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

Year Number of Results
1930 1
1943 1
1944 4
1945 4
1946 19
1947 6
1948 6
1949 7
1950 12
1951 10
1952 10
1953 22
1954 12
1955 11
1956 11
1957 14
1958 18
1959 16
1960 15
1961 18
1962 19
1963 26
1964 38
1965 39
1966 37
1967 53
1968 50
1969 61
1970 49
1971 54
1972 75
1973 63
1974 63
1975 112
1976 107
1977 132
1978 127
1979 164
1980 137
1981 149
1982 178
1983 195
1984 198
1985 190
1986 190
1987 208
1988 211
1989 268
1990 272
1991 296
1992 284
1993 327
1994 322
1995 329
1996 371
1997 355
1998 384
1999 398
2000 419
2001 397
2002 392
2003 470
2004 442
2005 562
2006 588
2007 640
2008 645
2009 649
2010 651
2011 734
2012 709
2013 788
2014 849
2015 830
2016 882
2017 852
2018 970
2019 1051
2020 1131
2021 1280
2022 1260
2023 1111
2024 423

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23,157 results

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Page 1
Altered glycosylation of IgG4 promotes lectin complement pathway activation in anti-PLA2R1-associated membranous nephropathy.
Haddad G, Lorenzen JM, Ma H, de Haan N, Seeger H, Zaghrini C, Brandt S, Kölling M, Wegmann U, Kiss B, Pál G, Gál P, Wüthrich RP, Wuhrer M, Beck LH, Salant DJ, Lambeau G, Kistler AD. Haddad G, et al. J Clin Invest. 2021 Mar 1;131(5):e140453. doi: 10.1172/JCI140453. J Clin Invest. 2021. PMID: 33351779 Free PMC article.
Primary membranous nephropathy (pMN) is a leading cause of nephrotic syndrome in adults. In most cases, this autoimmune kidney disease is associated with autoantibodies against the M-type phospholipase A2 receptor (PLA2R1) expressed on kidney podocytes, but t …
Primary membranous nephropathy (pMN) is a leading cause of nephrotic syndrome in adults. In most cases, this autoimmune kidney …
Genetics and CKD.
Vehaskari VM. Vehaskari VM. Adv Chronic Kidney Dis. 2011 Sep;18(5):317-23. doi: 10.1053/j.ackd.2011.07.001. Adv Chronic Kidney Dis. 2011. PMID: 21896372 Review.
Mutations affecting the integrity of the glomerular filtration barrier cause proteinuria or nephrotic syndrome; different types of Alport syndrome are caused by mutations in glomerular basement membrane type IV collagen; dysfunction of the primary cili …
Mutations affecting the integrity of the glomerular filtration barrier cause proteinuria or nephrotic syndrome; different type …
Developmental Abnormalities of Teeth in Children With Nephrotic Syndrome.
Piekoszewska-Ziętek P, Olczak-Kowalczyk D, Pańczyk-Tomaszewska M, Gozdowski D. Piekoszewska-Ziętek P, et al. Int Dent J. 2022 Aug;72(4):572-577. doi: 10.1016/j.identj.2021.11.014. Epub 2022 Mar 8. Int Dent J. 2022. PMID: 35277264 Free PMC article.
The aim was to assess the frequency and type of dental abnormalities and the correlation of their occurrence with a dosage of glucocorticoids and treatment time in children with idiopathic nephrotic syndrome. METHODS: The study group consisted of 31 pa …
The aim was to assess the frequency and type of dental abnormalities and the correlation of their occurrence with a dosage of …
NUP85 as a Neurodevelopmental Gene: From Podocyte to Neuron.
Gambadauro A, Mangano GD, Galletta K, Granata F, Riva A, Massella L, Guzzo I, Farello G, Scorrano G, Di Francesco L, Di Donato G, Ianni C, Di Ludovico A, La Bella S, Striano P, Efthymiou S, Houlden H, Nardello R, Chimenz R. Gambadauro A, et al. Genes (Basel). 2023 Nov 27;14(12):2143. doi: 10.3390/genes14122143. Genes (Basel). 2023. PMID: 38136965 Free PMC article. Review.
Pathogenic gene variants encoding nuclear pore complex (NPC) proteins were previously implicated in the pathogenesis of steroid-resistant nephrotic syndrome (SRNS). The NUP85 gene, encoding nucleoporin, is related to a very rare form of SRNS with limited genotype-ph …
Pathogenic gene variants encoding nuclear pore complex (NPC) proteins were previously implicated in the pathogenesis of steroid-resistant …
