Leschot NJ - Search Results

1

A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.

van der Kooi AJ, de Visser M, van Meegen M, Ginjaar HB, van Essen AJ, Jennekens FG, Jongen PJ, Leschot NJ, Bolhuis PA. van der Kooi AJ, et al. Among authors: leschot nj. Neuromuscul Disord. 1998 Jun;8(5):305-8. doi: 10.1016/s0960-8966(98)00040-6. Neuromuscul Disord. 1998. PMID: 9673983

2

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.

Hoogerwaard EM, van der Wouw PA, Wilde AA, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, van Essen AJ, Leschot NJ, de Visser M. Hoogerwaard EM, et al. Among authors: leschot nj. Neuromuscul Disord. 1999 Jul;9(5):347-51. doi: 10.1016/s0960-8966(99)00018-8. Neuromuscul Disord. 1999. PMID: 10407858

3

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy.

Schade van Westrum SM, Hoogerwaard EM, Dekker L, Standaar TS, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, van Essen AJ, Leschot NJ, Wilde AA, de Haan RJ, de Visser M, van der Kooi AJ. Schade van Westrum SM, et al. Among authors: leschot nj. Neurology. 2011 Jul 5;77(1):62-6. doi: 10.1212/WNL.0b013e318221ad14. Epub 2011 Jun 22. Neurology. 2011. PMID: 21700587

4

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study.

Hoogerwaard EM, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, Leschot NJ, Van Essen AJ, Brunner HG, van der Wouw PA, Wilde AA, de Visser M. Hoogerwaard EM, et al. Among authors: leschot nj. Lancet. 1999 Jun 19;353(9170):2116-9. doi: 10.1016/s0140-6736(98)10028-4. Lancet. 1999. PMID: 10382696

5

[The heartache of muscular dystrophy].

Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M. Hoogerwaard EM, et al. Among authors: leschot nj. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Ned Tijdschr Geneeskd. 2000. PMID: 11103252 Review. Dutch.

6

An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS.

Leschot NJ, Kanhai HH, van Asperen CJ, Wolf H, Boer K, van Prooijen-Knegt AC, Christiaens GC, Verjaal M, Briet E. Leschot NJ, et al. Clin Genet. 1990 Sep;38(3):211-7. doi: 10.1111/j.1399-0004.1990.tb03572.x. Clin Genet. 1990. PMID: 2225529

7

Heterogeneous nuclear ribonucleoprotein G-T (HNRNP G-T) mutations in men with impaired spermatogenesis.

Westerveld GH, Gianotten J, Leschot NJ, van der Veen F, Repping S, Lombardi MP. Westerveld GH, et al. Among authors: leschot nj. Mol Hum Reprod. 2004 Apr;10(4):265-9. doi: 10.1093/molehr/gah042. Epub 2004 Mar 2. Mol Hum Reprod. 2004. PMID: 14996998

8

Prenatal diagnosis in the Netherlands. Dutch Working Party of Prenatal Diagnosis.

Leschot NJ, Kloosterman MD. Leschot NJ, et al. Eur J Hum Genet. 1997;5 Suppl 1:51-6. Eur J Hum Genet. 1997. PMID: 9101180 Review.

9

Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage.

Franssen MT, Korevaar JC, Tjoa WM, Leschot NJ, Bossuyt PM, Knegt AC, Suykerbuyk RF, Hochstenbach R, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: leschot nj. Prenat Diagn. 2008 May;28(5):408-11. doi: 10.1002/pd.1960. Prenat Diagn. 2008. PMID: 18395875

10

Psycho-social counselling in predictive genetic testing for cancer: the association between number of supportive sessions and client characteristics as assessed by psycho-social workers.

Mollema ED, Smets EM, Richard ME, Schiphorst AM, Leschot NJ. Mollema ED, et al. Among authors: leschot nj. J Genet Couns. 2008 Oct;17(5):480-8. doi: 10.1007/s10897-008-9166-z. Epub 2008 Aug 27. J Genet Couns. 2008. PMID: 18751878

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