Results 71 to 80 of about 166,331,801 (189)

Genetic Determinants of Treatment‐Related Bone Toxicity in Pediatric Acute Lymphoblastic Leukemia

open access: yesClinical Pharmacology &Therapeutics, Volume 120, Issue 3, Page 786-794, September 2026.
Osteonecrosis and fractures are serious corticosteroid‐induced bone toxicities in children treated for acute lymphoblastic leukemia, yet their genetic determinants remain incompletely defined. In this study, we aimed to identify novel genetic contributors to bone toxicity and to evaluate the robustness of both newly identified and previously ...
Rachid Abaji   +14 more
wiley   +1 more source

Atypical presentation of Paget's disease with secondary osteomyelitis of mandible

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2017
Paget's disease (PD) is a chronic progressive disease of the bone characterized by abnormal bone resorption and deposition affecting either single bone (monostotic) or many bones (polyostotic).
Sadaksharam Jayachandran   +2 more
doaj   +1 more source

Paget’s disease of bone: a review [PDF]

open access: yesRheumatology International, 2008
Paget's disease of bone (PDB) is a condition of unknown etiology characterized by excessive and abnormal bone remodeling. It may be localized to one or several skeletal segments. The disease seldom appears before the age of 40 years, but its prevalence tends to double each decade from the age of 50 onwards, reaching about 10% after ninth decade.
COLINA, Matteo   +3 more
openaire   +3 more sources

Sodium Intake and Osteoporosis Risk: Evidence From NHANES and Mendelian Randomization Analysis

open access: yesFood Science &Nutrition, Volume 14, Issue 9, September 2026.
This study combined cross‐sectional data from the National Health and Nutrition Examination Survey (NHANES) with Mendelian Randomization (MR) analysis to systematically investigate the relationship between sodium intake and osteoporosis. The results showed that within a specific intake range (> 6150 mg/day), sodium intake was significantly negatively ...
Yunxiao Ji   +5 more
wiley   +1 more source

Doença de Paget Óssea: análise de 134 casos [PDF]

open access: yes, 2009
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Heiden, Glaucia Itamaro
core  

Tinnitus and Paget's disease of bone

open access: yes, 2006
Aim: To investigate the prevalence of tinnitus and deafness in subjects with Paget's disease of bone.Materials and methods: One hundred and thirty-four subjects in total (77 with Paget's disease) were identified and audiologically examined.
Fraser, W. D., Mackenzie, Ian, Young, C.
core   +1 more source

HLA Typing in Turkish Patients with Paget's Disease of Bone

open access: yesEndocrinology Research and Practice, 2022
Paget's disease of bone is a disorder of bone, primarily affecting elderly population. The disease causes a structural disorganisation of of bone tissue in affected sites. The etiology is unknown.
Gürcan Kısakol   +3 more
doaj   +2 more sources

S1 guideline sweat gland carcinoma

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 9, Page e1356-e1385, September 2026.
Summary The current classification of sweat gland carcinomas is based on histomorphological characteristics and distinguishes between more than 20 entities. Most patients are older, but some subtypes also affect middle‐aged and younger patients. The majority of tumors arise de novo. Sweat gland carcinomas have nonspecific clinical features.
Mirjana Ziemer   +19 more
wiley   +1 more source

Difficulties in diagnosis and treatment of Paget’s disease

open access: yesFamily Medicine & Primary Care Review, 2016
Paget’s disease is a rare finding in Poland. It is a disorder of the osteoarticular system, which, in adults, mostly affects people over 55 years of age.
Aleksandra Kawalec   +2 more
doaj   +1 more source

Craniodiaphyseal dysplasia, a very rare form of bone dysplasia

open access: yesOral and Maxillofacial Surgery Cases, 2020
Introduction: Craniodiaphyseal dysplasia is a very rare autosomal recessive disorder which is typically presented in infancy and characterised by severe form of bone dysplasia, massive bone sclerosis and hyperostosis.
Bayar Ahmed Qasim   +4 more
doaj   +1 more source

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