von der Lippe C - Search Results

1

G127R: A novel SOD1 mutation associated with rapidly evolving ALS and severe pain syndrome.

Holmøy T, Wilson JA, von der Lippe C, Andersen PM, Berg-Hansen P. Holmøy T, et al. Among authors: von der lippe c. Amyotroph Lateral Scler. 2010 Oct;11(5):478-80. doi: 10.3109/17482960903580315. Amyotroph Lateral Scler. 2010. PMID: 20192886

2

Primary Immunodeficiency Diseases and Gastrointestinal Distress: Coping Strategies and Dietary Experiences to Relieve Symptoms.

Brede KK, Wandel M, Wiig I, von der Lippe C. Brede KK, et al. Among authors: von der lippe c. Qual Health Res. 2021 Jan;31(2):361-372. doi: 10.1177/1049732320967908. Epub 2020 Nov 4. Qual Health Res. 2021. PMID: 33146080 Free PMC article.

3

Psychological reactions to predictive genetic testing for Huntington's disease: A qualitative study.

Tillerås KH, Kjoelaas SH, Dramstad E, Feragen KB, von der Lippe C. Tillerås KH, et al. Among authors: von der lippe c. J Genet Couns. 2020 Dec;29(6):1093-1105. doi: 10.1002/jgc4.1245. Epub 2020 Mar 12. J Genet Couns. 2020. PMID: 32162754

4

Treatment of hemophilia: A qualitative study of mothers' perspectives.

von der Lippe C, Frich JC, Harris A, Solbraekke KN. von der Lippe C, et al. Pediatr Blood Cancer. 2017 Jan;64(1):121-127. doi: 10.1002/pbc.26167. Epub 2016 Jul 29. Pediatr Blood Cancer. 2017. PMID: 27472376

5

Living with a rare disorder: a systematic review of the qualitative literature.

von der Lippe C, Diesen PS, Feragen KB. von der Lippe C, et al. Mol Genet Genomic Med. 2017 Nov;5(6):758-773. doi: 10.1002/mgg3.315. Epub 2017 Jul 23. Mol Genet Genomic Med. 2017. PMID: 29178638 Free PMC article. Review.

6

Children with a rare congenital genetic disorder: a systematic review of parent experiences.

von der Lippe C, Neteland I, Feragen KB. von der Lippe C, et al. Orphanet J Rare Dis. 2022 Oct 17;17(1):375. doi: 10.1186/s13023-022-02525-0. Orphanet J Rare Dis. 2022. PMID: 36253830 Free PMC article. Review.

7

Experiences of Being Heterozygous for Fabry Disease: a Qualitative Study.

von der Lippe C, Frich JC, Harris A, Solbrække KN. von der Lippe C, et al. J Genet Couns. 2016 Oct;25(5):1085-92. doi: 10.1007/s10897-016-9941-1. Epub 2016 Mar 7. J Genet Couns. 2016. PMID: 26948256

8

"It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

von der Lippe C, Frich JC, Harris A, Solbrække KN. von der Lippe C, et al. J Genet Couns. 2017 Dec;26(6):1324-1332. doi: 10.1007/s10897-017-0112-9. Epub 2017 May 26. J Genet Couns. 2017. PMID: 28547664

9

It's more than just lubrication of the skin: parents' experiences of caring for a child with ichthyosis.

Daae E, Feragen KB, Sitek JC, von der Lippe C. Daae E, et al. Among authors: von der lippe c. Health Psychol Behav Med. 2022 Apr 5;10(1):335-356. doi: 10.1080/21642850.2022.2053685. eCollection 2022. Health Psychol Behav Med. 2022. PMID: 35402085 Free PMC article.

10

The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease.

Sigurdardottir S, Bjerkely B, Jenssen TG, Mathisen P, von der Lippe C, Ørstavik K, Heimdal K, Dahle DO, Weedon-Fekjær MS, Solberg O, Pihlstrøm HK. Sigurdardottir S, et al. Among authors: von der lippe c. Orphanet J Rare Dis. 2021 Oct 12;16(1):427. doi: 10.1186/s13023-021-02066-y. Orphanet J Rare Dis. 2021. PMID: 34641933 Free PMC article.

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