Christoffer Ehrstedt
Forskare vid Institutionen för kvinnors och barns hälsa; Barnonkologisk och neurologisk forskning
- Telefon:
- 018-611 94 71
- Mobiltelefon:
- 070-940 97 89
- E-post:
- christoffer.ehrstedt@uu.se
- Besöksadress:
- MTC-huset, Dag Hammarskjölds väg 14B, 1 tr
752 37 Uppsala - Postadress:
- Akademiska sjukhuset
751 85 UPPSALA
Publikationer
Senaste publikationer
Ingår i Pediatric Neurology, s. 134-140, 2026
- DOI för The Lack of Broad Multidisciplinary Assessments in Children and Adolescents With Newly Diagnosed Idiopathic Intracranial Hypertension
- Ladda ner fulltext (pdf) av The Lack of Broad Multidisciplinary Assessments in Children and Adolescents With Newly Diagnosed Idiopathic Intracranial Hypertension
Risk Factors for Traumatic Lumbar Puncture in Children With ALL
Ingår i Acta Paediatrica, s. 2713-2715, 2025
- DOI för Risk Factors for Traumatic Lumbar Puncture in Children With ALL
- Ladda ner fulltext (pdf) av Risk Factors for Traumatic Lumbar Puncture in Children With ALL
Ingår i Acta Paediatrica, 2025
- DOI för Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
- Ladda ner fulltext (pdf) av Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
Ingår i Molecular Genetics and Metabolism, 2025
- DOI för 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
- Ladda ner fulltext (pdf) av 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
Ingår i Pediatric Neurology, s. 65-72, 2023
- DOI för Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension
- Ladda ner fulltext (pdf) av Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension
Alla publikationer
Artiklar i tidskrift
Ingår i Pediatric Neurology, s. 134-140, 2026
- DOI för The Lack of Broad Multidisciplinary Assessments in Children and Adolescents With Newly Diagnosed Idiopathic Intracranial Hypertension
- Ladda ner fulltext (pdf) av The Lack of Broad Multidisciplinary Assessments in Children and Adolescents With Newly Diagnosed Idiopathic Intracranial Hypertension
Risk Factors for Traumatic Lumbar Puncture in Children With ALL
Ingår i Acta Paediatrica, s. 2713-2715, 2025
- DOI för Risk Factors for Traumatic Lumbar Puncture in Children With ALL
- Ladda ner fulltext (pdf) av Risk Factors for Traumatic Lumbar Puncture in Children With ALL
Ingår i Acta Paediatrica, 2025
- DOI för Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
- Ladda ner fulltext (pdf) av Systematic follow‐ups were not associated with reduced acute ventriculoperitoneal shunt dysfunction in infancy
Ingår i Molecular Genetics and Metabolism, 2025
- DOI för 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
- Ladda ner fulltext (pdf) av 250 cases of "type 2 Gaucher disease": A novel system of clinical categorisation and evidence of genotype: Phenotype correlation
Ingår i Pediatric Neurology, s. 65-72, 2023
- DOI för Patient Delay, Lead Times, and Adherence to Diagnostic Guidelines in Children and Adolescents With Idiopathic Intracranial Hypertension
- Ladda ner fulltext (pdf) av 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
Ingår i Neuromuscular Disorders, s. 80-83, 2022
- DOI för Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report
- Ladda ner fulltext (pdf) av Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report
Ingår i Pediatric Blood & Cancer, 2022
- DOI för 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
- Ladda ner fulltext (pdf) av 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
Ingår i Child's Nervous System, s. 1479-1485, 2022
Ingår i Child's Nervous System, s. 3891-3895, 2021
- DOI för Acute disseminated encephalomyelitis with delayed onset and feasibility of the Miethke shunt and sensor reservoir system: a case report
- Ladda ner fulltext (pdf) av Acute disseminated encephalomyelitis with delayed onset and feasibility of the Miethke shunt and sensor reservoir system: a case report
Genotype-phenotype correlations in recessive titinopathies.
Ingår i Genetics in Medicine, s. 2029-2040, 2020
Somatostatin receptor expression and mTOR pathway activation in glioneuronal tumours of childhood
Ingår i Seizure, s. 123-130, 2020
Ingår i Epilepsy & Behavior, s. 59-66, 2018
Ingår i Neuro-Oncology, s. 161-161, 2018
Intrathecal baclofen treatment an option in X-linked adrenoleukodystrophy
Ingår i European journal of paediatric neurology, s. 178-181, 2018
Glioneuronal tumors in childhood - Before and after surgery. A long-term follow-up study
Ingår i Epilepsy & Behavior, s. 82-88, 2017
Ingår i European journal of paediatric neurology, s. 580-587, 2016
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
Ingår i Neuromuscular Disorders, s. 865-865, 2014
Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
Ingår i Neuromuscular Disorders, s. 713-720, 2014
Weekly vinblastine is a therapeutic option in recurrent/refractory pediatric low-grade gliomas
Ingår i Neuro-Oncology, 2012