Albena Jordanova

Albena Jordanova

UNVERIFIED PROFILE

Are you Albena Jordanova?   Register this Author

Register author
Albena Jordanova

Albena Jordanova

Publications by authors named "Albena Jordanova"

Are you Albena Jordanova?   Register this Author

89Publications

3705Reads

5Profile Views

Peripheral myelin protein 2 - a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy.

Orphanet J Rare Dis 2019 08 14;14(1):197. Epub 2019 Aug 14.

Molecular Neurogenomics group, VIB-UAntwerp Centre for Molecular Neurology, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
https://ojrd.biomedcentral.com/articles/10.1186/s13023-019-1
Publisher Site
http://dx.doi.org/10.1186/s13023-019-1162-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692960PMC
August 2019

Transthyretin familial amyloid polyneuropathy due to lle107Val mutation mimicking atypical chronic inflammatory demyelinating polyneuropathy: case report.

Acta Neurol Belg 2018 Dec 17. Epub 2018 Dec 17.

Molecular Neurogenomics Group, VIB-UAntwerp Center for Molecular Neurology, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s13760-018-01069-0
Publisher Site
http://dx.doi.org/10.1007/s13760-018-01069-0DOI Listing
December 2018

Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability.

Gene 2018 Aug 9;667:45-55. Epub 2018 May 9.

Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, 2 Zdrave str., 1431 Sofia, Bulgaria. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.gene.2018.05.015DOI Listing
August 2018

Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome.

Seizure 2018 Jan 28;54:41-44. Epub 2017 Nov 28.

Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical University - Sofia, Sofia, Bulgaria; VIB Department of Molecular Genetics, Molecular Neurogenomics Group, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2017.11.014DOI Listing
January 2018

Axonal neuropathy with neuromyotonia: there is a HINT.

Brain 2017 Apr;140(4):868-877

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB and University of Antwerp, Antwerpen 2610, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/aww301DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382946PMC
April 2017

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Hum Mutat 2017 03 19;38(3):297-309. Epub 2017 Jan 19.

Center for Molecular Neurology, VIB, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.23161DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324646PMC
March 2017

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.

View Article

Download full-text PDF

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

Creatine Deficiency Syndrome could be Missed Easily: A Case Report of Guanidinoacetate Methyltransferase Deficiency Presented with Neurodevelopmental Delay, Seizures, and Behavioral Changes, but Normal Structural MRI.

Ann Clin Lab Sci 2016 Sep;46(5):557-61

National Genetic Laboratory, University Hospital of Obstetrics and Gynecology, Sofia; Department of Analytical Chemistry, Sofia University "St. Kl. Ohridsky", Sofia, Bulgaria.

View Article

Download full-text PDF

Source
September 2016

Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

J Neurol 2016 Mar 2;263(3):467-76. Epub 2016 Jan 2.

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Universiteitsplein 1, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-015-7989-8DOI Listing
March 2016

NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype.

J Neurol 2016 Feb 8;263(2):361-369. Epub 2015 Dec 8.

Molecular Neurogenomics Group, VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-015-7985-zDOI Listing
February 2016

Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy.

Brain 2015 Nov 10;138(Pt 11):e392. Epub 2015 Jun 10.

2 Institute for Neuroscience and Muscle Research, Children's Hospital at Westmead, New South Wales, 2145, Australia 3 Discipline of Paediatrics and Child Health, Faculty of Medicine, The University of Sydney, Sydney, New South Wales, 2006, Australia 24 Murdoch Children's Research Institute. The Royal Children's Hospital. Parkville Victoria 3052 Australia 25 Department of Paediatrics, University of Melbourne Parkville Victoria 3010 Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awv160DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719680PMC
November 2015

Reply: Mutations in TUBB4A and spastic paraplegia.

Mov Disord 2015 Nov 19;30(13):1858-9. Epub 2015 Oct 19.

Medical University of Sofia, Faculty of Medicine, Department of Neurology, Clinic of Neurology, University Hospital Alexandrovska, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.26442DOI Listing
November 2015

Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia.

Mov Disord 2015 May 15;30(6):854-8. Epub 2015 Mar 15.

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.26196DOI Listing
May 2015

NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.

J Neurol 2015 May 1;262(5):1289-300. Epub 2015 Apr 1.

Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria (UC) and "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-015-7709-4DOI Listing
May 2015

A novel AARS mutation in a family with dominant myeloneuropathy.

