Results 71 to 80 of about 10,418 (205)

Osteopetrosis and Its Relevance for the Discovery of New Functions Associated with the Skeleton

open access: yesInternational Journal of Endocrinology, 2015
Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. Patients typically displayed spontaneous fractures, anemia, and in the most severe forms hepatosplenomegaly and compression of ...
Amélie E. Coudert   +3 more
doaj   +1 more source

Erratum: Chloride Channel CICN7 Mutations in a Korean Patient with Infantile Malignant Osteopetrosis Initially Presenting with Neonatal Thrombocytopenia [PDF]

open access: bronze, 2004
Youn Jeong Shin   +8 more
openalex   +1 more source

Low rates of endothelial cell dysfunction and transplant‐related mortality in 537 children receiving fludarabine–treosulfan conditioning for all transplant indications: A retrospective multicentre study on behalf of the UK Paediatric BMT group

open access: yes
British Journal of Haematology, Volume 207, Issue 2, Page 631-635, August 2025.
Thomas Altmann   +11 more
wiley   +1 more source

Osteopetrosis Case Series from Tanzania

open access: diamond, 2023
Lee Kapalisya Mwakalinga   +8 more
openalex   +1 more source

Osteopetrosis [PDF]

open access: yesArchives of Disease in Childhood, 1971
J S, Yu   +3 more
openaire   +2 more sources

Osteomyelitis in infantile osteopetrosis: A case report with review of literature

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2008
Osteopetrosis is a rare genetic disorder that causes generalized sclerosis of bone due to a defect in bone resorption and remodeling. Dental abnormality may be attributed to pathological changes in bone remodeling.
Roopashri R, Gopakumar R, Subhas B
doaj  

MALIGNANT INFANTILE OSTEOPETROSIS (MIOP)-A RARE CASE REPORT [PDF]

open access: hybrid, 2017
SunilKumar Agarwalla   +2 more
openalex   +1 more source

Unusual Intersecting Pathologies: Acute Myeloid Leukemia and Osteopetrosis

open access: yesArchives of Medicine and Health Sciences
Osteopetrosis, or marble bone disease, is a rare inherited skeletal disorder most often caused by mutations in the RANKL or RANK genes, resulting in defective osteoclast-mediated bone resorption and abnormally dense but fragile bones. While osteopetrosis
Tuphan Kanti Dolai   +2 more
doaj   +1 more source

Hypercalcemia and altered biochemical bone markers in post‐bone marrow transplantation osteopetrosis: A case report and literature review [PDF]

open access: bronze, 2011
Alisa Kulpiya   +4 more
openalex   +1 more source

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