Ontology type: schema:ScholarlyArticle
2002-05-09
AUTHORST. Hasegawa, T. Sasaki, T. Kimura, T. Sawai, K. Nose, S. Kamata, A. Okada, K. Wada, T. Kanzaki
ABSTRACT. Although prenatal ultrasonographic (US) diagnosis has been reported in biliary atresia (BA), most cases are type I (correctable with cystic dilatation). We report three prenatal cases of type IIId BA (uncorrectable with cystic dilatation). Routine fetal US at 22 to 24 weeks of gestation showed two communicating cystic lesions 12 to 16 mm in diameter. On color Doppler US, the lesions were separate from the portal vein or hepatic artery. The size did not change during the prenatal period in any case. Choledochal cyst (CC) was considered the most likely diagnosis, although BA with cystic lesions was also considered. After birth, the patients developed acholic stools and prolonged neonatal jaundice. Hepatobiliary scintigraphy showed negative passage. Duodenal fluid showed a negative or slightly positive Gmelin test. The neonates underwent laparotomy at the age of 36, 46, and 32 days, respectively. Intraoperative cholangiography showed the gallbladder and slightly-dilated common-bile duct without entering the proximal or distal bile ducts in all cases. They were classified as type IIId BA and underwent excision of the cystic lesions and dissection of the portal bile-duct remnants, followed by hepatic portoenterostomy. Case 1 showed persistent jaundice and finally underwent liver transplantation (LTx), case 2 became anicteric. Case 3 remained jaundiced and is to undergo LTx. In conclusion, type IIId BA may be one of the differential diagnoses when a cystic lesion is detected under the hepatic hilum by fetal US. However, prenatal diagnosis of BA is still difficult with respect to differentiation from a CC or type I BA. Early postnatal diagnosis followed by immediate treatment is important, especially in type IIId BA. More... »
PAGES425-428
http://scigraph.springernature.com/pub.10.1007/s00383-002-0843-y
DOIhttp://dx.doi.org/10.1007/s00383-002-0843-y
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1005340383
PUBMEDhttps://www.ncbi.nlm.nih.gov/pubmed/12415371
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/2008/11",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Medical and Health Sciences",
"type": "DefinedTerm"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/1114",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Paediatrics and Reproductive Medicine",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Bile Ducts",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Biliary Atresia",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Dilatation, Pathologic",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Humans",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Portoenterostomy, Hepatic",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Ultrasonography, Doppler, Color",
"type": "DefinedTerm"
},
{
"inDefinedTermSet": "https://www.nlm.nih.gov/mesh/",
"name": "Ultrasonography, Prenatal",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Hasegawa",
"givenName": "T.",
"id": "sg:person.01035261176.05",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01035261176.05"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Sasaki",
"givenName": "T.",
"id": "sg:person.01111055450.66",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01111055450.66"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Kimura",
"givenName": "T.",
"id": "sg:person.0774627050.82",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0774627050.82"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Sawai",
"givenName": "T.",
"id": "sg:person.01017103146.39",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01017103146.39"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Nose",
"givenName": "K.",
"id": "sg:person.01133331546.07",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01133331546.07"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Kamata",
"givenName": "S.",
"id": "sg:person.0634541346.04",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0634541346.04"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Okada",
"givenName": "A.",
"id": "sg:person.0725725344.49",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0725725344.49"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pediatrics, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Pediatrics, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Wada",
"givenName": "K.",
"id": "sg:person.01063727457.39",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01063727457.39"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Obstetrics and Gynecology, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan",
"id": "http://www.grid.ac/institutes/grid.136593.b",
"name": [
"Department of Obstetrics and Gynecology, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan"