Neurology 2015 May 22;84(20):2040-7. Epub 2015 Apr 22.

From the Department of Neurology (W.W.M., S.S.S.), Perelman School of Medicine, University of Pennsylvania, Philadelphia; the Cellular and Molecular Biology Program (L.B.G., A.A.), Medical Science Training Program (L.B.G.), and the Departments of Human Genetics (A.A.) and Neurology (A.A.), University of Michigan Medical School, Ann Arbor; the Neurogenetics Group (I.M., J.B., P.D.J.) and the Molecular Neurogenomics Group (E.D.V., A.J.), VIB, Department of Molecular Genetics, University of Antwerp; the Neurogenetics Laboratory (I.M., J.B., E.D.V., P.D.J., A.J.), Institute Born-Bunge, University of Antwerp; and the Department of Neurology (J.B., P.D.J.), Antwerp University Hospital, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000001583DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4442103PMC
May 2015

Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies.

Hum Mutat 2015 Mar;36(3):287-91

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.22744DOI Listing
March 2015

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2.

Brain 2015 Feb 14;138(Pt 2):293-310. Epub 2014 Dec 14.

2 Institute for Neuroscience and Muscle Research, Children's Hospital at Westmead, New South Wales, 2145, Australia 3 Discipline of Paediatrics and Child Health, Faculty of Medicine, The University of Sydney, Sydney, New South Wales, 2006, Australia 24 Murdoch Children's Research Institute. The Royal Children's Hospital, Parkville Victoria 3052 Australia 25 Department of Paediatrics, University of Melbourne Parkville Victoria 3010 Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awu356DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306822PMC
February 2015

Cognitive, neuropsychiatric, and motor features associated with apolipoprotein E ε4 allele in a sample of Bulgarian patients with late-onset Parkinson's disease.

Am J Alzheimers Dis Other Demen 2014 Nov 18;29(7):614-9. Epub 2014 Mar 18.

Clinic of Neurology, University Hospital Alexandrovska, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1533317514525655DOI Listing
November 2014

Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies.

Brain 2014 Nov 25;137(Pt 11):2879-96. Epub 2014 Jun 25.

1 Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerpen 2610, Belgium 2 Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerpen 2610, Belgium 4 Department of Medical Chemistry and Biochemistry, Molecular Medicine Centre, Medical University-Sofia, Sofia 1431, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awu169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208460PMC
November 2014

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:

View Article

Download full-text PDF

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

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

Acta Neuropathol 2014 Sep 5;128(3):397-410. Epub 2014 Jun 5.

Department of Molecular Genetics, VIB, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00401-014-1298-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131163PMC
September 2014

CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila.

Neurobiol Dis 2014 Aug 5;68:180-9. Epub 2014 May 5.

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, University of Antwerp, Antwerp 2610, Belgium; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp 2610, Belgium. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nbd.2014.04.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086162PMC
August 2014

Lack of neuropathy-related phenotypes in hint1 knockout mice.

J Neuropathol Exp Neurol 2014 Jul;73(7):693-701

From The Jackson Laboratory, Bar Harbor (KLS, KHM, RWB); Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono (KHM, RWB), Maine; and Vlaams Instituut voor Biotechnologie Department of Molecular Genetics (AJ) and Neurogenetics Laboratory, Institute Born-Bunge (AJ), University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/NEN.0000000000000085DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098130PMC
July 2014

Human Rab7 mutation mimics features of Charcot-Marie-Tooth neuropathy type 2B in Drosophila.

Neurobiol Dis 2014 May 9;65:211-9. Epub 2014 Feb 9.

Molecular Genetics Department, VIB, University of Antwerp, B-2610 Antwerpen, Belgium; Neurogenetics Laboratory, Institute Born Bunge, University of Antwerp, B-2610 Antwerpen, Belgium. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nbd.2014.01.021DOI Listing
May 2014

Biochemical and biophysical investigation of surfactant in neonatal gastric aspirate at birth.

Acta Med Port 2013 Jan-Feb;26(1):33-8. Epub 2013 Apr 24.

Faculty of Biology, University of Sofia, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
April 2014

Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy.

Hum Mol Genet 2013 Aug 4;22(15):2975-83. Epub 2013 Apr 4.

Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, Finland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddt149DOI Listing
August 2013

Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance.

