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Coating of PLA-nanoparticles with cyclic, arginine-rich cell penetrating peptides enables oral delivery of liraglutide

Nanomedicine, 2020-02, Vol.24, p.102132-102132, Article 102132

2020

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Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle

Journal of molecular medicine (Berlin, Germany), 2012-10, Vol.90 (10), p.1145-1160

2012

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Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

The Lancet (British edition), 1999-08, Vol.354 (9177), p.477-479

1999

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A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency

Human molecular genetics, 2000-05, Vol.9 (8), p.1245-1249

2000

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Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita

Acta neurologica Scandinavica, 2010-02, Vol.121 (2), p.131-135

2010

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Infliximab is an appropriate second‐line therapy in infants with steroid refractory pyoderma gangrenosum

Journal of the European Academy of Dermatology and Venereology, 2022-05, Vol.36 (5), p.e376-e378

2022

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Rapid development of life-threatening complete atrioventricular block in Kearns-Sayre syndrome

European journal of pediatrics, 2009-06, Vol.168 (6), p.757-759

2009

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Mutations in SURF1 are not specifically associated with Leigh syndrome

Journal of medical genetics, 2001-02, Vol.38 (2), p.109-113

2001

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A High Rate (20%–30%) of Parental Consanguinity in Cytochrome-Oxidase Deficiency

American journal of human genetics, 1998-08, Vol.63 (2), p.428-435

1998

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One-step single-chain Fv recombinant antibody-based purification of gp96 for vaccine development

Cancer research (Chicago, Ill.), 2000-08, Vol.60 (15), p.4175-4178

2000

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The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

European journal of pediatrics, 1999, Vol.158 (1), p.55-58

1999

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Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

The Journal of pediatrics, 2001-07, Vol.139 (1), p.111-116

2001

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ACOX1 Gain-of-Function Variant in Two German Pediatric Patients, in One Case Mimicking Autoimmune Inflammatory Disease

Neuropediatrics, 2024-04, Vol.55 (2), p.140

2024

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Mitochondriale Erkrankungen: Eine klinische und diagnostische Herausforderung

Medizinische Genetik, 2009-09, Vol.21 (3), p.358-366

2009

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Melan-A/MART1 analog peptide triggers anti-myeloma T-cells through crossreactivity with HM1.24

Journal of immunotherapy, 2009-07, Vol.32 (6), p.613-621

2009

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Ex vivo perfusion with mitomycin C containing solution prolongs heart graft survival in rats

Transplantation, 2006-12, Vol.82 (11), p.1537

2006

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Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency

The Journal of pediatrics, 2000-02, Vol.136 (2), p.209-214

2000

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Alice im digitalen Wunderland: pädiatrische Lehre in der COVID-19-Pandemie: Eine Umfrage und Stellungnahme der AG Lehre der Deutschen Gesellschaft für Kinder- und Jugendmedizin (DGKJ)

Monatsschrift Kinderheilkunde, 2021-02, Vol.169 (2), p.151-158

2021

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For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?

Mechanisms of ageing and development, 2000-04, Vol.114 (3), p.201-206

2000

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Iron overload and mitochondrial diseases

The Lancet (British edition), 1998-04, Vol.351 (9111), p.1286-1287

1998

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Suppressive dendritic cells as a tool for controlling allograft rejection in organ transplantation: Promises and difficulties

Human immunology, 2008-03, Vol.69 (3), p.165-173

2008

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Distinct phenotype of CD19-specific CAR T cells generated from healthy donor vs. patient lymphocytes using either IL-7/IL-15 or IL-2

Oncology research and treatment, 2017, Vol.40, p.213

2017

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T cell stimulation with different cytokines results in distinct phenotypes and cytotoxic activity of CD19-specific CART cells

Oncology research and treatment, 2016, Vol.39 (S3), p.136

2016

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Mitochondrial diseases - an expanding spectrum of disorders and affected genes

Experimental physiology, 2003-01, Vol.88 (1), p.155-166

2003

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Coating of PLA-nanoparticles with cyclic, arginine-rich cell penetrating peptides enables oral delivery of liraglutide

Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle

Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency

Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita

Infliximab is an appropriate second‐line therapy in infants with steroid refractory pyoderma gangrenosum

Rapid development of life-threatening complete atrioventricular block in Kearns-Sayre syndrome

Mutations in SURF1 are not specifically associated with Leigh syndrome

A High Rate (20%–30%) of Parental Consanguinity in Cytochrome-Oxidase Deficiency

One-step single-chain Fv recombinant antibody-based purification of gp96 for vaccine development

Mémoires des migrations, temps de l’histoire

The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

ACOX1 Gain-of-Function Variant in Two German Pediatric Patients, in One Case Mimicking Autoimmune Inflammatory Disease

Mitochondriale Erkrankungen: Eine klinische und diagnostische Herausforderung

Melan-A/MART1 analog peptide triggers anti-myeloma T-cells through crossreactivity with HM1.24

Ex vivo perfusion with mitomycin C containing solution prolongs heart graft survival in rats

Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency

Alice im digitalen Wunderland: pädiatrische Lehre in der COVID-19-Pandemie: Eine Umfrage und Stellungnahme der AG Lehre der Deutschen Gesellschaft für Kinder- und Jugendmedizin (DGKJ)

For debate: defective mitochondria, free radicals, cell death, aging-reality or myth-ochondria?

Iron overload and mitochondrial diseases

Suppressive dendritic cells as a tool for controlling allograft rejection in organ transplantation: Promises and difficulties

Distinct phenotype of CD19-specific CAR T cells generated from healthy donor vs. patient lymphocytes using either IL-7/IL-15 or IL-2

T cell stimulation with different cytokines results in distinct phenotypes and cytotoxic activity of CD19-specific CART cells

Mitochondrial diseases - an expanding spectrum of disorders and affected genes

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