Zobrazeno 1 - 10
of 145
pro vyhledávání: '"Caroli s disease"'
Publikováno v:
پزشکی بالینی ابن سینا, Vol 22, Iss 3, Pp 263-267 (2015)
Introduction: Caroli disease is a rare congenital disorder characterized by segmental, nonob-structive dilatation of intrahepatic bile ducts. The term Caroli syndrome is used for the asso-ciation of Caroli disease with congenital hepatic fibrosis. Ca
Externí odkaz:
https://doaj.org/article/16d9741deff447e1a1e0f63d582a3d17
Publikováno v:
Žurnal Infektologii, Vol 13, Iss 3, Pp 150-152 (2021)
In their medical practice doctors deal with rare diseases which present difficulties in making a clinical diagnosis, in this case additional diagnostic methods are required. One of these diseases is Caroli's disease (syndrome), characterized by cysti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a07b0d3c2b438134c2c2243bf2fc4f
https://journal.niidi.ru/jofin/article/view/1233
https://journal.niidi.ru/jofin/article/view/1233
Autor:
Abdullatif Almohtadi, Faisal Ahmed, Fawaz Mohammed, Morad Sanhan, Abdulghani Ghabisha, Lina Al-moliki
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Caroli´s disease is a congenital hepatic disorder characterized by nonobstructive saccular or fusiform dilatation of the intrahepatic bile ducts with the absence of congenital hepatic fibrosis. Caroli´s disease is rare, with few reported cases in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::e0c1b4abe849ef8fda6b8e028df1492a
https://www.ajol.info/index.php/pamj/article/view/240181
https://www.ajol.info/index.php/pamj/article/view/240181
Publikováno v:
Pediatric Oncall. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55b7d211aad62e06265911fb08049592
https://doi.org/10.7199/ped.oncall.2022.50
https://doi.org/10.7199/ped.oncall.2022.50
Publikováno v:
Scholars Journal of Medical Case Reports. :170-172
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d34b6086bdb3a3e4a22cdc8727545cd9
https://doi.org/10.36347/sjmcr.2020.v08i02.017
https://doi.org/10.36347/sjmcr.2020.v08i02.017
Autor:
Yassine Lemfadli
Publikováno v:
MOJ Clinical & Medical Case Reports. 10:81-83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59a115c8f66205e956670fa997639850
https://doi.org/10.15406/mojcr.2020.10.00349
https://doi.org/10.15406/mojcr.2020.10.00349
Publikováno v:
World Chinese Journal of Digestology. 27:535-538
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::818ad69494f2dbe32555040475d86a1e
https://doi.org/10.11569/wcjd.v27.i8.535
https://doi.org/10.11569/wcjd.v27.i8.535
Autor:
Wonho Lee, Do Young Kim
Publikováno v:
Clinical Ultrasound. 3:79-82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dbb7c9df1a05626d18ef989186de321
https://doi.org/10.18525/cu.2018.3.2.79
https://doi.org/10.18525/cu.2018.3.2.79
Autor:
Anitha Abimannane, Rakhee Kar, Thiagarajan Narayanasamy Rajavelu, Delhi Kumar Chinnaiah Govindhareddy, Smita Kayal
Publikováno v:
Journal of Pediatric Hematology/Oncology. 42:e620-e622
Langerhans' cell histiocytosis is an uncommon disease in children with varied clinical presentation. Multisystem form of this disorder usually affects organs like the bones, skin, liver, spleen, lungs, and the central nervous system. We describe here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c14ef2a86e42abf7cc244aaf9dcef41
https://doi.org/10.1097/mph.0000000000001495
https://doi.org/10.1097/mph.0000000000001495
Publikováno v:
ESGE Days 2019.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cfb588453d9ce213bcea66712bc7cd4
https://doi.org/10.1055/s-0039-1681852
https://doi.org/10.1055/s-0039-1681852