Zobrazeno 1 - 10
of 13
pro vyhledávání: '"R, Roukhsi"'
Publikováno v:
Scholars Journal of Medical Case Reports. 9:869-873
Pulmonary artery sarcoma is a rare tumor of the great vessels .It is aggressive and rapidly evolving disease, which is underdiagnosed and misunderstood. The diagnosis is usually made postoperatively or at autopsy a highly. Rapid recognition is needed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::211ee7516911fcf9fb7048d735487b77
https://doi.org/10.36347/sjmcr.2021.v09i09.011
https://doi.org/10.36347/sjmcr.2021.v09i09.011
Publikováno v:
Scholars Academic Journal of Pharmacy. 10:180-182
The urachus is a fibrous residue of the allantois that disappears after birth. In some cases, it may persist, which is called urachus abnormalities. This persistence of the urachus is manifested by abdominal pain and can be signalled by complications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::181e34aae0caa28e17b71f050bed14e4
https://doi.org/10.36347/sajp.2021.v10i10.004
https://doi.org/10.36347/sajp.2021.v10i10.004
Publikováno v:
Scholars Academic Journal of Pharmacy. 10:177-179
We report the case of a left pubic osteochondroma in a 55-year-old man, without any particular pathological history, which revealed itself as a painful left laterotesticular induration. This induration increased in volume and bothered the patient dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f20d1d9090c61630c858d8edddf117
https://doi.org/10.36347/sajp.2021.v10i10.003
https://doi.org/10.36347/sajp.2021.v10i10.003
Publikováno v:
Scholars Journal of Medical Case Reports. 9:974-976
Hydatid cyst (HC) disease is a serious health problem in endemic areas. It is a parasitic infection that commonly involves liver and lungs while muscular HC is rare. HC of abdominal wall was reported only six times. We reported a 75-year-old women pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2bd784290e2f0ccee0a06943080411a
https://doi.org/10.36347/sjmcr.2021.v09i10.013
https://doi.org/10.36347/sjmcr.2021.v09i10.013
Publikováno v:
La Revue de Médecine Interne. 43:746-747
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc8bf5a43f0993d2a75579997557a0a0
https://doi.org/10.1016/j.revmed.2022.07.001
https://doi.org/10.1016/j.revmed.2022.07.001
Publikováno v:
La Revue de medecine interne. 43(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::10d3a3d4f98c721c4e55d8daefe11c9f
https://pubmed.ncbi.nlm.nih.gov/35868990
https://pubmed.ncbi.nlm.nih.gov/35868990
Publikováno v:
International Journal of Advanced Research. 4:789-792
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90fc3baac01e6cf4a5f78033da6ae1e3
https://doi.org/10.21474/ijar01/1858
https://doi.org/10.21474/ijar01/1858
Publikováno v:
Journal d'imagerie diagnostique et interventionnelle. 2:228-229
Resume Introduction Le syndrome de Leri-Weill est une maladie hereditaire rare dont le diagnostic est a la fois clinique et radiologique, confirme par l’etude genetique. Cas clinique A travers cette observation, nous decrivons les aspects cliniques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c98c6af76704cccd5a8b856c7aee797
https://doi.org/10.1016/j.jidi.2019.04.005
https://doi.org/10.1016/j.jidi.2019.04.005
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Annales d'Endocrinologie. 75:346
Introduction Le syndrome de Fahr est une entite rare, caracterisee par des calcifications striato-pallido-dentelees, et par son polymorphisme clinique, aux etiologies dominees par les dysparathyroidies. Observations Nous rapportons deux cas de syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90b92c53b6c07fc906b9a906f27419ba
https://doi.org/10.1016/j.ando.2014.07.252
https://doi.org/10.1016/j.ando.2014.07.252