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

Year Number of Results
1806 1
1813 1
1818 2
1820 1
1825 1
1827 1
1828 1
1829 1
1830 1
1831 3
1832 1
1833 1
1835 3
1837 1
1838 1
1839 2
1840 2
1841 5
1842 3
1843 3
1844 5
1845 7
1846 7
1847 7
1848 1
1849 3
1850 2
1851 2
1852 2
1853 5
1854 3
1855 3
1856 7
1857 2
1858 7
1859 6
1860 2
1861 1
1862 4
1863 1
1864 2
1865 4
1866 2
1867 4
1868 6
1869 9
1870 3
1871 3
1872 4
1873 3
1874 6
1875 7
1876 6
1877 1
1878 9
1879 8
1880 4
1881 7
1882 8
1883 9
1884 13
1885 4
1886 7
1887 9
1888 13
1889 4
1890 10
1891 5
1892 12
1893 14
1894 12
1895 9
1896 13
1897 16
1898 11
1899 8
1900 5
1901 12
1902 10
1903 16
1904 15
1905 12
1906 11
1907 16
1908 22
1909 57
1910 40
1911 46
1912 47
1913 60
1914 49
1915 21
1916 24
1917 22
1918 20
1919 9
1920 29
1921 44
1922 28
1923 44
1924 41
1925 36
1926 53
1927 40
1928 49
1929 43
1930 58
1931 46
1932 49
1933 54
1934 47
1935 46
1936 31
1937 27
1938 44
1939 32
1940 31
1941 20
1942 17
1943 24
1944 29
1945 161
1946 466
1947 598
1948 690
1949 688
1950 968
1951 1147
1952 1209
1953 1462
1954 1986
1955 2066
1956 1750
1957 1483
1958 1970
1959 1494
1960 1283
1961 1501
1962 1875
1963 3204
1964 4186
1965 3027
1966 2364
1967 2621
1968 2959
1969 3168
1970 3213
1971 3629
1972 3452
1973 3225
1974 3574
1975 3787
1976 3660
1977 3714
1978 3618
1979 3726
1980 3645
1981 3708
1982 3823
1983 4105
1984 4372
1985 4550
1986 4425
1987 4519
1988 4891
1989 5155
1990 5485
1991 5300
1992 5468
1993 5797
1994 5535
1995 5430
1996 5813
1997 5907
1998 6471
1999 6932
2000 7564
2001 8287
2002 9163
2003 10016
2004 11035
2005 13059
2006 14541
2007 15625
2008 17213
2009 18609
2010 19984
2011 21873
2012 22997
2013 27027
2014 40988
2015 48876
2016 54840
2017 60560
2018 77817
2019 89433
2020 94135
2021 101992
2022 111955
2023 119585
2024 54829

