Issues with European guidelines for phenylketonuria

被引：22

作者：

Burgard, Peter ^{[1
]}

Ullrich, Kurt ^{[2
]}

Ballhausen, Diana ^{[3
]}

Hennermann, Julia B. ^{[4
]}

Hollak, Carla E. M. ^{[5
]}

Langeveld, Mirjam ^{[5
]}

Karall, Daniela ^{[6
]}

Konstantopoulou, Vassiliki ^{[7
]}

Maier, Esther M. ^{[8
]}

Lang, Frauke ^{[4
]}

Lachmann, Robin ^{[9
]}

Murphy, Elaine ^{[9
]}

Garbade, Sven ^{[1
]}

Hoffmann, Georg F. ^{[1
]}

Koelker, Stefan ^{[1
]}

Lindner, Martin ^{[10
]}

Zschocke, Johannes ^{[11
]}

机构：

[1] Heidelberg Univ Hosp, Div Neuropaediat & Metab Med, Ctr Paediat & Adolescent Med, D-69120 Heidelberg, Germany

[2] Univ Med Ctr Hamburg Eppendorf, Int Ctr Lysosomal Disorders, Univ Ctr Rare Dis, Hamburg, Germany

[3] CHUV BT 02 252, Serv Med Genet, Ctr Malad Mol, Lausanne, Switzerland

[4] Johannes Gutenberg Univ Mainz, Ctr Paediat & Adolescent Med, Mainz, Germany

[5] Acad Med Ctr, Div Clin Endocrinol & Metab, Amsterdam, Netherlands

[6] Med Univ Innsbruck, Pediat Clin, Inherited Metab Disorders, Innsbruck, Austria

[7] Med Univ Vienna, Dept Pediat & Adolescent Med, Vienna, Austria

[8] Univ Munich, Dr von Hauner Childrens Hosp, Munich, Germany

[9] Natl Hosp Neurol & Neurosurg, Charles Dent Metab Unit, London, England

[10] Univ Childrens Hosp Frankfurt, Frankfurt, Germany

[11] Med Univ Innsbruck, Div Human Genet, Innsbruck, Austria

来源：

LANCET DIABETES & ENDOCRINOLOGY | 2017年 / 5卷 / 09期

关键词：

RECOMMENDATIONS;

D O I：

10.1016/S2213-8587(17)30201-2

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：681 / 683

页数：4

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