Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 98

1.

Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.

Tanaka K, Sekijima Y, Yoshida K, Tamai M, Kosho T, Sakurai A, Wakui K, Ikeda S, Fukushima Y.

J Hum Genet. 2013 Aug;58(8):560-3. doi: 10.1038/jhg.2013.34. Epub 2013 May 2.

PMID:
23635952
2.

Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.

Yoshida K, Wada T, Sakurai A, Wakui K, Ikeda S, Fukushima Y.

J Hum Genet. 2007;52(8):675-9. Epub 2007 Jul 5.

PMID:
17611709
3.

[Current status of the predictive genetic testing for hereditary neurological diseases in Shinshu University Hospital].

Tanaka K, Sekijima Y, Yoshida K, Mizuuchi A, Yamashita H, Tamai M, Ikeda S, Fukushima Y.

Rinsho Shinkeigaku. 2013;53(3):196-204. Japanese.

PMID:
23524599
4.

[Survey on the attitude toward genetic testing of neurologists certified by the Japanese Society of Neurology].

Yoshida K, Ohata T, Muto K, Tsuchiya A, Sawada J, Hazama T, Ikeda S, Toda T.

Rinsho Shinkeigaku. 2013;53(5):337-44. Japanese.

PMID:
23719980
5.

A theoretical psychological perspective on predictive testing for late onset hereditary diseases.

Mularczyk E, Decruyenaere M, Denayer L, Evers-Kiebooms G.

Genet Couns. 2007;18(4):367-78. Review.

PMID:
18286817
6.

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y.

Rinsho Shinkeigaku. 2002 Feb;42(2):113-7. Japanese.

PMID:
12424959
7.
8.

Adult onset neurological disorders. Predictive genetic testing.

Delatycki M, Tassicker R.

Aust Fam Physician. 2001 Oct;30(10):948-52.

PMID:
11706602
9.

[Pediatric neurological disorders and genetic counseling].

Fukushima Y.

No To Hattatsu. 2003 Jul;35(4):285-91. Review. Japanese.

PMID:
12875203
11.

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup.

DudokdeWit AC, Tibben A, Duivenvoorden HJ, Frets PG, Zoeteweij MW, Losekoot M, van Haeringen A, Niermeijer MF, Passchier J.

J Med Genet. 1997 May;34(5):382-90.

12.

Attitudes regarding predictive genetic testing in minors: a survey of European clinical geneticists.

Borry P, Goffin T, Nys H, Dierickx K.

Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):78-83. doi: 10.1002/ajmg.c.30165.

PMID:
18200522
13.

Psychological consequences of predictive genetic testing: a systematic review.

Broadstock M, Michie S, Marteau T.

Eur J Hum Genet. 2000 Oct;8(10):731-8. Review.

14.

Clinical and therapeutic implications of presymptomatic gene testing for familial amyloidotic polyneuropathy (FAP).

Sales-Luís Mde L, Conceição I, de Carvalho M.

Amyloid. 2003 Aug;10 Suppl 1:26-31.

PMID:
14640039
15.

Perception of predictive testing for Huntington's disease by young women: preferring uncertainty to certainty?

Decruyenaere M, Evers-Kiebooms G, Van den Berghe H.

J Med Genet. 1993 Jul;30(7):557-61.

16.

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.

Misu Ki, Hattori N, Nagamatsu M, Ikeda Si, Ando Y, Nakazato M, Takei Yi, Hanyu N, Usui Y, Tanaka F, Harada T, Inukai A, Hashizume Y, Sobue G.

Brain. 1999 Oct;122 ( Pt 10):1951-62.

PMID:
10506096
17.

Psychosocial impact of predictive testing for myotonic dystrophy type 1.

Prévost C, Veillette S, Perron M, Laberge C, Tremblay C, Auclair J, Villeneuve J, Tremblay M, Mathieu J.

Am J Med Genet A. 2004 Apr 1;126A(1):68-77.

PMID:
15039975
18.

Survey of prenatal testing for genetic disorders in Japan: Recent report.

Nobuzane T, Yamada T, Miura K, Sawai H, Masuzaki H, Kudo Y.

J Obstet Gynaecol Res. 2016 Apr;42(4):375-9. doi: 10.1111/jog.12948. Epub 2016 Feb 18. Review.

PMID:
26890253
20.

Neurological disorders with autosomal dominant transmission.

Simpson JM.

J Neurosurg Nurs. 1984 Oct;16(5):262-9.

PMID:
6239015

Supplemental Content

Support Center