Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1580) 1580
Publication (124) 124
Newsletter (22) 22
Book Review (17) 17
Book Chapter (9) 9
Book / eBook (3) 3
Conference Proceeding (2) 2
Magazine Article (1) 1
Newspaper Article (1) 1
Paper (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1356) 1356
nephrotic syndrome (1008) 1008
male (934) 934
female (917) 917
index medicus (607) 607
urology & nephrology (572) 572
child (566) 566
adult (517) 517
adolescent (473) 473
nephrotic syndrome - epidemiology (432) 432
middle aged (419) 419
child, preschool (413) 413
risk factors (362) 362
retrospective studies (318) 318
children (310) 310
biopsy (301) 301
infant (287) 287
aged (268) 268
pediatrics (251) 251
nephrology (236) 236
kidney diseases (229) 229
glomerulonephritis (224) 224
incidence (212) 212
nephrotic syndrome - drug therapy (205) 205
prevalence (197) 197
prognosis (197) 197
proteinuria (191) 191
focal segmental glomerulosclerosis (187) 187
nephrotic syndrome - complications (181) 181
epidemiology (174) 174
kidney - pathology (173) 173
disease (167) 167
nephrotic syndrome - etiology (167) 167
treatment outcome (163) 163
nephrotic syndrome - pathology (156) 156
research (154) 154
medicine, general & internal (142) 142
diagnosis (135) 135
nephrotic syndrome - diagnosis (133) 133
care and treatment (128) 128
young adult (125) 125
transplantation (122) 122
glomerulonephritis - epidemiology (121) 121
medicine & public health (114) 114
glomerulosclerosis, focal segmental - epidemiology (113) 113
membranous nephropathy (113) 113
kidney diseases - epidemiology (111) 111
follow-up studies (110) 110
immunosuppressive agents - therapeutic use (110) 110
medicine (110) 110
nephropathy (105) 105
time factors (105) 105
age factors (102) 102
recurrence (102) 102
childhood (95) 95
analysis (93) 93
hypertension (92) 92
health aspects (90) 90
kidney failure, chronic - epidemiology (90) 90
adults (88) 88
glomerulosclerosis, focal segmental - pathology (88) 88
infant, newborn (88) 88
kidneys (88) 88
medical research (88) 88
animals (87) 87
disease progression (87) 87
nephrotic syndrome - genetics (87) 87
prospective studies (86) 86
cohort studies (84) 84
research article (82) 82
glomerulonephritis, membranous - epidemiology (80) 80
kidney transplantation (80) 80
risk (80) 80
medicine, experimental (79) 79
therapy (79) 79
glomerulonephritis - pathology (76) 76
kidney glomerulus - pathology (75) 75
iga nephropathy (74) 74
proteinuria - epidemiology (74) 74
development and progression (73) 73
patients (72) 72
proteinuria - etiology (72) 72
chronic kidney failure (71) 71
aged, 80 and over (70) 70
renal biopsy (70) 70
chronic kidney disease (69) 69
nephrotic syndrome - physiopathology (69) 69
complications and side effects (68) 68
age of onset (66) 66
chronic kidney-disease (66) 66
glucocorticoids - therapeutic use (66) 66
proteins (66) 66
diseases (65) 65
glomerular filtration rate (65) 65
nephrosis, lipoid - epidemiology (65) 65
kidney diseases - pathology (64) 64
mutation (63) 63
rodents (63) 63
comorbidity (62) 62
mortality (61) 61
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1478) 1478
French (29) 29
Japanese (23) 23
Spanish (18) 18
Russian (17) 17
German (12) 12
Chinese (8) 8
Polish (8) 8
Italian (5) 5
Portuguese (3) 3
Finnish (2) 2
Korean (2) 2
Romanian (2) 2
Turkish (2) 2
Bulgarian (1) 1
Croatian (1) 1
Hungarian (1) 1
Lithuanian (1) 1
Serbian (1) 1
Swedish (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Epidemiology and Pathophysiology of Nephrotic Syndrome–Associated Thromboembolic Disease
by Bryce A. Kerlin and Rose Ayoob and William E. Smoyer
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 03/2012, Volume 7, Issue 3, pp. 513 - 520
After infections, thromboembolism is considered by many experts to be the most significant life-threatening complication of nephrotic syndrome. The purpose of... 
