标题
Osteogenesis imperfecta
作者
关键词
-
出版物
Nature Reviews Disease Primers
Volume 3, Issue -, Pages 17052
出版商
Springer Nature
发表日期
2017-08-18
DOI
10.1038/nrdp.2017.52
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Osteogenesis imperfecta: new genes reveal novel mechanisms in bone dysplasia
- (2017) Heeseog Kang et al. Translational Research
- Single dose of bisphosphonate preserves gains in bone mass following cessation of sclerostin antibody in Brtl/+ osteogenesis imperfecta model
- (2016) Joseph E. Perosky et al. BONE
- Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations — genotype–phenotype correlations and effect of bisphosphonate treatment
- (2016) Atsuko Sato et al. BONE
- Mortality and Causes of Death in Patients With Osteogenesis Imperfecta: A Register-Based Nationwide Cohort Study
- (2016) Lars Folkestad et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Bone Material Properties in Osteogenesis Imperfecta
- (2016) Nick Bishop JOURNAL OF BONE AND MINERAL RESEARCH
- Evidence for a Role for Nanoporosity and Pyridinoline Content in Human Mild Osteogenesis Imperfecta
- (2016) Eleftherios P Paschalis et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization
- (2016) Nadja Fratzl-Zelman et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Orthopaedic Considerations for the Adult With Osteogenesis Imperfecta
- (2016) Timothy T. Roberts et al. JOURNAL OF THE AMERICAN ACADEMY OF ORTHOPAEDIC SURGEONS
- Osteogenesis imperfecta
- (2016) Antonella Forlino et al. LANCET
- Romosozumab Treatment in Postmenopausal Women with Osteoporosis
- (2016) Felicia Cosman et al. NEW ENGLAND JOURNAL OF MEDICINE
- Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
- (2016) Lucia Mauri et al. Orphanet Journal of Rare Diseases
- DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum
- (2016) G. Bardai et al. OSTEOPOROSIS INTERNATIONAL
- MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta
- (2016) Uschi Lindert et al. Nature Communications
- Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta
- (2016) Wayne A. Cabral et al. PLoS Genetics
- Experience of a skeletal dysplasia registry in Turkey: A five-years retrospective analysis
- (2015) Eda Didem Kurt-Sukur et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Quality of life in osteogenesis imperfecta: A mixed-methods systematic review
- (2015) N. Dahan-Oliel et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Nosology and classification of genetic skeletal disorders: 2015 revision
- (2015) Luisa Bonafe et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Multidisciplinary Treatment of Severe Osteogenesis Imperfecta: Functional Outcomes at Skeletal Maturity
- (2015) Kathleen Montpetit et al. ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
- Rapidly growing Brtl/+ mouse model of osteogenesis imperfecta improves bone mass and strength with sclerostin antibody treatment
- (2015) Benjamin P. Sinder et al. BONE
- Unique micro- and nano-scale mineralization pattern of human osteogenesis imperfecta type VI bone
- (2015) Nadja Fratzl-Zelman et al. BONE
- Fragility of Bone Material Controlled by Internal Interfaces
- (2015) Wolfgang Wagermaier et al. CALCIFIED TISSUE INTERNATIONAL
- Prevalence of Cardiovascular Disease and Cardiac Symptoms: Left and Right Ventricular Function in Adults With Osteogenesis Imperfecta
- (2015) Zoran Radunovic et al. CANADIAN JOURNAL OF CARDIOLOGY
- Zespół Brucka — rzadki zespół charakteryzujący się kruchością kości, przykurczami stawowymi i nowoodkrytą homozygotyczną mutacją FKBP10
- (2015) Hossein Moravej et al. Endokrynologia Polska
- Mutations in patients with osteogenesis imperfecta from consanguineous Indian families
- (2015) Joshi Stephen et al. European Journal of Medical Genetics
- Quality of life in caregivers of children and adolescents with Osteogenesis Imperfecta
- (2015) Ana Paula Vanz et al. Health and Quality of Life Outcomes
- Efficacy and Safety of Bisphosphonate Therapy in Children with Osteogenesis Imperfecta: A Systematic Review
- (2015) Ester B.G. Rijks et al. Hormone Research in Paediatrics
