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

Year Number of Results
1809 2
1818 1
1826 1
1828 2
1839 1
1848 2
1850 1
1852 2
1857 1
1858 2
1860 1
1861 2
1863 3
1866 1
1867 3
1870 2
1872 1
1873 1
1875 3
1876 3
1877 1
1878 1
1880 1
1882 2
1884 3
1885 4
1886 1
1887 1
1889 1
1890 1
1891 2
1894 1
1896 2
1897 7
1898 7
1899 2
1900 1
1901 1
1902 3
1905 3
1906 1
1907 4
1908 6
1909 4
1910 2
1911 4
1912 8
1913 2
1914 1
1915 7
1916 5
1917 8
1918 7
1919 7
1920 3
1921 2
1922 2
1923 3
1924 4
1925 4
1926 6
1927 18
1928 4
1929 7
1930 6
1931 7
1932 6
1933 7
1934 6
1935 10
1936 4
1937 4
1938 8
1939 7
1940 3
1941 3
1942 5
1944 6
1945 33
1946 84
1947 100
1948 152
1949 130
1950 188
1951 220
1952 213
1953 212
1954 181
1955 206
1956 208
1957 224
1958 196
1959 216
1960 234
1961 264
1962 315
1963 461
1964 597
1965 440
1966 342
1967 423
1968 515
1969 514
1970 447
1971 544
1972 502
1973 511
1974 523
1975 687
1976 722
1977 724
1978 717
1979 740
1980 713
1981 773
1982 782
1983 879
1984 818
1985 874
1986 835
1987 925
1988 976
1989 1146
1990 1149
1991 1078
1992 1233
1993 1359
1994 1341
1995 1572
1996 1604
1997 1631
1998 1940
1999 2010
2000 2148
2001 2133
2002 2087
2003 2172
2004 2303
2005 2395
2006 2625
2007 2570
2008 2724
2009 2731
2010 3018
2011 3244
2012 3517
2013 3785
2014 4040
2015 4157
2016 4202
2017 4153
2018 4433
2019 4749
2020 3778
2021 3
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Search Results

97,051 results
Results by year
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Page 1
Inherited hemolytic anemia: a possessive beginner's guide.
Mohandas N. Mohandas N. Hematology Am Soc Hematol Educ Program. 2018 Nov 30;2018(1):377-381. doi: 10.1182/asheducation-2018.1.377. Hematology Am Soc Hematol Educ Program. 2018. PMID: 30504335 Free PMC article. Review.
Membrane structural defects lead to hereditary spherocytosis (HS) and hereditary elliptocytosis (HE), whereas altered membrane transport function accounts for hereditary xerocytosis (HX) and hereditary overhydrated stomatocytosis (OHS). ...
Membrane structural defects lead to hereditary spherocytosis (HS) and hereditary elliptocytosis (HE), whereas altered membrane …
Hereditary Hemorrhagic Telangiectasia.
Kühnel T, Wirsching K, Wohlgemuth W, Chavan A, Evert K, Vielsmeier V. Kühnel T, et al. Otolaryngol Clin North Am. 2018 Feb;51(1):237-254. doi: 10.1016/j.otc.2017.09.017. Otolaryngol Clin North Am. 2018. PMID: 29217066 Review.
Hereditary hemorrhagic telangiectasia (HHT) describes the presenting manifestations of a disorder that is characterized by pathologic blood vessels. ...
Hereditary hemorrhagic telangiectasia (HHT) describes the presenting manifestations of a disorder that is characterized by pathologic
Red cell membrane disorders.
Narla J, Mohandas N. Narla J, et al. Int J Lab Hematol. 2017 May;39 Suppl 1:47-52. doi: 10.1111/ijlh.12657. Int J Lab Hematol. 2017. PMID: 28447420 Review.
