150 related articles for article (PubMed ID: 11909923)
1. A case of aceruloplasminaemia: abnormal serum ceruloplasmin protein without ferroxidase activity.
Takeuchi Y; Yoshikawa M; Tsujino T; Kohno S; Tsukamoto N; Shiroi A; Kikuchi E; Fukui H; Miyajima H
J Neurol Neurosurg Psychiatry; 2002 Apr; 72(4):543-5. PubMed ID: 11909923
[TBL] [Abstract][Full Text] [Related]
2. [A case of aceruloplasminemia presenting as cerebellar ataxia with homozygous mutation nt2602 delG].
Nagata M; Takiyama Y; Shimazaki H; Nakano I; Miyajima H
No To Shinkei; 2004 Oct; 56(10):885-9. PubMed ID: 15609677
[TBL] [Abstract][Full Text] [Related]
3. A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma.
Yonekawa M; Okabe T; Asamoto Y; Ohta M
Eur Neurol; 1999; 42(3):157-62. PubMed ID: 10529542
[TBL] [Abstract][Full Text] [Related]
4. [A case of hereditary ceruloplasmin deficiency with hemosiderosis].
Nakane S; Shirabe S; Suenaga A; Yoshimura T; Nakamura T
Rinsho Shinkeigaku; 1999; 39(2-3):347-51. PubMed ID: 10391079
[TBL] [Abstract][Full Text] [Related]
5. A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.
Yazaki M; Yoshida K; Nakamura A; Furihata K; Yonekawa M; Okabe T; Yamashita N; Ohta M; Ikeda S
J Neurol Sci; 1998; 156(1):30-4. PubMed ID: 9559983
[TBL] [Abstract][Full Text] [Related]
6. [A case of ceruloplasmin deficiency which showed dementia, ataxia and iron deposition in the brain].
Morita H; Inoue A; Yanagisawa N
Rinsho Shinkeigaku; 1992 May; 32(5):483-7. PubMed ID: 1458725
[TBL] [Abstract][Full Text] [Related]
7. Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia.
Kono S; Suzuki H; Takahashi K; Takahashi Y; Shirakawa K; Murakawa Y; Yamaguchi S; Miyajima H
Gastroenterology; 2006 Jul; 131(1):240-5. PubMed ID: 16831606
[TBL] [Abstract][Full Text] [Related]
8. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism.
Harris ZL; Takahashi Y; Miyajima H; Serizawa M; MacGillivray RT; Gitlin JD
Proc Natl Acad Sci U S A; 1995 Mar; 92(7):2539-43. PubMed ID: 7708681
[TBL] [Abstract][Full Text] [Related]
9. Hereditary ceruloplasmin deficiency with hemosiderosis.
Okamoto N; Wada S; Oga T; Kawabata Y; Baba Y; Habu D; Takeda Z; Wada Y
Hum Genet; 1996 Jun; 97(6):755-8. PubMed ID: 8641692
[TBL] [Abstract][Full Text] [Related]
10. Clinical, molecular, and PET study of a case of aceruloplasminaemia presenting with focal cranial dyskinesia.
Haemers I; Kono S; Goldman S; Gitlin JD; Pandolfo M
J Neurol Neurosurg Psychiatry; 2004 Feb; 75(2):334-7. PubMed ID: 14742624
[TBL] [Abstract][Full Text] [Related]
11. Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation.
Miyajima H; Kono S; Takahashi Y; Sugimoto M; Sakamoto M; Sakai N
Neurology; 2001 Dec; 57(12):2205-10. PubMed ID: 11756598
[TBL] [Abstract][Full Text] [Related]
12. Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox.
Lindner U; Schuppan D; Schleithoff L; Habeck JO; Grodde T; Kirchhof K; Stoelzel U
Horm Metab Res; 2015 Apr; 47(4):303-8. PubMed ID: 25089372
[TBL] [Abstract][Full Text] [Related]
13. Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease.
Takahashi Y; Miyajima H; Shirabe S; Nagataki S; Suenaga A; Gitlin JD
Hum Mol Genet; 1996 Jan; 5(1):81-84. PubMed ID: 8789443
[TBL] [Abstract][Full Text] [Related]
14. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.
Morita H; Ikeda S; Yamamoto K; Morita S; Yoshida K; Nomoto S; Kato M; Yanagisawa N
Ann Neurol; 1995 May; 37(5):646-56. PubMed ID: 7755360
[TBL] [Abstract][Full Text] [Related]
15. [Aceruloplasminemia].
Miyajima H
Rinsho Shinkeigaku; 2000 Dec; 40(12):1290-2. PubMed ID: 11464482
[TBL] [Abstract][Full Text] [Related]
16. New mutation of the ceruloplasmin gene in the case of a neurologically asymptomatic patient with microcytic anaemia, obesity and supposed Wilson's disease.
Ondrejkovičová M; Dražilová S; Drakulová M; Siles JL; Zemjarová Mezenská R; Jungová P; Fabián M; Rychlý B; Žigrai M
BMC Gastroenterol; 2020 Apr; 20(1):95. PubMed ID: 32264837
[TBL] [Abstract][Full Text] [Related]
17. The copper-iron connection: hereditary aceruloplasminemia.
Nittis T; Gitlin JD
Semin Hematol; 2002 Oct; 39(4):282-9. PubMed ID: 12382203
[TBL] [Abstract][Full Text] [Related]
18. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis.
Xu X; Pin S; Gathinji M; Fuchs R; Harris ZL
Ann N Y Acad Sci; 2004 Mar; 1012():299-305. PubMed ID: 15105274
[TBL] [Abstract][Full Text] [Related]
19. Hereditary caeruloplasmin deficiency: clinicopathological study of a patient.
Kawanami T; Kato T; Daimon M; Tominaga M; Sasaki H; Maeda K; Arai S; Shikama Y; Katagiri T
J Neurol Neurosurg Psychiatry; 1996 Nov; 61(5):506-9. PubMed ID: 8937346
[TBL] [Abstract][Full Text] [Related]
20. Looking for a partner: ceruloplasmin in protein-protein interactions.
Vasilyev VB
Biometals; 2019 Apr; 32(2):195-210. PubMed ID: 30895493
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]