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 Custom Filters

Edit custom filters

Results by year

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

Year Number of Results
1797 1
1799 1
1802 1
1806 1
1811 1
1835 1
1846 1
1847 2
1853 1
1858 1
1861 1
1865 2
1867 1
1869 2
1870 1
1875 1
1877 1
1878 1
1881 1
1882 2
1885 4
1886 1
1887 1
1889 1
1890 3
1892 2
1894 3
1895 1
1896 1
1898 2
1899 1
1900 2
1901 4
1902 2
1903 2
1905 1
1907 3
1908 2
1909 2
1910 1
1911 2
1912 4
1914 6
1915 3
1916 1
1917 5
1920 4
1921 3
1922 2
1923 3
1924 6
1925 4
1926 4
1927 12
1928 5
1929 2
1930 8
1931 5
1932 6
1933 7
1934 4
1935 4
1936 9
1937 4
1938 5
1939 1
1940 4
1941 4
1942 3
1943 3
1944 5
1945 9
1946 18
1947 63
1948 65
1949 56
1950 82
1951 117
1952 80
1953 168
1954 103
1955 115
1956 125
1957 139
1958 136
1959 82
1960 40
1961 54
1962 26
1963 74
1964 106
1965 145
1966 270
1967 364
1968 379
1969 358
1970 438
1971 406
1972 406
1973 496
1974 404
1975 635
1976 761
1977 704
1978 748
1979 886
1980 1069
1981 1135
1982 1263
1983 1438
1984 1809
1985 2070
1986 2028
1987 2305
1988 2732
1989 3062
1990 3221
1991 3362
1992 3567
1993 3973
1994 4088
1995 4051
1996 4671
1997 5073
1998 5440
1999 5878
2000 6852
2001 7420
2002 8376
2003 9078
2004 10461
2005 11871
2006 13003
2007 14739
2008 16006
2009 16971
2010 18789
2011 20285
2012 22560
2013 24610
2014 26881
2015 28154
2016 29097
2017 30019
2018 31160
2019 32995
2020 39246
2021 43156
2022 41947
2023 39474
2024 41077
2025 46025
2026 27099
2027 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

