BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

314 related articles for article (PubMed ID: 33910856)

  • 1. Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.
    Friedrich RE; Zustin J; Luebke AM; Rosenbaum T; Gosau M; Hagel C; Kohlrusch FK; Wieland I; Zenker M
    In Vivo; 2021; 35(3):1711-1736. PubMed ID: 33910856
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.
    Vannelli S; Buganza R; Runfola F; Mussinatto I; Andreacchio A; de Sanctis L
    Ital J Pediatr; 2020 May; 46(1):58. PubMed ID: 32393377
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent Mandibular Giant Cell Lesion in Neurofibromatosis Type 1: Second Hit Mutation on the
    Friedrich RE; Luebke AM; Schüller U; Hagel C; Kohlrusch FK; Wieland I; Zenker M
    Anticancer Res; 2022 Jun; 42(6):2945-2952. PubMed ID: 35641267
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurofibromatosis presenting with a cherubism phenotype.
    van Capelle CI; Hogeman PH; van der Sijs-Bos CJ; Heggelman BG; Idowu B; Slootweg PJ; Wittkampf AR; Flanagan AM
    Eur J Pediatr; 2007 Sep; 166(9):905-9. PubMed ID: 17120035
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetically confirmed coexistence of neurofibromatosis type 1 and Cherubism in a pediatric patient.
    Sarantou S; Marinakis NM; Traeger-Synodinos J; Siomou E; Ntinopoulos A; Serbis A
    Mol Biol Rep; 2024 Jan; 51(1):216. PubMed ID: 38281202
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unusual form of recurrent giant cell granuloma of the mandible and lower extremities in a patient with neurofibromatosis type 1.
    Ruggieri M; Pavone V; Polizzi A; Albanese S; Magro G; Merino M; Duray PH
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1999 Jan; 87(1):67-72. PubMed ID: 9927083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple non-ossifying fibromas as a cause of pathological femoral fracture in Jaffe-Campanacci syndrome.
    Cherix S; Bildé Y; Becce F; Letovanec I; Rüdiger HA
    BMC Musculoskelet Disord; 2014 Jun; 15():218. PubMed ID: 24965055
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg.
    Friedrich RE; Hagel C; Kohlrusch FK; Schanze I; Wieland I; Zenker M
    Anticancer Res; 2020 Jun; 40(6):3423-3427. PubMed ID: 32487640
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cherubism associated with neurofibromatosis type 1, and multiple osteolytic lesions of both femurs: a previously undescribed association of findings.
    Martínez-Tello FJ; Manjón-Luengo P; Martin-Pérez M; Montes-Moreno S
    Skeletal Radiol; 2005 Dec; 34(12):793-8. PubMed ID: 16096755
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent multilocular mandibular giant cell granuloma in neurofibromatosis type 1: Evidence for second hit mutation of NF1 gene in the jaw lesion and treatment with curettage and bone substitute materials.
    Friedrich RE; Grob TJ; Hollants S; Zustin J; Spaepen M; Mautner VF; Luebke AM; Hagel C; Legius E; Brems H
    J Craniomaxillofac Surg; 2016 Aug; 44(8):1054-60. PubMed ID: 27316856
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Idiopathic bilateral central giant cell reparative granuloma of jaws: a case report and literature review.
    Orhan E; Erol S; Deren O; Sevin A; Ekici O; Erdoğan B
    Int J Pediatr Otorhinolaryngol; 2010 May; 74(5):547-52. PubMed ID: 20219254
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Is Jaffe-Campanacci syndrome just a manifestation of neurofibromatosis type 1?
    Colby RS; Saul RA
    Am J Med Genet A; 2003 Nov; 123A(1):60-3. PubMed ID: 14556247
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bilateral Central Giant Cell Granuloma of the mandibular angle in three females from the same family.
    Tecco S; Caruso S; Nota A; Leocata P; Cipollone G; Gatto R; Cutilli T
    Head Face Med; 2018 Sep; 14(1):14. PubMed ID: 30180903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
    Yazdizadeh M; Tapia JL; Baharvand M; Radfar L
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Sep; 98(3):316-20. PubMed ID: 15356469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SH3BP2-encoding exons involved in cherubism are not associated with central giant cell granuloma.
    Teixeira RC; Horz HP; Damante JH; Garlet GP; Santos CF; Nogueira RL; Cavalcante RB; Conrads G
    Int J Oral Maxillofac Surg; 2011 Aug; 40(8):851-5. PubMed ID: 21680150
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neurofibromatosis type 1 associated with bilateral central giant cell granuloma of the mandible.
    Chrcanovic BR; Gomez RS; Freire-Maia B
    J Craniomaxillofac Surg; 2011 Oct; 39(7):538-43. PubMed ID: 21071237
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinically aggressive central giant cell granulomas in two patients with neurofibromatosis 1.
    Edwards PC; Fantasia JE; Saini T; Rosenberg TJ; Sachs SA; Ruggiero S
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Dec; 102(6):765-72. PubMed ID: 17138179
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multidisciplinary surgical management of cherubism complicated by neurofibromatosis type 1.
    Hachach-Haram N; Gerarchi P; Benyon SL; Saggar A; McLellan G; Kirkpatrick WN
    J Craniofac Surg; 2011 Nov; 22(6):2318-22. PubMed ID: 22134267
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unilateral Creeping Destruction of Deformed Mandibular Ramus and Angle Associated with Extensive Facial Plexiform Neurofibroma in Neurofibromatosis Type 1: A Case Report with Analysis of the Literature for Diagnosing Osteolytic Events of the Mandible in Tumor-suppressor Gene Syndrome.
    Friedrich RE; Scheuer HA
    Anticancer Res; 2018 Jul; 38(7):4083-4091. PubMed ID: 29970534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
    Messiaen L; Yao S; Brems H; Callens T; Sathienkijkanchai A; Denayer E; Spencer E; Arn P; Babovic-Vuksanovic D; Bay C; Bobele G; Cohen BH; Escobar L; Eunpu D; Grebe T; Greenstein R; Hachen R; Irons M; Kronn D; Lemire E; Leppig K; Lim C; McDonald M; Narayanan V; Pearn A; Pedersen R; Powell B; Shapiro LR; Skidmore D; Tegay D; Thiese H; Zackai EH; Vijzelaar R; Taniguchi K; Ayada T; Okamoto F; Yoshimura A; Parret A; Korf B; Legius E
    JAMA; 2009 Nov; 302(19):2111-8. PubMed ID: 19920235
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.