-
1
-
-
75449091572
-
Birth incidence and prevalence of tumor-prone syndromes: Estimates from a UK family genetic register service
-
Evans DG, Howard E, Giblin C, Clancy T, Spencer H, Huson SM, Lalloo F. Birth incidence and prevalence of tumor-prone syndromes: Estimates from a UK family genetic register service. Am J Med Genet 2010;152A:327e32.
-
(2010)
Am J Med Genet
, vol.152 A
, pp. 327-332
-
-
Evans, D.G.1
Howard, E.2
Giblin, C.3
Clancy, T.4
Spencer, H.5
Huson, S.M.6
Lalloo, F.7
-
2
-
-
0022599645
-
Long-term follow-up of von Recklinghausen neurofibromatosis: survival and malignant neoplasms
-
Sorensen SA, Mulvihill JJ, Nielsen A. Long-term follow-up of von Recklinghausen neurofibromatosis: survival and malignant neoplasms. N Engl J Med 1986;314:1010e15.
-
(1986)
N Engl J Med
, vol.314
, pp. 1010-1015
-
-
Sorensen, S.A.1
Mulvihill, J.J.2
Nielsen, A.3
-
3
-
-
0027486718
-
Neurofibromatosis type 1 and childhood cancer
-
Matsui I, Tanimura M, Kobayashi N, Sawada T, Nagahara N, Akatsuka J. Neurofibromatosis type 1 and childhood cancer. Cancer 1993;72:2746e54.
-
(1993)
Cancer
, vol.72
, pp. 2746-2754
-
-
Matsui, I.1
Tanimura, M.2
Kobayashi, N.3
Sawada, T.4
Nagahara, N.5
Akatsuka, J.6
-
4
-
-
0027974256
-
Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study
-
Stiller CA, Chessels JM, Fitchett M. Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study. Br J Cancer 1994;70:969e72.
-
(1994)
Br J Cancer
, vol.70
, pp. 969-972
-
-
Stiller, C.A.1
Chessels, J.M.2
Fitchett, M.3
-
5
-
-
0030960182
-
Malignant and benign tumours in patients with neurofibromatosis type 1 in a defined Swedish population
-
Zoller MET, Rembeck B, Oden A, Samuelsson M, Angervall L. Malignant and benign tumours in patients with neurofibromatosis type 1 in a defined Swedish population. Cancer 1997;79:2125e31.
-
(1997)
Cancer
, vol.79
, pp. 2125-2131
-
-
Zoller, M.E.T.1
Rembeck, B.2
Oden, A.3
Samuelsson, M.4
Angervall, L.5
-
8
-
-
0028902601
-
Life-expectancy, mortality and prognostic factors in neurofibromatosis type 1 a twelve-year follow-up of an epidemiological study in Goteborg Sweden
-
Zoller M, Rembeck B, Akesson H, Angervall L. Life-expectancy, mortality and prognostic factors in neurofibromatosis type 1: a twelve-year follow-up of an epidemiological study in Goteborg, Sweden. Acta Derm malignant nerve sheath tumoursenerol (stockh) 1995;75:136e40.
-
(1995)
Acta Derm malignant nerve sheath tumoursenerol (stockh)
, vol.75
, pp. 136-140
-
-
Zoller, M.1
Rembeck, B.2
Akesson, H.3
Angervall, L.4
-
9
-
-
0035025409
-
Mortality in neurofibromatosis1: an analysis using U S. death certificates
-
Rasmussen SA, Yang Q, Friedman JM. Mortality in neurofibromatosis1: an analysis using U.S. death certificates. Am J Hum Genet 2001;68:1110e18.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1110-1118
-
-
Rasmussen, S.A.1
Yang, Q.2
Friedman, J.M.3
-
10
-
-
80054829001
-
Mortality in neurofibromatosis 1 in North West England: an assessment of actuarial surival in a region of the UK since 1989
-
Evans DG, O'Hara C, Wilding A, Ingham SL, Howard E. Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial surival in a region of the UK since 1989. Eur J Hum Genet 2011;19:1187e91.
-
(2011)
Eur J Hum Genet
, vol.19
, pp. 1187-1191
-
-
Evans, D.G.1
O'Hara, C.2
Wilding, A.3
Ingham, S.L.4
Howard, E.5
-
11
-
-
77957189460
-
The impact of screening and genetic registration on mortality and colorectal cancer incidence in familial adenomatous polyposis
-
Mallinson EK, Newton KF, Bowen J, Lalloo F, Clancy T, Hill J, Evans DGR. The impact of screening and genetic registration on mortality and colorectal cancer incidence in familial adenomatous polyposis. Gut 2010;59:1378e82.
