Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency Latest Advances
Find the Latest Research About Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency
Last Updated: 02/24/2026
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Found 35 publications
Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 26, 2022
Identification of Δ-1-pyrroline-5-carboxylate derived biomarkers for hyperprolinemia type II.
Journal: Communications biology
Published: April 06, 2022
Metabolic epilepsy in hyperprolinemia type II due to a novel nonsense ALDH4A1 gene variant.
Journal: Metabolic brain disease
Published: April 07, 2021
Novel variants in a patient with late-onset hyperprolinemia type II: diagnostic key for status epilepticus and lactic acidosis.
Journal: BMC neurology
Published: September 11, 2019
Proline Accumulation Is Regulated by Transcription Factors Associated with Phosphate Starvation.
Journal: Plant physiology
Published: June 13, 2017
Structure, function, and mechanism of proline utilization A (PutA).
Journal: Archives of biochemistry and biophysics
Published: June 08, 2017
New developments in diagnosis and treatment update: Schizophrenia/first episode psychosis in children and adolescents.
Journal: Journal of child and adolescent mental health
Published: November 14, 2014
Long-term neuropsychiatric follow-up in hyperprolinemia type I.
Journal: Psychiatric genetics
Published: May 21, 2014
Biochemical and clinical features of hereditary hyperprolinemia.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 11, 2014
Hyperprolinemia induces DNA, protein and lipid damage in blood of rats: antioxidant protection.
Journal: The international journal of biochemistry & cell biology
Published: January 23, 2014
Vitamin D insufficiency and schizophrenia risk: evaluation of hyperprolinemia as a mediator of association.
Journal: Schizophrenia research
Published: July 23, 2013
Identification of PRODH mutations in Korean neonates with type I hyperprolinemia.
Journal: Annals of clinical and laboratory science
Published: March 07, 2013
Last Updated: 02/24/2026