-
1
-
-
0029117167
-
Multiple lentigines (Leopard) syndrome with Chiari I malformation
-
Agha A, Hashimoto K: Multiple lentigines (Leopard) syndrome with Chiari I malformation. J Dermatol 22:520-523, 1995
-
(1995)
J Dermatol
, vol.22
, pp. 520-523
-
-
Agha, A.1
Hashimoto, K.2
-
2
-
-
0027246570
-
Lipomyeloschisis associated with thoracic syringomyelia and Chiari I malformation
-
Aguilera Grijalvo C, Bank WO, Balériaux D, Matos C, Imaña FJ, Szliwowski HB, et al: Lipomyeloschisis associated with thoracic syringomyelia and Chiari I malformation. Neuroradiology 35:375-377, 1993
-
(1993)
Neuroradiology
, vol.35
, pp. 375-377
-
-
Aguilera Grijalvo, C.1
Bank, W.O.2
Balériaux, D.3
Matos, C.4
Imaña, F.J.5
Szliwowski, H.B.6
-
3
-
-
0029166346
-
Posterior fossa volume and response to suboccipital decompression in patients with Chiari I malformation
-
Badie B, Mendoza D, Batzdorf U: Posterior fossa volume and response to suboccipital decompression in patients with Chiari I malformation. Neurosurgery 37:214-218, 1995
-
(1995)
Neurosurgery
, vol.37
, pp. 214-218
-
-
Badie, B.1
Mendoza, D.2
Batzdorf, U.3
-
4
-
-
0029587580
-
Operative resection of 100 spinal lipomas in infants less than 1 year of age
-
Byrne RW, Hayes EA, George TM, McLone DG: Operative resection of 100 spinal lipomas in infants less than 1 year of age. Pediatr Neurosurg 23:182-187, 1995
-
(1995)
Pediatr Neurosurg
, vol.23
, pp. 182-187
-
-
Byrne, R.W.1
Hayes, E.A.2
George, T.M.3
McLone, D.G.4
-
5
-
-
0029030287
-
Chiari I malformation: association with hypophosphatemic rickets and MR imaging appearance
-
Caldemeyer KS, Boaz JC, Wappner RS, Moran CC, Smith RR, Quets JP: Chiari I malformation: association with hypophosphatemic rickets and MR imaging appearance. Radiology 195:733-738, 1995
-
(1995)
Radiology
, vol.195
, pp. 733-738
-
-
Caldemeyer, K.S.1
Boaz, J.C.2
Wappner, R.S.3
Moran, C.C.4
Smith, R.R.5
Quets, J.P.6
-
6
-
-
0033869375
-
Antley-Bixler syndrome associated with Arnold-Chiari malformation
-
Chang YT, Tsai FJ, Shen WC, Lin HC, Peng CT, Tsai CH: Antley-Bixler syndrome associated with Arnold-Chiari malformation. Acta Paediatr 89:737-739, 2000
-
(2000)
Acta Paediatr
, vol.89
, pp. 737-739
-
-
Chang, Y.T.1
Tsai, F.J.2
Shen, W.C.3
Lin, H.C.4
Peng, C.T.5
Tsai, C.H.6
-
7
-
-
34548002960
-
Veranderungen des kleinhirns infolge von hydrocephaliedes grosshirns
-
Chiari H: Veranderungen des kleinhirns infolge von hydrocephaliedes grosshirns. Deutsche Medicinische Wochenschrigt 17:1172-1175, 1891
-
(1891)
Deutsche Medicinische Wochenschrigt
, vol.17
, pp. 1172-1175
-
-
Chiari, H.1
-
8
-
-
0029101376
-
Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture
-
Cinalli G, Renier D, Sebag G, Sainte-Rose C, Arnaud E, Pierre-Kahn A: Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture. J Neurosurg 83:575-582, 1995
-
(1995)
J Neurosurg
, vol.83
, pp. 575-582
-
-
Cinalli, G.1
Renier, D.2
Sebag, G.3
Sainte-Rose, C.4
Arnaud, E.5
Pierre-Kahn, A.6
-
9
-
-
26044481756
-
Chiari malformation in craniosynostosis
-
Cinalli G, Spennato P, Sainte-Rose C, Arnaud E, Aliberti F, Brunelle F, et al: Chiari malformation in craniosynostosis. Childs Nerv Syst 21:889-901, 2005
-
(2005)
Childs Nerv Syst
, vol.21
, pp. 889-901
-
-
Cinalli, G.1
Spennato, P.2
Sainte-Rose, C.3