-
(2010)
Gut
, vol.59
, pp. 1378-1382
-
-
Mallinson, E.K.1
Newton, K.F.2
Bowen, J.3
Lalloo, F.4
Clancy, T.5
Hill, J.6
Evans, D.G.R.7
-
12
-
-
0032884657
-
Causes of death in familial adenomatous polyposis
-
Galle TS, Juel K, Bulow S. Causes of death in familial adenomatous polyposis. Scand J Gastroenterol 1999;34:808e12.
-
(1999)
Scand J Gastroenterol
, vol.34
, pp. 808-812
-
-
Galle, T.S.1
Juel, K.2
Bulow, S.3
-
14
-
-
0026746684
-
A clinical study of type 2 neurofibromatosis
-
Evans DG, Huson S, Donnai D, Neary N, Blair V, Newton V, Harris R. A clinical study of type 2 neurofibromatosis. Q J Med 1992;84:603e18.
-
(1992)
Q J Med
, vol.84
, pp. 603-618
-
-
Evans, D.G.1
Huson, S.2
Donnai, D.3
Neary, N.4
Blair, V.5
Newton, V.6
Harris, R.7
-
15
-
-
0036780708
-
Predictors of the risk of mortality in neurofibromatosis 2
-
Baser ME, Friedman JM, Aeschilman D, Joe H, Wallace AJ, Ramsden RT, Evans DG. Predictors of the risk of mortality in neurofibromatosis 2. Am J Hum Genet 2002;71:715e23.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 715-723
-
-
Baser, M.E.1
Friedman, J.M.2
Aeschilman, D.3
Joe, H.4
Wallace, A.J.5
Ramsden, R.T.6
Evans, D.G.7
-
16
-
-
70349706038
-
Neurofibromatosis 2 [Bilateral acoustic neurofibromatosis, central neurofibromatosis, NF2, neurofibromatosis type II
-
Evans DG. Neurofibromatosis 2 [Bilateral acoustic neurofibromatosis, central neurofibromatosis, NF2, neurofibromatosis type II. Genet Med 2009;11:599e610.
-
(2009)
Genet Med
, vol.11
, pp. 599-610
-
-
Evans, D.G.1
-
17
-
-
48549089799
-
Genetic evaluation of von HippeleLindau disease for early diagnosis and improved prognosis
-
Akcaglar S, Yavascaoglu I, Vuruskan H, Oktay B. Genetic evaluation of von HippeleLindau disease for early diagnosis and improved prognosis. Int Urol Nephrol 2008;40:615e20.
-
(2008)
Int Urol Nephrol
, vol.40
, pp. 615-620
-
-
Akcaglar, S.1
Yavascaoglu, I.2
Vuruskan, H.3
Oktay, B.4
-
18
-
-
19144371868
-
A genetic register for von Hippel-Lindau disease
-
Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG. A genetic register for von Hippel-Lindau disease. J Med Genet 1996;33:120e7.
-
(1996)
J Med Genet
, vol.33
, pp. 120-127
-
-
Maddock, I.R.1
Moran, A.2
Maher, E.R.3
Teare, M.D.4
Norman, A.5
Payne, S.J.6
Whitehouse, R.7
Dodd, C.8
Lavin, M.9
Hartley, N.10
Super, M.11
Evans, D.G.12
-
19
-
-
0025000210
-
Clinical features and natural history of von Hippel-Lindau disease
-
Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA. Clinical features and natural history of von Hippel-Lindau disease. Q J Med 1990;77:1151e63.
-
(1990)
Q J Med
, vol.77
, pp. 1151-1163
-
-
Maher, E.R.1
Yates, J.R.2
Harries, R.3
Benjamin, C.4
Harris, R.5
Moore, A.T.6
Ferguson-Smith, M.A.7
-
20
-
-
20244383434
-
Endolymphatic sac tumours A source of morbid hearing loss in von Hippel-Lindau disease
-
Manski TJ, Heffner DK, Glenn GM, Patronas NJ, Pikus AT, Katz D, lebovics R, Sledjeski K, Choyke PL, Zbar B, Linehan M, Oldfield EH. Endolymphatic sac tumours. A source of morbid hearing loss in von Hippel-Lindau disease. JAMA 1997;277:1461e6.
