Low ovarian reserve in girls with autosomal-recessive proximal spinal muscular atrophies type I-III

被引：0
|
作者：
Koelbel, H. [1 ]
Hauffa, B. [2 ]
Boukidis, A. [3 ]
Lutz, S. [1 ]
Della-Marina, A. [1 ]
Schara, U. [1 ]
机构：
[1] Univ Duisburg Essen, Dept Neuropediat, Dev Neurol, Essen, Germany
[2] Univ Duisburg Essen, Dept Pediat Endocrinol & Diabetol, Essen, Germany
[3] Univ Duisburg Essen, Dept Pediat Pulmonol, Essen, Germany
来源：
NEUROMUSCULAR DISORDERS | 2015年 / 25卷
关键词：
D O I：
10.1016/j.nmd.2015.06.046
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
G.P.31
引用
收藏
页码：S196 / S196
页数：1
相关论文
共 3 条
  • [1] Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
    Koelbel, Heike
    Hauffa, Berthold P.
    Wudy, Stefan A.
    Bouikidis, Anastasios
    Della Marina, Adela
    Schara, Ulrike
    PLOS ONE, 2017, 12 (03):
  • [2] Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III (vol 12, e0173144, 2017)
    Kolbel, Heike
    Hauffa, Berthold P.
    Wudy, Stefan A.
    Bouikidis, Anastasios
    Della Marina, Adela
    Schara, Ulrike
    PLOS ONE, 2017, 12 (04):
  • [3] Analysis of creatine kinase activity in 504 patients with proximal spinal muscular atrophy types I-III from the point of view of progression and severity
    Rudnik-Schöneborn, S
    Lützenrath, S
    Borkowska, J
    Karwanska, A
    Hausmanowa-Petrusewicz, I
    Zerres, K
    EUROPEAN NEUROLOGY, 1998, 39 (03) : 154 - 162
1