Arnaud, E.4
Aliberti, F.5
Brunelle, F.6
-
10
-
-
11344253459
-
Symptomatic Chiari I malformation in Kabuki syndrome
-
Ciprero KL, Clayton-Smith J, Donnai D, Zimmerman RA, Zackai EH, Ming JE: Symptomatic Chiari I malformation in Kabuki syndrome. Am J Med Genet A 132A:273-275, 2005
-
(2005)
Am J Med Genet A
, vol.132 A
, pp. 273-275
-
-
Ciprero, K.L.1
Clayton-Smith, J.2
Donnai, D.3
Zimmerman, R.A.4
Zackai, E.H.5
Ming, J.E.6
-
11
-
-
0032427328
-
Phacomatosis pigmentovascularis type II
-
Du LC, Delaporte E, Catteau B, Destee A, Piette F: Phacomatosis pigmentovascularis type II. Eur J Dermatol 8:569-572, 1998
-
(1998)
Eur J Dermatol
, vol.8
, pp. 569-572
-
-
Du, L.C.1
Delaporte, E.2
Catteau, B.3
Destee, A.4
Piette, F.5
-
12
-
-
0026747092
-
Chiari I malformations: clinical and radiologic reappraisal
-
Elster AD, Chen MY: Chiari I malformations: clinical and radiologic reappraisal. Radiology 183:347-353, 1992
-
(1992)
Radiology
, vol.183
, pp. 347-353
-
-
Elster, A.D.1
Chen, M.Y.2
-
13
-
-
34548756087
-
Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients
-
Ferrero GB, Biamino E, Sorasio L, Banaudi E, Peruzzi L, Forzano S, et al: Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients. Eur J Med Genet 50:327-337, 2007
-
(2007)
Eur J Med Genet
, vol.50
, pp. 327-337
-
-
Ferrero, G.B.1
Biamino, E.2
Sorasio, L.3
Banaudi, E.4
Peruzzi, L.5
Forzano, S.6
-
14
-
-
0028142517
-
Giant congenital melanocytic nevi: brain magnetic resonance findings in neurologically asymptomatic children
-
Frieden IJ, Williams ML, Barkovich AJ: Giant congenital melanocytic nevi: brain magnetic resonance findings in neurologically asymptomatic children. J Am Acad Dermatol 31: 423-429, 1994
-
(1994)
J Am Acad Dermatol
, vol.31
, pp. 423-429
-
-
Frieden, I.J.1
Williams, M.L.2
Barkovich, A.J.3
-
15
-
-
78651188990
-
Hydrodynamic mechanism of syringomyelia: its relationship to myelocele
-
Gardner WJ: Hydrodynamic mechanism of syringomyelia: its relationship to myelocele. J Neurol Neurosurg Psychiatry 28:247-259, 1965
-
(1965)
J Neurol Neurosurg Psychiatry
, vol.28
, pp. 247-259
-
-
Gardner, W.J.1
-
16
-
-
33749252898
-
Chiari type I malformation in four unrelated patients affected with Fabry disease
-
Germain DP, Benistan K, Halimi P: Chiari type I malformation in four unrelated patients affected with Fabry disease. Eur J Med Genet 49:419-425, 2006
-
(2006)
Eur J Med Genet
, vol.49
, pp. 419-425
-
-
Germain, D.P.1
Benistan, K.2
Halimi, P.3
-
17
-
-
0032546209
-
Shprintzen-Goldberg syndrome: a clinical analysis
-
Greally MT, Carey JC, Milewicz DM, Hudgins L, Goldberg RB, Shprintzen RJ, et al: Shprintzen-Goldberg syndrome: a clinical analysis. Am J Med Genet 76:202-212, 1998
-
(1998)
Am J Med Genet
, vol.76
, pp. 202-212
-
-
Greally, M.T.1
Carey, J.C.2
Milewicz, D.M.3
Hudgins, L.4
Goldberg, R.B.5
Shprintzen, R.J.6
-
18
-
-
0031045780
-
Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda
-
Gripp KW, Scott CI Jr, Nicholson L, Magram G, Grissom LE: Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda. Skeletal Radiol 26:131-133, 1997
-
(1997)
Skeletal Radiol
, vol.26
, pp. 131-133
-
-
Gripp, K.W.1
Scott Jr., C.I.2
Nicholson, L.3
Magram, G.4
Grissom, L.E.5
-
19
-
-
34247103211
-
CHERI: time to identify the syndrome?