],
"type": "Organization"
},
"familyName": "Kanzaki",
"givenName": "T.",
"id": "sg:person.0641500344.32",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0641500344.32"
],
"type": "Person"
}
],
"datePublished": "2002-05-09",
"datePublishedReg": "2002-05-09",
"description": "Abstract. Although prenatal ultrasonographic (US) diagnosis has been reported in biliary atresia (BA), most cases are type I (correctable with cystic dilatation). We report three prenatal cases of type IIId BA (uncorrectable with cystic dilatation). Routine fetal US at 22 to 24 weeks of gestation showed two communicating cystic lesions 12 to 16\u00a0mm in diameter. On color Doppler US, the lesions were separate from the portal vein or hepatic artery. The size did not change during the prenatal period in any case. Choledochal cyst (CC) was considered the most likely diagnosis, although BA with cystic lesions was also considered. After birth, the patients developed acholic stools and prolonged neonatal jaundice. Hepatobiliary scintigraphy showed negative passage. Duodenal fluid showed a negative or slightly positive Gmelin test. The neonates underwent laparotomy at the age of 36, 46, and 32 days, respectively. Intraoperative cholangiography showed the gallbladder and slightly-dilated common-bile duct without entering the proximal or distal bile ducts in all cases. They were classified as type IIId BA and underwent excision of the cystic lesions and dissection of the portal bile-duct remnants, followed by hepatic portoenterostomy. Case 1 showed persistent jaundice and finally underwent liver transplantation (LTx), case 2 became anicteric. Case 3 remained jaundiced and is to undergo LTx. In conclusion, type IIId BA may be one of the differential diagnoses when a cystic lesion is detected under the hepatic hilum by fetal US. However, prenatal diagnosis of BA is still difficult with respect to differentiation from a CC or type I BA. Early postnatal diagnosis followed by immediate treatment is important, especially in type IIId BA.",
"genre": "article",
"id": "sg:pub.10.1007/s00383-002-0843-y",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1096464",
"issn": [
"0179-0358",
"1437-9813"
],
"name": "Pediatric Surgery International",
"publisher": "Springer Nature",
"type": "Periodical"
},
{
"issueNumber": "5",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "18"
}
],
"keywords": [
"biliary atresia",
"choledochal cyst",
"cystic lesions",
"fetal US",
"type I biliary atresia",
"underwent liver transplantation",
"distal bile duct",
"common bile duct",
"weeks of gestation",
"bile duct remnants",
"color Doppler US",
"early postnatal diagnosis",
"prenatal ultrasonographic diagnosis",
"hepatic portoenterostomy",
"acholic stools",
"persistent jaundice",
"liver transplantation",
"hepatic hilum",
"hepatic artery",
"hepatobiliary scintigraphy",
"intraoperative cholangiography",
"bile duct",
"portal vein",
"immediate treatment",
"likely diagnosis",
"neonatal jaundice",
"differential diagnosis",
"ultrasonographic diagnosis",
"Doppler US",
"duodenal fluid",
"postnatal diagnosis",
"ultrasonographic appearance",
"prenatal period",
"lesions",
"diagnosis",
"Case 2",
"Case 1",
"Case 3",
"jaundice",
"prenatal diagnosis",
"atresia",
"type I",
"prenatal cases",
"duct",
"most cases",
"portoenterostomy",
"laparotomy",
"cholangiography",
"LTx",
"scintigraphy",
"patients",
"neonates",
"transplantation",
"artery",
"gestation",
"stool",
"gallbladder",
"excision",
"cases",
"cysts",
"hilum",
"dissection",
"weeks",
"birth",
"vein",
"age",
"treatment",
"days",
"conclusion",
"differentiation",
"period",
"appearance",
"test",
"uses",
"fluid",
"remnants",
"passage",
"diameter",
"size",
"respect"
],
"name": "Prenatal ultrasonographic appearance of type IIId (uncorrectable type with cystic dilatation) biliary atresia",
"pagination": "425-428",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1005340383"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1007/s00383-002-0843-y"
]
},
{
"name": "pubmed_id",
"type": "PropertyValue",
"value": [
"12415371"
]
}
],
"sameAs": [
"https://doi.org/10.1007/s00383-002-0843-y",
"https://app.dimensions.ai/details/publication/pub.1005340383"
],
"sdDataset": "articles",
"sdDatePublished": "2022-08-04T16:55",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220804/entities/gbq_results/article/article_361.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1007/s00383-002-0843-y"
}
]Download the RDF metadata as: json-ld nt turtle xml License info
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/s00383-002-0843-y'
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/s00383-002-0843-y'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s00383-002-0843-y'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s00383-002-0843-y'
This table displays all metadata directly associated to this object as RDF triples.
