Hereditary neuropathy with liability to pressure palsy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hereditary neuropathy with liability to pressure palsy" in English language version.

refsWebsite

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7nih.gov

4^th place

3doi.org

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3books.google.com

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2omim.org

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2worldcat.org

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1medlineplus.gov

1,581^st place

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1orpha.net

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1web.archive.org

1^st place

1nhs.uk

1,989^th place

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1semanticscholar.org

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1cmtausa.org

low place

books.google.com (Global: 3^rd place; English: 3^rd place)

Kuhlenbäumer, G.; Stögbauer, F.; Ringelstein, E. B.; Young, P. (2006-01-16). Hereditary Peripheral Neuropathies. Springer ScienceFatigue & Business Media. pp. 96, 126. ISBN 9783798515864.
Vallat, Jean-Michel; Weis, Joachim (2014-10-20). Peripheral Nerve Disorders: Pathology and Genetics. John Wiley & Sons. ISBN 9781118618431.
Sango, Kazunori; Yamauchi, Junji (2014-02-13). Schwann Cell Development and Pathology. Springer Science & Business Media. p. 83. ISBN 9784431547648. Retrieved 18 August 2016.

cmtausa.org (Global: low place; English: low place)

"Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)". Charcot–Marie–Tooth Association. Retrieved 2023-05-03.

doi.org (Global: 2^nd place; English: 2^nd place)

Watila MM, Balarabe SA (2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.
van Paassen, Barbara W; Kooi, Anneke J van der; Spaendonck-Zwarts, Karin Y van; Verhamme, Camiel; Baas, Frank; Visser, Marianne de (19 March 2014). "PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies". Orphanet Journal of Rare Diseases. 9 (1): 38. doi:10.1186/1750-1172-9-38. ISSN 1750-1172. PMC 3994927. PMID 24646194.
Park, Jong Eun; Noh, Seung-Jae; Oh, Mijin; Cho, Dae-Yeon; Kim, So Young; Ki, Chang-Seok (2018-03-15). "Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population". Orphanet Journal of Rare Diseases. 13 (1): 40. doi:10.1186/s13023-018-0779-5. ISSN 1750-1172. PMC 5856277. PMID 29544507.

medlineplus.gov (Global: 1,581^st place; English: 1,299^th place)

Genetics Home Reference (April 2007). "Hereditary neuropathy with liability to pressure palsies". NIH.gov. Retrieved 2020-02-09.

nhs.uk (Global: 1,989^th place; English: 1,528^th place)

"Hereditary neuropathy with pressure palsies (HNPP)". NHS. NHS.uk. Archived from the original on 11 September 2017. Retrieved 18 August 2016.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Bird, Thomas D. (1 January 1993). "Hereditary Neuropathy with Liability to Pressure Palsies". GeneReviews. PMID 20301566. Retrieved 6 August 2016.update 2014
Watila MM, Balarabe SA (2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.
van Paassen, Barbara W; Kooi, Anneke J van der; Spaendonck-Zwarts, Karin Y van; Verhamme, Camiel; Baas, Frank; Visser, Marianne de (19 March 2014). "PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies". Orphanet Journal of Rare Diseases. 9 (1): 38. doi:10.1186/1750-1172-9-38. ISSN 1750-1172. PMC 3994927. PMID 24646194.
Park, Jong Eun; Noh, Seung-Jae; Oh, Mijin; Cho, Dae-Yeon; Kim, So Young; Ki, Chang-Seok (2018-03-15). "Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population". Orphanet Journal of Rare Diseases. 13 (1): 40. doi:10.1186/s13023-018-0779-5. ISSN 1750-1172. PMC 5856277. PMID 29544507.

ncbi.nlm.nih.gov

Bird, Thomas D. (1 January 1993). "Hereditary Neuropathy with Liability to Pressure Palsies". GeneReviews. PMID 20301566. Retrieved 6 August 2016.update 2014
van Paassen, Barbara W; Kooi, Anneke J van der; Spaendonck-Zwarts, Karin Y van; Verhamme, Camiel; Baas, Frank; Visser, Marianne de (19 March 2014). "PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies". Orphanet Journal of Rare Diseases. 9 (1): 38. doi:10.1186/1750-1172-9-38. ISSN 1750-1172. PMC 3994927. PMID 24646194.
Park, Jong Eun; Noh, Seung-Jae; Oh, Mijin; Cho, Dae-Yeon; Kim, So Young; Ki, Chang-Seok (2018-03-15). "Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population". Orphanet Journal of Rare Diseases. 13 (1): 40. doi:10.1186/s13023-018-0779-5. ISSN 1750-1172. PMC 5856277. PMID 29544507.

omim.org (Global: 4,380^th place; English: 4,305^th place)

"OMIM Entry - # 162500 - NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP". www.omim.org. Retrieved 18 August 2016.
"OMIM Entry - * 601097 - PERIPHERAL MYELIN PROTEIN 22; PMP22". omim.org. Retrieved 2016-08-18.

orpha.net (Global: 3,537^th place; English: 7,177^th place)

RESERVED, INSERM US14 -- ALL RIGHTS. "Orphanet: Hereditary neuropathy with liability to pressure palsies". www.orpha.net. Retrieved 18 August 2016.{{cite web}}: CS1 maint: numeric names: authors list (link)

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Watila MM, Balarabe SA (2015). "Molecular and clinical features of inherited neuropathies due to PMP22 duplication". Journal of the Neurological Sciences. 355 (1–2): 18–24. doi:10.1016/j.jns.2015.05.037. PMID 26076881. S2CID 40080925.

web.archive.org (Global: 1^st place; English: 1^st place)

"Hereditary neuropathy with pressure palsies (HNPP)". NHS. NHS.uk. Archived from the original on 11 September 2017. Retrieved 18 August 2016.

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

van Paassen, Barbara W; Kooi, Anneke J van der; Spaendonck-Zwarts, Karin Y van; Verhamme, Camiel; Baas, Frank; Visser, Marianne de (19 March 2014). "PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies". Orphanet Journal of Rare Diseases. 9 (1): 38. doi:10.1186/1750-1172-9-38. ISSN 1750-1172. PMC 3994927. PMID 24646194.
Park, Jong Eun; Noh, Seung-Jae; Oh, Mijin; Cho, Dae-Yeon; Kim, So Young; Ki, Chang-Seok (2018-03-15). "Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population". Orphanet Journal of Rare Diseases. 13 (1): 40. doi:10.1186/s13023-018-0779-5. ISSN 1750-1172. PMC 5856277. PMID 29544507.

Hereditary neuropathy with liability to pressure palsy (English Wikipedia)

books.google.com (Global: 3rd place; English: 3rd place)

cmtausa.org (Global: low place; English: low place)

doi.org (Global: 2nd place; English: 2nd place)

medlineplus.gov (Global: 1,581st place; English: 1,299th place)

nhs.uk (Global: 1,989th place; English: 1,528th place)

nih.gov (Global: 4th place; English: 4th place)