Bjurulf B - Search Results

1

Severe ALG8-CDG (CDG-Ih) associated with homozygosity for two novel missense mutations detected by exome sequencing of candidate genes.

Sorte H, Mørkrid L, Rødningen O, Kulseth MA, Stray-Pedersen A, Matthijs G, Race V, Houge G, Fiskerstrand T, Bjurulf B, Lyle R, Prescott T. Sorte H, et al. Among authors: bjurulf b. Eur J Med Genet. 2012 Mar;55(3):196-202. doi: 10.1016/j.ejmg.2012.01.003. Epub 2012 Jan 16. Eur J Med Genet. 2012. PMID: 22306853

2

Niemann-Pick disease type C2 presenting as fatal pulmonary alveolar lipoproteinosis: morphological findings in lung and nervous tissue.

Bjurulf B, Spetalen S, Erichsen A, Vanier MT, Strøm EH, Strømme P. Bjurulf B, et al. Med Sci Monit. 2008 Aug;14(8):CS71-5. Med Sci Monit. 2008. PMID: 18668002

3

Effectiveness of the ketogenic diet used to treat resistant childhood epilepsy in Scandinavia.

Hallböök T, Sjölander A, Åmark P, Miranda M, Bjurulf B, Dahlin M. Hallböök T, et al. Among authors: bjurulf b. Eur J Paediatr Neurol. 2015 Jan;19(1):29-36. doi: 10.1016/j.ejpn.2014.09.005. Epub 2014 Oct 6. Eur J Paediatr Neurol. 2015. PMID: 25457511

4

Potassium citrate and metabolic acidosis in children with epilepsy on the ketogenic diet: a prospective controlled study.

Bjurulf B, Magnus P, Hallböök T, Strømme P. Bjurulf B, et al. Dev Med Child Neurol. 2020 Jan;62(1):57-61. doi: 10.1111/dmcn.14393. Epub 2019 Nov 19. Dev Med Child Neurol. 2020. PMID: 31745987 Free article. Clinical Trial.

5

Incidence rates of progressive childhood encephalopathy in Oslo, Norway: a population based study.

Stromme P, Kanavin OJ, Abdelnoor M, Woldseth B, Rootwelt T, Diderichsen J, Bjurulf B, Sommer F, Magnus P. Stromme P, et al. Among authors: bjurulf b. BMC Pediatr. 2007 Jun 27;7:25. doi: 10.1186/1471-2431-7-25. BMC Pediatr. 2007. PMID: 17597517 Free PMC article.

6

Caregiver reported seizure precipitants and measures to prevent seizures in children with Dravet syndrome.

Bjurulf B, Reilly C, Hallböök T. Bjurulf B, et al. Seizure. 2022 Dec;103:3-10. doi: 10.1016/j.seizure.2022.09.018. Epub 2022 Sep 30. Seizure. 2022. PMID: 36244183 Free article.

7

Dravet syndrome in children-A population-based study.

Bjurulf B, Reilly C, Sigurdsson GV, Thunström S, Kolbjer S, Hallböök T. Bjurulf B, et al. Epilepsy Res. 2022 May;182:106922. doi: 10.1016/j.eplepsyres.2022.106922. Epub 2022 Apr 8. Epilepsy Res. 2022. PMID: 35461153 Free article.

8

Neurological findings in aminoacylase 1 deficiency.

Sass JO, Olbrich H, Mohr V, Hart C, Woldseth B, Krywawych S, Bjurulf B, Lakhani PK, Buchdahl RM, Omran H. Sass JO, et al. Among authors: bjurulf b. Neurology. 2007 Jun 12;68(24):2151-3. doi: 10.1212/01.wnl.0000264933.56204.e8. Neurology. 2007. PMID: 17562838 No abstract available.

9

Diagnosis, epilepsy treatment and supports for neurodevelopment in children with Dravet Syndrome: Caregiver reported experiences and needs.

Soto Jansson J, Bjurulf B, Dellenmark Blom M, Hallböök T, Reilly C. Soto Jansson J, et al. Among authors: bjurulf b. Epilepsy Behav. 2024 Feb;151:109603. doi: 10.1016/j.yebeh.2023.109603. Epub 2024 Jan 1. Epilepsy Behav. 2024. PMID: 38168600

10

Do all individuals with Dravet syndrome have intellectual disability?

Reilly C, Bjurulf B, Hallböök T. Reilly C, et al. Among authors: bjurulf b. Epilepsia. 2023 Dec 14. doi: 10.1111/epi.17847. Online ahead of print. Epilepsia. 2023. PMID: 38093664 No abstract available.

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