229 TRIPLES
20 PREDICATES
112 URIs
104 LITERALS
14 BLANK NODES
| Subject | Predicate | Object | |
|---|---|---|---|
| 1 | sg:pub.10.1007/s00383-002-0843-y | schema:about | N3b1003989c7549669dda5206b852af3b |
| 2 | ″ | ″ | N7ceddd6124304021b4dacb3da156a3cf |
| 3 | ″ | ″ | N8a486cdf19b646329298ba80662c800d |
| 4 | ″ | ″ | Na0de8fe953124c97991e67323f65ad43 |
| 5 | ″ | ″ | Nbab81f6ec35342aa9b9f0d1b13085877 |
| 6 | ″ | ″ | Ne6a57d8875ee4038a6850282118c6096 |
| 7 | ″ | ″ | Ne95d20dd1bf142928a18eefc1d0a7b85 |
| 8 | ″ | ″ | anzsrc-for:11 |
| 9 | ″ | ″ | anzsrc-for:1114 |
| 10 | ″ | schema:author | Nb4a391f77dcc4b81b95f20143c2af0c9 |
| 11 | ″ | schema:datePublished | 2002-05-09 |
| 12 | ″ | schema:datePublishedReg | 2002-05-09 |
| 13 | ″ | schema:description | Abstract. Although prenatal ultrasonographic (US) diagnosis has been reported in biliary atresia (BA), most cases are type I (correctable with cystic dilatation). We report three prenatal cases of type IIId BA (uncorrectable with cystic dilatation). Routine fetal US at 22 to 24 weeks of gestation showed two communicating cystic lesions 12 to 16 mm in diameter. On color Doppler US, the lesions were separate from the portal vein or hepatic artery. The size did not change during the prenatal period in any case. Choledochal cyst (CC) was considered the most likely diagnosis, although BA with cystic lesions was also considered. After birth, the patients developed acholic stools and prolonged neonatal jaundice. Hepatobiliary scintigraphy showed negative passage. Duodenal fluid showed a negative or slightly positive Gmelin test. The neonates underwent laparotomy at the age of 36, 46, and 32 days, respectively. Intraoperative cholangiography showed the gallbladder and slightly-dilated common-bile duct without entering the proximal or distal bile ducts in all cases. They were classified as type IIId BA and underwent excision of the cystic lesions and dissection of the portal bile-duct remnants, followed by hepatic portoenterostomy. Case 1 showed persistent jaundice and finally underwent liver transplantation (LTx), case 2 became anicteric. Case 3 remained jaundiced and is to undergo LTx. In conclusion, type IIId BA may be one of the differential diagnoses when a cystic lesion is detected under the hepatic hilum by fetal US. However, prenatal diagnosis of BA is still difficult with respect to differentiation from a CC or type I BA. Early postnatal diagnosis followed by immediate treatment is important, especially in type IIId BA. |
| 14 | ″ | schema:genre | article |
| 15 | ″ | schema:isAccessibleForFree | false |
| 16 | ″ | schema:isPartOf | N0c70b9d37c084506ba2f1daefc5ef64b |
| 17 | ″ | ″ | N74f5bf12e0b347a78f54cd8ae14dc20d |
| 18 | ″ | ″ | sg:journal.1096464 |
| 19 | ″ | schema:keywords | Case 1 |
| 20 | ″ | ″ | Case 2 |
| 21 | ″ | ″ | Case 3 |
| 22 | ″ | ″ | Doppler US |
| 23 | ″ | ″ | LTx |
| 24 | ″ | ″ | acholic stools |
| 25 | ″ | ″ | age |
| 26 | ″ | ″ | appearance |
| 27 | ″ | ″ | artery |
| 28 | ″ | ″ | atresia |
| 29 | ″ | ″ | bile duct |
| 30 | ″ | ″ | bile duct remnants |
| 31 | ″ | ″ | biliary atresia |
| 32 | ″ | ″ | birth |
| 33 | ″ | ″ | cases |
| 34 | ″ | ″ | cholangiography |
| 35 | ″ | ″ | choledochal cyst |
| 36 | ″ | ″ | color Doppler US |
| 37 | ″ | ″ | common bile duct |
| 38 | ″ | ″ | conclusion |
