Respiratory failure in infants due to spinal muscular atrophy with respiratory distress type 1 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-09-09

AUTHORS

Alberto Giannini, Anna Maria Pinto, Giordano Rossetti, Edi Prandi, Danilo Tiziano, Christina Brahe, Nardo Nardocci

ABSTRACT

BackgroundSpinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn α-motoneurons and manifesting in the first 6 months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.SettingPediatric intensive care unit of tertiary care hospital.PatientsWe present two new cases of SMARD1 and report two new mutations in the gene IGHMBP2 which encodes immunoglobulin μ-binding protein 2 on chromosome 11q13.ConclusionsSMARD1 is a poor-prognosis disease that should be considered when acute respiratory insufficiency, of suspected neuromuscular or unclear cause, develops during the first 6 months of life. Diaphragmatic paralysis, manifesting as dyspnea and paradoxical respiration, is the most prominent presenting sign and diaphragmatic motility should be investigated early by fluoroscopy or ultrasound. Electromyography and nerve conduction studies revealing peripheral motor and sensory neuropathy then suggest the diagnosis which should be confirmed by genetic analysis. More... »

PAGES

1851-1855

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00134-006-0346-8

DOI

http://dx.doi.org/10.1007/s00134-006-0346-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1019226814

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16964485


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/2008/11", 
        "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/2008/1109", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Neurosciences", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "DNA-Binding Proteins", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Hereditary Sensory and Autonomic Neuropathies", 
        "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": "Infant, Newborn", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Male", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Mutation", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Respiration, Artificial", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Respiratory Paralysis", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Spinal Muscular Atrophies of Childhood", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Transcription Factors", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Giannini", 
        "givenName": "Alberto", 
        "id": "sg:person.0657155013.59", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0657155013.59"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy", 
          "id": "http://www.grid.ac/institutes/grid.8142.f", 
          "name": [
            "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Pinto", 
        "givenName": "Anna Maria", 
        "id": "sg:person.0761250567.64", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0761250567.64"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Rossetti", 
        "givenName": "Giordano", 
        "id": "sg:person.0611041613.50", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0611041613.50"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Prandi", 
        "givenName": "Edi", 
        "id": "sg:person.01245230041.51", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01245230041.51"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy", 
          "id": "http://www.grid.ac/institutes/grid.8142.f", 
          "name": [
            "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tiziano", 
        "givenName": "Danilo", 
        "id": "sg:person.0617721007.53", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0617721007.53"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy", 
          "id": "http://www.grid.ac/institutes/grid.8142.f", 
          "name": [
            "Institute of Medical Genetics, Universit\u00e0 Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Brahe", 
        "givenName": "Christina", 
        "id": "sg:person.0674700541.40", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0674700541.40"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Department of Child Neurology, Istituto Nazionale Neurologico C. Besta, Via Celoria 11, 20131, Milan, Italy", 
          "id": "http://www.grid.ac/institutes/grid.417894.7", 
          "name": [
            "Department of Child Neurology, Istituto Nazionale Neurologico C. Besta, Via Celoria 11, 20131, Milan, Italy"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Nardocci", 
        "givenName": "Nardo", 
        "id": "sg:person.01210313364.42", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01210313364.42"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s00247-005-1433-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1031053017", 
          "https://doi.org/10.1007/s00247-005-1433-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s11910-004-0016-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036160647", 