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1,114,376 results

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Page 1
Introduction.
Ross SA. Ross SA. Semin Perinatol. 2018 Apr;42(3):147-148. doi: 10.1053/j.semperi.2018.02.001. Epub 2018 Mar 9. Semin Perinatol. 2018. PMID: 29526384 No abstract available.
Severe congenital neutropenia.
Welte K, Zeidler C, Dale DC. Welte K, et al. Semin Hematol. 2006 Jul;43(3):189-95. doi: 10.1053/j.seminhematol.2006.04.004. Semin Hematol. 2006. PMID: 16822461 Review.
Severe congenital neutropenia (CN) includes a variety of hematologic disorders characterized by severe neutropenia, with absolute neutrophil counts (ANC) below 0.5 x 10(9)/L, and associated with severe systemic bacterial infections from early infancy. ...CN w …
Severe congenital neutropenia (CN) includes a variety of hematologic disorders characterized by severe neutropenia, with absol …
Molecular genetics of congenital cataracts.
Li J, Chen X, Yan Y, Yao K. Li J, et al. Exp Eye Res. 2020 Feb;191:107872. doi: 10.1016/j.exer.2019.107872. Epub 2019 Nov 23. Exp Eye Res. 2020. PMID: 31770519 Review.
Congenital cataracts, the most common cause of visual impairment and blindness in children worldwide, have diverse etiologies. According to statistics analysis, about one quarter of congenital cataracts caused by genetic defects. Various mutations of more than one h …
Congenital cataracts, the most common cause of visual impairment and blindness in children worldwide, have diverse etiologies. Accord …
Severe congenital neutropenia.
Welte K, Zeidler C. Welte K, et al. Hematol Oncol Clin North Am. 2009 Apr;23(2):307-20. doi: 10.1016/j.hoc.2009.01.013. Hematol Oncol Clin North Am. 2009. PMID: 19327585
Congenital neutropenia (CN) is a genetically heterogeneous bone marrow failure syndrome characterized by a maturation arrest of myelopoiesis at the level of the promyelocyte/myelocyte stage with peripheral blood absolute neutrophil counts below 0.5 x 10(9)/L. From e …
Congenital neutropenia (CN) is a genetically heterogeneous bone marrow failure syndrome characterized by a maturation arrest o …
Congenital neutropenias.
Zeidler C, Schwinzer B, Welte K. Zeidler C, et al. Rev Clin Exp Hematol. 2003 Mar;7(1):72-83. Rev Clin Exp Hematol. 2003. PMID: 14692235 Review.
The term congenital neutropenia (CN) has been used for a group of hematologic disorders characterized by severe neutropenia with absolute neutrophil counts (ANC) below 0.5 x 10(9)/L associated with increased susceptibility to bacterial infections. ...Recent pathogen …
The term congenital neutropenia (CN) has been used for a group of hematologic disorders characterized by severe neutropenia wi …
[Congenital neuroblastomas].
Luis AL, Martínez L, Hernández F, Sastre A, García P, Queizán A, Tovar JA. Luis AL, et al. Cir Pediatr. 2004 Apr;17(2):89-92. Cir Pediatr. 2004. PMID: 15285592 Spanish.
BACKGROUND: We consider congenital neuroblastomas (CN) those detected in pregnancy or at the very first hours of life. ...RESULTS: Among the 107 neural tumors managed during this period (89 neuroblastomas, 18 ganglioneuromas), 8 were congenital neuroblastomas …
BACKGROUND: We consider congenital neuroblastomas (CN) those detected in pregnancy or at the very first hours of life. ...RESU …
Congenital neutropenia in the era of genomics: classification, diagnosis, and natural history.
Donadieu J, Beaupain B, Fenneteau O, Bellanné-Chantelot C. Donadieu J, et al. Br J Haematol. 2017 Nov;179(4):557-574. doi: 10.1111/bjh.14887. Epub 2017 Sep 6. Br J Haematol. 2017. PMID: 28875503 Free article. Review.
This review focuses on the classification, diagnosis and natural history of congenital neutropenia (CN). CN encompasses a number of genetic disorders with chronic neutropenia and, for some, affecting other organ systems, such as the pancreas, central nervous …
This review focuses on the classification, diagnosis and natural history of congenital neutropenia (CN). CN encompasses …
Congenital epulis.
Olson JL, Marcus JR, Zuker RM. Olson JL, et al. J Craniofac Surg. 2005 Jan;16(1):161-4. doi: 10.1097/00001665-200501000-00033. J Craniofac Surg. 2005. PMID: 15699667 Review.
Congenital epulis is a rare benign hamartoma of the alveolar ridge found in the newborn. The clinical characteristics of this lesion show some variability, and opinion of its pathogenesis lacks consensus. Congenital epulis can cause feeding or respiratory compromise …
Congenital epulis is a rare benign hamartoma of the alveolar ridge found in the newborn. The clinical characteristics of this lesion …
RUNX1 Mutations in the Leukemic Progression of Severe Congenital Neutropenia.
Olofsen PA, Touw IP. Olofsen PA, et al. Mol Cells. 2020 Feb 29;43(2):139-144. doi: 10.14348/molcells.2020.0010. Mol Cells. 2020. PMID: 32041395 Free PMC article. Review.
This mini-review focusses on the role of RUNX1 mutations as the most common secondary leukemogenic hit in MDS/AML evolving from severe congenital neutropenia (SCN)....
This mini-review focusses on the role of RUNX1 mutations as the most common secondary leukemogenic hit in MDS/AML evolving from severe co …
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