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Osteoarthrosis Deformans -- See Osteoarthritis


A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans
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Osteoblasts -- See Also Osteoclasts


A large multinuclear cell associated with the BONE RESORPTION. An odontoclast, also called cementoclast, is cytomorphologically the same as an osteoclast and is involved in CEMENTUM resorption
  1
Osteoblasts. : Osteoblasts : morphology, functions and clinical implications / Hugo Scheurer  2013 1
Osteoblasts -- immunology.   2
Osteoblasts -- physiology.   2
 

Osteochondritis -- See Osteochondrosis


  1
 

Osteochondritis deformans juvenilis -- See Legg-Calvé-Perthes disease


  1
Osteochondritis Dissecans -- surgery. : Pediatric and adolescent knee surgery / editors, Frank A. Cordasco, MD, MS, Co-Medical Director, Leon Root Motion Analysis Laboratory, Attending Orthopedic Surgeon, Sports Medicine and Shoulder Service, Hospital for Special Surgery, Professor of Orthopaedic Surgery, Weill Cornell Medical College, New York, New York, Daniel W. Green, MD, MS, FAAP, FACS, Attending Orthopedic Surgeon, Pediatric Orthopedic Surgery Service, Hospital for Special Surgery, Professor of Clinical Orthopaedic Surgery, Weill Cornell Medical College, New York, New York  2015 1
Osteochondrodysplasias -- radiography. : Fetal radiology : a diagnostic atlas / Reinhard Schumacher, Laurie H. Seaver, Jürgen Spranger  2010 1
 

Osteochondroses -- See Osteochondrosis


Any of a group of bone disorders involving one or more ossification centers (EPIPHYSES). It is characterized by degeneration or NECROSIS followed by revascularization and reossification. Osteochondrosis often occurs in children causing varying degrees of discomfort or pain. There are many eponymic types for specific affected areas, such as tarsal navicular (Kohler disease) and tibial tuberosity (Osgood-Schlatter disease)
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Osteochondroses, Navicular -- See Osteochondrosis


Any of a group of bone disorders involving one or more ossification centers (EPIPHYSES). It is characterized by degeneration or NECROSIS followed by revascularization and reossification. Osteochondrosis often occurs in children causing varying degrees of discomfort or pain. There are many eponymic types for specific affected areas, such as tarsal navicular (Kohler disease) and tibial tuberosity (Osgood-Schlatter disease)
  1
 

Osteochondrosis -- See Also the narrower term Legg-Calvé-Perthes disease


  1
Osteochondrosis. : Talar osteochondral defects : diagnosis, planning, treatment, and rehabilitation / C. Niek van Dijk, John G. Kennedy, editors  2014 1
 

Osteochondrosis, Navicular -- See Osteochondrosis


Any of a group of bone disorders involving one or more ossification centers (EPIPHYSES). It is characterized by degeneration or NECROSIS followed by revascularization and reossification. Osteochondrosis often occurs in children causing varying degrees of discomfort or pain. There are many eponymic types for specific affected areas, such as tarsal navicular (Kohler disease) and tibial tuberosity (Osgood-Schlatter disease)
  1
Osteochondrosis -- Treatment. : Pediatric and adolescent knee surgery / editors, Frank A. Cordasco, MD, MS, Co-Medical Director, Leon Root Motion Analysis Laboratory, Attending Orthopedic Surgeon, Sports Medicine and Shoulder Service, Hospital for Special Surgery, Professor of Orthopaedic Surgery, Weill Cornell Medical College, New York, New York, Daniel W. Green, MD, MS, FAAP, FACS, Attending Orthopedic Surgeon, Pediatric Orthopedic Surgery Service, Hospital for Special Surgery, Professor of Clinical Orthopaedic Surgery, Weill Cornell Medical College, New York, New York  2015 1
 

