Pulmonary manifestations of prolidase deficiency-Reference-Cited by-同舟云学术

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Pulmonary manifestations of prolidase deficiency

Published:2016-05-01 Issue:11 Volume:51 Page:1229-1233
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol.

Author:

Nir Vered¹,Ilivitky Anat²,Hakim Fahed¹³,Yoseph Ronen Bar¹,Gur Michal¹,Mandel Hana⁴,Bentur Lea¹³

Affiliation:

1. Division of Pediatric Pulmonology, Ruth Children's Hospital; Rambam Health Care Campus; Haifa Israel

2. Pediatric Radiology; Ruth Children's Hospital; Rambam Health Care Campus; Haifa Israel

3. Rappaport Faculty of Medicine; Technion-Israel Institute of Technology; Haifa Israel

4. Hana Mandel, Metabolic Unit, Ruth Children's Hospital; Rambam Health Care Campus; Haifa Israel

Funder

none reported

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference22 articles.

1. A syndrome resembling lathyrism associated with iminodipeptiduria;Goodman;Am J Med,1968

2. Quebec neonatal mass urinary screening programme: from micromolecules to macromolecules;Auray-Blais;J Inherit Metab Dis,2007

3. Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations;Lupi;Amino Acids,2008

4. Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship;Lupi;J Hum Genet,2004

5. Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes;Jackson;CMAJ,1975

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1. Multiorgan Failure and Sepsis in an ICU Patient with Prolidase Enzyme Deficiency—The Specificity of Treatment and Care: A Case Report;Medicina;2024-06-20

2. An Infant With Interstitial Lung Disease of Rare Cause;Chest;2022-05

3. A case of prolidase deficiency in a male patient;Pediatric Dermatology;2021-12-09

4. Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases;Genetics in Medicine;2021-09

5. PROLIDASE: A Review from Discovery to its Role in Health and Disease;Frontiers in Molecular Biosciences;2021-08-31

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