Results 121 to 130 of about 743 (164)

Diverse learners: learning disabilities and quality of life following mind-body and health education interventions for adults with neurofibromatosis. [PDF]

J Neurooncol
Kanaya MR, Greenberg J, Bakhshaie J, Vranceanu AM.   +3 more
europepmc   +1 more source

Long-read genome sequencing resolves the breakpoints of a chromosome 8;22 balanced translocation in NF2-related schwannomatosis. [PDF]

Sci Rep
Montini M, Bonacchi L, Sidoti D, Cuccoli S, Pantaleo M, Peron A, Scuffi I, DosSantos MF, Nassini R, De Logu F, Papi L.   +10 more
europepmc   +1 more source

Long-standing retroperitoneal schwannoma in a 36-year-old female: A case report. [PDF]

Int J Surg Case Rep
Shah AK, Ghimire S, Gyawali B, Karki B, Neupane NP.   +4 more
europepmc   +1 more source

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Neurofibromatoses

Hematology/Oncology Clinics of North America, 2022
The neurofibromatoses are a group of genetic disorders that cause development of nervous system tumors as well as various other tumor and systemic manifestations. Neurofibromatosis type 1 is the most prevalent of these conditions and has the most variable phenotype and highest risk of malignant tumor formation.
Justin Jordan, Scott Plotkin
exaly   +3 more sources

Neurofibromatoses

2012
The studies of familial tumor predisposition syndromes have contributed immensely to our understanding of oncogenesis. Neurofibromatosis 1, neurofibromatosis 2 and schwannomatosis are inherited autosomal dominant neurocutaneous disorders with complete penetrance.
Pierre Wolkenstein, Bessis Didier, Laurence Valeyrie-Allanore   +2 more
exaly   +4 more sources