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- 2024
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Mark
Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management
(
- Contribution to journal › Article
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Mark
Clinical characteristics of children with Borrelia-related peripheral facial palsy and utility of cerebrospinal fluid testing
2024) In Acta Paediatrica, International Journal of Paediatrics(
- Contribution to journal › Article
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Mark
Manifestations of X-linked pyruvate dehydrogenase complex deficiency in female PDHA1 carriers
2024) In European Journal of Neurology(
- Contribution to journal › Article
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Mark
Overuse of EEG and ECG in children with breath-holding spells and its implication for the management of the spells
(
- Contribution to journal › Article
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Mark
Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy : A Systematic Review
(
- Contribution to journal › Scientific review
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Mark
Physician's conceptions of the decision-making process when managing febrile infants ≤ 60 days old : a phenomenographic qualitative study
(
- Contribution to journal › Article
- 2023
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Mark
Childhood tuberous sclerosis complex in southern Sweden: A paradigm shift in diagnosis and treatment.
(
- Contribution to journal › Article
- 2022
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Mark
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
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- Contribution to journal › Article
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Mark
Novel imaging findings in pyruvate dehydrogenase complex (PDHc) deficiency—Results from a nationwide population-based study
(
- Contribution to journal › Article
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Mark
Management and Outcome of Febrile Infants ≤60 days, With Emphasis on Infants ≤21 Days Old, in Swedish Pediatric Emergency Departments
(
- Contribution to journal › Article