-
Haapanen ML: CHERI: time to identify the syndrome? J Craniofac Surg 18:369-373, 2007
-
(2007)
J Craniofac Surg
, vol.18
, pp. 369-373
-
-
Haapanen, M.L.1
-
20
-
-
0031733089
-
Familial growth hormone deficiency associated with MRI abnormalities
-
Hamilton J, Chitayat D, Blaser S, Cohen LE, Phillips JA III, Daneman D: Familial growth hormone deficiency associated with MRI abnormalities. Am J Med Genet 80:128-132, 1998
-
(1998)
Am J Med Genet
, vol.80
, pp. 128-132
-
-
Hamilton, J.1
Chitayat, D.2
Blaser, S.3
Cohen, L.E.4
Phillips III, J.A.5
Daneman, D.6
-
22
-
-
0037404516
-
Rapid development of Chiari I malformation in an infant with Seckel syndrome and craniosynostosis. Case report and review of the literature
-
Hopkins TE, Haines SJ: Rapid development of Chiari I malformation in an infant with Seckel syndrome and craniosynostosis. Case report and review of the literature. J Neurosurg 98:1113-1115, 2003
-
(2003)
J Neurosurg
, vol.98
, pp. 1113-1115
-
-
Hopkins, T.E.1
Haines, S.J.2
-
23
-
-
17144474019
-
Paget's disease of bone and basilar impression associated with an Arnold-Chiari type I malformation
-
(Span)
-
Iglesias-Osma C, Gómez Sánchez JC, Suquia Múgica B, Querol Prieto R, de Portugal Alvarez J: [Paget's disease of bone and basilar impression associated with an Arnold-Chiari type I malformation.] An Med Interna 14:519-522, 1997 (Span)
-
(1997)
An Med Interna
, vol.14
, pp. 519-522
-
-
Iglesias-Osma, C.1
Gómez Sánchez, J.C.2
Suquia Múgica, B.3
Querol Prieto, R.4
de Portugal Alvarez, J.5
-
24
-
-
0027234483
-
Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes
-
Kreiborg S, Marsh JL, Cohen MM Jr, Liversage M, Pedersen H, Skovby F, et al: Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. J Craniomaxillofac Surg 21:181-188, 1993
-
(1993)
J Craniomaxillofac Surg
, vol.21
, pp. 181-188
-
-
Kreiborg, S.1
Marsh, J.L.2
Cohen Jr., M.M.3
Liversage, M.4
Pedersen, H.5
Skovby, F.6
-
25
-
-
0031969132
-
Chiari malformation associated with vitamin D-resistant rickets: case report
-
Kuether TA, Piatt JH: Chiari malformation associated with vitamin D-resistant rickets: case report. Neurosurgery 42:1168-1171, 1998
-
(1998)
Neurosurgery
, vol.42
, pp. 1168-1171
-
-
Kuether, T.A.1
Piatt, J.H.2
-
26
-
-
34248152560
-
Osteopetrosis with Arnold Chiari malformation type I and brain stem compression
-
Kulkarni ML, Marakkanavar SN, Sushanth S, Pradeep N, Ashok C, Balaji MD, et al: Osteopetrosis with Arnold Chiari malformation type I and brain stem compression. Indian J Pediatr 74:412-415, 2007
-
(2007)
Indian J Pediatr
, vol.74
, pp. 412-415
-
-
Kulkarni, M.L.1
Marakkanavar, S.N.2
Sushanth, S.3
Pradeep, N.4
Ashok, C.5
Balaji, M.D.6
-
27
-
-
0030934497
-
Interferon alpha-2a therapy for disseminatedintravascular coagulation in a patient with blue rubber bleb nevus syndrome. A case report
-
Kunishige M, Azuma H, Masuda K, Shigekiyo T, Arii Y, Kawai H, et al: Interferon alpha-2a therapy for disseminatedintravascular coagulation in a patient with blue rubber bleb nevus syndrome. A case report. Angiology 48:273-277, 1997
-
(1997)
Angiology
, vol.48
, pp. 273-277
-
-
Kunishige, M.1
Azuma, H.2
Masuda, K.3
Shigekiyo, T.4
Arii, Y.5
Kawai, H.6
-
28
-
-
0038607574
-
Pierre-Robin syndrome associated with Chiari type I malformation
-
Lee J, Hida K, Seki T, Kitamura J, Iwasaki Y: Pierre-Robin syndrome associated with Chiari type I malformation. Childs Nerv Syst 19:380-383, 2003
-
(2003)
Childs Nerv Syst
, vol.19
, pp. 380-383
-
-
