Results 121 to 130 of about 5,205 (214)

Urine microscopy revealing a metabolic disorder: a case report. [PDF]

BMC Nephrol
Santos D, Lança MB, Navarro D, Baltazar P, Jorge C, Pinheiro LC, Fonseca NM.   +6 more
europepmc   +1 more source

From recurrent flank pain to systemic oxalosis: a case of primary hyperoxaluria type 1 requiring dual organ transplantation. [PDF]

Ann Med Surg (Lond)
Hassan SMS, Amjad N, Rab M, Malik A, Jamal A, Fatima M, Sadiq MH, Khan A, Khalid M.   +8 more
europepmc   +1 more source

Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department. [PDF]

Pan Afr Med J
Bettaieb A, Hajji M, Kaaroud H, Ben Hamida F, Goucha R, Mrad R, Gargah T, Chakroun M, Bouzid K, Abderrahim E.   +9 more
europepmc   +1 more source

Acute renal failure after dietary change - a case report. [PDF]

BMC Nephrol
Jankowski E, Reindl J, Hauptmann L, Wiech T, Wolf G, Busch M.   +5 more
europepmc   +1 more source

[A case of primary hyperoxaluria].

Nihon Jinzo Gakkai shi, 1985
KATOH, SHUJI, AZUMA, AKIHIRO, OKUDA, JUNICHI, IDA, KAZUNORI, KOSUGA, TAKAHIKO, SHINODA, MASAAKI, YAMADA, SEIICHIRO, YAKANE, YOSHIHIRO, OKA, TAKAHIRO   +8 more
openaire   +2 more sources

Delayed Diagnosis of Primary Hyperoxaluria and Systemic Oxalosis in a Hemodialysis Patient: A Case Report and Literature Review. [PDF]

Cureus
Benali H, El Mansouri M, Ait Elkihal I, Hamouche N, Chettati M, Fadili W, Laouad I.   +6 more
europepmc   +1 more source

Severe Acute Kidney Injury Following Whipple Procedure. [PDF]

Kidney360
Akel H, Patel SK.
europepmc   +1 more source

Current status of primary hyperoxaluria type 1 in Japan. [PDF]

Urolithiasis
Ogawa T, Okamoto K, Yamamoto M, Sato Y, Ushijima K, Numahata D, Takeshita H, Inai H, Onozawa M, Miyazaki J, Takayama T.   +10 more
europepmc   +1 more source

The gut-kidney microbiome-oxalate axis in calcium oxalate nephrolithiasis: mechanisms and microbiome-based interventions. [PDF]

Front Cell Infect Microbiol
Pang S, Zhang Z, Ma Q, Liu Y, Wang S, Wang J, Bi Y.   +6 more
europepmc   +1 more source

Genetic aspects of primary hyperoxaluria: diagnostics and treatment

Primary hyperoxaluria is a group of inherited metabolic diseases characterized by increased formation of calcium-oxalate stones in kidneys with development of nephrolithiasis and chronic kidney disease.
Azova M.M., Subbotina T.I., Rudenko V.I., Gadzhieva Z.K., Shumikhina M.V., Asanov A.Y., Litvinova M.M., Alyaev Y.G., Filippova T.V., Svetlichnaya D.V.   +9 more
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