1
40
5
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.3109/00365599.2011.568954" target="_blank" rel="noreferrer noopener">http://doi.org/10.3109/00365599.2011.568954</a>
Rights
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
Pages
473-477
Issue
6
Volume
45
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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Waldenstrom's Macroglobulinemia And Nephrotic Syndrome With Membranous Nephropathy
Publisher
An entity responsible for making the resource available
Scandinavian Journal of Urology and Nephrology
Date
A point or period of time associated with an event in the lifecycle of the resource
2011
2011-12
Subject
The topic of the resource
antibody; glomerulonephritis; macroglobulinemia; membranous nephropathy; nephrotic syndrome; pathology; Urology & Nephrology; Waldenstrom's
Creator
An entity primarily responsible for making the resource
Lee B; Smith R S; Tanphaichitr N; Novak R; Robertson S; Haller N A
Description
An account of the resource
Renal complications of Waldenstrom's macroglobulinemia (WM) are rarely observed. Nephrotic syndrome in association with WM has most often been secondary to amyloidosis. This article reports a case of WM with nephrotic syndrome as a result of membranous nephropathy with immunoglobulin M (IgM) deposition. A 44-year-old male diagnosed with WM 4 years previously, presented with heavy proteinuria (7.8 g/24 h). Kidney biopsy revealed expanded mesangium, thickened capillary loops and epimembranous spikes, with no significant interstitial inflammation or thickened tubular basement membranes. Immunofluorescence examination demonstrated strong granular staining of IgM and l light chains, with weaker C3 and C1q staining. Electron microscopy showed many subepithelial dense deposits, and fewer large subendothelial dense deposits. Treatment was directed at the patient's WM with maintenance rituximab and fludarabine. Subsequently, decreases were seen in both the patient's serum IgM and serum viscosity. With therapy for WM and the addition of an angiotensin receptor blocker, the patient's proteinuria also improved, from 7.8 g to 4.8 g/24 h. The patient continued to follow up with his hematologist and in 2009 creatinine was 1 mg/dl (76.26 mu mol/l), with a 24 h urine protein excretion of 0.159 g.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.3109/00365599.2011.568954" target="_blank" rel="noreferrer noopener">10.3109/00365599.2011.568954</a>
Format
The file format, physical medium, or dimensions of the resource
Journal Article or Conference Abstract Publication
2011
antibody
Department of Internal Medicine
Glomerulonephritis
Haller N A
Journal Article or Conference Abstract Publication
Lee B
macroglobulinemia
membranous nephropathy
NEOMED College of Medicine
Nephrotic syndrome
Novak R
Pathology
Robertson S
Scandinavian Journal of Urology and Nephrology
Smith R S
Tanphaichitr N
Urology & Nephrology
Waldenstrom's
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
n/a
Rights
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
Pages
5P-5P
Issue
1
Volume
81
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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
From research literature to the clinical laboratory, problems in translation
Publisher
An entity responsible for making the resource available
Laboratory Investigation
Date
A point or period of time associated with an event in the lifecycle of the resource
2001
2001-01
Subject
The topic of the resource
Pathology; Research & Experimental Medicine
Creator
An entity primarily responsible for making the resource
Novak R
Identifier
An unambiguous reference to the resource within a given context
n/a
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2001
Journal Article
Laboratory Investigation
Novak R
Pathology
Research & Experimental Medicine
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
n/a
Rights
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
Pages
4P-4P
Issue
1
Volume
11
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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Crescentic glomerulonephritis in the pediatric population
Publisher
An entity responsible for making the resource available
Modern Pathology
Date
A point or period of time associated with an event in the lifecycle of the resource
1998
1998-01
Subject
The topic of the resource
Pathology
Creator
An entity primarily responsible for making the resource
Novak R; Agamanolis D; Dresner I
Identifier
An unambiguous reference to the resource within a given context
n/a
Format
The file format, physical medium, or dimensions of the resource
Journal Article
