| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Maria Demestre, Menderes Yusuf Terzi, Victor Mautner, Peter Vajkoczy, Andreas Kurtz, Ana Luisa Piñ. Effects of pigment epithelium derived factor (PEDF) on malignant peripheral nerve sheath tumours (MPNSTs). Journal of neuro-oncology. vol 115. issue 3. 2014-07-10. PMID:24078214. |
a prominent feature of nf1 is the formation of benign tumours of the peripheral nerve sheath (neurofibromas). |
2014-07-10 |
2023-08-12 |
mouse |
| H N Ozcan, M Karcaaltincaba, B Oguz, M Halilogl. Radiological manifestations of abdominopelvic nerve tumours seen in neurofibromatosis type 1. Clinical radiology. vol 69. issue 4. 2014-05-09. PMID:24361143. |
neurofibromas arise from schwann cells and fibroblasts and plexiform neurofibromas are pathognomonic for nf1, which may arise in any peripheral nerve. |
2014-05-09 |
2023-08-12 |
Not clear |
| Martino Ruggieri, Agata Polizzi, Vincenzo Salpietro, Gemma Incorpora, Francesco Nicita, Piero Pavone, Raffaele Falsaperla, Caterina Nucifora, Francesca Granata, Angela Distefano, Luca Padua, Rosario Caltabiano, Salvatore Lanzafame, Anna Lia Gabriele, Andrea Ortensi, Valerio D'Orazi, Andrea Panunzi, Pietro Milone, Kshitij Mankad, Nunzio Platania, Vincenzo Albanese, Vito Pavon. Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype. Neuropediatrics. vol 44. issue 5. 2014-05-08. PMID:23780384. |
familial spinal neurofibromatosis is a form of neurofibromatosis 1 (nf1), consisting of extensive, symmetrical, histologically proven, multiple neurofibromas of the spinal roots at every level and of all major peripheral nerves sometimes associated with typical nf1 stigmata; most cases underlie nf1 gene mutations. |
2014-05-08 |
2023-08-12 |
Not clear |
| P de Blank, K Cole, L Kersun, A Green, J J Wilkes, J Belasco, R Bagatell, L C Bailey, M J Fishe. fdg-pet in two cases of neurofibromatosis type 1 and atypical malignancies. Current oncology (Toronto, Ont.). vol 21. issue 2. 2014-04-25. PMID:24764718. |
although (18)f-fluorodeoxyglucose positron-emission tomography (fdg-pet) has been used to differentiate benign neurofibromas from malignant peripheral nerve sheath tumours, fdg-pet characteristics for more rare tumours have been poorly described in children with nf1. |
2014-04-25 |
2023-08-13 |
Not clear |
| Kenan Yılmaz, Ruhan Dusunsel, Ismail Dursun, Abdulhakim Coskun, Sirac Erten, Mustafa Kucukaydın, Sibel Yel, Zubeyde Gundu. Neurofibromas of the bladder in a child with neurofibromatosis type 1 causing chronic renal disease. Renal failure. vol 35. issue 7. 2014-04-08. PMID:23815393. |
neurofibromatosis type 1 (nf1) is an autosomal-dominant inherited disorder and its prominent feature is the neurofibroma and renal involvement includes renal artery stenosis and renal artery aneurysms causing renovascular hypertension. |
2014-04-08 |
2023-08-12 |
Not clear |
| M-J Descheemaeker, E Plasschaert, J-P Frijns, E Legiu. Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control group. Journal of intellectual disability research : JIDR. vol 57. issue 9. 2014-03-25. PMID:23095048. |
neurofibromatosis type 1 (nf1) is a common inherited autosomal dominant condition, characterised by multiple café-au-lait macules, axillary and/or inguinal freckling, iris lisch nodules and tumours of the nervous system such as neurofibromas and optic pathway gliomas. |
2014-03-25 |
2023-08-12 |
Not clear |
| David O Onu, Andrew W Hunn, Jens Peters-Willk. Charcot-Marie-Tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots. BMJ case reports. vol 2013. 2014-03-10. PMID:23853192. |
we describe a patient with both cmt and nf1, who had multiple neurofibromas involving the entire spinal neural axis. |
2014-03-10 |
2023-08-12 |
Not clear |
| David O Onu, Andrew W Hunn, Jens Peters-Willk. Charcot-Marie-Tooth syndrome and neurofibromatosis type 1 with multiple neurofibromas of the entire spinal nerve roots. BMJ case reports. vol 2013. 2014-03-10. PMID:23853192. |
to our knowledge, this is the first reported case of cmt syndrome coexisting with nf1 in which multiple neurofibromas involved the entire spinal nerve roots. |
2014-03-10 |
2023-08-12 |
Not clear |
| Shivani Ahlawat, Jaishri Blakeley, Elizabeth Montgomery, Rathan M Subramaniam, Allan Belzberg, Laura M Faya. Schwannoma in neurofibromatosis type 1: a pitfall for detecting malignancy by metabolic imaging. Skeletal radiology. vol 42. issue 9. 2014-02-20. PMID:23649401. |
neurofibromatosis type 1 (nf1) is a neurocutaneous syndrome characterized by the development of multiple peripheral nerve sheath tumors, the majority of which are benign neurofibromas. |
2014-02-20 |
2023-08-12 |
Not clear |
| Shivani Ahlawat, Jaishri Blakeley, Elizabeth Montgomery, Rathan M Subramaniam, Allan Belzberg, Laura M Faya. Schwannoma in neurofibromatosis type 1: a pitfall for detecting malignancy by metabolic imaging. Skeletal radiology. vol 42. issue 9. 2014-02-20. PMID:23649401. |