The current review summarizes these advances as they relate to defining the molecular and structural basis for disorders involving altered membrane structural organization (hereditary spherocytosis [HS] and hereditary elliptocytosis [HE]) and altered membrane transp …
The current review summarizes these advances as they relate to defining the molecular and structural basis for disorders involving altered m …
Hereditary hemorrhagic telangiectasia: diagnosis and management from the hematologist's perspective.
Kritharis A, Al-Samkari H, Kuter DJ. Kritharis A, et al. Haematologica. 2018 Sep;103(9):1433-1443. doi: 10.3324/haematol.2018.193003. Epub 2018 May 24. Haematologica. 2018. PMID: 29794143 Free PMC article. Review.
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes abnormal blood vessel formation. The diagnosis of hereditary hemorrhagic telangiectasia is clinical, based on the Curaçao criteria. G
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes
Advances in understanding the pathogenesis of red cell membrane disorders.
Iolascon A, Andolfo I, Russo R. Iolascon A, et al. Br J Haematol. 2019 Oct;187(1):13-24. doi: 10.1111/bjh.16126. Epub 2019 Jul 31. Br J Haematol. 2019. PMID: 31364155 Review.
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmembrane or cytoskeletal proteins of red blood cells. ...Red blood cell membrane defects encompass a heterogeneous group of haemolytic anaemias caused by either (i) altered mem
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmembrane or cytoskeletal proteins of
Hereditary Hemorrhagic Telangiectasia.
Schotland H, Denstaedt S. Schotland H, et al. N Engl J Med. 2019 Dec 26;381(26):2552. doi: 10.1056/NEJMicm1905896. N Engl J Med. 2019. PMID: 31881140 No abstract available.
Major hereditary gastrointestinal cancer syndromes: a narrative review.
Chintalacheruvu LM, Shaw T, Buddam A, Diab O, Kassim T, Mukherjee S, Lynch HT. Chintalacheruvu LM, et al. J Gastrointestin Liver Dis. 2017 Jun;26(2):157-163. doi: 10.15403/jgld.2014.1121.262.maj. J Gastrointestin Liver Dis. 2017. PMID: 28617886 Free article. Review.
Hereditary gastrointestinal cancer syndromes constitute about 5-10% of all cancers. About 20-25% of undiagnosed cases have a possible hereditary component, which is not yet established. ...In this review, we describe clinical manifestations, genetic testing and its
Hereditary gastrointestinal cancer syndromes constitute about 5-10% of all cancers. About 20-25% of undiagnosed cases have a possible
Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu syndrome).
Santos MA. Santos MA. J Gen Intern Med. 2017 Feb;32(2):218-219. doi: 10.1007/s11606-016-3870-4. Epub 2016 Oct 6. J Gen Intern Med. 2017. PMID: 27714648 Free PMC article. No abstract available.
Hereditary cancer syndromes, their testing and prevention.
Foretová L. Foretová L. Cas Lek Cesk. 2019 Spring;158(1):15-21. Cas Lek Cesk. 2019. PMID: 31046387 English.
So far, we know more than 200 hereditary cancer syndromes. The most frequently tested are hereditary breast and ovarian cancer syndrome, hereditary nonpolyposis colorectal cancer (Lynch syndrome), quite frequent are also hereditary gastrointestinal pol …
So far, we know more than 200 hereditary cancer syndromes. The most frequently tested are hereditary breast and ovarian cancer …
Hereditary optic neuropathies.
Newman NJ, Biousse V. Newman NJ, et al. Eye (Lond). 2004 Nov;18(11):1144-60. doi: 10.1038/sj.eye.6701591. Eye (Lond). 2004. PMID: 15534600 Free article. Review.
AIMS: To provide a clinical update on the hereditary optic neuropathies. METHODS: Review of the literature. RESULTS: The hereditary optic neuropathies comprise a group of disorders in which the cause of optic nerve dysfunction appears to be hereditable, based on fam …
AIMS: To provide a clinical update on the hereditary optic neuropathies. METHODS: Review of the literature. RESULTS: The hereditar
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