BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

631 related articles for article (PubMed ID: 30983397)

  • 1. [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]  

  • 2. [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]  

  • 3. Ehlers-Danlos Syndromes, Joint Hypermobility and Hypermobility Spectrum Disorders.
    Micale L; Fusco C; Castori M
    Adv Exp Med Biol; 2021; 1348():207-233. PubMed ID: 34807421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Ehlers-Danlos syndromes, rare types.
    Brady AF; Demirdas S; Fournel-Gigleux S; Ghali N; Giunta C; Kapferer-Seebacher I; Kosho T; Mendoza-Londono R; Pope MF; Rohrbach M; Van Damme T; Vandersteen A; van Mourik C; Voermans N; Zschocke J; Malfait F
    Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):70-115. PubMed ID: 28306225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The 2017 international classification of the Ehlers-Danlos syndromes.
    Malfait F; Francomano C; Byers P; Belmont J; Berglund B; Black J; Bloom L; Bowen JM; Brady AF; Burrows NP; Castori M; Cohen H; Colombi M; Demirdas S; De Backer J; De Paepe A; Fournel-Gigleux S; Frank M; Ghali N; Giunta C; Grahame R; Hakim A; Jeunemaitre X; Johnson D; Juul-Kristensen B; Kapferer-Seebacher I; Kazkaz H; Kosho T; Lavallee ME; Levy H; Mendoza-Londono R; Pepin M; Pope FM; Reinstein E; Robert L; Rohrbach M; Sanders L; Sobey GJ; Van Damme T; Vandersteen A; van Mourik C; Voermans N; Wheeldon N; Zschocke J; Tinkle B
    Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):8-26. PubMed ID: 28306229
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes.
    Gensemer C; Burks R; Kautz S; Judge DP; Lavallee M; Norris RA
    Dev Dyn; 2021 Mar; 250(3):318-344. PubMed ID: 32629534
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).
    Beighton P; De Paepe A; Steinmann B; Tsipouras P; Wenstrup RJ
    Am J Med Genet; 1998 Apr; 77(1):31-7. PubMed ID: 9557891
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome.
    Forghani I
    Balkan Med J; 2019 Jan; 36(1):12-16. PubMed ID: 30063214
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Molecular Genetics and Pathogenesis of Ehlers-Danlos Syndrome and Related Connective Tissue Disorders.
    Ritelli M; Colombi M
    Genes (Basel); 2020 May; 11(5):. PubMed ID: 32414079
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing.
    Cortini F; Villa C; Marinelli B; Combi R; Pesatori AC; Bassotti A
    Arch Dermatol Res; 2019 May; 311(4):265-275. PubMed ID: 30826961
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Diagnostic outcomes for molecular genetic testing in children with suspected Ehlers-Danlos syndrome.
    Damseh N; Dupuis L; O'Connor C; Oh RY; Wang YW; Stavropoulos DJ; Schwartz SB; Mendoza-Londono R
    Am J Med Genet A; 2022 May; 188(5):1376-1383. PubMed ID: 35128800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ehlers-Danlos syndrome: yet another type?
    Viljoen D; Goldblatt J; Thompson D; Beighton P
    Clin Genet; 1987 Sep; 32(3):196-201. PubMed ID: 3621666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural history.
    Tinkle B; Castori M; Berglund B; Cohen H; Grahame R; Kazkaz H; Levy H
    Am J Med Genet C Semin Med Genet; 2017 Mar; 175(1):48-69. PubMed ID: 28145611
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ehlers-Danlos syndrome--a historical review.
    Parapia LA; Jackson C
    Br J Haematol; 2008 Apr; 141(1):32-5. PubMed ID: 18324963
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type.
    Malfait F; Wenstrup RJ; De Paepe A
    Genet Med; 2010 Oct; 12(10):597-605. PubMed ID: 20847697
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heritable collagen disorders: the paradigm of the Ehlers-Danlos syndrome.
    Byers PH; Murray ML
    J Invest Dermatol; 2012 Nov; 132(E1):E6-11. PubMed ID: 23154631
    [No Abstract]   [Full Text] [Related]  

  • 20. [Ehlers-Danlos syndrome: Role of the dentist].
    Melou C; Taillard N; Chauvel-Lebret D
    Orthod Fr; 2021 Sep; 92(3):367-375. PubMed ID: 34583919
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.