149 related articles for article (PubMed ID: 33269527)
21. 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]
22. 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]
23. 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]
24. 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]
25. 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]
26. 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]
27. 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]
28. 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]
29. Neurofibromatosis and Schwannomatosis.
Plotkin SR; Wick A
Semin Neurol; 2018 Feb; 38(1):73-85. PubMed ID: 29548054
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. 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]
33. 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]
34. 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]
35. 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]
36. 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]
37. Schwannomatosis: the overlooked neurofibromatosis?
Koontz NA; Wiens AL; Agarwal A; Hingtgen CM; Emerson RE; Mosier KM
AJR Am J Roentgenol; 2013 Jun; 200(6):W646-53. PubMed ID: 23701098
[TBL] [Abstract][Full Text] [Related]
38. Multiple primary malignancies associated with a germline SMARCB1 pathogenic variant.
Eelloo JA; Smith MJ; Bowers NL; Ealing J; Hulse P; Wylie JP; Shenjere P; Clarke NW; Soh C; Whitehouse RW; Jones M; Duff C; Freemont A; Gareth Evans D
Fam Cancer; 2019 Oct; 18(4):445-449. PubMed ID: 31240424
[TBL] [Abstract][Full Text] [Related]
39. Schwannomatosis presenting as pancreatic and submandibular gland schwannoma.
Val-Bernal JF; Mayorga M; Sedano-Tous MJ
Pathol Res Pract; 2013 Dec; 209(12):817-22. PubMed ID: 24054034
[TBL] [Abstract][Full Text] [Related]
40. Epigenomic, genomic, and transcriptomic landscape of schwannomatosis.
Mansouri S; Suppiah S; Mamatjan Y; Paganini I; Liu JC; Karimi S; Patil V; Nassiri F; Singh O; Sundaravadanam Y; Rath P; Sestini R; Gensini F; Agnihotri S; Blakeley J; Ostrow K; Largaespada D; Plotkin SR; Stemmer-Rachamimov A; Ferrer MM; Pugh TJ; Aldape KD; Papi L; Zadeh G
Acta Neuropathol; 2021 Jan; 141(1):101-116. PubMed ID: 33025139
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
