Publications by authors named "Vedrana Milic Rasic"

30Publications

Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy.

Neurology 2017 Feb 11;88(6):533-542. Epub 2017 Jan 11.

From the Molecular Neurogenomics Group (D.A., B.E., A.E.-C., K.P., T.O., E.D.V., A.J.), VIB Department of Molecular Genetics (B.A.), University of Antwerp, Belgium; Clinic for Neurology and Psychiatry for Children and Youth (J.N.G), Belgrade, Serbia; Faculty of Medicine (V.M.R.), Clinic for Neurology and Psychiatry for Children and Youth, University of Belgrade, Serbia; Departments of Chemical Physiology and Cell and Molecular Biology (D.B., X.-L.Y.), The Scripps Research Institute, La Jolla, CA; and Institute of Clinical Chemistry (R.S., T.H.), University Hospital Zurich, University of Zurich, Switzerland.

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http://dx.doi.org/10.1212/WNL.0000000000003595DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5304460PMC
February 2017

Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients.

J Hum Genet 2015 Nov 27;60(11):723-8. Epub 2015 Aug 27.

Centre for Human Molecular Genetics, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

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http://dx.doi.org/10.1038/jhg.2015.104DOI Listing
November 2015

Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2.

Am J Hum Genet 2014 Nov 30;95(5):590-601. Epub 2014 Oct 30.

MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK; Department of Molecular Neurosciences, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.10.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225647PMC
November 2014

Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe.

J Neurol 2014 Jan 27;261(1):152-63. Epub 2013 Oct 27.

MRC Centre for Neuromuscular Diseases at Newcastle, Institute of Genetic Medicine, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK,

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http://link.springer.com/content/pdf/10.1007%2Fs00415-013-71
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http://www.rare-diseases.eu/wp-content/uploads/2013/08/41_t2
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http://link.springer.com/10.1007/s00415-013-7154-1
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http://dx.doi.org/10.1007/s00415-013-7154-1DOI Listing
January 2014

Further developments with antisense treatment for myasthenia gravis.

Ann N Y Acad Sci 2012 Dec;1275:13-6

Greater Manchester Neuroscience Centre, Manchester UK.

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http://dx.doi.org/10.1111/j.1749-6632.2012.06825.xDOI Listing
December 2012

Proteomic analysis in giant axonal neuropathy: new insights into disease mechanisms.

Muscle Nerve 2012 Aug;46(2):246-56

Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, De Pintelaan 185, B-9000 Ghent, Belgium.

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http://dx.doi.org/10.1002/mus.23306DOI Listing
August 2012

Community-based study of health-related quality of life in spinal cord injury, muscular dystrophy, multiple sclerosis, and cerebral palsy.

Disabil Rehabil 2012 12;34(15):1284-90. Epub 2012 Feb 12.

Clinic for Neurology and Psychiatry for Children and Youth, Belgrade, Serbia.

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http://dx.doi.org/10.3109/09638288.2011.641659DOI Listing
August 2012

Childhood cerebral X-linked adrenoleukodystrophy more than 5 years after hematopoietic cell transplantation: the first case from Serbia and southeastern Europe.

J Child Neurol 2010 Dec 22;25(12):1542-7. Epub 2010 Jul 22.

Clinic for Child Neurology and Psychiatry, Department of Child Neurology, Medical Faculty University of Belgrade, Belgrade, Serbia.

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http://journals.sagepub.com/doi/10.1177/0883073810375117
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http://dx.doi.org/10.1177/0883073810375117DOI Listing
December 2010

Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathy.

Neuromuscul Disord 2009 Feb 23;19(2):167-71. Epub 2009 Jan 23.

Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University, Ziemssenstr. 1a, 80336 München, Germany.

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http://dx.doi.org/10.1016/j.nmd.2008.11.010DOI Listing
February 2009

Arterial ischemic stroke in a child with beta-thalassemia trait and methylentetrahydrofolate reductase mutation.

J Child Neurol 2007 Feb;22(2):208-10

Clinic for Child Neurology and Psychiatry, Medical Faculty, University of Belgrade, Serbia.

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http://dx.doi.org/10.1177/0883073807300306DOI Listing
February 2007

The recurrence risk of ischemic stroke in childhood.

Med Princ Pract 2004 May-Jun;13(3):153-8

Clinic for Child Neurology and Psychiatry, Medical Faculty, University of Belgrade, Belgrade, Serbia and Montenegro.

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http://dx.doi.org/10.1159/000076955DOI Listing
July 2004