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Ophthalmology

Volumn 101, Issue 1, 1994, Pages 38-45

Pathology of Hereditary Retinal Degeneration Associated with Hypobetalipoproteinemia

(5) Brosnahan, Donal M a Kennedy, Susan M a Converse, Carolyn A b Lee, William R a Hammer, Harold M a

a UNIVERSITY OF GLASGOW (United Kingdom)

b UNIVERSITY OF STRATHCLYDE (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN B; CHOLESTEROL; LIPID; LIPOFUSCIN; LOW DENSITY LIPOPROTEIN; MELANIN;

AGED; ARTICLE; CASE REPORT; COLOR VISION; DEPIGMENTATION; FEMALE; HISTOPATHOLOGY; HUMAN; HYPOBETALIPOPROTEINEMIA; MACROPHAGE; NIGHT BLINDNESS; PHOTORECEPTOR; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA DEGENERATION;

EID: 0028157377 PISSN: 01616420 EISSN: None Source Type: Journal
DOI: 10.1016/S0161-6420(94)31358-3 Document Type: Article

Times cited : (26)

References (27)

1
- 50549088054
- Familial hypolipidaemia and retarded development without steatorrhoea. Another inborn error of metabolism?
- (1962) Helv Paediatr Acta , vol.17 , pp. 1-23
- Hooft, C¹ De Laey, P² Herpol, LJ³

2
- 0023712158
- Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred
- (1988) Journal of Clinical Investigation , vol.82 , pp. 847-851
- Leppert, M¹ Breslow, JL² Wu, L³

3
- 0025330127
- 100: genetic disorders associated with apolipoprotein B
- (1990) Curr Opin Lipidology , vol.1 , pp. 104-109
- Innerarity, TL¹

4
- 0014525935
- Familial hypobeta-lipoproteinemia: a genetic disorder of lipid metabolism with nervous system involvement
- (1969) Am J Med , vol.46 , pp. 886-900
- Mars, H¹ Lewis, LA² Robertson, AL³

5
- 0016085622
- Familial hypobetalipoproteinemia: report of a case with psychomotor retardation
- (1974) Pediatrics , vol.54 , pp. 111-113
- Brown, BJ¹ Lewis, LA² Mercer, RD³

6
- 0016136126
- Hypobetalipoproteinemia: clinical and biochemical description of a new kindred with ‘Friedreich's ataxia’
- (1974) Neurology , vol.24 , pp. 1051-1063
- Aggerbeck, LP¹ McMahon, JP² Scanu, AM³

7
- 0017188269
- Atypical retinitis pigmentosa in familial hypobetalipoproteinemia
- (1976) Am J Ophthalmol , vol.82 , pp. 64-71
- Yee, RD¹ Herbert, PN² Bergsma, DR³ Biemer, JJ⁴

8
- 0001298717
- Familial lipoprotein deficiency: abetalipoproteinemia, hypobetalipoproteinemia, and Tangier disease
- JB Stanbury, JB Wyngaarden, DS Fredrickson et al., 5th ed, McGraw-Hill, New York
- (1983) The Metabolic Basis of Inherited Disease , pp. 589-621
- Herbert, PN¹ Assmann, G² Gotto, AM³ Fredrickson, DS⁴

9
- 0026775222
- A novel truncated apolipoprotein B (apo B55) in a patient with familial hypobetalipoproteinemia and atypical retinitis pigmentosa
- (1992) Clin Genet , vol.42 , pp. 62-70
- Talmud, PJ¹ Converse, C² Krul, E³

10
- 0024269064
- Retinitis pigmentosa
- (1988) Surv Ophthalmol , vol.33 , pp. 137-177
- Pagon, RA¹

11
- 0022596325
- Extensive subretinal pigment epithelial deposit in two brothers suffering from dominant retinitis pigmentosa. A histopathological study
- (1986) Graefes Arch Clin Exp Ophthalmol , vol.224 , pp. 299-309
- Duvall, J¹ McKechnie, NM² Lee, WR³

