Pinckers AJ[au] - Search Results

Year	Number of Results
1969	1
1972	1
1974	2
1976	1
1977	1
1978	2
1979	1
1980	1
1982	4
1983	1
1984	1
1985	2
1986	2
1987	1
1988	1
1990	3
1991	2
1992	2
1995	7
1996	4
1997	7
1998	4
1999	4
2001	1
2002	1
2024	0

1

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.

Bergen AA, Pinckers AJ. Bergen AA, et al. Among authors: pinckers aj. Am J Hum Genet. 1997 Jun;60(6):1468-73. doi: 10.1086/515458. Am J Hum Genet. 1997. PMID: 9199568 Free PMC article.

2

Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) gene.

van den Hurk JA, Schwartz M, van Bokhoven H, van de Pol TJ, Bogerd L, Pinckers AJ, Bleeker-Wagemakers EM, Pawlowitzki IH, Rüther K, Ropers HH, Cremers FP. van den Hurk JA, et al. Among authors: pinckers aj. Hum Mutat. 1997;9(2):110-7. doi: 10.1002/(SICI)1098-1004(1997)9:2<110::AID-HUMU2>3.0.CO;2-D. Hum Mutat. 1997. PMID: 9067750 Free article. Review.

3

Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndrome.

Rump P, Hamel BC, Pinckers AJ, van Dop PA. Rump P, et al. Among authors: pinckers aj. J Med Genet. 1997 Sep;34(9):767-71. doi: 10.1136/jmg.34.9.767. J Med Genet. 1997. PMID: 9321767 Free PMC article. Review.

4

[Hydrophilic contact lenses].

Pinckers AJ. Pinckers AJ. Ned Tijdschr Geneeskd. 1974 Jun 15;118(24):922-3. Ned Tijdschr Geneeskd. 1974. PMID: 4603273 Review. Dutch. No abstract available.

5

Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.

Hamel BC, Draaisma JM, Pinckers AJ, Boetes C, Hoppe RL, Ropers HH, Brunner HG. Hamel BC, et al. Among authors: pinckers aj. Am J Med Genet. 1995 Apr 10;56(3):312-6. doi: 10.1002/ajmg.1320560320. Am J Med Genet. 1995. PMID: 7778598 Free article. Review.

6

Ophthalmologic findings in Usher syndrome type 2A.

Van Aarem A, Wagenaar M, Pinckers AJ, Huygen PL, Bleeker-Wagemakers EM, Kimberling BJ, Cremers CW. Van Aarem A, et al. Among authors: pinckers aj. Ophthalmic Genet. 1995 Dec;16(4):151-8. doi: 10.3109/13816819509057856. Ophthalmic Genet. 1995. PMID: 8749051

7

Gyrate atrophy and choroidal neovascularization.

Marano F, Deutman AF, Pinckers AJ, Aandekerk AL. Marano F, et al. Among authors: pinckers aj. Arch Ophthalmol. 1996 Oct;114(10):1295. doi: 10.1001/archopht.1996.01100140495035. Arch Ophthalmol. 1996. PMID: 8859105 Free article. No abstract available.

8

Dominantly inherited cystoid macular edema.

Deutman AF, Pinckers AJ, Aan de Kerk AL. Deutman AF, et al. Among authors: pinckers aj. Am J Ophthalmol. 1976 Oct;82(4):540-8. doi: 10.1016/0002-9394(76)90540-7. Am J Ophthalmol. 1976. PMID: 970419

9

Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis).

Taschner PE, de Vos N, Post JG, Meijers-Heijboer EJ, Hofman I, Loonen MC, Pinckers AJ, Bleeker-Wagemakers EM, Gardiner RM, Breuning MH. Taschner PE, et al. Among authors: pinckers aj. Am J Med Genet. 1995 Jun 5;57(2):333-7. doi: 10.1002/ajmg.1320570246. Am J Med Genet. 1995. PMID: 7668358 Free article.

10

Atypical Cogan's syndrome: an autoimmune disease?

Peeters GJ, Cremers CW, Pinckers AJ, Hoefnagels WH. Peeters GJ, et al. Among authors: pinckers aj. Ann Otol Rhinol Laryngol. 1986 Mar-Apr;95(2 Pt 1):173-5. doi: 10.1177/000348948609500213. Ann Otol Rhinol Laryngol. 1986. PMID: 3963689

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