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Refinado por: autor: Finsterer, Josef remover
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31
Neuromuscular Aspects of Channelopathies With Left-Ventricular Hypertrabeculation/Noncompaction
Neuromuscular Aspects of Channelopathies With Left-Ventricular Hypertrabeculation/Noncompaction
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Neuromuscular Aspects of Channelopathies With Left-Ventricular Hypertrabeculation/Noncompaction

Stöllberger, Claudia ; Finsterer, Josef

Pediatric cardiology, 2012-10, Vol.33 (7), p.1235-1237 [Periódico revisado por pares]

New York: Springer-Verlag

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32
Noncompaction in Healthy Subjects, Dilated and Hypertrophic Cardiomyopathy, and Neuromuscular Disorders Is the Same Entity
Noncompaction in Healthy Subjects, Dilated and Hypertrophic Cardiomyopathy, and Neuromuscular Disorders Is the Same Entity
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Noncompaction in Healthy Subjects, Dilated and Hypertrophic Cardiomyopathy, and Neuromuscular Disorders Is the Same Entity

Stollberger, Claudia ; Finsterer, Josef

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2015-04, Vol.25 (2), p.e511-e511 [Periódico revisado por pares]

Iran: Tehran University of Medical Sciences

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33
Thromboembolism and ventricular thrombus in non-neuromuscular noncompaction
Thromboembolism and ventricular thrombus in non-neuromuscular noncompaction
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Thromboembolism and ventricular thrombus in non-neuromuscular noncompaction

Stöllberger, Claudia ; Kolussi, Thomas ; Umschaden, Heinz Werner ; Finsterer, Josef

International journal of cardiology, 2011-08, Vol.151 (1), p.124-125 [Periódico revisado por pares]

Shannon: Elsevier Ireland Ltd

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34
Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”
Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”
Material Type:
Artigo 		Adicionar ao Meu Espaço

Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”

Finsterer, Josef ; Zarrouk-Mahjoub, Sinda

Circulation. Cardiovascular genetics, 2016-12, Vol.9 (6), p.579-579 [Periódico revisado por pares]

United States: American Heart Association, Inc

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35
Is Surgical Removal of the Noncompacted Layer the Clue to Treat Left Ventricular Hypertrabeculation/Noncompaction?
Is Surgical Removal of the Noncompacted Layer the Clue to Treat Left Ventricular Hypertrabeculation/Noncompaction?
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Is Surgical Removal of the Noncompacted Layer the Clue to Treat Left Ventricular Hypertrabeculation/Noncompaction?

Stöllberger, Claudia ; Finsterer, Josef

Journal of cardiac surgery, 2014-11, Vol.29 (6), p.837-838 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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36
Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder
Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder
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Trifunctional Protein Deficiency Due to HADHB Mutations Is a Multisystem, β-Oxidation Disorder

Finsterer, Josef ; Zarrouk-Mahjoub, Sinda

Archives of Iranian medicine, 2017-12, Vol.20 (12), p.767 [Periódico revisado por pares]

Iran: Academy of Medical Sciences of I.R. Iran

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37
Letter by Stollberger and Finsterer regarding article, "mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center"
Letter by Stollberger and Finsterer regarding article, "mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center"
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Letter by Stollberger and Finsterer regarding article, "mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center"

Stöllberger, Claudia ; Finsterer, Josef

Circulation (New York, N.Y.), 2014-01, Vol.129 (3), p.e299-e299 [Periódico revisado por pares]

United States

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38
Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy
Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy
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Corticosteroid treatment retards development of ventricular dysfunction in Duchenne muscular dystrophy

Finsterer, Josef ; Stöllberger, Claudia

Neuromuscular disorders : NMD, 2009-01, Vol.19 (1), p.74-74 [Periódico revisado por pares]

England: Elsevier B.V

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39
Thorough search for myopathy increases the prevalence of noncompaction
Thorough search for myopathy increases the prevalence of noncompaction
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Thorough search for myopathy increases the prevalence of noncompaction

Finsterer, Josef ; Stöllberger, Claudia

International journal of cardiology, 2010-09, Vol.144 (1), p.64-65 [Periódico revisado por pares]

Netherlands: Elsevier Ireland Ltd

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40
Noncompaction in Neuromuscular Disorders Is Not at Variance From Noncompaction in Chromosomal Disorders, Congenital, or Non-Hereditary Disease
Noncompaction in Neuromuscular Disorders Is Not at Variance From Noncompaction in Chromosomal Disorders, Congenital, or Non-Hereditary Disease
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Noncompaction in Neuromuscular Disorders Is Not at Variance From Noncompaction in Chromosomal Disorders, Congenital, or Non-Hereditary Disease

Finsterer, Josef, MD, PhD ; Stöllberger, Claudia, MD

The American journal of cardiology, 2012-04, Vol.109 (7), p.1083-1084 [Periódico revisado por pares]

United States: Elsevier Inc

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