-
(1997)
JAMA
, vol.277
, pp. 1461-1466
-
-
Manski, T.J.1
Heffner, D.K.2
Glenn, G.M.3
Patronas, N.J.4
Pikus, A.T.5
Katz, D.6
lebovics, R.7
Sledjeski, K.8
Choyke, P.L.9
Zbar, B.10
Linehan, M.11
Oldfield, E.H.12
-
21
-
-
0027231001
-
Complications of the naevoid basal cell carcinoma syndrome: results of a population based study
-
Evans DG, Ladusans E, Rimmer S, Burnell LD, Thakker N, Farndon PA. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. J Med Genet 1993;30:460e4.
-
(1993)
J Med Genet
, vol.30
, pp. 460-464
-
-
Evans, D.G.1
Ladusans, E.2
Rimmer, S.3
Burnell, L.D.4
Thakker, N.5
Farndon, P.A.6
-
22
-
-
0030913738
-
The gene for naevoid basal cell carcinoma (Gorlin) syndrome acts as a tumour supressor gene in medulloblastoma
-
Cowan R, Hoban P, Kelsey A, Birch JM, Evans DG. The gene for naevoid basal cell carcinoma (Gorlin) syndrome acts as a tumour supressor gene in medulloblastoma. Br J Cancer 1997;76:141e5.
-
(1997)
Br J Cancer
, vol.76
, pp. 141-145
-
-
Cowan, R.1
Hoban, P.2
Kelsey, A.3
Birch, J.M.4
Evans, D.G.5
-
23
-
-
71149116390
-
Basal cell nevus syndrome: clinical and genetic, diagnosis
-
García de Marcos JA, Dean-Ferrer A, Rodríguez SA, Calderón-Polanco J, Francisco J, Granados A, Poblet E. Basal cell nevus syndrome: clinical and genetic diagnosis. Oral Maxillofac Surg 2009;13:225e30.
-
(2009)
Oral Maxillofac, Surg
, vol.13
, pp. 225-230
-
-
García de Marcos, J.A.1
Dean-Ferrer, A.2
Rodríguez, S.A.3
Calderón-Polanco, J.4
Francisco, J.5
Granados, A.6
Poblet, E.7
-
24
-
-
0027366528
-
Life-expectancy after colectomy and ileorectal anastamosis for familial adenomatous polyposis
-
NugentT KP, Spigelman AD, Phillips RK. Life-expectancy after colectomy and ileorectal anastamosis for familial adenomatous polyposis. Dis colon rectum 1993;36:1059e62.
-
(1993)
Dis colon rectum
, vol.36
, pp. 1059-1062
-
-
Nugentt, K.P.1
Spigelman, A.D.2
Phillips, R.K.3
-
25
-
-
34250772785
-
Malignant peripheral nerve sheath tumors (MPNST) in NF1-affected children
-
Friedrich RE, Hartmann M, Mautner VF. Malignant peripheral nerve sheath tumors (MPNST) in NF1-affected children. Anticancer Res 2007;27:1957e60.
-
(2007)
Anticancer Res
, vol.27
, pp. 1957-1960
-
-
Friedrich, R.E.1
Hartmann, M.2
Mautner, V.F.3
-
26
-
-
0037226349
-
Prognostic factors of CNS Tumours in Neurofibromatosis 1 (NF1): a retrospective study of 104 patients
-
Guillamo JS, Creange A, Kalifa C, Grill J, Rodriguez D, Doz F, Barbarot S, Zerah M, Sanson M, Bastuji-Garin S, Wolkenstein P. Prognostic factors of CNS Tumours in Neurofibromatosis 1 (NF1): a retrospective study of 104 patients. Brain 2003;126:152e60.
-
(2003)
Brain
, vol.126
, pp. 152-160
-
-
Guillamo, J.S.1
Creange, A.2
Kalifa, C.3
Grill, J.4
Rodriguez, D.5
Doz, F.6
Barbarot, S.7
Zerah, M.8
Sanson, M.9
Bastuji-Garin, S.10
Wolkenstein, P.11
-
27
-
-
33947236808
-
Histopathology and clinical outcomes of NF1-associated vs. sporadic malignant peripheral nerve sheath tumors
-
Hagel C, Zils U, Peiper M, Kluwe L, Gottard S, Friedrich RE, Zurakowski D, von Deimling A, Mautner VF. Histopathology and clinical outcomes of NF1-associated vs. sporadic malignant peripheral nerve sheath tumors. J Neurooncol 2006;82:187e92.
-
(2006)
J Neurooncol
, vol.82
, pp. 187-192
-
-
Hagel, C.1
Zils, U.2
Peiper, M.3
Kluwe, L.4
Gottard, S.5
Friedrich, R.E.6
Zurakowski, D.7
von Deimling, A.8
Mautner, V.F.9
-
28
-
-
33947514688
-
Soft-tissue sarcomas in children and adolescents with neurofibromatosis type 1
-
Ferrai A, Bisogno G, Macaluso A, Casanova M, D'Angelo P, Pierani P, Zanetti I, Alaggio R, Cecchetto G, Carli M. Soft-tissue sarcomas in children and adolescents with neurofibromatosis type 1. Cancer 2007;109:1406e12.
