X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (91) 91
nphs1 (89) 89
humans (85) 85
congenital nephrotic syndrome (64) 64
nephrin (60) 60
urology & nephrology (54) 54
male (50) 50
nephrotic syndrome (49) 49
nephrotic syndrome - genetics (49) 49
female (46) 46
membrane proteins - genetics (45) 45
mutations (43) 43
mutation (42) 42
infant (39) 39
pediatrics (38) 38
nephrotic syndrome - congenital (35) 35
finnish type (34) 34
gene (34) 34
infant, newborn (30) 30
glomerular protein (29) 29
child (27) 27
children (27) 27
focal segmental glomerulosclerosis (27) 27
child, preschool (25) 25
podocin (25) 25
slit diaphragm (23) 23
wt1 (23) 23
nphs2 (22) 22
genetics & heredity (20) 20
nphs1 gene (20) 20
genotype (19) 19
proteinuria (19) 19
medicine & public health (18) 18
nephrology (18) 18
phenotype (17) 17
dna mutational analysis (16) 16
transplantation (16) 16
expression (15) 15
genetic disorders (15) 15
proteins - genetics (15) 15
adolescent (14) 14
membrane proteins (14) 14
nephrin gene (14) 14
nephrotic syndrome - diagnosis (14) 14
protein (14) 14
spectrum (14) 14
genetic aspects (13) 13
kidney - pathology (13) 13
adult (12) 12
kidney transplantation (12) 12
podocytes (12) 12
recurrence (12) 12
animals (11) 11
biochemistry & molecular biology (11) 11
diffuse mesangial sclerosis (11) 11
disease (11) 11
intracellular signaling peptides and proteins - genetics (11) 11
kidney (11) 11
nephrotic syndrome - pathology (11) 11
pedigree (11) 11
podocyte (11) 11
genes (10) 10
genetic predisposition to disease (10) 10
kidney diseases (10) 10
mechanisms (10) 10
nephrotic syndrome - surgery (10) 10
biopsy (9) 9
diagnosis (9) 9
disease progression (9) 9
glomerular slit diaphragm (9) 9
heterozygote (9) 9
nephrectomy (9) 9
nephrotic syndrome - therapy (9) 9
treatment outcome (9) 9
urology (9) 9
cohort studies (8) 8
congenital diseases (8) 8
genetics (8) 8
kidney - metabolism (8) 8
lamb2 (8) 8
molecular sequence data (8) 8
mutation, missense (8) 8
prognosis (8) 8
childhood (7) 7
gene mutations (7) 7
genetic research (7) 7
genotype/phenotype correlations (7) 7
membrane proteins - metabolism (7) 7
missense mutations (7) 7
mutation - genetics (7) 7
mutation analysis (7) 7
nephrotic syndrome - metabolism (7) 7
nephrotic syndrome - physiopathology (7) 7
nphs2 mutations (7) 7
podocytes - metabolism (7) 7
proteinuria - etiology (7) 7
research (7) 7
retrospective studies (7) 7
steroid-resistant nephrotic syndrome (7) 7
1st year (6) 6
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (120) 120
Spanish (4) 4
French (3) 3
Chinese (2) 2
German (1) 1
Korean (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Sadowski, Carolin E and Lovric, Svjetlana and Ashraf, Shazia and Pabst, Werner L and Gee, Heon Yung and Kohl, Stefan and Engelmann, Susanne and Vega-Warner, Virginia and Fang, Humphrey and Halbritter, Jan and Somers, Michael J and Tan, Weizhen and Shril, Shirlee and Fessi, Inès and Lifton, Richard P and Bockenhauer, Detlef and El-Desoky, Sherif and Kari, Jameela A and Zenker, Martin and Kemper, Markus J and Mueller, Dominik and Fathy, Hanan M and Soliman, Neveen A and Hildebrandt, Friedhelm and Repetto, H.A and MacTaggart, P and Johnstone, L and Alexander, S and Hodson, E and Mache, C and Jungraithmayr, T.C and Aufricht, C and Arbeiter, K and Lilova, M and Sweeny, C and Filler, G and Licht, C and Chan, S.Y and Skalova, S and Seeman, T and Nuutinen, M