INFERIOR VENA-CAVA | FREE PROTEIN-S | RISK-FACTORS | INTERNATIONAL CONSENSUS STATEMENT | VENOUS THROMBOEMBOLISM | DEFINITE ANTIPHOSPHOLIPID SYNDROME | ANTITHROMBOTIC THERAPY | UROLOGY & NEPHROLOGY | MEMBRANOUS NEPHROPATHY | RENAL-VEIN THROMBOSIS | CLASSIFICATION CRITERIA | Risk Assessment | Humans | Risk Factors | Child, Preschool | Anticoagulants - therapeutic use | Infant | Treatment Outcome | Nephrotic Syndrome - drug therapy | Thromboembolism - epidemiology | Animals | Thromboembolism - blood | Blood Coagulation - drug effects | Nephrotic Syndrome - physiopathology | Fibrinolytic Agents - therapeutic use | Thrombolytic Therapy | Nephrotic Syndrome - epidemiology | Adult | Thromboembolism - drug therapy | Thromboembolism - physiopathology | Nephrotic Syndrome - blood | Child | In-Depth Review
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Spectrum of steroid-resistant and congenital nephrotic syndrome in children: The podoNet registry cohort
by Trautmann, Agnes and Bodria, Monica and Ozaltin, Fatih and Gheisari, Alaleh and Melk, Anette and Azocar, Marta and Anarat, Ali and Caliskan, Salim and Emma, Francesco and Gellermann, Jutta and Oh, Jun and Baskin, Esra and Ksiazek, Joanna and Remuzzi, Giuseppe and Erdogan, Ozlem and Akman, Sema and Dusek, Jiri and Davitaia, Tinatin and Özkaya, Ozan and Papachristou, Fotios and Firszt-Adamczyk, Agnieszka and Urasinski, Tomasz and Testa, Sara and Krmar, Rafael T and Hyla-Klekot, Lidia and Pasini, Andrea and Özcakar, Z. Birsin and Sallay, Peter and Cakar, Nilgun and Galanti, Monica and Terzic, Joelle and Aoun, Bilal and Afonso, Alberto Caldas and Szymanik-Grzelak, Hanna and Lipska, Beata S and Schnaidt, Sven and Schaefer, Franz and PodoNet Consortium
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 2015, Volume 10, Issue 4, pp. 592 - 600
Background and objectives Steroid-resistant nephrotic syndrome is a rare kidney disease involving either immune-mediated or genetic alterations of podocyte... 
UROLOGY & NEPHROLOGY | PATTERNS | THERAPY | MUTATIONS | CYCLOPHOSPHAMIDE | NPHS2 | Recurrence | Age Distribution | Prospective Studies | Glomerulosclerosis, Focal Segmental - genetics | Humans | Immunosuppressive Agents - therapeutic use | Nephrosis, Lipoid - epidemiology | Child, Preschool | Infant | Male | Nephrotic Syndrome - genetics | Nephrotic Syndrome - congenital | Young Adult | DNA Mutational Analysis | Female | Registries | Nephrotic Syndrome - therapy | Retrospective Studies | Child | Nephrotic Syndrome - diagnosis | Infant, Newborn | Latin America - epidemiology | Genetic Predisposition to Disease | Nephrosis, Lipoid - diagnosis | Glomerulosclerosis, Focal Segmental - epidemiology | Risk Factors | Europe - epidemiology | Treatment Outcome | Kidney Transplantation | Nephrosis, Lipoid - therapy | Genetic Markers | Nephrosis, Lipoid - genetics | Glomerulonephritis, Membranoproliferative - therapy | Remission Induction | Glomerulosclerosis, Focal Segmental - diagnosis | Glomerulonephritis, Membranoproliferative - genetics | Middle East - epidemiology | Phenotype | Biopsy | Adolescent | Age of Onset | Nephrotic Syndrome - epidemiology | Glomerulonephritis, Membranoproliferative - diagnosis | Glomerulosclerosis, Focal Segmental - therapy | Mutation | Glomerulonephritis, Membranoproliferative - epidemiology | podocytopathies | nephrin | children | WT1 | Original | podocin
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome
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
Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of ESRD in the first two decades of life. Effective treatment is lacking. First... 
