-
1
-
-
59449101518
-
Neurofibromatosis type 1 revisited
-
PID: 19117870
-
Williams VC, Lucas J, Babcock MA, et al. Neurofibromatosis type 1 revisited. Pediatrics. 2009;123:124–33.
-
(2009)
Pediatrics
, vol.123
, pp. 124-133
-
-
Williams, V.C.1
Lucas, J.2
Babcock, M.A.3
-
2
-
-
84911191642
-
Update from the 2013 international neurofibromatosis conference
-
Plotkin SR, Albers AC, Babovic-Vuksanovic D, et al. Update from the 2013 international neurofibromatosis conference. Am J Med Genet A. 2014;164:2969–78.
-
(2014)
Am J Med Genet A
, vol.164
, pp. 2969-2978
-
-
Plotkin, S.R.1
Albers, A.C.2
Babovic-Vuksanovic, D.3
-
3
-
-
84904263293
-
Neurofibromatosis type 1: a multidisciplinary approach to care
-
PID: 25030515
-
Hirbe AC, Gutmann DH. Neurofibromatosis type 1: a multidisciplinary approach to care. Lancet Neurol. 2014;13:834–43.
-
(2014)
Lancet Neurol
, vol.13
, pp. 834-843
-
-
Hirbe, A.C.1
Gutmann, D.H.2
-
4
-
-
33645285906
-
Neurofibromatosis type 1: new insights into neurocognitive issues
-
COI: 1:CAS:528:DC%2BD28Xjt12ntLg%3D, PID: 16522267
-
Acosta MT, Gioia GA, Silva AJ. Neurofibromatosis type 1: new insights into neurocognitive issues. Curr Neurol Neurosci Rep. 2006;6:136–43.
-
(2006)
Curr Neurol Neurosci Rep
, vol.6
, pp. 136-143
-
-
Acosta, M.T.1
Gioia, G.A.2
Silva, A.J.3
-
5
-
-
80052778711
-
Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I study
-
PID: 21907886
-
Acosta MT, Kardel PG, Walsh KS, et al. Lovastatin as treatment for neurocognitive deficits in neurofibromatosis type 1: phase I study. Pediatr Neurol. 2011;45:241–5.
-
(2011)
Pediatr Neurol
, vol.45
, pp. 241-245
-
-
Acosta, M.T.1
Kardel, P.G.2
Walsh, K.S.3
-
6
-
-
84866402145
-
The adverse influence of attention-deficit disorder with or without hyperactivity on cognition in neurofibromatosis type 1
-
PID: 22881119
-
Lidzba K, Granstrom S, Lindenau J, Mautner VF. The adverse influence of attention-deficit disorder with or without hyperactivity on cognition in neurofibromatosis type 1. Dev Med Child Neurol. 2012;54:892–7.
-
(2012)
Dev Med Child Neurol
, vol.54
, pp. 892-897
-
-
Lidzba, K.1
Granstrom, S.2
Lindenau, J.3
Mautner, V.F.4
-
7
-
-
84860283040
-
Developmental delays in children with neurofibromatosis type 1
-
PID: 22190506
-
Soucy EA, Gao F, Gutmann DH, Dunn CM. Developmental delays in children with neurofibromatosis type 1. J Child Neurol. 2012;27:641–4.
-
(2012)
J Child Neurol
, vol.27
, pp. 641-644
-
-
Soucy, E.A.1
Gao, F.2
Gutmann, D.H.3
Dunn, C.M.4
-
8
-
-
84898448300
-
Relationship between cognitive dysfunction, gait, and motor impairment in children and adolescents with neurofibromatosis type 1
-
PID: 24387687
-
Champion JA, Rose KJ, Payne JM, Burns J, North KN. Relationship between cognitive dysfunction, gait, and motor impairment in children and adolescents with neurofibromatosis type 1. Dev Med Child Neurol. 2014;56:468–74.
-
(2014)
Dev Med Child Neurol
, vol.56
, pp. 468-474
-
-
Champion, J.A.1
Rose, K.J.2
Payne, J.M.3
Burns, J.4
North, K.N.5
-
9
-
-
2642683203
-
Magnetic resonance imaging lesion analysis in neurofibromatosis type 1
-
PID: 9561977
-
DiMario Jr FJ, Ramsby G. Magnetic resonance imaging lesion analysis in neurofibromatosis type 1. Arch Neurol. 1998;55:500–5.
