Zobrazeno 1 - 10
of 2 155
pro vyhledávání: '"microlithiasis"'
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
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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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
Autor:
Amir Mohammad Hashem Asnaashari, Davood Attaran, Soroush Attaran, Parastou Asnaashari, Sahar Ravanshad, Sepide Hejazi
Publikováno v:
Journal of Cardio-Thoracic Medicine, Vol 10, Iss 3, Pp 1039-1043 (2022)
Pulmonary alveolar microlithiasis (PAM) is a rare inherited pulmonary disease characterized by the deposition of intra-alveolar calcium deposits. In most of the Asian and European countries, PAM is usually misdiagnosed as pulmonary tuberculosis and s
Externí odkaz:
https://doaj.org/article/3f693e0ac8a648aeaf11f846aed36493
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
Akademický článek
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