| 39 | ″ | ″ | cystic lesions |
| 40 | ″ | ″ | cysts |
| 41 | ″ | ″ | days |
| 42 | ″ | ″ | diagnosis |
| 43 | ″ | ″ | diameter |
| 44 | ″ | ″ | differential diagnosis |
| 45 | ″ | ″ | differentiation |
| 46 | ″ | ″ | dissection |
| 47 | ″ | ″ | distal bile duct |
| 48 | ″ | ″ | duct |
| 49 | ″ | ″ | duodenal fluid |
| 50 | ″ | ″ | early postnatal diagnosis |
| 51 | ″ | ″ | excision |
| 52 | ″ | ″ | fetal US |
| 53 | ″ | ″ | fluid |
| 54 | ″ | ″ | gallbladder |
| 55 | ″ | ″ | gestation |
| 56 | ″ | ″ | hepatic artery |
| 57 | ″ | ″ | hepatic hilum |
| 58 | ″ | ″ | hepatic portoenterostomy |
| 59 | ″ | ″ | hepatobiliary scintigraphy |
| 60 | ″ | ″ | hilum |
| 61 | ″ | ″ | immediate treatment |
| 62 | ″ | ″ | intraoperative cholangiography |
| 63 | ″ | ″ | jaundice |
| 64 | ″ | ″ | laparotomy |
| 65 | ″ | ″ | lesions |
| 66 | ″ | ″ | likely diagnosis |
| 67 | ″ | ″ | liver transplantation |
| 68 | ″ | ″ | most cases |
| 69 | ″ | ″ | neonatal jaundice |
| 70 | ″ | ″ | neonates |
| 71 | ″ | ″ | passage |
| 72 | ″ | ″ | patients |
| 73 | ″ | ″ | period |
| 74 | ″ | ″ | persistent jaundice |
| 75 | ″ | ″ | portal vein |
| 76 | ″ | ″ | portoenterostomy |
| 77 | ″ | ″ | postnatal diagnosis |
| 78 | ″ | ″ | prenatal cases |
| 79 | ″ | ″ | prenatal diagnosis |
| 80 | ″ | ″ | prenatal period |
| 81 | ″ | ″ | prenatal ultrasonographic diagnosis |
| 82 | ″ | ″ | remnants |
| 83 | ″ | ″ | respect |
| 84 | ″ | ″ | scintigraphy |
| 85 | ″ | ″ | size |
| 86 | ″ | ″ | stool |
| 87 | ″ | ″ | test |
| 88 | ″ | ″ | transplantation |
| 89 | ″ | ″ | treatment |
| 90 | ″ | ″ | type I |
| 91 | ″ | ″ | type I biliary atresia |
| 92 | ″ | ″ | ultrasonographic appearance |
| 93 | ″ | ″ | ultrasonographic diagnosis |
| 94 | ″ | ″ | underwent liver transplantation |
| 95 | ″ | ″ | uses |
| 96 | ″ | ″ | vein |
| 97 | ″ | ″ | weeks |
| 98 | ″ | ″ | weeks of gestation |
| 99 | ″ | schema:name | Prenatal ultrasonographic appearance of type IIId (uncorrectable type with cystic dilatation) biliary atresia |
| 100 | ″ | schema:pagination | 425-428 |
| 101 | ″ | schema:productId | N1d192d329b484342ab138a91e631cb52 |
| 102 | ″ | ″ | N46a036c76dbb45d89df0d5d07f7cd2b6 |
| 103 | ″ | ″ | Nd9d99a38f98b4bb6b817eb5b1c854a4e |
| 104 | ″ | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1005340383 |
| 105 | ″ | ″ | https://doi.org/10.1007/s00383-002-0843-y |
| 106 | ″ | schema:sdDatePublished | 2022-08-04T16:55 |
| 107 | ″ | schema:sdLicense | https://scigraph.springernature.com/explorer/license/ |
| 108 | ″ | schema:sdPublisher | N451a46f8c8fe4c57a0a5ef86a924bf07 |
| 109 | ″ | schema:url | https://doi.org/10.1007/s00383-002-0843-y |
| 110 | ″ | sgo:license | sg:explorer/license/ |
| 111 | ″ | sgo:sdDataset | articles |
| 112 | ″ | rdf:type | schema:ScholarlyArticle |
| 113 | N0c70b9d37c084506ba2f1daefc5ef64b | schema:volumeNumber | 18 |
| 114 | ″ | rdf:type | schema:PublicationVolume |
| 115 | N13f022c956c54db58f12deb172cf002f | rdf:first | sg:person.01133331546.07 |
| 116 | ″ | rdf:rest | Nb1007e6b1750470e845307e5a0b7e27d |
| 117 | N1d192d329b484342ab138a91e631cb52 | schema:name | pubmed_id |
| 118 | ″ | schema:value | 12415371 |
| 119 | ″ | rdf:type | schema:PropertyValue |
| 120 | N286f4002b65d4e80be3b8696c627e1fe | rdf:first | sg:person.0725725344.49 |
| 121 | ″ | rdf:rest | Nc12b2103301744ffa4cfab9e0176666d |