1998
Agamanolis D
Dresner I
Journal Article
Modern Pathology
Novak R
Pathology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1080/08860220802213062" target="_blank" rel="noreferrer noopener">http://doi.org/10.1080/08860220802213062</a>
Rights
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
Pages
759-762
Issue
7
Volume
30
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Dublin Core
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Title
A name given to the resource
Fibrillary glomerulonephritis with hepatitis C viral infection and hypocomplementemia
Publisher
An entity responsible for making the resource available
Renal Failure
Date
A point or period of time associated with an event in the lifecycle of the resource
2008
2008
Subject
The topic of the resource
deposits; entity; features; fibrillary glomerulonephritis; hepatitis C infection; hypocomplementemia; immunofluorescence; immunotactoid glomerulopathy; Urology & Nephrology
Creator
An entity primarily responsible for making the resource
Ray S; Rouse K; Appis A; Novak R; Haller N A
Description
An account of the resource
Fibrillary glomerulonephritis (FGN) is a relatively rare cause of renal disease, found in only 0.6-1.5% of native renal biopsies. The pathogenesis of FGN is not well described, and very few associations with disease processes other than hepatitis C virus (HCV) have been made. We describe a case that provides evidence in support of the FGN-HCV association, as well as introduces the association of FGN-HCV and hypocomplementemia. The case is a 53-year-old African-American female demonstrating a classical presentation of FGN complicated by a concomitant HCV infection. Treating an HCV infection with alpha-interferon has been shown to result in subsequent improvement in the nephrotic syndrome and renal function. However, this patient is unique in that she is complicated with hypocomplementemia, creating a complex treatment situation.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1080/08860220802213062" target="_blank" rel="noreferrer noopener">10.1080/08860220802213062</a>
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2008
Appis A
deposits
entity
features
fibrillary glomerulonephritis
Haller N A
hepatitis C infection
hypocomplementemia
immunofluorescence
immunotactoid glomerulopathy
Journal Article
Novak R
Ray S
Renal failure
Rouse K
Urology & Nephrology
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
URL Address
<a href="http://doi.org/10.1080/107710497175056" target="_blank" rel="noreferrer noopener">http://doi.org/10.1080/107710497175056</a>
Rights
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
Pages
99-103
Issue
1
Volume
17
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Dublin Core
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Title
A name given to the resource
Trisomy 8 is a characteristic finding in pleuropulmonary blastoma
Publisher
An entity responsible for making the resource available
Pediatric Pathology & Laboratory Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
1997
1997-01
Subject
The topic of the resource
aberrations; childhood; chromosomal-abnormalities; mosaicism; Pathology; Pediatrics; pleuropulmonary blastoma; pulmonary blastoma; trisomy 8; tumors
Creator
An entity primarily responsible for making the resource
Novak R; Dasu S; Agamanolis D; Herold W; Malone J; Waterson J
Description
An account of the resource
The cytogenetic findings in pleuropulmonary blastoma (PPB) have not been widely studied and reported and are of interest in view of the implications that PPB has for additional tumors in the patient and the patient's relatives. Using standard tumor cytogenetic methodology, we investigated three cases of PPB encountered in our institution over a 5-year period. Trisomy 8 was the only karyotypic abnormality in a localized type 2 PPB and was present with other abnormalities in another type 2 PPB and a massive type 3 PPB. Review of the literature yielded three additional karyotyped PPBs; all had trisomy 8 as part of the abnormalities detected. Trisomy 8 appears to be a characteristic of PPB and may be related to the development of PPB and related tumors.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1080/107710497175056" target="_blank" rel="noreferrer noopener">10.1080/107710497175056</a>
Format
The file format, physical medium, or dimensions of the resource
Journal Article
1997
aberrations
Agamanolis D
childhood
chromosomal-abnormalities
Dasu S
Herold W
Journal Article
Malone J
mosaicism
Novak R
Pathology
Pediatric Pathology & Laboratory Medicine
Pediatrics
pleuropulmonary blastoma
pulmonary blastoma
trisomy 8
tumors
Waterson J