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 *

170 related articles for article (PubMed ID: 35657380)

  • 1. Pubertal growth in osteogenesis imperfecta caused by pathogenic variants in COL1A1/COL1A2.
    Robinson ME; Rauch D; Glorieux FH; Rauch F
    Genet Med; 2022 Sep; 24(9):1920-1926. PubMed ID: 35657380
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Longitudinal growth curves for children with classical osteogenesis imperfecta (types III and IV) caused by structural pathogenic variants in type I collagen.
    Barber LA; Abbott C; Nakhate V; Do AND; Blissett AR; Marini JC
    Genet Med; 2019 May; 21(5):1233-1239. PubMed ID: 30270360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Standardized growth charts for children with osteogenesis imperfecta.
    Robinson ME; Rauch D; Glorieux FH; Rauch F
    Pediatr Res; 2023 Sep; 94(3):1075-1082. PubMed ID: 36922619
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles.
    Rauch D; Robinson ME; Seiltgens C; Sutton VR; Lee B; Glorieux F; Rauch F
    Bone; 2020 Nov; 140():115547. PubMed ID: 32730936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta.
    Ho Duy B; Zhytnik L; Maasalu K; Kändla I; Prans E; Reimann E; Märtson A; Kõks S
    Hum Genomics; 2016 Aug; 10(1):27. PubMed ID: 27519266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types I or III.
    Augusciak-Duma A; Witecka J; Sieron AL; Janeczko M; Pietrzyk JJ; Ochman K; Galicka A; Borszewska-Kornacka MK; Pilch J; Jakubowska-Pietkiewicz E
    Acta Biochim Pol; 2018; 65(1):79-86. PubMed ID: 29543922
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unequal Impact of
    Yamaguti PM; de La Dure-Molla M; Monnot S; Cardozo-Amaya YJ; Baujat G; Michot C; Fournier BPJ; Riou MC; Caldas Rosa ECC; Soares de Lima Y; Dos Santos PAC; Alcaraz G; Guerra ENS; Castro LC; de Oliveira SF; Pogue R; Berdal A; de Paula LM; Mazzeu JF; Cormier-Daire V; Acevedo AC
    J Dent Res; 2023 Jun; 102(6):616-625. PubMed ID: 36951356
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects.
    Yang L; Liu B; Dong X; Wu J; Sun C; Xi L; Cheng R; Wu B; Wang H; Tong S; Wang D; Luo F
    Osteoporos Int; 2022 Jun; 33(6):1373-1384. PubMed ID: 35044492
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.
    Hartikka H; Kuurila K; Körkkö J; Kaitila I; Grénman R; Pynnönen S; Hyland JC; Ala-Kokko L
    Hum Mutat; 2004 Aug; 24(2):147-54. PubMed ID: 15241796
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with Pamidronate.
    Lindahl K; Kindmark A; Rubin CJ; Malmgren B; Grigelioniene G; Söderhäll S; Ljunggren Ö; Åström E
    Bone; 2016 Jun; 87():11-8. PubMed ID: 26957348
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.
    Sato A; Ouellet J; Muneta T; Glorieux FH; Rauch F
    Bone; 2016 May; 86():53-7. PubMed ID: 26927310
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta.
    Xi L; Zhang H; Zhang ZL
    J Bone Miner Metab; 2021 May; 39(3):416-422. PubMed ID: 33070251
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.
    Zhang H; Yue H; Wang C; Hu W; Gu J; He J; Fu W; Hu Y; Li M; Zhang Z
    Mol Med Rep; 2016 Nov; 14(5):4918-4926. PubMed ID: 27748872
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.
    Ohata Y; Takeyari S; Nakano Y; Kitaoka T; Nakayama H; Bizaoui V; Yamamoto K; Miyata K; Yamamoto K; Fujiwara M; Kubota T; Michigami T; Yamamoto K; Yamamoto T; Namba N; Ebina K; Yoshikawa H; Ozono K
    Osteoporos Int; 2019 Nov; 30(11):2333-2342. PubMed ID: 31363794
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum.
    Bardai G; Moffatt P; Glorieux FH; Rauch F
    Osteoporos Int; 2016 Dec; 27(12):3607-3613. PubMed ID: 27509835
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Skeletal phenotypes in adult patients with osteogenesis imperfecta-correlations with COL1A1/COL1A2 genotype and collagen structure.
    Hald JD; Folkestad L; Harsløf T; Lund AM; Duno M; Jensen JB; Neghabat S; Brixen K; Langdahl B
    Osteoporos Int; 2016 Nov; 27(11):3331-3341. PubMed ID: 27256333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes.
    Malmgren B; Andersson K; Lindahl K; Kindmark A; Grigelioniene G; Zachariadis V; Dahllöf G; Åström E
    Oral Dis; 2017 Jan; 23(1):42-49. PubMed ID: 27510842
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic analysis in Japanese patients with osteogenesis imperfecta: Genotype and phenotype spectra in 96 probands.
    Higuchi Y; Hasegawa K; Futagawa N; Yamashita M; Tanaka H; Tsukahara H
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1675. PubMed ID: 33939306
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparing Clinical and Genetic Characteristics of
    Mei Y; Zhang H; Zhang Z
    Front Endocrinol (Lausanne); 2022; 13():935905. PubMed ID: 35909573
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study.
    Machol K; Hadley TD; Schmidt J; Cuthbertson D; Traboulsi H; Silva RC; Citron C; Khan S; Citron K; Carter E; Brookler K; Shapiro JR; Steiner RD; Byers PH; Glorieux FH; Durigova M; Smith P; Bober MB; Sutton VR; Lee BH; ; Nagamani SCS; Raggio C
    Am J Med Genet A; 2020 Apr; 182(4):697-704. PubMed ID: 31876392
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.