-
(2007)
Cancer
, vol.109
, pp. 1406-1412
-
-
Ferrai, A.1
Bisogno, G.2
Macaluso, A.3
Casanova, M.4
D'Angelo, P.5
Pierani, P.6
Zanetti, I.7
Alaggio, R.8
Cecchetto, G.9
Carli, M.10
-
29
-
-
0036096489
-
Malignant peripheral nerve sheath tumours in neurofibromatosis 1
-
Evans DG, Baser ME, McGraughran J, Sharif S, Howard E, Moran A. Malignant peripheral nerve sheath tumours in neurofibromatosis 1. J Med Genet 2002;39:311e14.
-
(2002)
J Med Genet
, vol.39
, pp. 311-314
-
-
Evans, D.G.1
Baser, M.E.2
McGraughran, J.3
Sharif, S.4
Howard, E.5
Moran, A.6
-
30
-
-
0025455386
-
Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis) An update
-
Mulvihill JJ, Parry DM, Sherman JL, Pikus A, Kaiser-Kupfer MI, Eldridge R. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update. Ann Intern Med 1990;113:39e52.
-
(1990)
Ann Intern Med
, vol.113
, pp. 39-52
-
-
Mulvihill, J.J.1
Parry, D.M.2
Sherman, J.L.3
Pikus, A.4
Kaiser-Kupfer, M.I.5
Eldridge, R.6
-
31
-
-
0023885121
-
Neurofibromatosis conference, statement
-
National Institutes of Health Consensus Development, Conference
-
National Institutes of Health Consensus Development Conference. Neurofibromatosis conference statement. Arch Neurol 1988;45:575e8.
-
(1988)
Arch Neurol
, vol.45
, pp. 575-578
-
-
-
32
-
-
0037058777
-
Evaluation of diagnostic criteria for neurofibromatosis 2
-
Baser ME, Friedman JM, Wallace AJ, Ramsden RT, Joe H, Evans DGR. Evaluation of diagnostic criteria for neurofibromatosis 2. Neurology 2002;59:1759e65.
-
(2002)
Neurology
, vol.59
, pp. 1759-1765
-
-
Baser, M.E.1
Friedman, J.M.2
Wallace, A.J.3
Ramsden, R.T.4
Joe, H.5
Evans, D.G.R.6
-
33
-
-
42549165647
-
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
-
Vasen HF, Moslein G, Alonso A, Aretz S, Bernstein I, Bertario L, Blanco I, Bulow S, Burn J, Capella G, Colas C, Frayling I, Friedl W, Hes FJ, Hodgson S, Jarvinen H, Mecklin JP, Moller P, Myrhoi T, Nagengast FM, Parc Y, Phillips R, Clark SK, de Leon MP, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Teipar S, Thomas HJ, Wijnen J. Guidelines for the clinical management of familial adenomatous polyposis (FAP). Gut 2008;57:704e13.
-
(2008)
Gut
, vol.57
, pp. 704-713
-
-
Vasen, H.F.1
Moslein, G.2
Alonso, A.3
Aretz, S.4
Bernstein, I.5
Bertario, L.6
Blanco, I.7
Bulow, S.8
Burn, J.9
Capella, G.10
Colas, C.11
Frayling, I.12
Friedl, W.13
Hes, F.J.14
Hodgson, S.15
Jarvinen, H.16
Mecklin, J.P.17
Moller, P.18
Myrhoi, T.19
Nagengast, F.M.20
Parc, Y.21
Phillips, R.22
Clark, S.K.23
de Leon, M.P.24
Renkonen-Sinisalo, L.25
Sampson, J.R.26
Stormorken, A.27
Teipar, S.28
Thomas, H.J.29
Wijnen, J.30
more..
-
34
-
-
0025741681
-
Von Hippel-Lindau disease. A genetic study
-
Maher ER, Iselius L, Yates JR, Littler M, Benjamin C, Harris R, Sampson J, Williams A, Ferguson-Smith MA, Morton N. Von Hippel-Lindau disease. A genetic study. J Med Genet 1991;28:443e7.
