1
40
8
-
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/10.1007/s00240-019-01133-1" target="_blank" rel="noreferrer noopener">http://doi.org/10.1007/s00240-019-01133-1</a>
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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
Adolescents with urinary stones have elevated urine levels of inflammatory mediators
Publisher
An entity responsible for making the resource available
Urolithiasis
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-04
Subject
The topic of the resource
Biomarker; Cytokine; Innate immunity; Interleukin
Creator
An entity primarily responsible for making the resource
Kusumi Kirsten; Ketz John; Saxena Vijay; Spencer John David; Safadi Fayez; Schwaderer Andrew
Description
An account of the resource
Urinary stones are increasing in children, primarily during adolescence. Although urinary stones are often viewed in the context of intermittent stone events, increasing evidence indicates that stones are a metabolic process associated with chronic kidney disease and cardiovascular disease. These aforementioned stone-associated conditions may have pediatric origins. To compare urine inflammatory markers in otherwise healthy stone forming children versus matched controls. Urine samples were collected from 12 adolescents with urinary stones along with 15 controls. The levels of 30 urine cytokines were measured using a Mesoscale 30-Plex Human Cytokine panel and normalized to urine creatinine levels. Macrophage inflammatory protein 1β and interleukin 13 levels were significantly elevated in the urine of the stone forming adolescents compared to controls. Interleukin 17A was elevated in the urine of controls. This study indicates that urine levels of cytokines involved in chronic inflammation and fibrosis are elevated in urinary stone formers as early as adolescence. Because stone formers are at risk for chronic kidney disease, macrophage inflammatory protein 1β and interleukin 13 represent investigative targets.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1007/s00240-019-01133-1" target="_blank" rel="noreferrer noopener">10.1007/s00240-019-01133-1</a>
2019
Biomarker
Cytokine
Department of Pediatrics
Innate immunity
Interleukin
June 2019 Update
Ketz John
Kusumi Kirsten
NEOMED College of Medicine
Safadi Fayez
Saxena Vijay
Schwaderer Andrew
Spencer John David
urolithiasis
-
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/10.1093/neuonc/noz175.767" target="_blank" rel="noreferrer noopener">http://doi.org/10.1093/neuonc/noz175.767</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
S57-S58
Issue
4, SI
Volume
66
ISSN
1545-5009
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<a href="http://ezproxy.neomed.idm.oclc.org/login?url=http://doi.org/10.1093/neuonc/noz175.767" target="_blank" rel="noreferrer noopener">NEOMED Full-text Holding (if available) - Proxy DOI: 10.1093/neuonc/noz175.767</a>
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Title
A name given to the resource
Chemotherapy Strategies for Young Children Newly-Diagnosed with Medulloblastoma up to the Era of Molecular Profiling - A Comparative Outcomes Analysis
Publisher
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Pediatric Blood & Cancer
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-12
Creator
An entity primarily responsible for making the resource
Finlay J; Mynarek M; Dhall G; Lafay-Cousin L; Mazewski C M; Ashley D; Cohen B H; von Bueren A O; Gerber N; Leary S; Geyer J R; Tait D; Gajjar A; Rutkowski S
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1093/neuonc/noz175.767" target="_blank" rel="noreferrer noopener">10.1093/neuonc/noz175.767</a>
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2019
Akron Children's Hospital
Ashley D
Cohen B H
Department of Integrative Medical Sciences
Department of Pediatrics
Dhall G
Finlay J
Gajjar A
Gerber N
Geyer J R
Journal Article
Lafay-Cousin L
Leary S
Mazewski C M
Mynarek M
NEOMED College of Medicine
November 2019 Update
Pediatric blood & cancer
Rutkowski S
Tait D
von Bueren A O
-
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/10.1136/jmedgenet-2018-105800" target="_blank" rel="noreferrer noopener">http://doi.org/10.1136/jmedgenet-2018-105800</a>
Pages
123–130
Issue
3
Volume
56
NEOMED College
NEOMED College of Medicine
NEOMED Department
Department of Pediatrics; Department of Integrative Medical Sciences
Affiliated Hospital
Akron Children's Hospital
Dublin Core
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Title
A name given to the resource
Diagnosis of 'possible' mitochondrial disease: an existential crisis.