- Heart disease in patients with osteogenesis imperfecta — A systematic review
- (2015) Hamoun Ashournia et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
- Molecular Consequences of theSERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta
- (2015) Uschi Lindert et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- An Investigation of the Mineral in Ductile and Brittle Cortical Mouse Bone
- (2015) Naiara Rodriguez-Florez et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to BiallelicBMP1Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta
- (2015) Delfien Syx et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Bisphosphonates for the Prevention of Fractures in Osteogenesis Imperfecta: Meta-Analysis of Placebo-Controlled Trials
- (2015) Jannie D Hald et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Structure–mechanics relationships of collagen fibrils in the osteogenesis imperfecta mouse model
- (2015) O. G. Andriotis et al. Journal of the Royal Society Interface
- BMP-1/tolloid-like proteinases synchronize matrix assembly with growth factor activation to promote morphogenesis and tissue remodeling
- (2015) Sandrine Vadon-Le Goff et al. MATRIX BIOLOGY
- Clinical Presentation and Alternative Diagnoses in the Adult Population
- (2015) Ulrich Batzdorf NEUROSURGERY CLINICS OF NORTH AMERICA
- LRP receptor family member associated bone disease
- (2015) N. Lara-Castillo et al. REVIEWS IN ENDOCRINE & METABOLIC DISORDERS
- Treatment options for osteogenesis imperfecta
- (2015) Roberta Besio et al. Expert Opinion on Orphan Drugs
- Femoral non-elongating rodding in osteogenesis imperfecta - The importance of purchasing epiphyseal plate
- (2015) Chia-Hsieh Chang et al. Biomedical Journal
- Implementing family health history risk stratification in primary care: Impact of guideline criteria on populations and resource demand
- (2014) Lori A. Orlando et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Skeletal characteristics associated with homozygous and heterozygous WNT1 mutations
- (2014) Telma Palomo et al. BONE
- Effect of sclerostin antibody treatment in a mouse model of severe osteogenesis imperfecta
- (2014) Andreas Roschger et al. BONE
- Targeted Sequencing of a Pediatric Metabolic Bone Gene Panel Using a Desktop Semiconductor Next-Generation Sequencer
- (2014) Frank Rauch et al. CALCIFIED TISSUE INTERNATIONAL
- THERAPY OF ENDOCRINE DISEASE: Treatment of osteogenesis imperfecta in adults
- (2014) Katarina Lindahl et al. EUROPEAN JOURNAL OF ENDOCRINOLOGY
- Quality of life in children and adolescents with Osteogenesis Imperfecta: a qualitative interview based study
- (2014) Claire L Hill et al. Health and Quality of Life Outcomes
- Transcatheter Mitral Valve Repair in Osteogenesis Imperfecta Associated Mitral Valve Regurgitation
- (2014) Frank van der Kley et al. Heart Lung and Circulation
- How Tough Is Brittle Bone? Investigating Osteogenesis Imperfecta in Mouse Bone
- (2014) Alessandra Carriero et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Targeting the LRP5 Pathway Improves Bone Properties in a Mouse Model of Osteogenesis Imperfecta
- (2014) Christina M Jacobsen et al. JOURNAL OF BONE AND MINERAL RESEARCH
- A NovelIFITM5Mutation in Severe Atypical Osteogenesis Imperfecta Type VI Impairs Osteoblast Production of Pigment Epithelium-Derived Factor
- (2014) Charles R Farber et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Evaluation of teriparatide treatment in adults with osteogenesis imperfecta
- (2014) Eric S. Orwoll et al. JOURNAL OF CLINICAL INVESTIGATION
- Osteogenesis imperfecta in adults
- (2014) Nick J. Bishop et al. JOURNAL OF CLINICAL INVESTIGATION
- Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta
- (2014) Ingo Grafe et al. NATURE MEDICINE
- Update on the Evaluation and Treatment of Osteogenesis Imperfecta
- (2014) Jennifer Harrington et al. PEDIATRIC CLINICS OF NORTH AMERICA
- Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients
- (2014) Peiran Zhou et al. PLoS One
