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

Year Number of Results
1962 1
1963 1
1965 1
1966 2
1967 2
1968 1
1969 5
1970 2
1971 7
1972 1
1973 3
1974 3
1975 2
1976 3
1977 5
1978 2
1979 2
1980 1
1981 1
1982 2
1984 5
1985 1
1988 2
1989 1
1990 1
1992 1
1993 1
1994 5
1995 3
1996 3
1997 1
1999 1
2000 3
2002 1
2011 1
2012 2
2013 1
2014 1
2015 2
2022 1
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Search Results

83 results
Results by year
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Page 1
Oculodentodigital dysplasia.
Reisner SH, Kott E, Bornstein B, Salinger H, Kaplan I, Gorlin RJ. Reisner SH, et al. Among authors: kott e. Am J Dis Child. 1969 Oct;118(4):600-7. doi: 10.1001/archpedi.1969.02100040602013. Am J Dis Child. 1969. PMID: 5820606 No abstract available.
[Post-shock optic neuropathy].
Kesler A, Telman G, Kotas-Neuman R, Kott E. Kesler A, et al. Among authors: kott e. Harefuah. 1996 Nov 1;131(9):305-7, 374. Harefuah. 1996. PMID: 8981796 Hebrew.
Oncocytoma of kidney.
Akhtar M, Kott E. Akhtar M, et al. Among authors: kott e. Urology. 1979 Oct;14(4):397-400. doi: 10.1016/0090-4295(79)90091-8. Urology. 1979. PMID: 494472
[Septic cavernous sinus thrombosis].
Avraham S, Berco E, Sinnreich Z, Kott E, Ophir D. Avraham S, et al. Among authors: kott e. Harefuah. 1992 Mar 15;122(6):369-71, 406. Harefuah. 1992. PMID: 1582628 Hebrew.
Excretion of dopa metabolites.
Kott E, Bornstein B, Eichhorn F. Kott E, et al. N Engl J Med. 1971 Feb 18;284(7):395. doi: 10.1056/nejm197102182840725. N Engl J Med. 1971. PMID: 5539935 No abstract available.
Idiopathic intracranial hypertension and anticardiolipin antibodies.
Kesler A, Ellis MH, Reshef T, Kott E, Gadoth N. Kesler A, et al. Among authors: kott e. J Neurol Neurosurg Psychiatry. 2000 Mar;68(3):379-80. doi: 10.1136/jnnp.68.3.379. J Neurol Neurosurg Psychiatry. 2000. PMID: 10675226 Free PMC article.
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.
Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek AM, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S. Kott E, et al. Am J Hum Genet. 2013 Sep 5;93(3):561-70. doi: 10.1016/j.ajhg.2013.07.013. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993197 Free PMC article.
Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia.
Blanchon S, Legendre M, Copin B, Duquesnoy P, Montantin G, Kott E, Dastot F, Jeanson L, Cachanado M, Rousseau A, Papon JF, Beydon N, Brouard J, Crestani B, Deschildre A, Désir J, Dollfus H, Leheup B, Tamalet A, Thumerelle C, Vojtek AM, Escalier D, Coste A, de Blic J, Clément A, Escudier E, Amselem S. Blanchon S, et al. Among authors: kott e. J Med Genet. 2012 Jun;49(6):410-6. doi: 10.1136/jmedgenet-2012-100867. J Med Genet. 2012. PMID: 22693285
83 results