Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease: Expanding the spectrum

被引:0
|
作者
Alonso-Canovas, A.
Katschnig, P.
Tucci, A.
Carecchio, M.
Wood, N.
Edwards, M.
Martinez-Castrillo, J. C.
Burke, D.
Heales, S.
Bhatia, K.
机构
关键词
D O I
暂无
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:S494 / S494
页数:1
相关论文
共 50 条
  • [41] Corticobasal syndrome in a man with type 1 Gaucher disease: Expansion of the understanding of the neurological spectrum
    Flueckinger, Lauren B.
    Potnis, Kunal C.
    DeArmey, Stephanie M.
    Alcalay, Roy N.
    Cooney, Jeffrey W.
    Kishnani, Priya S.
    MOLECULAR GENETICS AND METABOLISM, 2019, 126 (02) : S55 - S55
  • [42] Subtle neuropsychological abnormalities in patients with type I Gaucher disease.
    Elstein, D
    Guedalia, J
    Rosenberg, P
    Antebi, V
    Arnon, Y
    Zimran, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 449 - 449
  • [43] Abnormalities in the cerebral cortex in Gaucher disease type 1: Findings from the ENIGMA storage disease working group
    Karkashadze, George
    Namazova-Baranova, Leyla
    Belyaev, Mikhail
    Anikin, Anatoly
    Gundobina, Olga
    Vashakmadze, Nato
    Karkashadze, Magda
    Kapilushniy, Dmitry
    Gogberashvili, Tina
    Movsisyan, Goar
    Ermolina, Julia
    Konstsantinidi, Tatiana
    Solovieva, Anastasia
    Firumyants, Alexey
    Khrameeva, Ekaterina
    Gutman, Boris
    Zelman, Vladimir
    Thompson, Paul
    Baranov, Alexander
    MOLECULAR GENETICS AND METABOLISM, 2020, 129 (02) : S84 - S84
  • [44] Oculomotor findings and their correlation with clinical abnormalities in Gaucher disease type 3
    Bremova, T.
    Schiffmann, R.
    Patterson, M.
    Belmatoug, N.
    Bardins, S.
    Malinova, V.
    Mengel, E.
    Reinke, J.
    Strupp, M.
    EUROPEAN JOURNAL OF NEUROLOGY, 2016, 23 : 453 - 454
  • [45] High incidence of cholesterol gallstone disease in type 1 Gaucher disease: characterizing the biliary phenotype of type 1 Gaucher disease
    Taddei, Tamar H.
    Dziura, James
    Chen, Shu
    Yang, Ruhua
    Hyogo, Hideyuki
    Sullards, Cameron
    Cohen, David E.
    Pastores, Gregory
    Mistry, Pramod K.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 (03) : 291 - 300
  • [46] Kufor Rakeb disease: Autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia
    Williams, DR
    Hadeed, A
    Al-Din, ASN
    Wreikat, AL
    Lees, AJ
    MOVEMENT DISORDERS, 2005, 20 (10) : 1264 - 1271
  • [47] Positive filipin staining in patients with progressive supranuclear palsy: Expanding the phenotypic spectrum of Niemann-Pick disease type C?
    Giugni, J. C.
    Micheli, F. E.
    Perandones, C.
    Raina, G. B.
    Pellene, L. A.
    Calvo, D. S.
    Gonzalez Aleman, G.
    Bruni, D. N.
    Farini, V. L.
    Radrizzani, M.
    MOVEMENT DISORDERS, 2013, 28 : S352 - S352
  • [48] The neurological manifestations of Gaucher disease type 1: the French Observatoire on Gaucher disease (FROG)
    Cherin, P.
    Rose, C.
    de Roux-Serratrice, C.
    Tardy, D.
    Dobbelaere, D.
    Grosbois, B.
    Hachulla, E.
    Jaussaud, R.
    Javier, R. -M.
    Noel, E.
    Clerson, P.
    Hartmann, A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 (04) : 331 - 338
  • [49] Eliglustat: A Review in Gaucher Disease Type 1
    Scott, Lesley J.
    DRUGS, 2015, 75 (14) : 1669 - 1678
  • [50] GLYCOSYLATED FERRITIN IN TYPE 1 GAUCHER DISEASE
    Stirnemann, J.
    Heraoui, D.
    Boutenn, A.
    Fain, O.
    Fantin, B.
    Belmatoug, N.
    CLINICAL THERAPEUTICS, 2009, 31 : S208 - S209