These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 30098238)

  • 1. [Analysis of NF1 gene mutations among eleven sporadic patients with neurofibromatosis type 1].
    Peng C; Ma S; Tang X; Yang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):480-483. PubMed ID: 30098238
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Analysis of NF1 gene mutations in two sporadic patients with neurofibromatosis type 1].
    Zhao X; Zhou Q; Cai L; Zhao Z; Zhang L; Wang P; Zhang G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):489-492. PubMed ID: 30098240
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Comprehensive Overview of NF1 Mutations in Iranian Patients.
    Savad S; Modarressi MH; Younesi S; Seifi-Alan M; Samadaian N; Masoomy M; Dianatpour M; Norouzi S; Amidi S; Boroumand A; Ashrafi MR; Ronagh A; Eslami M; Hashemnejad M; Nourian S; Mohammadi S; Taheri Amin MM; Heidari M; Seifi-Alan M; Shojaaldini Ardakani H; Aghamahdi F; Khalilian S; Ghafouri-Fard S
    Neuromolecular Med; 2024 Jul; 26(1):28. PubMed ID: 38954284
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Identification of a novel NF1 mutation in a Chinese family affected with neurofibromatosis type I].
    Zhang Q; Liang Y; Gao A; Duan C; Ding Y; Pan Y; Qiao L; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):132-135. PubMed ID: 30703230
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1.
    Xiao H; Yuan L; Xu H; Yang Z; Huang F; Song Z; Yang Y; Zeng C; Deng H
    J Mol Neurosci; 2018 Aug; 65(4):557-563. PubMed ID: 30046999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Molecular diagnosis as a strategy for differential diagnosis and at early ages of neurofibromatosis type 1 (NF1)].
    Gómez M; Batista O
    Rev Med Chil; 2015 Oct; 143(10):1320-30. PubMed ID: 26633276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.
    Palma Milla C; Lezana Rosales JM; López Montiel J; Andrés Garrido LD; Sánchez Linares C; Carmona Tamajón S; Torres Fernández C; Sánchez González P; Franco Freire S; Benito López C; López Siles J
    Ann Hum Genet; 2018 Nov; 82(6):425-436. PubMed ID: 30014477
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism.
    Trevisson E; Forzan M; Salviati L; Clementi M
    Clin Genet; 2014 Apr; 85(4):386-9. PubMed ID: 23621909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of NF1 gene variant in a sporadic case with neurofibromatosis type 1].
    Zhao X; Cai L; Zhang L; Wang P; Zhang G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):871-874. PubMed ID: 32761598
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole Exome Sequencing of Growing and Non-Growing Cutaneous Neurofibromas from a Single Patient with Neurofibromatosis Type 1.
    Faden DL; Asthana S; Tihan T; DeRisi J; Kliot M
    PLoS One; 2017; 12(1):e0170348. PubMed ID: 28099461
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.
    Jeong SY; Park SJ; Kim HJ
    J Korean Med Sci; 2006 Feb; 21(1):107-12. PubMed ID: 16479075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.
    Ko JM; Sohn YB; Jeong SY; Kim HJ; Messiaen LM
    Pediatr Neurol; 2013 Jun; 48(6):447-53. PubMed ID: 23668869
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics and NF1 gene mutation analysis of three successive generations in three different Indian families with neurofibromatosis type 1 and peripheral nerve sheath tumours.
    Prasad BCM; Chandra VVR; Sudarsan A; Kumar PS; Sarma PVGK
    J Clin Neurosci; 2018 Jul; 53():62-68. PubMed ID: 29680440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel and recurrent mutations in the NF1 gene in Italian patients with neurofibromatosis type 1.
    De Luca A; Schirinzi A; Buccino A; Bottillo I; Sinibaldi L; Torrente I; Ciavarella A; Dottorini T; Porciello R; Giustini S; Calvieri S; Dallapiccola B
    Hum Mutat; 2004 Jun; 23(6):629. PubMed ID: 15146469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy.
    Pourirahim M; Houshmand G; Abdolkarimi L; Maleki M; Kalayinia S
    BMC Cardiovasc Disord; 2024 Apr; 24(1):220. PubMed ID: 38654147
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel diagnostic method to detect truncated neurofibromin in neurofibromatosis 1.
    Esposito T; Piluso G; Saracino D; Uccello R; Schettino C; Dato C; Capaldo G; Giugliano T; Varriale B; Paolisso G; Di Iorio G; Melone MA
    J Neurochem; 2015 Dec; 135(6):1123-8. PubMed ID: 26478990
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular analysis of two pediatric cases with sporadic neurofibromatosis type 1].
    Zhang J; Li M; Yao Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):200-2. PubMed ID: 27060315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Simultaneous Detection of
    Bianchessi D; Ibba MC; Saletti V; Blasa S; Langella T; Paterra R; Cagnoli GA; Melloni G; Scuvera G; Natacci F; Cesaretti C; Finocchiaro G; Eoli M
    Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32575496
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Patterns of Novel Alleles and Genotype/Phenotype Correlations Resulting from the Analysis of 108 Previously Undetected Mutations in Patients Affected by Neurofibromatosis Type I.
    Bonatti F; Adorni A; Matichecchia A; Mozzoni P; Uliana V; Pisani F; Garavelli L; Graziano C; Gnoli M; Carli D; Bigoni S; Boschi E; Martorana D; Percesepe A
    Int J Mol Sci; 2017 Sep; 18(10):. PubMed ID: 28961165
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel, heterozygous, pathogenic variant (c.4272delA: p.I1426Ffs*2) for the NF1 gene in a large Chinese family with neurofibromatosis type 1.
    Yang L; Fu J; Cheng J; Zhou B; Liu X; Anuchapreeda S; Fu J
    Mol Biol Rep; 2023 Feb; 50(2):1117-1123. PubMed ID: 36401065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.