Lee, J.1
Hida, K.2
Seki, T.3
Kitamura, J.4
Iwasaki, Y.5
-
29
-
-
85031525070
-
Growth hormone deficiency in Costello syndrome: a possible explanation for the short stature
-
Legault L, Gagnon C, Lapointe N: Growth hormone deficiency in Costello syndrome: a possible explanation for the short stature. J Pediatr 138:151-152, 2001
-
(2001)
J Pediatr
, vol.138
, pp. 151-152
-
-
Legault, L.1
Gagnon, C.2
Lapointe, N.3
-
30
-
-
0020580505
-
Chiari malformation presenting in adults: a surgical experience in 127 cases
-
Levy WJ, Mason L, Hahn JF: Chiari malformation presenting in adults: a surgical experience in 127 cases. Neurosurgery 12:377-390, 1983
-
(1983)
Neurosurgery
, vol.12
, pp. 377-390
-
-
Levy, W.J.1
Mason, L.2
Hahn, J.F.3
-
31
-
-
44949163238
-
Hans Chiari (1851-1916)
-
Loukas M, Noordeh N, Shoja MM, Pugh J, Oakes WJ, Tubbs RS: Hans Chiari (1851-1916). Childs Nerv Syst 24:407-409, 2008
-
(2008)
Childs Nerv Syst
, vol.24
, pp. 407-409
-
-
Loukas, M.1
Noordeh, N.2
Shoja, M.M.3
Pugh, J.4
Oakes, W.J.5
Tubbs, R.S.6
-
32
-
-
0019455844
-
Morphogenesis of experimentally induced Arnold-Chiari malformation
-
Marin-Padilla M, Marin-Padilla TM: Morphogenesis of experimentally induced Arnold-Chiari malformation. J Neurol Sci 50:29-55, 1981
-
(1981)
J Neurol Sci
, vol.50
, pp. 29-55
-
-
Marin-Padilla, M.1
Marin-Padilla, T.M.2
-
33
-
-
0030390182
-
Jugular foraminal stenosis in Crouzon syndrome
-
Martinez-Perez D, Vander Woude DL, Barnes PD, Scott RM, Mulliken JB: Jugular foraminal stenosis in Crouzon syndrome. Pediatr Neurosurg 25:252-255, 1996
-
(1996)
Pediatr Neurosurg
, vol.25
, pp. 252-255
-
-
Martinez-Perez, D.1
Vander Woude, D.L.2
Barnes, P.D.3
Scott, R.M.4
Mulliken, J.B.5
-
34
-
-
0034117079
-
Asymptomatic Chiari Type I malformations identified on magnetic resonance imaging
-
Meadows J, Kraut M, Guarnieri M, Haroun RI, Carson BS: Asymptomatic Chiari Type I malformations identified on magnetic resonance imaging. J Neurosurg 92:920-926, 2000
-
(2000)
J Neurosurg
, vol.92
, pp. 920-926
-
-
Meadows, J.1
Kraut, M.2
Guarnieri, M.3
Haroun, R.I.4
Carson, B.S.5
-
35
-
-
37349101954
-
Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue
-
Milhorat TH, Bolognese PA, Nishikawa M, McDonnell NB, Francomano CA: Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue. J Neurosurg Spine 7:601-609, 2007
-
(2007)
J Neurosurg Spine
, vol.7
, pp. 601-609
-
-
Milhorat, T.H.1
Bolognese, P.A.2
Nishikawa, M.3
McDonnell, N.B.4
Francomano, C.A.5
-
36
-
-
0032907185
-
Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients
-
Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, et al: Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44:1005-1017, 1999
-
(1999)
Neurosurgery
, vol.44
, pp. 1005-1017
-
-
Milhorat, T.H.1
Chou, M.W.2
Trinidad, E.M.3
Kula, R.W.4
Mandell, M.5
Wolpert, C.6
-
38
-
-
0029078213
-
A case of achondroplasia with downward displacement of the brain stem
-
Nakai T, Asato R, Miki Y, Tanaka F, Matsumoto S, Konishi J: A case of achondroplasia with downward displacement of the brain stem. Neuroradiology 37:293-294, 1995
-
(1995)
Neuroradiology
, vol.37
, pp. 293-294
-
-
Nakai, T.1
Asato, R.2
Miki, Y.3
Tanaka, F.4
Matsumoto, S.5
Konishi, J.6
-
39
-
-
0033663937
-
Chiari type I malformation in children and adolescents with cystic fibrosis
-
Needleman JP, Panitch HB, Bierbrauer KS, Schidlow DV: Chiari type I malformation in children and adolescents with cystic fibrosis. Pediatr Pulmonol 30:490-492, 2000
-
(2000)
