Christoffer Ehrstedt

Risk Factors for Traumatic Lumbar Puncture in Children With ALL

Setänen, Sirkku; Harila, Arja; Metsistö, Viola; Ehrstedt, Christoffer

Part of Acta Paediatrica, p. 2713-2715, 2025

• DOI for Risk Factors for Traumatic Lumbar Puncture in Children With ALL
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Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy

Liminga, Gunnar; Ahlbäck, Benjamin; Abu Hamdeh, Sami; Nilsson, Pelle et al.

Part of Acta Paediatrica, 2025

• DOI for Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
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250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation

Donald, A.; Brothwell, S.; Cabello, B. M.; Ehrstedt, Christoffer et al.

Part of Molecular Genetics and Metabolism, 2025

• DOI for 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
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Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension

Ehrstedt, Christoffer; Lehtonen, Mira; Liminga, Gunnar

Part of Pediatric Neurology, p. 65-72, 2023

• DOI for Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension
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Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report

Ehrstedt, Christoffer; Liu, Wei-Wei; Frykholm, Carina; Beeson, David et al.

Part of Neuromuscular Disorders, p. 80-83, 2022

• DOI for Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report
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Risk Factors for Traumatic Lumbar Puncture in Children With ALL

Setänen, Sirkku; Harila, Arja; Metsistö, Viola; Ehrstedt, Christoffer

Part of Acta Paediatrica, p. 2713-2715, 2025

• DOI for Risk Factors for Traumatic Lumbar Puncture in Children With ALL
• Download full text (pdf) of Risk Factors for Traumatic Lumbar Puncture in Children With ALL

Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy

Liminga, Gunnar; Ahlbäck, Benjamin; Abu Hamdeh, Sami; Nilsson, Pelle et al.

Part of Acta Paediatrica, 2025

• DOI for Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
• Download full text (pdf) of Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy

250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation

Donald, A.; Brothwell, S.; Cabello, B. M.; Ehrstedt, Christoffer et al.

Part of Molecular Genetics and Metabolism, 2025

• DOI for 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
• Download full text (pdf) of 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation

Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension

Ehrstedt, Christoffer; Lehtonen, Mira; Liminga, Gunnar

Part of Pediatric Neurology, p. 65-72, 2023

• DOI for Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension
• Download full text (pdf) of Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension

Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report

Ehrstedt, Christoffer; Liu, Wei-Wei; Frykholm, Carina; Beeson, David et al.

Part of Neuromuscular Disorders, p. 80-83, 2022

• DOI for Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report
• Download full text (pdf) of Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report

Prospective registration of symptoms and times to diagnosis in children and adolescents with central nervous system tumors: A study of the Swedish Childhood Cancer Registry

Rask, Olof; Nilsson, Fredrik; Lahteenmaki, Paivi; Ehrstedt, Christoffer et al.

Part of Pediatric Blood & Cancer, 2022

• DOI for Prospective registration of symptoms and times to diagnosis in children and adolescents with central nervous system tumors: A study of the Swedish Childhood Cancer Registry
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Left-handedness should not be overrated as a risk factor for postoperative speech impairment in children after posterior fossa tumour surgery: a prospective European multicentre study

Gronbaek, Jonathan Kjaer; Laustsen, Aske Foldbjerg; Toescu, Sebastian; Pizer, Barry et al.

Part of Child's Nervous System, p. 1479-1485, 2022

• DOI for Left-handedness should not be overrated as a risk factor for postoperative speech impairment in children after posterior fossa tumour surgery: a prospective European multicentre study

Acute disseminated encephalomyelitis with delayed onset and feasibility of the Miethke shunt and sensor reservoir system: a case report

Liminga, Gunnar; Grabowska, Anna; Petursdottir, Dyrleif; Cesarini, Kristina G et al.

Part of Child's Nervous System, p. 3891-3895, 2021

• DOI for Acute disseminated encephalomyelitis with delayed onset and feasibility of the Miethke shunt and sensor reservoir system: a case report
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Genotype-phenotype correlations in recessive titinopathies.

