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Ruler Visibility and Popular Belonging in the Ottoman Empire, 1808-1908

Stephanov, Darin N

1, 2018

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Ruler Visibility and Popular Belonging in the Ottoman Empire, 1808-1908

Darin N. Stephanov

2018

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Drug-induced hyperthermia with rhabdomyolysis in CLN3 disease

European journal of paediatric neurology, 2022-07, Vol.39, p.74-78

2022

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Product Unbundling in the Travel Industry: The Economics of Airline Bag Fees

Journal of economics & management strategy, 2015-09, Vol.24 (3), p.457-484

2015

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The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interaction

Genes and immunity, 2017-03, Vol.18 (2), p.75-81

2017

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A novel mutation in EPG5 cause Vici syndrome with vacuolar myopathy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S192-S193

2016

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Using the method of biotesting to assess the toxicity of waste medical and biological practices containing nanomaterials

IOP conference series. Earth and environmental science, 2019-11, Vol.337 (1), p.12012

2019

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Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1

European journal of neurology, 2017-04, Vol.24 (4), p.587-593

2017

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Congenital mitochondrial encephalomyopathy with complex I deficiency due to mutations in sideroflexin 4 (SFXN4)

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S175-S175

2016

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Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden

Neuromuscular disorders : NMD, 2000-01, Vol.10 (1), p.1-9

2000

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Cerebrospinal fluid neurofilament light protein as a diagnostic and prognostic biomarker in mitochondrial diseases with CNS involvement

European journal of paediatric neurology, 2017-06, Vol.21, p.e1-e1

2017

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Ophthalmological findings in children and young adults with genetically verified mitochondrial disease

British journal of ophthalmology, 2010-01, Vol.94 (1), p.121-127

2010

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New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7

Neurology, 2007-06, Vol.68 (23), p.2041

2007

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Metal−Olefin Bond Energies in M(CO)5(C2H4-n Cl n ) M = Cr, Mo, W; n = 0−4: Electron-Withdrawing Olefins Do Not Increase the Bond Strength

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2009-09, Vol.113 (35), p.9692-9699

2009

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Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I

European journal of paediatric neurology, 2007-11, Vol.11 (6), p.353-357

2007

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New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations

Neurology, 2008-12, Vol.71 (23), p.1896

2008

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S.P.31 What was the age and cause of death in patients with Duchenne muscular dystrophy in Sweden during 2000–2010?

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.880-881

2012

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Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes

Journal of inherited metabolic disease, 2017-03, Vol.40 (2), p.237-245

2017

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P5.76 Muscular dystrophies and congenital myopathies in childhood

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.746-747

2011

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ALLIANCES, CODESHARING, ANTITRUST IMMUNITY, AND INTERNATIONAL AIRFARES: DO PREVIOUS PATTERNS PERSIST?

Journal of competition law & economics, 2011-09, Vol.7 (3), p.573-602

2011

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Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

Molecular genetics and metabolism, 2002-09, Vol.77 (1-2), p.21-30

2002

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OP5 – 2696: Pyruvate dehydrogenase complex deficiency: Phenotype–genotype, phenotype–neuroimaging associations and treatment outcomes

European journal of paediatric neurology, 2015-05, Vol.19, p.S2-S2

2015

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OP6 – 2631: Decreased free-thiamine in cerebro spinal fluid and fibroblasts is a sensitive marker of thiamine transporter 2 deficiency in Leigh syndrome patients

European journal of paediatric neurology, 2015-05, Vol.19, p.S2-S3

2015

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D.I.2 Myosin myopathies and distal arthrogryposis syndromes

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.635-635

2010

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Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients

Journal of medical genetics, 2018-01, Vol.55 (1), p.21

2018

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Ruler Visibility and Popular Belonging in the Ottoman Empire, 1808-1908

Ruler Visibility and Popular Belonging in the Ottoman Empire, 1808-1908

Drug-induced hyperthermia with rhabdomyolysis in CLN3 disease

Product Unbundling in the Travel Industry: The Economics of Airline Bag Fees

The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene-environment interaction

A novel mutation in EPG5 cause Vici syndrome with vacuolar myopathy

Using the method of biotesting to assess the toxicity of waste medical and biological practices containing nanomaterials

Benign mitochondrial myopathy with exercise intolerance in a large multigeneration family due to a homoplasmic m.3250T>C mutation in MTTL1

Congenital mitochondrial encephalomyopathy with complex I deficiency due to mutations in sideroflexin 4 (SFXN4)

Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden

Cerebrospinal fluid neurofilament light protein as a diagnostic and prognostic biomarker in mitochondrial diseases with CNS involvement

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease

New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7

Metal−Olefin Bond Energies in M(CO)5(C2H4-n Cl n ) M = Cr, Mo, W; n = 0−4: Electron-Withdrawing Olefins Do Not Increase the Bond Strength

Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I

New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations

S.P.31 What was the age and cause of death in patients with Duchenne muscular dystrophy in Sweden during 2000–2010?

Ketogenic diet in pyruvate dehydrogenase complex deficiency: short- and long-term outcomes

P5.76 Muscular dystrophies and congenital myopathies in childhood

ALLIANCES, CODESHARING, ANTITRUST IMMUNITY, AND INTERNATIONAL AIRFARES: DO PREVIOUS PATTERNS PERSIST?

Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits

OP5 – 2696: Pyruvate dehydrogenase complex deficiency: Phenotype–genotype, phenotype–neuroimaging associations and treatment outcomes

OP6 – 2631: Decreased free-thiamine in cerebro spinal fluid and fibroblasts is a sensitive marker of thiamine transporter 2 deficiency in Leigh syndrome patients

D.I.2 Myosin myopathies and distal arthrogryposis syndromes

Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients

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