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

Year Number of Results
1959 1
1962 1
1964 2
1965 1
1967 1
1968 1
1973 1
1975 2
1977 2
1984 4
1986 1
1987 2
1988 4
1989 5
1990 2
1991 9
1992 6
1993 11
1994 5
1995 17
1996 7
1997 8
1998 4
1999 6
2000 3
2001 2
2002 5
2003 6
2004 10
2005 11
2006 6
2007 6
2008 1
2009 4
2010 8
2011 1
2012 2
2013 3
2014 6
2015 4
2016 2
2017 3
2018 6
2019 8
2020 1
2021 3
2022 1
2023 2
2024 0

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Search Results

198 results

Results by year

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Page 1
Facioscapulohumeral muscular dystrophy.
Padberg GW, van Engelen BG. Padberg GW, et al. Curr Opin Neurol. 2009 Oct;22(5):539-42. doi: 10.1097/WCO.0b013e328330a572. Curr Opin Neurol. 2009. PMID: 19724227 Review.
Facioscapulohumeral muscular dystrophy.
van der Maarel SM, Frants RR, Padberg GW. van der Maarel SM, et al. Among authors: padberg gw. Biochim Biophys Acta. 2007 Feb;1772(2):186-94. doi: 10.1016/j.bbadis.2006.05.009. Epub 2006 Jun 6. Biochim Biophys Acta. 2007. PMID: 16837171 Free article. Review.
[Facioscapulohumeral muscular dystrophy].
Wilbers J, Frants RR, van Engelen BG, Padberg GW, van der Maarel SM. Wilbers J, et al. Among authors: padberg gw. Ned Tijdschr Tandheelkd. 2010 Jan;117(1):11-4. Ned Tijdschr Tandheelkd. 2010. PMID: 20180344 Free article. Review. Dutch.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: padberg gw. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
Chorea and polycythaemia.
Bruyn GW, Padberg G. Bruyn GW, et al. Among authors: padberg g. Eur Neurol. 1984;23(1):26-33. doi: 10.1159/000115674. Eur Neurol. 1984. PMID: 6370700 Review.
Molecular genetics of facioscapulohumeral muscular dystrophy.
Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ. Wijmenga C, et al. Among authors: padberg gw. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):487-91. doi: 10.1016/0960-8966(93)90102-p. Neuromuscul Disord. 1993. PMID: 8186699 Review.
Ophthalmological findings in facioscapulohumeral dystrophy.
Goselink RJM, Schreur V, van Kernebeek CR, Padberg GW, van der Maarel SM, van Engelen BGM, Erasmus CE, Theelen T. Goselink RJM, et al. Among authors: padberg gw. Brain Commun. 2019 Oct 11;1(1):fcz023. doi: 10.1093/braincomms/fcz023. eCollection 2019. Brain Commun. 2019. PMID: 32954265 Free PMC article.
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data.
Goselink RJM, Voermans NC, Okkersen K, Brouwer OF, Padberg GW, Nikolic A, Tupler R, Dorobek M, Mah JK, van Engelen BGM, Schreuder THA, Erasmus CE. Goselink RJM, et al. Among authors: padberg gw. Neuromuscul Disord. 2017 Dec;27(12):1077-1083. doi: 10.1016/j.nmd.2017.09.007. Epub 2017 Sep 21. Neuromuscul Disord. 2017. PMID: 29102079 Free article. Review.
198 results