136 related articles for article (PubMed ID: 9773037)
1. [Cerebral hemosiderosis related to hereditary ceruloplasmin deficiency. Clinical familial case study].
Servan J; Elghozi D; Gaynot S; Duclos H
Rev Neurol (Paris); 1998 Feb; 154(2):158-62. PubMed ID: 9773037
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. [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]
4. 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]
5. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus.
Logan JI; Harveyson KB; Wisdom GB; Hughes AE; Archbold GP
QJM; 1994 Nov; 87(11):663-70. PubMed ID: 7820540
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. 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]
9. Aceruloplasminemia in an asymptomatic patient with a new mutation. Diagnosis and family genetic analysis.
Pérez-Aguilar F; Burguera JA; Benlloch S; Berenguer M; Rayón JM
J Hepatol; 2005 Jun; 42(6):947-9. PubMed ID: 15885371
[TBL] [Abstract][Full Text] [Related]
10. Identification and in silico characterization of a novel compound heterozygosity associated with hereditary aceruloplasminemia.
Hofmann WP; Welsch C; Takahashi Y; Miyajima H; Mihm U; Krick C; Zeuzem S; Sarrazin C
Scand J Gastroenterol; 2007 Sep; 42(9):1088-94. PubMed ID: 17710675
[TBL] [Abstract][Full Text] [Related]
11. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.
Yoshida K; Furihata K; Takeda S; Nakamura A; Yamamoto K; Morita H; Hiyamuta S; Ikeda S; Shimizu N; Yanagisawa N
Nat Genet; 1995 Mar; 9(3):267-72. PubMed ID: 7539672
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Aceruloplasminemia].
Miyajima H
Rinsho Shinkeigaku; 2000 Dec; 40(12):1290-2. PubMed ID: 11464482
[TBL] [Abstract][Full Text] [Related]
14. [The onset of psychiatric disorders and Wilson's disease].
Benhamla T; Tirouche YD; Abaoub-Germain A; Theodore F
Encephale; 2007 Dec; 33(6):924-32. PubMed ID: 18789784
[TBL] [Abstract][Full Text] [Related]
15. Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.
Fasano A; Colosimo C; Miyajima H; Tonali PA; Re TJ; Bentivoglio AR
Mov Disord; 2008 Apr; 23(5):751-5. PubMed ID: 18200628
[TBL] [Abstract][Full Text] [Related]
16. High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.
Chen Q; Chen XP; Zou L; Zhou D; Gong QY; Burgunder JM; Shang HF
Mov Disord; 2008 Apr; 23(6):916-7. PubMed ID: 18311828
[No Abstract] [Full Text] [Related]
17. [A case of cerebellar degeneration with schizophrenia-like psychosis, severe iron deficiency, hypoceruloplasminemia and abnormal electroretinography: a new syndrome?].
Kimura A; Yoshino H; Yuasa T
Rinsho Shinkeigaku; 2001 Aug; 41(8):507-11. PubMed ID: 11889836
[TBL] [Abstract][Full Text] [Related]
18. Hallervorden-Spatz syndrome in two siblings diagnosed by clinical features and magnetic resonance imaging.
Tiamkao S; Nitinavakarn B; Jitpimolmard S
J Med Assoc Thai; 2000 Dec; 83(12):1535-40. PubMed ID: 11253896
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A 70-year-old man with extrapyramidal symptoms, dementia and hemosiderosis.
Chrétien F; Servan J; Mikol J; Trierweiller M; Elghozi D; Gray F
Brain Pathol; 2006 Jul; 16(3):235-6. PubMed ID: 16911481
[No Abstract] [Full Text] [Related]
[Next] [New Search]