1085-1104
-
-
Volpe, J.J.1
-
60
-
-
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(7):1659-67.
-
(2005)
AJNR Am J Neuroradiol.
, vol.26
, Issue.7
, pp. 1659-1667
-
-
Messerschmidt, A.1
Brugger, P.C.2
Boltshauser, E.3
Zoder, G.4
Sterniste, W.5
Birnbacher, R.6
-
61
-
-
84894265209
-
Injury to the premature cerebellum: outcome is related to remote cortical development
-
Limperopoulos C, Chilingaryan G, Sullivan N, Guizard N, Robertson RL, du Plessis AJ. Injury to the premature cerebellum: outcome is related to remote cortical development. Cereb Cortex. 2014;24(3):728-36.
-
(2014)
Cereb Cortex.
, vol.24
, Issue.3
, pp. 728-736
-
-
Limperopoulos, C.1
Chilingaryan, G.2
Sullivan, N.3
Guizard, N.4
Robertson, R.L.5
du Plessis, A.J.6
-
62
-
-
33644680177
-
Impaired trophic interactions between the cerebellum and the cerebrum among preterm infants
-
Limperopoulos C, Soul JS, Haidar H, Huppi PS, Bassan H, Warfield SK, et al. Impaired trophic interactions between the cerebellum and the cerebrum among preterm infants. Pediatrics. 2005;116(4):844-50.
-
(2005)
Pediatrics.
, vol.116
, Issue.4
, pp. 844-850
-
-
Limperopoulos, C.1
Soul, J.S.2
Haidar, H.3
Huppi, P.S.4
Bassan, H.5
Warfield, S.K.6
-
63
-
-
43149108450
-
Disrupted cerebellar development in preterm infants is associated with impaired neurodevelopmental outcome
-
Messerschmidt A, Fuiko R, Prayer D, Brugger PC, Boltshauser E, Zoder G, et al. Disrupted cerebellar development in preterm infants is associated with impaired neurodevelopmental outcome. Eur J Pediatr. 2008;167(10):1141-7.
-
(2008)
Eur J Pediatr.
, vol.167
, Issue.10
, pp. 1141-1147
-
-
Messerschmidt, A.1
Fuiko, R.2
Prayer, D.3
Brugger, P.C.4
Boltshauser, E.5
Zoder, G.6
-
64
-
-
84925465507
-
Developmental cerebellar cognitive affective syndrome in ex-preterm survivors following cerebellar injury
-
Brossard-Racine M, du Plessis AJ, Limperopoulos C. Developmental cerebellar cognitive affective syndrome in ex-preterm survivors following cerebellar injury. Cerebellum. 2015;14(2):151-64.
-
(2015)
Cerebellum.
, vol.14
, Issue.2
, pp. 151-164
-
-
Brossard-Racine, M.1
du Plessis, A.J.2
Limperopoulos, C.3
-
65
-
-
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(3):717-24.
-
(2005)
Pediatrics.
, vol.116
, Issue.3
, pp. 717-724
-
-
Limperopoulos, C.1
Benson, C.B.2
Bassan, H.3
Disalvo, D.N.4
Kinnamon, D.D.5
Moore, M.6
-
66
-
-
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(6):E62.
-
(1998)
Pediatrics.
, vol.102
, Issue.6
, pp. E62
-
-
Merrill, J.D.1
Piecuch, R.E.2
Fell, S.C.3
Barkovich, A.J.4
Goldstein, R.B.5
-
67
-
-
84892396450
-
Small cerebellar hemorrhage in preterm infants: perinatal and postnatal factors and outcome
-
Steggerda SJ, De Bruine FT, van den Berg-Huysmans AA, Rijken M, Leijser LM, Walther FJ, et al. Small cerebellar hemorrhage in preterm infants: perinatal and postnatal factors and outcome. Cerebellum. 2013;12(6):794-801.
-
(2013)
Cerebellum.
, vol.12
, Issue.6
, pp. 794-801
-
-
Steggerda, S.J.1
De Bruine, F.T.2
van den Berg-Huysmans, A.A.3
Rijken, M.4
Leijser, L.M.5
Walther, F.J.6
-
68
-
-
66349100970
-
Cerebellar injury in term infants: clinical characteristics, magnetic resonance imaging findings, and outcome
-
Limperopoulos C, Robertson RL, Sullivan NR, Bassan H, du Plessis AJ. Cerebellar injury in term infants: clinical characteristics, magnetic resonance imaging findings, and outcome. Pediatr Neurol. 2009;41(1):1-8.
