These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis. Kehrer-Sawatzki H; Farschtschi S; Mautner VF; Cooper DN Hum Genet; 2017 Feb; 136(2):129-148. PubMed ID: 27921248 [TBL] [Abstract][Full Text] [Related]
24. Creation of an international registry to support discovery in schwannomatosis. Ostrow KL; Bergner AL; Blakeley J; Evans DG; Ferner R; Friedman JM; Harris GJ; Jordan JT; Korf B; Langmead S; Leschziner G; Mautner V; Merker VL; Papi L; Plotkin SR; Slopis JM; Smith MJ; Stemmer-Rachamimov A; Yohay K; Belzberg AJ Am J Med Genet A; 2017 Feb; 173(2):407-413. PubMed ID: 27759912 [TBL] [Abstract][Full Text] [Related]
25. Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria. Plotkin SR; Blakeley JO; Evans DG; Hanemann CO; Hulsebos TJ; Hunter-Schaedle K; Kalpana GV; Korf B; Messiaen L; Papi L; Ratner N; Sherman LS; Smith MJ; Stemmer-Rachamimov AO; Vitte J; Giovannini M Am J Med Genet A; 2013 Mar; 161A(3):405-16. PubMed ID: 23401320 [TBL] [Abstract][Full Text] [Related]
26. Broadening the spectrum of SMARCB1-associated malignant tumors: a case of uterine leiomyosarcoma in a patient with schwannomatosis. Paganini I; Sestini R; Cacciatore M; Capone GL; Candita L; Paolello C; Sbaraglia M; Dei Tos AP; Rossi S; Papi L Hum Pathol; 2015 Aug; 46(8):1226-31. PubMed ID: 26001331 [TBL] [Abstract][Full Text] [Related]
27. Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants. Hutter S; Piro RM; Reuss DE; Hovestadt V; Sahm F; Farschtschi S; Kehrer-Sawatzki H; Wolf S; Lichter P; von Deimling A; Schuhmann MU; Pfister SM; Jones DT; Mautner VF Acta Neuropathol; 2014 Sep; 128(3):449-52. PubMed ID: 25008767 [No Abstract] [Full Text] [Related]
28. An unusual case of schwannomatosis with bilateral maxillary sinus schwannomas and a novel SMARCB1 gene mutation. Toms J; Harrison J; Richard H; Childers A; Reiter ER; Graham RS J Neurosurg Spine; 2016 Jan; 24(1):160-6. PubMed ID: 26431068 [TBL] [Abstract][Full Text] [Related]
29. A deep intronic SMARCB1 variant associated with schwannomatosis. Smith MJ; Bowers NL; Banks C; Coates-Brown R; Morris KA; Ewans L; Wilson M; Pinner J; Bhaskar SS; Cammarata-Scalisi F; Wallace AJ; Evans DGR Clin Genet; 2020 Feb; 97(2):376-377. PubMed ID: 31502250 [No Abstract] [Full Text] [Related]
30. Schwannoma of the posterior tibial nerve in a patient with schwannomatosis and a novel mutation of the LZTR1 gene. Herrero San Martín A; Alcalá-Galiano A Neurologia (Engl Ed); 2020; 35(9):657-659. PubMed ID: 31892430 [No Abstract] [Full Text] [Related]
31. WP1066 induces cell death in a schwannomatosis patient-derived schwannoma cell line. Allaf A; Victoria B; Rosario R; Misztal C; Humayun Gultekin S; Dinh CT; Fernandez-Valle C Cold Spring Harb Mol Case Stud; 2022 Jun; 8(4):. PubMed ID: 35732500 [TBL] [Abstract][Full Text] [Related]
32. Neurofibromatosis and Schwannomatosis. Plotkin SR; Wick A Semin Neurol; 2018 Feb; 38(1):73-85. PubMed ID: 29548054 [TBL] [Abstract][Full Text] [Related]
33. A rare occurrence and management of familial schwannomatosis. Reddy RG; Banda VR; Gunadal S; Banda NR BMJ Case Rep; 2013 Apr; 2013():. PubMed ID: 23595180 [TBL] [Abstract][Full Text] [Related]
34. Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders. Evans DGR; Salvador H; Chang VY; Erez A; Voss SD; Druker H; Scott HS; Tabori U Clin Cancer Res; 2017 Jun; 23(12):e54-e61. PubMed ID: 28620005 [TBL] [Abstract][Full Text] [Related]
35. Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis. Smith MJ; Kulkarni A; Rustad C; Bowers NL; Wallace AJ; Holder SE; Heiberg A; Ramsden RT; Evans DG Am J Med Genet A; 2012 Jan; 158A(1):215-9. PubMed ID: 22105938 [TBL] [Abstract][Full Text] [Related]
36. Hereditary intraspinal schwannomatosis with SMARCB1 gene mutation: A case report. Li Y; Chen L; Shao D; Zhang B; Xie S; Zheng X; Jiang Z J Clin Lab Anal; 2022 Jun; 36(6):e24448. PubMed ID: 35446994 [TBL] [Abstract][Full Text] [Related]
37. Neurofibromas in LZTR1 schwannomatosis. Groen JL; Moghadasi S; Spruijt L; Korpershoek E; van Ierland Y; van Wezel JT; van Duinen S; Malessy MJA; Lesnik Oberstein SAJ Clin Genet; 2022 May; 101(5-6):571-572. PubMed ID: 35178712 [No Abstract] [Full Text] [Related]
38. Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis. Smith MJ; Wallace AJ; Bowers NL; Rustad CF; Woods CG; Leschziner GD; Ferner RE; Evans DG Neurogenetics; 2012 May; 13(2):141-5. PubMed ID: 22434358 [TBL] [Abstract][Full Text] [Related]
39. Distinctive low epidermal nerve fiber density in schwannomatosis patients provides a major parameter for diagnosis and differential diagnosis. Farschtschi SC; Kluwe L; Schön G; Friedrich RE; Matschke J; Glatzel M; Weis J; Hagel C; Mautner VF Brain Pathol; 2020 Mar; 30(2):386-391. PubMed ID: 31424590 [TBL] [Abstract][Full Text] [Related]