-
1
-
-
0016156388
-
The giant melanosome: A model of deranged melanosome morphogenesis
-
Konrad K, Wolff K, Hönigsmann H: The giant melanosome: A model of deranged melanosome morphogenesis. J Ultrastruct Res 1974;48:102-123.
-
(1974)
J. Ultrastruct. Res
, vol.48
, pp. 102-123
-
-
Konrad, K.1
Wolff, K.2
Hönigsmann, H.3
-
2
-
-
0017057195
-
Giant and "granular melanosomes" in LEOPARD syndrome: An ultrastructural study
-
Bhawan J, Purtilo D, Riordan J, et al: Giant and "granular melanosomes" in LEOPARD syndrome: An ultrastructural study. J Cutan Pathol 1976;3:207-216.
-
(1976)
J. Cutan. Pathol
, vol.3
, pp. 207-216
-
-
Bhawan, J.1
Purtilo, D.2
Riordan, J.3
-
3
-
-
0021829487
-
Melanin macroglobules as a cellular marker of neurofibromatosis: A quantitative study
-
Martuza R, Phillippe I, Fitzpatrick T, et al: Melanin macroglobules as a cellular marker of neurofibromatosis: A quantitative study. J Invest Dermatol 1985;85:347-350.
-
(1985)
J. Invest. Dermatol
, vol.85
, pp. 347-350
-
-
Martuza, R.1
Phillippe, I.2
Fitzpatrick, T.3
-
4
-
-
0019764447
-
Neuropathological findings and the biology of neurofibromatosis
-
Lott I, Richardson E: Neuropathological findings and the biology of neurofibromatosis. Adv Neurol 1981;29:23-32.
-
(1981)
Adv. Neurol
, vol.29
, pp. 23-32
-
-
Lott, I.1
Richardson, E.2
-
5
-
-
0033605480
-
Plexiform neurofibromas
-
Korf B: Plexiform neurofibromas. Am J Med Genet 1999;89:31-37.
-
(1999)
Am. J. Med. Genet
, vol.89
, pp. 31-37
-
-
Korf, B.1
-
7
-
-
0033605452
-
Pathology of tumors of the peripheral nerve sheath in type 1 neurofibroimatosis
-
Woodruff J: Pathology of tumors of the peripheral nerve sheath in type 1 neurofibroimatosis. Am J Med Genet 1999;89:23-30.
-
(1999)
Am. J. Med. Genet
, vol.89
, pp. 23-30
-
-
Woodruff, J.1
-
9
-
-
0019433931
-
Von Recklinghausen neurofibromatosis: Incidence of iris hamartomata
-
Lewis R, Riccardi V: Von Recklinghausen neurofibromatosis: Incidence of iris hamartomata. Ophthalmology 1981;88:348-354.
-
(1981)
Ophthalmology
, vol.88
, pp. 348-354
-
-
Lewis, R.1
Riccardi, V.2
-
10
-
-
0019834061
-
Von Recklinghausen neurofibromatosis
-
Riccardi V: Von Recklinghausen neurofibromatosis. N Engl J Med 1981;305:1617-1627.
-
(1981)
N. Engl. J. Med
, vol.305
, pp. 1617-1627
-
-
Riccardi, V.1
-
11
-
-
0000068572
-
Tumors of the optic pathway
-
Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): 3rd ed. Baltimore, Johns Hopkins University Press
-
Listenick R, Gutmann DH: Tumors of the optic pathway, in Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): Neurofibromatosis: Phenotype, Natural History, and Pathogenesis. 3rd ed. Baltimore, Johns Hopkins University Press, 1999,203-230.
-
(1999)
Neurofibromatosis: Phenotype, Natural History, and Pathogenesis
, pp. 203-230
-
-
Listenick, R.1
Gutmann, D.H.2
-
13
-
-
0004265579
-
Über die Multiplen Fibrome der Haut und Ihre Beziehungen zu Multiplen Neuromen
-
Berlin, August Hirschwald
-
Von Recklinghausen F: Über die Multiplen Fibrome der Haut und Ihre Beziehungen zu Multiplen Neuromen. Berlin, August Hirschwald, 1882.