Publisher
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Journal of medical genetics
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-03
Subject
The topic of the resource
clinical genetics; diagnosis; evidence based practice; metabolic disorders
Creator
An entity primarily responsible for making the resource
Parikh Sumit; Karaa Amel; Goldstein Amy; Bertini Enrico Silvio; Chinnery Patrick F; Christodoulou John; Cohen Bruce H; Davis Ryan L; Falk Marni J; Fratter Carl; Horvath Rita; Koenig Mary Kay; Mancuso Michaelangelo; McCormack Shana; McCormick Elizabeth M; McFarland Robert; Nesbitt Victoria; Schiff Manuel; Steele Hannah; Stockler Silvia; Sue Carolyn; Tarnopolsky Mark; Thorburn David R; Vockley Jerry; Rahman Shamima
Description
An account of the resource
Primary genetic mitochondrial diseases are often difficult to diagnose, and the term 'possible' mitochondrial disease is used frequently by clinicians when such a diagnosis is suspected. There are now many known phenocopies of mitochondrial disease. Advances in genomic testing have shown that some patients with a clinical phenotype and biochemical abnormalities suggesting mitochondrial disease may have other genetic disorders. In instances when a genetic diagnosis cannot be confirmed, a diagnosis of 'possible' mitochondrial disease may result in harm to patients and their families, creating anxiety, delaying appropriate diagnosis and leading to inappropriate management or care. A categorisation of 'diagnosis uncertain', together with a specific description of the metabolic or genetic abnormalities identified, is preferred when a mitochondrial disease cannot be genetically confirmed.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1136/jmedgenet-2018-105800" target="_blank" rel="noreferrer noopener">10.1136/jmedgenet-2018-105800</a>
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Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
2019
Akron Children's Hospital
Bertini Enrico Silvio
Chinnery Patrick F
Christodoulou John
clinical genetics
Cohen Bruce H
Davis Ryan L
Department of Integrative Medical Sciences
Department of Pediatrics
Diagnosis
evidence based practice
Falk Marni J
Fratter Carl
Goldstein Amy
Horvath Rita
Journal of medical genetics
Karaa Amel
Koenig Mary Kay
Mancuso Michaelangelo
McCormack Shana
McCormick Elizabeth M
McFarland Robert
metabolic disorders
NEOMED College of Medicine
Nesbitt Victoria
Parikh Sumit
Rahman Shamima
Schiff Manuel
Steele Hannah
Stockler Silvia
Sue Carolyn
Tarnopolsky Mark
Thorburn David R
Vockley Jerry
-
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/10.1136/jmedgenet-2018-105800" target="_blank" rel="noreferrer noopener">http://doi.org/10.1136/jmedgenet-2018-105800</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
123-130
Issue
3
Volume
56
NEOMED College
NEOMED College of Medicine
NEOMED Department
Department of Pediatrics; Department of Integrative Medical Sciences
Affiliated Hospital
Akron Children's Hospital
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
Diagnosis of 'possible' mitochondrial disease: an existential crisis.
Publisher
An entity responsible for making the resource available
Journal of medical genetics
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-03
Subject
The topic of the resource
clinical genetics; diagnosis; evidence based practice; metabolic disorders
Creator
An entity primarily responsible for making the resource
Parikh Sumit; Karaa Amel; Goldstein Amy; Bertini Enrico Silvio; Chinnery Patrick F; Christodoulou John; Cohen Bruce H; Davis Ryan L; Falk Marni J; Fratter Carl; Horvath Rita; Koenig Mary Kay; Mancuso Michaelangelo; McCormack Shana; McCormick Elizabeth M; McFarland Robert; Nesbitt Victoria; Schiff Manuel; Steele Hannah; Stockler Silvia; Sue Carolyn; Tarnopolsky Mark; Thorburn David R; Vockley Jerry; Rahman Shamima
Description
An account of the resource
Primary genetic mitochondrial diseases are often difficult to diagnose, and the term 'possible' mitochondrial disease is used frequently by clinicians when such a diagnosis is suspected. There are now many known phenocopies of mitochondrial disease. Advances in genomic testing have shown that some patients with a clinical phenotype and biochemical abnormalities suggesting mitochondrial disease may have other genetic disorders. In instances when a genetic diagnosis cannot be confirmed, a diagnosis of 'possible' mitochondrial disease may result in harm to patients and their families, creating anxiety, delaying appropriate diagnosis and leading to inappropriate management or care. A categorisation of 'diagnosis uncertain', together with a specific description of the metabolic or genetic abnormalities identified, is preferred when a mitochondrial disease cannot be genetically confirmed.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1136/jmedgenet-2018-105800" target="_blank" rel="noreferrer noopener">10.1136/jmedgenet-2018-105800</a>
