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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1951 2
1953 1
1955 4
1956 2
1957 1
1959 1
1964 2
1966 1
1967 1
1968 1
1969 1
1970 4
1971 1
1972 2
1973 6
1974 4
1975 4
1976 6
1977 4
1978 3
1979 3
1980 5
1981 4
1982 8
1983 9
1984 14
1985 11
1986 12
1987 7
1988 15
1989 9
1990 8
1991 7
1992 9
1993 17
1994 14
1995 16
1996 15
1997 9
1998 12
1999 14
2000 16
2001 13
2002 9
2003 15
2004 16
2005 26
2006 15
2007 19
2008 17
2009 15
2010 14
2011 23
2012 44
2013 34
2014 41
2015 40
2016 36
2017 34
2018 37
2019 28
2020 31
2021 39
2022 38
2023 43
2024 10

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834 results

Results by year

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Page 1
Glomerulonephritis Histopathological Pattern Change.
AlYousef A, AlSahow A, AlHelal B, Alqallaf A, Abdallah E, Abdellatif M, Nawar H, Elmahalawy R. AlYousef A, et al. BMC Nephrol. 2020 May 18;21(1):186. doi: 10.1186/s12882-020-01836-3. BMC Nephrol. 2020. PMID: 32423387 Free PMC article.
It helps in identifying the exact specific diagnosis, assessing the level of disease activity and severity, and hence aids in proper therapy and helps predicting prognosis. There is a global change of pattern of glomerular disease over the last five decades. ...
It helps in identifying the exact specific diagnosis, assessing the level of disease activity and severity, and hence aids in proper therapy …
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group; Hildebrandt F. Sadowski CE, et al. J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27. J Am Soc Nephrol. 2015. PMID: 25349199 Free PMC article.
Deaths: Leading Causes for 2020.
Curtin SC, Tejada-Vera B, Bastian BA. Curtin SC, et al. Natl Vital Stat Rep. 2023 Dec;72(13):1-115. Natl Vital Stat Rep. 2023. PMID: 38085308 Free article.
MicroRNAs in childhood nephrotic syndrome.
Dhandapani MC, Venkatesan V, Pricilla C. Dhandapani MC, et al. J Cell Physiol. 2021 Oct;236(10):7186-7210. doi: 10.1002/jcp.30374. Epub 2021 Apr 5. J Cell Physiol. 2021. PMID: 33819345 Review.
Because of their conservative feature in evolution and important role in the physiological function, microRNAs could be treated as predictors for disease classification and clinical process based on the specific expression. ...
Because of their conservative feature in evolution and important role in the physiological function, microRNAs could be treated as predic …
Deaths: Leading Causes for 2018.
Heron M. Heron M. Natl Vital Stat Rep. 2021 May;70(4):1-115. Natl Vital Stat Rep. 2021. PMID: 34029179
Idiopathic Nephrotic Syndrome in Pediatrics: An Up-to-date.
da Silva Filha R, Burini K, Pires LG, Brant Pinheiro SV, Simões E Silva AC. da Silva Filha R, et al. Curr Pediatr Rev. 2022;18(4):251-264. doi: 10.2174/1573396318666220314142713. Curr Pediatr Rev. 2022. PMID: 35289253 Review.
There are several gaps in the etiopathogenesis, response to treatment and clinical course of INS that justify further investigation. Novel advances include the recent understanding of the role of podocytes in INS and the identification of genes associated with the disease. …
There are several gaps in the etiopathogenesis, response to treatment and clinical course of INS that justify further investigation. …
Age of Onset and Disease Course in Biopsy-Proven Minimal Change Disease: An Analysis From the Cure Glomerulonephropathy Network.
Chen DP, Helmuth ME, Smith AR, Canetta PA, Ayoub I, Mucha K, Kallash M, Kopp JB, Gbadegesin R, Gillespie BW, Greenbaum LA, Parekh RS, Hunley TE, Sperati CJ, Selewski DT, Kidd J, Chishti A, Reidy K, Mottl AK, Gipson DS, Srivastava T, Twombley KE; CureGN Consortium. Chen DP, et al. Am J Kidney Dis. 2023 Jun;81(6):695-706.e1. doi: 10.1053/j.ajkd.2022.11.012. Epub 2023 Jan 3. Am J Kidney Dis. 2023. PMID: 36608921 Free PMC article.
RATIONALE & OBJECTIVE: Adolescent- and adult-onset minimal change disease (MCD) may have a clinical course distinct from childhood-onset disease. We characterized the course of children and adults with MCD in the Cure Glomerulonephropathy Network (CureGN) and as …
RATIONALE & OBJECTIVE: Adolescent- and adult-onset minimal change disease (MCD) may have a clinical course distinct from childhoo …
834 results