BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 34627224)

  • 1. Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene.
    Liu Y; Zeng X; Ding Y; Xu Y; Duan D
    BMC Oral Health; 2021 Oct; 21(1):508. PubMed ID: 34627224
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.
    Zhu Y; Du X; Sun L; Wang H; Wang D; Wu B
    Mol Genet Genomic Med; 2022 Aug; 10(8):e1993. PubMed ID: 35726349
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.
    Härter B; Benedicenti F; Karall D; Lausch E; Schweigmann G; Stanzial F; Superti-Furga A; Scholl-Bürgi S
    Mol Genet Genomic Med; 2020 Jun; 8(6):e1203. PubMed ID: 32196989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hyaline fibromatosis syndrome: A case report.
    Pereira TDSF; Sales JF; Travassos DV; Lanza CR; Castro WH; Gomes CC; Fonseca FP; Silva TA; Gomez RS
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2020 Dec; 130(6):e328-e335. PubMed ID: 32771412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations in the ANTXR2 gene in a Chinese patient suffering from hyaline fibromatosis syndrome: A case report.
    Gao Y; Bai J; Wang J; Liu X
    Mol Med Rep; 2018 Oct; 18(4):4004-4008. PubMed ID: 30152846
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.
    Haidar Z; Temanni R; Chouery E; Jithesh P; Liu W; Al-Ali R; Wang E; Marincola FM; Jalkh N; Haddad S; Haidar W; Chouchane L; Mégarbané A
    BMC Genet; 2017 Jan; 18(1):3. PubMed ID: 28103792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system.
    Denadai R; Raposo-Amaral CE; Bertola D; Kim C; Alonso N; Hart T; Han S; Stelini RF; Buzzo CL; Raposo-Amaral CA; Hart PS
    Am J Med Genet A; 2012 Apr; 158A(4):732-42. PubMed ID: 22383261
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.
    Jaouad IC; Guaoua S; Hajjioui A; Sefiani A
    J Med Case Rep; 2014 Sep; 8():291. PubMed ID: 25186005
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.
    Casas-Alba D; Martínez-Monseny A; Pino-Ramírez RM; Alsina L; Castejón E; Navarro-Vilarrubí S; Pérez-Dueñas B; Serrano M; Palau F; García-Alix A
    Hum Mutat; 2018 Dec; 39(12):1752-1763. PubMed ID: 30176098
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports.
    Ismail MM; Musa SA; Hassan SS; Abdullah MA
    J Med Case Rep; 2023 Jun; 17(1):244. PubMed ID: 37264371
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome.
    Cozma C; Hovakimyan M; Iurașcu MI; Makhseed N; Selim LA; Alhashem AM; Ben-Omran T; Mahmoud IG; Al Menabawy NM; Al-Mureikhi M; Martin M; Demuth L; Yüksel Z; Beetz C; Bauer P; Rolfs A
    Orphanet J Rare Dis; 2019 Aug; 14(1):209. PubMed ID: 31455396
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series.
    Youssefian L; Vahidnezhad H; Touati A; Ziaee V; Saeidian AH; Pajouhanfar S; Zeinali S; Uitto J
    BMC Med Genet; 2018 May; 19(1):87. PubMed ID: 29801470
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome.
    Daşar T; Gönen HN; Kösemehmetoğlu K; Tekşam Ö; Boduroğlu K; Utine GE; Şimşek Kiper PÖ
    Turk J Pediatr; 2024 May; 66(2):205-214. PubMed ID: 38814306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome.
    Knežević P; Tarle M; Fratrić LI; Tarle A; Knežević-Krajina H; Macan D
    Acta Stomatol Croat; 2020 Mar; 54(1):69-74. PubMed ID: 32523159
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder.
    Mantri MD; Pradeep MM; Kalpesh PO; Pranavsinh RJ
    Indian J Dermatol; 2016; 61(5):580. PubMed ID: 27688461
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Systemic Hyalinosis With Heterozygous CMG2 Mutations: A Case Report and Review of Literature.
    Rahvar M; Teng J; Kim J
    Am J Dermatopathol; 2016 May; 38(5):e60-3. PubMed ID: 26885603
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multisystemic Manifestations of Hyaline Fibromatosis Syndrome: Implications for Diagnosis and Management.
    Albusta N; Isa HM; Al-Jowder HE
    Cureus; 2023 Oct; 15(10):e47250. PubMed ID: 37859675
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of novel compound heterozygous mutations in the ANTXR2 gene in a Chinese patient with juvenile hyaline fibromatosis].
    Zhang Y; Li R; Li Y; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):866-869. PubMed ID: 29188618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur.
    Soni JP; Puri RD; Jetha K; Bhavani GS; Chaudhary M; Kohli S; Verma IC
    Indian J Pediatr; 2016 Nov; 83(11):1341-1345. PubMed ID: 27753005
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.