however, malignant peripheral nerve sheath tumors (mpnsts) occur with a 10 % lifetime risk in patients with nf1, often developing within a neurofibroma. |
2014-02-20 |
2023-08-12 |
Not clear |
| Ashish Kumar, Srinivas Vinjamuri, Sahu P Barad. Posterior approach for giant S1 neurofibroma in Von Recklinghausen's disease: Is total resection realistic? Journal of neurosciences in rural practice. vol 4. issue 4. 2013-12-18. PMID:24347959. |
bilateral sacral neurofibromas are uncommonly seen in neurofibromatosis type 1 (nf1) also known as von recklinghausen's disease. |
2013-12-18 |
2023-08-12 |
Not clear |
| Ashish Kumar, Srinivas Vinjamuri, Sahu P Barad. Posterior approach for giant S1 neurofibroma in Von Recklinghausen's disease: Is total resection realistic? Journal of neurosciences in rural practice. vol 4. issue 4. 2013-12-18. PMID:24347959. |
we report a case of bilateral s1 neurofibromas in a patient of nf1 where she had a giant left-sided neurofibroma with extensive bone erosion and a small fusiform neurofibroma on the right side. |
2013-12-18 |
2023-08-12 |
Not clear |
| Yi Zhen Chiang, Firas Al-Niaimi, Janice Ferguson, Paul Jeffrey August, Vishal Mada. Carbon dioxide laser treatment of cutaneous neurofibromas. Dermatology and therapy. vol 2. issue 1. 2013-12-09. PMID:23205330. |
neurofibromatosis type 1 (nf1) is an autosomal dominant disorder, with multisystem involvement, including cutaneous manifestations of hyperpigmentation and neurofibromas. |
2013-12-09 |
2023-08-12 |
Not clear |
| Yilun Koethe, Brigitte C Widemann, Fouad Hajjar, Bradford J Wood, Aradhana M Venkatesa. PET-guided biopsy with needle navigation facilitates diagnosis of angiosarcoma in neurofibromatosis type 1. Pediatric blood & cancer. vol 60. issue 12. 2013-11-26. PMID:23922330. |
navigation with multi-modality (pet, ct, and ultrasound) image fusion facilitated the successful biopsy and diagnosis of angiosarcoma arising from a pelvic neurofibroma in a patient with nf1. |
2013-11-26 |
2023-08-12 |
Not clear |
| Miriam J Smith, Sonia Esparza, Vanessa L Merker, Alona Muzikansky, Miriam A Bredella, Gordon J Harris, Ara Kassarjian, Wenli Cai, James A Walker, Victor F Mautner, Scott R Plotki. Plasma S100β is not a useful biomarker for tumor burden in neurofibromatosis. Clinical biochemistry. vol 46. issue 7-8. 2013-09-30. PMID:23261835. |
neurofibromatosis 1 (nf1), nf2, and schwannomatosis are characterized by a predisposition to develop multiple neurofibromas and schwannomas. |
2013-09-30 |
2023-08-12 |
Not clear |
| Kursat bora Carman, Ayten Yakut, Banu Anlar, Sukriye Ayte. Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case. BMJ case reports. vol 2013. 2013-09-24. PMID:23417386. |
we report a young patient whose classical nf1 stigmata and numerous spinal neurofibromas matched both groups. |
2013-09-24 |
2023-08-12 |
Not clear |
| Ciğdem Usul Afşar, Ismail Oğuz Kara, Banu Kara Kozat, Haluk Demiryürek, Berna Bozkurt Duman, Figen Dora. Neurofibromatosis type 1, gastrointestinal stromal tumor, leiomyosarcoma and osteosarcoma: four cases of rare tumors and a review of the literature. Critical reviews in oncology/hematology. vol 86. issue 2. 2013-09-23. PMID:23218951. |
patients with nf1 develop multiple neurofibromas that can transform into aggressive sarcomas known as malignant peripheral nerve sheath tumors. |
2013-09-23 |
2023-08-12 |
Not clear |
| Carlos E Prada, Edwin Jousma, Tilat A Rizvi, Jianqiang Wu, R Scott Dunn, Debra A Mayes, Jose A Cancelas, Eva Dombi, Mi-Ok Kim, Brian L West, Gideon Bollag, Nancy Ratne. Neurofibroma-associated macrophages play roles in tumor growth and response to pharmacological inhibition. Acta neuropathologica. vol 125. issue 1. 2013-08-06. PMID:23099891. |
we tested the effects of plx3397, a dual kit/fms kinase inhibitor that blocks macrophage infiltration, in the dhh-cre; nf1(flox/flox) mouse model of gem grade i neurofibroma. |
2013-08-06 |
2023-08-12 |
mouse |
| Bhavya Shetty, Y Umesh, K Kranti, Hema Sesha. Periodontal manifestations of von Recklinghausen neuro fibromatosis. Journal of Indian Society of Periodontology. vol 17. issue 2. 2013-07-22. PMID:23869137. |
neurofibroma is an uncommon benign tumor of the oral cavity derived from the cells that constitute the nerve sheath neurofibromatosis type 1 (nf1), also known as von recklinghausen's disease, is the most common type of neurofibromatosis and accounts for about 90% of all cases. |
2013-07-22 |
2023-08-12 |
human |
| Kavitha Nutakki, Cynthia M Hingtgen, Patrick Monahan, James W Varni, Nancy L Swigonsk. Development of the adult PedsQL™ neurofibromatosis type 1 module: initial feasibility, reliability and validity. Health and quality of life outcomes. vol 11. 2013-07-12. PMID:23432799. |
research in understanding the pathogenetic mechanisms of neurofibroma development has led to the use of new clinical trials for the treatment of nf1. |
2013-07-12 |
2023-08-12 |
Not clear |