Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1971 1
1973 1
1976 1
1977 1
1983 1
1985 1
1987 1
1988 2
1989 2
1991 1
1994 1
1997 1
1998 1
2001 2
2004 1
2006 2
2007 2
2008 1
2012 1
2013 1
2015 1
2019 1
2020 1
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

28 results

Results by year

Filters applied: . Clear all
Page 1
Premature Loss of Deciduous Teeth as a Symptom of Systemic Disease: A Narrative Literature Review.
Spodzieja K, Olczak-Kowalczyk D. Spodzieja K, et al. Int J Environ Res Public Health. 2022 Mar 13;19(6):3386. doi: 10.3390/ijerph19063386. Int J Environ Res Public Health. 2022. PMID: 35329073 Free PMC article. Review.
RESULTS: In this study, 16 systemic diseases were linked to premature primary tooth loss in children: Papillon-Lefevre syndrome, mucocutaneous dyskeratosis, Coffin-Lowry syndrome, congenital adrenal hyperplasia, Langerhans cell histiocytosis, cherubism, hypophosphatasia, acata
RESULTS: In this study, 16 systemic diseases were linked to premature primary tooth loss in children: Papillon-Lefevre syndrome, mucocutaneo …
Role of Catalase in Oxidative Stress- and Age-Associated Degenerative Diseases.
Nandi A, Yan LJ, Jana CK, Das N. Nandi A, et al. Oxid Med Cell Longev. 2019 Nov 11;2019:9613090. doi: 10.1155/2019/9613090. eCollection 2019. Oxid Med Cell Longev. 2019. PMID: 31827713 Free PMC article. Review.
This paper describes the direct and indirect involvement of deficiency and/or modification of catalase in the pathogenesis of some important diseases such as diabetes mellitus, Alzheimer's disease, Parkinson's disease, vitiligo, and acatalasemia. Details on the efforts exp …
This paper describes the direct and indirect involvement of deficiency and/or modification of catalase in the pathogenesis of some important …
[Acatalasemia and type 2 diabetes mellitus].
Góth L, Nagy T, Káplár M. Góth L, et al. Orv Hetil. 2015 Mar 8;156(10):393-8. doi: 10.1556/OH.2015.30095. Orv Hetil. 2015. PMID: 25726767 Review. Hungarian.
Hydrogen peroxide is a highly reactive small molecule and its excessive concentration may cause significant damages to proteins, deoxyribonucleic acid, ribonucleic acid and lipids. Acatalasemia refers to inherited deficiency of the catalase enzyme. In this review the autho …
Hydrogen peroxide is a highly reactive small molecule and its excessive concentration may cause significant damages to proteins, deoxyribonu …
Acatalasemia and diabetes mellitus.
Góth L, Nagy T. Góth L, et al. Arch Biochem Biophys. 2012 Sep 15;525(2):195-200. doi: 10.1016/j.abb.2012.02.005. Epub 2012 Feb 16. Arch Biochem Biophys. 2012. PMID: 22365890 Review.
Low levels in muscle cells, facilitate insulin signaling. Acatalasemia is a result of the homozygous mutations in the catalase gene, has a worldwide distribution with 12 known mutations. ...
Low levels in muscle cells, facilitate insulin signaling. Acatalasemia is a result of the homozygous mutations in the catalase gene, …
Peroxisomes and aging.
Terlecky SR, Koepke JI, Walton PA. Terlecky SR, et al. Biochim Biophys Acta. 2006 Dec;1763(12):1749-54. doi: 10.1016/j.bbamcr.2006.08.017. Epub 2006 Aug 23. Biochim Biophys Acta. 2006. PMID: 17027095 Free PMC article. Review.
Acatalasemia.
Ogata M. Ogata M. Hum Genet. 1991 Feb;86(4):331-40. doi: 10.1007/BF00201829. Hum Genet. 1991. PMID: 1999334 Review.
The abnormalities in acatalasemia at the gene level as well as properties of the residual catalase in Japanese acatalasemia are historically reviewed. ...
The abnormalities in acatalasemia at the gene level as well as properties of the residual catalase in Japanese acatalasemia ar …
Prenatal and perinatal diagnosis of peroxisomal disorders.
Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H. Schutgens RB, et al. J Inherit Metab Dis. 1989;12 Suppl 1:118-34. doi: 10.1007/BF01799291. J Inherit Metab Dis. 1989. PMID: 2509803 Review.
Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified into three groups: (1) disorders of peroxisome biogenesis with a generalized loss of peroxisomal functions (Zellweger syndrome, neonatal adrenoleukodystrophy, infantile Refsum …
Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified into three groups: (1) disorders of …
Molecular basis of D-bifunctional protein deficiency.
Möller G, van Grunsven EG, Wanders RJ, Adamski J. Möller G, et al. Mol Cell Endocrinol. 2001 Jan 22;171(1-2):61-70. doi: 10.1016/s0303-7207(00)00388-9. Mol Cell Endocrinol. 2001. PMID: 11165012 Review.
The phenotypes vary widely: affected humans may die very early in life within a few days to several months as a result of the impairment in essential peroxisomal functions as, for example, in Zellweger syndrome, or they may show only minor disabilities as is in acatalasemia
The phenotypes vary widely: affected humans may die very early in life within a few days to several months as a result of the impairment in …
Peroxisomal disorders: clinical commentary and future prospects.
Wilson GN, Holmes RD, Hajra AK. Wilson GN, et al. Am J Med Genet. 1988 Jul;30(3):771-92. doi: 10.1002/ajmg.1320300311. Am J Med Genet. 1988. PMID: 2461077 Review.
These disorders are associated with diverse metabolic abnormalities which are useful in pre- or postnatal diagnosis and distinguish these disorders from others such as X-linked adrenoleukodystrophy, adult Refsum disease, hyperoxaluria type I, and acatalasemia. Peroxisome s …
These disorders are associated with diverse metabolic abnormalities which are useful in pre- or postnatal diagnosis and distinguish these di …
New approaches in peroxisomal disorders.
Moser HW. Moser HW. Dev Neurosci. 1987;9(1):1-18. doi: 10.1159/000111604. Dev Neurosci. 1987. PMID: 3297624 Review.
Here the peroxisomal structure is intact, but there is deficient function of several peroxisomal enzymes. The third group includes X-linked adrenoleukodystrophy, acatalasemia and 'adult' Refsum's disease. The peroxisomal structure is intact, and the defect in each instance …
Here the peroxisomal structure is intact, but there is deficient function of several peroxisomal enzymes. The third group includes X-linked …
28 results