- Muscle Strength, Joint Range of Motion, and Gait in Children and Adolescents With Osteogenesis Imperfecta
- (2014) Evelise Brizola et al. Pediatric Physical Therapy
- Osteogenesis Imperfecta: Diagnosis and Treatment
- (2014) A. Biggin et al. Current Osteoporosis Reports
- WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta
- (2013) Shawna M. Pyott et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in WNT1 Cause Different Forms of Bone Fragility
- (2013) Katharina Keupp et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype-phenotype correlations
- (2013) José A. Caparrós-Martin et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Osteogénesis imperfecta: estudio de la calidad de vida en los niños
- (2013) Virginia Fano Archivos Argentinos de Pediatria
- A molecular ensemble in the rER for procollagen maturation
- (2013) Yoshihiro Ishikawa et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- The impact of severe osteogenesis imperfecta on the lives of young patients and their parents – a qualitative analysis
- (2013) Maman Joyce Dogba et al. BMC Pediatrics
- Mineral particle size in children with osteogenesis imperfecta type I is not increased independently of specific collagen mutations
- (2013) Nadja Fratzl-Zelman et al. BONE
- Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta
- (2013) David R. Eyre et al. CALCIFIED TISSUE INTERNATIONAL
- An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk
- (2013) Ye Cheng et al. HUMAN MOLECULAR GENETICS
- Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype ofFKBP10 Mutations
- (2013) Aileen M. Barnes et al. HUMAN MUTATION
- A NonclassicalIFITM5Mutation Located in the Coding Region Causes Severe Osteogenesis Imperfecta With Prenatal Onset
- (2013) Heike Hoyer-Kuhn et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Valvular Heart Disease in Patients with Osteogenesis Imperfecta
- (2013) Mohammad Q. Najib et al. JOURNAL OF CARDIAC SURGERY
- New Genes in Bone Development: What's New in Osteogenesis Imperfecta
- (2013) Joan C. Marini et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Musculoskeletal Functional Outcomes in Children With Osteogenesis Imperfecta
- (2013) Ted Sousa et al. JOURNAL OF PEDIATRIC ORTHOPAEDICS
- Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial
- (2013) Nick Bishop et al. LANCET
- WNT signaling in bone homeostasis and disease: from human mutations to treatments
- (2013) Roland Baron et al. NATURE MEDICINE
- WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta
- (2013) Christine M. Laine et al. NEW ENGLAND JOURNAL OF MEDICINE
- Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome
- (2013) Fransiska Malfait et al. Orphanet Journal of Rare Diseases
- Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
- (2013) Sofie Symoens et al. Orphanet Journal of Rare Diseases
- Potential of Human Fetal Chorionic Stem Cells for the Treatment of Osteogenesis Imperfecta
- (2013) Gemma N. Jones et al. STEM CELLS AND DEVELOPMENT
- A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V
- (2012) Tae-Joon Cho et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Attenuated BMP1 Function Compromises Osteogenesis, Leading to Bone Fragility in Humans and Zebrafish
- (2012) P.V. Asharani et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Mutation in the 5′-UTR of IFITM5 Creates an In-Frame Start Codon and Causes Autosomal-Dominant Osteogenesis Imperfecta Type V with Hyperplastic Callus
- (2012) Oliver Semler et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Analysis of skeletal dysplasias in the Utah population
- (2012) David A. Stevenson et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Peptidyl 3-Hydroxyproline Binding Properties of Type I Collagen Suggest a Function in Fibril Supramolecular Assembly
- (2012) David M. Hudson et al. BIOCHEMISTRY
- Transplanted bone marrow mononuclear cells and MSCs impart clinical benefit to children with osteogenesis imperfecta through different mechanisms
- (2012) S. Otsuru et al. BLOOD
- Ultra-structural defects cause low bone matrix stiffness despite high mineralization in osteogenesis imperfecta mice
