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
1963 7
1964 14
1965 10
1966 10
1967 15
1968 20
1969 17
1970 26
1971 26
1972 33
1973 33
1974 30
1975 25
1976 38
1977 21
1978 24
1979 37
1980 30
1981 24
1982 36
1983 32
1984 34
1985 32
1986 28
1987 31
1988 44
1989 43
1990 44
1991 41
1992 41
1993 55
1994 53
1995 63
1996 61
1997 82
1998 115
1999 103
2000 100
2001 97
2002 116
2003 80
2004 102
2005 101
2006 99
2007 87
2008 73
2009 86
2010 86
2011 81
2012 77
2013 80
2014 69
2015 66
2016 61
2017 95
2018 88
2019 75
2020 70
2021 66
2022 56
2023 69
2024 19

Text availability

Article attribute

Article type

Publication date

Search Results

3,212 results

Results by year

Filters applied: . Clear all
Page 1
Wilson's disease and other neurological copper disorders.
Bandmann O, Weiss KH, Kaler SG. Bandmann O, et al. Lancet Neurol. 2015 Jan;14(1):103-13. doi: 10.1016/S1474-4422(14)70190-5. Lancet Neurol. 2015. PMID: 25496901 Free PMC article. Review.
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hepatic and neurological deficits, including dystonia and parkinsonism. ...Furthermore, Wilson's disease needs to be differentiated from other conditions tha …
The copper metabolism disorder Wilson's disease was first defined in 1912. Wilson's disease can present with hepatic and neuro …
Pseudohypoparathyroidism.
Linglart A, Levine MA, Jüppner H. Linglart A, et al. Endocrinol Metab Clin North Am. 2018 Dec;47(4):865-888. doi: 10.1016/j.ecl.2018.07.011. Epub 2018 Oct 12. Endocrinol Metab Clin North Am. 2018. PMID: 30390819 Free PMC article. Review.
Hemochromatosis.
Olynyk JK, Ramm GA. Olynyk JK, et al. N Engl J Med. 2022 Dec 8;387(23):2159-2170. doi: 10.1056/NEJMra2119758. N Engl J Med. 2022. PMID: 36477033 Review. No abstract available.
Review of the Diagnosis and Treatment of Periodic Paralysis.
Statland JM, Fontaine B, Hanna MG, Johnson NE, Kissel JT, Sansone VA, Shieh PB, Tawil RN, Trivedi J, Cannon SC, Griggs RC. Statland JM, et al. Muscle Nerve. 2018 Apr;57(4):522-530. doi: 10.1002/mus.26009. Epub 2017 Nov 29. Muscle Nerve. 2018. PMID: 29125635 Free PMC article. Review.
ACG Clinical Guideline: Hereditary Hemochromatosis.
Kowdley KV, Brown KE, Ahn J, Sundaram V. Kowdley KV, et al. Am J Gastroenterol. 2019 Aug;114(8):1202-1218. doi: 10.14309/ajg.0000000000000315. Am J Gastroenterol. 2019. PMID: 31335359 Review.
Diagnosis and management of hereditary haemochromatosis.
Murphree CR, Nguyen NN, Raghunathan V, Olson SR, DeLoughery T, Shatzel JJ. Murphree CR, et al. Vox Sang. 2020 May;115(4):255-262. doi: 10.1111/vox.12896. Epub 2020 Feb 20. Vox Sang. 2020. PMID: 32080859 Review.
Hereditary hemochromatosis.
Pietrangelo A. Pietrangelo A. Biochim Biophys Acta. 2006 Jul;1763(7):700-10. doi: 10.1016/j.bbamcr.2006.05.013. Epub 2006 May 27. Biochim Biophys Acta. 2006. PMID: 16891003 Free article. Review.
Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment.
Whyte MP. Whyte MP. Nat Rev Endocrinol. 2016 Apr;12(4):233-46. doi: 10.1038/nrendo.2016.14. Epub 2016 Feb 19. Nat Rev Endocrinol. 2016. PMID: 26893260 Review.
Hypophosphatasia is the inborn error of metabolism characterized by low serum alkaline phosphatase activity (hypophosphatasaemia). ...
Hypophosphatasia is the inborn error of metabolism characterized by low serum alkaline phosphatase activity (hypophosphatasaem …
3,212 results