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 *

415 related articles for article (PubMed ID: 31250196)

  • 61. Joint hypermobility and headache: understanding the glue that binds the two together--part 1.
    Neilson D; Martin VT
    Headache; 2014 Sep; 54(8):1393-402. PubMed ID: 25040892
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigations.
    Angwin C; Ghali N; Baker D; Brady AF; Pope FM; Vandersteen A; Wagner B; Ferguson DJP; van Dijk FS
    Br J Dermatol; 2020 Mar; 182(3):698-707. PubMed ID: 31141158
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB gene.
    Al-Harbi TM; Al-Rammah H; Al-Zahrani N; Liu Y; Sleiman PMA; Dridi W; Hakonarson H
    Am J Med Genet A; 2022 Feb; 188(2):618-623. PubMed ID: 34636138
    [TBL] [Abstract][Full Text] [Related]  

  • 64. COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap.
    Morlino S; Micale L; Ritelli M; Rohrbach M; Zoppi N; Vandersteen A; Mackay S; Agolini E; Cocciadiferro D; Sasaki E; Madeo A; Ferraris A; Reardon W; Di Rocco M; Novelli A; Grammatico P; Malfait F; Mazza T; Hakim A; Giunta C; Colombi M; Castori M
    Clin Genet; 2020 Mar; 97(3):396-406. PubMed ID: 31794058
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders.
    Salles Rosa Neto N; Pereira IA; Sztajnbok FR; Azevedo VF
    Adv Rheumatol; 2024 Apr; 64(1):32. PubMed ID: 38664779
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Delineation of Ehlers-Danlos syndrome phenotype due to the c.934C>T, p.(Arg312Cys) mutation in COL1A1: Report on a three-generation family without cardiovascular events, and literature review.
    Colombi M; Dordoni C; Venturini M; Zanca A; Calzavara-Pinton P; Ritelli M
    Am J Med Genet A; 2017 Feb; 173(2):524-530. PubMed ID: 28102596
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives.
    Ritelli M; Venturini M; Cinquina V; Chiarelli N; Colombi M
    Orphanet J Rare Dis; 2020 Jul; 15(1):197. PubMed ID: 32736638
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Identification of the novel COL5A1 c.3369_3431dup, p.(Glu1124_Gly1144dup) variant in a patient with incomplete classical Ehlers-Danlos syndrome: The importance of phenotype-guided genetic testing.
    Ritelli M; Cinquina V; Venturini M; Colombi M
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1422. PubMed ID: 32720758
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Neurodevelopmental atypisms in the context of joint hypermobility, hypermobility spectrum disorders, and Ehlers-Danlos syndromes.
    Baeza-Velasco C
    Am J Med Genet C Semin Med Genet; 2021 Dec; 187(4):491-499. PubMed ID: 34741402
    [TBL] [Abstract][Full Text] [Related]  

  • 70. [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]  

  • 71. Gonosomal Mosaicism for a Novel
    Micale L; Foiadelli T; Russo F; Cinque L; Bassanese F; Granatiero M; Fusco C; Savasta S; Castori M
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946877
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Successful treatment with the Smith-Hodge pessary of cervical incompetence due to defective connective tissue in Ehlers-Danlos syndrome.
    Leduc L; Wasserstrum N
    Am J Perinatol; 1992 Jan; 9(1):25-7. PubMed ID: 1550628
    [TBL] [Abstract][Full Text] [Related]  

  • 73. High Prevalence of Connective Tissue Gene Variants in Professional Ballet.
    Vera AM; Peterson LE; Dong D; Haghshenas V; Yetter TR; Delgado DA; McCulloch PC; Varner KE; Harris JD
    Am J Sports Med; 2020 Jan; 48(1):222-228. PubMed ID: 31765226
    [TBL] [Abstract][Full Text] [Related]  

  • 74. [The Ehlers Danlos syndrome : a rare disease although commonly suspected].
    Docampo E; Lehane F; Ribbens C
    Rev Med Liege; 2023 Nov; 78(11):626-633. PubMed ID: 37955292
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Uterine torsion as an elusive obstetrical emergency in pregnancy: is there an association between gravid uterus torsion and Ehlers-Danlos syndrome?: a case report.
    Ghalandarpoor-Attar SN; Ghalandarpoor-Attar SM
    J Med Case Rep; 2022 May; 16(1):210. PubMed ID: 35578307
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Vascular Ehlers-Danlos syndrome.
    Germain DP; Herrera-Guzman Y
    Ann Genet; 2004; 47(1):1-9. PubMed ID: 15127738
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Ehlers-Danlos syndrome associated with glycosaminoglycan abnormalities.
    Miyake N; Kosho T; Matsumoto N
    Adv Exp Med Biol; 2014; 802():145-59. PubMed ID: 24443026
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Application of the 2017 criteria for vascular Ehlers-Danlos syndrome in 50 patients ascertained according to the Villefranche nosology.
    Ritelli M; Rovati C; Venturini M; Chiarelli N; Cinquina V; Castori M; Colombi M
    Clin Genet; 2020 Feb; 97(2):287-295. PubMed ID: 31600821
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The molecular genetics of the Ehlers-Danlos syndrome.
    Burrows NP
    Clin Exp Dermatol; 1999 Mar; 24(2):99-106. PubMed ID: 10233664
    [TBL] [Abstract][Full Text] [Related]  

  • 80. The clinical presentation of Ehlers-Danlos syndrome.
    Lawrence EJ
    Adv Neonatal Care; 2005 Dec; 5(6):301-14. PubMed ID: 16338669
    [TBL] [Abstract][Full Text] [Related]  

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