-
(1998)
Arch Neurol
, vol.55
, pp. 500-505
-
-
DiMario, F.J.1
Ramsby, G.2
-
10
-
-
84894254334
-
Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year study
-
PID: 24357578
-
Payne JM, Pickering T, Porter M, et al. Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year study. Am J Med Genet A. 2014;164A:661–5.
-
(2014)
Am J Med Genet A
, vol.164A
, pp. 661-665
-
-
Payne, J.M.1
Pickering, T.2
Porter, M.3
-
11
-
-
66349094869
-
Gliomas in patients with neurofibromatosis type 1
-
PID: 19344304
-
Albers AC, Gutmann DH. Gliomas in patients with neurofibromatosis type 1. Expert Rev Neurother. 2009;9:535–9.
-
(2009)
Expert Rev Neurother
, vol.9
, pp. 535-539
-
-
Albers, A.C.1
Gutmann, D.H.2
-
12
-
-
84892462598
-
Functional outcome measures for NF1-associated optic pathway glioma clinical trials
-
COI: 1:CAS:528:DC%2BC3sXhvVSmsbfO, PID: 24249802
-
Fisher MJ, Avery RA, Allen JC, et al. Functional outcome measures for NF1-associated optic pathway glioma clinical trials. Neurology. 2013;81:S15–24.
-
(2013)
Neurology
, vol.81
, pp. 15-24
-
-
Fisher, M.J.1
Avery, R.A.2
Allen, J.C.3
-
13
-
-
83855163457
-
Neurofibromatosis type 1 and cerebellar T2-hyperintensities: the relationship to cognitive functioning
-
PID: 22107256
-
Piscitelli O, Digilio MC, Capolino R, Longo D, Di Ciommo V. Neurofibromatosis type 1 and cerebellar T2-hyperintensities: the relationship to cognitive functioning. Dev Med Child Neurol. 2012;54:49–51.
-
(2012)
Dev Med Child Neurol
, vol.54
, pp. 49-51
-
-
Piscitelli, O.1
Digilio, M.C.2
Capolino, R.3
Longo, D.4
Di Ciommo, V.5
-
14
-
-
78649323197
-
Posterior fossa tumors in children with neurofibromatosis type 1 (NF1)
-
PID: 20464401
-
Pascual-Castroviejo I, Pascual-Pascual SI, Viano J, et al. Posterior fossa tumors in children with neurofibromatosis type 1 (NF1). Childs Nerv Syst. 2010;26:1599–603.
-
(2010)
Childs Nerv Syst
, vol.26
, pp. 1599-1603
-
-
Pascual-Castroviejo, I.1
Pascual-Pascual, S.I.2
Viano, J.3
-
15
-
-
0004265328
-
-
The Johns Hopkins University Press, Baltimore
-
Riccardi VM. Neurofibromatosis. Baltimore: The Johns Hopkins University Press; 1992. p. 63.
-
(1992)
Neurofibromatosis
, pp. 63
-
-
Riccardi, V.M.1
-
17
-
-
42149107052
-
Differential diagnosis of cerebellar atrophy in childhood
-
PID: 17869142
-
Poretti A, Wolf NI, Boltshauser E. Differential diagnosis of cerebellar atrophy in childhood. Eur J Paediatr Neurol. 2008;12:155–67.
-
(2008)
Eur J Paediatr Neurol
, vol.12
, pp. 155-167
-
-
Poretti, A.1
Wolf, N.I.2
Boltshauser, E.3
-
18
-
-
84905829707
-
Cerebellar dysplasia
-
Boltshauser E, Schmahmann JD, (eds), Mac Keith Press, London
-
Poretti A, Boltshauser E. Cerebellar dysplasia. In: Boltshauser E, Schmahmann JD, editors. Cerebellar disorders in children. London: Mac Keith Press; 2012. p. 172–6.
-
(2012)
Cerebellar disorders in children
, pp. 172-176
-
-
Poretti, A.1
Boltshauser, E.2
-
19
-
-
84890288912
-
Cerebellar hypoplasia in a case with neurofibromatosis type 1
-
Isikay S. Cerebellar hypoplasia in a case with neurofibromatosis type 1. BMJ Case Rep 2013;2013.
