Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency A follow-up EMG study of 12 patients (vol 20, pg 38, 2016)

被引：0
|
作者：
Immonen, Tuuli [1 ]
Ahola, Emilia [1 ]
Toppila, Jussi [2 ]
Lapatto, Risto [1 ]
Tyni, Tiina [1 ]
Lauronen, Leena [2 ]
机构：
[1] Univ Helsinki, Helsinki Univ Hosp, Childrens Hosp, Helsinki, Finland
[2] Univ Helsinki, Childrens Hosp, Dept Clin Neurophysiol, HUS Med Imaging Ctr, Helsinki, Finland
来源：
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY | 2019年 / 23卷 / 01期
关键词：
D O I：
10.1016/j.ejpn.2017.12.001
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：228 / 228
页数：1
相关论文
共 50 条
  • [31] Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    Harding, CO
    Gillingham, MB
    van Calcar, SC
    Wolff, JA
    Verhoeve, JN
    Mills, MD
    JOURNAL OF INHERITED METABOLIC DISEASE, 1999, 22 (03) : 276 - 280
  • [32] Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    Lund, AM
    Dixon, MA
    Vreken, P
    Leonard, JV
    Morris, AAM
    JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (04) : 410 - 412
  • [33] Ophthalmic Symptoms of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency: A Report of Three Cases
    Lange, Natalia
    Bodetko, Aleksandra Maria
    Mozrzymas, Renata
    Kowal-Lange, Agnieszka
    CASE REPORTS IN OPHTHALMOLOGY, 2024, 15 (01): : 310 - 319
  • [34] Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    Amirkhan, RH
    Timmons, CF
    Brown, KO
    Weinberger, MJ
    Bennett, MJ
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 1997, 121 (07) : 730 - 734
  • [35] What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?
    Lund, AM
    Dixon, MA
    Vreken, P
    Leonard, JV
    Morris, AAM
    JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (04) : 353 - 360
  • [36] Long-chain hydroxyacyl-CoA dehydrogenase deficiency - LCHAD defect. Two-year follow-up of two patients
    Korenke, GC
    Marquardt, I
    Motz, R
    Voges, A
    Wanders, RJA
    Steuerwald, U
    Sander, J
    MONATSSCHRIFT KINDERHEILKUNDE, 2005, 153 (07) : 657 - 663
  • [37] Ornithine transcarbamylase deficiency with organic acid pattern mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    Kostalova, E.
    Stastna, S.
    Pospisilova, E.
    Dvorakova, L.
    Zeman, J.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 : 127 - 127
  • [38] Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey
    Gillingham, M
    Van Calcar, S
    Ney, D
    Wolff, J
    Harding, C
    JOURNAL OF INHERITED METABOLIC DISEASE, 1999, 22 (02) : 123 - 131
  • [39] Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of two new mutations
    IJlst, L
    Oostheim, W
    Ruiter, JPN
    Wanders, RJA
    JOURNAL OF INHERITED METABOLIC DISEASE, 1997, 20 (03) : 420 - 422
  • [40] Serial fatty acid profiles in a preterm infant with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
    Suganuma, Hiroki
    McPhee, Andrew J.
    Bratkovic, Drago
    Gibson, Robert A.
    Andersen, Chad C.
    PEDIATRICS INTERNATIONAL, 2019, 61 (04) : 415 - 416
12345