Search

Your search keyword '"Kano, Hiroki"' showing total 169 results

Search Constraints

Start Over You searched for: Author "Kano, Hiroki" Remove constraint Author: "Kano, Hiroki"
169 results on '"Kano, Hiroki"'

Search Results

2. Optical holonomic single quantum gates with a geometric spin under a zero field

3. Multifocal motor neuropathy in Japan: A nationwide survey on prevalence, clinical profiles, and treatment.

6. Prevalence and clinical profiles of anti‐myelin‐associated glycoprotein neuropathy in Japan: A nationwide survey study of 133 patients

7. Diagnostic utility of Gold Coast criteria for amyotrophic lateral sclerosis in Asia

8. Susceptibility of Ugandan Plasmodium falciparum Isolates to the Antimalarial Drug Pipeline

11. Combined Therapy with Ixazomib, Lenalidomide, and Dexamethasone for Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes Syndrome

12. Relationship between motor cortical and peripheral axonal hyperexcitability in amyotrophic lateral sclerosis

13. Decreased initial compound muscle action potential amplitudes in myasthenia gravis

14. Different patterns of sensory nerve involvement in chronic inflammatory demyelinating polyneuropathy subtypes

20. Molecular pathogenesis of Spondylocheirodysplastic Ehlers‐Danlos syndrome caused by mutant ZIP13 proteins

25. Dispersion of mean consecutive differences in single‐fiber electromyography increases diagnostic sensitivity for myasthenia gravis

26. Quantum teleportation-based state transfer of photon polarization into a carbon spin in diamond

29. Impaired neuromuscular transmission in facial muscles of amyotrophic lateral sclerosis: A single‐fiber electromyography study.

34. L1 retrotransposition can occur early in human embryonic development

37. Optical holonomic single quantum gates with a geometric spin under a zero field

41. Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex

44. FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst

47. Biology of mammalian mobile DNA

50. Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy

Catalog

Books, media, physical & digital resources