Literature DB >> 15069249

Satoyoshi syndrome.

R Ashalatha1, A Kishore, C Sarada, M D Nair.   

Abstract

Satoyoshi syndrome (Komuragaeri disease) is a rare disorder of presumed autoimmune etiology, characterized by painful muscle spasms, alopecia, diarrhea, endocrinopathy with amenorrhoea and secondary skeletal abnormalities. Most of the previous reports are of the Japanese people. We report the first case from India.

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Year:  2004        PMID: 15069249

Source DB:  PubMed          Journal:  Neurol India        ISSN: 0028-3886            Impact factor:   2.117


  4 in total

1.  Adult-onset Satoyoshi syndrome and response to plasmapheresis.

Authors:  Rajeshwari Aghoram; P R Srijithesh; Sudheeran Kannoth
Journal:  Ann Indian Acad Neurol       Date:  2016 Jan-Mar       Impact factor: 1.383

Review 2.  Gastrointestinal manifestations in Satoyoshi syndrome: a systematic review.

Authors:  Julián Solís-García Del Pozo; Carlos de Cabo; Javier Solera
Journal:  Orphanet J Rare Dis       Date:  2020-05-19       Impact factor: 4.123

Review 3.  Treatment of Satoyoshi syndrome: a systematic review.

Authors:  Julián Solís-García Del Pozo; Carlos de Cabo; Javier Solera
Journal:  Orphanet J Rare Dis       Date:  2019-06-19       Impact factor: 4.123

4.  Oromandibular Dystonia - A Systematic Review.

Authors:  Udit Saraf; Mitesh Chandarana; K P Divya; Syam Krishnan
Journal:  Ann Indian Acad Neurol       Date:  2021-10-22       Impact factor: 1.383

  4 in total

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