Pediatr Pulmonol
, vol.30
, pp. 490-492
-
-
Needleman, J.P.1
Panitch, H.B.2
Bierbrauer, K.S.3
Schidlow, D.V.4
-
40
-
-
0025557184
-
Chiari I malformation: a review of 43 patients
-
Nohria V, Oakes WJ: Chiari I malformation: a review of 43 patients. Pediatr Neurosurg 16:222-227, 1990-1991
-
(1990)
Pediatr Neurosurg
, vol.16
, pp. 222-227
-
-
Nohria, V.1
Oakes, W.J.2
-
41
-
-
0034056709
-
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies
-
Nye JS, Hayes EA, Amendola M, Vaughn D, Charrow J, McLone DG, et al: Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies. Teratology 61:165-171, 2000
-
(2000)
Teratology
, vol.61
, pp. 165-171
-
-
Nye, J.S.1
Hayes, E.A.2
Amendola, M.3
Vaughn, D.4
Charrow, J.5
McLone, D.G.6
-
42
-
-
0003383022
-
Chiari malformations, hydromyelia, syringomyelia
-
Wilkins RH, Rengachary SS (eds): ed 2. New York: McGraw-Hill
-
Oakes WJ: Chiari malformations, hydromyelia, syringomyelia, in Wilkins RH, Rengachary SS (eds): Neurosurgery, ed, New York: McGraw-Hill, 1996, pp 3593-3616
-
(1996)
Neurosurgery
, pp. 3593-3616
-
-
Oakes, W.J.1
-
43
-
-
0001707285
-
The Chiari malformations of the child
-
Menezes AH, Sonntag VKH (eds): New York: McGraw-Hill
-
Oakes WJ: The Chiari malformations of the child, in Menezes AH, Sonntag VKH (eds): Principles of Spinal Surgery. New York: McGraw-Hill, 1996, Vol 1, pp 379-394
-
(1996)
Principles of Spinal Surgery
, vol.1
, pp. 379-394
-
-
Oakes, W.J.1
-
44
-
-
1842836249
-
Chiari malformations
-
Winn HR (ed): ed 5. Philadelphia: Saunders
-
Oakes WJ, Tubbs RS: Chiari malformations, in Winn HR (ed): Youmans Neurological Surgery, ed 5. Philadelphia: Saunders, 2004, pp 3347-3361
-
(2004)
Youmans Neurological Surgery
, pp. 3347-3361
-
-
Oakes, W.J.1
Tubbs, R.S.2
-
45
-
-
0031034034
-
Resolution of acquired tonsillar herniation after resection of supratentorial meningioma. Case illustration
-
Onesti ST, Ashkenazi E, Miller AM, Michelsen WJ: Resolution of acquired tonsillar herniation after resection of supratentorial meningioma. Case illustration. J Neurosurg 86:572, 1997
-
(1997)
J Neurosurg
, vol.86
, pp. 572
-
-
Onesti, S.T.1
Ashkenazi, E.2
Miller, A.M.3
Michelsen, W.J.4
-
46
-
-
0029004086
-
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
-
Park WJ, Meyers GA, Li X, Theda C, Day D, Orlow SJ, et al: Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability. Hum Mol Genet 4:1229-1233, 1995
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1229-1233
-
-
Park, W.J.1
Meyers, G.A.2
Li, X.3
Theda, C.4
Day, D.5
Orlow, S.J.6
-
47
-
-
0020693645
-
Arnold-Chiari malformation. Review of 71 cases
-
Paul KS, Lye RH, Strang FA, Dutton J: Arnold-Chiari malformation. Review of 71 cases. J Neurosurg 58:183-187, 1983
-
(1983)
J Neurosurg
, vol.58
, pp. 183-187
-
-
Paul, K.S.1
Lye, R.H.2
Strang, F.A.3
Dutton, J.4
-
48
-
-
0028942218
-
Association of Chiari I malformation and Williams syndrome
-
Pober BR, Filiano JJ: Association of Chiari I malformation and Williams syndrome. Pediatr Neurol 12:84-88, 1995
-
(1995)
Pediatr Neurol
, vol.12
, pp. 84-88
-
-
Pober, B.R.1
Filiano, J.J.2
-
49
-
-
33846898033
-
Chiari-like tonsillar herniation associated with intracranial hypotension in Marfan syndrome. Case report
-
Puget S, Kondageski C, Wray A, Boddaert N, Roujeau T, Di Rocco F, et al: Chiari-like tonsillar herniation associated with intracranial hypotension in Marfan syndrome. Case report. J Neurosurg 106 (1 Suppl):48-52, 2007
-
(2007)
J Neurosurg
, vol.106
, Issue.1 SUPPL.
