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

Year Number of Results
1966 1
1969 1
1970 2
1971 3
1972 1
1975 6
1976 5
1977 2
1978 1
1981 1
1982 5
1983 4
1985 5
1986 3
1987 4
1988 1
1989 1
1990 5
1991 3
1992 8
1993 5
1994 5
1995 7
1996 5
1997 5
1998 10
1999 6
2000 8
2001 7
2002 7
2003 6
2004 3
2005 3
2006 1
2007 1
2008 4
2009 1
2010 2
2012 2
2013 2
2014 1
2015 2
2022 1
2023 0

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156 results

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Page 1
[Marfan syndrome].
Kaitila I, Jokinen E, Kokkonen J. Kaitila I, et al. Duodecim. 2012;128(5):503-13. Duodecim. 2012. PMID: 22486066 Review. Finnish.
Cartilage-hair hypoplasia.
Mäkitie O, Sulisalo T, de la Chapelle A, Kaitila I. Mäkitie O, et al. Among authors: kaitila i. J Med Genet. 1995 Jan;32(1):39-43. doi: 10.1136/jmg.32.1.39. J Med Genet. 1995. PMID: 7897625 Free PMC article. Review. No abstract available.
Dysosteosclerosis.
Leisti J, Kaitila I, Lachman RS, Asch MJ, Rimoin DL. Leisti J, et al. Among authors: kaitila i. Birth Defects Orig Artic Ser. 1975;11(6):349-51. Birth Defects Orig Artic Ser. 1975. PMID: 1201343 No abstract available.
Mesomelic skeletal dysplasias.
Kaitila I, Leisti JT, Rimoin DL. Kaitila I, et al. Clin Orthop Relat Res. 1976 Jan-Feb;(114):94-106. Clin Orthop Relat Res. 1976. PMID: 1261139
Craniodiaphyseal dysplasia.
Kaitila I, Stewart RE, Landow E, Lachman R, Rimoin DL. Kaitila I, et al. Birth Defects Orig Artic Ser. 1975;11(6):359-62. Birth Defects Orig Artic Ser. 1975. PMID: 1201347 No abstract available.
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.
Collod-Béroud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, Béroud C, Boileau C. Collod-Béroud G, et al. Among authors: kaitila i. Hum Mutat. 2003 Sep;22(3):199-208. doi: 10.1002/humu.10249. Hum Mutat. 2003. PMID: 12938084 Review.
Safety of laronidase delivered into the spinal canal for treatment of cervical stenosis in mucopolysaccharidosis I.
Dickson PI, Kaitila I, Harmatz P, Mlikotic A, Chen AH, Victoroff A, Passage MB, Madden J, Le SQ, Naylor DE; Mucopolysaccharidosis I Intrathecal Research Collaborative. Dickson PI, et al. Among authors: kaitila i. Mol Genet Metab. 2015 Sep-Oct;116(1-2):69-74. doi: 10.1016/j.ymgme.2015.07.005. Epub 2015 Jul 26. Mol Genet Metab. 2015. PMID: 26260077 Free PMC article. Clinical Trial.
Growth in diastrophic dysplasia.
Mäkitie O, Kaitila I. Mäkitie O, et al. Among authors: kaitila i. J Pediatr. 1997 Apr;130(4):641-6. doi: 10.1016/s0022-3476(97)70250-6. J Pediatr. 1997. PMID: 9108864
156 results