Hemolytic uremic syndrome associated with Denys-Drash syndrome View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2000-09

AUTHORS

J. R. Sherbotie, V. van Heyningen, R. Axton, K. Williamson, L. S. Finn, B. S. Kaplan

ABSTRACT

The Denys-Drash syndrome is defined by the occurrence of combinations of pseudohermaphroditism, nephrotic syndrome with diffuse mesangial sclerosis, Wilms' tumor, and constitutional mutations in the WT1 suppressor gene. Most patients develop end-stage renal failure. Atypical hemolytic uremic syndrome (HUS) is defined by onset of acute hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and renal failure in the absence of a gastrointestinal prodromal illness of bloody diarrhea. The purpose of this report is to describe the occurrence of features of atypical HUS and Denys-Drash syndrome in two African-American boys aged 13 and 16 months. Each had nephrotic syndrome, diffuse mesangial sclerosis, and WT1 point mutations. Both had grade III hypospadias and undescended testes. They had normal serum creatinine concentrations and hematology a month before presenting with HUS. Stool cultures for Escherichia coli O157:H7 were negative. Each patient has been transplanted with cadaver kidneys without recurrence of HUS. More... »

PAGES

1092-1097

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s004670000389

DOI

http://dx.doi.org/10.1007/s004670000389

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030868834

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/11045393


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

JSON-LD is the canonical representation for SciGraph data.

TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

[
  {
    "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
    "about": [
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/1103", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Clinical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/11", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Medical and Health Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Base Sequence", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "DNA", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "DNA-Binding Proteins", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Disorders of Sex Development", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Glomerular Mesangium", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Glomerulosclerosis, Focal Segmental", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Hemolytic-Uremic Syndrome", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Humans", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Infant", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Kidney", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Kidney Failure, Chronic", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Male", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Molecular Sequence Data", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Mutation", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Nephrotic Syndrome", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Syndrome", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Transcription Factors", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "WT1 Proteins", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Wilms Tumor", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "University of Pennsylvania", 
          "id": "https://www.grid.ac/institutes/grid.25879.31", 
          "name": [
            "Division of Nephrology, Department of Pediatrics, The Children\u2019s Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA 19104, USA e-mail: kaplanb@email.CHOP.edu Tel.: +1-215-5902451, Fax: +1-215-5903705, US"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sherbotie", 
        "givenName": "J. R.", 
        "id": "sg:person.0720257377.64", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0720257377.64"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Western General Hospital", 
          "id": "https://www.grid.ac/institutes/grid.417068.c", 
          "name": [
            "MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK, GB"
          ], 
          "type": "Organization"
        }, 
        "familyName": "van Heyningen", 
        "givenName": "V.", 
        "id": "sg:person.0606020600.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0606020600.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Western General Hospital", 
          "id": "https://www.grid.ac/institutes/grid.417068.c", 
          "name": [
            "MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK, GB"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Axton", 
        "givenName": "R.", 
        "id": "sg:person.0676331043.26", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0676331043.26"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Western General Hospital", 
          "id": "https://www.grid.ac/institutes/grid.417068.c", 
          "name": [
            "MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK, GB"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Williamson", 
        "givenName": "K.", 
        "id": "sg:person.015724717252.45", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015724717252.45"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Pennsylvania", 
          "id": "https://www.grid.ac/institutes/grid.25879.31", 
          "name": [
            "Department of Pathology, The Children\u2019s Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA, US"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Finn", 
        "givenName": "L. S.", 
        "id": "sg:person.0624412532.68", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0624412532.68"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Pennsylvania", 
          "id": "https://www.grid.ac/institutes/grid.25879.31", 
          "name": [
            "Division of Nephrology, Department of Pediatrics, The Children\u2019s Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA 19104, USA e-mail: kaplanb@email.CHOP.edu Tel.: +1-215-5902451, Fax: +1-215-5903705, US"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kaplan", 
        "givenName": "B. S.", 
        "id": "sg:person.01236112435.64", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01236112435.64"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2000-09", 
    "datePublishedReg": "2000-09-01", 
    "description": "The Denys-Drash syndrome is defined by the occurrence of combinations of pseudohermaphroditism, nephrotic syndrome with diffuse mesangial sclerosis, Wilms' tumor, and constitutional mutations in the WT1 suppressor gene. Most patients develop end-stage renal failure. Atypical hemolytic uremic syndrome (HUS) is defined by onset of acute hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and renal failure in the absence of a gastrointestinal prodromal illness of bloody diarrhea. The purpose of this report is to describe the occurrence of features of atypical HUS and Denys-Drash syndrome in two African-American boys aged 13 and 16 months. Each had nephrotic syndrome, diffuse mesangial sclerosis, and WT1 point mutations. Both had grade III hypospadias and undescended testes. They had normal serum creatinine concentrations and hematology a month before presenting with HUS. Stool cultures for Escherichia coli O157:H7 were negative. Each patient has been transplanted with cadaver kidneys without recurrence of HUS.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s004670000389", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isFundedItemOf": [
      {
        "id": "sg:grant.2762005", 
        "type": "MonetaryGrant"
      }
    ], 
    "isPartOf": [
      {
        "id": "sg:journal.1097267", 
        "issn": [
          "0931-041X", 
          "1432-198X"
        ], 
        "name": "Pediatric Nephrology", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "12", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "14"
      }
    ], 
    "name": "Hemolytic uremic syndrome associated with Denys-Drash syndrome", 
    "pagination": "1092-1097", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "930e15357562d996370db988e47fd7b9946a94f0d1768e164863e57c1bc0b750"
        ]
      }, 
      {
        "name": "pubmed_id", 
        "type": "PropertyValue", 
        "value": [
          "11045393"
        ]
      }, 
      {
        "name": "nlm_unique_id", 
        "type": "PropertyValue", 
        "value": [
          "8708728"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s004670000389"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1030868834"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s004670000389", 
      "https://app.dimensions.ai/details/publication/pub.1030868834"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T14:55", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000001_0000000264/records_8663_00000489.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007/s004670000389"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/s004670000389'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/s004670000389'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s004670000389'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s004670000389'


