Haim M - Search Results

1

Retinitis pigmentosa: problems associated with genetic classification.

Haim M. Haim M. Clin Genet. 1993 Aug;44(2):62-70. doi: 10.1111/j.1399-0004.1993.tb03848.x. Clin Genet. 1993. PMID: 8275561

2

Epidemiology of retinitis pigmentosa in Denmark.

Haim M. Haim M. Acta Ophthalmol Scand Suppl. 2002;(233):1-34. doi: 10.1046/j.1395-3907.2002.00001.x. Acta Ophthalmol Scand Suppl. 2002. PMID: 11921605

3

Retinitis pigmentosa and allied disorders in Denmark. IV. Ophthalmic features in systemic and non-systemic cases.

Haim M, Rosenberg T. Haim M, et al. Acta Ophthalmol (Copenh). 1993 Oct;71(5):597-605. doi: 10.1111/j.1755-3768.1993.tb04648.x. Acta Ophthalmol (Copenh). 1993. PMID: 8109205

4

Autosomal dominant stationary night-blindness. A large family rediscovered.

Rosenberg T, Haim M, Piczenik Y, Simonsen SE. Rosenberg T, et al. Among authors: haim m. Acta Ophthalmol (Copenh). 1991 Dec;69(6):694-702. doi: 10.1111/j.1755-3768.1991.tb02046.x. Acta Ophthalmol (Copenh). 1991. PMID: 1789082

5

Prevalence of retinitis pigmentosa and allied disorders in Denmark. I Main results.

Haim M, Holm NV, Rosenberg T. Haim M, et al. Acta Ophthalmol (Copenh). 1992 Apr;70(2):178-86. doi: 10.1111/j.1755-3768.1992.tb04121.x. Acta Ophthalmol (Copenh). 1992. PMID: 1609565

6

A population survey of retinitis pigmentosa and allied disorders in Denmark. Completeness of registration and quality of data.

Haim M, Holm NV, Rosenberg T. Haim M, et al. Acta Ophthalmol (Copenh). 1992 Apr;70(2):165-77. doi: 10.1111/j.1755-3768.1992.tb04120.x. Acta Ophthalmol (Copenh). 1992. PMID: 1609564

7

Prevalence of retinitis pigmentosa and allied disorders in Denmark. II. Systemic involvement and age at onset.

Haim M. Haim M. Acta Ophthalmol (Copenh). 1992 Aug;70(4):417-26. doi: 10.1111/j.1755-3768.1992.tb02109.x. Acta Ophthalmol (Copenh). 1992. PMID: 1414285

8

Prevalence of retinitis pigmentosa and allied disorders in Denmark. III. Hereditary pattern.

Haim M. Haim M. Acta Ophthalmol (Copenh). 1992 Oct;70(5):615-24. doi: 10.1111/j.1755-3768.1992.tb02142.x. Acta Ophthalmol (Copenh). 1992. PMID: 1471485

9

Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa.

Haim M, Grundmann K, Gal A, Rosenberg T. Haim M, et al. Ophthalmic Genet. 1996 Dec;17(4):193-7. doi: 10.3109/13816819609057893. Ophthalmic Genet. 1996. PMID: 9010870

10

X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.

Schwartz M, Haim M, Skarsholm D. Schwartz M, et al. Among authors: haim m. Clin Genet. 1990 Oct;38(4):281-6. Clin Genet. 1990. PMID: 1980096

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