BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

415 related articles for article (PubMed ID: 31250196)

  • 41. Biomarkers for Ehlers-Danlos Syndromes: There Is a Role?
    Caliogna L; Guerrieri V; Annunziata S; Bina V; Brancato AM; Castelli A; Jannelli E; Ivone A; Grassi FA; Mosconi M; Pasta G
    Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34576312
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Up-to-date classification and multidisciplinary symptoms of Ehlers-Danlos syndromes].
    Ralovich FV; Kiss N; Horváth K; Kárpáti S; Medvecz M
    Orv Hetil; 2019 Apr; 160(16):603-612. PubMed ID: 30983397
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The Ehlers-Danlos syndromes.
    Malfait F; Castori M; Francomano CA; Giunta C; Kosho T; Byers PH
    Nat Rev Dis Primers; 2020 Jul; 6(1):64. PubMed ID: 32732924
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Ehlers-Danlos syndromes].
    Germain DP
    Ann Dermatol Venereol; 2017 Dec; 144(12):744-758. PubMed ID: 29032848
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Ehlers-Danlos syndromes: importance of defining the type.
    van Dijk FS; Ghali N; Chandratheva A
    Pract Neurol; 2024 Mar; 24(2):90-97. PubMed ID: 38160052
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Ehlers-Danlos syndrome type IV.
    Germain DP
    Orphanet J Rare Dis; 2007 Jul; 2():32. PubMed ID: 17640391
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Considerations for lactation with Ehlers-Danlos syndrome: a narrative review.
    Francis J; Dickton DD
    Int Breastfeed J; 2022 Jan; 17(1):4. PubMed ID: 34983567
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report.
    Cortini F; Marinelli B; Seia M; De Giorgio B; Pesatori AC; Montano N; Bassotti A
    J Med Case Rep; 2016 Oct; 10(1):303. PubMed ID: 27799058
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Ehlers-Danlos syndrome presenting with primary nocturnal enuresis.
    Cunha M; Matias M; Marques I
    BMJ Case Rep; 2020 Feb; 13(2):. PubMed ID: 32024714
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A review of Ehlers-Danlos syndrome.
    Miller E; Grosel JM
    JAAPA; 2020 Apr; 33(4):23-28. PubMed ID: 32175940
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Linkage of the gene that encodes the alpha 1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II).
    Loughlin J; Irven C; Hardwick LJ; Butcher S; Walsh S; Wordsworth P; Sykes B
    Hum Mol Genet; 1995 Sep; 4(9):1649-51. PubMed ID: 8541855
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
    Schalkwijk J; Zweers MC; Steijlen PM; Dean WB; Taylor G; van Vlijmen IM; van Haren B; Miller WL; Bristow J
    N Engl J Med; 2001 Oct; 345(16):1167-75. PubMed ID: 11642233
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Urogenital and pelvic complications in the Ehlers-Danlos syndromes and associated hypermobility spectrum disorders: A scoping review.
    Gilliam E; Hoffman JD; Yeh G
    Clin Genet; 2020 Jan; 97(1):168-178. PubMed ID: 31420870
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Clinical and genetic features of vascular Ehlers-Danlos syndrome.
    Germain DP
    Ann Vasc Surg; 2002 May; 16(3):391-7. PubMed ID: 12016538
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Peripartum Iliac Arterial Aneurysm and Rupture in a Patient with Vascular Ehlers-Danlos Syndrome Diagnosed by Next-Generation Sequencing.
    Koitabashi N; Yamaguchi T; Fukui D; Nakano T; Umeyama A; Toda K; Funada R; Ishikawa M; Kawamura R; Okada K; Hatamochi A; Kosho T; Kurabayashi M
    Int Heart J; 2018 Sep; 59(5):1180-1185. PubMed ID: 30158381
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Ehlers-Danlos syndrome: case report and an electron microscopy study.
    Carlesimo M; Cortesi G; Gamba A; Narcisi A; Turturro F; Raffa S; Torrisi MR; Camplone G
    Rheumatol Int; 2012 Jun; 32(6):1507-10. PubMed ID: 21305297
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The Genetics of Soft Connective Tissue Disorders.
    Vanakker O; Callewaert B; Malfait F; Coucke P
    Annu Rev Genomics Hum Genet; 2015; 16():229-55. PubMed ID: 26002060
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Ehlers-Danlos syndrome--diagnosis and subclassification].
    Rand-Hendriksen S; Wekre LL; Paus B
    Tidsskr Nor Laegeforen; 2006 Aug; 126(15):1903-7. PubMed ID: 16915311
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type: a study of intrafamilial and interfamilial variability in 23 Italian pedigrees.
    Castori M; Dordoni C; Valiante M; Sperduti I; Ritelli M; Morlino S; Chiarelli N; Celletti C; Venturini M; Camerota F; Calzavara-Pinton P; Grammatico P; Colombi M
    Am J Med Genet A; 2014 Dec; 164A(12):3010-20. PubMed ID: 25338840
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification of Two Independent
    Bauer A; Bateman JF; Lamandé SR; Hanssen E; Kirejczyk SGM; Yee M; Ramiche A; Jagannathan V; Welle M; Leeb T; Bateman FL
    Genes (Basel); 2019 Sep; 10(10):. PubMed ID: 31546637
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.