Ruggieri M, Huson SM, « The neurofibromatoses. An overview », Ital J Neurol Sci, vol. 20, no 2, , p. 89–108 (PMID10933430, DOI10.1007/s100720050017)
Melean G, Sestini R, Ammannati F, Papi L, « Genetic insights into familial tumors of the nervous system », Am J Med Genet C Semin Med Genet, vol. 129C, no 1, , p. 74–84 (PMID15264275, DOI10.1002/ajmg.c.30022)
Hanemann CO, Evans DG, « News on the genetics, epidemiology, medical care and translational research of Schwannomas », J. Neurol., vol. 253, no 12, , p. 1533–41 (PMID17219030, DOI10.1007/s00415-006-0347-0)
MacCollin M, Woodfin W, Kronn D, Short MP, « Schwannomatosis: a clinical and pathologic study », Neurology, vol. 46, no 4, , p. 1072–9 (PMID8780094, DOI10.1212/wnl.46.4.1072)
MacCollin M, Chiocca EA, Evans DG, Friedman JM, Horvitz R, Jaramillo D, Lev M, Mautner VF, Niimura M, Plotkin SR, Sang CN, Stemmer-Rachamimov A, Roach ES, « Diagnostic criteria for schwannomatosis », Neurology, vol. 64, no 11, , p. 1838–45 (PMID15955931, DOI10.1212/01.WNL.0000163982.78900.AD)
Westhout FD, Mathews M, Paré LS, Armstrong WB, Tully P, Linskey ME, « Recognizing schwannomatosis and distinguishing it from neurofibromatosis type 1 or 2 », J Spinal Disord Tech, vol. 20, no 4, , p. 329–32 (PMID17538359, DOI10.1097/BSD.0b013e318033ee0f)
Senchenkov A, Kriegel A, Staren ED, Allison DC, « Use of intraoperative ultrasound in excision of multiple schwannomas of the thigh », J Clin Ultrasound, vol. 33, no 7, , p. 360–3 (PMID16196005, DOI10.1002/jcu.20161)
Lunsford LD, Niranjan A, Flickinger JC, Maitz A, Kondziolka D, « Radiosurgery of vestibular schwannomas: summary of experience in 829 cases », J. Neurosurg., vol. 102, no Suppl, , p. 195–9 (PMID15662809, DOI10.3171/jns.2005.102.s_supplement.0195)
(en) Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P, « Germline mutation of INI1/SMARCB1 in familial schwannomatosis », Am. J. Hum. Genet., vol. 80, no 4, , p. 805–10 (PMID17357086, PMCIDPMC1852715, DOI10.1086/513207)
(en) Sestini R, Bacci C, Provenzano A, Genuardi M, Papi L, « Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas », Hum. Mutat., vol. 29, no 2, , p. 227–31 (PMID18072270, DOI10.1002/humu.20679)
Ruggieri M, Huson SM, « The neurofibromatoses. An overview », Ital J Neurol Sci, vol. 20, no 2, , p. 89–108 (PMID10933430, DOI10.1007/s100720050017)
Melean G, Sestini R, Ammannati F, Papi L, « Genetic insights into familial tumors of the nervous system », Am J Med Genet C Semin Med Genet, vol. 129C, no 1, , p. 74–84 (PMID15264275, DOI10.1002/ajmg.c.30022)
Hanemann CO, Evans DG, « News on the genetics, epidemiology, medical care and translational research of Schwannomas », J. Neurol., vol. 253, no 12, , p. 1533–41 (PMID17219030, DOI10.1007/s00415-006-0347-0)
MacCollin M, Woodfin W, Kronn D, Short MP, « Schwannomatosis: a clinical and pathologic study », Neurology, vol. 46, no 4, , p. 1072–9 (PMID8780094, DOI10.1212/wnl.46.4.1072)
MacCollin M, Chiocca EA, Evans DG, Friedman JM, Horvitz R, Jaramillo D, Lev M, Mautner VF, Niimura M, Plotkin SR, Sang CN, Stemmer-Rachamimov A, Roach ES, « Diagnostic criteria for schwannomatosis », Neurology, vol. 64, no 11, , p. 1838–45 (PMID15955931, DOI10.1212/01.WNL.0000163982.78900.AD)
Westhout FD, Mathews M, Paré LS, Armstrong WB, Tully P, Linskey ME, « Recognizing schwannomatosis and distinguishing it from neurofibromatosis type 1 or 2 », J Spinal Disord Tech, vol. 20, no 4, , p. 329–32 (PMID17538359, DOI10.1097/BSD.0b013e318033ee0f)
Senchenkov A, Kriegel A, Staren ED, Allison DC, « Use of intraoperative ultrasound in excision of multiple schwannomas of the thigh », J Clin Ultrasound, vol. 33, no 7, , p. 360–3 (PMID16196005, DOI10.1002/jcu.20161)
Lunsford LD, Niranjan A, Flickinger JC, Maitz A, Kondziolka D, « Radiosurgery of vestibular schwannomas: summary of experience in 829 cases », J. Neurosurg., vol. 102, no Suppl, , p. 195–9 (PMID15662809, DOI10.3171/jns.2005.102.s_supplement.0195)
(en) Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P, « Germline mutation of INI1/SMARCB1 in familial schwannomatosis », Am. J. Hum. Genet., vol. 80, no 4, , p. 805–10 (PMID17357086, PMCIDPMC1852715, DOI10.1086/513207)
(en) Sestini R, Bacci C, Provenzano A, Genuardi M, Papi L, « Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas », Hum. Mutat., vol. 29, no 2, , p. 227–31 (PMID18072270, DOI10.1002/humu.20679)