Delleman JW - Search Results

1

The intraocular straylight function in some hereditary corneal dystrophies.

van den Berg TJ, Hwan BS, Delleman JW. van den Berg TJ, et al. Among authors: delleman jw. Doc Ophthalmol. 1993;85(1):13-9. doi: 10.1007/BF01268096. Doc Ophthalmol. 1993. PMID: 8181422

2

Goniodysgenesis in familial primary open-angle glaucoma.

Verbraak FD, vd Berg W, Delleman JW, Greve EL. Verbraak FD, et al. Among authors: delleman jw. Acta Ophthalmol (Copenh). 1994 Feb;72(1):98-102. doi: 10.1111/j.1755-3768.1994.tb02745.x. Acta Ophthalmol (Copenh). 1994. PMID: 8017205

3

DNA carrier detection in X-linked progressive cone dystrophy.

Bergen AA, Meire F, Schuurman EJ, Delleman JW. Bergen AA, et al. Among authors: delleman jw. Clin Genet. 1994 May;45(5):236-40. doi: 10.1111/j.1399-0004.1994.tb04148.x. Clin Genet. 1994. PMID: 8076408

4

The honeycomb type of Reis-Bücklers' dystrophy of the cornea: biometrics and an interpretation.

Wittebol-Post D, van Bijsterveld OP, Delleman JW. Wittebol-Post D, et al. Among authors: delleman jw. Ophthalmologica. 1987;194(2-3):65-70. doi: 10.1159/000309737. Ophthalmologica. 1987. PMID: 3497370

5

Crystalline cataract and uncombable hair. Ultrastructural and biochemical findings.

de Jong PT, Bleeker-Wagemakers EM, Vrensen GF, Broekhuyse RM, Peereboom-Wynia JD, Delleman JW. de Jong PT, et al. Among authors: delleman jw. Ophthalmology. 1990 Sep;97(9):1181-7. doi: 10.1016/s0161-6420(90)32438-7. Ophthalmology. 1990. PMID: 2234851

6

Meesmann's epithelial dystrophy of the cornea. Biometrics and a hypothesis.

Wittebol-Post D, van Bijsterveld OP, Delleman JW. Wittebol-Post D, et al. Among authors: delleman jw. Ophthalmologica. 1987;194(1):44-9. doi: 10.1159/000309733. Ophthalmologica. 1987. PMID: 3495763

7

[Reis-Bücklers corneal dystrophy].

Winkelman JE, Wittebol-Post D, Delleman JW. Winkelman JE, et al. Among authors: delleman jw. Klin Monbl Augenheilkd. 1986 Feb;188(2):143-7. doi: 10.1055/s-2008-1050600. Klin Monbl Augenheilkd. 1986. PMID: 3520120 German.

8

Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3.

Bergen AA, Meire F, ten Brink J, Schuurman EJ, van Ommen GJ, Delleman JW. Bergen AA, et al. Among authors: delleman jw. Genomics. 1993 Nov;18(2):463-4. doi: 10.1006/geno.1993.1504. Genomics. 1993. PMID: 8288262 No abstract available.

9

X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis.

Meire FM, Bergen AA, De Rouck A, Leys M, Delleman JW. Meire FM, et al. Among authors: delleman jw. Br J Ophthalmol. 1994 Feb;78(2):103-8. doi: 10.1136/bjo.78.2.103. Br J Ophthalmol. 1994. PMID: 8123616 Free PMC article.

10

Autosomal dominant congenital miosis with megalocornea.

Meire FM, Delleman JW. Meire FM, et al. Among authors: delleman jw. Ophthalmic Paediatr Genet. 1992 Jun;13(2):123-9. doi: 10.3109/13816819209087612. Ophthalmic Paediatr Genet. 1992. PMID: 1495762

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