Literature DB >> 30327957

Decreasing 123I-ioflupane SPECT accumulation and 123I-MIBG myocardial scintigraphy uptake in a patient with a novel homozygous mutation in the ZFYVE26 gene.

Kishin Koh1, Mai Tsuchiya1, Takamura Nagasaka1, Kazumasa Shindo1, Yoshihisa Takiyama2.   

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Year:  2018        PMID： 30327957     DOI： 10.1007/s10072-018-3603-z

Source DB:  PubMed          Journal:  Neurol Sci        ISSN： 1590-1874            Impact factor:   3.307


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  6 in total

1.  SPG15: a cause of juvenile atypical levodopa responsive parkinsonism.

Authors:  Martial Mallaret; Ouhaid Lagha-Boukbiza; Saskia Biskup; Izzie Jacques Namer; Gabrielle Rudolf; Mathieu Anheim; Christine Tranchant
Journal:  J Neurol       Date:  2013-12-24       Impact factor: 4.849

2.  Atypical juvenile parkinsonism in a consanguineous SPG15 family.

Authors:  Julia Schicks; Matthis Synofzik; Hjörvar Pétursson; Johanna Huttenlocher; Matthias Reimold; Ludger Schöls; Peter Bauer
Journal:  Mov Disord       Date:  2011-01-06       Impact factor: 10.338

3.  Reduced cardiac 123I-MIBG uptake reflects cardiac sympathetic dysfunction in de novo Parkinson's disease.

Authors:  Hisayoshi Oka; Chizuko Toyoda; Makiko Yogo; Soichiro Mochio
Journal:  J Neural Transm (Vienna)       Date:  2011-02-18       Impact factor: 3.575

4.  Cardiac 123I-MIBG scintigraphy can assess the disease severity and phenotype of PD.

Authors:  Shinji Saiki; Genjiro Hirose; Koichiro Sakai; Satoshi Kataoka; Ariyuki Hori; Misuzu Saiki; Muichi Kaito; Kotaro Higashi; Suzuka Taki; Kazuo Kakeshita; Susumu Fujino; Miho Miaki
Journal:  J Neurol Sci       Date:  2004-05-15       Impact factor: 3.181

5.  SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.

Authors:  C Goizet; A Boukhris; D Maltete; L Guyant-Maréchal; J Truchetto; E Mundwiller; S Hanein; P Jonveaux; F Roelens; J Loureiro; E Godet; S Forlani; J Melki; M Auer-Grumbach; J C Fernandez; P Martin-Hardy; I Sibon; G Sole; I Orignac; C Mhiri; P Coutinho; A Durr; A Brice; G Stevanin
Journal:  Neurology       Date:  2009-10-06       Impact factor: 9.910

6.  Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.

Authors:  Benoît Renvoisé; Jaerak Chang; Rajat Singh; Sayuri Yonekawa; Edmond J FitzGibbon; Ami Mankodi; Adeline Vanderver; Alice Schindler; Camilo Toro; William A Gahl; Don J Mahuran; Craig Blackstone; Tyler Mark Pierson
Journal:  Ann Clin Transl Neurol       Date:  2014-06-01       Impact factor: 4.511
  6 in total
  1 in total

1.  Rare Neurologic Diseases and Neurological Sciences: a report for the celebration of the 2020 Rare Diseases Day.

Authors:  Antonio Federico
Journal:  Neurol Sci       Date:  2020-03       Impact factor: 3.307
  1 in total

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