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「"Glorieux FH "[Author]」の検索結果

282件中 21件~40件表示    検索結果をPubMedで見る PubMedで見る

DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum.

Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization.

Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - Genotype-phenotype correlations and effect of bisphosphonate treatment.

Effect of high-dose vitamin D supplementation on bone density in youth with osteogenesis imperfecta: A randomized controlled trial.

Osteogenesis Imperfecta Type VI in Individuals from Northern Canada.

Involving Families with Osteogenesis Imperfecta in Health Service Research: Joint Development of the OI/ECE Questionnaire.

Evidence for a Role for Nanoporosity and Pyridinoline Content in Human Mild Osteogenesis Imperfecta.

Body Composition in Children and Adolescents with Osteogenesis Imperfecta.

Prevention and consequences of vitamin D deficiency in pregnant and lactating women and children: A symposium to prioritise vitamin D on the global agenda.

Osteogenesis Imperfecta Type I Caused by COL1A1 Deletions.

Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta.

Evaluation of a Modified Pamidronate Protocol for the Treatment of Osteogenesis Imperfecta.

Aging vs Postmenopausal Osteoporosis: Bone Composition and Maturation Kinetics at Actively Forming Trabecular Surfaces of Female Subjects Aged 1 to 84 Years Old.

Multidisciplinary Treatment of Severe Osteogenesis Imperfecta - Functional Outcomes at Skeletal Maturity.

Pharmacokinetics and pharmacodynamics of a human monoclonal anti-FGF23 antibody (KRN23) in the first multiple ascending dose trial treating adults with X-linked hypophosphatemia.

Intravenous Bisphosphonate Therapy of Young Children with Osteogenesis Imperfecta: Skeletal Findings during Follow Up Throughout the Growing Years.

[The 1990 years].

The functional muscle-bone unit in patients with osteogenesis imperfecta type I.

Prolonged correction of serum phosphorus in adults with X-linked hypophosphatemia using monthly doses of KRN23.

The Effect of SERPINF1 In-Frame Mutations in Osteogenesis Imperfecta Type VI.

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