, pp. 48-52
-
-
Puget, S.1
Kondageski, C.2
Wray, A.3
Boddaert, N.4
Roujeau, T.5
Di Rocco, F.6
-
50
-
-
77952822481
-
Chiari type 1 malformation in an infant with type 2 Pfeiffer syndrome: further evidence of acquired pathogenesis
-
Ranger A, Al-Hayek A, Matic D: Chiari type 1 malformation in an infant with type 2 Pfeiffer syndrome: further evidence of acquired pathogenesis. J Craniofac Surg 21:427-431, 2010
-
(2010)
J Craniofac Surg
, vol.21
, pp. 427-431
-
-
Ranger, A.1
Al-Hayek, A.2
Matic, D.3
-
51
-
-
0030930503
-
Craniocephalic disproportion with increased intracranial pressure and brain herniation: a new clinical syndrome in anemic patients: report of two cases
-
Rengachary SS, Blount J, Heros D, Bowers S, Truwit C: Craniocephalic disproportion with increased intracranial pressure and brain herniation: a new clinical syndrome in anemic patients: report of two cases. Neurosurgery 41:297-304, 1997
-
(1997)
Neurosurgery
, vol.41
, pp. 297-304
-
-
Rengachary, S.S.1
Blount, J.2
Heros, D.3
Bowers, S.4
Truwit, C.5
-
52
-
-
0031203577
-
Oxycephaly, a severe craniosynostosis. Apropos of a series of 129 cases
-
(Fr)
-
Renier D, Cinalli G, Lajeunie E, Arnaud E, Marchac D: [Oxycephaly, a severe craniosynostosis. Apropos of a series of 129 cases.] Arch Pediatr 4:722-729, 1997 (Fr)
-
(1997)
Arch Pediatr
, vol.4
, pp. 722-729
-
-
Renier, D.1
Cinalli, G.2
Lajeunie, E.3
Arnaud, E.4
Marchac, D.5
-
53
-
-
0035118066
-
Paget's disease causing an Arnold-Chiari Type 1 malformation: radiographic findings
-
Richards PS, Bargiota A, Corrall RJ: Paget's disease causing an Arnold-Chiari Type 1 malformation: radiographic findings. AJR Am J Roentgenol 176:816-817, 2001
-
(2001)
AJR Am J Roentgenol
, vol.176
, pp. 816-817
-
-
Richards, P.S.1
Bargiota, A.2
Corrall, R.J.3
-
54
-
-
0025147378
-
Analysis of craniofacial growth in Crouzon syndrome using landmark data
-
Richtsmeier JT, Lele S: Analysis of craniofacial growth in Crouzon syndrome using landmark data. J Craniofac Genet Dev Biol 10:39-62, 1990
-
(1990)
J Craniofac Genet Dev Biol
, vol.10
, pp. 39-62
-
-
Richtsmeier, J.T.1
Lele, S.2
-
55
-
-
31344477933
-
Tethered cord syndrome
-
Rinaldi F, Cioffi FA, Columbano L, Krasagakis G, Bernini FP: Tethered cord syndrome. J Neurosurg Sci 49:131-135, 2005
-
(2005)
J Neurosurg Sci
, vol.49
, pp. 131-135
-
-
Rinaldi, F.1
Cioffi, F.A.2
Columbano, L.3
Krasagakis, G.4
Bernini, F.P.5
-
57
-
-
70349218593
-
Neuroradiologic manifestations of Loeys-Dietz syndrome type 1
-
Rodrigues VJ, Elsayed S, Loeys BL, Dietz HC, Yousem DM: Neuroradiologic manifestations of Loeys-Dietz syndrome type 1. AJNR Am J Neuroradiol 30:1614-1619, 2009
-
(2009)
AJNR Am J Neuroradiol
, vol.30
, pp. 1614-1619
-
-
Rodrigues, V.J.1
Elsayed, S.2
Loeys, B.L.3
Dietz, H.C.4
Yousem, D.M.5
-
59
-
-
0023491178
-
The incidence of craniocervical bony anomalies in the adult Chiari malformation
-
Schady W, Metcalfe RA, Butler P: The incidence of craniocervical bony anomalies in the adult Chiari malformation. J Neurol Sci 82:193-203, 1987
-
(1987)
J Neurol Sci
, vol.82
, pp. 193-203
-
-
Schady, W.1
Metcalfe, R.A.2
Butler, P.3
-
60
-
-
34548672877
-
The co-occurrence of Chiari type 1 malformation with syringomyelia and total situs inversus
-
Serarslan Y, Melek IM, Duman T, Eraslan T, Akdemir G, Yalçin F: The co-occurrence of Chiari type 1 malformation with syringomyelia and total situs inversus. Med Sci Monit 13:CS110-CS113, 2007
-
(2007)
Med Sci Monit
, vol.13
-
-
Serarslan, Y.1
Melek, I.M.2
Duman, T.3
Eraslan, T.4
Akdemir, G.5
Yalçin, F.6
-
61
-
-
38549122393
-
Foramen magnum decompression and expansile duroplasty for acquired Chiari type I malformation in craniometaphyseal dysplasia
-
Sewell MD, Akram H, Wadley J: Foramen magnum decompression and expansile duroplasty for acquired Chiari type I malformation in craniometaphyseal dysplasia. Br J Neurosurg 22:83-85, 2008
-
(2008)
Br J Neurosurg
, vol.22
, pp. 83-85
-
-
Sewell, M.D.1
Akram, H.2
Wadley, J.3
-
62
-
-
38449103894
-
Skull base growth in children with Chiari malformation Type I
-
Sgouros S, Kountouri M, Natarajan K: Skull base growth in children with Chiari malformation Type I. J Neurosurg 107 (3 Suppl):188-192, 2007
-
(2007)
J Neurosurg
, vol.107
, Issue.3 SUPPL.
