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1973
2025

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

Year Number of Results
1973 1
1976 1
1978 2
1979 6
1980 3
1981 5
1982 6
1983 5
1984 2
1985 6
1986 6
1987 4
1988 2
1989 3
1990 1
1991 1
1992 1
1993 5
1994 5
1995 5
1996 9
1997 6
1998 12
1999 16
2000 5
2001 5
2002 6
2003 4
2004 4
2005 3
2006 3
2007 6
2008 4
2009 7
2010 7
2011 6
2012 4
2013 5
2014 6
2015 5
2016 2
2017 4
2018 4
2019 2
2020 2
2022 1
2023 2
2024 1
2025 0

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200 results

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Page 1
Nutrition and hair: deficiencies and supplements.
Finner AM. Finner AM. Dermatol Clin. 2013 Jan;31(1):167-72. doi: 10.1016/j.det.2012.08.015. Epub 2012 Oct 18. Dermatol Clin. 2013. PMID: 23159185 Review.
The diagnosis is established through a careful history, clinical examination of hair loss activity, and hair quality and confirmed through targeted laboratory tests. Examples of genetic hair disorders caused by reduced nutritional components are zinc deficien …
The diagnosis is established through a careful history, clinical examination of hair loss activity, and hair quality and confi …
Menkes disease.
Tümer Z, Møller LB. Tümer Z, et al. Eur J Hum Genet. 2010 May;18(5):511-8. doi: 10.1038/ejhg.2009.187. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888294 Free PMC article. Review.
Menkes disease (MD) is a lethal multisystemic disorder of copper metabolism. Progressive neurodegeneration and connective tissue disturbances, together with the peculiar 'kinky' hair are the main manifestations. ...
Menkes disease (MD) is a lethal multisystemic disorder of copper metabolism. Progressive neurodegeneration and connective tissue dist
The molecular mechanisms of copper metabolism and its roles in human diseases.
Chen J, Jiang Y, Shi H, Peng Y, Fan X, Li C. Chen J, et al. Pflugers Arch. 2020 Oct;472(10):1415-1429. doi: 10.1007/s00424-020-02412-2. Epub 2020 Jun 7. Pflugers Arch. 2020. PMID: 32506322 Review.
A hereditary or acquired copper unbalance, including deficiency, overload, or misdistribution, may cause or aggravate certain diseases such as Menkes disease, Wilson disease, neurodegenerative diseases, anemia, metabolic syndrome, cardiovascular diseases, and cancer …
A hereditary or acquired copper unbalance, including deficiency, overload, or misdistribution, may cause or aggravate certain diseases such …
Ataxia telangiectasia, Menkes kinky hair disease and neurocutaneous melanosis.
Caccavale S, Bove D, Bove RM, LA Montagna M. Caccavale S, et al. G Ital Dermatol Venereol. 2017 Feb;152(1):58-65. doi: 10.23736/S0392-0488.16.05083-5. Epub 2016 Mar 22. G Ital Dermatol Venereol. 2017. PMID: 27002302 Review.
In this review, different aspects of ataxia telangiectasia, Menkes kinky hair disease and neurocutaneous melanosis are examined: clinical features, genetic defect, mutation spectrum, pathogenesis, and neurobiological basis; indications for clinical practice a …
In this review, different aspects of ataxia telangiectasia, Menkes kinky hair disease and neurocutaneous melanosis are …
Cellular copper transport.
Vulpe CD, Packman S. Vulpe CD, et al. Annu Rev Nutr. 1995;15:293-322. doi: 10.1146/annurev.nu.15.070195.001453. Annu Rev Nutr. 1995. PMID: 8527222 Review.
Study of two human disorders of copper transport, Menkes disease and Wilson disease, led to the identification of an important category of proteins mediating cell copper export. The Menkes and Wilson disease gene products are copper-transporting ATPases of the P typ …
Study of two human disorders of copper transport, Menkes disease and Wilson disease, led to the identification of an important catego …
Copper deficiency.
Madsen E, Gitlin JD. Madsen E, et al. Curr Opin Gastroenterol. 2007 Mar;23(2):187-92. doi: 10.1097/MOG.0b013e32801421bb. Curr Opin Gastroenterol. 2007. PMID: 17268249 Review.
PURPOSE OF REVIEW: Reports of the neurologic findings in adults with acquired copper deficiency as well as the development of novel models for Menkes disease have permitted a greater understanding of the role of copper in the central nervous system. ...Chemical genetic stu …
PURPOSE OF REVIEW: Reports of the neurologic findings in adults with acquired copper deficiency as well as the development of novel models f …
Menkes's kinky hair syndrome.
[No authors listed] [No authors listed] Nutr Rev. 1973 Jan;31(1):17. doi: 10.1111/j.1753-4887.1973.tb05140.x. Nutr Rev. 1973. PMID: 4571253 Review. No abstract available.
Menkes disease.
Bertini I, Rosato A. Bertini I, et al. Cell Mol Life Sci. 2008 Jan;65(1):89-91. doi: 10.1007/s00018-007-7439-6. Cell Mol Life Sci. 2008. PMID: 17989919 Free PMC article. Review.
Menkes disease is caused by mutations in the copper-transporting P(1B)-type ATPase ATP7A. ...
Menkes disease is caused by mutations in the copper-transporting P(1B)-type ATPase ATP7A. ...
Menkes syndrome and animal models.
Mercer JF. Mercer JF. Am J Clin Nutr. 1998 May;67(5 Suppl):1022S-1028S. doi: 10.1093/ajcn/67.5.1022S. Am J Clin Nutr. 1998. PMID: 9587146 Review.
Menkes syndrome is an X-linked genetic copper deficiency that is usually fatal in early childhood. ...Copper-resistant cells overexpress MNK and can efflux more copper than parental cells, consistent with the copper efflux role proposed for MNK. Patients with Men
Menkes syndrome is an X-linked genetic copper deficiency that is usually fatal in early childhood. ...Copper-resistant cells o
Lysyl oxidase.
Siegel RC. Siegel RC. Int Rev Connect Tissue Res. 1979;8:73-118. doi: 10.1016/b978-0-12-363708-6.50009-6. Int Rev Connect Tissue Res. 1979. PMID: 41816 Review. No abstract available.
200 results