          "https://doi.org/10.1007/s11910-004-0016-6"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1038/sj.sc.3101889", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010839790", 
          "https://doi.org/10.1038/sj.sc.3101889"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1038/ng703", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1015912598", 
          "https://doi.org/10.1038/ng703"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s00401-005-1056-y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1016819693", 
          "https://doi.org/10.1007/s00401-005-1056-y"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2006-09-09", 
    "datePublishedReg": "2006-09-09", 
    "description": "BackgroundSpinal muscular atrophy with respiratory distress type 1 (SMARD1) is a\u00a0rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn \u03b1-motoneurons and manifesting in the first 6\u202fmonths of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.SettingPediatric intensive care unit of tertiary care hospital.PatientsWe present two new cases of SMARD1 and report two new mutations in the gene IGHMBP2 which encodes immunoglobulin\u202f\u03bc-binding protein 2 on chromosome 11q13.ConclusionsSMARD1 is a\u00a0poor-prognosis disease that should be considered when acute respiratory insufficiency, of suspected neuromuscular or unclear cause, develops during the first 6\u202fmonths of life. Diaphragmatic paralysis, manifesting as dyspnea and paradoxical respiration, is the most prominent presenting sign and diaphragmatic motility should be investigated early by fluoroscopy or ultrasound. Electromyography and nerve conduction studies revealing peripheral motor and sensory neuropathy then suggest the diagnosis which should be confirmed by genetic analysis.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s00134-006-0346-8", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1313639", 
        "issn": [
          "0342-4642", 
          "1432-1238"
        ], 
        "name": "Intensive Care Medicine", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "11", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "32"
      }
    ], 
    "keywords": [
      "respiratory distress type 1", 
      "months of life", 
      "diaphragmatic paralysis", 
      "sensory neuropathy", 
      "muscular atrophy", 
      "type 1", 
      "peripheral sensory neuropathy", 
      "tertiary care hospital", 
      "acute respiratory insufficiency", 
      "nerve conduction studies", 
      "poor prognosis disease", 
      "autosomal recessive neuromuscular disease", 
      "intensive care unit", 
      "BackgroundSpinal muscular atrophy", 
      "recessive neuromuscular disease", 
      "spinal muscular atrophy", 
      "diaphragmatic motility", 
      "respiratory insufficiency", 
      "respiratory failure", 
      "care hospital", 
      "presenting sign", 
      "peripheral motor", 
      "care unit", 
      "paradoxical respiration", 
      "conduction studies", 
      "muscular weakness", 
      "unclear cause", 
      "muscle atrophy", 
      "unknown prevalence", 
      "neuromuscular disease", 
      "new cases", 
      "atrophy", 
      "neuropathy", 
      "protein 2", 
      "paralysis", 
      "disease", 
      "months", 
      "new mutations", 
      "PatientsWe", 
      "dyspnea", 
      "SMARD1", 
      "hospital", 
      "infants", 
      "motoneurons", 
      "insufficiency", 
      "prevalence", 
      "degeneration", 
      "immunoglobulin", 
      "diagnosis", 
      "fluoroscopy", 
      "electromyography", 
      "IGHMBP2", 
      "ultrasound", 
      "cause", 
      "signs", 
      "life", 
      "genetic analysis", 
      "motility", 
      "failure", 
      "mutations", 
      "cases", 
      "study", 
      "weakness", 
      "respiration", 
      "units", 
      "analysis", 
      "motor"
    ], 
    "name": "Respiratory failure in infants due to spinal muscular atrophy with respiratory distress type 1", 
    "pagination": "1851-1855", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1019226814"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s00134-006-0346-8"
        ]
      }, 
      {
        "name": "pubmed_id", 
        "type": "PropertyValue", 
        "value": [
          "16964485"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s00134-006-0346-8", 
      "https://app.dimensions.ai/details/publication/pub.1019226814"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-06-01T22:04", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220601/entities/gbq_results/article/article_417.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s00134-006-0346-8"
  }
]
 

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/s00134-006-0346-8'

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/s00134-006-0346-8'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s00134-006-0346-8'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s00134-006-0346-8'


 