, pp. 188-192
-
-
Sgouros, S.1
Kountouri, M.2
Natarajan, K.3
-
63
-
-
0009837288
-
Chiari malformation (chronic tonsillar herniation) and syringomyelia in Crouzon's syndrome
-
(Jpn)
-
Shigeta H, Sakai K: [Chiari malformation (chronic tonsillar herniation) and syringomyelia in Crouzon's syndrome.] Nerv Syst Child 21:395-401, 1996 (Jpn)
-
(1996)
Nerv Syst Child
, vol.21
, pp. 395-401
-
-
Shigeta, H.1
Sakai, K.2
-
64
-
-
0030896624
-
Syringomyelia associated with a posterior fossa cyst. Illustration of two cases
-
Tokime T, Okamoto S, Yamagata S, Konishi T: Syringomyelia associated with a posterior fossa cyst. Illustration of two cases. J Neurosurg 86:907, 1997
-
(1997)
J Neurosurg
, vol.86
, pp. 907
-
-
Tokime, T.1
Okamoto, S.2
Yamagata, S.3
Konishi, T.4
-
65
-
-
79952954466
-
Institutional experience with 500 cases of surgically treated pediatric Chiari malformation Type I. Clinical article
-
Tubbs RS, Beckman J, Naftel RP, Chern JJ, Wellons JC III, Rozzelle CJ, et al: Institutional experience with 500 cases of surgically treated pediatric Chiari malformation Type I. Clinical article. J Neurosurg Pediatr 7:248-256, 2011
-
(2011)
J Neurosurg Pediatr
, vol.7
, pp. 248-256
-
-
Tubbs, R.S.1
Beckman, J.2
Naftel, R.P.3
Chern, J.J.4
Wellons III, J.C.5
Rozzelle, C.J.6
-
66
-
-
0034775126
-
Preliminary observations on the association between simple metopic ridging in children without trigonocephaly and the Chiari I malformation
-
Tubbs RS, Elton S, Blount JP, Oakes WJ: Preliminary observations on the association between simple metopic ridging in children without trigonocephaly and the Chiari I malformation. Pediatr Neurosurg 35:136-139, 2001
-
(2001)
Pediatr Neurosurg
, vol.35
, pp. 136-139
-
-
Tubbs, R.S.1
Elton, S.2
Blount, J.P.3
Oakes, W.J.4
-
67
-
-
34648835207
-
The pediatric Chiari I malformation: a review
-
Tubbs RS, Lyerly MJ, Loukas M, Shoja MM, Oakes WJ: The pediatric Chiari I malformation: a review. Childs Nerv Syst 23:1239-1250, 2007
-
(2007)
Childs Nerv Syst
, vol.23
, pp. 1239-1250
-
-
Tubbs, R.S.1
Lyerly, M.J.2
Loukas, M.3
Shoja, M.M.4
Oakes, W.J.5
-
68
-
-
33644672818
-
Beckwith-Wiedemann syndrome in a child with Chiari I malformation. Case report
-
Tubbs RS, Oakes WJ: Beckwith-Wiedemann syndrome in a child with Chiari I malformation. Case report. J Neurosurg 103 (2 Suppl):172-174, 2005
-
(2005)
J Neurosurg
, vol.103
, Issue.2 SUPPL.
