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
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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
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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
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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
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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
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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
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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
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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
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Ingår i Child's Nervous System, s. 1479-1485, 2022
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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
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Genotype-phenotype correlations in recessive titinopathies.
Ingår i Genetics in Medicine, s. 2029-2040, 2020
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Somatostatin receptor expression and mTOR pathway activation in glioneuronal tumours of childhood
Ingår i Seizure, s. 123-130, 2020
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Ingår i Epilepsy & Behavior, s. 59-66, 2018
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Ingår i Neuro-Oncology, s. 161-161, 2018
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Intrathecal baclofen treatment an option in X-linked adrenoleukodystrophy
Ingår i European journal of paediatric neurology, s. 178-181, 2018
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Glioneuronal tumors in childhood - Before and after surgery. A long-term follow-up study
Ingår i Epilepsy & Behavior, s. 82-88, 2017
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Ingår i European journal of paediatric neurology, s. 580-587, 2016
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Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
Ingår i Neuromuscular Disorders, s. 865-865, 2014
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Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
Ingår i Neuromuscular Disorders, s. 713-720, 2014
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Weekly vinblastine is a therapeutic option in recurrent/refractory pediatric low-grade gliomas
Ingår i Neuro-Oncology, 2012