Comparison of clinical expression of type 2 (juvenile) and type 3 hemochromatosis.

被引:0
|
作者
De Gobbi, M
Roetto, A
Daraio, F
Alberti, F
Piga, A
Girelli, D
Camaschella, C
机构
[1] Univ Turin, I-10124 Turin, Italy
[2] Univ Verona, I-37100 Verona, Italy
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
1732
引用
收藏
页码:447A / 447A
页数:1
相关论文
共 50 条
  • [1] Mutations in the HFE2A gene cause juvenile hemochromatosis.
    Goldberg, P
    Papanikolaou, G
    Ludwig, E
    MacDonald, M
    Andres, L
    Dube, MP
    Franchini, P
    Babakaiff, R
    Risler, J
    Zaborowska, C
    Pimstone, S
    Brissot, P
    Lockitch, G
    Hayden, M
    Samuels, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 205 - 205
  • [2] Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature
    Nicholas G. Angelopoulos
    Anastasia K. Goula
    George Papanikolaou
    George Tolis
    Osteoporosis International, 2006, 17 : 150 - 155
  • [3] Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature
    Angelopoulos, NG
    Goula, AK
    Papanikolaou, G
    Tolis, G
    OSTEOPOROSIS INTERNATIONAL, 2006, 17 (01) : 150 - 155
  • [4] Type 3 hemochromatosis and β-thalassemia trait
    Riva, A
    Mariani, R
    Bovo, G
    Pelucchi, S
    Arosio, C
    Salvioni, A
    Vergani, A
    Piperno, A
    EUROPEAN JOURNAL OF HAEMATOLOGY, 2004, 72 (05) : 370 - 374
  • [5] Hemochromatosis gene in type 2 diabetes
    Mack, R
    Raghuwanshi, M
    Bachl, B
    DIABETES, 2000, 49 : A399 - A399
  • [6] Studies in Hemochromatosis Type 3: How Does TfR2 Control Hepatic Hepcidin Expression?
    Schranz, Melanie
    Dorn, Livia
    Strasser, Michael P.
    Baumgartner, Nadia
    Pietrangelo, Antonello
    Vogel, Wolfgang
    Zoller, Heinz M.
    HEPATOLOGY, 2012, 56 : 829A - 829A
  • [7] Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene
    Girelli, D
    Bozzini, C
    Roetto, A
    Alberti, F
    Daraio, F
    Colombari, R
    Olivieri, O
    Corrocher, R
    Camaschella, C
    GASTROENTEROLOGY, 2002, 122 (05) : 1295 - 1302
  • [8] Mutations in transferrin receptor-2 in hemochromatosis type 3.
    Roetto, A
    Camaschella, C
    Cali, A
    De Gobbi, M
    Carella, M
    Majorano, N
    Totaro, A
    Gasparini, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 385 - 385
  • [9] New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
    Roetto, A
    Totaro, A
    Piperno, A
    Piga, A
    Longo, F
    Garozzo, G
    Calì, A
    De Gobbi, M
    Gasparini, P
    Camaschella, C
    BLOOD, 2001, 97 (09) : 2555 - 2560
  • [10] Clinical Expression in Pfeiffer Syndrome Type 2 and 3: Surveillance in Japan
    Koga, Hiroshi
    Suga, Naohiro
    Nakamoto, Takato
    Tanaka, Koichi
    Takahashi, Noboru
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (10) : 2506 - 2510