, pp. 172-174
-
-
Tubbs, R.S.1
Oakes, W.J.2
-
69
-
-
33750463053
-
Chiari I malformation, caudal regression syndrome, and Pierre Robin Syndrome: a previously unreported combination
-
Tubbs RS, Oakes WJ: Chiari I malformation, caudal regression syndrome, and Pierre Robin Syndrome: a previously unreported combination. Childs Nerv Syst 22:1507-1508, 2006
-
(2006)
Childs Nerv Syst
, vol.22
, pp. 1507-1508
-
-
Tubbs, R.S.1
Oakes, W.J.2
-
70
-
-
0041922399
-
Costello syndrome and Chiari I malformation: apropos of a case with a review of the literature regarding a potential association
-
Tubbs RS, Oakes WJ: Costello syndrome and Chiari I malformation: apropos of a case with a review of the literature regarding a potential association. J Child Neurol 18:496-498, 2003
-
(2003)
J Child Neurol
, vol.18
, pp. 496-498
-
-
Tubbs, R.S.1
Oakes, W.J.2
-
71
-
-
1842850801
-
Chiari I malformation and neurofibromatosis type 1
-
Tubbs RS, Rutledge SL, Kosentka A, Bartolucci AA, Oakes WJ: Chiari I malformation and neurofibromatosis type 1. Pediatr Neurol 30:278-280, 2004
-
(2004)
Pediatr Neurol
, vol.30
, pp. 278-280
-
-
Tubbs, R.S.1
Rutledge, S.L.2
Kosentka, A.3
Bartolucci, A.A.4
Oakes, W.J.5
-
72
-
-
0042823476
-
Chiari I malformation and cloacal exstrophy: report of a patient with both defects of blastogenesis
-
Tubbs RS, Smyth MD, Oakes WJ: Chiari I malformation and cloacal exstrophy: report of a patient with both defects of blastogenesis. Am J Med Genet A 119A:231-233, 2003
-
(2003)
Am J Med Genet A
, vol.119 A
, pp. 231-233
-
-
Tubbs, R.S.1
Smyth, M.D.2
Oakes, W.J.3
-
73
-
-
0242474427
-
Cutaneous manifestations and the Chiari I malformation
-
Tubbs RS, Smyth MD, Wellons JC, Blount JP, Oakes WJ: Cutaneous manifestations and the Chiari I malformation. Pediatr Neurol 29:250-252, 2003
-
(2003)
Pediatr Neurol
, vol.29
, pp. 250-252
-
-
Tubbs, R.S.1
Smyth, M.D.2
Wellons, J.C.3
Blount, J.P.4
Oakes, W.J.5
-
74
-
-
3543038802
-
Posterior cranial fossa volume in patients with rickets: insights into the increased occurrence of Chiari I malformation in metabolic bone disease
-
Tubbs RS, Webb D, Abdullatif H, Conklin M, Doyle S, Oakes WJ: Posterior cranial fossa volume in patients with rickets: insights into the increased occurrence of Chiari I malformation in metabolic bone disease. Neurosurgery 55:380-384, 2004
-
(2004)
Neurosurgery
, vol.55
, pp. 380-384
-
-
Tubbs, R.S.1
Webb, D.2
Abdullatif, H.3
Conklin, M.4
Doyle, S.5
Oakes, W.J.6
-
76
-
-
0038322131
-
Occipital encephalocele, lipomeningomyelocele, and Chiari I malformation: case report and review of the literature
-
Tubbs RS, Wellons JC III, Oakes WJ: Occipital encephalocele, lipomeningomyelocele, and Chiari I malformation: case report and review of the literature. Childs Nerv Syst 19:50-53, 2003
-
(2003)
Childs Nerv Syst
, vol.19
, pp. 50-53
-
-
Tubbs, R.S.1
Wellons III, J.C.2
Oakes, W.J.3
-
77
-
-
0037236416
-
Reformation of the posterior atlanto-occipital membrane following posterior fossa decompression with subsequent constriction at the craniocervical junction
-
Tubbs RS, Wellons JC III, Oakes WJ, Blount JP: Reformation of the posterior atlanto-occipital membrane following posterior fossa decompression with subsequent constriction at the craniocervical junction. Pediatr Neurosurg 38:219-221, 2003
-
(2003)
Pediatr Neurosurg
, vol.38
, pp. 219-221
-
-
Tubbs, R.S.1
Wellons III, J.C.2
Oakes, W.J.3
Blount, J.P.4
-
78
-
-
0037531535
-
Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa
-
Tubbs RS, Wellons JC III, Smyth MD, Bartolucci AA, Blount JP, Oakes WJ, et al: Children with growth hormone deficiency and Chiari I malformation: a morphometric analysis of the posterior cranial fossa. Pediatr Neurosurg 38:324-328, 2003
-
(2003)
Pediatr Neurosurg
, vol.38
, pp. 324-328
-
-
Tubbs, R.S.1
Wellons III, J.C.2
Smyth, M.D.3
Bartolucci, A.A.4
Blount, J.P.5
Oakes, W.J.6
-
79
-
-
0025053197
-
Basichondrocranium anomalies in adult Chiari type I malformation: a morphometric study
-
Vega A, Quintana F, Berciano J: Basichondrocranium anomalies in adult Chiari type I malformation: a morphometric study. J Neurol Sci 99:137-145, 1990
-
(1990)
J Neurol Sci
, vol.99
, pp. 137-145
-
-
Vega, A.1
Quintana, F.2
Berciano, J.3
-
80
-
-
80052762980
-
Chiari malformations and syringohydromyelia
-
Rengachary SS, Ellenbogen RG (eds): ed 2. Edinburgh: Elsevier Mosby
-
Wellons JC III, Tubbs RS, Oakes WJ: Chiari malformations and syringohydromyelia, in Rengachary SS, Ellenbogen RG (eds): Principles of Neurosurgery, ed 2. Edinburgh: Elsevier Mosby, 2005, pp 181-195
-
(2005)
Principles of Neurosurgery
, pp. 181-195
-
-
Wellons III, J.C.1
Tubbs, R.S.2
Oakes, W.J.3
|