Literature DB >> 20896937

A Contribution to the Study of Alkaptonuria.

A E Garrod.   

Abstract

Entities:  

Year:  1899        PMID： 20896937      PMCID： PMC2036698          DOI： 10.1177/095952879908200119

Source DB:  PubMed          Journal:  Med Chir Trans        ISSN： 0959-5287


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  5 in total

1.  Sir Archibald Garrod's inborn errors of metabolism. II. Alkaptonuria.

Authors:  W E KNOX
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

Review 2.  Inborn errors of metabolism: Garrod's legacy.

Authors:  A G Bearn
Journal:  Mol Med       Date:  1996-05       Impact factor: 6.354

3.  Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy.

Authors:  Martina Nemethova; Jan Radvanszky; Ludevit Kadasi; David B Ascher; Douglas E V Pires; Tom L Blundell; Berardino Porfirio; Alessandro Mannoni; Annalisa Santucci; Lia Milucci; Silvia Sestini; Gianfranco Biolcati; Fiammetta Sorge; Caterina Aurizi; Robert Aquaron; Mohammed Alsbou; Charles Marques Lourenço; Kanakasabapathi Ramadevi; Lakshminarayan R Ranganath; James A Gallagher; Christa van Kan; Anthony K Hall; Birgitta Olsson; Nicolas Sireau; Hana Ayoob; Oliver G Timmis; Kim-Hanh Le Quan Sang; Federica Genovese; Richard Imrich; Jozef Rovensky; Rangan Srinivasaraghavan; Shruthi K Bharadwaj; Ronen Spiegel; Andrea Zatkova
Journal:  Eur J Hum Genet       Date:  2015-03-25       Impact factor: 4.246

Review 4.  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

Review 5.  Dominant versus recessive: molecular mechanisms in metabolic disease.

Authors:  Johannes Zschocke
Journal:  J Inherit Metab Dis       Date:  2008-10-21       Impact factor: 4.982
  5 in total

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