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Medicinski Glasnik : Official Publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina
|
October 13, 2025
Effectiveness of Hemodialysis with hemoperfusion as a therapeutic modality in pediatric chronic kidney disease
Ahmedz Widiasta, Rini Rossanti, Dedi Rachmadi, et al.
Pediatric Nephrology (Berlin, Germany)
|
December 6, 2025
Early detection of proteinuria to prevent kidney fibrosis and progression to kidney failure: lessons from the School Urine Screening Program in Japan
Rini Rossanti, Kimiko Honda, Masataka Honda, et al.
Urology Case Reports
|
December 11, 2023
2,8-Dihydroxyadenine nephrolithiasis with chronic kidney disease in children: A case report and review of literature
Rizky Ramdhani, Akhmad Mustafa, Safendra Siregar, et al.
European Journal of Medical Research
|
May 1, 2025
Prevalence of systemic lupus erythematosus in autoimmune hemolytic anemia patients based on coombs test results
Raja Iqbal Mulya Harahap, Tiara Ardiningrum, Yunisa Pamela, et al.
International Journal of Nephrology and Renovascular Disease
|
November 4, 2022
Factors Affecting Neurocognitive Function in Children with Chronic Kidney Disease: A Systematic Review
Elrika A Wijaya, Purboyo Solek, Dzulfikar D L Hakim, et al.
Scientific Reports
|
December 31, 2024
Use of large language models as artificial intelligence tools in academic research and publishing among global clinical researchers
Tanisha Mishra, Edward Sutanto, Rini Rossanti, et al.
CEN Case Reports
|
September 9, 2020
FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child
Rini Rossanti, Toshio Watanabe, China Nagano, et al.
Kidney360
|
April 4, 2022
Heterozygous Urinary Abnormality-Causing Variants of <i>COL4A3</i> and <i>COL4A4</i> Affect Severity of Autosomal Recessive Alport Syndrome
Tomoko Horinouchi, Tomohiko Yamamura, China Nagano, et al.
American Journal of Medical Genetics. Part A
|
July 5, 2022
Detecting pathogenic deep intronic variants in Gitelman syndrome
Rini Rossanti, Tomoko Horinouchi, Nana Sakakibara, et al.
Clinical and Experimental Nephrology
|
March 24, 2020
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.
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Search research articles
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Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
Medicinski Glasnik : Official Publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina
|
October 13, 2025
Effectiveness of Hemodialysis with hemoperfusion as a therapeutic modality in pediatric chronic kidney disease
Ahmedz Widiasta, Rini Rossanti, Dedi Rachmadi, et al.
Pediatric Nephrology (Berlin, Germany)
|
December 6, 2025
Early detection of proteinuria to prevent kidney fibrosis and progression to kidney failure: lessons from the School Urine Screening Program in Japan
Rini Rossanti, Kimiko Honda, Masataka Honda, et al.
Urology Case Reports
|
December 11, 2023
2,8-Dihydroxyadenine nephrolithiasis with chronic kidney disease in children: A case report and review of literature
Rizky Ramdhani, Akhmad Mustafa, Safendra Siregar, et al.
European Journal of Medical Research
|
May 1, 2025
Prevalence of systemic lupus erythematosus in autoimmune hemolytic anemia patients based on coombs test results
Raja Iqbal Mulya Harahap, Tiara Ardiningrum, Yunisa Pamela, et al.
International Journal of Nephrology and Renovascular Disease
|
November 4, 2022
Factors Affecting Neurocognitive Function in Children with Chronic Kidney Disease: A Systematic Review
Elrika A Wijaya, Purboyo Solek, Dzulfikar D L Hakim, et al.
Scientific Reports
|
December 31, 2024
Use of large language models as artificial intelligence tools in academic research and publishing among global clinical researchers
Tanisha Mishra, Edward Sutanto, Rini Rossanti, et al.
CEN Case Reports
|
September 9, 2020
FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child
Rini Rossanti, Toshio Watanabe, China Nagano, et al.
Kidney360
|
April 4, 2022
Heterozygous Urinary Abnormality-Causing Variants of <i>COL4A3</i> and <i>COL4A4</i> Affect Severity of Autosomal Recessive Alport Syndrome
Tomoko Horinouchi, Tomohiko Yamamura, China Nagano, et al.
American Journal of Medical Genetics. Part A
|
July 5, 2022
Detecting pathogenic deep intronic variants in Gitelman syndrome
Rini Rossanti, Tomoko Horinouchi, Nana Sakakibara, et al.
Clinical and Experimental Nephrology
|
March 24, 2020
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
Tomohiko Inoue, China Nagano, Masafumi Matsuo, et al.
Page
of 4