-
(2009)
Pediatr Neurol.
, vol.41
, Issue.1
, pp. 1-8
-
-
Limperopoulos, C.1
Robertson, R.L.2
Sullivan, N.R.3
Bassan, H.4
du Plessis, A.J.5
-
69
-
-
78651473197
-
Cerebellar hemorrhage on magnetic resonance imaging in preterm newborns associated with abnormal neurologic outcome
-
Tam EW, Rosenbluth G, Rogers EE, Ferriero DM, Glidden D, Goldstein RB, et al. Cerebellar hemorrhage on magnetic resonance imaging in preterm newborns associated with abnormal neurologic outcome. J Pediatr. 2011; 158(2):245-50.
-
(2011)
J Pediatr.
, vol.158
, Issue.2
, pp. 245-250
-
-
Tam, E.W.1
Rosenbluth, G.2
Rogers, E.E.3
Ferriero, D.M.4
Glidden, D.5
Goldstein, R.B.6
-
70
-
-
34548383985
-
Does cerebellar injury in premature infants contribute to the high prevalence of long-term cognitive, learning, and behavioral disability in survivors?
-
Limperopoulos C, Bassan H, Gauvreau K, Robertson Jr RL, Sullivan NR, Benson CB, et al. Does cerebellar injury in premature infants contribute to the high prevalence of long-term cognitive, learning, and behavioral disability in survivors? Pediatrics. 2007;120(3):584-93.
-
(2007)
Pediatrics.
, vol.120
, Issue.3
, pp. 584-593
-
-
Limperopoulos, C.1
Bassan, H.2
Gauvreau, K.3
Robertson, R.L.4
Sullivan, N.R.5
Benson, C.B.6
-
71
-
-
80051770628
-
Neonatal cerebral sinovenous thrombosis: neuroimaging and long-term follow-up
-
Kersbergen KJ, Groenendaal F, Benders MJ, de Vries LS. Neonatal cerebral sinovenous thrombosis: neuroimaging and long-term follow-up. J Child Neurol. 2011;26(9):1111-20.
-
(2011)
J Child Neurol.
, vol.26
, Issue.9
, pp. 1111-1120
-
-
Kersbergen, K.J.1
Groenendaal, F.2
Benders, M.J.3
de Vries, L.S.4
-
72
-
-
0035833493
-
Cerebral sinovenous thrombosis in children
-
deVeber G, Andrew M, Adams C, Bjornson B, Booth F, Buckley DJ, et al. Cerebral sinovenous thrombosis in children. N Engl J Med. 2001;345(6):417-23.
-
(2001)
N Engl J Med.
, vol.345
, Issue.6
, pp. 417-423
-
-
deVeber, G.1
Andrew, M.2
Adams, C.3
Bjornson, B.4
Booth, F.5
Buckley, D.J.6
-
73
-
-
77954174188
-
Neonatal cerebral sinovenous thrombosis from symptom to outcome
-
Berfelo FJ, Kersbergen KJ, van Ommen CH, Govaert P, van Straaten HL, Poll-The BT, et al. Neonatal cerebral sinovenous thrombosis from symptom to outcome. Stroke. 2010;41(7):1382-8.
-
(2010)
Stroke.
, vol.41
, Issue.7
, pp. 1382-1388
-
-
Berfelo, F.J.1
Kersbergen, K.J.2
van Ommen, C.H.3
Govaert, P.4
van Straaten, H.L.5
Poll-The, B.T.6
-
74
-
-
80051707058
-
A prospective outcome study of neonatal cerebral sinovenous thrombosis
-
Moharir MD, Shroff M, Pontigon AM, Askalan R, Yau I, Macgregor D, et al. A prospective outcome study of neonatal cerebral sinovenous thrombosis. J Child Neurol. 2011;26(9):1137-44.
-
(2011)
J Child Neurol.
, vol.26
, Issue.9
, pp. 1137-1144
-
-
Moharir, M.D.1
Shroff, M.2
Pontigon, A.M.3
Askalan, R.4
Yau, I.5
Macgregor, D.6
-
75
-
-
0036557950
-
Cerebellar infarction: an unrecognized complication of very low birthweight
-
Johnsen SD, Tarby TJ, Lewis KS, Bird R, Prenger E. Cerebellar infarction: an unrecognized complication of very low birthweight. J Child Neurol. 2002;17(5):320-4.
-
(2002)
J Child Neurol.
