| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Fahad Aljindan, Lamiaa Aljehani, Bayan Alsharif, Hatan Mortad. Management of Neurofibromatosis of the Nipple-Areolar Complex. Case reports in surgery. vol 2021. 2021-08-24. PMID:34422429. |
several case series of patients with nf1 have been reported, but there are only a few published reports on neurofibromas of the nipple-areolar complexes. |
2021-08-24 |
2023-08-13 |
Not clear |
| Samira Foji, Eesa Mohammadi, Akram Sanagoo, Leila Jouybar. The Patients' Experiences of Burden of Neurofibromatosis: A Qualitative Study. Iranian journal of nursing and midwifery research. vol 26. issue 4. 2021-08-24. PMID:34422615. |
neurofibromatosis type 1 (nf1) is a common autosomal disorder; the criteria for the diagnosis of nf1 includes café au lait spots, freckling, and neurofibromas (nf). |
2021-08-24 |
2023-08-13 |
Not clear |
| Maud Jalabert, Salah Ferkal, Jean-Claude Souberbielle, Emilie Sbidian, Arthur Mageau, Florent Eymard, Philippe Le Corvoisier, Laurence Allanore, Xavier Chevalier, Pierre Wolkenstein, Sandra Guignar. Bone Status According to Neurofibromatosis Type 1 Phenotype: A Descriptive Study of 60 Women in France. Calcified tissue international. vol 108. issue 6. 2021-08-18. PMID:33558959. |
we included 60 nf1 women, 18-51 years old, non-menopausal, divided in 2 groups: «at risk phenotype» (arp) composed by 30 patients with at least 2 subcutaneous neurofibromas (sc-nf) and «classical phenotype» (cp) composed by 30 patients with none or 1 sc-nf. |
2021-08-18 |
2023-08-13 |
Not clear |
| Xi-Wei Cui, Jie-Yi Ren, Yi-Hui Gu, Qing-Feng Li, Zhi-Chao Wan. NF1, Neurofibromin and Gene Therapy: Prospects of Next-Generation Therapy. Current gene therapy. vol 20. issue 2. 2021-08-16. PMID:32767931. |
nf1 is well known for its various clinical manifestations, including café-au-late macules, lisch nodules, bone deformity and neurofibromas. |
2021-08-16 |
2023-08-13 |
Not clear |
| Francisco Javier García-Martínez, Daniel Azorín, Anna Duat-Rodríguez, Ángela Hernández-Martí. Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancy. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG. vol 19. issue 1. 2021-08-09. PMID:33448128. |
clinicopathological features of cutaneous neurofibromas presenting as large irregularly shaped congenital café-au-lait macules (calm) in neurofibromatosis type 1 (nf1) patients have not been well characterized. |
2021-08-09 |
2023-08-13 |
Not clear |
| Roope A Kallionpää, Kaisa Ahramo, Marianna Aaltonen, Paula Pennanen, Juha Peltonen, Sirkku Peltone. Circulating free DNA in the plasma of individuals with neurofibromatosis type 1. American journal of medical genetics. Part A. vol 185. issue 4. 2021-08-06. PMID:33484105. |
individuals with nf1 are likely to be followed up using this method, but the effects of nf1 and neurofibromas on cfdna levels are not known. |
2021-08-06 |
2023-08-13 |
Not clear |
| Charlie N Nelson, Eva Dombi, Jared S Rosenblum, Markku M Miettinen, Tanya J Lehky, Patricia O Whitcomb, Christina Hayes, Gretchen Scott, Sarah Benzo, Brigitte C Widemann, Prashant Chittiboin. Safe marginal resection of atypical neurofibromas in neurofibromatosis type 1. Journal of neurosurgery. 2021-07-30. PMID:31653805. |
patients with neurofibromatosis type 1 (nf1) are predisposed to visceral neurofibromas, some of which can progress to premalignant atypical neurofibromas (anfs) and malignant peripheral nerve sheath tumors (mpnsts). |
2021-07-30 |
2023-08-13 |
Not clear |
| Hui Li Kwong, Yong-Kwang Tay, Ene-Choo Ta. Case Report: Mosaicism of a novel nonsense variant in the neurofibromin gene underlies a mosaic generalized NF1 phenotype. F1000Research. vol 10. 2021-07-27. PMID:34164111. |
neurofibromatosis 1 (nf1) is a neurocutaneous syndrome characterized by multiple café-au-lait macules, cutaneous neurofibromas or plexiform neurofibromas, iris lisch nodules, axillary and inguinal freckling. |
2021-07-27 |
2023-08-13 |
Not clear |
| Ricci Allen, Monica Epelman, Omar Cruz-Diaz, Pamela Ellswort. Pelvic plexiform neurofibroma during bowel/bladder dysfunction in an NF1 pediatric patient: A case report. Urology case reports. vol 38. 2021-07-27. PMID:34307048. |
we present a 15-year-old patient with nf1 with a large unresectable neurofibroma located between the prostate and bladder discovered incidentally on renal/bladder ultrasound during the evaluation of bowel/bladder dysfunction. |
2021-07-27 |
2023-08-13 |
Not clear |
| Roope A Kallionpää, Kaisa Ahramo, Eija Martikkala, Elnaz Fazeli, Pekka Haapaniemi, Anne Rokka, Ilmo Leivo, Ilkka T Harvima, Juha Peltonen, Sirkku Peltone. Mast Cells in Human Cutaneous Neurofibromas: Density, Subtypes, and Association with Clinical Features in Neurofibromatosis 1. Dermatology (Basel, Switzerland). 2021-07-08. PMID:34237737. |
cutaneous neurofibromas (cnfs) are hallmarks of neurofibromatosis 1 (nf1) and cause the main disease burden in adults with nf1. |
2021-07-08 |
2023-08-13 |
human |