 

This table displays all metadata directly associated to this object as RDF triples.

186 TRIPLES      20 PREDICATES      48 URIs      40 LITERALS      28 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s004670000389 schema:about N0762ce9157a84f86a8d0757db729f3b6
2 N0a30c35927af4382a1300b4693939588
3 N18ebdaac3acb4dbd85d204bd3d1b5299
4 N2ab77dd8ce0b45c7a4192504db46940e
5 N31c9264b5b164c25afbe07bbf0b9b7ee
6 N31ccf4f673c1464b84deab608a1bb569
7 N63286ae1972941e4b7c24749b253d2ea
8 N7f6dc2e8ae27437d9e4e10f8509090ae
9 N805d42350db74292a28ce1dafe320791
10 Nb1c23152623047a1a015c6fbfe6058a2
11 Nb5da4625f43f4210b773127517ebf1ce
12 Nb641b0c165ec44a58525f9d11ac40223
13 Nc6f86212c82e4a9cb6ccdafd77b66195
14 Ncdbbde7cc56142a8b973b8a147099804
15 Ncf3ca97386dd45769259c29246536e08
16 Nd01cf9bf3eb54e1a96c9d94d2213a127
17 Nd1c0c9885ddb4523988be0a34ff640cb
18 Nde1f2dca13934d36aa3a8176bb2ebd94
19 Nfac2263576794cf385d28fb8423ce26d
20 anzsrc-for:11
21 anzsrc-for:1103
22 schema:author Nafe584cbf6e34a1ba265dd1e32af6c24
23 schema:datePublished 2000-09
24 schema:datePublishedReg 2000-09-01
25 schema:description The Denys-Drash syndrome is defined by the occurrence of combinations of pseudohermaphroditism, nephrotic syndrome with diffuse mesangial sclerosis, Wilms' tumor, and constitutional mutations in the WT1 suppressor gene. Most patients develop end-stage renal failure. Atypical hemolytic uremic syndrome (HUS) is defined by onset of acute hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and renal failure in the absence of a gastrointestinal prodromal illness of bloody diarrhea. The purpose of this report is to describe the occurrence of features of atypical HUS and Denys-Drash syndrome in two African-American boys aged 13 and 16 months. Each had nephrotic syndrome, diffuse mesangial sclerosis, and WT1 point mutations. Both had grade III hypospadias and undescended testes. They had normal serum creatinine concentrations and hematology a month before presenting with HUS. Stool cultures for Escherichia coli O157:H7 were negative. Each patient has been transplanted with cadaver kidneys without recurrence of HUS.
26 schema:genre research_article
27 schema:inLanguage en
28 schema:isAccessibleForFree false
29 schema:isPartOf N9c261302e881416596e53db9d75cafba
30 Ncbc29affd4f14282bca8ace9c291d051
31 sg:journal.1097267
32 schema:name Hemolytic uremic syndrome associated with Denys-Drash syndrome
33 schema:pagination 1092-1097
34 schema:productId N2d37ff85eabd4407b1d4e826c7f07109
35 N7f7492e3ba6d4103bcce637bde6b8476
36 N9c78f8c6faa14b85a3a472c975c9b887
37 Na218462fa895473abf652a26116215f8
38 Na22c3da79bcc475aac3423903663a6ac
39 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030868834
40 https://doi.org/10.1007/s004670000389
41 schema:sdDatePublished 2019-04-10T14:55
42 schema:sdLicense https://scigraph.springernature.com/explorer/license/
43 schema:sdPublisher N381121932873414f896ce330333ebdfe
44 schema:url http://link.springer.com/10.1007/s004670000389
45 sgo:license sg:explorer/license/
46 sgo:sdDataset articles
47 rdf:type schema:ScholarlyArticle
48 N0762ce9157a84f86a8d0757db729f3b6 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
49 schema:name Mutation
50 rdf:type schema:DefinedTerm
51 N0a30c35927af4382a1300b4693939588 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
52 schema:name DNA-Binding Proteins
53 rdf:type schema:DefinedTerm
54 N18ebdaac3acb4dbd85d204bd3d1b5299 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
