Literature DB >> 5383982

The excretion of amino acids by cystinuric patients and their relatives.

J C Crawhall, P Purkiss, R W Watts, E P Young.   

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Year:  1969        PMID： 5383982     DOI： 10.1111/j.1469-1809.1969.tb01641.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  6 in total

Review 1.  Factors governing urinary tract stone disease.

Authors:  R W Watts
Journal:  Pediatr Nephrol       Date:  1989-07       Impact factor: 3.714

2.  Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers.

Authors:  N P Cavanagh; J Bicknell; F Howard
Journal:  Arch Dis Child       Date:  1974-08       Impact factor: 3.791

Review 3.  Garrod's Croonian Lectures (1908) and the charter 'Inborn Errors of Metabolism': albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008.

Authors:  Charles R Scriver
Journal:  J Inherit Metab Dis       Date:  2008-10-12       Impact factor: 4.982

4.  Cystine crystalluria and urinary saturation in cystine and non-cystine stone formers.

Authors:  M Labeeuw; C Gerbaulet; N Pozet; P Zech; J Traeger
Journal:  Urol Res       Date:  1981

5.  Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital.

Authors:  G C Yadav; P C Reavey
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

6.  Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.

Authors:  P Purkiss; R A Chalmers; O Borud
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982
  6 in total

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