Osteoclast -- See Osteoclasts


A large multinuclear cell associated with the BONE RESORPTION. An odontoclast, also called cementoclast, is cytomorphologically the same as an osteoclast and is involved in CEMENTUM resorption
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Osteoclastic Bone Loss -- See Bone Resorption


Bone loss due to osteoclastic activity
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Osteoclastic Bone Losses -- See Bone Resorption


Bone loss due to osteoclastic activity
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Osteoclastogeneses -- See Osteogenesis


The process of bone formation. Histogenesis of bone including ossification
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Osteoclastogenesis -- See Osteogenesis


The process of bone formation. Histogenesis of bone including ossification
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Osteoclasts -- See Also Bone Resorption


Bone loss due to osteoclastic activity
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Osteoclasts.   7
Osteoclasts -- immunology.   2
Osteoclasts -- Pathophysiology. : Osteoclasts : cell biology, functions and related diseases / by Cecelia Reeves, editor  2016 1
Osteoclasts -- physiology. : Nucleotides and regulation of bone cell function / edited by Geoffrey Burnstock, Timothy R. Arnett  2007 1
 

Osteoconduction -- See Bone Regeneration


Renewal or repair of lost bone tissue. It excludes BONY CALLUS formed after BONE FRACTURES but not yet replaced by hard bone
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Osteocyte -- See Osteocytes


Mature osteoblasts that have become embedded in the BONE MATRIX. They occupy a small cavity, called lacuna, in the matrix and are connected to adjacent osteocytes via protoplasmic projections called canaliculi
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Osteocytes.   4
 

Osteodystrophies, Renal -- See Chronic Kidney Disease-Mineral and Bone Disorder


Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders
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Osteodystrophy, Renal -- See Chronic Kidney Disease-Mineral and Bone Disorder


Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders
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Osteogeneses, Distraction -- See Osteogenesis, Distraction


Bone lengthening by gradual mechanical distraction. An external fixation device produces the distraction across the bone plate. The technique was originally applied to long bones but in recent years the method has been adapted for use with mandibular implants in maxillofacial surgery
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  Osteogenesis -- 2 Related Subjects   2
Osteogenesis.   8
  Osteogenesis, Distraction -- 2 Related Subjects   2
Osteogenesis, Distraction. : Distraction osteogenesis of the facial skeleton / [edited by] William H. Bell, César A. Guerrero  2007 1
Osteogenesis imperfecta.   3
Osteogenesis imperfecta -- China. : Journalist on the Spot. China Dolls : fragile bodies, strong minds / director, Benny Yip ; producer, Kwok Fong  2011 1
 

Osteogenesis imperfecta congenita -- See Osteogenesis imperfecta


  1
Osteogenesis imperfecta -- Nursing. : Osteogenesis imperfecta : a guide for nurses  2003 1
Osteogenesis imperfecta -- Patients. : The Undateables: Matthew/Heather/Gareth - Series 2, Ep 4 Of 5 / Director: McLaughlin, Chris  2013 1
Osteogenesis imperfecta -- Surgery : Osteogenesis imperfecta : a case-based guide to surgical decision-making and care / Richard W. Kruse, editor  2020 1
  Osteogenesis imperfecta tarda -- 2 Related Subjects   2
 

Osteogenesis Imperfecta Tardas -- See Osteogenesis Imperfecta


COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I
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Osteogenesis Imperfecta, Type 1 -- See Osteogenesis Imperfecta


COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I
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Osteogenesis Imperfecta, Type I -- See Osteogenesis Imperfecta


COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I
  1
 

Osteogenesis Imperfecta with Blue Sclerae -- See Osteogenesis Imperfecta


COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I
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Osteogenesis -- physiology. : Age estimation of the human skeleton / edited by Krista E. Latham and Michael Finnegan ; with a foreword by Stanley J. Rhine  2010 1
  Osteogenic sarcoma -- 2 Related Subjects   2
 

Osteogenic Sarcomas -- See Osteosarcoma


A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed)
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Osteoid sarcoma -- See Osteosarcoma


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