Similar articles for PMID: 8781450

Year	Number of Results
1995	3
1996	2
1997	6
1998	4
1999	5
2000	5
2001	8
2002	7
2003	7
2004	8
2005	4
2006	6
2007	6
2008	1
2009	4
2010	3
2011	4
2013	2
2014	3
2015	1
2016	2
2017	2
2018	2
2019	1
2020	2
2021	1
2022	2
2023	1
2024	0

1

A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome.

Aguilar-Martinez P, Biron C, Masmejean C, Jeanjean P, Schved JF. Aguilar-Martinez P, et al. Blood. 1996 Sep 1;88(5):1895. Blood. 1996. PMID: 8781450 Free article. No abstract available.

2

[Hyperferritinemia cataract syndrome].

Kessler LJ, Auffarth GU, Khoramnia R. Kessler LJ, et al. Ophthalmologie. 2023 Mar;120(3):237. doi: 10.1007/s00347-022-01787-0. Epub 2022 Dec 22. Ophthalmologie. 2023. PMID: 36547669 German. No abstract available.

3

Brazilian family with hyperferritinemia-cataract syndrome: case report.

Alvarenga AM, Silva NKD, Cançado RD, Carvalho LEMR, Santos PCJL. Alvarenga AM, et al. Einstein (Sao Paulo). 2022 Oct 24;20:eRC0076. doi: 10.31744/einstein_journal/2022RC0076. eCollection 2022. Einstein (Sao Paulo). 2022. PMID: 36287435 Free PMC article.

4

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.

Celma Nos F, Hernández G, Ferrer-Cortès X, Hernandez-Rodriguez I, Navarro-Almenzar B, Fuster JL, Bermúdez Cortés M, Pérez-Montero S, Tornador C, Sanchez M. Celma Nos F, et al. Int J Mol Sci. 2021 May 21;22(11):5451. doi: 10.3390/ijms22115451. Int J Mol Sci. 2021. PMID: 34064225 Free PMC article.

5

Why and How Is Hyperferritinemic Sepsis Different From Sepsis Without Hyperferritinemia?

Carcillo JA, Kernan KK, Horvat CM, Simon DW, Aneja RK. Carcillo JA, et al. Pediatr Crit Care Med. 2020 May;21(5):509-512. doi: 10.1097/PCC.0000000000002285. Pediatr Crit Care Med. 2020. PMID: 32358338 Free PMC article. No abstract available.

6

Children with extreme hyperferritinemia are at risk of receiving more chemotherapy than necessary.

Han SB, Lee SY. Han SB, et al. Turk J Pediatr. 2020;62(1):165-166. doi: 10.24953/turkjped.2020.01.026. Turk J Pediatr. 2020. PMID: 32253886 Free article. No abstract available.

7

Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome.

Aslan D, Akata RF, Atalay HT, Üçgül AY. Aslan D, et al. Pediatr Hematol Oncol. 2019 Sep;36(6):390-393. doi: 10.1080/08880018.2019.1621972. Epub 2019 Sep 14. Pediatr Hematol Oncol. 2019. PMID: 31522592

8

FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family.

Ferro E, Capra AP, Zirilli G, Meduri A, Urso M, Briuglia S, La Rosa MA. Ferro E, et al. Pediatr Dev Pathol. 2018 Sep-Oct;21(5):456-460. doi: 10.1177/1093526618755200. Epub 2018 Feb 9. Pediatr Dev Pathol. 2018. PMID: 29426274

9

A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome.

Mattila RM, Sainio A, Järveläinen M, Pursiheimo J, Järveläinen H. Mattila RM, et al. Acta Ophthalmol. 2018 Feb;96(1):95-99. doi: 10.1111/aos.13492. Epub 2017 Jun 21. Acta Ophthalmol. 2018. PMID: 28636169 Free article.

10

Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome.

Yazar S, Franchina M, Craig JE, Burdon KP, Mackey DA. Yazar S, et al. Ophthalmic Genet. 2017 Mar-Apr;38(2):171-174. doi: 10.3109/13816810.2016.1164195. Epub 2016 Apr 20. Ophthalmic Genet. 2017. PMID: 27096259 Free article.

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