-
(1882)
-
-
Von Recklinghausen, F.1
-
14
-
-
0023885121
-
Neurofibromatosis: Conference statement
-
National Institutes of Health Consensus Development Conference
-
National Institutes of Health Consensus Development Conference: Neurofibromatosis: Conference statement. Arch Neurol 1988;45:575-578.
-
(1988)
Arch. Neurol
, vol.45
, pp. 575-578
-
-
-
15
-
-
0025297599
-
Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients
-
Wallace M, Marchuk D, Andersen LB, et al: Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients. Science 1990;249:181-186.
-
(1990)
Science
, vol.249
, pp. 181-186
-
-
Wallace, M.1
Marchuk, D.2
Andersen, L.B.3
-
16
-
-
0025369709
-
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
-
Viskochil D, Buchberg A, Xu G, et al: Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus. Cell 1990;62:187-192.
-
(1990)
Cell
, vol.62
, pp. 187-192
-
-
Viskochil, D.1
Buchberg, A.2
Xu, G.3
-
17
-
-
0025326726
-
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
-
Cawthon R, Weiss R, Xu G, et al: A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 1990;62:193-201.
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.1
Weiss, R.2
Xu, G.3
-
18
-
-
0030957310
-
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
-
Gutmann D, Aylsworth A, Carey J, et al: The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 1997;278:51-57.
-
(1997)
JAMA
, vol.278
, pp. 51-57
-
-
Gutmann, D.1
Aylsworth, A.2
Carey, J.3
-
19
-
-
0034094731
-
Use of the National Institutes of Health criteria for diagnosis of neurofibromatosis 1 in children
-
DeBella K, Szudek J, Friedman JM: Use of the National Institutes of Health criteria for diagnosis of neurofibromatosis 1 in children. Pediatrics 2000; 105:608-614.
-
(2000)
Pediatrics
, vol.105
, pp. 608-614
-
-
DeBella, K.1
Szudek, J.2
Friedman, J.M.3
-
20
-
-
0029905849
-
Neurofibromatosis type 1 An update and review for the primary pediatrician
-
Goldberg Y, Dibbern K, Klein J, et al: Neurofibromatosis type 1 An update and review for the primary pediatrician. Clin Pediatr (Phila) 1996;35:545-561.
-
(1996)
Clin. Pediatr. (Phila)
, vol.35
, pp. 545-561
-
-
Goldberg, Y.1
Dibbern, K.2
Klein, J.3
-
21
-
-
0030966414
-
Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients
-
Friedman J, Birch P: Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients. Am J Med Genet 1997;70:138-143.
-
(1997)
Am. J. Med. Genet
, vol.70
, pp. 138-143
-
-
Friedman, J.1
Birch, P.2
-
22
-
-
0031890253
-
MRI diagnosis of NF1 in children without café-au-lait skin lesions
-
Curless R, Siatkowski M, Glaser J, Shatz N: MRI diagnosis of NF1 in children without café-au-lait skin lesions. Pediatr Neurol 1998;18:269-271.
-
(1998)
Pediatr. Neurol
, vol.18
, pp. 269-271
-
-
Curless, R.1
Siatkowski, M.2
Glaser, J.3
Shatz, N.4
-
23
-
-
0030016355
-
MRI findings in children with neurofibromatosis type 1: A prospective study
-
Van Es S, North K, McHugh K, De Silva M: MRI findings in children with neurofibromatosis type 1: A prospective study. Pediatr Radiol 1996;26:478-487.
-
(1996)
Pediatr. Radiol
, vol.26
, pp. 478-487
-
-
Van Es, S.1
North, K.2
McHugh, K.3
De Silva, M.4
-
24
-
-
0027522490
-
Neurofibromatosis type 1: Magnetic resonance imaging findings
-
DiMario F, Ramsby G, Greenstein R, et al: Neurofibromatosis type 1: Magnetic resonance imaging findings. J Child Neurol 1993;18:32-39.
