• A case of fetal osteogenesis imperfecta type 2A: longitudinal observation of natural course in utero and pitfalls for prenatal ultrasound diagnosis
• A case of osteogenesis imperfecta congenita (osteopsathyrosis)
• A case of osteogenesis imperfecta congenita diagnosed in utero
• A Case of Osteogenesis Imperfecta Type II With Additional Balanced Translocation t(1;20)(p13;p11.2)
• A histochemical study of long bones in osteogenesis imperfecta congenita
• A novel homozygous variant in SERPINH1 associated with a severe, lethal presentation of osteogenesis imperfecta with hydranencephaly
• A prenatal case of osteogenesis imperfecta diagnosed with next-generation sequencing
• A Rare Case of Bruck Syndrome Type 2 in Siblings With Broad Phenotypic Variability
• A study of Vrolik's osteogenesis imperfecta congenita
• Acetabular fracture and central hip dislocation in osteogenesis imperfecta child treated surgically with bone grafts augmented by recombinant human bone morphogenetic protein-2: A rare case report
• Acetabular Protrusio in Patients With Osteogenesis Imperfecta: Risk Factors and Progression
• Altered collagen I and premature pulmonary embryonic differentiation in patients with OI type II
• Anesthetic management of a patient with osteogenesis imperfecta combined with mandibular defect
• Anesthetic management of ventricular-peritoneal shunt implantation in osteogenesis imperfecta type IIB: A case report
• Attempts to use gene therapy for reducing connective tissue disorders--osteogenesis imperfecta
• Bone formation in osteogenesis imperfecta congenita
• BPS804 Anti-Sclerostin Antibody in Adults With Moderate Osteogenesis Imperfecta: Results of a Randomized Phase 2a Trial
• Case of osteogenesis imperfecta congenita
• Case Report: A novel <em>de novo</em> variant of <em>COL1A1</em> in fetal genetic osteogenesis imperfecta
• COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta
• Comparative X-ray morphometry of prenatal osteogenesis imperfecta type 2 and thanatophoric dysplasia: a contribution to prenatal differential diagnosis
• Congenital osteogenesis imperfecta (Vrolik's disease)
• Contribution to the study of osteogenesis imperfecta congenita precoce
• Cyclic intravenous pamidronate for an infant with osteogenesis imperfecta type II
• Delivering a Home-Based Exercise Program to Youth With Osteogenesis Imperfecta: Protocol for a Comparative-Approach Study
• Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype-phenotype correlation
• Design and validation of bending test method for characterization of miniature pediatric cortical bone specimens
• Detection of point mutations in type I collagen by RNase digestion of RNA/RNA hybrids
• Determination of a Newborn with Lethal Type II Osteogenesis Imperfecta and Other Anomalies Using Autopsy and Postmortem MSCT--A Case Report
• Direct sequencing of PCR products for mutation detection in osteogenesis imperfecta
• Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies
• Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2
• Family osteogenesis imperfecta (type Vrolik) and its treatment with vitamin D shock
• Fetal Skeletal Lethal Dysplasia: Case Report
• Fetal therapy of skeletal dysplasias
• Gene expression profiling of bone marrow mesenchymal stem cells from Osteogenesis Imperfecta patients during osteoblast differentiation
• Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation
• Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II
• Identification of pathogenic variant and preimplantation genetic testing for a Chinese family affected with osteogenesis imperfecta
• Late oto-neuroophthalmological manifestations in a case of osteogenesis imperfecta congenita
• Lethal osteogenesis imperfecta-like condition with cutis laxa and arterial tortuosity in MZ twins due to a homozygous fibulin-4 mutation
• Lobstein's syndrome; osteogenesis imperfecta congenita
• Management of hangman's fractures and a subaxial compression fracture in two children with osteogenesis imperfecta
• Mutation Analysis of COL1A1 and COL1A2 in Fetuses with Osteogenesis Imperfecta Type II/III
• Next-generation sequencing of common osteogenesis imperfecta-related genes in clinical practice
• Normalization of ossification processes in a case of osteogenesis imperfecta congenita treated with thymus extracts potentiated with liver extracts
• ON A CASE OF EARLY OSTEOGENESIS IMPERFECTA CONGENITA
• On congenital imperfections in the osteogenesis (osteogenesis imperfecta congenita)
• Osteogenesis imperfecta and primary open angle glaucoma: genotypic analysis of a new phenotypic association
• Osteogenesis imperfecta congenita
• Osteogenesis imperfecta congenita
• Osteogenesis imperfecta congenita
• OSTEOGENESIS IMPERFECTA CONGENITA
• Osteogenesis imperfecta congenita (Periosteal dysplasia of Porak and Durante)
• Osteogenesis imperfecta congenita (Vrolick) and congenital rickets--osteogenesis imperfecta tarda (Lobstein) and oxycephaly
• Osteogenesis imperfecta congenita and blue sclerotics; a clinicopathologic study
• Osteogenesis imperfecta congenita in consecutive siblings
• Osteogenesis imperfecta congenita in dizygotic twin
• Osteogenesis imperfecta congenita in dizygotic twins
• OSTEOGENESIS IMPERFECTA CONGENITA OF THE VROLIK TYPE
• Osteogenesis imperfecta congenita, Vrolik's disease
• Osteogenesis imperfecta congenita; report of a case in a Negro infant
• Osteogenesis imperfecta congenita: a connective tissue diathesis
• Osteogenesis imperfecta congenita: report of a case discovered in utero
• OSTEOGENESIS IMPERFECTA CONGENITA: REVIEW OF THE LITERATURE AND A CASE REPORT
• Osteogenesis imperfecta congenita. A presentation of 16 cases and review of the literature
• OSTEOGENESIS IMPERFECTA CONGENITA. CLINICAL, PATHOLOGICAL AND HISTOCHEMICAL STUDY
• Osteogenesis imperfecta congenita. Report of a case
• Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation
• Osteogenesis Imperfecta: Current and Prospective Therapies
• Perinatal lethal type II osteogenesis imperfecta: a case report
• Retinal hemorrhages in type I osteogenesis imperfecta after minor trauma
• Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta
• Rosemary Extract-Induced Autophagy and Decrease in Accumulation of Collagen Type I in Osteogenesis Imperfecta Skin Fibroblasts
• Simultaneous occurrence of osteogenesis imperfecta congenita (Vrolik) and congenital rickets. Osteogenesis imperfecta tarda (Lobstein) and acrocephaly
• Splice receptor-site mutation c.697-2A&gt;G of the <em>COL1A1</em> gene in a Chinese family with osteogenesis imperfecta
• Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report
• Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey
• THE ANTEPARTUM DIAGNOSIS OF OSTEOGENESIS IMPERFECTA CONGENITA: A REPORT OF TWO CASES RECOGNIZED IN UTERO
• The dentin phosphoprotein repeat region and inherited defects of dentin
• The mistaken diagnosis of child abuse: a three-year USAF Medical Center analysis and literature review
• The Stimulating Effect of Rosmarinic Acid and Extracts from Rosemary and Lemon Balm on Collagen Type I Biosynthesis in Osteogenesis Imperfecta Type I Skin Fibroblasts
• The temporal bone in osteogenesis imperfecta congenita. A contribution to the question of the etiology of otosclerosis
• Vrolika's osteogenesis imperfecta congenita