Literature DB >> 15723447

Hyperhydroxyprolinaemia: a new case diagnosed during neonatal screening with tandem mass spectrometry.

Giancarlo la Marca, Sabrina Malvagia, Elisabetta Pasquini, Maria Alice Donati, Serena Gasperini, Elena Procopio, Enrico Zammarchi.   

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Year:  2005        PMID： 15723447     DOI： 10.1002/rcm.1861

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN： 0951-4198            Impact factor:   2.419


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  2 in total

1.  Genetic cause and prevalence of hydroxyprolinemia.

Authors:  Christian Staufner; Tobias B Haack; Patrik Feyh; Gwendolyn Gramer; Deepthi Ediga Raga; Caterina Terrile; Sven Sauer; Jürgen G Okun; Junmin Fang-Hoffmann; Ertan Mayatepek; Holger Prokisch; Georg F Hoffmann; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2016-05-02       Impact factor: 4.982

2.  Recall rate and positive predictive value of MSUD screening is not influenced by hydroxyproline.

Authors:  Ralph Fingerhut
Journal:  Eur J Pediatr       Date:  2008-08-06       Impact factor: 3.183
  2 in total

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