-
(1993)
J. Child Neurol
, vol.18
, pp. 32-39
-
-
DiMario, F.1
Ramsby, G.2
Greenstein, R.3
-
25
-
-
0027752275
-
Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1
-
Balestri P, Calistri L, Vivarelli R, et al: Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1. Childs Nerv Syst 1993;9:448-451.
-
(1993)
Childs Nerv. Syst
, vol.9
, pp. 448-451
-
-
Balestri, P.1
Calistri, L.2
Vivarelli, R.3
-
26
-
-
0034091759
-
Use of unidentified bright objects on MRI for diagnosis of neurofibromatosis 1 in children
-
DeBella Y, Poskitt K, Szudek J, Friedman JM: Use of unidentified bright objects on MRI for diagnosis of neurofibromatosis 1 in children. Neurology 2000;54:1646-1651.
-
(2000)
Neurology
, vol.54
, pp. 1646-1651
-
-
DeBella, Y.1
Poskitt, K.2
Szudek, J.3
Friedman, J.M.4
-
27
-
-
0016169528
-
The neurocristopathies: A unifying concept of disease arising in neural crest development
-
Bolande R: The neurocristopathies: A unifying concept of disease arising in neural crest development. Hum Pathol 1974;5:409-429.
-
(1974)
Hum. Pathol
, vol.5
, pp. 409-429
-
-
Bolande, R.1
-
28
-
-
0019749883
-
Neurofibromatosis-The quintessential neurocristopathy: Pathogenic concepts and relationships
-
Bolande R: Neurofibromatosis-The quintessential neurocristopathy: Pathogenic concepts and relationships. Adv Neurol 1981;29:67-75.
-
(1981)
Adv. Neurol
, vol.29
, pp. 67-75
-
-
Bolande, R.1
-
29
-
-
0029101184
-
Regulated expression of neurofibromin in migrating neural crest cells of avian embryos
-
Stocker K, Baizer L, Coston T, et al: Regulated expression of neurofibromin in migrating neural crest cells of avian embryos. J Neurobiol 1995;27:535-552.
-
(1995)
J. Neurobiol
, vol.27
, pp. 535-552
-
-
Stocker, K.1
Baizer, L.2
Coston, T.3
-
30
-
-
0033670127
-
Insights into the pathogenesis of neurofibromatosis 1 vasculopathy
-
Hamilton SJ, Friedman JM: Insights into the pathogenesis of neurofibromatosis 1 vasculopathy. Clin Genet 2000;58:341-,344.
-
(2000)
Clin. Genet
, vol.58
, pp. 341-344
-
-
Hamilton, S.J.1
Friedman, J.M.2
-
32
-
-
0000953960
-
Other malignancies
-
Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): 3rd ed. Baltimore, Johns Hopkins University Press
-
Gutmann D, Gurney J: Other malignancies, in Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, 3rd ed. Baltimore, Johns Hopkins University Press, 1999, 231-249.
-
(1999)
Neurofibromatosis: Phenotype, Natural History, and Pathogenesis
, pp. 231-249
-
-
Gutmann, D.1
Gurney, J.2
-
33
-
-
0003165967
-
Neurofibromas and malignant tumors of the peripheral nerve sheath
-
Friedman J, Gutmann D, MacCollin M, Riccardi V (eds): 3rd ed. Baltimore, Johns Hopkins University Press
-
Korf B: Neurofibromas and malignant tumors of the peripheral nerve sheath, in Friedman J, Gutmann D, MacCollin M, Riccardi V (eds): Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, 3rd ed. Baltimore, Johns Hopkins University Press, 1999, 142-161.
