Results 11 to 20 of about 2,380 (140)

Remimazolam Ameliorates Autistic-Like Behaviors via Suppression of Ferroptosis in VTA Dopaminergic Neurons in a Mouse Model of ASD. [PDF]

open access: yesAdv Sci (Weinh)
The ultra‐short‐acting sedative remimazolam has a sustained therapeutic effect on the core symptoms of VPA‐exposed mice. Remimazolam, a GABA agonist, exerts its therapeutic effects by protecting dopamine neurons in the VTA of VPA‐exposed mice. Meanwhile, ferroptosis is the critical mechanism by which remimazolam protects VTA dopaminergic neurons and ...
Zhang Y   +7 more
europepmc   +2 more sources

Clinical, genetic aspects and molecular pathogenesis of osteopetrosis

open access: yesВавиловский журнал генетики и селекции, 2023
Osteopetrosis (“marble bone”, ICD-10-78.2) includes a group of hereditary bone disorders distinguished by clinical variability and genetic heterogeneity.
D. D. Nadyrshina, R. I. Khusainova
doaj   +1 more source

Left Hindquarter Amputation due to High-Grade Pleomorphic Sarcoma of the Groin: A Case Report

open access: yesIndonesian Journal of Cancer, 2023
Introduction:Hindquarter amputation or known as hemipelvectomy is a surgical technique that is primarily used for the eradication of malignant primary soft tissue and bone tumors of the pelvis, hip, and upper thigh regions.
Muhammad Zaki Abdul Hafiz   +2 more
doaj   +1 more source

Clinical masks of marble disease

open access: yesСовременная ревматология, 2023
Marble disease, or osteopetrosis (OPT), is rare in the practice of a rheumatologist, internist or pediatrician. This group of hereditary diseases is based on a defect in the formation, development and functioning of osteoclasts (OCL), which leads to ...
O. G. Radaikina   +4 more
doaj   +1 more source

Benign osteopetrosis with secondary osteomyelitic changes in the mandible: A report of two rare cases

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2009
Osteopetrosis is a name given to a group of diseases that affect the growth and remodeling of the bone. It is characterized by overgrowth and sclerosis of bone, with a resultant thickening of bony cortices and narrowing of marrow cavities throughout the ...
S Jayachandran   +2 more
doaj   +1 more source

Osteopetrosis as a rare cause of anaemia in paediatric patients: a case report

open access: yesPediatria i Medycyna Rodzinna, 2019
Anaemia is a common manifestation in paediatric patients. The most common cause of anaemia is iron deficiency. In differential diagnosis not only the most common diseases resulting in haemoglobin decrease should be considered, but also those less common.
Anna Fałkowska   +3 more
doaj   +1 more source

Osteopetrosis Ditinjau dari Bidang Kedokteran Gigi (Laporan Kasus)

open access: yesJournal of Dentistry Indonesia, 2015
Osteopetrosis or Albers Schonberg Disease or Marble Bone Disease is bone dysplasia hardness and brittleness of the bone as a result because of bone resorbtion and calcification of chondroid due to a failure of osteoclast function.
Heriandi Sutadi
doaj   +1 more source

Infantile malignant osteopetrosis: A case report with review of literature

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2008
Osteopetrosis is a rare hereditary, generalized disorder of bone characterized by a significant increase in the density of the skeletal tissues usually manifesting in two basic forms: an autosomal dominant benign form (osteopetrosis tarda) and an ...
Sunil Chaudhary, Arun Sharma
doaj   +1 more source

Neurosurgical considerations in osteopetrosis

open access: yesInterdisciplinary Neurosurgery, 2020
Osteopetrosis is a metabolic bone disease resulting in skeletal hyper-sclerosis. Three major genetic subtypes of the disease are phenotypically expressed into three distinguishable forms of the disease, each dictating specific management.
Adrian Kelly   +2 more
doaj   +1 more source

Osteopetrosis: classification, pathomorphology, genetic disorders, clinical manifestations (literature review and clinical case report)

open access: yesBolʹ, Sustavy, Pozvonočnik, 2019
Osteopetrosis is a hereditary disease with an autosomal recessive or autosomal dominant type of inheritance, caused by a disruption in the functional activity of osteoclasts due to gene mutation. The article systematizes data on etiology, classification,
V.V. Povoroznyuk   +3 more
doaj   +1 more source

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