| 122 | N3b1003989c7549669dda5206b852af3b | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 123 | ″ | schema:name | Portoenterostomy, Hepatic |
| 124 | ″ | rdf:type | schema:DefinedTerm |
| 125 | N430738cdb34d478ea2f9a04d6e0452a5 | rdf:first | sg:person.01111055450.66 |
| 126 | ″ | rdf:rest | N7bfb5b880c014b3aa155697fb9b7bd71 |
| 127 | N451a46f8c8fe4c57a0a5ef86a924bf07 | schema:name | Springer Nature - SN SciGraph project |
| 128 | ″ | rdf:type | schema:Organization |
| 129 | N46a036c76dbb45d89df0d5d07f7cd2b6 | schema:name | dimensions_id |
| 130 | ″ | schema:value | pub.1005340383 |
| 131 | ″ | rdf:type | schema:PropertyValue |
| 132 | N66fb273ca35140b28b6627f89df936d1 | rdf:first | sg:person.01017103146.39 |
| 133 | ″ | rdf:rest | N13f022c956c54db58f12deb172cf002f |
| 134 | N74f5bf12e0b347a78f54cd8ae14dc20d | schema:issueNumber | 5 |
| 135 | ″ | rdf:type | schema:PublicationIssue |
| 136 | N7bfb5b880c014b3aa155697fb9b7bd71 | rdf:first | sg:person.0774627050.82 |
| 137 | ″ | rdf:rest | N66fb273ca35140b28b6627f89df936d1 |
| 138 | N7ceddd6124304021b4dacb3da156a3cf | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 139 | ″ | schema:name | Bile Ducts |
| 140 | ″ | rdf:type | schema:DefinedTerm |
| 141 | N8a486cdf19b646329298ba80662c800d | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 142 | ″ | schema:name | Ultrasonography, Doppler, Color |
| 143 | ″ | rdf:type | schema:DefinedTerm |
| 144 | Na0de8fe953124c97991e67323f65ad43 | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 145 | ″ | schema:name | Dilatation, Pathologic |
| 146 | ″ | rdf:type | schema:DefinedTerm |
| 147 | Nb1007e6b1750470e845307e5a0b7e27d | rdf:first | sg:person.0634541346.04 |
| 148 | ″ | rdf:rest | N286f4002b65d4e80be3b8696c627e1fe |
| 149 | Nb4a391f77dcc4b81b95f20143c2af0c9 | rdf:first | sg:person.01035261176.05 |
| 150 | ″ | rdf:rest | N430738cdb34d478ea2f9a04d6e0452a5 |
| 151 | Nbab81f6ec35342aa9b9f0d1b13085877 | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 152 | ″ | schema:name | Biliary Atresia |
| 153 | ″ | rdf:type | schema:DefinedTerm |
| 154 | Nc12b2103301744ffa4cfab9e0176666d | rdf:first | sg:person.01063727457.39 |
| 155 | ″ | rdf:rest | Nfe329be193e24575b06b4ba206423a8d |
| 156 | Nd9d99a38f98b4bb6b817eb5b1c854a4e | schema:name | doi |
| 157 | ″ | schema:value | 10.1007/s00383-002-0843-y |
| 158 | ″ | rdf:type | schema:PropertyValue |
| 159 | Ne6a57d8875ee4038a6850282118c6096 | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 160 | ″ | schema:name | Humans |
| 161 | ″ | rdf:type | schema:DefinedTerm |
| 162 | Ne95d20dd1bf142928a18eefc1d0a7b85 | schema:inDefinedTermSet | https://www.nlm.nih.gov/mesh/ |
| 163 | ″ | schema:name | Ultrasonography, Prenatal |
| 164 | ″ | rdf:type | schema:DefinedTerm |
| 165 | Nfe329be193e24575b06b4ba206423a8d | rdf:first | sg:person.0641500344.32 |
| 166 | ″ | rdf:rest | rdf:nil |
| 167 | anzsrc-for:11 | schema:inDefinedTermSet | anzsrc-for: |
| 168 | ″ | schema:name | Medical and Health Sciences |
| 169 | ″ | rdf:type | schema:DefinedTerm |
| 170 | anzsrc-for:1114 | schema:inDefinedTermSet | anzsrc-for: |
| 171 | ″ | schema:name | Paediatrics and Reproductive Medicine |
| 172 | ″ | rdf:type | schema:DefinedTerm |
| 173 | sg:journal.1096464 | schema:issn | 0179-0358 |
| 174 | ″ | ″ | 1437-9813 |
| 175 | ″ | schema:name | Pediatric Surgery International |
