106 related articles for article (PubMed ID: 14735856)
1. [Hereditary hyperferritinaemia-cataract syndrome].
Simsek S; Nanayakkara PW
Ned Tijdschr Geneeskd; 2003 Dec; 147(51):2557; author reply 2557-8. PubMed ID: 14735856
[No Abstract] [Full Text] [Related]
2. Two Dutch families with hereditary hyperferritinaemia-cataract syndrome and heterozygosity for an HFE-related haemochromatosis gene mutation.
Simsek S; Nanayakkara PW; Keek JM; Faber LM; Bruin KF; Pals G
Neth J Med; 2003 Sep; 61(9):291-5. PubMed ID: 14692443
[TBL] [Abstract][Full Text] [Related]
3. [Hereditary hyperferritinaemia-cataract syndrome].
van der Klooster JM
Ned Tijdschr Geneeskd; 2003 Sep; 147(39):1923-8. PubMed ID: 14560693
[TBL] [Abstract][Full Text] [Related]
4. Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene.
Arosio C; Fossati L; Viganò M; Trombini P; Cazzaniga G; Piperno A
Haematologica; 1999 Jun; 84(6):560-1. PubMed ID: 10366804
[No Abstract] [Full Text] [Related]
5. Hereditary hyperferritinemia-cataract syndrome: a novel mutation in the iron-responsive element of the L-ferritin gene in a French family.
Garderet L; Hermelin B; Gorin NC; Rosmorduc O
Am J Med; 2004 Jul; 117(2):138-9. PubMed ID: 15234655
[No Abstract] [Full Text] [Related]
6. [Hereditary hyperferritinemia-cataract syndrome].
Merkt J
Dtsch Med Wochenschr; 1997 Apr; 122(16):504-6. PubMed ID: 9162623
[TBL] [Abstract][Full Text] [Related]
7. Onset of cataract in early infancy associated with a 32G-->C transition in the iron responsive element of L-ferritin.
Campagnoli MF; Pimazzoni R; Bosio S; Zecchina G; DeGobbi M; Bosso P; Oldani B; Ramenghi U
Eur J Pediatr; 2002 Sep; 161(9):499-502. PubMed ID: 12200611
[TBL] [Abstract][Full Text] [Related]
8. [Molecular genetics of hereditary cataract-hyperferritinemia syndrome].
Milon B; Beaumont C
Ann Biol Clin (Paris); 1998 Jul; 56 Spec No():36-40. PubMed ID: 9827213
[No Abstract] [Full Text] [Related]
9. Hyperferritinaemia-cataract syndrome.
Lindberg K; Hellebostad M
Acta Ophthalmol Scand; 1999 Aug; 77(4):478-80. PubMed ID: 10463429
[TBL] [Abstract][Full Text] [Related]
10. Gene symbol: FTL. Disease: Hyperferritinemia-cataract syndrome.
Piperno A; Pelucchi S
Hum Genet; 2004 Mar; 114(4):406. PubMed ID: 15046083
[No Abstract] [Full Text] [Related]
11. Granulocyte function in patients with L-ferritin iron-responsive element (IRE) 39C-->T-positive hereditary hyperferritinaemia-cataract syndrome.
Fritsche-Polanz R; Wallner M; Cohen G; Eberle C; Sunder-Plassmann G; Födinger M
Eur J Clin Invest; 2004 Oct; 34(10):701-8. PubMed ID: 15473895
[TBL] [Abstract][Full Text] [Related]
12. Clinical features and molecular analysis of seven British kindreds with hereditary hyperferritinaemia cataract syndrome.
Lachlan KL; Temple IK; Mumford AD
Eur J Hum Genet; 2004 Oct; 12(10):790-6. PubMed ID: 15280904
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract.
Bozzini C; Galbiati S; Tinazzi E; Aldigeri R; De Matteis G; Girelli D
Haematologica; 2003 Feb; 88(2):219-20. PubMed ID: 12604412
[No Abstract] [Full Text] [Related]
14. The lens in hereditary hyperferritinaemia cataract syndrome contains crystalline deposits of L-ferritin.
Mumford AD; Cree IA; Arnold JD; Hagan MC; Rixon KC; Harding JJ
Br J Ophthalmol; 2000 Jul; 84(7):697-700. PubMed ID: 10873976
[TBL] [Abstract][Full Text] [Related]
15. [Genetics of iron overloads and hereditary hyperferritinemia cataract syndrome].
García-Erce JA; Salvador Osuna C
An Med Interna; 2003 Apr; 20(4):213-4. PubMed ID: 12768838
[No Abstract] [Full Text] [Related]
16. A family with hereditary hyperferritinaemia cataract syndrome: evidence of incomplete penetrance and clinical heterogeneity.
Gonzalez-Huerta L; Ramirez-Sanchez V; Rivera-Vega M; Messina-Baas O; Cuevas-Covarrubias S
Br J Haematol; 2008 Nov; 143(4):596-8. PubMed ID: 18710380
[No Abstract] [Full Text] [Related]
17. A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome.
Cazzola M; Foglieni B; Bergamaschi G; Levi S; Lazzarino M; Arosio P
Br J Haematol; 2002 Mar; 116(3):667-70. PubMed ID: 11849230
[TBL] [Abstract][Full Text] [Related]
18. Description of a new mutation in the L-ferrin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family.
Balas A; Aviles MJ; Garcia-Sanchez F; Vicario JL
Blood; 1999 Jun; 93(11):4020-1. PubMed ID: 10383191
[No Abstract] [Full Text] [Related]
19. Identification of a novel mutation in the L ferritin iron-responsive element causing hereditary hyperferritinemia-cataract syndrome.
Messa E; Pellegrino RM; Palmieri A; Carturan S; Cilloni D; Saglio G; Roetto A
Acta Haematol; 2009; 122(4):223-5. PubMed ID: 19887780
[No Abstract] [Full Text] [Related]
20. [Pair of siblings of Italian ethnicity with hyperferritinemia and cataract].
Volkmann M; Schiff JH; Hör M; Hentze MW; Fiehn W; Merkt J
Internist (Berl); 2000 Apr; 41(4):381-4. PubMed ID: 10798187
[No Abstract] [Full Text] [Related]
[Next] [New Search]
