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kw.\*:("Schwannomatosis")

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Schwannomatosis, sporadic schwannomatosis, and familial schwannomatosis: a surgical series with long-term follow-up: Clinical articleGONZALVO, Augusto; FOWLER, Adam; COOK, Raymond John et al.Journal of neurosurgery. 2011, Vol 114, Num 3, pp 756-762, issn 0022-3085, 7 p.Article

News on the genetics, epidemiology, medical care and translational research of SchwannomasHANEMANN, C. O; EVANS, D. G.Journal of neurology. 2006, Vol 253, Num 12, pp 1533-1541, issn 0340-5354, 9 p.Article

Frequency of SMARCB1 mutations in familial and sporadic schwannomatosisSMITH, Miriam J; WALLACE, Andrew J; BOWERS, Naomi L et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 2, pp 141-145, issn 1364-6745, 5 p.Article

Vestibular Schwannomas Occur in Schwannomatosis and Should not be Considered an Exclusion Criterion for Clinical DiagnosisSMITH, Miriam J; KULKARNI, Anjana; RUSTAD, Cecilie et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 215-219, issn 1552-4825, 5 p.Article

Aberrant axon neurofilaments in schwannomas associated with phacomatosesWECHSLER, Janine; LANTIERI, Laurent; ZELLER, Jacques et al.Virchows Archiv. 2003, Vol 443, Num 6, pp 768-773, issn 0945-6317, 6 p.Article

Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebriDEN MUNCKHOF, Pepijn Van; CHRISTIAANS, Imke; KENTER, Susan B et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 1, pp 1-7, issn 1364-6745, 7 p.Article

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationBACCI, Costanza; SESTINI, Roberta; PROVENZANO, Aldesia et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 1, pp 73-80, issn 1364-6745, 8 p.Article

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosisBOYD, C; SMITH, M. J; KLUWE, L et al.Clinical genetics. 2008, Vol 74, Num 4, pp 358-366, issn 0009-9163, 9 p.Article

Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomasHADFIELD, K. D; SMITH, M. J; URQUHART, J. E et al.Oncogene (Basingstoke). 2010, Vol 29, Num 47, pp 6216-6221, issn 0950-9232, 6 p.Article

Multiple unilateral schwannomas: segmental neurofibromatosis type 2 or schwannomatosis?LEVERKUS, M; KLUWE, L; RÖLL, E-M et al.British journal of dermatology (1951). 2003, Vol 148, Num 4, pp 804-809, issn 0007-0963, 6 p.Article

Multiple schwannomas of the sciatic nerveHUANG, J; MOBBS, R; TEO, C et al.Journal of clinical neuroscience. 2003, Vol 10, Num 3, pp 391-393, issn 0967-5868, 3 p.Article

RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomasMELEAN, German; VELASCO, Ana; HERNANDEZ-IMAZ, Elisabete et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 267-274, issn 1364-6745, 8 p.Article

Schwannomatosis : Multiple schwannomas of the upper limbHASHAM, S; MATTEUCCI, P; STANLEY, P. R. W et al.Journal of hand surgery. British and european volume. 2006, Vol 31, Num 2, pp 182-184, 3 p.Article

Management of patients with schwannomatosis: Report of six cases and review of the literature. CommentaryHUANG, Jason H; SIMON, Scott L; NAGPAL, Seema et al.Surgical neurology. 2004, Vol 62, Num 4, pp 353-361, issn 0090-3019, 9 p.Article

Segmental Neurofibromatosis of the Hand and Upper Extremity : A Case ReportILYAS, Asif M; NOURISSAT, Geoffroy; JUPITER, Jesse B et al.The Journal of hand surgery (St. Louis, Mo.). 2007, Vol 32A, Num 10, pp 1538-1542, issn 0363-5023, 5 p.Article

Genetic insights into familial tumors of the nervous systemMELEAN, German; SESTINI, Roberta; AMMANNATI, Franco et al.American journal of medical genetics. 2004, Vol 129C, Num 1, pp 74-84, issn 0148-7299, 11 p.Article

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