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pro vyhledávání: '"Urine copper level"'
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Publikováno v:
Chinese Journal of Contemporary Pediatrics; Jun2023, Vol. 25 Issue 6, p612-618, 7p
Publikováno v:
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 6, Iss 21, Pp 43-45 (2015)
Wilson’s disease is an autosomal recessive disorder of copper metabolism characterized by excessive amount of copper in liver, brain, eye and other body tissues. Diagnosis is based on the presence of Kayser-Fleischer rings, typical neurological sym
Publikováno v:
Journal of Toxicology: Clinical Toxicology. 30:99-108
Despite widespread industrial use of copper naphthenate, there are no reports of the relationship of copper naphthenate and copper absorption in humans or animals. We report a family of three individuals who lived in a home where copper naphthenate w
Autor:
Talaei, Afsaneh1 afsanehtalaeii@yahoo.com, Jabari, Saber2, Bigdeli, Mohamad Hasan2, Farahani, Heidar3, Siavash, Mansour4
Publikováno v:
Indian Journal of Endocrinology & Metabolism. Oct2011, Vol. 15 Issue 4, p316-319. 4p.
Autor:
Gok, Veysel1 (AUTHOR), Ozcan, Alper1 (AUTHOR), Ozer, Sinem2 (AUTHOR), Karaman, Filiz3 (AUTHOR), Aykutlu, Esra1 (AUTHOR), Yilmaz, Ebru1 (AUTHOR), Karakukcu, Musa1 (AUTHOR), Bisgin, Atil2 (AUTHOR), Unal, Ekrem1,4,5 (AUTHOR)
Publikováno v:
Pediatric Hematology & Oncology. 2023, Vol. 40 Issue 7, p673-681. 9p.
Autor:
Uppicherla, Suchitra1, Shaik, Hazira Farheen1, Shaik, Rahila Iram1, Chavakala, Bhaskar Rao2 suchitrauppicherla@gmail.com, Padmakar, Somanaboina1, Cuddapah, Rajaram1
Publikováno v:
Journal of Dr. NTR University of Health Sciences. Oct-Dec2023, Vol. 12 Issue 4, p373-377. 5p.
Publikováno v:
Movement Disorders Clinical Practice. May2022 Supplement S1, Vol. 9, pS8-S73. 66p.
Publikováno v:
Annals of Laboratory Medicine; 2020, Vol. 40 Issue 6, p500-503, 4p