Zobrazeno 1 - 10
of 2 157
pro vyhledávání: '"Microlithiasis"'
Publikováno v:
Basic and Clinical Andrology, Vol 34, Iss 1, Pp 1-14 (2024)
Abstract Background Testicular microlithiasis (TM) is characterised by microcalcifications in the testes and has been associated with infertility. This has led to studies of semen analysis in men with the condition. This systematic review aimed to co
Externí odkaz:
https://doaj.org/article/9061ea9770c24f7391cadc4d7885bf47
Autor:
Corrado Tagliati, Daniele Veri, Andrea Pietra, Giuseppe Lanni, Davide Battista, Marco Fogante, Giulio Argalia, Cecilia Lanza, Stefano Pantano, Francesca Collini, Maria Di Sabatino, Pietro Ripani
Publikováno v:
Clinical Case Reports, Vol 12, Iss 10, Pp n/a-n/a (2024)
Key Clinical Message Gallstones, microlithiasis, gallbladder sludge, and micro‐gallbladder are frequently reported in cystic fibrosis patients, and modulators could modify gallbladder disease, probably reducing biliary secretions viscosity.
Externí odkaz:
https://doaj.org/article/cd0a08a8313d47d78ae36b92b259c238
Akademický článek
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Publikováno v:
Arquivo Brasileiro de Medicina Veterinária e Zootecnia, Vol 76, Iss 2, Pp 275-281 (2024)
ABSTRACT Anatomical and ultrasonographic diagnostic work-up of testicular abscesses (n = 2) and testicular microlithiasis (n = 3) in Kazakh rams is described. For testicular abscesses, the localized symptoms include enlargement of the testicle and de
Externí odkaz:
https://doaj.org/article/047689ae0766449babe99cf7b2b9d31e
Autor:
Parviz Mardani, Reyhaneh Naseri, Reza Shahriarirad, Hadiseh Mahram, Masoud Shafi, Tahmoores Niknam, Mohammad Bagher Khosravi, Mohammad Javad Fallahi, Armin Amirian
Publikováno v:
The Clinical Respiratory Journal, Vol 18, Iss 5, Pp n/a-n/a (2024)
Abstract Background Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive genetic disorder with approximately 1000 known cases worldwide, in which calcium phosphate microliths deposit in the alveolar air spaces. As of writing this rep
Externí odkaz:
https://doaj.org/article/a13caadefc2c4bc893ca7f0ef6852985
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundPulmonary alveolar microlithiasis (PAM) is a rare disease whose clinical and imaging manifestations are non-specific, characterized by the deposition of microliths, which primarily consist of calcium and phosphorus, within the alveoli. In t
Externí odkaz:
https://doaj.org/article/2ed51e895194455c85dd3a339fc792ee
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Manizheh Mostafa Gharehbaghi, Fakhralsadat Mortazavi, Hanieh Hosseinzadeh-Asl, Iman Bagheri Gahvechi, Razieh Parizad, Samira Jafarisis, Shahab Masoumi
Publikováno v:
Iranian Journal of Neonatology, Vol 14, Iss 3, Pp 6-12 (2023)
Background: Renal microlithiasis includes renal hyperechogenic deposits in the calyces, pelvis, or ureter with a diameter of less than 2-3 mm by ultrasound. Currently, there is no information about the outcome and possible complications of renal calc
Externí odkaz:
https://doaj.org/article/de515da961ca4dcf9926582f83a0c0ab
Autor:
Åsa Lina M. Jönsson, Ole Hilberg, Ulf Simonsen, Jane Hvarregaard Christensen, Elisabeth Bendstrup
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-15 (2023)
Abstract Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive lung disease caused by variants in the SLC34A2 gene encoding the sodium-dependent phosphate transport protein 2B, NaPi-2b. PAM is characterized by deposition of calcium ph
Externí odkaz:
https://doaj.org/article/eda338914ccf4ad78ba9a4d7be092085
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message We reported a case of a 7‐year‐old boy with pulmonary alveolar microlithiasis (PAM) and detected two novel compound heterozygous mutations of solute carrier family 34 member 2 (SLC34A2), EXON:2–6 duplication and c.1218 (EXO
Externí odkaz:
https://doaj.org/article/768226287c754bdeb567c2dd1032671e