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

241 TRIPLES      22 PREDICATES      109 URIs      96 LITERALS      18 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s00134-006-0346-8 schema:about N0b9824fff7744712a012ffdc79f0dd21
2 N2b15726dff7c45a7a641734c7a512e8f
3 N4bd0f460f73345f68efa42b09387ab41
4 N4be74fc1a2714eb9ac0c50b5e8869162
5 N4c666ea06f9844709e77140d9a894baf
6 N71aec88f93474016a56235e1d546b20a
7 N94f6867e3fc449d8b8fa8ac585b5302d
8 N99eff8eb72324aeca07105b04b8278f3
9 Nc19bcfb55653460d9c0d8f2671f0fd6f
10 Ndae7eb028e214a2c9117438193bf4c60
11 Nf21f042f87fd441ba09806b5cf4f5e63
12 anzsrc-for:11
13 anzsrc-for:1109
14 schema:author Nb3258308487f40899450b0d8fed36961
15 schema:citation sg:pub.10.1007/s00247-005-1433-7
16 sg:pub.10.1007/s00401-005-1056-y
17 sg:pub.10.1007/s11910-004-0016-6
18 sg:pub.10.1038/ng703
19 sg:pub.10.1038/sj.sc.3101889
20 schema:datePublished 2006-09-09
21 schema:datePublishedReg 2006-09-09
22 schema:description BackgroundSpinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn α-motoneurons and manifesting in the first 6 months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.SettingPediatric intensive care unit of tertiary care hospital.PatientsWe present two new cases of SMARD1 and report two new mutations in the gene IGHMBP2 which encodes immunoglobulin μ-binding protein 2 on chromosome 11q13.ConclusionsSMARD1 is a poor-prognosis disease that should be considered when acute respiratory insufficiency, of suspected neuromuscular or unclear cause, develops during the first 6 months of life. Diaphragmatic paralysis, manifesting as dyspnea and paradoxical respiration, is the most prominent presenting sign and diaphragmatic motility should be investigated early by fluoroscopy or ultrasound. Electromyography and nerve conduction studies revealing peripheral motor and sensory neuropathy then suggest the diagnosis which should be confirmed by genetic analysis.
23 schema:genre article
24 schema:inLanguage en
25 schema:isAccessibleForFree false
26 schema:isPartOf N523a06912fa04fb9a76ba98f73d25c4b
27 N7d9e99043365436f86b4706e5f976f11
28 sg:journal.1313639
29 schema:keywords BackgroundSpinal muscular atrophy
30 IGHMBP2
31 PatientsWe
32 SMARD1
33 acute respiratory insufficiency
34 analysis
35 atrophy
36 autosomal recessive neuromuscular disease
37 care hospital
38 care unit
39 cases
40 cause
41 conduction studies
42 degeneration
43 diagnosis
44 diaphragmatic motility
45 diaphragmatic paralysis
46 disease
47 dyspnea
48 electromyography
49 failure
50 fluoroscopy
51 genetic analysis
52 hospital
53 immunoglobulin
54 infants
55 insufficiency
56 intensive care unit
57 life
58 months
59 months of life
60 motility
61 motoneurons
62 motor
63 muscle atrophy
64 muscular atrophy
65 muscular weakness
66 mutations
67 nerve conduction studies
68 neuromuscular disease
69 neuropathy
70 new cases
71 new mutations
72 paradoxical respiration
73 paralysis
74 peripheral motor
75 peripheral sensory neuropathy
76 poor prognosis disease
77 presenting sign
78 prevalence
79 protein 2
80 recessive neuromuscular disease
81 respiration
82 respiratory distress type 1
83 respiratory failure
84 respiratory insufficiency
85 sensory neuropathy
86 signs
87 spinal muscular atrophy
88 study
89 tertiary care hospital
90 type 1
91 ultrasound
92 unclear cause
93 units
94 unknown prevalence
95 weakness
96 schema:name Respiratory failure in infants due to spinal muscular atrophy with respiratory distress type 1
97 schema:pagination 1851-1855
98 schema:productId N1ef01f6387f442e680a3d610e796f9f3
99 N55e3e743dee44c1a92bfd828151a1127
100 Nec88cc93b4c14f5599fa1888bc735d75
101 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019226814