-
(1999)
Neurofibromatosis: Phenotype, Natural History, and Pathogenesis
, pp. 142-161
-
-
Korf, B.1
-
34
-
-
0034837027
-
Loss of NF1 alleles distinguish sporadic from NFl-associated pilocytic astrocytomas
-
Kluwe L, Hagel C, Tatagiba M, et al: Loss of NF1 alleles distinguish sporadic from NFl-associated pilocytic astrocytomas. J Neuropathol Exp Neurol 2001;60:917-920.
-
(2001)
J. Neuropathol. Exp. Neurol
, vol.60
, pp. 917-920
-
-
Kluwe, L.1
Hagel, C.2
Tatagiba, M.3
-
35
-
-
0033864837
-
Loss of neurofibromatosis 1 (NF1) gene expression in NF1-associated pilocytic astrocytomas
-
Gutmann DH, Donahoe J, Brown T, et al: Loss of neurofibromatosis 1 (NF1) gene expression in NF1-associated pilocytic astrocytomas. Neuropathol Appl Neurobiol 2000;26: 361-367.
-
(2000)
Neuropathol. Appl. Neurobiol
, vol.26
, pp. 361-367
-
-
Gutmann, D.H.1
Donahoe, J.2
Brown, T.3
-
36
-
-
0034530244
-
Growth in North American white children with neurofibromatosis 1 (NF1)
-
Szudek J, Birch P, Friedman JM: Growth in North American white children with neurofibromatosis 1 (NF1). J Med Genet 2000;37:933-938.
-
(2000)
J. Med. Genet
, vol.37
, pp. 933-938
-
-
Szudek, J.1
Birch, P.2
Friedman, J.M.3
-
37
-
-
0027320496
-
Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules
-
Gregory P, Gutmann D, Mitchell A, et al: Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules. Somat Cell Mol Genet 1993; 19:265-274.
-
(1993)
Somat. Cell Mol. Genet
, vol.19
, pp. 265-274
-
-
Gregory, P.1
Gutmann, D.2
Mitchell, A.3
-
38
-
-
0027310225
-
Characterization of full-length neurofibromin: Tubulin inhibits Ras GAP activity
-
Bollag G, McCormick F Clark R: Characterization of full-length neurofibromin: Tubulin inhibits Ras GAP activity EMBO J 1993;12:1923-1927.
-
(1993)
EMBO J
, vol.12
, pp. 1923-1927
-
-
Bollag, G.1
McCormick, F.2
Clark, R.3
-
39
-
-
0034708076
-
A neurofibromatosis-1-regulated pathway is required for learning in Drosophila
-
Guo H, Tong J, Hannan F, et al: A neurofibromatosis-1-regulated pathway is required for learning in Drosophila. Nature 2000;403:895-898.
-
(2000)
Nature
, vol.403
, pp. 895-898
-
-
Guo, H.1
Tong, J.2
Hannan, F.3
-
40
-
-
0034598363
-
Genetic and biochemical evidence that haploinsufficiency of the NF1 tumor suppressor gene modulates melanocyte and mast cell fates in vivo
-
Ingrain DA, Yang FC, Travers JB, et al: Genetic and biochemical evidence that haploinsufficiency of the NF1 tumor suppressor gene modulates melanocyte and mast cell fates in vivo. J Exp Med 2000;191:181-188.
-
(2000)
J. Exp. Med
, vol.191
, pp. 181-188
-
-
Ingrain, D.A.1
Yang, F.C.2
Travers, J.B.3
-
41
-
-
0033527061
-
Haploinsufficiency for the neurofibromatosis 1 (NF1) tumor suppressor results in increased astrocyte proliferation
-
Gutmann DH, Loehr A, Zhang Y, et al: Haploinsufficiency for the neurofibromatosis 1 (NF1) tumor suppressor results in increased astrocyte proliferation. Oncogene 1999;18:4450-4459.
-
(1999)
Oncogene
, vol.18
, pp. 4450-4459
-
-
Gutmann, D.H.1
Loehr, A.2
Zhang, Y.3
-
42
-
-
0002321373
-
Clinical and epidemiological features
-
Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): 3rd ed. Baltimore, Johns Hopkins University Press
-
Friedman JM, Riccardi VM: Clinical and epidemiological features, in Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, 3rd ed. Baltimore, Johns Hopkins University Press, 1999,29-86.
