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

Year Number of Results
1989 1
1990 4
1992 3
1993 3
1995 5
1996 1
1997 1
1998 1
1999 1
2000 4
2001 5
2002 2
2003 1
2004 3
2005 8
2006 4
2007 2
2008 1
2012 1
2013 1
2024 0

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Page 1
Molecular biology of diabetes insipidus.
Fujiwara TM, Morgan K, Bichet DG. Fujiwara TM, et al. Annu Rev Med. 1995;46:331-43. doi: 10.1146/annurev.med.46.1.331. Annu Rev Med. 1995. PMID: 7541187 Review.
Molecular biology of hereditary diabetes insipidus.
Fujiwara TM, Bichet DG. Fujiwara TM, et al. J Am Soc Nephrol. 2005 Oct;16(10):2836-46. doi: 10.1681/ASN.2005040371. Epub 2005 Aug 10. J Am Soc Nephrol. 2005. PMID: 16093448 Review.
Bowen-Conradi syndrome: a clinical and genetic study.
Lowry RB, Innes AM, Bernier FP, McLeod DR, Greenberg CR, Chudley AE, Chodirker B, Marles SL, Crumley MJ, Loredo-Osti JC, Morgan K, Fujiwara TM. Lowry RB, et al. Among authors: fujiwara tm. Am J Med Genet A. 2003 Jul 30;120A(3):423-8. doi: 10.1002/ajmg.a.20059. Am J Med Genet A. 2003. PMID: 12838567
Autosomal recessive cerebellar hypoplasia in the Hutterite population.
Glass HC, Boycott KM, Adams C, Barlow K, Scott JN, Chudley AE, Fujiwara TM, Morgan K, Wirrell E, McLeod DR. Glass HC, et al. Among authors: fujiwara tm. Dev Med Child Neurol. 2005 Oct;47(10):691-5. doi: 10.1017/S0012162205001404. Dev Med Child Neurol. 2005. PMID: 16174313 Free article.
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
Hrebícek M, Mrázová L, Seyrantepe V, Durand S, Roslin NM, Nosková L, Hartmannová H, Ivánek R, Cízkova A, Poupetová H, Sikora J, Urinovská J, Stranecký V, Zeman J, Lepage P, Roquis D, Verner A, Ausseil J, Beesley CE, Maire I, Poorthuis BJ, van de Kamp J, van Diggelen OP, Wevers RA, Hudson TJ, Fujiwara TM, Majewski J, Morgan K, Kmoch S, Pshezhetsky AV. Hrebícek M, et al. Among authors: fujiwara tm. Am J Hum Genet. 2006 Nov;79(5):807-19. doi: 10.1086/508294. Epub 2006 Sep 8. Am J Hum Genet. 2006. PMID: 17033958 Free PMC article.
A locus for Bowen-Conradi syndrome maps to chromosome region 12p13.3.
Lamont RE, Loredo-Osti J, Roslin NM, Mauthe J, Coghlan G, Nylen E, Frappier D, Innes AM, Lemire EG, Lowry RB, Greenberg CR, Triggs-Raine BL, Morgan K, Wrogemann K, Fujiwara TM, Zelinski T. Lamont RE, et al. Among authors: fujiwara tm. Am J Med Genet A. 2005 Jan 15;132A(2):136-43. doi: 10.1002/ajmg.a.30420. Am J Med Genet A. 2005. PMID: 15578624
49 results