-
(2013)
BMJ Case Rep
, pp. 2013
-
-
Isikay, S.1
-
20
-
-
61849186040
-
Neurofibromatosis type 1 & related disorders
-
Ruggieri M, Pascual-Castroviejo I, Rocco C, (eds), Springer, New York
-
Ruggieri M, Upadhyaya M, Di Rocco C, Gabriele A, Pascual-Castroviejo I. Neurofibromatosis type 1 & related disorders. In: Ruggieri M, Pascual-Castroviejo I, Di Rocco C, editors. Neurocutaneous disorders. New York: Springer; 2008. p. 51–151.
-
(2008)
Neurocutaneous disorders
, pp. 51-151
-
-
Ruggieri, M.1
Upadhyaya, M.2
Di Rocco, C.3
Gabriele, A.4
Pascual-Castroviejo, I.5
-
21
-
-
35348813837
-
[Unilateral facial and cerebral hyperplasia associated with neurofibromatosis type 1. Report of four patients]
-
COI: 1:STN:280:DC%2BD28rlsFansg%3D%3D, PID: 16981165
-
Pascual-Castroviejo I, Pascual-Pascual SI, Burgueno M, et al. [Unilateral facial and cerebral hyperplasia associated with neurofibromatosis type 1. Report of four patients]. Rev Neurol. 2006;43:346–52.
-
(2006)
Rev Neurol
, vol.43
, pp. 346-352
-
-
Pascual-Castroviejo, I.1
Pascual-Pascual, S.I.2
Burgueno, M.3
-
22
-
-
44449118891
-
[Cerebellar hypoplasia and vertebral indentations in a case of neurofibromatosis type I]
-
COI: 1:STN:280:DC%2BD1czgtlOksw%3D%3D, PID: 18465703
-
Al-Hail H, Ruiz-Miyares F, Deleu D, Mesraoua B. [Cerebellar hypoplasia and vertebral indentations in a case of neurofibromatosis type I]. Rev Neurol. 2008;46:626–7.
-
(2008)
Rev Neurol
, vol.46
, pp. 626-627
-
-
Al-Hail, H.1
Ruiz-Miyares, F.2
Deleu, D.3
Mesraoua, B.4
-
23
-
-
70349257973
-
Cerebral arteriopathy in children with neurofibromatosis type 1
-
PID: 19706560
-
Rea D, Brandsema JF, Armstrong D, et al. Cerebral arteriopathy in children with neurofibromatosis type 1. Pediatrics. 2009;124:e476–83.
-
(2009)
Pediatrics
, vol.124
, pp. 476-483
-
-
Rea, D.1
Brandsema, J.F.2
Armstrong, D.3
-
24
-
-
84871582891
-
Cerebral vasculopathy in children with neurofibromatosis type 1
-
PID: 22532547
-
Ghosh PS, Rothner AD, Emch TM, Friedman NR, Moodley M. Cerebral vasculopathy in children with neurofibromatosis type 1. J Child Neurol. 2013;28:95–101.
-
(2013)
J Child Neurol
, vol.28
, pp. 95-101
-
-
Ghosh, P.S.1
Rothner, A.D.2
Emch, T.M.3
Friedman, N.R.4
Moodley, M.5
-
25
-
-
84885931961
-
Spectrum and prevalence of vasculopathy in pediatric neurofibromatosis type 1
-
PID: 22832780
-
Kaas B, Huisman TA, Tekes A, et al. Spectrum and prevalence of vasculopathy in pediatric neurofibromatosis type 1. J Child Neurol. 2013;28:561–9.
-
(2013)
J Child Neurol
, vol.28
, pp. 561-569
-
-
Kaas, B.1
Huisman, T.A.2
Tekes, A.3
-
26
-
-
84908432902
-
NF1 regulation of RAS/ERK signaling is required for appropriate granule neuron progenitor expansion and migration in cerebellar development
-
PID: 25367036
-
Sanchez-Ortiz E, Cho W, Nazarenko I, et al. NF1 regulation of RAS/ERK signaling is required for appropriate granule neuron progenitor expansion and migration in cerebellar development. Genes Dev. 2014;28:2407–20.
-
(2014)
Genes Dev
, vol.28
, pp. 2407-2420
-
-
Sanchez-Ortiz, E.1
Cho, W.2
Nazarenko, I.3
-
27
-
-
79952707970
-
Unilateral cerebellar hypoplasia with different clinical features
-
PID: 20967575
-
Benbir G, Kara S, Yalcinkaya BC, et al. Unilateral cerebellar hypoplasia with different clinical features. Cerebellum. 2011;10:49–60.
