SCOPUS 정보 검색 플랫폼

Deutsche Medizinische Wochenschrift

Volumn 122, Issue 16, 1997, Pages 504-506

Hereditary hyperferritinaemia-cataract syndrome;Hereditares Hyperferritinamie-Katarakt-Syndrom

(1) Merkt, J a,b

a Cemeinschaftspraxis Gastroenterologie (Germany)

b Am Wollhaus 1 (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN;

ADULT; ARTICLE; AUTOSOMAL DISORDER; CASE REPORT; CATARACT; DIFFERENTIAL DIAGNOSIS; FAMILY STUDY; FEMALE; FERRITIN BLOOD LEVEL; HUMAN; MALE; BLOOD; GENETICS; IRON METABOLISM DISORDER; PEDIGREE; SYNDROME;

ADULT; CATARACT; FEMALE; FERRITINS; HUMANS; IRON METABOLISM DISORDERS; MALE; PEDIGREE; SYNDROME;

EID: 0031576914 PISSN: 00120472 EISSN: None Source Type: Journal
DOI: 10.1055/s-2008-1047644 Document Type: Article

Times cited : (12)

References (5)

1
- 0028881134
- Mutation in the iron responsive element of the L-ferritin mRNA in a family with dominant hyperferritinaemia and cataract
- Beaumont, C., P. Leneuve, J. Devaux, J.-Y. Scoazec, M. Berthier, M.-N. Loiseau, B. Grandchamp. D. Bonneau Mutation in the iron responsive element of the L-ferritin mRNA in a family with dominant hyperferritinaemia and cataract. Nature genetics 11 (1995), 444-446.
- (1995) Nature Genetics , vol.11 , pp. 444-446
- Beaumont, C.¹ Leneuve, P.² Devaux, J.³ Scoazec, J.-Y.⁴ Berthier, M.⁵ Loiseau, M.-N.⁶ Grandchamp, B.⁷ Bonneau, D.⁸

2
- 0029156805
- Bilateral cataract and high serum ferritin. a new dominant genetic disorder?
- Bonneau, D., I. Winter-Fuseau, M.-N. Loiseau, P. Amati, M. Berthier, D. Oriot, C. Beaumont Bilateral cataract and high serum ferritin. A new dominant genetic disorder?], med. Genet. 32 (1995), 778-779.
- (1995) Med. Genet. , vol.32 , pp. 778-779
- Bonneau, D.¹ Winter-Fuseau, I.² Loiseau, M.-N.³ Amati, P.⁴ Berthier, M.⁵ Oriot, D.⁶ Beaumont, C.⁷

3
- 0029148586
- A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract
- Girelli, D., O. Olivieri, L de Franceschi, R. Corrocher, G. Bergamaschi, M. Cazzola A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract. Brit. J. Haematol. 9 (1995), 931 -934.
- (1995) Brit. J. Haematol. , vol.9 , pp. 931-934
- Girelli, D.¹ Olivieri, O.² De Franceschi, L.³ Corrocher, R.⁴ Bergamaschi, G.⁵ Cazzola, M.⁶

4
- 0028788201
- Molecular basis for the recently described hereditary Hyperferritinemia-Cataract Syndrome. a mutation in the iron-responsive element of ferritin L-subunit gene the »Verona Mutation«
- Girelli, D., R. Corrocher, L Bisceglia, O. Olivieri, L. de Fanceschi, I. Zelante, P. Gasparini Molecular basis for the recently described hereditary Hyperferritinemia-Cataract Syndrome. A mutation in the iron-responsive element of ferritin L-subunit gene (the »Verona Mutation« Blood 86 (1995), 4050-4053.
- (1995) Blood , vol.86 , pp. 4050-4053
- Girelli, D.¹ Corrocher, R.² Bisceglia, L.³ Olivieri, O.⁴ De Fanceschi, L.⁵ Zelante, I.⁶ Gasparini, P.⁷

5
- 0030011316
- Mojecular basis for the hereditary hyperferritinemia-cataract-syndrome (letter)
- Girelli, D., O. Olivieri, P. Gasparini, R. Corrocher Mojecular basis for the hereditary hyperferritinemia-cataract-syndrome (letter). Blood 87 (1996), 4912-4913.
- (1996) Blood , vol.87 , pp. 4912-4913
- Girelli, D.¹ Olivieri, O.² Gasparini, P.³ Corrocher, R.⁴

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