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Cerebral blood flow and glucose metabolism in mitochondrial disorders

Neurology, 2000-08, Vol.55 (4), p.544-548

2000

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Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy

Neuropathology and applied neurobiology, 2014-04, Vol.40 (3), p.345-350

2014

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Myotonic dystrophy in two European grey wolves (Canis lupus)

Acta veterinaria Hungarica (Budapest. 1983), 2007-03, Vol.55 (1), p.87-95

2007

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The typical MERRF (A8344G) mutation of the mitochondrial DNA associated with depressive mood disorders

Journal of neurology, 2009-02, Vol.256 (2), p.264-265

2009

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Peripheral nerve and skeletal muscle involvement in CADASIL

Acta neuropathologica, 2005-12, Vol.110 (6), p.587-599

2005

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Marked phenotypic variation in a family with a new myelin protein zero mutation

Neuromuscular disorders : NMD, 2005-11, Vol.15 (11), p.760-763

2005

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Cerebrotendinous xanthomatosis with the c.379 C > T (p. R 127 W ) mutation in the CYP27A1 gene associated with premature age‐associated limbic tauopathy

Neuropathology and applied neurobiology, 2014-04, Vol.40 (3), p.345-350

2014

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Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes

Acta neurologica Scandinavica, 2010-10, Vol.122 (4), p.252-256

2010

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A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases

Annals of the rheumatic diseases, 2013-03, Vol.72 (Suppl 1), p.A49-A49

2013

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Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes

Acta neurologica Scandinavica, 2010-10, Vol.122 (4), p.252-256

2010

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Molecular therapy for genetic muscle diseases : status 1999

Clinical genetics, 1999, Vol.55 (1), p.1-8

1999

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Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature

Clinical neuropathology, 2008-09, Vol.27 (5), p.289-294

2008

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Challenging previous conceptions of vegetarianism and eating disorders

Eating and weight disorders, 2006-12, Vol.11 (4), p.195-200

2006

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The effect of the CYP 2C192 polymorphism on stroke care

Acta physiologica Hungarica, 2012-03, Vol.99 (1), p.33-39

2012

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Factors Influencing the Efficacy, Longevity, and Safety of Electroporation-Assisted Plasmid-Based Gene Transfer into Mouse Muscles

Molecular therapy, 2004-09, Vol.10 (3), p.447-455

2004

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Complement fragments and the pathogenesis of polymyositis

Molecular immunology, 2011-08, Vol.48 (14), p.1731-1731

2011

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Lighting for greenhouse vegetable production--an overview

Canadian journal of plant science, 1989-10, Vol.69 (4), p.1309-1326

1989

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Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes: New mitochondrial tRNALys mutation with dystonia

Acta neurologica Scandinavica, 2010-10, Vol.122 (4), p.252-256

2010

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Novel heteroplasmic mutation in the Lys anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes

Acta neurologica Scandinavica, 2010, Vol.122 (4), p.252-256

2010

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The prion protein in human neuromuscular diseases

The Journal of pathology, 2004-11, Vol.204 (3), p.241-247

2004

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A7.4Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases

Annals of the rheumatic diseases, 2013-03, Vol.72 (Suppl 1), p.A49-A49

2013

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Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy

Neuropathology and applied neurobiology, 2014, Vol.40 (3), p.345-350

2014

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Beneficial effect of epidural anesthesia on oxygen consumption in a parturient with adult respiratory distress syndrome

Southern medical journal (Birmingham, Ala.), 1993-03, Vol.86 (3), p.361-363

1993

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Studies of the rooting of cuttings of Hydrangea macrophylla : enzyme changes

Canadian journal of botany, 1972-02, Vol.50 (2), p.315-322

1972

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Growth of Crystalline Silicon Carbide by CVD Using Chlorosilane Gases

MRS proceedings, 2006, Vol.911, Article 0911-B02-03

2006

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Cerebral blood flow and glucose metabolism in mitochondrial disorders

Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy

Myotonic dystrophy in two European grey wolves (Canis lupus)

The typical MERRF (A8344G) mutation of the mitochondrial DNA associated with depressive mood disorders

Peripheral nerve and skeletal muscle involvement in CADASIL

Marked phenotypic variation in a family with a new myelin protein zero mutation

Cerebrotendinous xanthomatosis with the c.379 C > T (p. R 127 W ) mutation in the CYP27A1 gene associated with premature age‐associated limbic tauopathy

Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes

A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases

Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes

Molecular therapy for genetic muscle diseases : status 1999

Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature

Challenging previous conceptions of vegetarianism and eating disorders

The effect of the CYP 2C192 polymorphism on stroke care

Factors Influencing the Efficacy, Longevity, and Safety of Electroporation-Assisted Plasmid-Based Gene Transfer into Mouse Muscles

Complement fragments and the pathogenesis of polymyositis

Lighting for greenhouse vegetable production--an overview

Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes: New mitochondrial tRNALys mutation with dystonia

Novel heteroplasmic mutation in the Lys anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes

The prion protein in human neuromuscular diseases

A7.4Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases

Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy

Beneficial effect of epidural anesthesia on oxygen consumption in a parturient with adult respiratory distress syndrome

Studies of the rooting of cuttings of Hydrangea macrophylla : enzyme changes

Growth of Crystalline Silicon Carbide by CVD Using Chlorosilane Gases

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