Am J Hum Genet 2013 Jun 9;92(6):955-64. Epub 2013 May 9.

Molecular Neurogenomics Group, Department of Molecular Genetics, VIB, Antwerp 2610, Belgium; Neurogenetics Laboratory, Institute Born-Bunge, University of Antwerp, Antwerp 2610, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2013.04.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675262PMC
June 2013

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

Authors:
Julie van der Zee Ilse Gijselinck Lubina Dillen Tim Van Langenhove Jessie Theuns Sebastiaan Engelborghs Stéphanie Philtjens Mathieu Vandenbulcke Kristel Sleegers Anne Sieben Veerle Bäumer Githa Maes Ellen Corsmit Barbara Borroni Alessandro Padovani Silvana Archetti Robert Perneczky Janine Diehl-Schmid Alexandre de Mendonça Gabriel Miltenberger-Miltenyi Sónia Pereira José Pimentel Benedetta Nacmias Silvia Bagnoli Sandro Sorbi Caroline Graff Huei-Hsin Chiang Marie Westerlund Raquel Sanchez-Valle Albert Llado Ellen Gelpi Isabel Santana Maria Rosário Almeida Beatriz Santiago Giovanni Frisoni Orazio Zanetti Cristian Bonvicini Matthis Synofzik Walter Maetzler Jennifer Müller Vom Hagen Ludger Schöls Michael T Heneka Frank Jessen Radoslav Matej Eva Parobkova Gabor G Kovacs Thomas Ströbel Stayko Sarafov Ivailo Tournev Albena Jordanova Adrian Danek Thomas Arzberger Gian Maria Fabrizi Silvia Testi Eric Salmon Patrick Santens Jean-Jacques Martin Patrick Cras Rik Vandenberghe Peter Paul De Deyn Marc Cruts Christine Van Broeckhoven Julie van der Zee Ilse Gijselinck Lubina Dillen Tim Van Langenhove Jessie Theuns Stéphanie Philtjens Kristel Sleegers Veerle Bäumer Githa Maes Ellen Corsmit Marc Cruts Christine Van Broeckhoven Julie van der Zee Ilse Gijselinck Lubina Dillen Tim Van Langenhove Stéphanie Philtjens Jessie Theuns Kristel Sleegers Veerle Bäumer Githa Maes Marc Cruts Christine Van Broeckhoven Sebastiaan Engelborghs Peter P De Deyn Patrick Cras Sebastiaan Engelborghs Peter P De Deyn Mathieu Vandenbulcke Mathieu Vandenbulcke Barbara Borroni Alessandro Padovani Silvana Archetti Robert Perneczky Janine Diehl-Schmid Matthis Synofzik Walter Maetzler Jennifer Müller Vom Hagen Ludger Schöls Matthis Synofzik Walter Maetzler Jennifer Müller Vom Hagen Ludger Schöls Michael T Heneka Frank Jessen Alfredo Ramirez Delia Kurzwelly Carmen Sachtleben Wolfgang Mairer Alexandre de Mendonça Gabriel Miltenberger-Miltenyi Sónia Pereira Clara Firmo José Pimentel Raquel Sanchez-Valle Albert Llado Anna Antonell Jose Molinuevo Ellen Gelpi Caroline Graff Huei-Hsin Chiang Marie Westerlund Caroline Graff Anne Kinhult Ståhlbom Håkan Thonberg Inger Nennesmo Anne Börjesson-Hanson Benedetta Nacmias Silvia Bagnoli Sandro Sorbi Valentina Bessi Irene Piaceri Isabel Santana Beatriz Santiago Isabel Santana Maria Helena Ribeiro Maria Rosário Almeida Catarina Oliveira João Massano Carolina Garret Paula Pires Giovanni Frisoni Orazio Zanetti Cristian Bonvicini Stayko Sarafov Ivailo Tournev Albena Jordanova Ivailo Tournev Gabor G Kovacs Thomas Ströbel Michael T Heneka Frank Jessen Alfredo Ramirez Delia Kurzwelly Carmen Sachtleben Wolfgang Mairer Frank Jessen Radoslav Matej Eva Parobkova Adrian Danel Thomas Arzberger Gian Maria Fabrizi Silvia Testi Sergio Ferrari Tiziana Cavallaro Eric Salmon Patrick Santens Patrick Cras

Hum Mutat 2013 Feb 4;34(2):363-73. Epub 2013 Jan 4.