-
(1999)
Neurofibromatosis: Phenotype, Natural History, and Pathogenesis
, pp. 29-86
-
-
Friedman, J.M.1
Riccardi, V.M.2
-
43
-
-
0030786387
-
An association between optic glioma and other tumours of the central nervous system in neurofibromatosis type 1
-
Friedman JM, Birch P: An association between optic glioma and other tumours of the central nervous system in neurofibromatosis type 1. Neuropediatrics 1997;28:131-132.
-
(1997)
Neuropediatrics
, vol.28
, pp. 131-132
-
-
Friedman, J.M.1
Birch, P.2
-
44
-
-
0010978774
-
Logistic regresssive models of neurofibromatosis 1 (NF1 clinical features
-
Submitted
-
Szudek J, Evans D, Friedman J: Logistic regresssive models of neurofibromatosis 1 (NF1 clinical features. Submitted.
-
-
-
Szudek, J.1
Evans, D.2
Friedman, J.3
-
45
-
-
0033712016
-
Associations of clinical features in neurofibromatosis 1 (NF1)
-
Szudek J, Birch P, Riccardi VM, et al: Associations of clinical features in neurofibromatosis 1 (NF1). Genet Epidemiol 2000;19:429-439.
-
(2000)
Genet. Epidemiol
, vol.19
, pp. 429-439
-
-
Szudek, J.1
Birch, P.2
Riccardi, V.M.3
-
46
-
-
0027029581
-
Analysis of mutations at the neurofibromatosis (NF1) locus
-
Upadhaya M, Shen M, Chenyson A, et al: Analysis of mutations at the neurofibromatosis (NF1) locus. Hum Mot Genet 1992;1:735-740.
-
(1992)
Hum. Mot. Genet
, vol.1
, pp. 735-740
-
-
Upadhaya, M.1
Shen, M.2
Chenyson, A.3
-
47
-
-
0026048268
-
Watson syndrome: Is it a subtype of type 1 neurofibromatosis?
-
Allanson J, Upadhaya M, Watson G, et al: Watson syndrome: Is it a subtype of type 1 neurofibromatosis? J Med Genet 1991;28:752-756.
-
(1991)
J. Med. Genet
, vol.28
, pp. 752-756
-
-
Allanson, J.1
Upadhaya, M.2
Watson, G.3
-
48
-
-
0028971493
-
Familial cafe au lait spots: A variant of neurofibromatosis type 1
-
Abeliovich D, Gelman-Kohan Z, Silverstein S, et al: Familial cafe au lait spots: A variant of neurofibromatosis type 1. J Med Genet 1995;32:985-986.
-
(1995)
J. Med. Genet
, vol.32
, pp. 985-986
-
-
Abeliovich, D.1
Gelman-Kohan, Z.2
Silverstein, S.3
-
49
-
-
0031899827
-
A clinical variant of neurofibromatosis type 1: Familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene
-
Ars E, Kruyer H, Gaona A, et al: A clinical variant of neurofibromatosis type 1: Familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene. Am J Hum Genet 1998;62:834-841.
-
(1998)
Am. J. Hum. Genet
, vol.62
, pp. 834-841
-
-
Ars, E.1
Kruyer, H.2
Gaona, A.3
-
50
-
-
0026335083
-
Familial spinal neurofibromatosis: Clinical and DNA linkage analysis
-
Pulst SM, Riccardi VM, Fain P, Korenberg JR: Familial spinal neurofibromatosis: Clinical and DNA linkage analysis. Neurology 1991;41:1923-1927.
