557 results on '"Kuniyoshi, Kazuki"'
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2. Genetic etiology and clinical features of achromatopsia in Japan
3. Genetic and Clinical Features of ABCA4-Associated Retinopathy in a Japanese Nationwide Cohort
4. Fundus autofluorescence, optical coherence tomography and electroretinography abnormalities in a patient with digoxin retinopathy that resemble those in KCNV2-associated retinopathy
5. Amalric triangular sign and carotid Doppler ultrasonographic findings in central retinal artery occlusion
6. Necl-1/CADM3 regulates cone synapse formation in the mouse retina
7. A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
8. The Effect of an Additional Core Suture During Pulvertaft Tendon Repair: A Fresh-Frozen Cadaver Study
9. Reply
10. Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis
11. A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
12. EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS
13. Biomechanical Evaluation of Opponensplasty for Low Median Palsy: A Cadaver Study
14. The Effect of Flexor Digitorum Profundus Dynamic Tenodesis on the Distal Interphalangeal Joint: A Cadaver Study
15. Incidence of Axillary Nerve Injury After Arthroscopic Shoulder Stabilization
16. Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis
17. Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
18. Leber Congenital Amaurosis/Early-Onset Retinal Dystrophy in Japanese Population
19. Complete Visual Recovery From Severe Outer Retinitis After Tonsillitis
20. ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME
21. Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association
22. Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies
23. Ultrasonography could be used to predict extended insertion of the EPB tendon noninvasively
24. Re: Iwahashi et al.:Efficacy of inner wall retinectomy for bullous schisis cavity hanging over or threatening the macula in patients with congenital X-linked retinoschisis
25. Systemic impact on preterm infants during treatment for retinopathy of prematurity: A comparison of retinal photocoagulation and intravitreal injection of anti-vascular endothelial growth factor drugs
26. Anatomical Cadaver Study of the Hotchkiss Over-the-Top Approach for Exposing the Anteromedial Facet of the Ulnar Coronoid Process: Critical Measurements and Implications for Protecting the Median Nerve
27. A Cadaver Study of Median-to-Radial Nerve Transfer for Radial Nerve Injuries
28. Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
29. Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis
30. Long-Term Visual Prognosis of Patients Following Lens-Sparing Vitrectomy for Stage 4A Retinopathy of Prematurity
31. Biomechanical Study of the Digital Flexor Tendon Sliding Lengthening Technique
32. The Effects of Generally Administered Anti–Nerve Growth Factor Receptor (p75NTR) Antibody on Pain-Related Behavior, Dorsal Root Ganglia, and Spinal Glia Activation in a Rat Model of Brachial Plexus Avulsion
33. Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing
34. Variant course of extensor pollicis brevis tendon in the third extensor compartment
35. Anatomic study of the first extensor compartment and the relationship between the extensor tendon width and its distal insertion
36. Radiographic evaluation of indirect decompression of mini-open anterior retroperitoneal lumbar interbody fusion: oblique lateral interbody fusion for degenerated lumbar spondylolisthesis
37. New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome
38. STRUCTURAL OUTCOME AFTER SURGERY FOR STAGE 5 RETINOPATHY OF PREMATURITY BASED ON THE NEW INTERNATIONAL CLASSIFICATION
39. The Effect of an Additional Core Suture During Pulvertaft Tendon Repair: A Fresh-Frozen Cadaver Study
40. EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS
41. The Effects of Locally Injected Triamcinolone on Entrapment Neuropathy in a Rat Chronic Constriction Injury Model
42. Relationship between traction force of the flexor tendon and flexion force of the finger output based on the Jamar dynamometer
43. Smithʼs fracture generally occurs after falling on the palm of the hand
44. Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy
45. Long-lasting, dense scotoma under light-adapted conditions in patient with multiple evanescent white dot syndrome
46. Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia
47. Recurrent proliferative vitreoretinopathy in a patient with morning glory syndrome and intellectual disability
48. Activation of Astrocytes and Microglia in the C3–T4 Dorsal Horn by Lower Trunk Avulsion in a Rat Model of Neuropathic Pain
49. Fractional Fowler Tenotomy for Chronic Mallet Finger: A Cadaveric Biomechanical Study
50. Anti-RANKL antibodies decrease CGRP expression in dorsal root ganglion neurons innervating injured lumbar intervertebral discs in rats
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