Elevated Soluble Podoplanin Associates with Hypercoagulability in Patients with Nephrotic Syndrome.
Ji Y, Wang YL, Xu F, Jia XB, Mu SH, Lyu HY, Yuan XY, Na SP, Bao YS. Ji Y, et al. Clin Appl Thromb Hemost. 2022 Jan-Dec;28:10760296221108967. doi: 10.1177/10760296221108967. Clin Appl Thromb Hemost. 2022. PMID: 35862263 Free PMC article.
The aim of this study is to investigate the association of soluble PDPN/CLEC-2 with hypercoagulability in nephrotic syndrome. Thirty-five patients with nephrotic syndrome and twenty-seven healthy volunteers were enrolled. ...When serum PDPN was > …
The aim of this study is to investigate the association of soluble PDPN/CLEC-2 with hypercoagulability in nephrotic syndrome. …
Down syndrome.
Catalano RA. Catalano RA. Surv Ophthalmol. 1990 Mar-Apr;34(5):385-98. doi: 10.1016/0039-6257(90)90116-d. Surv Ophthalmol. 1990. PMID: 2139246 Review.
Down syndrome is the most common chromosome abnormality of man. The isolated occurrence of any one of the most of the protean systemic and ocular features of Down syndrome is not specific to the disorder. ...Associated ocular disorders can signi …
Down syndrome is the most common chromosome abnormality of man. The isolated occurrence of any one of the most of the protean …
Management of patients with nephrotic syndrome.
de Seigneux S, Martin PY. de Seigneux S, et al. Swiss Med Wkly. 2009 Jul 25;139(29-30):416-22. doi: 10.4414/smw.2009.12477. Swiss Med Wkly. 2009. PMID: 19680831 Free article. Review.
Nephrotic syndrome is characterised by proteinuria >3.5 g/24h, oedema, hypoalbuminaemia and hyperlipidaemia. Several glomerular diseases, either primary or secondary, may lead to nephrotic syndrome. Investigations for nephrotic synd …
Nephrotic syndrome is characterised by proteinuria >3.5 g/24h, oedema, hypoalbuminaemia and hyperlipidaemia. Several …
Sphingosine phosphate lyase insufficiency syndrome: a systematic review.
Pournasiri Z, Madani A, Nazarpack F, Sayer JA, Chavoshzadeh Z, Nili F, Tran P, Saba JD, Jamee M. Pournasiri Z, et al. World J Pediatr. 2023 May;19(5):425-437. doi: 10.1007/s12519-022-00615-4. Epub 2022 Nov 12. World J Pediatr. 2023. PMID: 36371483 Review.
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused by biallelic mutations in SGPL1. ...Kidney disorders (42, 80.8%) were mainly in the form of steroid-resistant nephrotic syndrome …
BACKGROUND: Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) or nephrotic syndrome type-14 is caused …
Global glomerulosclerosis with nephrotic syndrome; the clinical importance of age adjustment.
Hommos MS, Zeng C, Liu Z, Troost JP, Rosenberg AZ, Palmer M, Kremers WK, Cornell LD, Fervenza FC, Barisoni L, Rule AD. Hommos MS, et al. Kidney Int. 2018 May;93(5):1175-1182. doi: 10.1016/j.kint.2017.09.028. Epub 2017 Dec 19. Kidney Int. 2018. PMID: 29273332 Free PMC article.
To evaluate this, we identified patients with a glomerulopathy that often presents with nephrotic syndrome (focal segmental glomerulosclerosis, membranous nephropathy, or minimal change disease) in the setting of the Nephrotic Syndrome Study Network (N …
To evaluate this, we identified patients with a glomerulopathy that often presents with nephrotic syndrome (focal segmental gl …
Childhood nephrotic syndrome in tropical Africa: then and now.
Olowu WA, Ademola A, Ajite AB, Saad YM. Olowu WA, et al. Paediatr Int Child Health. 2017 Nov;37(4):259-268. doi: 10.1080/20469047.2017.1374002. Epub 2017 Sep 26. Paediatr Int Child Health. 2017. PMID: 28949280 Review.
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic syndrome (NS) in tropical Africa (TpAfr). In the 1960s to 1980s, corticosteroid-resistant non-minimal change disease (nMCD) includ …
This descriptive and comparative review examines the changing epidemiology, treatment, renal and patient outcome of childhood nephrotic …
23,157 results
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