-
(2011)
Cerebellum
, vol.10
, pp. 49-60
-
-
Benbir, G.1
Kara, S.2
Yalcinkaya, B.C.3
-
28
-
-
68349096178
-
Morphological spectrum of prenatal cerebellar disruptions
-
PID: 18945628
-
Poretti A, Prayer D, Boltshauser E. Morphological spectrum of prenatal cerebellar disruptions. Eur J Paediatr Neurol. 2009;13:397–407.
-
(2009)
Eur J Paediatr Neurol
, vol.13
, pp. 397-407
-
-
Poretti, A.1
Prayer, D.2
Boltshauser, E.3
-
30
-
-
84908208916
-
Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis
-
COI: 1:STN:280:DC%2BC2c7itFalsg%3D%3D, PID: 24185815
-
Massoud M, Cagneaux M, Garel C, et al. Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis. Ultrasound Obstet Gynecol. 2014;44:447–54.
-
(2014)
Ultrasound Obstet Gynecol
, vol.44
, pp. 447-454
-
-
Massoud, M.1
Cagneaux, M.2
Garel, C.3
-
31
-
-
0037056366
-
Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)
-
COI: 1:STN:280:DC%2BD38vmt1emtA%3D%3D, PID: 12221173
-
Gutmann DH, Rasmussen SA, Wolkenstein P, et al. Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1). Neurology. 2002;59:759–61.
-
(2002)
Neurology
, vol.59
, pp. 759-761
-
-
Gutmann, D.H.1
Rasmussen, S.A.2
Wolkenstein, P.3
-
32
-
-
77951704065
-
Clinicopathologic study of glioblastoma in children with neurofibromatosis type 1
-
PID: 20310005
-
Huttner AJ, Kieran MW, Yao X, et al. Clinicopathologic study of glioblastoma in children with neurofibromatosis type 1. Pediatr Blood Cancer. 2010;54:890–6.
-
(2010)
Pediatr Blood Cancer
, vol.54
, pp. 890-896
-
-
Huttner, A.J.1
Kieran, M.W.2
Yao, X.3
-
33
-
-
84946488601
-
Glioblastoma in a patient with neurofibromatosis type 1: a case report and review of the literature
-
PID: 24926470
-
Jeong TS, Yee GT. Glioblastoma in a patient with neurofibromatosis type 1: a case report and review of the literature. Brain Tumor Res Treat. 2014;2:36–8.
-
(2014)
Brain Tumor Res Treat
, vol.2
, pp. 36-38
-
-
Jeong, T.S.1
Yee, G.T.2
-
34
-
-
84982235592
-
Disrupting LIN28 in atypical teratoid rhabdoid tumors reveals the importance of the mitogen activated protein kinase pathway as a therapeutic target
-
Weingart MF, Roth JJ, Hutt-Cabezas M, et al. Disrupting LIN28 in atypical teratoid rhabdoid tumors reveals the importance of the mitogen activated protein kinase pathway as a therapeutic target. Oncotarget 2014.
-
(2014)
Oncotarget
-
-
Weingart, M.F.1
Roth, J.J.2
Hutt-Cabezas, M.3
-
36
-
-
0036700297
-
Cognitive deficits in neurofibromatosis 1
-
PID: 12403559, discussion 27–9, 46–51
-
North K, Hyman S, Barton B. Cognitive deficits in neurofibromatosis 1. J Child Neurol. 2002;17:605–12. discussion 27–9, 46–51.
-
(2002)
J Child Neurol
, vol.17
, pp. 605-612
-
-
North, K.1
Hyman, S.2
Barton, B.3
-
37
-
-
33751109941
-
Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder
-
PID: 17109785
-
Hyman SL, Arthur Shores E, North KN. Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder. Dev Med Child Neurol. 2006;48:973–7.
-
(2006)
Dev Med Child Neurol
, vol.48
, pp. 973-977
-
-
Hyman, S.L.1
Arthur Shores, E.2
North, K.N.3
-
38
-
-
79952575099
-
Mental, motor, and language development of toddlers with neurofibromatosis type 1
-
PID: 21094952
-
Lorenzo J, Barton B, Acosta MT, North K. Mental, motor, and language development of toddlers with neurofibromatosis type 1. J Pediatr. 2011;158:660–5.
-
(2011)
J Pediatr
, vol.158
, pp. 660-665
-
-
Lorenzo, J.1
Barton, B.2
Acosta, M.T.3
North, K.4
|