N. Kawamoto

ORCID: 0009-0006-9166-4911
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About
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Research Areas
  • Black Holes and Theoretical Physics
  • Neurological diseases and metabolism
  • Noncommutative and Quantum Gravity Theories
  • Hereditary Neurological Disorders
  • Quantum Chromodynamics and Particle Interactions
  • Particle physics theoretical and experimental studies
  • Cosmology and Gravitation Theories
  • Skin and Cellular Biology Research

The University of Tokyo
1976-2023

Hereditary neuropathy with liability to pressure palsies (HNPP) is a peripheral autosomal dominant inheritance. Diagnosis can be made from the characteristic abnormalities determined by nerve conduction studies (NCS), including subclinical deficits at physiological compression sites. Heterozygous deletion of chromosome 17p11.2-p12 region myelin protein 22 gene (PMP22) cause in majority cases. However, loss function PMP22 due frameshift-causing insertion/deletion, missense, nonsense, or...

10.1111/jns.12558 article EN Journal of the Peripheral Nervous System 2023-05-12

The possible existence of heavy leptons and several schemes to accommodate these are investigated. We first study the problems related lepton number assignment weak angles. A violation e-µ universality its experimental consequences examined. Guided by a lepton-hadron analogy, we also discuss sextet scheme hadrons based on (p, p′, p″, n, λ, λ′) which was previously studied in connection with ψ-particles. Several version scheme, in, particular, structure hadron currents SU(2)L × U(1) gauge...

10.1143/ptp.55.1960 article EN Progress of Theoretical Physics 1976-06-01
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