102 https://doi.org/10.1007/s00134-006-0346-8
103 schema:sdDatePublished 2022-06-01T22:04
104 schema:sdLicense https://scigraph.springernature.com/explorer/license/
105 schema:sdPublisher Nb5eabb1496e24921a5282cc4a06974ae
106 schema:url https://doi.org/10.1007/s00134-006-0346-8
107 sgo:license sg:explorer/license/
108 sgo:sdDataset articles
109 rdf:type schema:ScholarlyArticle
110 N0b9824fff7744712a012ffdc79f0dd21 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
111 schema:name Infant, Newborn
112 rdf:type schema:DefinedTerm
113 N1ef01f6387f442e680a3d610e796f9f3 schema:name doi
114 schema:value 10.1007/s00134-006-0346-8
115 rdf:type schema:PropertyValue
116 N2b15726dff7c45a7a641734c7a512e8f schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
117 schema:name Humans
118 rdf:type schema:DefinedTerm
119 N335c2e747926417799a67774d63c5370 rdf:first sg:person.0674700541.40
120 rdf:rest Nad3d5d57f36e405c8f5d52ab481bb1f0
121 N4bd0f460f73345f68efa42b09387ab41 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
122 schema:name DNA-Binding Proteins
123 rdf:type schema:DefinedTerm
124 N4be74fc1a2714eb9ac0c50b5e8869162 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
125 schema:name Spinal Muscular Atrophies of Childhood
126 rdf:type schema:DefinedTerm
127 N4c666ea06f9844709e77140d9a894baf schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
128 schema:name Mutation
129 rdf:type schema:DefinedTerm
130 N523a06912fa04fb9a76ba98f73d25c4b schema:issueNumber 11
131 rdf:type schema:PublicationIssue
132 N55e3e743dee44c1a92bfd828151a1127 schema:name dimensions_id
133 schema:value pub.1019226814
134 rdf:type schema:PropertyValue
135 N5f3728aae49f49049515461ae9a09a73 rdf:first sg:person.0611041613.50
136 rdf:rest Nbeb9f05e765f4085ba454a64c40b121f
137 N71aec88f93474016a56235e1d546b20a schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
138 schema:name Hereditary Sensory and Autonomic Neuropathies
139 rdf:type schema:DefinedTerm
140 N7d9e99043365436f86b4706e5f976f11 schema:volumeNumber 32
141 rdf:type schema:PublicationVolume
142 N821b6f79e35e4b28be7cb2a7013c2d82 rdf:first sg:person.0617721007.53
143 rdf:rest N335c2e747926417799a67774d63c5370
144 N94f6867e3fc449d8b8fa8ac585b5302d schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
145 schema:name Transcription Factors
146 rdf:type schema:DefinedTerm
147 N99eff8eb72324aeca07105b04b8278f3 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
148 schema:name Respiration, Artificial
149 rdf:type schema:DefinedTerm
150 Nad3d5d57f36e405c8f5d52ab481bb1f0 rdf:first sg:person.01210313364.42
151 rdf:rest rdf:nil
152 Nb3258308487f40899450b0d8fed36961 rdf:first sg:person.0657155013.59
153 rdf:rest Ncbd93ec3a8424470857555da4100488a
154 Nb5eabb1496e24921a5282cc4a06974ae schema:name Springer Nature - SN SciGraph project
155 rdf:type schema:Organization
156 Nbeb9f05e765f4085ba454a64c40b121f rdf:first sg:person.01245230041.51
157 rdf:rest N821b6f79e35e4b28be7cb2a7013c2d82
158 Nc19bcfb55653460d9c0d8f2671f0fd6f schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
159 schema:name Male
160 rdf:type schema:DefinedTerm
161 Ncbd93ec3a8424470857555da4100488a rdf:first sg:person.0761250567.64
162 rdf:rest N5f3728aae49f49049515461ae9a09a73
163 Ndae7eb028e214a2c9117438193bf4c60 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
164 schema:name Respiratory Paralysis
165 rdf:type schema:DefinedTerm
166 Nec88cc93b4c14f5599fa1888bc735d75 schema:name pubmed_id
167 schema:value 16964485
168 rdf:type schema:PropertyValue
169 Nf21f042f87fd441ba09806b5cf4f5e63 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
170 schema:name Infant
171 rdf:type schema:DefinedTerm
172 anzsrc-for:11 schema:inDefinedTermSet anzsrc-for:
173 schema:name Medical and Health Sciences
174 rdf:type schema:DefinedTerm
175 anzsrc-for:1109 schema:inDefinedTermSet anzsrc-for:
176 schema:name Neurosciences
177 rdf:type schema:DefinedTerm
178 sg:journal.1313639 schema:issn 0342-4642
179 1432-1238
180 schema:name Intensive Care Medicine
181 schema:publisher Springer Nature
182 rdf:type schema:Periodical
183 sg:person.01210313364.42 schema:affiliation grid-institutes:grid.417894.7
184 schema:familyName Nardocci
185 schema:givenName Nardo
186 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01210313364.42
187 rdf:type schema:Person
188 sg:person.01245230041.51 schema:affiliation grid-institutes:None
189 schema:familyName Prandi
190 schema:givenName Edi
191 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01245230041.51
192 rdf:type schema:Person
193 sg:person.0611041613.50 schema:affiliation grid-institutes:None
194 schema:familyName Rossetti
195 schema:givenName Giordano
196 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0611041613.50
197 rdf:type schema:Person
198 sg:person.0617721007.53 schema:affiliation grid-institutes:grid.8142.f
199 schema:familyName Tiziano
200 schema:givenName Danilo
201 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0617721007.53
202 rdf:type schema:Person
203 sg:person.0657155013.59 schema:affiliation grid-institutes:None
204 schema:familyName Giannini
205 schema:givenName Alberto
206 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0657155013.59
207 rdf:type schema:Person
208 sg:person.0674700541.40 schema:affiliation grid-institutes:grid.8142.f
209 schema:familyName Brahe
210 schema:givenName Christina
211 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0674700541.40
212 rdf:type schema:Person
213 sg:person.0761250567.64 schema:affiliation grid-institutes:grid.8142.f
214 schema:familyName Pinto
215 schema:givenName Anna Maria
216 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0761250567.64
217 rdf:type schema:Person
218 sg:pub.10.1007/s00247-005-1433-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1031053017
219 https://doi.org/10.1007/s00247-005-1433-7
220 rdf:type schema:CreativeWork
221 sg:pub.10.1007/s00401-005-1056-y schema:sameAs https://app.dimensions.ai/details/publication/pub.1016819693
222 https://doi.org/10.1007/s00401-005-1056-y
223 rdf:type schema:CreativeWork
224 sg:pub.10.1007/s11910-004-0016-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036160647
225 https://doi.org/10.1007/s11910-004-0016-6
226 rdf:type schema:CreativeWork
227 sg:pub.10.1038/ng703 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015912598
228 https://doi.org/10.1038/ng703
229 rdf:type schema:CreativeWork
230 sg:pub.10.1038/sj.sc.3101889 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010839790
231 https://doi.org/10.1038/sj.sc.3101889
232 rdf:type schema:CreativeWork
233 grid-institutes:None schema:alternateName Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy
234 schema:name Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy
235 rdf:type schema:Organization
236 grid-institutes:grid.417894.7 schema:alternateName Department of Child Neurology, Istituto Nazionale Neurologico C. Besta, Via Celoria 11, 20131, Milan, Italy
237 schema:name Department of Child Neurology, Istituto Nazionale Neurologico C. Besta, Via Celoria 11, 20131, Milan, Italy
238 rdf:type schema:Organization
239 grid-institutes:grid.8142.f schema:alternateName Institute of Medical Genetics, Università Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy
240 schema:name Institute of Medical Genetics, Università Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy
241 rdf:type schema:Organization
 




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


...