55 schema:name Hemolytic-Uremic Syndrome
56 rdf:type schema:DefinedTerm
57 N2ab77dd8ce0b45c7a4192504db46940e schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
58 schema:name Infant
59 rdf:type schema:DefinedTerm
60 N2d37ff85eabd4407b1d4e826c7f07109 schema:name readcube_id
61 schema:value 930e15357562d996370db988e47fd7b9946a94f0d1768e164863e57c1bc0b750
62 rdf:type schema:PropertyValue
63 N31c9264b5b164c25afbe07bbf0b9b7ee schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
64 schema:name WT1 Proteins
65 rdf:type schema:DefinedTerm
66 N31ccf4f673c1464b84deab608a1bb569 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
67 schema:name Glomerulosclerosis, Focal Segmental
68 rdf:type schema:DefinedTerm
69 N381121932873414f896ce330333ebdfe schema:name Springer Nature - SN SciGraph project
70 rdf:type schema:Organization
71 N3bbbf2d5cbff4e90ba28ca1b28576b5c rdf:first sg:person.0606020600.49
72 rdf:rest Nb6e50e143fef4bab8922fb877de4978b
73 N63286ae1972941e4b7c24749b253d2ea schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
74 schema:name Kidney Failure, Chronic
75 rdf:type schema:DefinedTerm
76 N7f6dc2e8ae27437d9e4e10f8509090ae schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
77 schema:name Syndrome
78 rdf:type schema:DefinedTerm
79 N7f7492e3ba6d4103bcce637bde6b8476 schema:name nlm_unique_id
80 schema:value 8708728
81 rdf:type schema:PropertyValue
82 N805d42350db74292a28ce1dafe320791 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
83 schema:name Transcription Factors
84 rdf:type schema:DefinedTerm
85 N9c261302e881416596e53db9d75cafba schema:issueNumber 12
86 rdf:type schema:PublicationIssue
87 N9c78f8c6faa14b85a3a472c975c9b887 schema:name pubmed_id
88 schema:value 11045393
89 rdf:type schema:PropertyValue
90 Na218462fa895473abf652a26116215f8 schema:name doi
91 schema:value 10.1007/s004670000389
92 rdf:type schema:PropertyValue
93 Na22c3da79bcc475aac3423903663a6ac schema:name dimensions_id
94 schema:value pub.1030868834
95 rdf:type schema:PropertyValue
96 Na8a214f3d5f04e3ca8dd64529cd40906 rdf:first sg:person.0624412532.68
97 rdf:rest Nc022a76e3c1947b993d1ffcdbb1ea902
98 Nafe584cbf6e34a1ba265dd1e32af6c24 rdf:first sg:person.0720257377.64
99 rdf:rest N3bbbf2d5cbff4e90ba28ca1b28576b5c
100 Nb1c23152623047a1a015c6fbfe6058a2 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
101 schema:name Humans
102 rdf:type schema:DefinedTerm
103 Nb5da4625f43f4210b773127517ebf1ce schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
104 schema:name Nephrotic Syndrome
105 rdf:type schema:DefinedTerm
106 Nb641b0c165ec44a58525f9d11ac40223 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
107 schema:name Base Sequence
108 rdf:type schema:DefinedTerm
109 Nb6e50e143fef4bab8922fb877de4978b rdf:first sg:person.0676331043.26
110 rdf:rest Nb7ab316fd1b64fe9a4f3bfe3fd8a053c
111 Nb7ab316fd1b64fe9a4f3bfe3fd8a053c rdf:first sg:person.015724717252.45
112 rdf:rest Na8a214f3d5f04e3ca8dd64529cd40906
113 Nc022a76e3c1947b993d1ffcdbb1ea902 rdf:first sg:person.01236112435.64
114 rdf:rest rdf:nil
115 Nc6f86212c82e4a9cb6ccdafd77b66195 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
116 schema:name Wilms Tumor
117 rdf:type schema:DefinedTerm
118 Ncbc29affd4f14282bca8ace9c291d051 schema:volumeNumber 14
119 rdf:type schema:PublicationVolume
120 Ncdbbde7cc56142a8b973b8a147099804 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
121 schema:name Kidney
122 rdf:type schema:DefinedTerm