MUTATION ANALYSIS | GENOTYPE/PHENOTYPE CORRELATION | POSTTRANSPLANT | WORLDWIDE COHORT | UROLOGY & NEPHROLOGY | WT1 MUTATIONS | PODOCIN | NPHS1 MUTATIONS | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | DIFFUSE MESANGIAL SCLEROSIS | AGE-OF-ONSET | Humans | Middle Aged | Child, Preschool | Infant | Male | Nephrotic Syndrome - genetics | Nephrotic Syndrome - congenital | Incidence | Young Adult | Adult | Female | Retrospective Studies | Genetic Predisposition to Disease - epidemiology | Child | Intracellular Signaling Peptides and Proteins - genetics | Real-Time Polymerase Chain Reaction | Genetic Association Studies | Risk Assessment | Membrane Proteins - genetics | Genotype | Phenotype | Genes, Wilms Tumor | Nephrotic Syndrome - physiopathology | Pedigree | Adolescent | Age of Onset | Nephrotic Syndrome - epidemiology | Heterozygote | Mutation | Cohort Studies | SRNS | steroid-resistant nephrotic syndrome | kidney failure | FSGS | nephrosis | genetic disease | Basic Research
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach
by Gadegbeku, Crystal A and Gipson, Debbie S and Holzman, Lawrence B and Ojo, Akinlolu O and Song, Peter X.K and Barisoni, Laura and Sampson, Matthew G and Kopp, Jeffrey B and Lemley, Kevin V and Nelson, Peter J and Lienczewski, Chrysta C and Adler, Sharon G and Appel, Gerald B and Cattran, Daniel C and Choi, Michael J and Contreras, Gabriel and Dell, Katherine M and Fervenza, Fernando C and Gibson, Keisha L and Greenbaum, Larry A and Hernandez, Joel D and Hewitt, Stephen M and Hingorani, Sangeeta R and Hladunewich, Michelle and Hogan, Marie C and Hogan, Susan L and Kaskel, Frederick J and Lieske, John C and Meyers, Kevin E.C and Nachman, Patrick H and Nast, Cynthia C and Neu, Alicia M and Reich, Heather N and Sedor, John R and Sethna, Christine B and Trachtman, Howard and Tuttle, Katherine R and Zhdanova, Olga and Zilleruelo, Gastòn E and Kretzler, Matthias
Kidney International, ISSN 0085-2538, 04/2013, Volume 83, Issue 4, pp. 749 - 756
The Nephrotic Syndrome Study Network (NEPTUNE) is a North American multicenter collaborative consortium established to develop a translational research... 
clinical trial | focal segmental glomerulosclerosis | membranous nephropathy | nephrotic syndrome | CLINICAL SPECTRUM | BIOLOGY | UROLOGY & NEPHROLOGY | GENETIC-HETEROGENEITY | CLASSIFICATION | RENAL-DISEASE | IDIOPATHIC MEMBRANOUS NEPHROPATHY | Predictive Value of Tests | Glomerulonephritis - therapy | Prognosis | Prospective Studies | Age Factors | Glomerulosclerosis, Focal Segmental - genetics | Humans | Nephrosis, Lipoid - epidemiology | Glomerulonephritis, Membranous - genetics | Glomerulonephritis, Membranous - epidemiology | Nephrotic Syndrome - genetics | Systems Biology | Time Factors | Adult | Registries | Surveys and Questionnaires | Nephrotic Syndrome - therapy | Translational Medical Research - methods | Child | Glomerulonephritis, Membranous - therapy | Glomerulonephritis - epidemiology | Glomerulosclerosis, Focal Segmental - epidemiology | Glomerulonephritis, Membranous - pathology | Risk Factors | Glomerulonephritis - genetics | Cooperative Behavior | Nephrotic Syndrome - pathology | Genotype | Nephrosis, Lipoid - therapy | Nephrosis, Lipoid - genetics | Phenotype | Pilot Projects | Nephrosis, Lipoid - pathology | Biopsy | Glomerulonephritis - pathology | Nephrotic Syndrome - epidemiology | Glomerulosclerosis, Focal Segmental - therapy | North America - epidemiology | Longitudinal Studies | Research Design | Glomerulosclerosis, Focal Segmental - pathology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text AKI in children hospitalized with nephrotic syndrome
by Rheault, Michelle N and Zhang, Lei and Selewski, David T and Kallash, Mahmoud and Tran, Cheryl L and Seamon, Meredith and Katsoufis, Chryso and Ashoor, Isa and Hernandez, Joel and Supe-Markovina, Katarina and D’alessandri-Silva, Cynthia and Dejesus-Gonzalez, Nilka and Vasylyeva, Tetyana L and Formeck, Cassandra and Woll, Christopher and Gbadegesin, Rasheed and Geier, Pavel and Devarajan, Prasad and Carpenter, Shannon L and Kerlin, Bryce A and Smoyer, William E and Midwest Pediat Nephrology Consorti and Midwest Pediatric Nephrology Consortium
Clinical Journal of the American Society of Nephrology, ISSN 1555-9041, 12/2015, Volume 10, Issue 12, pp. 2110 - 2118
Background and objectives Children with nephrotic syndrome can develop life-threatening complications, including infection and thrombosis. While AKI is... 
