Hypokalemic periodic paralysis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hypokalemic periodic paralysis" in English language version.

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10nih.gov

4^th place

8doi.org

2^nd place

2worldcat.org

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2semanticscholar.org

11^th place

8^th place

1medlineplus.gov

1,581^st place

1,299^th place

1omim.org

4,380^th place

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1uni-ulm.de

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1books.google.com

3^rd place

books.google.com

Encyclopedia of the Neurological Sciences. Academic Press. 2014-04-29. ISBN 9780123851581.

doi.org

Kung AW (July 2006). "Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge". J. Clin. Endocrinol. Metab. 91 (7): 2490–5. doi:10.1210/jc.2006-0356. PMID 16608889.
Jurkat-Rott, K.; Lehmann-Horn, F. (April 2007). "Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis". Neurotherapeutics. 4 (2): 216–24. doi:10.1016/j.nurt.2007.02.001. PMID 17395131.
Rüdel R, Lehmann-Horn F, Ricker K, Küther G (February 1984). "Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parameters". Muscle Nerve. 7 (2): 110–20. doi:10.1002/mus.880070205. PMID 6325904. S2CID 25705002.
Jurkat-Rott K, Lehmann-Horn F (August 2005). "Muscle channelopathies and critical points in functional and genetic studies". J. Clin. Invest. 115 (8): 2000–9. doi:10.1172/JCI25525. PMC 1180551. PMID 16075040.
Kim, SJ; Lee, YJ; Kim, JB (January 2010). "Reduced expression and abnormal localization of the KATP channel subunit SUR2A in patients with familial hypokalemic periodic paralysis". Biochemical and Biophysical Research Communications. 391 (1): 974–8. doi:10.1016/j.bbrc.2009.11.177. PMID 19962959.
Kim, JB; Kim, MH (December 2007). "The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis". J Korean Med Sci. 22 (6): 946–51. doi:10.3346/jkms.2007.22.6.946. PMC 2694642. PMID 18162704.
Finsterer, J. (2008-03-01). "Primary periodic paralyses". Acta Neurologica Scandinavica. 117 (3): 145–158. doi:10.1111/j.1600-0404.2007.00963.x. ISSN 1600-0404. PMID 18031562. S2CID 22496999.
Walker MB (1935). "Potassium chloride in myasthenia gravis". Lancet. 2 (5836): 47. doi:10.1016/S0140-6736(01)09382-5.

medlineplus.gov

"Hypokalemic periodic paralysis: MedlinePlus Genetics". medlineplus.gov. U.S. National Library of Medicine. Retrieved 26 October 2020. This article incorporates text from this source, which is in the public domain.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kung AW (July 2006). "Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge". J. Clin. Endocrinol. Metab. 91 (7): 2490–5. doi:10.1210/jc.2006-0356. PMID 16608889.
Jurkat-Rott, K.; Lehmann-Horn, F. (April 2007). "Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis". Neurotherapeutics. 4 (2): 216–24. doi:10.1016/j.nurt.2007.02.001. PMID 17395131.
Rüdel R, Lehmann-Horn F, Ricker K, Küther G (February 1984). "Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parameters". Muscle Nerve. 7 (2): 110–20. doi:10.1002/mus.880070205. PMID 6325904. S2CID 25705002.
Jurkat-Rott K, Lehmann-Horn F (August 2005). "Muscle channelopathies and critical points in functional and genetic studies". J. Clin. Invest. 115 (8): 2000–9. doi:10.1172/JCI25525. PMC 1180551. PMID 16075040.
Kim, SJ; Lee, YJ; Kim, JB (January 2010). "Reduced expression and abnormal localization of the KATP channel subunit SUR2A in patients with familial hypokalemic periodic paralysis". Biochemical and Biophysical Research Communications. 391 (1): 974–8. doi:10.1016/j.bbrc.2009.11.177. PMID 19962959.
Kim, JB; Kim, MH (December 2007). "The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis". J Korean Med Sci. 22 (6): 946–51. doi:10.3346/jkms.2007.22.6.946. PMC 2694642. PMID 18162704.
Finsterer, J. (2008-03-01). "Primary periodic paralyses". Acta Neurologica Scandinavica. 117 (3): 145–158. doi:10.1111/j.1600-0404.2007.00963.x. ISSN 1600-0404. PMID 18031562. S2CID 22496999.

ncbi.nlm.nih.gov

Jurkat-Rott K, Lehmann-Horn F (August 2005). "Muscle channelopathies and critical points in functional and genetic studies". J. Clin. Invest. 115 (8): 2000–9. doi:10.1172/JCI25525. PMC 1180551. PMID 16075040.
"Sternberg D et al. (2009) Hypokalemic Periodic Paralysis, in GeneReviews "
Kim, JB; Kim, MH (December 2007). "The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis". J Korean Med Sci. 22 (6): 946–51. doi:10.3346/jkms.2007.22.6.946. PMC 2694642. PMID 18162704.

omim.org

Online Mendelian Inheritance in Man (OMIM): 604433

semanticscholar.org

api.semanticscholar.org

Rüdel R, Lehmann-Horn F, Ricker K, Küther G (February 1984). "Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane parameters". Muscle Nerve. 7 (2): 110–20. doi:10.1002/mus.880070205. PMID 6325904. S2CID 25705002.
Finsterer, J. (2008-03-01). "Primary periodic paralyses". Acta Neurologica Scandinavica. 117 (3): 145–158. doi:10.1111/j.1600-0404.2007.00963.x. ISSN 1600-0404. PMID 18031562. S2CID 22496999.

uni-ulm.de

"Segal MM, Jurkat-Rott K, Levitt J, Lehmann-Horn F, Hypokalemic periodic paralysis - an owner's manual"

worldcat.org

Harrison's principles of internal medicine. Jameson, J. Larry; Kasper, Dennis L.; Longo, Dan L. (Dan Louis), 1949-; Fauci, Anthony S., 1940-; Hauser, Stephen L.; Loscalzo, Joseph (20th ed.). New York. 13 August 2018. p. 307. ISBN 978-1-259-64403-0. OCLC 1029074059.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
Finsterer, J. (2008-03-01). "Primary periodic paralyses". Acta Neurologica Scandinavica. 117 (3): 145–158. doi:10.1111/j.1600-0404.2007.00963.x. ISSN 1600-0404. PMID 18031562. S2CID 22496999.