12
- 0020417782
- Dominant retinitis pigmentosa. A clinicopathologic correlation
- (1982) Ophthalmology , vol.89 , pp. 1414-1424
- Meyer, KT¹ Heckenlively, JR² Spitznas, M³ Foos, RY⁴

13
- 0020365239
- A histopathologic study of retinitis pigmentosa
- (1982) Ophthalmic Paediatr Genet , vol.1 , pp. 151-168
- Santos-Anderson, RM¹ Tso, MOM² Fishman, GA³

14
- 0020532994
- Clinical-ultrastructural study of a retinal dystrophy
- (1983) Invest Ophthalmol Vis Sci , vol.24 , pp. 458-469
- Bunt-Milam, AH¹ Kalina, RE² Pagon, RA³

15
- 0016169602
- Electron microscopic observations of human retinitis pigmentosa, dominantly inherited
- (1974) Invest Ophthalmol , vol.13 , pp. 487-498
- Kolb, H¹ Gouras, P²

16
- 0021964847
- Dominantly inherited retinitis pigmentosa. Ultrastructure and biochemical analysis
- (1985) Ophthalmology , vol.92 , pp. 1165-1172
- Rodrigues, MM¹ Wiggert, B² Hackett, J³

17
- 0017762737
- Retinal ultrastructure in advanced retinitis pigmentosa
- (1977) Invest Ophthalmol Vis Sci , vol.16 , pp. 947-962
- Szamier, RB¹ Berson, EL²

18
- 0021948505
- Retinal histopathology of a carrier of x-chromosome-linked retinitis pigmentosa
- (1985) Ophthalmology , vol.92 , pp. 271-278
- Szamier, RB¹ Berson, EL²

19
- 0018411075
- Sex-linked retinitis pigmentosa: ultrastructure of photoreceptors and pigment epithelium
- (1979) Invest Ophthalmol Vis Sci , vol.18 , pp. 145-160
- Szamier, RB¹ Berson, EL² Klein, R³ Meyers, S⁴

20
- 0014064266
- Studies on the human macula. IV. Ageing changes in Bruch's membrane
- (1967) Arch Ophthalmol , vol.77 , pp. 410-420
- Hogan, MJ¹ Alvarado, J²

21
- 0017078404
- Ageing and degeneration in the macular region: a clinico-pathological study
- (1976) Br J Ophthalmol , vol.60 , pp. 324-341
- Sarks, SH¹

22
- 0019253913
- Softening of drusen and subretinal neovascularization
- (1980) Trans Ophthalmol Soc U K , vol.100 , pp. 414-422
- Sarks, SH¹ Van Driel, D² Maxwell, L³ Killingsworth, M⁴

23
- 0023018702
- Basal linear deposit in the human macula
- (1986) Graefe's Archive for Clinical and Experimental Ophthalmology , vol.224 , pp. 493-501
- Löfller, KU¹ Lee, WR²

24
- 0026508815
- Histologic features of the early stages of age-related macular degeneration. A statistical analysis
- (1992) Ophthalmology , vol.99 , pp. 278-286
- van der Schaft, TL¹ Mooy, CM² de Bruijn, WC³

25
- 0026082831
- Is basal laminar deposit unique for age-related macular degeneration?
- (1991) Arch Ophthalmol , vol.109 , pp. 420-425
- van der Schaft, TL¹ de Bruijn, WC² Mooy, CM³

26
- 0021125834
- Ocular abnormalities in abetalipoproteinemia. A clinicopathologic correlation
- (1984) Ophthalmology , vol.91 , pp. 991-998
- Cogan, DG¹ Rodrigues, M² Chu, FC³ Schaefer, EJ⁴

27
- 0026343685
- Ageing of the retinal pigment epitheium
- (1991) Prog Retinal Res , vol.11 , pp. 125-151
- Boulton, M¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.