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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
2022 0
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49 results
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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 Free article. Review.
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.
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
Cystic fibrosis mutations in the Hutterite Brethren.
Klinger K, Horn GT, Stanislovitis P, Schwartz RH, Fujiwara TM, Morgan K. Klinger K, et al. Among authors: fujiwara tm. Am J Hum Genet. 1990 May;46(5):983-7. Am J Hum Genet. 1990. PMID: 2339696 Free PMC 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.
Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status.
Asai Y, Greenwood C, Hull PR, Alizadehfar R, Ben-Shoshan M, Brown SJ, Campbell L, Michel DL, Bussières J, Rousseau F, Fujiwara TM, Morgan K, Irvine AD, McLean WH, Clarke A. Asai Y, et al. Among authors: fujiwara tm. J Allergy Clin Immunol. 2013 Jul;132(1):239-42. doi: 10.1016/j.jaci.2013.03.043. Epub 2013 May 16. J Allergy Clin Immunol. 2013. PMID: 23684069 Free PMC article. No abstract available.
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, Morel CF, Fujiwara TM, Moras E, Hosack AR, Dunbar GV, Antonicka H, Forgetta V, Dobson CM, Leclerc D, Gravel RA, Shoubridge EA, Coulton JW, Lepage P, Rommens JM, Morgan K, Rosenblatt DS. Lerner-Ellis JP, et al. Among authors: fujiwara tm. Nat Genet. 2006 Jan;38(1):93-100. doi: 10.1038/ng1683. Epub 2005 Nov 27. Nat Genet. 2006. PMID: 16311595
49 results