van Osch LD - Search Results

1

Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.

van Osch LD, Oranje AP, Keukens FM, van Voorst Vader PC, Veldman E. van Osch LD, et al. J Med Genet. 1992 Jan;29(1):36-40. doi: 10.1136/jmg.29.1.36. J Med Genet. 1992. PMID: 1552542 Free PMC article.

2

Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch family.

Oosterwijk JC, Nelen M, Van Zandvoort PM, Van Osch LD, Oranje AP, Wittebol-Post D, Van Oost BA. Oosterwijk JC, et al. Among authors: van osch ld. Ophthalmic Paediatr Genet. 1992 Mar;13(1):27-30. doi: 10.3109/13816819209070050. Ophthalmic Paediatr Genet. 1992. PMID: 1350668

3

Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.

Oosterwijk JC, Nelen M, van Zandvoort PM, van Osch LD, Oranje AP, Wittebol-Post D, van Oost BA. Oosterwijk JC, et al. Among authors: van osch ld. Am J Hum Genet. 1992 Apr;50(4):801-7. Am J Hum Genet. 1992. PMID: 1550124 Free PMC article.

4

[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research].

Oosterwijk JC, van Osch LD, Wittebol-Post D, Nelen M, van Zandvoort P, Oranje AP, van Oost BA. Oosterwijk JC, et al. Among authors: van osch ld. Klin Monbl Augenheilkd. 1992 Dec;201(6):412-3. Klin Monbl Augenheilkd. 1992. PMID: 1287362 German. No abstract available.

5

Keratosis pilaris atrophicans. One heterogeneous disease or a symptom in different clinical entities?

Oranje AP, van Osch LD, Oosterwijk JC. Oranje AP, et al. Among authors: van osch ld. Arch Dermatol. 1994 Apr;130(4):500-2. doi: 10.1001/archderm.130.4.500. Arch Dermatol. 1994. PMID: 8166489 Free article. No abstract available.

6

Golden tapetal reflex in male patients with X-linked retinitis pigmentosa. Case report and practical implications.

van Osch L, van Schooneveld M, Bleekerwagemakers EM. van Osch L, et al. Ophthalmic Paediatr Genet. 1990 Dec;11(4):287-91. doi: 10.3109/13816819009015715. Ophthalmic Paediatr Genet. 1990. PMID: 2096357

7

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Bergen AA, Samanns C, Schuurman EJ, van Osch L, van Dorp DB, Pinckers AJ, Bakker E, Gal A, van Ommen GJ, Bleeker-Wagemakers EM. Bergen AA, et al. Hum Genet. 1991 Dec;88(2):162-6. doi: 10.1007/BF00206065. Hum Genet. 1991. PMID: 1684563

8

Age and sex distribution of the incidence of contact sensitivity to standard allergens.

Young E, van Weelden H, van Osch L. Young E, et al. Contact Dermatitis. 1988 Oct;19(4):307-8. doi: 10.1111/j.1600-0536.1988.tb02935.x. Contact Dermatitis. 1988. PMID: 3219843 No abstract available.

9

Does and should breast cancer genetic counselling include lifestyle advice?

Albada A, Vernooij M, van Osch L, Pijpe A, van Dulmen S, Ausems MG. Albada A, et al. Fam Cancer. 2014 Mar;13(1):35-44. doi: 10.1007/s10689-013-9672-5. Fam Cancer. 2014. PMID: 23934600

10

Does action planning moderate the intention-habit interaction in the exercise domain? A three-way interaction analysis investigation.

de Bruijn GJ, Rhodes RE, van Osch L. de Bruijn GJ, et al. J Behav Med. 2012 Oct;35(5):509-19. doi: 10.1007/s10865-011-9380-2. Epub 2011 Oct 8. J Behav Med. 2012. PMID: 21979328 Free PMC article.

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