石河 慎也

Liposomal nanocarriers of preassembled glycocalyx restore normal venular permeability and shear stress sensitivity in sepsis: assessed quantitatively with a novel microchamber system. 

American journal of physiology. Heart and circulatory physiology 327(2) H390-H398 2024年8月1日  

Long-term efficacy of liposomal nanocarriers of preassembled glycocalyx in restoring cerebral endothelial glycocalyx in sepsis. 

Microvascular research 154 104684-104684 2024年7月  

All reported non-canonical splice site variants in GLA cause aberrant splicing. 

Clinical and experimental nephrology 27(9) 737-746 2023年9月  

Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease. 

Kidney international reports 8(9) 1811-1821 2023年9月  

Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866. 

Kidney international reports 8(5) 1127-1129 2023年5月  

Detecting pathogenic deep intronic variants in Gitelman syndrome. 

American journal of medical genetics. Part A 188(9) 2576-2583 2022年9月  

Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis. 

Kidney360 3(8) 1384-1393 2022年8月25日  

早期の遺伝学的検査が治療方針選択に有用であったステロイド抵抗性ネフローゼ症候群の1例 

日本小児腎不全学会雑誌 42 97-100 2022年8月  

Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch-Schönlein purpura nephritis of moderate severity. 

Pediatric nephrology (Berlin, Germany) 37(8) 1845-1853 2022年8月  

Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population. 

Journal of human genetics 67(7) 427-440 2022年7月  

Efficacy of combination therapy for childhood complicated focal IgA nephropathy. 

Clinical and experimental nephrology 26(6) 561-570 2022年6月  

Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease. 

Kidney international reports 7(4) 857-866 2022年4月  

Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants. 

Kidney360 3(3) 497-505 2022年3月31日  

Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes. 

Clinical and experimental nephrology 26(2) 140-153 2022年2月  

Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome. 

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 37(2) 262-270 2022年1月25日  

Epidemiological impact of universal varicella vaccination on consecutive emergency department visits for varicella and its economic impact among children in Kobe City, Japan. 

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 28(1) 35-40 2022年1月  

Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing. 

Kidney international reports 7(1) 108-116 2022年1月  

Ways and Means of Cellular Reconditioning for Kidney Regeneration. 

American journal of nephrology 53(2-3) 96-107 2022年