-
(1991)
J Med Genet
, vol.28
, pp. 443-447
-
-
Maher, E.R.1
Iselius, L.2
Yates, J.R.3
Littler, M.4
Benjamin, C.5
Harris, R.6
Sampson, J.7
Williams, A.8
Ferguson-Smith, M.A.9
Morton, N.10
-
35
-
-
79955824816
-
Progress in Nephron Sparing Therapy for Renal Cell Carcinoma and von Hippel-Lindau disease
-
Joly D, Mejean A, Correas J-M, Timsit M-C, Verkarre V, Deveaux S, Landais P, Grunfield JP, Richard S. Progress in Nephron Sparing Therapy for Renal Cell Carcinoma and von Hippel-Lindau disease. J Urol 2011;185:2056e60.
-
(2011)
J Urol
, vol.185
, pp. 2056-2060
-
-
Joly, D.1
Mejean, A.2
Correas, J.-M.3
Timsit, M.-C.4
Verkarre, V.5
Deveaux, S.6
Landais, P.7
Grunfield, J.P.8
Richard, S.9
-
36
-
-
67651173054
-
Hearing improvement after bevacizumab in patients with neurofibromatosis type 2
-
Plotkin SR, Stemmer-Rachamimov AO, Barker FG, Halpin C, Padera TP, Tyrrell A, Sorensen AG, Jain RK, di Tomaso E. Hearing improvement after bevacizumab in patients with neurofibromatosis type 2. NEJM 2009;361:358e67.
-
(2009)
NEJM
, vol.361
, pp. 358-367
-
-
Plotkin, S.R.1
Stemmer-Rachamimov, A.O.2
Barker, F.G.3
Halpin, C.4
Padera, T.P.5
Tyrrell, A.6
Sorensen, A.G.7
Jain, R.K.8
di Tomaso, E.9
-
37
-
-
68149180536
-
Consensus Recommendations to accelerate Clinical Trials for Neurofibromatosis type 2
-
Evans DG, Kalamarides M, Hunter-Schaedle K, Blakeley J, Allen J, Babovic-Vuskanovic D, Belzberg A, Bollag G, Chen R, DiTomaso E, Golfinos J, Harris G, Jacod A, Kalpana G, Karajannis M, Korf B, Kurzrock R, Law M, McClatchey A, Packer R, Roehm P, Rubenstein A, Slattery W 3rd, Tonsgard H, Welling DB, Widemann B, Yohay K, Giovannini M. Consensus Recommendations to accelerate Clinical Trials for Neurofibromatosis type 2. Clin Cancer Res 2009;15:5032e9.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 5032-5039
-
-
Evans, D.G.1
Kalamarides, M.2
Hunter-Schaedle, K.3
Blakeley, J.4
Allen, J.5
Babovic-Vuskanovic, D.6
Belzberg, A.7
Bollag, G.8
Chen, R.9
DiTomaso, E.10
Golfinos, J.11
Harris, G.12
Jacod, A.13
Kalpana, G.14
Karajannis, M.15
Korf, B.16
Kurzrock, R.17
Law, M.18
McClatchey, A.19
Packer, R.20
Roehm, P.21
Rubenstein, A.22
Slattery III, W.23
Tonsgard, H.24
Welling, D.B.25
Widemann, B.26
Yohay, K.27
Giovannini, M.28
more..
-
38
-
-
0029018288
-
Diagnostic issues in a family with late onset type 2 neurofibromatosis
-
Evans DG, Bourn D, Wallace A, Ramsden RT, Mitchell JD, Strachan T. Diagnostic issues in a family with late onset type 2 neurofibromatosis. J Med Genet 1995;32:470e4.
-
(1995)
J Med Genet
, vol.32
, pp. 470-474
-
-
Evans, D.G.1
Bourn, D.2
Wallace, A.3
Ramsden, R.T.4
Mitchell, J.D.5
Strachan, T.6
-
39
-
-
20444448454
-
Management of the patient and family with neurofibromatosis 2 a consensus conference statement
-
Evans DG, Baser ME, O'Reilly B, Rowe J, Gleeson M, Saeed S, King A, Huson SM, Kerr R, Thomas N, Irving R, MacFarlane R, Ferner R, McLeod R, Moffat D, Ramsden R. Management of the patient and family with neurofibromatosis 2: a consensus conference statement. Brit J Neurosurg 2005;19:5e12.
-
(2005)
Brit J Neurosurg
, vol.19
, pp. 5-12
-
-
Evans, D.G.1
Baser, M.E.2
O'Reilly, B.3
Rowe, J.4
Gleeson, M.5
Saeed, S.6
King, A.7
Huson, S.M.8
Kerr, R.9
Thomas, N.10
Irving, R.11
MacFarlane, R.12
Ferner, R.13
McLeod, R.14
Moffat, D.15
Ramsden, R.16
|