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Results by year

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

Year Number of Results
1947 1
1948 1
1949 2
1951 1
1953 2
1954 2
1955 5
1957 2
1958 5
1959 9
1960 5
1961 3
1962 1
1963 5
1964 1
1965 3
1967 2
1968 1
1969 2
1970 3
1971 1
1972 2
1973 2
1974 5
1975 2
1976 3
1977 11
1978 6
1979 6
1980 1
1981 3
1982 1
1983 4
1984 4
1985 4
1987 3
1988 1
1989 4
1990 5
1991 1
1992 7
1993 8
1994 3
1995 6
1996 9
1997 10
1998 4
1999 15
2000 6
2001 5
2002 14
2003 12
2004 20
2005 12
2006 17
2007 28
2008 22
2009 20
2010 16
2011 14
2012 9
2013 15
2014 17
2015 18
2016 18
2017 9
2018 17
2019 9
2020 10
2021 16
2022 15
2023 9

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494 results

Results by year

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Page 1
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.
Oza AM, DiStefano MT, Hemphill SE, Cushman BJ, Grant AR, Siegert RK, Shen J, Chapin A, Boczek NJ, Schimmenti LA, Murry JB, Hasadsri L, Nara K, Kenna M, Booth KT, Azaiez H, Griffith A, Avraham KB, Kremer H, Rehm HL, Amr SS, Abou Tayoun AN; ClinGen Hearing Loss Clinical Domain Working Group. Oza AM, et al. Among authors: kremer h. Hum Mutat. 2018 Nov;39(11):1593-1613. doi: 10.1002/humu.23630. Hum Mutat. 2018. PMID: 30311386 Free PMC article.
Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations.
Dulla K, Slijkerman R, van Diepen HC, Albert S, Dona M, Beumer W, Turunen JJ, Chan HL, Schulkens IA, Vorthoren L, den Besten C, Buil L, Schmidt I, Miao J, Venselaar H, Zang J, Neuhauss SCF, Peters T, Broekman S, Pennings R, Kremer H, Platenburg G, Adamson P, de Vrieze E, van Wijk E. Dulla K, et al. Among authors: kremer h. Mol Ther. 2021 Aug 4;29(8):2441-2455. doi: 10.1016/j.ymthe.2021.04.024. Epub 2021 Apr 23. Mol Ther. 2021. PMID: 33895329 Free PMC article.
Genetics of Hearing Impairment.
Kremer H, Del Castillo I. Kremer H, et al. Genes (Basel). 2022 May 11;13(5):852. doi: 10.3390/genes13050852. Genes (Basel). 2022. PMID: 35627237 Free PMC article.
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Brandsma R, Verschuuren-Bemelmans CC, Amrom D, Barisic N, Baxter P, Bertini E, Blumkin L, Brankovic-Sreckovic V, Brouwer OF, Bürk K, Catsman-Berrevoets CE, Craiu D, de Coo IFM, Gburek J, Kennedy C, de Koning TJ, Kremer HPH, Kumar R, Macaya A, Micalizzi A, Mirabelli-Badenier M, Nemeth A, Nuovo S, Poll-The B, Lerman-Sagie T, Steinlin M, Synofzik M, Tijssen MAJ, Vasco G, Willemsen MAAP, Zanni G, Valente EM, Boltshauser E, Sival DA. Brandsma R, et al. Among authors: kremer hph. Eur J Paediatr Neurol. 2019 Sep;23(5):692-706. doi: 10.1016/j.ejpn.2019.08.004. Epub 2019 Aug 10. Eur J Paediatr Neurol. 2019. PMID: 31481303 Review.
Reviewing the genetic causes of spastic-ataxias.
de Bot ST, Willemsen MA, Vermeer S, Kremer HP, van de Warrenburg BP. de Bot ST, et al. Among authors: kremer hp. Neurology. 2012 Oct 2;79(14):1507-14. doi: 10.1212/WNL.0b013e31826d5fb0. Neurology. 2012. PMID: 23033504 Review.
Spermatogenesis of Drosophila hydei.
Hennig W, Kremer H. Hennig W, et al. Among authors: kremer h. Int Rev Cytol. 1990;123:129-75. doi: 10.1016/s0074-7696(08)60673-7. Int Rev Cytol. 1990. PMID: 2289847 Review. No abstract available.
A Medical Mystery.
Kremer H. Kremer H. N Engl J Med. 1997 Mar 20;336(12):846. doi: 10.1056/NEJM199703203361206. N Engl J Med. 1997. PMID: 9062094 Free article. No abstract available.
Listening to bluetooth beacons for epidemic risk mitigation.
Barthe G, Viti R, Druschel P, Garg D, Gomez-Rodriguez M, Ingo P, Kremer H, Lentz M, Lorch L, Mehta A, Schölkopf B. Barthe G, et al. Among authors: kremer h. Sci Rep. 2022 Apr 1;12(1):5558. doi: 10.1038/s41598-022-09440-1. Sci Rep. 2022. PMID: 35365709 Free PMC article.
494 results