Results 101 to 110 of about 1,245 (197)

The Roots of Neurofibromas in Neurofibromatosis 1 — A Question of Multipotency, Differentiation and Hiding [PDF]

open access: yes, 2012
Neurofibromatosis type 1 (NF1) is an autosomal dominant cancer predisposition syndrome that affects about 1 in 3500 individuals worldwide. NF1 is caused by mutations in the NF1 gene that encodes the tumor suppressor protein neurofibromin, an ...
Jouhilahti, Eeva-Mari
core   +1 more source

Neurofibromatose de von Recklinghausen.

open access: yesActa Médica Portuguesa, 1989
Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered.
Ventura, A   +4 more
openaire   +2 more sources

Neurofibromatosis type 1: natural history and impact on quality of life [PDF]

open access: yes, 2016
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal dominant genetic disorders, with a worldwide incidence of approximately 1 in 3000 live births. NF1 can occur as either an inherited defect or as a spontaneous
Obagi, Zaidal
core   +1 more source

Correction to: Surgical management of peripheral nerve sheath tumours in children, with special consideration of neurofibromatoses. [PDF]

open access: yesChilds Nerv Syst, 2021
Zipfel J   +9 more
europepmc   +1 more source

Effect of Mind-Body Skills Training on Quality of Life for Geographically Diverse Adults With Neurofibromatosis: A Fully Remote Randomized Clinical Trial.

open access: yesJAMA Netw Open, 2023
Vranceanu AM   +9 more
europepmc   +1 more source

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