Ken Saida

Ken Saida

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Ken Saida

Ken Saida

Publications by authors named "Ken Saida"

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Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.

J Hum Genet 2019 Dec 17;64(12):1173-1186. Epub 2019 Sep 17.

Department of Human Genetics, Graduate school of medicine, Yokohama City University, Yokohama, Japan.

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http://dx.doi.org/10.1038/s10038-019-0667-4DOI Listing
December 2019

Autosomal dominant Alport syndrome due to a COL4A4 mutation with an additional ESPN variant detected by whole-exome analysis.

CEN Case Rep 2019 Nov 1. Epub 2019 Nov 1.

Department of Nephrology, Kumamoto University Graduate School of Medical Sciences, 1-1-1 Honjo, Chuo-ku, Kumamoto, Kumamoto, 860-8556, Japan.

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http://dx.doi.org/10.1007/s13730-019-00429-wDOI Listing
November 2019

A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease.

CEN Case Rep 2019 Sep 19. Epub 2019 Sep 19.

Division of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

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http://dx.doi.org/10.1007/s13730-019-00419-yDOI Listing
September 2019

SOFT syndrome in a patient from Chile.

Am J Med Genet A 2019 03 20;179(3):338-340. Epub 2018 Dec 20.

Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.

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http://doi.wiley.com/10.1002/ajmg.a.61015
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http://dx.doi.org/10.1002/ajmg.a.61015DOI Listing
March 2019

Treatment of hemolytic uremic syndrome related to Bordetella pertussis infection -is plasma exchange or eculizumab use necessary?

BMC Nephrol 2018 12 17;19(1):365. Epub 2018 Dec 17.

Division of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

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http://dx.doi.org/10.1186/s12882-018-1168-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297948PMC
December 2018

Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 gene.

Brain Dev 2018 Aug 17;40(7):566-569. Epub 2018 Apr 17.

Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.

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http://dx.doi.org/10.1016/j.braindev.2018.03.012DOI Listing
August 2018

Successful therapy switch from eculizumab to mycophenolate mofetil in a girl with DEAP-HUS.

Pediatr Nephrol 2017 10 12;32(10):1997-1998. Epub 2017 Jul 12.

Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1007/s00467-017-3738-9DOI Listing
October 2017

Ampicillin- and ampicillin/sulbactam-resistant Escherichia coli infection in a neonatal intensive care unit in Japan.

Pediatr Int 2016 Jun;58(6):537-9

Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.

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http://dx.doi.org/10.1111/ped.12984DOI Listing
June 2016

Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan.

Clin Exp Nephrol 2016 Apr 9;20(2):265-72. Epub 2015 Jul 9.

Division of Nephrology and Rheumatology, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

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http://dx.doi.org/10.1007/s10157-015-1142-yDOI Listing
April 2016

Exfoliative toxin A staphylococcal scalded skin syndrome in preterm infants.

Eur J Pediatr 2015 Apr 7;174(4):551-5. Epub 2014 Sep 7.

Department of Pediatrics Shinshu, University School of Medicine, 3-1-1 Asahi, Matsumoto, 390-8621, Japan,

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http://dx.doi.org/10.1007/s00431-014-2414-3DOI Listing
April 2015

Rituximab-associated agranulocytosis in children with refractory idiopathic nephrotic syndrome: case series and review of literature.

Nephrol Dial Transplant 2015 Jan 1;30(1):91-6. Epub 2014 Aug 1.

Department of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.

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http://dx.doi.org/10.1093/ndt/gfu258DOI Listing
January 2015

A case of adult Dent disease in Japan with advanced chronic kidney disease.

CEN Case Rep 2014 Nov 2;3(2):132-138. Epub 2013 Nov 2.

Department of Pediatrics, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano, Japan.

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http://dx.doi.org/10.1007/s13730-013-0102-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411561PMC
November 2014

A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.

Brain Dev 2014 Sep 26;36(8):721-4. Epub 2013 Nov 26.

Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.

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http://dx.doi.org/10.1016/j.braindev.2013.10.013DOI Listing
September 2014

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.

J Dermatol Sci 2013 Nov 28;72(2):193-5. Epub 2013 Jun 28.

Department of Dermatology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.

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http://dx.doi.org/10.1016/j.jdermsci.2013.06.008DOI Listing
November 2013

Successful unrelated cord blood transplantation using a reduced-intensity conditioning regimen in a 6-month-old infant with congenital neutropenia complicated by severe pneumonia.

Int J Hematol 2004 Oct;80(3):287-90

Department of Pediatrics, Reconstructive Medicine and Tissue Engineering, Shinshu University School of Medicine, Matsumoto, Japan.

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http://dx.doi.org/10.1532/ijh97.04079DOI Listing
October 2004