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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1962 1
1964 2
1965 1
1967 2
1968 5
1969 4
1970 6
1971 4
1972 3
1973 1
1974 9
1975 3
1976 6
1977 2
1978 3
1979 3
1980 1
1982 1
1984 2
1985 2
1987 2
1988 2
1989 3
1990 2
1991 2
1992 2
1993 1
1996 2
1997 4
1998 3
1999 3
2000 8
2001 5
2002 1
2003 7
2004 2
2005 9
2006 5
2007 8
2008 6
2009 4
2010 3
2011 9
2012 7
2013 7
2014 7
2015 8
2016 4
2017 8
2018 3
2019 5
2020 1
2021 6
2022 2
2023 6
2024 2
2025 1

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207 results

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Page 1
Psychiatric phenotypes associated with hyperprolinemia: A systematic review.
Namavar Y, Duineveld DJ, Both GIA, Fiksinski AM, Vorstman JAS, Verhoeven-Duif NM, Zinkstok JR. Namavar Y, et al. Am J Med Genet B Neuropsychiatr Genet. 2021 Jul;186(5):289-317. doi: 10.1002/ajmg.b.32869. Epub 2021 Jul 24. Am J Med Genet B Neuropsychiatr Genet. 2021. PMID: 34302426
Hyperprolinemia Type I and II are genetic metabolic disorders caused by disrupted proline degradation. ...More studies are needed to clarify whether hyperprolinemia is a primary causal factor underlying the increased risk of developing psychiatric disorders seen in …
Hyperprolinemia Type I and II are genetic metabolic disorders caused by disrupted proline degradation. ...More studies are needed to …
[Hyperprolinemia].
Endo F. Endo F. Ryoikibetsu Shokogun Shirizu. 2001;(33):838-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462711 Review. Japanese. No abstract available.
Disorders affecting vitamin B6 metabolism.
Wilson MP, Plecko B, Mills PB, Clayton PT. Wilson MP, et al. J Inherit Metab Dis. 2019 Jul;42(4):629-646. doi: 10.1002/jimd.12060. Epub 2019 Mar 20. J Inherit Metab Dis. 2019. PMID: 30671974 Review.
This includes pyridox(am)ine phosphate oxidase deficiency (a disorder affecting PLP synthesis and recycling), disorders affecting PLP import into the brain (hypophosphatasia and glycosylphosphatidylinositol anchor synthesis defects), a disorder of an intracellular PLP-binding pro …
This includes pyridox(am)ine phosphate oxidase deficiency (a disorder affecting PLP synthesis and recycling), disorders affecting PLP import …
[Hyperprolinemia type II].
Endo F. Endo F. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):155-7. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590014 Review. Japanese. No abstract available.
[Hyperprolinemia type I].
Endo F. Endo F. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):152-4. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590013 Review. Japanese. No abstract available.
[Hyperprolinemia].
Matsumura R. Matsumura R. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):389. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11031977 Review. Japanese. No abstract available.
Hyperprolinemia type I caused by homozygous p.T466M mutation in PRODH.
Hama R, Kido J, Sugawara K, Nakamura T, Nakamura K. Hama R, et al. Hum Genome Var. 2021 Jul 20;8(1):28. doi: 10.1038/s41439-021-00159-5. Hum Genome Var. 2021. PMID: 34285201 Free PMC article.
Hyperprolinemia type I (HPI) is an autosomal recessive metabolic disorder caused by defects in proline oxidase. ...
Hyperprolinemia type I (HPI) is an autosomal recessive metabolic disorder caused by defects in proline oxidase. ...
Myoclonus-Ataxia Syndrome Associated with Hyperprolinemia Type I.
Ong TL, Lau YH, Ngu LH, Hadi D, Lau KM, Mawardi AS. Ong TL, et al. Mov Disord Clin Pract. 2023 Aug 24;10(Suppl 3):S38-S40. doi: 10.1002/mdc3.13780. eCollection 2023 Aug. Mov Disord Clin Pract. 2023. PMID: 37636236 Free PMC article. No abstract available.
Hyperprolinemia type II.
Applegarth DA, Ingram P, Hingston J, Hardwick DF. Applegarth DA, et al. Clin Biochem. 1974 Mar;7(1):14-28. doi: 10.1016/s0009-9120(74)90174-x. Clin Biochem. 1974. PMID: 4825691 No abstract available.
207 results