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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 0

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Search Results

199 results

Results by year

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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. MD is inherited as an X-linked recessive trait, …
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.
Multiple proteins mediate intracellular transfers in bacteria, and glutathione may play a major role in cytosolic copper delivery to cuproenzymes in mammalian cells. Study of two human disorders of copper transport, Menkes disease and Wilson disease, led to the identificat …
Multiple proteins mediate intracellular transfers in bacteria, and glutathione may play a major role in cytosolic copper delivery to cuproen …
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. ...RECENT FINDINGS: Acq …
PURPOSE OF REVIEW: Reports of the neurologic findings in adults with acquired copper deficiency as well as the development of novel models f …
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes.
De Feyter S, Beyens A, Callewaert B. De Feyter S, et al. J Inherit Metab Dis. 2023 Mar;46(2):163-173. doi: 10.1002/jimd.12590. Epub 2023 Feb 3. J Inherit Metab Dis. 2023. PMID: 36692329 Review.
We recorded data on the phenotype and genotype in 162 individuals with a molecularly confirmed ATP7A-related disorder in order to identify differentiating clinical criteria, evaluate genotype-phenotype correlations and propose management guidelines. Early seizures are specific fo …
We recorded data on the phenotype and genotype in 162 individuals with a molecularly confirmed ATP7A-related disorder in order to identify d …
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.
Neuroimaging Changes in Menkes Disease, Part 2.
Manara R, Rocco MC, D'agata L, Cusmai R, Freri E, Giordano L, Darra F, Procopio E, Toldo I, Peruzzi C, Vittorini R, Spalice A, Fusco C, Nosadini M, Longo D, Sartori S; Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases. Manara R, et al. AJNR Am J Neuroradiol. 2017 Oct;38(10):1858-1865. doi: 10.3174/ajnr.A5192. Epub 2017 May 11. AJNR Am J Neuroradiol. 2017. PMID: 28495940 Free PMC article. Review.
This is the second part of a retrospective and review MR imaging study aiming to define the frequency rate, timing, imaging features, and evolution of gray matter changes in Menkes disease, a rare multisystem X-linked disorder of copper metabolism characterized by early, s …
This is the second part of a retrospective and review MR imaging study aiming to define the frequency rate, timing, imaging features, and ev …
199 results