, vol.17
, Issue.5
, pp. 320-324
-
-
Johnsen, S.D.1
Tarby, T.J.2
Lewis, K.S.3
Bird, R.4
Prenger, E.5
-
76
-
-
41849085134
-
Very early arterial ischemic stroke in premature infants
-
Golomb MR, Garg BP, Edwards-Brown M, Williams LS. Very early arterial ischemic stroke in premature infants. Pediatr Neurol. 2008;38(5):329-34.
-
(2008)
Pediatr Neurol.
, vol.38
, Issue.5
, pp. 329-334
-
-
Golomb, M.R.1
Garg, B.P.2
Edwards-Brown, M.3
Williams, L.S.4
-
77
-
-
84865596546
-
Neonatal encephalopathy: an inadequate term for hypoxicischemic encephalopathy
-
Volpe JJ. Neonatal encephalopathy: an inadequate term for hypoxicischemic encephalopathy. Ann Neurol. 2012;72(2):156-66.
-
(2012)
Ann Neurol.
, vol.72
, Issue.2
, pp. 156-166
-
-
Volpe, J.J.1
-
78
-
-
0346102595
-
Marked reduction of brainstem blood flow in artificially ventilated newborn piglets during normoxia and normocapnic hypoxia
-
Zwiener U, Walter B, Kratzsch B, Bauer R. Marked reduction of brainstem blood flow in artificially ventilated newborn piglets during normoxia and normocapnic hypoxia. Intensive Care Med. 2003;29(12):2277-84.
-
(2003)
Intensive Care Med.
, vol.29
, Issue.12
, pp. 2277-2284
-
-
Zwiener, U.1
Walter, B.2
Kratzsch, B.3
Bauer, R.4
-
79
-
-
33846420662
-
Selective vulnerability and the cerebellum in neonates
-
Castillo M. Selective vulnerability and the cerebellum in neonates. AJNR Am J Neuroradiol. 2007;28(1):20-1.
-
(2007)
AJNR Am J Neuroradiol.
, vol.28
, Issue.1
, pp. 20-21
-
-
Castillo, M.1
-
80
-
-
84940540191
-
Injury to the cerebellum in term asphyxiated newborns treated with hypothermia
-
Kwan S, Boudes E, Gilbert G, Saint-Martin C, Albrecht S, Shevell M, et al. Injury to the cerebellum in term asphyxiated newborns treated with hypothermia. AJNR Am J Neuroradiol. 2015;36(8):1542-9.
-
(2015)
AJNR Am J Neuroradiol.
, vol.36
, Issue.8
, pp. 1542-1549
-
-
Kwan, S.1
Boudes, E.2
Gilbert, G.3
Saint-Martin, C.4
Albrecht, S.5
Shevell, M.6
-
81
-
-
2942694514
-
Cerebellar vermian atrophy after neonatal hypoxic-ischemic encephalopathy
-
Sargent MA, Poskitt KJ, Roland EH, Hill A, Hendson G. Cerebellar vermian atrophy after neonatal hypoxic-ischemic encephalopathy. AJNR Am J Neuroradiol. 2004;25(6):1008-15.
-
(2004)
AJNR Am J Neuroradiol.
, vol.25
, Issue.6
, pp. 1008-1015
-
-
Sargent, M.A.1
Poskitt, K.J.2
Roland, E.H.3
Hill, A.4
Hendson, G.5
-
82
-
-
33846415492
-
Involvement of the anterior lobe of the cerebellar vermis in perinatal profound hypoxia
-
Connolly DJ, Widjaja E, Griffiths PD. Involvement of the anterior lobe of the cerebellar vermis in perinatal profound hypoxia. AJNR Am J Neuroradiol. 2007;28(1):16-9.
-
(2007)
AJNR Am J Neuroradiol.
, vol.28
, Issue.1
, pp. 16-19
-
-
Connolly, D.J.1
Widjaja, E.2
Griffiths, P.D.3
-
83
-
-
1642278075
-
MR imaging quantification of cerebellar growth following hypoxic-ischemic injury to the neonatal brain
-
Le Strange E, Saeed N, Cowan FM, Edwards AD, Rutherford MA. MR imaging quantification of cerebellar growth following hypoxic-ischemic injury to the neonatal brain. AJNR Am J Neuroradiol. 2004;25(3):463-8.
-
(2004)
AJNR Am J Neuroradiol.