Savarese, Marco; Vihola, Anna; Oates, Emily C; Barresi, Rita et al.

Part of Genetics in Medicine, p. 2029-2040, 2020

• DOI for Genotype-phenotype correlations in recessive titinopathies.

Somatostatin receptor expression and mTOR pathway activation in glioneuronal tumours of childhood

Ehrstedt, Christoffer; Ahlsten, Gunnar; Strömberg, Bo; Lindskog, Cecilia et al.

Part of Seizure, p. 123-130, 2020

• DOI for Somatostatin receptor expression and mTOR pathway activation in glioneuronal tumours of childhood

Cognition, health-related quality of life, and mood in children and young adults diagnosed with a glioneuronal tumor in childhood

Ehrstedt, Christoffer; Rydell, Ann-Margret; Hallsten, Marina Gabert; Strömberg, Bo et al.

Part of Epilepsy & Behavior, p. 59-66, 2018

• DOI for Cognition, health-related quality of life, and mood in children and young adults diagnosed with a glioneuronal tumor in childhood

Cognition, Health-Related Quality Of Life and Mood in Children and Young Adults Diagnosed with a Glioneuronal Tumor in Childhood

Ehrstedt, Christoffer; Rydell, Ann-Margret; Hallsten, Marina Gabert; Strömberg, Bo et al.

Part of Neuro-Oncology, p. 161-161, 2018

• DOI for Cognition, Health-Related Quality Of Life and Mood in Children and Young Adults Diagnosed with a Glioneuronal Tumor in Childhood

Intrathecal baclofen treatment an option in X-linked adrenoleukodystrophy

Hjartarson, Helgi Thor; Ehrstedt, Christoffer; Tedroff, Kristina

Part of European journal of paediatric neurology, p. 178-181, 2018

• DOI for Intrathecal baclofen treatment an option in X-linked adrenoleukodystrophy

Glioneuronal tumors in childhood - Before and after surgery. A long-term follow-up study

Ehrstedt, Christoffer; Canto Moreira, Nuno; Casar Borota, Olivera; Strömberg, Bo et al.

Part of Epilepsy & Behavior, p. 82-88, 2017

• DOI for Glioneuronal tumors in childhood - Before and after surgery. A long-term follow-up study

Clinical characteristics and late effects in CNS tumours of childhood: Do not forget long term follow-up of the low grade tumours

Ehrstedt, Christoffer; Kristiansen, Ingela; Ahlsten, Gunnar; Casar Borota, Olivera et al.

Part of European journal of paediatric neurology, p. 580-587, 2016

• DOI for Clinical characteristics and late effects in CNS tumours of childhood: Do not forget long term follow-up of the low grade tumours

Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations

Roos, S.; Lindgren, U.; Ehrstedt, Christoffer; Moslemi, A. R. et al.

Part of Neuromuscular Disorders, p. 865-865, 2014

• DOI for Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations

Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations

Roos, S.; Lindgren, U.; Ehrstedt, Christoffer; Moslemi, A. R. et al.

Part of Neuromuscular Disorders, p. 713-720, 2014

• DOI for Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations

Weekly vinblastine is a therapeutic option in recurrent/refractory pediatric low-grade gliomas

Ehrstedt, Christoffer; Laurencikas, Evaldas; Björklund, Ann-Christin; Strömberg, Bo et al.

Part of Neuro-Oncology, 2012

• DOI for Weekly vinblastine is a therapeutic option in recurrent/refractory pediatric low-grade gliomas

Glioneuronal tumours in childhood: Clinical picture, long-term outcome and possible new treatments

Ehrstedt, Christoffer

2019

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Somatostatin receptor expression, mTOR pathway activation and BRAFV600E mutational status in glioneuronal tumours of childhood

Ehrstedt, Christoffer; Ahlsten, Gunnar; Strömberg, Bo; Lindskog, C et al.