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pro vyhledávání: '"Medhat Abdul Halim"'
Autor:
Prasad Nair, Torki Al-Otaibi, Narayanan Nampoory, Wafa′a Al-Qabandi, Tarek Said, Medhat Abdul Halim, Osama Gheith
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 24, Iss 5, Pp 969-975 (2013)
Primary hyperoxaluria type-1 (PH-1) is a rare autosomal recessive metabolic disorder leading to excessive oxalate production, deposition of calcium oxalate crystals in the kidney, nephrocalcinosis, progressive renal failure and systemic deposition of
Externí odkaz:
https://doaj.org/article/8ec13ebdbbdb4a6185c459b5f5572bba
