Literature DB >> 3771038

Prolidase deficiency. A metabolic disorder presenting with dermatologic signs.

B J Freij, V M Der Kaloustian.   

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Year:  1986        PMID： 3771038     DOI： 10.1111/j.1365-4362.1986.tb03446.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN： 0011-9059            Impact factor:   2.736


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  3 in total

1.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

2.  Spurious Elevation of Multiple Urine Amino Acids by Ion-Exchange Chromatography in Patients with Prolidase Deficiency.

Authors:  Carlos R Ferreira; Kristina Cusmano-Ozog
Journal:  JIMD Rep       Date:  2016-04-12

3.  Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins.

Authors:  Nora Alrumayyan; Drew Slauenwhite; Sarah M McAlpine; Sarah Roberts; Thomas B Issekutz; Adam M Huber; Zaiping Liu; Beata Derfalvi
Journal:  Allergy Asthma Clin Immunol       Date:  2022-02-23       Impact factor: 3.406
  3 in total

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