| 176 | ″ | schema:publisher | Springer Nature |
| 177 | ″ | rdf:type | schema:Periodical |
| 178 | sg:person.01017103146.39 | schema:affiliation | grid-institutes:grid.136593.b |
| 179 | ″ | schema:familyName | Sawai |
| 180 | ″ | schema:givenName | T. |
| 181 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01017103146.39 |
| 182 | ″ | rdf:type | schema:Person |
| 183 | sg:person.01035261176.05 | schema:affiliation | grid-institutes:grid.136593.b |
| 184 | ″ | schema:familyName | Hasegawa |
| 185 | ″ | schema:givenName | T. |
| 186 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01035261176.05 |
| 187 | ″ | rdf:type | schema:Person |
| 188 | sg:person.01063727457.39 | schema:affiliation | grid-institutes:grid.136593.b |
| 189 | ″ | schema:familyName | Wada |
| 190 | ″ | schema:givenName | K. |
| 191 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01063727457.39 |
| 192 | ″ | rdf:type | schema:Person |
| 193 | sg:person.01111055450.66 | schema:affiliation | grid-institutes:grid.136593.b |
| 194 | ″ | schema:familyName | Sasaki |
| 195 | ″ | schema:givenName | T. |
| 196 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01111055450.66 |
| 197 | ″ | rdf:type | schema:Person |
| 198 | sg:person.01133331546.07 | schema:affiliation | grid-institutes:grid.136593.b |
| 199 | ″ | schema:familyName | Nose |
| 200 | ″ | schema:givenName | K. |
| 201 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01133331546.07 |
| 202 | ″ | rdf:type | schema:Person |
| 203 | sg:person.0634541346.04 | schema:affiliation | grid-institutes:grid.136593.b |
| 204 | ″ | schema:familyName | Kamata |
| 205 | ″ | schema:givenName | S. |
| 206 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0634541346.04 |
| 207 | ″ | rdf:type | schema:Person |
| 208 | sg:person.0641500344.32 | schema:affiliation | grid-institutes:grid.136593.b |
| 209 | ″ | schema:familyName | Kanzaki |
| 210 | ″ | schema:givenName | T. |
| 211 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0641500344.32 |
| 212 | ″ | rdf:type | schema:Person |
| 213 | sg:person.0725725344.49 | schema:affiliation | grid-institutes:grid.136593.b |
| 214 | ″ | schema:familyName | Okada |
| 215 | ″ | schema:givenName | A. |
| 216 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0725725344.49 |
| 217 | ″ | rdf:type | schema:Person |
| 218 | sg:person.0774627050.82 | schema:affiliation | grid-institutes:grid.136593.b |
| 219 | ″ | schema:familyName | Kimura |
| 220 | ″ | schema:givenName | T. |
| 221 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0774627050.82 |
| 222 | ″ | rdf:type | schema:Person |
| 223 | grid-institutes:grid.136593.b | schema:alternateName | Department of Obstetrics and Gynecology, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 224 | ″ | ″ | Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 225 | ″ | ″ | Department of Pediatrics, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 226 | ″ | schema:name | Department of Obstetrics and Gynecology, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 227 | ″ | ″ | Department of Pediatric Surgery, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 228 | ″ | ″ | Department of Pediatrics, Osaka University Medical School, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan |
| 229 | ″ | rdf:type | schema:Organization |