-
(1991)
Neurology
, vol.41
, pp. 1923-1927
-
-
Pulst, S.M.1
Riccardi, V.M.2
Fain, P.3
Korenberg, J.R.4
-
53
-
-
0026734892
-
Malignant peripheral nerve sheath turnors (malignant schwannomas) in children
-
Meis J, Enzinger F, Martz K, Neal J: Malignant peripheral nerve sheath turnors (malignant schwannomas) in children. Am J Surg Pathol 1992;16:694-707.
-
(1992)
Am. J. Surg. Pathol
, vol.16
, pp. 694-707
-
-
Meis, J.1
Enzinger, F.2
Martz, K.3
Neal, J.4
-
54
-
-
0028176825
-
Neurofibromatosis type I and malignancy: Review of 32 pediatric cases treated at a single institution
-
Shearer P Parham D, Kovnar E, et al: Neurofibromatosis type I and malignancy: Review of 32 pediatric cases treated at a single institution. Med Pediatr Oncol 1994;22:78-83.
-
(1994)
Med. Pediatr. Oncol
, vol.22
, pp. 78-83
-
-
Shearer, P.1
Parham, D.2
Kovnar, E.3
-
55
-
-
0029993451
-
Neurofibromatosis/Noonan phenotype: A variable feature of type 1 neurofibromatosis
-
Colley A, Donnai D, Evans DG: Neurofibromatosis/Noonan phenotype: A variable feature of type 1 neurofibromatosis. Clin Genet 1996;49:59-64.
-
(1996)
Clin. Genet
, vol.49
, pp. 59-64
-
-
Colley, A.1
Donnai, D.2
Evans, D.G.3
-
56
-
-
0028082464
-
Deletions spanning the neurofibromatosis 1 gene: Identification and phenotype of five patients
-
Kayes L, Burke W, Riccardi V, et al: Deletions spanning the neurofibromatosis 1 gene: Identification and phenotype of five patients. Am J Hum Genet 1994;54:424-436.
-
(1994)
Am. J. Hum. Genet
, vol.54
, pp. 424-436
-
-
Kayes, L.1
Burke, W.2
Riccardi, V.3
-
57
-
-
0026583146
-
Clinical variability of type 1 neurofibromatosis: Is there a neurofibromatosis-Noonan syndrome?
-
Stern H, Saal H, Lee J, et al: Clinical variability of type 1 neurofibromatosis: Is there a neurofibromatosis-Noonan syndrome? J Med Genet 1992;29:184-187.
-
(1992)
J. Med. Genet
, vol.29
, pp. 184-187
-
-
Stern, H.1
Saal, H.2
Lee, J.3
-
58
-
-
0027363277
-
Tandem duplication within a neurofibromatosis type I (NFI) gene exon in a family with features of Watson syndrome and Noonan syndrome
-
Tassabehji M, Strachan T, Sharland M, et al: Tandem duplication within a neurofibromatosis type I (NFI) gene exon in a family with features of Watson syndrome and Noonan syndrome. Am J Hum Genet 1993;53:90-95.
-
(1993)
Am. J. Hum. Genet
, vol.53
, pp. 90-95
-
-
Tassabehji, M.1
Strachan, T.2
Sharland, M.3
-
59
-
-
0031968762
-
Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome
-
van Asperen CJ, Overweg-Plandsoen WC, Cnossen MH, et al: Familial neurofibromatosis type 1 associated with an overgrowth syndrome resembling Weaver syndrome. J Med Genet 1998;35:323-327.
-
(1998)
J. Med. Genet
, vol.35
, pp. 323-327
-
-
van Asperen, C.J.1
Overweg-Plandsoen, W.C.2
Cnossen, M.H.3
-
60
-
-
0027379865
-
An analysis of variation in expression of neurofibromatosis (NF) type I (NF1): Evidence for modifying genes
-
Easton D, Ponder M, Huson S, Ponder B: An analysis of variation in expression of neurofibromatosis (NF) type I (NF1): Evidence for modifying genes. Am J Hum Genet 1993;53:305-313.