Department of Molecular Genetics, VIB, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.22244DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638346PMC
February 2013

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Hum Mol Genet 2012 Dec 4;21(24):5359-72. Epub 2012 Sep 4.

Institute for Medical Biometry, Informatic and Epidemiology, University of Bonn, Bonn, Germany.

View Article

Download full-text PDF

Source
http://hmg.oxfordjournals.org/content/21/24/5359.full.pdf
Web Search
http://www.hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/dds373
Publisher Site
http://dx.doi.org/10.1093/hmg/dds373DOI Listing
December 2012

Drosophila as a platform to predict the pathogenicity of novel aminoacyl-tRNA synthetase mutations in CMT.

Amino Acids 2012 May 8;42(5):1661-8. Epub 2011 Mar 8.

Department of Molecular Genetics, VIB, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00726-011-0868-4DOI Listing
May 2012

Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation.

J Neurol 2011 Aug 19;258(8):1413-21. Epub 2011 Feb 19.

Service of Neurology, University Hospital "Marqués de Valdecilla" (IFIMAV), "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas" (CIBERNED), University of Cantabria (UC), 39008 Santander, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-011-5947-7DOI Listing
August 2011

Surface chemistry study of the interactions of benzalkonium chloride with films of meibum, corneal cells lipids, and whole tears.

Invest Ophthalmol Vis Sci 2011 Jun 28;52(7):4645-54. Epub 2011 Jun 28.

Department of Biochemistry, Faculty of Biology, University of Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1167/iovs.10-6271DOI Listing
June 2011

Alterations in the content and physiological role of sphingomyelin in plasma membranes of cells cultured in three-dimensional matrix.

Mol Cell Biochem 2010 Jul 23;340(1-2):215-22. Epub 2010 Feb 23.

Department of Lipid-Protein Interactions, Institute of Biophysics, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11010-010-0420-yDOI Listing
July 2010

The SCN1A variant database: a novel research and diagnostic tool.

Hum Mutat 2009 Oct;30(10):E904-20

Neurogenetics Group, VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.21083DOI Listing
October 2009

Surface properties and behavior of lipid extracts from plasma membranes of cells cultured as monolayer and in tissue-like conditions.

Cell Biochem Biophys 2009 30;54(1-3):47-55. Epub 2009 May 30.

Department of Lipid-Protein Interactions, Institute of Biophysics, Bulgarian Academy of Sciences, 1113, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12013-009-9050-yDOI Listing
August 2009

Influence of surfactant protein C on the interfacial behavior of phosphatidylethanolamine monolayers.

Eur Biophys J 2009 Apr 1;38(4):369-79. Epub 2008 Nov 1.

Department of Lipid-Protein Interactions, Institute of Biophysics, Bulgarian Academy of Sciences, 1113, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00249-008-0380-2DOI Listing
April 2009

Unraveling the genetics of distal hereditary motor neuronopathies.

Neuromolecular Med 2006 ;8(1-2):131-46

Peripheral Neuropathy Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerpen, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1385/nmm:8:1-2:131DOI Listing
March 2007

Rhamnolipid biosurfactants produced by Renibacterium salmoninarum 27BN during growth on n-hexadecane.

Z Naturforsch C J Biosci 2004 Jan-Feb;59(1-2):70-4

Institute of Microbiology, Bulgarian Academy of Sciences, Acad. G. Bonchev str, bl 26, 1113 Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1515/znc-2004-1-215DOI Listing
May 2004

Effect of halothane on lung carcinoma cells A 549.

Chem Biol Interact 2003 Oct;146(2):191-200

Department of Cell biology, Faculty of Biology, Sofia University, St. Kliment Ohridski, 8 Dragan Tsankov blv, 1164 Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cbi.2003.08.002DOI Listing
October 2003

Formation of monolayers and bilayer foam films from lamellar, inverted hexagonal and cubic lipid phases.

Eur Biophys J 2003 Feb 1;31(8):626-32. Epub 2002 Nov 1.

Institute of Biophysics, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00249-002-0263-xDOI Listing
February 2003

Spinal muscular atrophy among the Roma (Gypsies) in Bulgaria and Hungary.

Neuromuscul Disord 2002 May;12(4):378-85

Laboratory of Molecular Pathology, Sofia Medical University, Sofia, Bulgaria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0960-8966(01)00283-8DOI Listing
May 2002