and Antignac, C and Briese, S and Querfeld, U and Franke, I and Bachmann, H and Kirschstein, M and Weber, L.T and Hoppe, B and Beck, B.B and Habbig, S and Mayer, B and Büscher, R and Mallmann, R and Vester, U and Latta, K and Pohl, M and Häffner, K and Patzer, L and Henne, T and Pape, L and Schiffer, M and Schwarz, A and Kiepe, D and Schäfer, F and Tönshoff, B and Rönnefarth, G and Strehlau, J.S and Schumacher, M and Beetz, R and Klaus, G and Fehrenbach, H and Kuwertz-Broeking, E and Konrad, M and Schulze-Everding, A and Benz, M.R and Griebel, M and Hoefele, J and Muscheistes, J and Wigger, M and Bald, M and Leichter, H and Reusz, G and Louis, D and Senguttuvan, P and Aravind, R and Padmaraj, R and Manorajan, M and Nampoothiri, S and Sharma, J.S and Bagga, A and Choudry, S and Schreiber, R and Frishberg, Y and Cleper, R and Chenin, G and Gianviti, A and Al-Kandari, F and Tasic, V and Ch'ng, G.S and ... and SRNS Study Grp and SRNS Study Group and the SRNS Study Group
Journal of the American Society of Nephrology, ISSN 1046-6673, 06/2015, Volume 26, Issue 6, pp. 1279 - 1289
Journal Article
Kidney International, ISSN 0085-2538, 12/2009, Volume 76, Issue 12, pp. 1268 - 1276
Journal Article
Néphrologie & Thérapeutique, ISSN 1769-7255, 12/2013, Volume 9, Issue 7, pp. 494 - 496
Rapporter le premier cas de syndrome néphrotique congénital type finlandais (SNCF) au Togo associé à une nouvelle mutation du gène . Notre observation a porté... 
NPHS1 mutation | Togo | SNC Finnish | SNC finlandais | Mutation NPHS1
Journal Article
Medical Journal of Chinese People's Liberation Army, ISSN 0577-7402, 07/2015, Volume 40, Issue 7, pp. 578 - 581
Journal Article
Journal Article
Nephrologie et Therapeutique, ISSN 1769-7255, 12/2013, Volume 9, Issue 7, pp. 494 - 496
Objective To report the first case of congenital nephrotic syndrome of the Finnish type (SNCF) in Togo associated with a new mutation of NPHS1. Observation Our... 
NPHS1 mutation | SNC Finnish | Togo
Journal Article
解放军医学杂志, ISSN 0577-7402, 2015, Volume 40, Issue 7, pp. 578 - 581
Journal Article
Journal Article
Jie Fang Jun Yi Xue Za Zhi, ISSN 0577-7402, 01/2015, Volume 40, Issue 7, pp. 578 - 581
Objective To analyze the mutations and characteristics of NPHS1 and NPHS2 genes in a child with congenital nephrotic syndrome (CNS). Methods Mutation analysis... 
Urinalysis | Genes | Mutation | mutation | genes NPHS1 | nephrotic syndrome
Journal Article
NEFROLOGIA, ISSN 0211-6995, 2014, Volume 34, Issue 2, pp. 268 - 270
Journal Article
Meta Gene, ISSN 2214-5400, 02/2017, Volume 11, pp. 98 - 103
Nephrotic syndrome (NS) is the prevailing kidney disease caused by mutations in Nephrosis-1-congenital, finish type ( ) gene. gene encodes for nephrin protein,... 
Single nucleotide polymorphisms (SNPs) | Nephrotic syndrome | Computational analysis | NPHS1 gene
Journal Article
Journal Article
Pediatrics, ISSN 0031-4005, 04/2007, Volume 119, Issue 4, pp. e907 - e919
Journal Article
FRONTIERS IN PEDIATRICS, ISSN 2296-2360, 08/2019, Volume 7, pp. 341 - 341
From January 1995 to June 2018, 14 patients with congenital nephrotic syndrome (CNS) were diagnosed in the Department of Pediatrics, Peking University First... 
NPHS1 | WT1 | clinical manifestation | PEDIATRICS | CYTOMEGALOVIRUS-INFECTION | congenital nephrotic syndrome | MUTATIONS | cytomegalovirus infection | genetic defect | prognosis
Journal Article