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Results by year

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

Year Number of Results
1967 1
1970 6
1971 2
1972 5
1973 6
1974 5
1975 4
1976 1
1977 5
1978 5
1979 5
1980 1
1981 1
1982 4
1983 3
1984 2
1985 5
1986 2
1987 5
1989 5
1990 5
1991 2
1992 8
1993 2
1994 1
1995 2
1996 5
1997 3
1998 4
1999 4
2000 3
2001 2
2002 7
2003 2
2004 3
2005 4
2006 8
2007 7
2008 6
2009 5
2010 2
2011 3
2013 2
2014 3
2015 4
2016 1
2020 1
2022 1
2023 1
2024 0

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164 results

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Page 1
[Microdeletion syndromes].
Seemanová E. Seemanová E. Cas Lek Cesk. 2002 Jun 21;141(12):363-70. Cas Lek Cesk. 2002. PMID: 12238021 Czech.
The Neu-Laxova syndrome.
Seemanová E, Rudolf R. Seemanová E, et al. Am J Med Genet. 1985 Jan;20(1):13-5. doi: 10.1002/ajmg.1320200103. Am J Med Genet. 1985. PMID: 3970065 No abstract available.
[Homocystinuria].
Hyánek J, Kavka J, Seemanová E, Laufbergerová J, Dvorak J, Huslarová A, Hermanská Z, Kopejtková H, Hádek J. Hyánek J, et al. Among authors: seemanova e. Cesk Pediatr. 1972 Aug;27(8):394-6. Cesk Pediatr. 1972. PMID: 5051737 Czech. No abstract available.
[Hyperphenylalaninemia].
Hyánek J, Seemanová E, Sádlová I, Mrastíková H, Wünschová N, Hoza J, Zelingerová J. Hyánek J, et al. Among authors: seemanova e. Cas Lek Cesk. 1971;110(15):337-41. Cas Lek Cesk. 1971. PMID: 5554915 Czech. No abstract available.
[The Zimmermann-Laband syndrome].
Pfeiffer RA, Seemanova E, Süss J, Müssig D, Tietze HU. Pfeiffer RA, et al. Among authors: seemanova e. Klin Padiatr. 1992 Jan-Feb;204(1):1-5. doi: 10.1055/s-2007-1025313. Klin Padiatr. 1992. PMID: 1740896 German.
[Mosaic phenotypes].
Seemanová E. Seemanová E. Cas Lek Cesk. 2002 Jul 19;141(14):439-44. Cas Lek Cesk. 2002. PMID: 12238251 Czech.
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects.
Kessler K, Wunderlich I, Uebe S, Falk NS, Gießl A, Brandstätter JH, Popp B, Klinger P, Ekici AB, Sticht H, Dörr HG, Reis A, Roepman R, Seemanová E, Thiel CT. Kessler K, et al. Among authors: seemanova e. Sci Rep. 2015 Jul 1;5:11649. doi: 10.1038/srep11649. Sci Rep. 2015. PMID: 26130459 Free PMC article.
Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy.
Van Maldergem L, Magré J, Khallouf TE, Gedde-Dahl T Jr, Delépine M, Trygstad O, Seemanova E, Stephenson T, Albott CS, Bonnici F, Panz VR, Medina JL, Bogalho P, Huet F, Savasta S, Verloes A, Robert JJ, Loret H, De Kerdanet M, Tubiana-Rufi N, Mégarbané A, Maassen J, Polak M, Lacombe D, Kahn CR, Silveira EL, D'Abronzo FH, Grigorescu F, Lathrop M, Capeau J, O'Rahilly S. Van Maldergem L, et al. Among authors: seemanova e. J Med Genet. 2002 Oct;39(10):722-33. doi: 10.1136/jmg.39.10.722. J Med Genet. 2002. PMID: 12362029 Free PMC article.
164 results