Results 101 to 110 of about 91,488 (232)

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

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, Lixue Huang, Xia Li, Yuting Zhou, Hui Zhang, Yeming Wang, Dan Cui, Ting Yu, Yimin Wang, Bin Cao   +9 more
wiley   +1 more source

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

Journal 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, Gaurav Nepal, Yow Ka Shing, Hari Prasad Panthi, Suman Baral   +4 more
doaj   +1 more source

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

JEADV Clinical Practice, Volume 4, Issue 1, Page 277-280, March 2025.
Tomoya Takegami, Takashi Nomura, Satoru Yonekura, Akiyoshi Senda, Kazue Yoshida, Atsuhito Seki, Kazuhiko Nakabayashi, Tadakazu Hisamatsu, Hiroki Kitamoto, Shuji Yamamoto, Yusuke Honzawa, Hiroshi Seno, Hironori Niizeki, Kenji Kabashima   +13 more
wiley   +1 more source

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

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, Antônio César Paulillo de Cillo, Bárbara Campolina C. Silva, Catarina Brasil DÁlva, Érico Higino de Carvalho, Juliana M. C. M. de Almeida, Larissa L. M. Marques, Marcia Ribeiro, Mauro Borghi M. da Silva, Paula Frassinetti V. de Medeiros, Pedro Henrique Mendes   +10 more
wiley   +1 more source

HYPERTROPHIC PULMONARY OSTEOARTHROPATHY [PDF]

The Journal of Thoracic and Cardiovascular Surgery, 1963
H E, HOLLING, G K, DANIELSON, R W, HAMILTON, W S, BLAKEMORE, R S, BRODEY   +4 more
openaire   +4 more sources

THYROID ACROPACHY [PDF]

, 2017
No ...
Koeva, L.
core   +2 more sources

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

, 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

Gastric Juvenile Polyposis with High-Grade Dysplasia in Pachydermoperiostosis [PDF]

, 2011
Pachydermoperiostosis (PDP) is the primary form of hypertrophic osteoarthropathy. It is a very rare disease consisting of pachydermia, digital clubbing and radiologic periostosis.
Baert AL, C. Neuzillet, Castori M, Cooper RG, Covarrubias DJ, Hizawa K, Ikeda F, Jajic I, Jajic Z, Jass JR, L. de Mestier, Lakshmi TS, Lam SK, Li M, Liu Z, Martinez-Lavin M, Matsui Y, Okten A, P. Hammel, P. Ruszniewski, Pignone A, Prieto G, Rodríguez NG, S. Moreau, Sethuraman G, Seung-Chul L, Simpson EL, Staalman CR, Tanaka H, Uppal S, Y. Panis, Yüksel-Konuk B   +31 more
core   +3 more sources

Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)

Nepal Journal of Dermatology, Venereology & Leprology, 2013
DOI: http://dx.doi.org/10.3126/njdvl.v11i1.7937 Nepal Journal of Dermatology, Venereology & Leprology Vol.11(1) 2013 pp.64 ...
R Sharma, S Pandey, D Choudhary, DB Pokhrel   +3 more
doaj   +3 more sources

Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

JPRAS Open, 2019
Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat, Papassorn Limsuvan   +1 more
doaj   +1 more source