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Results by year

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

Year Number of Results
1948 1
1955 2
1972 2
1973 3
1974 6
1975 3
1976 6
1977 4
1978 5
1979 4
1980 1
1981 5
1982 8
1983 7
1984 5
1985 10
1986 2
1987 5
1988 5
1989 3
1990 8
1991 10
1992 10
1993 7
1994 14
1995 10
1996 11
1997 17
1998 14
1999 12
2000 12
2001 3
2002 7
2003 12
2004 8
2005 6
2006 13
2007 10
2008 9
2009 25
2010 17
2011 28
2012 23
2013 25
2014 22
2015 20
2016 12
2017 11
2018 12
2019 12
2020 23
2021 21
2022 19
2023 26
2024 5

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Article attribute

Article type

Publication date

Search Results

519 results

Results by year

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Page 1
Nosology of genetic skeletal disorders: 2023 revision.
Unger S, Ferreira CR, Mortier GR, Ali H, Bertola DR, Calder A, Cohn DH, Cormier-Daire V, Girisha KM, Hall C, Krakow D, Makitie O, Mundlos S, Nishimura G, Robertson SP, Savarirayan R, Sillence D, Simon M, Sutton VR, Warman ML, Superti-Furga A. Unger S, et al. Among authors: calder a. Am J Med Genet A. 2023 May;191(5):1164-1209. doi: 10.1002/ajmg.a.63132. Epub 2023 Feb 13. Am J Med Genet A. 2023. PMID: 36779427 Free PMC article.
Imaging in osteopetrosis.
Calder AD, Arulkumaran S, D'Arco F. Calder AD, et al. Bone. 2022 Dec;165:116560. doi: 10.1016/j.bone.2022.116560. Epub 2022 Sep 15. Bone. 2022. PMID: 36116759 Review.
Laryngeal cleft: A literature review.
Martha VV, Vontela S, Calder AN, Martha RR, Sataloff RT. Martha VV, et al. Among authors: calder an. Am J Otolaryngol. 2021 Nov-Dec;42(6):103072. doi: 10.1016/j.amjoto.2021.103072. Epub 2021 Apr 20. Am J Otolaryngol. 2021. PMID: 33957543 Review.
Disgust discussed.
Calder AJ. Calder AJ. Ann Neurol. 2003 Apr;53(4):427-8. doi: 10.1002/ana.10565. Ann Neurol. 2003. PMID: 12666109 Review. No abstract available.
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay.
Marom R, Burrage LC, Venditti R, Clément A, Blanco-Sánchez B, Jain M, Scott DA, Rosenfeld JA, Sutton VR, Shinawi M, Mirzaa G, DeVile C, Roberts R, Calder AD, Allgrove J, Grafe I, Lanza DG, Li X, Joeng KS, Lee YC, Song IW, Sliepka JM, Batkovskyte D, Washington M, Dawson BC, Jin Z, Jiang MM, Chen S, Chen Y, Tran AA, Emrick LT, Murdock DR, Hanchard NA, Zapata GE, Mehta NR, Weis MA, Scott AA, Tremp BA, Phillips JB, Wegner J, Taylor-Miller T, Gibbs RA, Muzny DM, Jhangiani SN, Hicks J, Stottmann RW, Dickinson ME, Seavitt JR, Heaney JD, Eyre DR; Undiagnosed Diseases Network; Westerfield M, De Matteis MA, Lee B. Marom R, et al. Among authors: calder ad. Am J Hum Genet. 2021 Sep 2;108(9):1710-1724. doi: 10.1016/j.ajhg.2021.08.002. Epub 2021 Aug 26. Am J Hum Genet. 2021. PMID: 34450031 Free PMC article.
Sedaghatian spondylometaphyseal dysplasia in two siblings.
Peshimam N, Farah H, Caswell R, Ellard S, Jan W, Calder AD, Cobben J, Kariholu U, Leitch HG. Peshimam N, et al. Among authors: calder ad. Eur J Med Genet. 2022 Aug;65(8):104541. doi: 10.1016/j.ejmg.2022.104541. Epub 2022 Jun 16. Eur J Med Genet. 2022. PMID: 35718083 Free article.
Lung infections in immunocompromised children.
Calder AD, Perucca G, Johnson SM, Pandey AR, Moshal K, Kusters MA. Calder AD, et al. Pediatr Radiol. 2024 Apr;54(4):530-547. doi: 10.1007/s00247-023-05735-1. Epub 2023 Aug 17. Pediatr Radiol. 2024. PMID: 37589764 Review.
Achondroplasia: Really rhizomelic?
Shelmerdine SC, Brittain H, Arthurs OJ, Calder AD. Shelmerdine SC, et al. Among authors: calder ad. Am J Med Genet A. 2016 Aug;170(8):2039-43. doi: 10.1002/ajmg.a.37776. Epub 2016 Jun 3. Am J Med Genet A. 2016. PMID: 27257098
519 results