BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 33570693)

  • 1. Imaging of pediatric bone and growth disorders: Of diagnostic workhorses and new horizons.
    Mehany SN; Patsch JM
    Wien Med Wochenschr; 2021 Apr; 171(5-6):102-110. PubMed ID: 33570693
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oral health-related quality of life in X-linked hypophosphataemia and osteogenesis imperfecta.
    Gjørup H; Beck-Nielsen SS; Hald JD; Haubek D
    J Oral Rehabil; 2021 Feb; 48(2):160-168. PubMed ID: 33058298
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Circulating sclerostin in children and young adults with heritable bone disorders.
    Palomo T; Glorieux FH; Rauch F
    J Clin Endocrinol Metab; 2014 May; 99(5):E920-5. PubMed ID: 24512494
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Transition of young adults with metabolic bone diseases to adult care.
    Ross J; Bowden MR; Yu C; Diaz-Thomas A
    Front Endocrinol (Lausanne); 2023; 14():1137976. PubMed ID: 37008909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.
    Forestier-Zhang L; Watts L; Turner A; Teare H; Kaye J; Barrett J; Cooper C; Eastell R; Wordsworth P; Javaid MK; Pinedo-Villanueva R
    Orphanet J Rare Dis; 2016 Nov; 11(1):160. PubMed ID: 27894323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The muscle-bone relationship in X-linked hypophosphatemic rickets.
    Veilleux LN; Cheung MS; Glorieux FH; Rauch F
    J Clin Endocrinol Metab; 2013 May; 98(5):E990-5. PubMed ID: 23526465
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis and management of pediatric metabolic bone diseases associated with skeletal fragility.
    Charoenngam N; Cevik MB; Holick MF
    Curr Opin Pediatr; 2020 Aug; 32(4):560-573. PubMed ID: 32692054
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Evaluation of bone mineral density in selected regions of the skeleton in children with osteogenesis imperfecta and hypophosphatemic rickets].
    Olszaniecka M; Lebiedowski M; Matusik H; Rowińska E; Wieczorek E; Lorenc R
    Pol Tyg Lek; 1995 Nov; 50(44-47):32-4. PubMed ID: 8643422
    [No Abstract]   [Full Text] [Related]  

  • 9. Multidisciplinary patient care in X-linked hypophosphatemic rickets: one challenge, many perspectives.
    Raimann A; Mindler GT; Kocijan R; Bekes K; Zwerina J; Haeusler G; Ganger R
    Wien Med Wochenschr; 2020 Apr; 170(5-6):116-123. PubMed ID: 31993875
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Type III osteogenesis imperfecta associated with hypophosphatemic vitamin D-resistant rickets].
    Menzel D; Monnens L
    Monatsschr Kinderheilkd; 1986 Oct; 134(10):755-7. PubMed ID: 3025669
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Changes in adipose bone marrow and bone morphology in X-linked hypophosphatemic rickets.
    Nguyen-Khac V; Bonnet-Lebrun A; Skalli W; Adamsbaum C; Linglart A; Wicart P
    Orthop Traumatol Surg Res; 2023 May; 109(3):103529. PubMed ID: 36565743
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of bone mineral density and microarchitectural parameters by DXA and HR-pQCT in 37 children and adults with X-linked hypophosphatemic rickets.
    Colares Neto GP; Pereira RM; Alvarenga JC; Takayama L; Funari MF; Martin RM
    Osteoporos Int; 2017 May; 28(5):1685-1692. PubMed ID: 28194480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscle-Bone Interactions in Pediatric Bone Diseases.
    Veilleux LN; Rauch F
    Curr Osteoporos Rep; 2017 Oct; 15(5):425-432. PubMed ID: 28856575
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Material matters: a mechanostat-based perspective on bone development in osteogenesis imperfecta and hypophosphatemic rickets.
    Rauch F
    J Musculoskelet Neuronal Interact; 2006; 6(2):142-6. PubMed ID: 16849823
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Diseases revealed by the mouth].
    Opsahl-Vital S; Gaucher C; Bardet C; Courson F; Linglart A; Chaussain C
    Arch Pediatr; 2015 May; 22(5 Suppl 1):151-2. PubMed ID: 26112566
    [No Abstract]   [Full Text] [Related]  

  • 16. [Rare bone disorders and respective treatments].
    Seefried L; Jakob F
    Internist (Berl); 2021 May; 62(5):486-495. PubMed ID: 33779789
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lack of circulating pigment epithelium-derived factor is a marker of osteogenesis imperfecta type VI.
    Rauch F; Husseini A; Roughley P; Glorieux FH; Moffatt P
    J Clin Endocrinol Metab; 2012 Aug; 97(8):E1550-6. PubMed ID: 22669302
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Usefulness of X-rays in the Differential Diagnosis of Hypophosphataemic Rickets.
    Martel-Villagrán J; Arias-Medina A; García-Mardones G
    Adv Ther; 2020 May; 37(Suppl 2):89-94. PubMed ID: 32236877
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of FGFR Signaling Partially Rescues Hypophosphatemic Rickets in HMWFGF2 Tg Male Mice.
    Xiao L; Du E; Homer-Bouthiette C; Hurley MM
    Endocrinology; 2017 Oct; 158(10):3629-3646. PubMed ID: 28938491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. What every clinical geneticist should know about testing for osteogenesis imperfecta in suspected child abuse cases.
    Pepin MG; Byers PH
    Am J Med Genet C Semin Med Genet; 2015 Dec; 169(4):307-13. PubMed ID: 26566591
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.