Yasutomo Ito
Nagoya, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
A Child with Epidermolytic Ichthyosis from a Parent with Epidermolytic Nevus: Risk Evaluation of Transmission from Mosaic to Germline.
Journal: The Journal of investigative dermatology
Published: January 26, 2017
Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.
Journal: The Journal of investigative dermatology
Published: August 23, 2015
Functional characteristics of L1156F-CFTR associated with alcoholic chronic pancreatitis in Japanese.
Journal: American journal of physiology. Gastrointestinal and liver physiology
Published: January 10, 2014
LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner.
Journal: Human molecular genetics
Published: November 16, 2013
Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.
Journal: Journal of dermatological science
Published: May 08, 2013
Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families.
Journal: International journal of dermatology
Published: April 30, 2013
TLR4-MD-2 complex is negatively regulated by an endogenous ligand, globotetraosylceramide.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 09, 2013
The majority of generalized pustular psoriasis without psoriasis vulgaris is caused by deficiency of interleukin-36 receptor antagonist.
Journal: The Journal of investigative dermatology
Published: January 18, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026