Alternating hemiplegia of childhood (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alternating hemiplegia of childhood" in Dutch language version.

refsWebsite

Global rank Dutch rank

4^th place

12^th place

5^th place

28^th place

2^nd place

8^th place

1^st place

234^th place

128^th place

doi.org

Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay Sisodiya (26 september 2015). Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet Journal of Rare Diseases 10: 123. ISSN: 1750-1172. PMID 26410222. PMC PMC4583741. DOI: 10.1186/s13023-015-0335-5. Gearchiveerd van origineel op 22 maart 2019.
(en) Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries (September 2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nature Genetics 44 (9): 1030–1034. ISSN: 1061-4036. DOI: 10.1038/ng.2358.

(en) Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries (September 2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nature Genetics 44 (9): 1030–1034. ISSN: 1061-4036. DOI: 10.1038/ng.2358.

Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay Sisodiya (26 september 2015). Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet Journal of Rare Diseases 10: 123. ISSN: 1750-1172. PMID 26410222. PMC PMC4583741. DOI: 10.1186/s13023-015-0335-5. Gearchiveerd van origineel op 22 maart 2019.
ATP1A3 ATPase Na+/K+ transporting subunit alpha 3 [Homo sapiens (human) - Gene - NCBI]. www.ncbi.nlm.nih.gov. Gearchiveerd op 3 oktober 2016. Geraadpleegd op 18 september 2017.

Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay Sisodiya (26 september 2015). Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet Journal of Rare Diseases 10: 123. ISSN: 1750-1172. PMID 26410222. PMC PMC4583741. DOI: 10.1186/s13023-015-0335-5. Gearchiveerd van origineel op 22 maart 2019.
ATP1A3 ATPase Na+/K+ transporting subunit alpha 3 [Homo sapiens (human) - Gene - NCBI]. www.ncbi.nlm.nih.gov. Gearchiveerd op 3 oktober 2016. Geraadpleegd op 18 september 2017.

Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay Sisodiya (26 september 2015). Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet Journal of Rare Diseases 10: 123. ISSN: 1750-1172. PMID 26410222. PMC PMC4583741. DOI: 10.1186/s13023-015-0335-5. Gearchiveerd van origineel op 22 maart 2019.
(en) Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries (September 2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nature Genetics 44 (9): 1030–1034. ISSN: 1061-4036. DOI: 10.1038/ng.2358.