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Pseudotumor cerebri in childhood and adolescence -- results of a Germany-wide ESPED-survey

Klinische Padiatrie, 2013-03, Vol.225 (2), p.81

2013

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Neuromyelitis optica and pregnancy during therapeutic B cell depletion: infant exposure to anti-AQP4 antibody and prevention of rebound relapses with low-dose rituximab postpartum

Multiple sclerosis, 2013-10, Vol.19 (11), p.1544-1547

2013

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Paraneoplastic limbic encephalitis with SOX1 and PCA2 antibodies and relapsing neurological symptoms in an adolescent with Hodgkin lymphoma

European journal of paediatric neurology, 2017-07, Vol.21 (4), p.661-665

2017

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Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations

European journal of paediatric neurology, 2017-06, Vol.21, p.e128-e129

2017

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PP04.10 – 2544: Trichothiodystrophy presenting with cardiomyopathy and recurrent arterial ischemic strokes

European journal of paediatric neurology, 2015-05, Vol.19, p.S44-S44

2015

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Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency

Cell calcium (Edinburgh), 2008-07, Vol.44 (1), p.123-133

2008

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Phytanic acid impairs mitochondrial respiration through protonophoric action

Cellular and molecular life sciences : CMLS, 2007-12, Vol.64 (24), p.3271-3281

2007

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Granulocyte colony stimulating factor for treatment of neutropenia-associated infection in Pearson syndrome

Klinische Padiatrie, 2014-05, Vol.226 (3), p.190

2014

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Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration

Brain (London, England : 1878), 2016-02, Vol.139 (Pt 2), p.346-354

2016

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Seasonal Variation and Atypical Presentation of Idiopathic Intracranial Hypertension in Pre-Pubertal Children

Cephalalgia, 2007-11, Vol.27 (11), p.1261-1264

2007

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Sedation of children during measurement of CSF opening pressure: lack of standardisation in German children with pseudotumor cerebri

Klinische Padiatrie, 2012-01, Vol.224 (1), p.40-42

2012

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Papilledema in children with an CSF opening pressure below 28 cm H sub(2)O. Is it pseudotumor cerebri though?

Canadian journal of neurological sciences, 2014-05, Vol.41 (3), p.S14-S14

2014

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Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease

Brain (London, England : 1878), 2009-04, Vol.132 (4), p.833-842

2009

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Seltene Erkrankungen mit symmetrischer Beteiligung der Basalganglien

RöFo : Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebende Verfahren, 2013, Vol.185 (9)

2013

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Pseudotumor Cerebri in Childhood and Adolescence - Results of a Germany-wide ESPED-survey

Klinische Pädiatrie, 2013-03, Vol.225 (2), p.81-85

2013

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Antiepileptic Treatment in Paediatric Oncology - An Interdisciplinary Challenge

Klinische Pädiatrie, 2006-11, Vol.218 (6), p.340-349

2006

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Trolox-sensitive reactive oxygen species regulate mitochondrial morphology, oxidative phosphorylation and cytosolic calcium handling in healthy cells

Antioxidants & redox signaling, 2012-12, Vol.17 (12), p.1657-1669

2012

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Mitochondrial dysfunction in primary human fibroblasts triggers an adaptive cell survival program that requires AMPK-α

Biochimica et biophysica acta, 2015-03, Vol.1852 (3), p.529-540

2015

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Granulocyte Colony Stimulating Factor for Treatment of Neutropenia-associated Infection in Pearson Syndrome

Klinische Pädiatrie, 2014-03, Vol.226 (3), p.190-191

2014

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Detection of 6-demethoxyubiquinone in CoQ10 deficiency disorders: Insights into enzyme interactions and identification of potential therapeutics

Molecular genetics and metabolism, 2017-07, Vol.121 (3), p.216-223

2017

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Trichothiodystrophy Presenting with Cardiomyopathy and Recurrent Stroke Episodes

Neuropediatrics, 2014, Vol.45 (S 01)

2014

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Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Rare Causes of Childhood Stroke: A Single-Center Experience

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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Fatal hypertensive crisis as presentation of mitochondrial complex I deficiency

Neuropediatrics, 2007-06, Vol.38 (3), p.148-150

2007

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Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Pseudotumor cerebri in childhood and adolescence -- results of a Germany-wide ESPED-survey

Neuromyelitis optica and pregnancy during therapeutic B cell depletion: infant exposure to anti-AQP4 antibody and prevention of rebound relapses with low-dose rituximab postpartum

Paraneoplastic limbic encephalitis with SOX1 and PCA2 antibodies and relapsing neurological symptoms in an adolescent with Hodgkin lymphoma

Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations

PP04.10 – 2544: Trichothiodystrophy presenting with cardiomyopathy and recurrent arterial ischemic strokes

Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency

Phytanic acid impairs mitochondrial respiration through protonophoric action

Granulocyte colony stimulating factor for treatment of neutropenia-associated infection in Pearson syndrome

Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration

Seasonal Variation and Atypical Presentation of Idiopathic Intracranial Hypertension in Pre-Pubertal Children

Sedation of children during measurement of CSF opening pressure: lack of standardisation in German children with pseudotumor cerebri

Papilledema in children with an CSF opening pressure below 28 cm H sub(2)O. Is it pseudotumor cerebri though?

Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease

Seltene Erkrankungen mit symmetrischer Beteiligung der Basalganglien

Pseudotumor Cerebri in Childhood and Adolescence - Results of a Germany-wide ESPED-survey

Antiepileptic Treatment in Paediatric Oncology - An Interdisciplinary Challenge

Trolox-sensitive reactive oxygen species regulate mitochondrial morphology, oxidative phosphorylation and cytosolic calcium handling in healthy cells

Mitochondrial dysfunction in primary human fibroblasts triggers an adaptive cell survival program that requires AMPK-α

Granulocyte Colony Stimulating Factor for Treatment of Neutropenia-associated Infection in Pearson Syndrome

Detection of 6-demethoxyubiquinone in CoQ10 deficiency disorders: Insights into enzyme interactions and identification of potential therapeutics

Trichothiodystrophy Presenting with Cardiomyopathy and Recurrent Stroke Episodes

Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency

Rare Causes of Childhood Stroke: A Single-Center Experience

Fatal hypertensive crisis as presentation of mitochondrial complex I deficiency

Reversible Epileptic Encephalopathy upon Uridine Treatment in Patients with CAD Mutations

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