Results 61 to 70 of about 87,294 (214)
Кубанский научный медицинский вестник, 2015 The hypertrophic osteoarthropathy (HOA) may occur as isolated finding or is often part of the syndrome which is characterized by periostosis of the long bones and occasional painful joint enlargement.
M. V. Potapova +4 more
doaj
Animal models of tendon calcification: Past, present, and future
Animal Models and Experimental Medicine, Volume 7, Issue 4, Page 471-483, August 2024.Various modeling methods for experimental animal models of tendon calcification are shown in the figure: the methods of modeling tendon calcification in experimental animals as shown in the figure can be mainly classified as trauma induced, tissue factor injections, dietary or pharmacological modifications, and gene knockouts.
Ruichen Li +8 more
wiley +1 more source
A Case Report of Primary Hypertrophic Osteoarthropathy
罕见病研究Primary hypertrophic osteoarthropathy(PHO) is a rare disease also known as pachydermoperiostosis. We reported a painless case whose diagnosis was confirmed by genetic test. A 24-year-old male presented a series of symptoms that first began at 14.
ZHAO Zongxuan +7 more
doaj +1 more source
Recurrent hypertrophic pulmonary osteoarthropathy in an adult with bronchiectasis
Respirology Case Reports, 2020 Hypertrophic pulmonary osteoarthropathy (HPOA) is a well‐documented complication of pulmonary malignancy and cystic fibrosis (CF). However, HPOA associated with exacerbations of non‐CF bronchiectasis has only been reported once previously in an ...
Amelia Tekiteki +4 more
doaj +1 more source
Pseudoacromegaly—A challenging entity in the endocrine clinic: A systematic review
Clinical Endocrinology, Volume 100, Issue 6, Page 542-557, June 2024.Abstract Objective Pseudoacromegaly encompasses conditions with features of acromegaly/gigantism, but no growth hormone (GH) or insulin‐like growth factor‐1 (IGF‐1) excess. We aimed to review published pseudoacromegaly cases evaluated due to clinical suspicion of acromegaly.
Pedro Marques +2 more
wiley +1 more source
The seminal role played by Pierre Marie in Neurology and Internal Medicine
Arquivos de Neuro-Psiquiatria, 2015 The authors review the most important contributions of Pierre Marie to the elucidation and description of several neurological diseases, such as Charcot-Marie-Tooth’s disease and hereditary cerebellar ataxia, as well as his contributions to Internal ...
Gustavo M Almeida +2 more
doaj +1 more source
Hypertrophic Osteoarthropathy in Eisenmenger Syndrome
Congenital Heart Disease, 2012 Hypertrophic osteoarthropathy secondary to Eisenmenger syndrome can produce severe disabling pain. We report two cases treated by intravenous pamidronate infusion with good symptomatic relief. Such therapy can greatly improve the quality of life of end-stage cyanotic congenital heart patients.
Wijesekera, Vishva A. +1 more
openaire +4 more sources
Influenza and Other Respiratory Viruses, Volume 18, Issue 3, March 2024.ABSTRACT Background Abnormal changes of monocytes have been observed in acute COVID‐19, whereas associations of monocyte count with long COVID were not sufficiently elucidated. Methods A cohort study was conducted among COVID‐19 survivors discharged from hospital. The primary outcomes were core symptoms of long COVID, distance walked in 6 min, and lung
Xiaoying Gu +9 more
wiley +1 more source
Rheumatic manifestations associated with lung diseases [PDF]
Einstein (São Paulo), 2008 Rheumatic manifestations in the more prevalent lung diseasessuch as asthma, chronic pulmonary disease or pneumonia are notfrequent. Exceptions to this rule are represented by lung cancerand sarcoidosis, where the appearance of the digital clubbing ...
Marco Aurelio Scarpinella Bueno +1 more
doaj
Molecular Genetics &Genomic Medicine, Volume 12, Issue 2, February 2024.Abstract Background Disease‐related variants in PHEX cause XLH by an increase of fibroblast growth factor 23 (FGF23) circulating levels, resulting in hypophosphatemia and 1,25(OH)2 vitamin D deficiency. XLH manifests in early life with rickets and persists in adulthood with osseous and extraosseous manifestations.
Maria Helena Vaisbich +10 more
wiley +1 more source