, vol.25
, Issue.3
, pp. 463-468
-
-
Le Strange, E.1
Saeed, N.2
Cowan, F.M.3
Edwards, A.D.4
Rutherford, M.A.5
-
84
-
-
2442486655
-
The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infection
-
de Vries LS, Gunardi H, Barth PG, Bok LA, Verboon-Maciolek MA, Groenendaal F. The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infection. Neuropediatrics. 2004;35(2):113-9.
-
(2004)
Neuropediatrics.
, vol.35
, Issue.2
, pp. 113-119
-
-
de Vries, L.S.1
Gunardi, H.2
Barth, P.G.3
Bok, L.A.4
Verboon-Maciolek, M.A.5
Groenendaal, F.6
-
85
-
-
84925389915
-
Neuro-imaging findings in infants with congenital cytomegalovirus infection: relation to trimester of infection
-
Oosterom N, Nijman J, Gunkel J, Wolfs TF, Groenendaal F, Verboon-Maciolek MA, et al. Neuro-imaging findings in infants with congenital cytomegalovirus infection: relation to trimester of infection. Neonatology. 2015;107(4):289-96.
-
(2015)
Neonatology.
, vol.107
, Issue.4
, pp. 289-296
-
-
Oosterom, N.1
Nijman, J.2
Gunkel, J.3
Wolfs, T.F.4
Groenendaal, F.5
Verboon-Maciolek, M.A.6
-
86
-
-
41149084449
-
Imaging findings of neonatal herpes simplex virus type 2 encephalitis
-
Vossough A, Zimmerman RA, Bilaniuk LT, Schwartz EM. Imaging findings of neonatal herpes simplex virus type 2 encephalitis. Neuroradiology. 2008; 50(4):355-66.
-
(2008)
Neuroradiology.
, vol.50
, Issue.4
, pp. 355-366
-
-
Vossough, A.1
Zimmerman, R.A.2
Bilaniuk, L.T.3
Schwartz, E.M.4
-
87
-
-
0021307174
-
The neonatal cerebellum: the highest level of glucocorticoid receptors in the brain
-
Pavlik A, Buresova M. The neonatal cerebellum: the highest level of glucocorticoid receptors in the brain. Brain Res. 1984;314(1):13-20.
-
(1984)
Brain Res.
, vol.314
, Issue.1
, pp. 13-20
-
-
Pavlik, A.1
Buresova, M.2
-
88
-
-
84941196295
-
Glucocorticoid induced cerebellar toxicity in the developing neonate: implications for glucocorticoid therapy during bronchopulmonary dysplasia
-
Noguchi KK. Glucocorticoid induced cerebellar toxicity in the developing neonate: implications for glucocorticoid therapy during bronchopulmonary dysplasia. Cells. 2014;3(1):36-52.
-
(2014)
Cells.
, vol.3
, Issue.1
, pp. 36-52
-
-
Noguchi, K.K.1
-
89
-
-
33947161432
-
Postnatal dexamethasone therapy and cerebral tissue volumes in extremely low birth weight infants
-
Parikh NA, Lasky RE, Kennedy KA, Moya FR, Hochhauser L, Romo S, et al. Postnatal dexamethasone therapy and cerebral tissue volumes in extremely low birth weight infants. Pediatrics. 2007;119(2):265-72.
-
(2007)
Pediatrics.
, vol.119
, Issue.2
, pp. 265-272
-
-
Parikh, N.A.1
Lasky, R.E.2
Kennedy, K.A.3
Moya, F.R.4
Hochhauser, L.5
Romo, S.6
-
90
-
-
80054790955
-
Preterm cerebellar growth impairment after postnatal exposure to glucocorticoids
-
Tam EW, Chau V, Ferriero DM, Barkovich AJ, Poskitt KJ, Studholme C, et al. Preterm cerebellar growth impairment after postnatal exposure to glucocorticoids. Sci Transl Med. 2011;3(105):105ra.
-
(2011)
Sci Transl Med.
, vol.3
, Issue.105
, pp. 105ra
-
-
Tam, E.W.1
Chau, V.2
Ferriero, D.M.3
Barkovich, A.J.4
Poskitt, K.J.5
Studholme, C.6
-
91
-
-
0141520486
-
Fetal brain tumors
-
Cavalheiro S, Moron AF, Hisaba W, Dastoli P, Silva NS. Fetal brain tumors. Childs Nerv Syst. 2003;19(7-8):529-36.
-
(2003)
Childs Nerv Syst.
, vol.19
, Issue.7-8
, pp. 529-536
-
-
Cavalheiro, S.1
Moron, A.F.2
Hisaba, W.3
Dastoli, P.4
Silva, N.S.5
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