BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 29149593)

  • 21. Hajdu-Cheney Syndrome: A Systematic Review of the Literature.
    Cortés-Martín J; Díaz-Rodríguez L; Piqueras-Sola B; Rodríguez-Blanque R; Bermejo-Fernández A; Sánchez-García JC
    Int J Environ Res Public Health; 2020 Aug; 17(17):. PubMed ID: 32854429
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review.
    Zeng C; Lin Y; Lu Z; Chen Z; Jiang X; Mao X; Liu Z; Lu X; Zhang K; Yu Q; Wang X; Huang Y; Liu L
    BMC Musculoskelet Disord; 2020 Mar; 21(1):154. PubMed ID: 32143606
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.
    Efstathiadou ZA; Kostoulas C; Polyzos SA; Adamidou F; Georgiou I; Kita M
    Endocrine; 2021 Jan; 71(1):208-215. PubMed ID: 32772338
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An Antibody to Notch2 Reverses the Osteopenic Phenotype of Hajdu-Cheney Mutant Male Mice.
    Canalis E; Sanjay A; Yu J; Zanotti S
    Endocrinology; 2017 Apr; 158(4):730-742. PubMed ID: 28323963
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Progress and Current Status in Hajdu-Cheney Syndrome with Focus on Novel Genetic Research.
    Aida N; Ohno T; Azuma T
    Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232677
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A very rare cause of acro-osteolysis: Hajdu-Cheney syndrome.
    Deprouw C; Feydy A; Giraudet Le Quintrec JS; Ruiz B; Kahan A; Allanore Y
    Joint Bone Spine; 2015 Dec; 82(6):455-9. PubMed ID: 26184537
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fracture healing in a mouse model of Hajdu-Cheney-Syndrome with high turnover osteopenia results in decreased biomechanical stability.
    Ballhause TM; Jiang S; Xie W; Sevecke J; Dowling C; Dust T; Brandt S; Mertens PR; Yorgan TA; Schinke T; Frosch KH; Baranowsky A; Keller J
    Sci Rep; 2023 Jul; 13(1):11418. PubMed ID: 37452111
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel NOTCH2 mutation identified in a Korean family with Hajdu-Cheney syndrome showing phenotypic diversity.
    Han MS; Ko JM; Cho TJ; Park WY; Cheong HI
    Ann Clin Lab Sci; 2015; 45(1):110-4. PubMed ID: 25696021
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical consequences in truncating mutations in exon 34 of NOTCH2: report of six patients with Hajdu-Cheney syndrome and a patient with serpentine fibula polycystic kidney syndrome.
    Narumi Y; Min BJ; Shimizu K; Kazukawa I; Sameshima K; Nakamura K; Kosho T; Rhee Y; Chung YS; Kim OH; Fukushima Y; Park WY; Nishimura G
    Am J Med Genet A; 2013 Mar; 161A(3):518-26. PubMed ID: 23401378
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A mutation in NOTCH2 gene in a Chinese patient with Hajdu-Cheney syndrome.
    Gu JM; Hu YQ; Zhang H; Wang C; Hu WW; Yue H; Liu YJ; Zhang ZL
    Joint Bone Spine; 2013 Oct; 80(5):548-9. PubMed ID: 23566664
    [No Abstract]   [Full Text] [Related]  

  • 31. Bisphosphonate therapy for spinal osteoporosis in Hajdu-Cheney syndrome - new data and literature review.
    Pittaway JFH; Harrison C; Rhee Y; Holder-Espinasse M; Fryer AE; Cundy T; Drake WM; Irving MD
    Orphanet J Rare Dis; 2018 Apr; 13(1):47. PubMed ID: 29618366
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotypic presentations of Hajdu-Cheney syndrome according to age - 5 distinct clinical presentations.
    Graversen L; Handrup MM; Irving M; Hove H; Diness BR; Risom L; Svaneby D; Aagaard MM; Vogel I; Gjørup H; Davidsen M; Hellfritzsch MB; Lauridsen E; Gregersen PA
    Eur J Med Genet; 2020 Feb; 63(2):103650. PubMed ID: 30980954
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal and postnatal findings in serpentine fibula polycystic kidney syndrome and a review of the NOTCH2 spectrum disorders.
    Martin BM; Ivanova MH; Sarukhanov A; Kim A; Power P; Pugash D; Popescu OE; Lachman RS; Krakow D; Patel MS
    Am J Med Genet A; 2014 Oct; 164A(10):2490-5. PubMed ID: 24995648
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The Hajdu Cheney Mutation Is a Determinant of B-Cell Allocation of the Splenic Marginal Zone.
    Yu J; Zanotti S; Walia B; Jellison E; Sanjay A; Canalis E
    Am J Pathol; 2018 Jan; 188(1):149-159. PubMed ID: 29037852
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Induction of the Hajdu-Cheney Syndrome Mutation in CD19 B Cells in Mice Alters B-Cell Allocation but Not Skeletal Homeostasis.
    Yu J; Zanotti S; Schilling L; Schoenherr C; Economides AN; Sanjay A; Canalis E
    Am J Pathol; 2018 Jun; 188(6):1430-1446. PubMed ID: 29545197
    [TBL] [Abstract][Full Text] [Related]  

  • 36. NOTCH2 related disorders: Description and review of the fetal presentation.
    Deb W; Joubert M; Cogné B; Vincent M; Ghesh L; Bézieau S; Le Vaillant C; Beneteau C
    Eur J Med Genet; 2023 Jul; 66(7):104769. PubMed ID: 37121269
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital Glaucoma: a Novel Ocular Manifestation of Hajdu-Cheney Syndrome.
    Swan L; Gole G; Sabesan V; Cardinal J; Coman D
    Case Rep Genet; 2018; 2018():2508345. PubMed ID: 30420927
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Exploratory use of romosozumab for osteoporosis in a patient with Hajdu-Cheney syndrome: a case report.
    Kim KJ; Hong N; Lee S; Shin S; Rhee Y
    Osteoporos Int; 2023 May; 34(5):1005-1009. PubMed ID: 36622389
    [TBL] [Abstract][Full Text] [Related]  

  • 39. First case of Hajdu-Cheney syndrome in Lithuania caused by novel NOTCH2 gene likely pathogenic variant.
    Tėvelytė I; Bertašius P; Aleknavičienė K; Jonikas R; Klimaitė J; Jašinskienė E; Traberg R
    Eur J Med Genet; 2024 Apr; 69():104938. PubMed ID: 38580081
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome.
    Sakka S; Gafni RI; Davies JH; Clarke B; Tebben P; Samuels M; Saraff V; Klaushofer K; Fratzl-Zelman N; Roschger P; Rauch F; Högler W
    J Clin Endocrinol Metab; 2017 Nov; 102(11):4163-4172. PubMed ID: 28938420
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.