ACUTE KIDNEY INJURY | INTENSIVE-CARE-UNIT | ADOLESCENTS | RENAL-FAILURE | UROLOGY & NEPHROLOGY | COHORT | CRITICALLY-ILL CHILDREN | OUTCOMES | LENGTH-OF-STAY | STRATIFICATION | EPIDEMIOLOGY | Multivariate Analysis | Age Factors | Humans | Child, Preschool | Infant | Male | Incidence | Time Factors | Female | Nephrotic Syndrome - therapy | Retrospective Studies | Odds Ratio | Child | Nephrotic Syndrome - diagnosis | Length of Stay | Risk Factors | Medical Records | Linear Models | Treatment Outcome | Hospitalization | Drug-Related Side Effects and Adverse Reactions - epidemiology | Acute Kidney Injury - diagnosis | Adolescent | Nephrotic Syndrome - epidemiology | Acute Kidney Injury - therapy | Acute Kidney Injury - epidemiology | North America - epidemiology | Drug-Related Side Effects and Adverse Reactions - diagnosis | Drug-Related Side Effects and Adverse Reactions - therapy | Index Medicus | dialysis | risk factors | nephrotoxicity | hospitalization | length of stay | acute kidney injury | Original | humans | incidence | nephrotic syndrome | child
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Epidemiology of idiopathic nephrotic syndrome in children: endemic or epidemic?
by Dossier, Claire and Lapidus, Nathanael and Bayer, Florian and Sellier-Leclerc, Anne-Laure and Boyer, Olivia and de Pontual, Loic and May, Adrien and Nathanson, Sylvie and Orzechowski, Christine and Simon, Tabassome and Carrat, Fabrice and Deschênes, Georges
Pediatric Nephrology, ISSN 0931-041X, 12/2016, Volume 31, Issue 12, pp. 2299 - 2308
The etiology of idiopathic nephrotic syndrome (INS) remains partially unknown. Viral infections have been reported to be associated with INS onset and relapse.... 
Pediatrics | Nephrology | Medicine & Public Health | Childhood | Cluster | Nephrotic syndrome | Seasonal periodicity | Epidemiology | Urology | ASIANS | UROLOGY & NEPHROLOGY | PEDIATRICS | ONSET | Epidemics | Prospective Studies | Age Factors | Humans | Child, Preschool | Infant | Male | Nephrotic Syndrome - drug therapy | Socioeconomic Factors | Incidence | Endemic Diseases | Nephrotic Syndrome - virology | Adolescent | Nephrotic Syndrome - epidemiology | Female | Steroids - therapeutic use | Seasons | Child | Cluster Analysis | Cohort Studies | Paris - epidemiology | Diagnosis | Research | Demographic aspects | Risk factors | Prevalence studies (Epidemiology)
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Phospholipase A2 receptor autoantibodies and clinical outcome in patients with primary membranous nephropathy
by Hoxha, Elion and Hoxha, Elion and Thiele, Ina and Thiele, Ina and Zahner, Gunther and Zahner, Gunther and Panzer, Ulf and Panzer, Ulf and Harendza, Sigrid and Harendza, Sigrid and Stahl, Rolf A.K and Stahl, Rolf A K
Journal of the American Society of Nephrology : JASN, ISSN 1046-6673, 2014, Volume 25, Issue 6, pp. 1357 - 1366
Membranous nephropathy (MN) is the most common cause of nephrotic syndrome in adults, with an uncertain clinical outcome. The characterization of the... 
