Skip to Main Content (Press Enter)

×
Home
Persone
Pubblicazioni
Strutture
Competenze

UNI-FIND

|

UNI-FIND

cnr.it

×
Home
Persone
Pubblicazioni
Strutture
Competenze

Pubblicazioni

JOURNAL OF BONE AND MINERAL RESEARCH

Rivista

Codice:

E090767

ISSN:

0884-0431

Dati Generali

Dati Generali

Pubblicazioni (42)

Ordina Pubblicazioni:

ascendente
decrescente

A New Familial Sclerosing Bone Dysplasia

Articolo

A new familial sclerosing bone dysplasia.

Articolo

A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease

Articolo

A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.

Articolo

A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease

Articolo

Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss

Articolo

As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene

Articolo

Bone Mineral Density Predicts Fractures in Chronic Kidney Disease

Traduzione

Bone quality in hip fractures and hip osteoarthritis.

Abstract

Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis.

Articolo

Characterization of Extracellular Vesicles in Osteoporotic Patients Compared to Osteopenic and Healthy Controls

Articolo

Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patients.

Articolo

Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis

Articolo

Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone.

Articolo

Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.

Articolo

Comparison of intravenous and intramuscular neridronate regimens for the treatment of paget's disease of bone.

Articolo

In Vitro Differentiation of CD14 Cells From Osteopetrotic Subjects: Contrasting Phenotypes With TCIRG1, CLCN7, and Attachment Defects.

Articolo

Increased Risk of Bone Fractures in Hemodialysis Patients Treated with Proton Pump Inhibitors in Real World: Results from the Dialysis Outcomes and Practice Patterns Study (DOPPS)

Articolo

Klotho Variants and Chronic Hemodialysis Mortality.

Articolo

Large Collaborative Study on Geographic Variation of SQSTM1 Mutations in Paget's Disease of Bone in Italy

Contributo in Atti di convegno

Muscle microstructure: a new point of view on osteoporosis-related muscle atrophy.

Contributo in Atti di convegno

Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.

Articolo

Oral Calcitriol Use, Vertebral Fractures, and Vitamin K in Hemodialysis Patients: A Cross-Sectional Study

Articolo

Osteopetrosis rescue upon RANKL administration to Rankl -/- mice: A new therapy for human RANKL-dependent ARO

Articolo

Overexpression of Deaminase Acting on RNA-2 enzyme ADAR2 Reduces Osteosarcoma Progression

Abstract

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived from Structural and Functional Analysis of 14 ClC-7 Mutants

Articolo

Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women.

Articolo

RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations.

Articolo

Relationship Between Low Bone Mineral Density and Fractures With Incident Cardiovascular Disease: A Systematic Review and Meta-Analysis

Articolo

Romosozumab Use and Cardiovascular Events

Articolo

SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.

Articolo

SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone

Articolo

Sclerostin Regulation, Microarchitecture, and Advanced Glycation End-Products in the Bone of Elderly Women With Type 2 Diabetes

Articolo

Sevelamer Use, Vitamin K Levels, Vascular Calcifications, and Vertebral Fractures in Hemodialysis Patients: Results from the VIKI Study

Articolo

Severe Malignant Osteopetrosis Caused by a GL Gene Mutation.

Articolo

Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis.

Articolo

Transfer, analysis and reversion of the fibrous dysplasia cellular phenotype in human skeletal progenitors

Articolo

Urokinase plasminogen activator receptor affects bone homeostasis by regulating osteoblast and osteoclast

Articolo

Vitamin D Receptor (VDR) gene polymorphism is associated with Left Ventricular (LV) mass and predicts Left Ventricular Hypertrophy (LVH) progression in End-Stage Renal Disease (ESRD) patients

Articolo

Vitamin K, vertebral fractures, vascular calcifications and mortality: Vitamin K Italian (VIKI) dialysis study.

Articolo

Vitamin K, vertebral fractures, vascular calcifications, and mortality: VItamin K Italian (VIKI) dialysis study.

Articolo

ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology

Articolo

No Results Found

«
‹

{pageNumber}

›
»

{startItem} - {endItem} di {itemsNumber}

Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.1.0 | Sorgente dati: PREPROD (Ribaltamento disabilitato)