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

Year Number of Results
1965 2
1968 2
1969 2
1970 6
1971 1
1972 2
1973 2
1974 5
1975 1
1976 3
1977 3
1978 4
1979 4
1980 1
1981 3
1982 2
1983 4
1984 6
1985 3
1986 2
1987 4
1988 7
1989 4
1990 2
1991 5
1992 4
1993 5
1994 3
1995 9
1996 5
1997 13
1998 7
1999 8
2000 8
2001 1
2002 9
2003 4
2004 6
2005 9
2006 6
2007 4
2008 6
2009 5
2010 4
2011 5
2012 2
2013 5
2014 3
2016 1
2017 3
2018 1
2020 5
2021 1
2024 0

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217 results

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Page 1
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.
van Trotsenburg P, Stoupa A, Léger J, Rohrer T, Peters C, Fugazzola L, Cassio A, Heinrichs C, Beauloye V, Pohlenz J, Rodien P, Coutant R, Szinnai G, Murray P, Bartés B, Luton D, Salerno M, de Sanctis L, Vigone M, Krude H, Persani L, Polak M. van Trotsenburg P, et al. Among authors: pohlenz j. Thyroid. 2021 Mar;31(3):387-419. doi: 10.1089/thy.2020.0333. Thyroid. 2021. PMID: 33272083 Free PMC article. Review.
Serotypes of bovine astrovirus.
Woode GN, Gourley NE, Pohlenz JF, Liebler EM, Mathews SL, Hutchinson MP. Woode GN, et al. Among authors: pohlenz jf. J Clin Microbiol. 1985 Oct;22(4):668-70. doi: 10.1128/jcm.22.4.668-670.1985. J Clin Microbiol. 1985. PMID: 3935665 Free PMC article.
Clinical features of pediatric Graves' orbitopathy.
Eha J, Pitz S, Pohlenz J. Eha J, et al. Among authors: pohlenz j. Int Ophthalmol. 2010 Dec;30(6):717-21. doi: 10.1007/s10792-010-9351-6. Epub 2010 Feb 27. Int Ophthalmol. 2010. PMID: 20191374
Familial Central Hypothyroidism Caused by a Novel IGSF1 Gene Mutation.
Tenenbaum-Rakover Y, Turgeon MO, London S, Hermanns P, Pohlenz J, Bernard DJ, Bercovich D. Tenenbaum-Rakover Y, et al. Among authors: pohlenz j. Thyroid. 2016 Dec;26(12):1693-1700. doi: 10.1089/thy.2015.0672. Epub 2016 Jul 25. Thyroid. 2016. PMID: 27310681
217 results