GLOMERULONEPHRITIS | ANTIBODIES | TARGET | RITUXIMAB | UROLOGY & NEPHROLOGY | CYCLOSPORINE | ELISA | Prognosis | Prospective Studies | Follow-Up Studies | Receptors, Phospholipase A2 - immunology | Humans | Middle Aged | Male | Seroepidemiologic Studies | Glomerulonephritis, Membranous - epidemiology | Nephrotic Syndrome - drug therapy | Glomerulonephritis, Membranous - immunology | Adult | Female | Immunosuppressive Agents - administration & dosage | Proteinuria - epidemiology | Proteinuria - immunology | Risk Factors | Treatment Outcome | Nephrotic Syndrome - immunology | Autoantibodies - immunology | Proteinuria - drug therapy | Glomerulonephritis, Membranous - drug therapy | Nephrotic Syndrome - epidemiology | Aged | Serum Albumin - metabolism | Clinical Research
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Global glomerulosclerosis with nephrotic syndrome; the clinical importance of age adjustment
by Hommos, Musab S and Zeng, Caihong and Liu, Zhihong and Troost, Jonathan P and Rosenberg, Avi Z and Palmer, Matthew and Kremers, Walter K and Cornell, Lynn D and Fervenza, Fernando C and Barisoni, Laura and Rule, Andrew D
Kidney International, ISSN 0085-2538, 05/2018, Volume 93, Issue 5, pp. 1175 - 1182
Globally sclerotic glomeruli (GSG) occur with both normal aging and kidney disease. However, it is unknown whether any GSG or only GSG exceeding that expected... 
FSGS | global glomerulosclerosis | age-based threshold | minimal change disease | membranous nephropathy | nephrotic syndrome | PROGNOSIS | CLASSIFICATION | BIOPSY SPECIMENS | NEPHROPATHY | AGING KIDNEY | FUNCTIONAL-CHANGES | UROLOGY & NEPHROLOGY | CHRONIC KIDNEY-DISEASE | RENAL BIOPSY | PROGRESSION | NEPHROSCLEROSIS | Age Distribution | Prognosis | Age Factors | Kidney - pathology | Humans | Middle Aged | Nephrosis, Lipoid - epidemiology | Male | Glomerulonephritis, Membranous - epidemiology | Glomerulonephritis, Membranous - physiopathology | Incidence | Young Adult | Time Factors | Adult | Female | Glomerulosclerosis, Focal Segmental - physiopathology | Nephrotic Syndrome - diagnosis | Kidney - physiopathology | Kidney Failure, Chronic - physiopathology | Glomerular Filtration Rate | Kidney Failure, Chronic - diagnosis | Nephrosis, Lipoid - diagnosis | Glomerulosclerosis, Focal Segmental - epidemiology | Risk Factors | China - epidemiology | Disease Progression | Nephrosis, Lipoid - physiopathology | Glomerulosclerosis, Focal Segmental - diagnosis | Kidney Failure, Chronic - epidemiology | Biopsy | Nephrotic Syndrome - physiopathology | Adolescent | Glomerulonephritis, Membranous - diagnosis | Nephrotic Syndrome - epidemiology | Aged | North America - epidemiology | Hypertension | End-stage renal disease | Kidneys | Diabetes mellitus | Nephrotic syndrome | Patients | Glomerular filtration rate | Body mass index | Nephropathy | Membranous nephropathy | Arteriosclerosis | Fibrosis | Aging | Diabetes | Kidney diseases | Age | Proteinuria
