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

Year Number of Results
1972 1
1973 1
1974 1
1975 1
1976 3
1977 3
1978 4
1979 8
1980 2
1981 3
1982 3
1983 2
1984 3
1985 1
1986 1
1987 1
1988 5
1989 2
1991 1
1992 1
1993 3
1994 2
1995 2
1996 3
1997 1
1998 2
1999 2
2000 2
2001 3
2002 3
2003 1
2004 1
2005 4
2006 3
2008 2
2009 2
2010 2
2011 3
2012 7
2013 3
2014 10
2015 6
2016 2
2017 2
2018 2
2019 6
2024 0

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118 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.
A caloric deprivation or deficiency of several components, such as proteins, minerals, essential fatty acids, and vitamins, caused by inborn errors or reduced uptake, can lead to structural abnormalities, pigmentation changes, or hair loss, although exact data are often lacking. …
A caloric deprivation or deficiency of several components, such as proteins, minerals, essential fatty acids, and vitamins, caused by inborn …
A systematic review and evidence-based guideline for diagnosis and treatment of Menkes disease.
Vairo FPE, Chwal BC, Perini S, Ferreira MAP, de Freitas Lopes AC, Saute JAM. Vairo FPE, et al. Mol Genet Metab. 2019 Jan;126(1):6-13. doi: 10.1016/j.ymgme.2018.12.005. Epub 2018 Dec 11. Mol Genet Metab. 2019. PMID: 30594472
In conclusion, our guideline can contribute to standardize some aspects of the clinical care of patients with Menkes disease, especially reducing disease burden and mortality and providers' and families' anxiety....
In conclusion, our guideline can contribute to standardize some aspects of the clinical care of patients with Menkes disease, especia …
Menkes' kinky-hair syndrome.
Danks DM, Campbell PE, Walker-Smith J, Stevens BJ, Gillespie JM, Blomfield J, Turner B. Danks DM, et al. Lancet. 1972 May 20;1(7760):1100-2. doi: 10.1016/s0140-6736(72)91433-x. Lancet. 1972. PMID: 4112576 No abstract available.
Diagnosis and therapy of Menkes syndrome, a genetic form of copper deficiency.
Kaler SG. Kaler SG. Am J Clin Nutr. 1998 May;67(5 Suppl):1029S-1034S. doi: 10.1093/ajcn/67.5.1029S. Am J Clin Nutr. 1998. PMID: 9587147 Review.
In the 25 y since copper deficiency was first delineated in persons with Menkes syndrome, advances in our understanding of the clinical, biochemical, and molecular aspects of this rare disorder have surpassed progress in the design of effective therapies. ...This abnormal …
In the 25 y since copper deficiency was first delineated in persons with Menkes syndrome, advances in our understanding of the clinical
Inborn errors of copper metabolism.
Kaler SG. Kaler SG. Handb Clin Neurol. 2013;113:1745-54. doi: 10.1016/B978-0-444-59565-2.00045-9. Handb Clin Neurol. 2013. PMID: 23622398 Free PMC article. Review.
Clinical manifestations and treatment of Menkes disease and its variants.
Kodama H, Murata Y, Kobayashi M. Kodama H, et al. Pediatr Int. 1999 Aug;41(4):423-9. doi: 10.1046/j.1442-200x.1999.01095.x. Pediatr Int. 1999. PMID: 10453199 Review.
The clinical manifestations of classical Menkes disease, mild Menkes disease and occipital horn syndrome are reviewed. ...Mild Menkes disease and occipital horn syndrome, which show milder forms than Menkes disease, have been identified as genetic disorders resulting from …
The clinical manifestations of classical Menkes disease, mild Menkes disease and occipital horn syndrome are reviewed. ...Mild Menkes …
Acquired Pili Torti.
Evans JB, Hastings JG, Kaffenberger BH. Evans JB, et al. JAMA Dermatol. 2019 Apr 1;155(4):488. doi: 10.1001/jamadermatol.2018.4677. JAMA Dermatol. 2019. PMID: 30810707 No abstract available.
Copper comes of age in Melbourne.
Mercer JF, Camakaris J. Mercer JF, et al. Metallomics. 2016 Sep 1;8(9):816-23. doi: 10.1039/c6mt90022d. Epub 2016 Jul 11. Metallomics. 2016. PMID: 27399171
Copper deficiency in humans.
Williams DM. Williams DM. Semin Hematol. 1983 Apr;20(2):118-28. Semin Hematol. 1983. PMID: 6410510 Review.
This x-linked abnormality is associated with copper deficiency due to impaired gastrointestinal copper absorption. However, the clinical disorder cannot be corrected readily with copper replacement, thus suggesting that Menkes' syndrome may reflect more than simple copper …
This x-linked abnormality is associated with copper deficiency due to impaired gastrointestinal copper absorption. However, the clinical
118 results