BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 24958419)

  • 1. Isolated fetal macrodactyly: phenotypic and genetic disparities in mosaic overgrowth syndrome.
    Bornstein E; Bacino CA; Maliszewski K; Delaney K; Moyal R; Divon MY
    J Ultrasound Med; 2014 Jul; 33(7):1305-7. PubMed ID: 24958419
    [No Abstract]   [Full Text] [Related]  

  • 2. Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly.
    Tripolszki K; Knox R; Parker V; Semple R; Farkas K; Sulák A; Horváth E; Széll M; Nagy N
    Eur J Med Genet; 2016 Apr; 59(4):223-6. PubMed ID: 26851524
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly.
    Rios JJ; Paria N; Burns DK; Israel BA; Cornelia R; Wise CA; Ezaki M
    Hum Mol Genet; 2013 Feb; 22(3):444-51. PubMed ID: 23100325
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An investigation of PIK3CA mutations in isolated macrodactyly.
    Wu J; Tian W; Tian G; Sumner K; Hutchinson DT; Ji Y
    J Hand Surg Eur Vol; 2018 Sep; 43(7):756-760. PubMed ID: 29661094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Insights into the pathogenesis of macrodactyly.
    Ezaki M
    J Hand Surg Eur Vol; 2019 Jan; 44(1):25-31. PubMed ID: 30086673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gait disturbance and lower limb pain in a patient with PIK3CA-related disorder.
    Cappuccio G; Alagia M; D'Anna M; Ranieri C; Di Tommaso S; Bruno C; Fiorillo C; Pedemonte M; Loconte D; Della Casa R; Strisciuglio P; Ginocchio MI; Pinelli M; Resta N; Brunetti-Pierri N
    Eur J Med Genet; 2017 Dec; 60(12):655-657. PubMed ID: 28867506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Macrodactyly: decision-making and surgery timing.
    Ezaki M; Beckwith T; Oishi SN
    J Hand Surg Eur Vol; 2019 Jan; 44(1):32-42. PubMed ID: 30208752
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants.
    Tian W; Huang Y; Sun L; Guo Y; Zhao S; Lin M; Dong X; Zhong W; Yin Y; Chen Z; Zhang N; Zhang Y; Wang L; Lin J; Yan Z; Yang X; Zhao J; Qiu G; Zhang J; Wu Z; Wu N;
    Orphanet J Rare Dis; 2020 Oct; 15(1):288. PubMed ID: 33054853
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GRIN3A and MAPT stimulate nerve overgrowth in macrodactyly.
    Shi X; Lu L; Jin X; Liu B; Sun X; Lu L; Jiang Y
    Mol Med Rep; 2016 Dec; 14(6):5637-5643. PubMed ID: 27840953
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [
    Wu JH; Tian W; Tian GL; Tian MM; Chen SL; Tian W
    Zhonghua Wai Ke Za Zhi; 2018 Jul; 56(7):538-542. PubMed ID: 30032537
    [No Abstract]   [Full Text] [Related]  

  • 11. Surgical Treatment of Macrodactyly.
    Gluck JS; Ezaki M
    J Hand Surg Am; 2015 Jul; 40(7):1461-8. PubMed ID: 26050204
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macrodactyly as a Presenting Sign of Maffucci Syndrome.
    Ghosh SK; Gangopadhyay A
    J Pediatr; 2015 Nov; 167(5):1159-9.e1. PubMed ID: 26364983
    [No Abstract]   [Full Text] [Related]  

  • 13. Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization.
    Wu CJ; Su YN; Lin TH; Tseng LH; Chao KH
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):92-4. PubMed ID: 25675931
    [No Abstract]   [Full Text] [Related]  

  • 14. Limb overgrowth--clinical observations and nosological considerations.
    Pearn J; Viljoen D; Beighton P
    S Afr Med J; 1983 Nov; 64(23):905-8. PubMed ID: 6314563
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Macrodactyly with a complex glomuvenous malformation in congenital lipomatous overgrowth with vascular malformations, epidermal naevi and skeletal anomalies (CLOVES) syndrome.
    Song W; Kwee TC; Suurmeijer AJ
    Histopathology; 2018 Oct; 73(4):705-708. PubMed ID: 29882992
    [No Abstract]   [Full Text] [Related]  

  • 16. Prenatal diagnosis of Roberts syndrome.
    Sharma AK; Jain A; Phadke SR; Srivastava S
    Indian Pediatr; 1994 Oct; 31(10):1261-4. PubMed ID: 7875788
    [No Abstract]   [Full Text] [Related]  

  • 17. Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: prenatal diagnosis and literature review.
    Chen CP; Su YN; Lin TH; Chang TY; Su JW; Wang W
    Taiwan J Obstet Gynecol; 2013 Dec; 52(4):580-5. PubMed ID: 24411048
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital difference of the hand and foot: Pediatric macrodactyly.
    Shen XF; Gasteratos K; Spyropoulou GA; Yin F; Rui YJ
    J Plast Reconstr Aesthet Surg; 2022 Nov; 75(11):4054-4062. PubMed ID: 36175329
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Macrodactyly - options and outcomes.
    Hardwicke J; Khan MA; Richards H; Warner RM; Lester R
    J Hand Surg Eur Vol; 2013 Mar; 38(3):297-303. PubMed ID: 22736742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial Pallister-Hall syndrome: three affected offspring.
    Sills IN; Rapaport R; Desposito F; Lieber C
    Am J Med Genet; 1994 Aug; 52(2):251. PubMed ID: 7802025
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.