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Clinical Journal of the American Society of Nephrology : CJASN
|
March 31, 2015
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1
Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, et al.
Kidney International
|
May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants
Kathrin Burgmaier, Leonie Brinker, Florian Erger, et al.
Kidney International
|
June 1, 2022
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
Stefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
Kidney International
|
April 28, 2022
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy
Stefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Page
of 3
Search research articles
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Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Clinical Journal of the American Society of Nephrology : CJASN
|
March 31, 2015
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1
Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, et al.
Kidney International
|
May 3, 2021
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants
Kathrin Burgmaier, Leonie Brinker, Florian Erger, et al.
Kidney International
|
June 1, 2022
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
Stefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
Kidney International
|
April 28, 2022
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy
Stefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.
American Journal of Human Genetics
|
January 28, 2021
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis
Patricia L Weng, Amar J Majmundar, Kamal Khan, et al.
Page
of 3