Results 71 to 80 of about 2,266 (189)

Rheumatic manifestations associated with lung diseases [PDF]

open access: yesEinstein (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  

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

Tuberculosis in Retrospective: Review of Current Knowledge and its Application in the Study of Skeletal Remains [PDF]

open access: yes, 2012
La tuberculosis fue en el pasado, al igual que en la actualidad, una enfermedad con una alta morbilidad y mortalidad. Sin embargo, su detección en el registro arqueológico humano es relativamente infrecuente.
Santos, Ana Luisa, Suby, Jorge Alejandro
core  

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

Assessing the Reliability of Stable Isotopes in Fossil Bone: A Unique Case Study of Prehistoric Lung Pathology. [PDF]

open access: yes, 2013
Mammals at Ashfall Fossil Beds State Historical Park (NE Nebraska) offer a unique opportunity to test for the preservation of primary isotopic signatures in fossilized materials.
Bundy, Kathleen, Matson, Samuel D
core   +1 more source

Acetaminophen as a possible safer alternative for reducing prostaglandin E2‐major urinary metabolites concentrations and alleviating joint pain in pachydermoperiostosis

open access: yes
JEADV Clinical Practice, Volume 4, Issue 1, Page 277-280, March 2025.
Tomoya Takegami   +13 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

Hypertrophic pulmonary osteoarthropathy with primary lung cancer

open access: yesOncology Letters, 2014
Hypertrophic pulmonary osteoarthropathy (HPO) is a rare paraneoplastic syndrome that is frequently associated with lung cancer; however, the incidence of clinically apparent HPO is not well known. The clinical data of 6,151 patients with advanced lung cancer between January 1996 and December 2008 were retrospectively analyzed in Zhejiang Cancer ...
QIAN, XINYU, QIN, JING
openaire   +3 more sources

Arthroscopic synovectomy and radiosynoviorthesis: a treatment option for recurrent arthritis symptoms in patients with pachydermoperiostosis

open access: yesReumatismo, 2013
Pachydermoperiostosis as the primary form of hypertrophic osteoarthropathy is a rare hereditary disorder with a number of characteristic findings, e.g. periosteal hypertrophy, digital clubbing and pachydermia.
S. Warwas   +3 more
doaj   +1 more source

Primary hypertrophic osteoarthropathy.

open access: yesJPMA. The Journal of the Pakistan Medical Association, 2014
We describe two cases of familial primary hypertrophic osteoarthropathy. In this family, brother and a sister were affected with history of similar features in father.
Abdul, Khalid, Muhammad Tariq, Baqai
openaire   +1 more source

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