649,456 results

Results by year

Filters applied: . Clear all
The following terms were not found in PubMed: Anthocyanins+Extraction+Mulberry, marc+Pathological+Type
Page 1
Wolfram Syndrome: Diagnosis, Management, and Treatment.
Urano F. Urano F. Curr Diab Rep. 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6. Curr Diab Rep. 2016. PMID: 26742931 Free PMC article. Review.
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus, optic nerve atrophy, hearing loss, and neurodegeneration. ...
Wolfram syndrome is a rare genetic disorder characterized by juvenile-onset diabetes mellitus, diabetes insipidus …
Diabetes insipidus in infants and children.
Dabrowski E, Kadakia R, Zimmerman D. Dabrowski E, et al. Best Pract Res Clin Endocrinol Metab. 2016 Mar;30(2):317-28. doi: 10.1016/j.beem.2016.02.006. Epub 2016 Feb 27. Best Pract Res Clin Endocrinol Metab. 2016. PMID: 27156767 Review.
Diabetes insipidus, the inability to concentrate urine resulting in polyuria and polydipsia, can have different manifestations and management considerations in infants and children compared to adults. Central diabetes insipidus, secondary to lack of va …
Diabetes insipidus, the inability to concentrate urine resulting in polyuria and polydipsia, can have different manifestations …
[Association between central diabetes insipidus and type 2 diabetes mellitus].
Palumbo C, Nicolaci N, La Manna AA, Branek N, Pissano MN. Palumbo C, et al. Medicina (B Aires). 2018;78(2):127-130. Medicina (B Aires). 2018. PMID: 29659364 Free article. Spanish.
Central diabetes insipidus is a rare disease of the hypothalamus and neurohypophysis. It is very unusually found in the adult with type 2 diabetes mellitus. ...The case of a 72-year-old male with type 2 diabetes mellitus wit …
Central diabetes insipidus is a rare disease of the hypothalamus and neurohypophysis. It is very unusually found in the adult …
Diabetes or endocrinopathy admitted in the COVID-19 ward.
Clotman K, Twickler MB. Clotman K, et al. Eur J Clin Invest. 2020 Jul;50(7):e13262. doi: 10.1111/eci.13262. Epub 2020 May 24. Eur J Clin Invest. 2020. PMID: 32383239 Free PMC article.
The last weeks we built experience and gathered knowledge while giving hospital care to patients who had a pre-existent endocrine disease (and diabetes; most patients suffered from a type two diabetes). In our contribution we presented our insights obtained from thi …
The last weeks we built experience and gathered knowledge while giving hospital care to patients who had a pre-existent endocrine disease (a …
Monogenic diabetes syndromes: Locus-specific databases for Alstrom, Wolfram, and Thiamine-responsive megaloblastic anemia.
Astuti D, Sabir A, Fulton P, Zatyka M, Williams D, Hardy C, Milan G, Favaretto F, Yu-Wai-Man P, Rohayem J, López de Heredia M, Hershey T, Tranebjaerg L, Chen JH, Chaussenot A, Nunes V, Marshall B, McAfferty S, Tillmann V, Maffei P, Paquis-Flucklinger V, Geberhiwot T, Mlynarski W, Parkinson K, Picard V, Bueno GE, Dias R, Arnold A, Richens C, Paisey R, Urano F, Semple R, Sinnott R, Barrett TG. Astuti D, et al. Hum Mutat. 2017 Jul;38(7):764-777. doi: 10.1002/humu.23233. Epub 2017 Jun 1. Hum Mutat. 2017. PMID: 28432734 Free PMC article.
We developed a variant database for diabetes syndrome genes, using the Leiden Open Variation Database platform, containing observed phenotypes matched to the genetic variations. ...The development of the database as a repository for monogenic diabetes gene variants …
We developed a variant database for diabetes syndrome genes, using the Leiden Open Variation Database platform, containing observed p …
Arginine vasopressin deficiency: diagnosis, management and the relevance of oxytocin deficiency.
Atila C, Refardt J, Christ-Crain M. Atila C, et al. Nat Rev Endocrinol. 2024 Aug;20(8):487-500. doi: 10.1038/s41574-024-00985-x. Epub 2024 May 1. Nat Rev Endocrinol. 2024. PMID: 38693275 Review.
Polyuria-polydipsia syndrome can be caused by central diabetes insipidus, nephrogenic diabetes insipidus or primary polydipsia. To avoid confusion with diabetes mellitus, the name 'central diabetes insipidus' was changed in …
Polyuria-polydipsia syndrome can be caused by central diabetes insipidus, nephrogenic diabetes insipidus or prim …
Delineating Wolfram-like syndrome: A systematic review and discussion of the WFS1-associated disease spectrum.
de Muijnck C, Brink JBT, Bergen AA, Boon CJF, van Genderen MM. de Muijnck C, et al. Surv Ophthalmol. 2023 Jul-Aug;68(4):641-654. doi: 10.1016/j.survophthal.2023.01.012. Epub 2023 Feb 9. Surv Ophthalmol. 2023. PMID: 36764396 Free article.
The most common phenotype consisted of the combination of optic atrophy (87%) and hearing impairment (94%). Diabetes mellitus was seen in 44% of the patients. Nineteen percent developed cataract. Patients with missense mutations in WFS1 had a lower number of clinica …
The most common phenotype consisted of the combination of optic atrophy (87%) and hearing impairment (94%). Diabetes mellitus …
New developments and concepts in the diagnosis and management of diabetes insipidus (AVP-deficiency and resistance).
Angelousi A, Alexandraki KI, Mytareli C, Grossman AB, Kaltsas G. Angelousi A, et al. J Neuroendocrinol. 2023 Jan;35(1):e13233. doi: 10.1111/jne.13233. Epub 2023 Jan 22. J Neuroendocrinol. 2023. PMID: 36683321 Review.
Diabetes insipidus (DI) is a disorder characterised by the excretion of large amounts of hypotonic urine, with a prevalence of 1 per 25,000 population. ...Although the pathogenesis of NDI is unclear, more than 280 disease-causing mutations affecting the AVP2 protein …
Diabetes insipidus (DI) is a disorder characterised by the excretion of large amounts of hypotonic urine, with a prevalence of …
The genetic and clinical characteristics of WFS1 related diabetes in Chinese early onset type 2 diabetes.
Li Y, Gong S, Li M, Cai X, Liu W, Zhang S, Ma Y, Luo Y, Zhou L, Zhang X, Huang X, Gao X, Hu M, Li Y, Ren Q, Wang Y, Zhou X, Han X, Ji L. Li Y, et al. Sci Rep. 2023 Jun 5;13(1):9127. doi: 10.1038/s41598-023-36334-7. Sci Rep. 2023. PMID: 37277527 Free PMC article.
We aimed to explore the prevalence of WFS1-related diabetes (WFS1-DM) and its clinical characteristics in a Chinese population with early-onset type 2 diabetes (EOD). ...WFS1-DM is usually mistakenly diagnosed as type 2 diabetes, and genetic tes …
We aimed to explore the prevalence of WFS1-related diabetes (WFS1-DM) and its clinical characteristics in a Chinese population with e …
Diabetes insipidus.
Verbalis JG. Verbalis JG. Rev Endocr Metab Disord. 2003 May;4(2):177-85. doi: 10.1023/a:1022946220908. Rev Endocr Metab Disord. 2003. PMID: 12766546 Review. No abstract available.
649,456 results
You have reached the last available page of results. Please see the User Guide for more information.