Pirinen S[au] - Search Results

Year	Number of Results
1994	1
1995	3
1996	5
1997	6
1998	4
1999	5
2000	2
2001	4
2002	2
2003	2
2004	1
2005	1
2006	1
2007	1
2009	1
2011	1
2012	1
2013	1
2023	0

1

Pirinen S. Pirinen S. Acta Odontol Scand. 1998 Dec;56(6):356-9. doi: 10.1080/000163598428310. Acta Odontol Scand. 1998. PMID: 10066116 Review.

2

Endocrine regulation of craniofacial growth.

Pirinen S. Pirinen S. Acta Odontol Scand. 1995 Jun;53(3):179-85. doi: 10.3109/00016359509005969. Acta Odontol Scand. 1995. PMID: 7572094 Review.

3

Recessively inherited lower incisor hypodontia.

Pirinen S, Kentala A, Nieminen P, Varilo T, Thesleff I, Arte S. Pirinen S, et al. J Med Genet. 2001 Aug;38(8):551-6. doi: 10.1136/jmg.38.8.551. J Med Genet. 2001. PMID: 11494968 Free PMC article. No abstract available.

4

Characteristics of incisor-premolar hypodontia in families.

Arte S, Nieminen P, Apajalahti S, Haavikko K, Thesleff I, Pirinen S. Arte S, et al. Among authors: pirinen s. J Dent Res. 2001 May;80(5):1445-50. doi: 10.1177/00220345010800051201. J Dent Res. 2001. PMID: 11437217

5

Craniofacial structure in diastrophic dysplasia--a cephalometric study.

Karlstedt E, Kaitila I, Pirinen S. Karlstedt E, et al. Among authors: pirinen s. Am J Med Genet. 1997 Oct 31;72(3):266-74. doi: 10.1002/(sici)1096-8628(19971031)72:3<266::aid-ajmg3>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9332652

6

Craniofacial and dental characteristics of Silver-Russell syndrome.

Kotilainen J, Hölttä P, Mikkonen T, Arte S, Sipilä I, Pirinen S. Kotilainen J, et al. Among authors: pirinen s. Am J Med Genet. 1995 Mar 27;56(2):229-36. doi: 10.1002/ajmg.1320560223. Am J Med Genet. 1995. PMID: 7625451

7

Impaired oral health in patients with aspartylglucosaminuria.

Arvio P, Arvio M, Wolf J, Lukinmaa PL, Saxen L, Pirinen S. Arvio P, et al. Among authors: pirinen s. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998 Nov;86(5):562-8. doi: 10.1016/s1079-2104(98)90346-8. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998. PMID: 9830648

8

A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.

Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P. Lammi L, et al. Among authors: pirinen s. Eur J Hum Genet. 2003 Nov;11(11):866-71. doi: 10.1038/sj.ejhg.5201060. Eur J Hum Genet. 2003. PMID: 14571272

9

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S. Nieminen P, et al. Among authors: pirinen s. Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715. Eur J Hum Genet. 2001. PMID: 11781684

10

Premolar hypodontia is a common feature in Sotos syndrome with a mutation in the NSD1 gene.

Kotilainen J, Pohjola P, Pirinen S, Arte S, Nieminen P. Kotilainen J, et al. Among authors: pirinen s. Am J Med Genet A. 2009 Nov;149A(11):2409-14. doi: 10.1002/ajmg.a.33062. Am J Med Genet A. 2009. PMID: 19876911

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