- (2012) Maximilien Vanleene et al. BONE
- Atrioventricular valve development: New perspectives on an old theme
- (2012) Annemarieke de Vlaming et al. DIFFERENTIATION
- A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta
- (2012) Wayne A. Cabral et al. GENETICS IN MEDICINE
- Suspected collagen disorders in the bleeding disorder clinic: A case-control study
- (2012) S. C. Jackson et al. HAEMOPHILIA
- Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms
- (2012) Frank Thiele et al. HUMAN MOLECULAR GENETICS
- Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum
- (2012) Maria Trinidad Puig-Hervás et al. HUMAN MUTATION
- Sclerostin antibody improves skeletal parameters in a Brtl/+ mouse model of osteogenesis imperfecta
- (2012) Benjamin P Sinder et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: A proteomic approach
- (2012) Laura Bianchi et al. Journal of Proteomics
- Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta: A New Target for Osteogenesis Imperfecta Pharmacological Therapy
- (2012) Roberta Gioia et al. STEM CELLS
- Wnt Proteins
- (2012) K. Willert et al. Cold Spring Harbor Perspectives in Biology
- Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta
- (2011) Jutta Becker et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Transition to adult care for children with chronic neurological disorders
- (2011) Peter Camfield et al. ANNALS OF NEUROLOGY
- Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
- (2011) Ortrud K Steinlein et al. BMC Medical Genetics
- A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect
- (2011) Giacomo Venturi et al. BONE
- EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta
- (2011) Fleur S van Dijk et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A novel homozygous 5bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient
- (2011) E.D. Setijowati et al. European Journal of Medical Genetics
- Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes
- (2011) Shawna M. Pyott et al. HUMAN MOLECULAR GENETICS
- Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta
- (2011) Víctor Martínez-Glez et al. HUMAN MUTATION
- Mutations in SERPINF1 cause osteogenesis imperfecta type VI
- (2011) Erica P Homan et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Predictors and Correlates of Vitamin D Status in Children and Adolescents with Osteogenesis Imperfecta
- (2011) Thomas Edouard et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- New perspectives on osteogenesis imperfecta
- (2011) Antonella Forlino et al. Nature Reviews Endocrinology
- Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype
- (2011) Freya KR Swinnen et al. Orphanet Journal of Rare Diseases
- Audiologic Phenotype of Osteogenesis Imperfecta
- (2011) Freya K. R. Swinnen et al. OTOLOGY & NEUROTOLOGY
- Fassier–Duval femoral rodding in children with osteogenesis imperfecta receiving bisphosphonates: functional outcomes at one year
- (2011) Joanne Ruck et al. Journal of Childrens Orthopaedics
- Cardiovascular abnormalities in adults with osteogenesis imperfecta
- (2010) Zoran Radunovic et al. AMERICAN HEART JOURNAL
- Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
- (2010) Pablo Lapunzina et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
- (2010) Yasemin Alanay et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta
- (2010) Helena E. Christiansen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Molecular and structural mapping of collagen fibril interactions
- (2010) J. P. R. O. Orgel et al. CONNECTIVE TISSUE RESEARCH
- Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
- (2010) Brian P Kelley et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Alendronate for the Treatment of Pediatric Osteogenesis Imperfecta: A Randomized Placebo-Controlled Study
- (2010) L. M. Ward et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Alteraciones cardiacas en la osteogénesis imperfecta. Estudio ecocardiográfico de casos y controles
- (2010) Vanesa Bonilla Jiménez et al. MEDICINA CLINICA
- Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding
- (2010) Aileen M. Barnes et al. NEW ENGLAND JOURNAL OF MEDICINE
- Lethal/Severe Osteogenesis Imperfecta in a Large Family: A Novel Homozygous LEPRE1 Mutation and Bone Histological Findings
- (2010) Fleur S. van Dijk et al. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
- Ankle Strength and Functional Limitations in Children and Adolescents With Type I Osteogenesis Imperfecta
- (2010) Angela Caudill et al. Pediatric Physical Therapy
- PPIB Mutations Cause Severe Osteogenesis Imperfecta
- (2009) Fleur S. van Dijk et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Osteogenesis Imperfecta and Aortic Dissection
- (2009) Shawn Chillag et al. AMERICAN JOURNAL OF THE MEDICAL SCIENCES
- PEDF regulates osteoclasts via osteoprotegerin and RANKL
- (2009) Toru Akiyama et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII
- (2009) N. Fratzl-Zelman et al. BONE
- Essential role of the TRIC-B channel in Ca2+ handling of alveolar epithelial cells and in perinatal lung maturation
- (2009) D. Yamazaki et al. DEVELOPMENT
- Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex
- (2009) Weizhong Chang et al. HUMAN MOLECULAR GENETICS
- Biochemical Characterization of the Prolyl 3-Hydroxylase 1·Cartilage-associated Protein·Cyclophilin B Complex
- (2009) Yoshihiro Ishikawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Location of 3-Hydroxyproline Residues in Collagen Types I, II, III, and V/XI Implies a Role in Fibril Supramolecular Assembly
- (2009) Mary Ann Weis et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A randomized, controlled dose-ranging study of risedronate in children with moderate and severe osteogenesis imperfecta
- (2009) Nick Bishop et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta
- (2009) Freya K.R. Swinnen et al. LARYNGOSCOPE
- Autophagic Elimination of Misfolded Procollagen Aggregates in the Endoplasmic Reticulum as a Means of Cell Protection
- (2009) Yoshihito Ishida et al. MOLECULAR BIOLOGY OF THE CELL
- Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation
- (2009) Tomohiko Murakami et al. NATURE CELL BIOLOGY
- Evidence that Abnormal High Bone Mineralization in Growing Children with Osteogenesis Imperfecta is not Associated with Specific Collagen Mutations
- (2008) Paul Roschger et al. CALCIFIED TISSUE INTERNATIONAL
- Results of a prospective pilot trial on mobility after whole body vibration in children and adolescents with osteogenesis imperfecta
- (2008) Oliver Semler et al. CLINICAL REHABILITATION
- Impairment of diastolic function in adult patients affected by osteogenesis imperfecta clinically asymptomatic for cardiac disease: Casuality or causality?
- (2008) Silvia Migliaccio et al. INTERNATIONAL JOURNAL OF CARDIOLOGY
- Defective C-propeptides of the Proα2(I) Chain of Type I Procollagen Impede Molecular Assembly and Result in Osteogenesis Imperfecta
- (2008) James M. Pace et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates
- (2008) Shawn M. Sweeney et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Rough Endoplasmic Reticulum-resident FK506-binding Protein FKBP65 Is a Molecular Chaperone That Interacts with Collagens
- (2008) Yoshihiro Ishikawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Impaired pyridinoline cross-link formation in patients with osteogenesis imperfecta
- (2008) Kosei Hasegawa et al. JOURNAL OF BONE AND MINERAL METABOLISM
- Alendronate Treatment of the Brtl Osteogenesis Imperfecta Mouse Improves Femoral Geometry and Load Response Before Fracture but Decreases Predicted Material Properties and Has Detrimental Effects on Osteoblasts and Bone Formation
- (2008) Thomas E Uveges et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Neurosurgical implications of osteogenesis imperfecta in children
- (2008) Deanna Sasaki-Adams et al. Journal of Neurosurgery-Pediatrics
- Physical Training in Children with Osteogenesis Imperfecta
- (2007) Marco Van Brussel et al. JOURNAL OF PEDIATRICS
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