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

Year Number of Results
1952 1
1953 1
1962 1
1966 4
1967 6
1968 3
1969 1
1970 2
1971 1
1972 6
1973 17
1974 6
1975 25
1976 9
1977 15
1978 10
1979 17
1980 14
1981 5
1982 12
1983 3
1984 12
1985 7
1986 10
1987 11
1988 6
1989 10
1990 8
1991 11
1992 7
1993 13
1994 11
1995 16
1996 13
1997 16
1998 18
1999 9
2000 14
2001 21
2002 12
2003 17
2004 18
2005 15
2006 17
2007 18
2008 14
2009 33
2010 17
2011 27
2012 26
2013 37
2014 28
2015 32
2016 39
2017 31
2018 37
2019 39
2020 43
2021 36
2022 31
2023 30
2024 42

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Search Results

908 results

Results by year

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Page 1
Classification and pharmacology of progestins.
Schindler AE, Campagnoli C, Druckmann R, Huber J, Pasqualini JR, Schweppe KW, Thijssen JH. Schindler AE, et al. Maturitas. 2003 Dec 10;46 Suppl 1:S7-S16. doi: 10.1016/j.maturitas.2003.09.014. Maturitas. 2003. PMID: 14670641 Review.
Endometriosis--a European perspective.
Schindler AE, Druckmann R. Schindler AE, et al. Gynecol Endocrinol. 2009 Nov;25(11):693. doi: 10.3109/09513590903230143. Gynecol Endocrinol. 2009. PMID: 19903046 Free article. No abstract available.
Dydrogesterone--a unique progestogen.
Schindler AE. Schindler AE. Maturitas. 2009 Dec;65 Suppl 1:S1. doi: 10.1016/j.maturitas.2009.09.002. Epub 2009 Sep 24. Maturitas. 2009. PMID: 19781875 No abstract available.
Autosomal Dominant TRPV4 Disorders.
McCray BA, Schindler A, Hoover-Fong JE, Sumner CJ. McCray BA, et al. Among authors: schindler a. 2014 May 15 [updated 2020 Sep 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2014 May 15 [updated 2020 Sep 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24830047 Free Books & Documents. Review.
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Diarra S, Ghosh S, Cissé L, Coulibaly T, Yalcouyé A, Harmison G, Diallo S, Diallo SH, Coulibaly O, Schindler A, Cissé CAK, Maiga AB, Bamba S, Samassekou O, Khokha MK, Mis EK, Lakhani SA, Donovan FX, Jacobson S, Blackstone C, Guinto CO, Landouré G, Bonifacino JS, Fischbeck KH, Grunseich C. Diarra S, et al. Among authors: schindler a. Neurobiol Dis. 2024 Aug;198:106537. doi: 10.1016/j.nbd.2024.106537. Epub 2024 May 19. Neurobiol Dis. 2024. PMID: 38772452 Free article.
A review of genetic counseling for Charcot Marie Tooth disease (CMT).
Siskind CE, Panchal S, Smith CO, Feely SM, Dalton JC, Schindler AB, Krajewski KM. Siskind CE, et al. Among authors: schindler ab. J Genet Couns. 2013 Aug;22(4):422-36. doi: 10.1007/s10897-013-9584-4. Epub 2013 Apr 21. J Genet Couns. 2013. PMID: 23604902 Review.
Childhood obesity.
Schindler AM. Schindler AM. J Pediatr. 1984 Jun;104(6):959-60. doi: 10.1016/s0022-3476(84)80516-8. J Pediatr. 1984. PMID: 6726536 No abstract available.
908 results