123 Ncf3ca97386dd45769259c29246536e08 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
124 schema:name Male
125 rdf:type schema:DefinedTerm
126 Nd01cf9bf3eb54e1a96c9d94d2213a127 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
127 schema:name Molecular Sequence Data
128 rdf:type schema:DefinedTerm
129 Nd1c0c9885ddb4523988be0a34ff640cb schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
130 schema:name Glomerular Mesangium
131 rdf:type schema:DefinedTerm
132 Nde1f2dca13934d36aa3a8176bb2ebd94 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
133 schema:name DNA
134 rdf:type schema:DefinedTerm
135 Nfac2263576794cf385d28fb8423ce26d schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
136 schema:name Disorders of Sex Development
137 rdf:type schema:DefinedTerm
138 anzsrc-for:11 schema:inDefinedTermSet anzsrc-for:
139 schema:name Medical and Health Sciences
140 rdf:type schema:DefinedTerm
141 anzsrc-for:1103 schema:inDefinedTermSet anzsrc-for:
142 schema:name Clinical Sciences
143 rdf:type schema:DefinedTerm
144 sg:grant.2762005 http://pending.schema.org/fundedItem sg:pub.10.1007/s004670000389
145 rdf:type schema:MonetaryGrant
146 sg:journal.1097267 schema:issn 0931-041X
147 1432-198X
148 schema:name Pediatric Nephrology
149 rdf:type schema:Periodical
150 sg:person.01236112435.64 schema:affiliation https://www.grid.ac/institutes/grid.25879.31
151 schema:familyName Kaplan
152 schema:givenName B. S.
153 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01236112435.64
154 rdf:type schema:Person
155 sg:person.015724717252.45 schema:affiliation https://www.grid.ac/institutes/grid.417068.c
156 schema:familyName Williamson
157 schema:givenName K.
158 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015724717252.45
159 rdf:type schema:Person
160 sg:person.0606020600.49 schema:affiliation https://www.grid.ac/institutes/grid.417068.c
161 schema:familyName van Heyningen
162 schema:givenName V.
163 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0606020600.49
164 rdf:type schema:Person
165 sg:person.0624412532.68 schema:affiliation https://www.grid.ac/institutes/grid.25879.31
166 schema:familyName Finn
167 schema:givenName L. S.
168 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0624412532.68
169 rdf:type schema:Person
170 sg:person.0676331043.26 schema:affiliation https://www.grid.ac/institutes/grid.417068.c
171 schema:familyName Axton
172 schema:givenName R.
173 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0676331043.26
174 rdf:type schema:Person
175 sg:person.0720257377.64 schema:affiliation https://www.grid.ac/institutes/grid.25879.31
176 schema:familyName Sherbotie
177 schema:givenName J. R.
178 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0720257377.64
179 rdf:type schema:Person
180 https://www.grid.ac/institutes/grid.25879.31 schema:alternateName University of Pennsylvania
181 schema:name Department of Pathology, The Children’s Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA, US
182 Division of Nephrology, Department of Pediatrics, The Children’s Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA 19104, USA e-mail: kaplanb@email.CHOP.edu Tel.: +1-215-5902451, Fax: +1-215-5903705, US
183 rdf:type schema:Organization
184 https://www.grid.ac/institutes/grid.417068.c schema:alternateName Western General Hospital
185 schema:name MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK, GB
186 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...