Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness

Kandai Nozu, Tetsuji Inagaki, Xue Jun Fu, +9

Journal of Medical Genetics

The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies

Kandai Nozu, Kazumoto Iijima, Kyoko Kanda, +16

The Journal of Clinical Endocrinology & Metabolism

Treatment strategies for Henoch-Schönlein purpura nephritis by histological and clinical severity

Takeshi Ninchoji, Hiroshi Kaito, Kandai Nozu, +10

Pediatric Nephrology

GlomerulonephritisUrologyHenoch-schönlein Purpura NephritisRenal PathologyPathology +5

Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR

Kandai Nozu, Xue Jun Fu, Koichi Nakanishi, +12

Pediatric Research

Mendelian DisorderGenetic DisorderGeneticsPathogenesisMolecular Analysis +6

The effect of aldosterone blockade in patients with Alport syndrome

Hiroshi Kaito, Kandai Nozu, Kazumoto Iijima, +6

Pediatric Nephrology

MedicinePhysiologyPharmacologyAldosterone BlockadeAldosterone Physiology +1

Oral health behavior of children and guardians’ beliefs about children’s dental caries in Vientiane, Lao People’s Democratic Republic (Lao PDR)

Somphone Phanthavong, Daisuke Nonaka, Thongsavanh Phonaphone, +7

PLoS ONE

East Asian StudiesPrimary Care DentistryPreventive DentistryMedical AnthropologyLanguage Studies +15

Evolution of the response patterns to dietary carbohydrates and the developmental differentiation of gene expression of ?-amylase in Drosophila

Nobuyuki Inomata, Kyoko Kanda, Marie‐Louise Cariou, +2

Journal of Molecular Evolution

BiologyEnergy MetabolismDevelopmental BiologyMedicineGenetics +8

Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome.

Hiroshi Kaito, Kandai Nozu, Xue Jun Fu, +8

PubMed

The relationship between arginine vasopressin levels and hyponatremia following a percutaneous renal biopsy in children receiving hypotonic or isotonic intravenous fluids

Kyoko Kanda, Kandai Nozu, Hiroshi Kaito, +7

Pediatric Nephrology

Electrolyte DisorderRenal FunctionAcute Kidney InjuryRenal PharmacologyMedicine +5

A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism

Kandai Nozu, Xue Jun Fu, Hiroshi Kaito, +7

Pediatric Nephrology

Novel MutationBartter Syndrome CasePathologyMedicinePotassium Homeostasis