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A peer-reviewed clinical and translational neurology open access journal
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The Helix
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Year
Year
-Year
2011
2012
2013
2014
2015
2016
2017
2018
2019
Article
Deleterious mutation in
GPR88
is associated with chorea, speech delay, and learning disabilities
Fadi
Alkufri
,
Avraham
Shaag
,
Bassam
Abu-Libdeh
, et al.
March 09, 2016
Article
Clinical course and prognosis in patients with Gaucher disease and parkinsonism
Grisel
Lopez
,
Jenny
Kim
,
Edythe
Wiggs
, et al.
March 04, 2016
Article
New susceptible variant of
COQ2
gene in Japanese patients with sporadic multiple system atrophy
Zhuoran
Sun
,
Yasuyuki
Ohta
,
Toru
Yamashita
, et al.
March 03, 2016
Article
Compound heterozygote mutations in
SPG7
in a family with adult-onset primary lateral sclerosis
Yi
Yang
,
Lei
Zhang
,
David R.
Lynch
, et al.
March 03, 2016
Clinical/Scientific Notes
“Fork and bracket” syndrome expands the spectrum of
SBF1
-related sensory motor polyneuropathies
Marta
Romani
,
Cybel
Mehawej
,
Tommaso
Mazza
, et al.
March 03, 2016
Article
Homozygous deletion in
MICU1
presenting with fatigue and lethargy in childhood
David
Lewis-Smith
,
Kimberli J.
Kamer
,
Helen
Griffin
, et al.
March 03, 2016
Article
Stabilization of the thermolabile variant S113L of carnitine palmitoyltransferase II
Leila
Motlagh
,
Ralph
Golbik
,
Wolfgang
Sippl
, et al.
February 25, 2016
Clinical/Scientific Notes
Exonic deletion of
SLC9A9
in autism with epilepsy
Meeta
Cardon
,
Karen D.
Evankovich
,
J. Lloyd
Holder
February 25, 2016
Article
Long-term follow-up and sudden unexpected death in Gaucher disease type 3 in Egypt
Magy
Abdelwahab
,
Derek
Blankenship
,
Raphael
Schiffmann
February 25, 2016
The Helix
Genetics of neurodegenerative diseases
Stefan M.
Pulst
February 18, 2016
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