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text HLA-DQA1 and PLCG2 are candidate risk loci for childhood-onset steroid-sensitive nephrotic syndrome
by Gbadegesin, Rasheed A and Adeyemo, Adebowale and Webb, Nicholas J. A and Greenbaum, Larry A and Abeyagunawardena, Asiri and Thalgahagoda, Shenal and Kale, Arundhati and Gipson, Debbie and Srivastava, Tarak and Lin, Jen-Jar and Chand, Deepa and Hunley, Tracy E and Brophy, Patrick D and Bagga, Arvind and Sinha, Aditi and Rheault, Michelle N and Ghali, Joanna and Nicholls, Kathy and Abraham, Elizabeth and Janjua, Halima S and Omoloja, Abiodun and Barletta, Gina-Marie and Cai, Yi and Milford, David D and O'Brien, Catherine and Awan, Atif and Belostotsky, Vladimir and Smoyer, William E and Homstad, Alison and Hall, Gentzon and Wu, Guanghong and Nagaraj, Shashi and Wigfall, Delbert and Foreman, John and Winn, Michelle P and Mid-West Pediat Nephrology Consort and Mid-West Pediatric Nephrology Consortium and Members of the Mid-West Pediatric Nephrology Consortium
Journal of the American Society of Nephrology, ISSN 1046-6673, 07/2015, Volume 26, Issue 7, pp. 1701 - 1710
Steroid-sensitive nephrotic syndrome (SSNS) accounts for >80% of cases of nephrotic syndrome in childhood. However, the etiology and pathogenesis of SSNS... 
TESTS | METAANALYSIS | RARE | ANTIGENS | glomerular disease | VARIANT | nephrotic syndrome | genetic renal disease | children | AUTOIMMUNITY | DISEASE | MUTATION | UROLOGY & NEPHROLOGY | COMMON | ASSOCIATION | Sri Lanka - epidemiology | Age Distribution | Humans | Child, Preschool | Genotype | Male | Nephrotic Syndrome - genetics | Mutation, Missense | Nephrotic Syndrome - drug therapy | HLA-DQ alpha-Chains - genetics | Case-Control Studies | Incidence | Age of Onset | Alleles | Phospholipase C gamma - genetics | Nephrotic Syndrome - epidemiology | Sex Distribution | Female | Steroids - therapeutic use | Genetic Predisposition to Disease - epidemiology | Child | Cohort Studies | Clinical Research
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Genotype–phenotype associations in WT1 glomerulopathy
by Lipska, Beata S and Ranchin, Bruno and Iatropoulos, Paraskevas and Gellermann, Jutta and Melk, Anette and Ozaltin, Fatih and Caridi, Gianluca and Seeman, Tomas and Tory, Kalman and Jankauskiene, Augustina and Zurowska, Aleksandra and Szczepanska, Maria and Wasilewska, Anna and Harambat, Jerome and Trautmann, Agnes and Peco-Antic, Amira and Borzecka, Halina and Moczulska, Anna and Saeed, Bassam and Bogdanovic, Radovan and Kalyoncu, Mukaddes and Simkova, Eva and Erdogan, Ozlem and Vrljicak, Kristina and Teixeira, Ana and Azocar, Marta and Schaefer, Franz and PodoNet Consortium
Kidney International, ISSN 0085-2538, 05/2014, Volume 85, Issue 5, pp. 1169 - 1178
mutations cause a wide spectrum of renal and extrarenal manifestations. Here we evaluated disease prevalence, phenotype spectrum, and genotype–phenotype... 