| Eric Legius, Hilde Brem. Genetic basis of neurofibromatosis type 1 and related conditions, including mosaicism. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 36. issue 10. 2021-06-21. PMID:32601904. |
neurofibromatosis type 1 (nf1) is a frequent autosomal dominant disorder characterised by café-au-lait maculae (calm), skinfold freckling, iris lisch nodules and benign peripheral nerve sheath tumours (neurofibromas). |
2021-06-21 |
2023-08-13 |
Not clear |
| Rafaela E Rozza-de-Menezes, Lilian M Almeida, Raquel M Andrade-Losso, Gustavo de Souza Vieira, Orlando H K Siqueira, Carolina I Brum, Vincent M Riccardi, Karin S Cunh. A Clinicopathologic Study on the Role of Estrogen, Progesterone, and Their Classical and Nonclassical Receptors in Cutaneous Neurofibromas of Individuals With Neurofibromatosis 1. American journal of clinical pathology. vol 155. issue 5. 2021-06-15. PMID:33289020. |
to evaluate the expression of progesterone receptor (pr), estrogen receptor (er), and g protein-coupled estrogen receptor 1 (gper-1) in cutaneous neurofibromas (cnfs) and their correlation with demographic, clinical, and laboratory data of individuals with neurofibromatosis 1 (nf1). |
2021-06-15 |
2023-08-13 |
Not clear |
| Mika M Tabata, Shufeng Li, Pamela Knight, Annette Bakker, Kavita Y Sari. Phenotypic heterogeneity of neurofibromatosis type 1 in a large international registry. JCI insight. vol 5. issue 16. 2021-06-11. PMID:32814709. |
phenotypic clustering revealed 6 phenotypic patient cluster subtypes: mild, freckling predominant, neurofibroma predominant, skeletal predominant, late-onset neural severe, and early-onset neural severe, highlighting potential phenotypic subtypes within nf1. |
2021-06-11 |
2023-08-13 |
Not clear |
| C Iacovino, E Miraglia, A Moramarco, G Corbo, A Lambiase, S Giustin. Ectropion Uveae in neurofibromatosis type 1: a new manifestation. La Clinica terapeutica. vol 172. issue 3. 2021-06-08. PMID:33956037. |
diagnosis of nf1 is made with at least two of the following diagnostic criteria: six or more cafè-au-lait spots, two neurofibromas or one plexiform neurofibroma, axillary or groin freckling, optic glioma, two lisch nodules, bone dysplasia and first-degree relative with nf1. |
2021-06-08 |
2023-08-13 |
Not clear |
| Vincent Roy, Rémy Lamontagne, Matthieu Talagas, Lydia Touzel-Deschênes, Hélène T Khuong, Stéphan Saikali, Nicolas Dupré, François Gros-Loui. Biofabrication of a three dimensional human-based personalized neurofibroma model. Biotechnology journal. vol 16. issue 6. 2021-06-07. PMID:33689228. |
neurofibromas are the most characteristic feature of neurofibromatosis type 1 (nf1), a multisystemic disorder caused by aberrations in the neurofibromin gene (nf1). |
2021-06-07 |
2023-08-13 |
Not clear |
| Vincent Roy, Rémy Lamontagne, Matthieu Talagas, Lydia Touzel-Deschênes, Hélène T Khuong, Stéphan Saikali, Nicolas Dupré, François Gros-Loui. Biofabrication of a three dimensional human-based personalized neurofibroma model. Biotechnology journal. vol 16. issue 6. 2021-06-07. PMID:33689228. |
we describe the first in vitro three dimensional neurofibroma model-directly derived from nf1 patients presenting with histopathological features-having an ecm protein expression profile quite similar to that of a native tumor. |
2021-06-07 |
2023-08-13 |
Not clear |
| Qin Du, Hongxi Chen, Hongyu Zho. Deletion of the whole NF1 gene in a three-generation family with neurofibromatosis type 1. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2021-06-05. PMID:34089417. |
neurofibromatosis type 1 (nf1) is an autosomal dominant neurocutaneous disorder characterized by café-au-lait macules (calms), skinfold freckling, lisch nodules, and neurofibromas. |
2021-06-05 |
2023-08-13 |
Not clear |
| César Bimbi, Vincent M Riccardi, Dimitra Koumoundourou, Georgia Kyriako. Ketotifen, mast cells and NF1 cutaneous neurofibromas: Compelling human data. Dermatologic therapy. vol 33. issue 4. 2021-05-14. PMID:32449281. |
ketotifen, mast cells and nf1 cutaneous neurofibromas: compelling human data. |
2021-05-14 |
2023-08-13 |
human |
| Hiroaki Sakai, Kosuke Kawata, Jun Masuoka, Tomohisa Nishimura, Hiroshi Enaid. Diagnosis and clinical course of ocular ischemic syndrome with retinal vascular abnormalities due to unilateral ocular artery and internal carotid artery stenosis in a child with neurofibromatosis type 1: a case report. BMC ophthalmology. vol 20. issue 1. 2021-05-14. PMID:33097012. |
neurofibromatosis type 1 (nf1) is a hereditary disease that causes neurofibromas generally, but it has been reported to sometimes be associated with various forms of blood vessel stenosis, occlusion and vascular abnormalities of unknown mechanism. |
2021-05-14 |
2023-08-13 |
Not clear |
| Bethany Cartwright, Kenneth Corsa. Neurofibroma of the hard palate. BMJ case reports. vol 14. issue 4. 2021-05-14. PMID:33827870. |
neurofibromas can occur as part of neurofibromatosis, type 1 (nf1) or type 2 (nf2). |
2021-05-14 |
2023-08-13 |
Not clear |