Persistence of elevated aminotransferases in Wilson's disease despite adequate therapy

被引：12

作者：

Iorio, R ^{[1
]}

D'Ambrosi, M ^{[1
]}

Marcellini, M ^{[1
]}

Barbera, C ^{[1
]}

Maggiore, G ^{[1
]}

Zancan, L ^{[1
]}

Giacchino, R ^{[1
]}

Vajro, P ^{[1
]}

Marazzi, MG ^{[1
]}

Francavilla, R ^{[1
]}

Michielutti, F ^{[1
]}

Resti, M ^{[1
]}

Frediani, T ^{[1
]}

Pastore, M ^{[1
]}

Vegnente, A ^{[1
]}

机构：

[1] Univ Naples Federico II, Dept Pediat, Naples, Italy

来源：

HEPATOLOGY | 2004年 / 39卷 / 04期

关键词：

D O I：

10.1002/hep.20165

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：1173 / 1174

页数：2

共 9 条

[1] VALUE OF URINARY COPPER EXCRETION AFTER PENICILLAMINE CHALLENGE IN THE DIAGNOSIS OF WILSONS-DISEASE [J].

DACOSTA, CM ;

BALDWIN, D ;

PORTMANN, B ;

LOLIN, Y ;

MOWAT, AP ;

MIELIVERGANI, G .

HEPATOLOGY, 1992, 15 (04) :609-615

[2] Early occurrence of hypertransaminasemia in a 13-month-old child with Wilson disease [J].

Iorio, R ;

D'Ambrosi, M ;

Mazzarella, G ;

Varrella, F ;

Vecchione, R ;

Vegnente, A .

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2003, 36 (05) :637-638

[3] A practice guideline on Wilson disease [J].

Roberts, EA ;

Schilsky, ML .

HEPATOLOGY, 2003, 37 (06) :1475-1492

[4] PRESENTING SYMPTOMS AND NATURAL-HISTORY OF WILSON DISEASE [J].

SAITO, T .

EUROPEAN JOURNAL OF PEDIATRICS, 1987, 146 (03) :261-265

[5] A high index of suspicion:: The key to an early diagnosis of Wilson's disease in childhood [J].

Sánchez-Albisua, I ;

Garde, T ;

Hierro, L ;

Camarena, C ;

Frauca, E ;

de la Vega, A ;

Díaz, MC ;

Larrauri, J ;

Jara, P .

JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1999, 28 (02) :186-190

[6] PERSISTENT TRANS-AMINASEMIA AND FATTY LIVER - THEIR USE IN THE DIAGNOSIS OF PRESYMPTOMATIC WILSONS-DISEASE [J].

STILLMAN, AE ;

ROHR, LR .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1982, 136 (03) :242-244

[7] WILSON DISEASE - CLINICAL PRESENTATION, TREATMENT, AND SURVIVAL [J].

STREMMEL, W ;

MEYERROSE, KW ;

NIEDERAU, C ;

HEFTER, H ;

KREUZPAINTNER, G ;

STROHMEYER, G .

ANNALS OF INTERNAL MEDICINE, 1991, 115 (09) :720-726

[8] THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGY TO THE MENKES DISEASE GENE [J].

TANZI, RE ;

PETRUKHIN, K ;

CHERNOV, I ;

PELLEQUER, JL ;

WASCO, W ;

ROSS, B ;

ROMANO, DM ;

PARANO, E ;

PAVONE, L ;

BRZUSTOWICZ, LM ;

DEVOTO, M ;

PEPPERCORN, J ;

BUSH, AI ;

STERNLIEB, I ;

PIRASTU, M ;

GUSELLA, JF ;

EVGRAFOV, O ;

PENCHASZADEH, GK ;

HONIG, B ;

EDELMAN, IS ;

SOARES, MB ;

SCHEINBERG, IH ;

GILLIAM, TC .

NATURE GENETICS, 1993, 5 (04) :344-350

[9]

WALSHE JM, 1986, LANCET, V1, P845

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