Denys–Drash syndrome | diffuse mesangial sclerosis | Frasier syndrome | steroid-resistant nephrotic syndrome | focal segmental glomerulosclerosis | WT1 | Denys-Drash syndrome | Steroid-resistant nephrotic syndrome | Diffuse mesangial sclerosis | Focal segmental glomerulosclerosis | STEROID-RESISTANT | SPLICE-SITE MUTATIONS | RESISTANT NEPHROTIC SYNDROME | BINDING ACTIVITY | SUPPRESSOR GENE WT1 | WILMS-TUMOR | PROTEIN WT1 | UROLOGY & NEPHROLOGY | FRASIER-SYNDROME | EXPRESSION | Prevalence | Prognosis | Glomerulosclerosis, Focal Segmental - genetics | Humans | Child, Preschool | Infant | Male | Nephrotic Syndrome - genetics | Genetic Testing - methods | Nephrotic Syndrome - congenital | Incidence | Renal Insufficiency, Chronic - epidemiology | Renal Insufficiency, Chronic - therapy | Time Factors | DNA Mutational Analysis | Renal Insufficiency, Chronic - genetics | Female | Registries | Renal Insufficiency, Chronic - diagnosis | Nephrotic Syndrome - therapy | Child | Nephrotic Syndrome - diagnosis | WT1 Proteins - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Glomerulosclerosis, Focal Segmental - epidemiology | Risk Factors | Disease Progression | Glomerulosclerosis, Focal Segmental - diagnosis | Phenotype | Age of Onset | Nephrotic Syndrome - epidemiology | Glomerulosclerosis, Focal Segmental - therapy | Mutation
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Epidemiology and Risk Factors for Thromboembolic Complications of Childhood Nephrotic Syndrome: A Midwest Pediatric Nephrology Consortium (MWPNC) Study
by Kerlin, Bryce A., MD and Blatt, Neal B., MD and Fuh, Beng, MD and Zhao, Shuang and Lehman, Amy, PhD and Blanchong, Carol, MD and Mahan, John D., MD and Smoyer, William E., MD
Journal of Pediatrics, The, ISSN 0022-3476, 2009, Volume 155, Issue 1, pp. 105 - 110.e1
Objectives To identify clinical variables predictive of the risk of thromboembolism (TE), and to confirm the incidence of TE in primary and secondary childhood... 
Pediatrics | SYSTEMIC-LUPUS-ERYTHEMATOSUS | INTERNATIONAL CONSENSUS STATEMENT | REVISED CRITERIA | DEFINITE ANTIPHOSPHOLIPID SYNDROME | THROMBOSIS | ADOLESCENTS | DISEASE | PEDIATRICS | COHORT | CLASSIFICATION CRITERIA | CHILDREN | Multivariate Analysis | Age Factors | Follow-Up Studies | Humans | Child, Preschool | Infant | Male | Thromboembolism - epidemiology | Incidence | Young Adult | Female | Retrospective Studies | Ohio - epidemiology | Child | Infant, Newborn | Severity of Illness Index | Proteinuria - epidemiology | Risk Factors | Catheterization, Central Venous | Creatinine - urine | Adolescent | Age of Onset | Nephrotic Syndrome - epidemiology | Michigan - epidemiology | Cohort Studies | Lupus | Medical colleges | Medical research | Nephrotic syndrome | Transplantation | Antiphospholipid antibodies | Epidemiology | Risk factors | Pulmonary embolism | Consortia | Complications and side effects | Antithrombin III | Bone marrow | Medicine, Experimental | Protein S | Venous thrombosis | Thromboembolism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome
by Machuca, Eduardo and Benoit, Geneviève and Nevo, Fabien and Tête, Marie-Josèphe and Gribouval, Olivier and Pawtowski, Audrey and Brandström, Per and Loirat, Chantal and Niaudet, Patrick and Gubler, Marie-Claire and Antignac, Corinne
Journal of the American Society of Nephrology, ISSN 1046-6673, 2010, Volume 21, Issue 7, pp. 1209 - 1217
Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which... 
DISTINCT EYE ABNORMALITIES | NEPHRIN MUTATIONS | GENOTYPE/PHENOTYPE CORRELATIONS | DIPHOSPHATE SYNTHASE SUBUNIT-2 | GLOMERULAR PROTEIN | PIERSON-SYNDROME | RENAL PATHOLOGY | UROLOGY & NEPHROLOGY | MISSENSE MUTATIONS | DIFFUSE MESANGIAL SCLEROSIS | AGE-OF-ONSET | Genetic Testing | Kidney - pathology | Humans | Child, Preschool | Infant | Male | Nephrotic Syndrome - genetics | Nephrotic Syndrome - congenital | Kidney Failure, Chronic - pathology | Female | Retrospective Studies | Intracellular Signaling Peptides and Proteins - genetics | Infant, Newborn | Membrane Proteins - genetics | Kaplan-Meier Estimate | Europe - epidemiology | Genotype | Mutation - genetics | Disease Progression | Phenotype | Turkey - epidemiology | Biopsy | Nephrotic Syndrome - epidemiology | Africa, Northern - epidemiology | Cohort Studies | Clinical Research
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights