Results 251 to 260 of about 8,821 (269)
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[Cystinuria].

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2010
Cystinuria is an autosomal recessive disorder characterized by impairment of the proximal renal tubules which are unable to reabsorb cystine and dibasic amino acids, leading to the formation of recurrent kidney stones. According to the most recent genetic knowledge, there are two types of cystinuria.
Luca, Dello Strologo   +2 more
openaire   +1 more source

Cystinuria

New England Journal of Medicine, 1986
openaire   +2 more sources

Covalent post-synthetic modification of MOFs as a fluorescent sensor for the efficient detection of the biomarker of cystinuria

Microchimica Acta
Hao Guo   +8 more
semanticscholar   +1 more source

Cystinuria

The American Journal of Medicine, 1957
H, HARRIS, E B, ROBSON
openaire   +2 more sources

Attenuated total reflection-fourier transform infrared spectroscopy (ATR-FTIR) detection as a rapid and convenient screening test for cystinuria.

Clinica chimica acta; international journal of clinical chemistry, 2021
A. Primiano   +8 more
semanticscholar   +1 more source

Challenges in diagnosis and treatment of cystinuria patients with Urolithiasis: multicenter patient centered study

World journal of urology
W. Kamal   +11 more
semanticscholar   +1 more source

[Cystinuria].

Néphrologie & Thérapeutique, 2021
C. Prot-Bertoye   +7 more
semanticscholar   +1 more source

CYSTINURIA

Nutrition Reviews, 2009
openaire   +2 more sources

IATROGENIC CYSTINURIA

The Lancet, 1970
A, Hill, W A, Zaleski
openaire   +2 more sources

Heterozygotes for cystinuria

Annals of Human Genetics, 1966
J C, Crawhall   +2 more
openaire   +2 more sources

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