Results 171 to 180 of about 33,507 (210)

Neurofibromatosis type 1 with bladder neurofibroma followed by retroperitoneal malignant peripheral nerve sheath tumor: a case report. [PDF]

Urol Case Rep
Ishii N, Yamamoto H, Kobayashi T, Hamaya T, Kodama H, Fujita N, Okamoto T, Hirabayashi T, Hatakeyama S.   +8 more
europepmc   +1 more source

Tips and Pitfalls of Surgical Techniques for Scoliotic Deformities in Neurofibromatosis Type 1. [PDF]

J Clin Med
Kaspiris A, Lianou I, Marouglianis V, Afrati RS, Sakellariou E, Morakis A, Karampinas P, Vasilisadis ES, Pneumaticos SG.   +8 more
europepmc   +1 more source

Coexisting Optic Pathway and Posterior Fossa Gliomas in an Adult With Previously Undiagnosed Neurofibromatosis Type 1. [PDF]

Cureus
Pinto C, Santos AP, Faia J, Pinheiro IS, Martins AS.   +4 more
europepmc   +1 more source

Diagnosis and treatment of neurofibromatosis type 1 with malignant transformation and multiple gastrointestinal stromal tumors: a case report and literature review. [PDF]

Front Med (Lausanne)
Wang H, Liu J, Huang B, Lai Z, Fang Y, Fu G.   +5 more
europepmc   +1 more source

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Von Recklinghausen's neurofibromatosis: neurofibromatosis type 1

Lancet, The, 2003
Rebecca M Reynolds, I W Campbell, Rm Reynolds   +2 more
exaly   +3 more sources

Neurofibromatosis type 1

Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2000
Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity.
openaire   +4 more sources

Neurofibromatosis type 1

Nature Reviews Disease Primers, 2017
Neurofibromatosis type 1 is a complex autosomal dominant disorder caused by germline mutations in the NF1 tumour suppressor gene. Nearly all individuals with neurofibromatosis type 1 develop pigmentary lesions (café-au-lait macules, skinfold freckling and Lisch nodules) and dermal neurofibromas.
David H, Gutmann, Rosalie E, Ferner, Robert H, Listernick, Bruce R, Korf, Pamela L, Wolters, Kimberly J, Johnson   +5 more
openaire   +2 more sources

Neurofibromatosis type 1 and pregnancy

American Journal of Medical Genetics, 1996
Neurofibromatosis Type 1 (NF-1) is an autosomal dominant condition which has markedly variable clinical expression, with manifestations ranging from mild cutaneous lesions to severe orthopedic complications and functional impairment. The current obstetrical literature indicates that women with NF-1 have increased complications associated with pregnancy.
L, Dugoff, E, Sujansky
openaire   +2 more sources

Neurofibromatosis type 1

2015
Neurofibromatosis type 1 (NF1), previously known as von Recklinghausen disease, is a neurogenetic disorder distinct from neurofibromatosis type 2 (NF2). Approximately 1:2500 to 1:3500 individuals worldwide are affected, regardless of ethnicity or race.
Jacqueline L, Anderson, David H, Gutmann
openaire   +2 more sources

Pathophysiology of Neurofibromatosis Type 1

Annals of Internal Medicine, 2006
Neurofibromatoses are inherited disorders, designated as neurofibromatosis type 1 (NF1), neurofibromatosis type 2, and schwannomatosis, that tend to result in benign tumors of the nerve sheath.
Amy, Theos, Bruce R, Korf
openaire   +2 more sources