-
(1993)
Am. J. Hum. Genet
, vol.53
, pp. 305-313
-
-
Easton, D.1
Ponder, M.2
Huson, S.3
Ponder, B.4
-
61
-
-
0036668720
-
Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1)
-
(in press)
-
Szudek J, Joe H, Friedman JM: Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1). Genet Epidemiol (in press).
-
Genet. Epidemiol
-
-
Szudek, J.1
Joe, H.2
Friedman, J.M.3
-
62
-
-
0034085541
-
Cost evaluation of the medical management of neurofibromatosis 1: A prospective study on 201 patients
-
Wolkenstein P, Durand-Zaleski I, Moreno J, et al: Cost evaluation of the medical management of neurofibromatosis 1: A prospective study on 201 patients. Br J Dermatol 2000; 142:1166-1170.
-
(2000)
Br. J. Dermatol
, vol.142
, pp. 1166-1170
-
-
Wolkenstein, P.1
Durand-Zaleski, I.2
Moreno, J.3
-
63
-
-
0035025409
-
Mortality in neurofibromatosis 1: An analysis using U.S. death certificates
-
Rasmussen S, Yang Q, Friedman J: Mortality in neurofibromatosis 1: An analysis using U.S. death certificates. Am J Hum Genet 2001;68:1110-1118.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 1110-1118
-
-
Rasmussen, S.1
Yang, Q.2
Friedman, J.3
-
64
-
-
0000306102
-
Malignant peripheral nerve sheath tumors in neurofibromatosis 1
-
Evans DG, Baser M, McGaughran J, et al: Malignant peripheral nerve sheath tumors in neurofibromatosis 1. Am J Hum Genet 2001;69:307.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 307
-
-
Evans, D.G.1
Baser, M.2
McGaughran, J.3
-
65
-
-
0004042176
-
Abnormalities of the nervous system
-
Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): 3rd ed. Baltimore, Johns Hopkins University Press,
-
Gutmann D: Abnormalities of the nervous system, in Friedman JM, Gutmann DH, MacCollin M, Riccardi VM (eds): Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, 3rd ed. Baltimore, Johns Hopkins University Press, 1999, 190-202.
-
Neurofibromatosis: Phenotype, Natural History, and Pathogenesis
, vol.1999
, pp. 190-202
-
-
Gutmann, D.1
-
66
-
-
0022599645
-
Long-term follow-up of von Recklinghausen neurofibromatosis: Survival and malignant neoplasms
-
Sørensen S, Mulvihill J, Nielsen A. Long-term follow-up of von Recklinghausen neurofibromatosis: Survival and malignant neoplasms. N Engl J Med 1986;314:1010-1015.
-
(1986)
N. Engl. J. Med
, vol.314
, pp. 1010-1015
-
-
Sørensen, S.1
Mulvihill, J.2
Nielsen, A.3
-
67
-
-
0023894373
-
Cerebrovascular disorders associated with von Recklinghausen's neurofibromatosis: A case report
-
Sobata E, Ohkuma H, Suzuki S: Cerebrovascular disorders associated with von Recklinghausen's neurofibromatosis: A case report. Neurosurgery 1988;22:544-549.
-
(1988)
Neurosurgery
, vol.22
, pp. 544-549
-
-
Sobata, E.1
Ohkuma, H.2
Suzuki, S.3
-
68
-
-
0021323044
-
Von Recklinghausen's vasculopathy
-
Zochodne D: Von Recklinghausen's vasculopathy. Am J Med Sci 1984;287:64-65.
-
(1984)
Am. J. Med. Sci
, vol.287
, pp. 64-65
-
-
Zochodne, D.1
-
70
-
-
0028348890
-
Neurovascular manifestations of heritable connective tissue disorders. A review
-
Schievink W, Michels V, Piepgras D: Neurovascular manifestations of heritable connective tissue disorders. A review. Stroke 1994;25: 889-903.
-
(1994)
Stroke
, vol.25
, pp. 889-903
-
-
Schievink, W.1
Michels, V.2
Piepgras, D.3
|