Results 61 to 70 of about 4,325,288 (187)

The Clinical Spectrum of Pachydermoperiostosis (Primary Hypertrophic Osteoarthropathy)

open access: yesMedicine, 1991
The clinical spectrum of pachydermoperiostosis (primary hypertrophic osteoarthropathy).
MATUCCI CERINIC, MARCO   +5 more
openaire   +4 more sources

Radiofrequency ablation: mechanisms and clinical applications

open access: yesMedComm, Volume 5, Issue 10, October 2024.
Radiofrequency ablation (RFA) is a type of thermal ablation that induces coagulation necrosis of tumors by raising temperatures above 60°C. However, compared with complete RFA, because the ablation area cannot completely cover the entire tumor, insufficient RFA (iRFA) can lead to rapid local tumor progression, metastasis, and even further malignant ...
Jianhua Wu   +10 more
wiley   +1 more source

Hypertrophic osteoarthropathy in a child with chronic liver disease [PDF]

open access: yes, 2014
Hypertrophic osteoarthropathy (HOA) is an uncommon condition in children, consisting of a triad of digital clubbing, non-inflammatory joint effusions and radiographic evidence of periostitis affecting the hands, feet and distal long bones.
Wittenberg, Dankwart F.   +2 more
core   +1 more source

Hypertrophic osteoarthropathy associated with lung cancer: a case report

open access: yes, 2007
Malignant neoplasms are sometimes associated with a variety of paraneoplastic rheumatic syndromes. Hypertrophic osteoarthropathy is one of these syndromes and the vast majority of cases are associated with intra thoracic neoplasms mainly broncogenic ...
Ozen, Alaattin   +6 more
core   +2 more sources

Animal models of tendon calcification: Past, present, and future

open access: yesAnimal 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

Pseudoacromegaly—A challenging entity in the endocrine clinic: A systematic review

open access: yesClinical 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

Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel SLCO2A1 Mutation and Imaging Findings [PDF]

open access: yes, 2019
Primary hypertrophic osteoarthropathy (PHO), also known as pachydermoperiostosis, is a rare, multisystemic, autosomal recessive condition typically presenting with digital clubbing, osteoarthropathy, and various skin manifestations.
Durmaz, Ceren D.   +6 more
core   +1 more source

Association of Monocyte Count With Lung Function and Exercise Capacity Among Hospitalized COVID‐19 Survivors: A 2‐Year Cohort Study

open access: yesInfluenza 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

Pachydermoperiostosis (Touraine–Solente–Gole syndrome): a case report

open access: yesJournal of Medical Case Reports, 2019
Background Pachydermoperiostosis (PDP) is a rare disorder characterized by clubbing of the fingers, thickening of the skin (pachyderma), and excessive sweating (hyperhidrosis).
Amir Joshi   +4 more
doaj   +1 more source

Real‐world data of Brazilian adults with X‐linked hypophosphatemia (XLH) treated with burosumab and comparison with other worldwide cohorts

open access: yesMolecular 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

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