2019
Akron Children's Hospital
Bertini Enrico Silvio
Chinnery Patrick F
Christodoulou John
clinical genetics
Cohen Bruce H
Davis Ryan L
Department of Integrative Medical Sciences
Department of Pediatrics
Diagnosis
evidence based practice
Falk Marni J
Fratter Carl
Goldstein Amy
Horvath Rita
Journal of medical genetics
Karaa Amel
Koenig Mary Kay
Mancuso Michaelangelo
McCormack Shana
McCormick Elizabeth M
McFarland Robert
metabolic disorders
NEOMED College of Medicine
Nesbitt Victoria
Parikh Sumit
Rahman Shamima
Schiff Manuel
Steele Hannah
Stockler Silvia
Sue Carolyn
Tarnopolsky Mark
Thorburn David R
Vockley Jerry
-
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/10.1136/annrheumdis-2019-216040" target="_blank" rel="noreferrer noopener">http://doi.org/10.1136/annrheumdis-2019-216040</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
1722-1731
Issue
12
Volume
78
ISSN
1468-2060
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<a href="http://ezproxy.neomed.idm.oclc.org/login?url=http://doi.org/10.1136/annrheumdis-2019-216040" target="_blank" rel="noreferrer noopener">NEOMED Full-text Holding (if available) - Proxy DOI: 10.1136/annrheumdis-2019-216040</a>
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Title
A name given to the resource
Emergent high fatality lung disease in systemic juvenile arthritis
Publisher
An entity responsible for making the resource available
Annals Of The Rheumatic Diseases
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-12
Subject
The topic of the resource
treatment; inflammation; adult onset still's disease; DMARDs (biologic); juvenile idiopathic arthritis
Creator
An entity primarily responsible for making the resource
Saper Vivian E; Chen Guangbo; Deutsch Gail H; Guillerman R Paul; Birgmeier Johannes; Jagadeesh Karthik; Canna Scott; Schulert Grant; Deterding Robin; Xu Jianpeng; Leung Ann N; Bouzoubaa Layla; Abulaban Khalid; Baszis Kevin; Behrens Edward M; Birmingham James; Casey Alicia; Cidon Michal; Cron Randy Q; De Aliva; De Benedetti Fabrizio; Ferguson Ian; Fishman Martha P; Goodman Steven I; Graham T Brent; Grom Alexei A; Haines Kathleen; Hazen Melissa; Henderson Lauren A; Ho Assunta; Ibarra Maria; Inman Christi J; Jerath Rita; Khawaja Khulood; Kingsbury Daniel J; Klein-Gitelman Marisa; Lai Khanh; Lapidus Sivia; Lin Clara; Lin Jenny; Liptzin Deborah R; Milojevic Diana; Mombourquette Joy; Onel Karen; Ozen Seza; Perez Maria; Phillippi Kathryn; Prahalad Sampath; Radhakrishna Suhas; Reinhardt Adam; Riskalla Mona; Rosenwasser Natalie; Roth Johannes; Schneider Rayfel; Schonenberg-Meinema Dieneke; Shenoi Susan; Smith Judith A; Sönmez Hafize Emine; Stoll Matthew L; Towe Christopher; Vargas Sara O; Vehe Richard K; Young Lisa R; Yang Jacqueline; Desai Tushar; Balise Raymond; Lu Ying; Tian Lu; Bejerano Gill; Davis Mark M; Khatri Purvesh; Mellins Elizabeth D; Childhood Arthritis and Rheumatology Research Alliance Registry Investigators
Description
An account of the resource
OBJECTIVE: To investigate the characteristics and risk factors of a novel parenchymal lung disease (LD), increasingly detected in systemic juvenile idiopathic arthritis (sJIA). METHODS: In a multicentre retrospective study, 61 cases were investigated using physician-reported clinical information and centralised analyses of radiological, pathological and genetic data. RESULTS: LD was associated with distinctive features, including acute erythematous clubbing and a high frequency of anaphylactic reactions to the interleukin (IL)-6 inhibitor, tocilizumab. Serum ferritin elevation and/or significant lymphopaenia preceded LD detection. The most prevalent chest CT pattern was septal thickening, involving the periphery of multiple lobes ± ground-glass opacities. The predominant pathology (23 of 36) was pulmonary alveolar proteinosis and/or endogenous lipoid pneumonia (PAP/ELP), with atypical features including regional involvement and concomitant vascular changes. Apparent severe delayed drug hypersensitivity occurred in some cases. The 5-year survival was 42%. Whole exome sequencing (20 of 61) did not identify a novel monogenic defect or likely causal PAP-related or macrophage activation syndrome (MAS)-related mutations. Trisomy 21 and young sJIA onset increased LD risk. Exposure to IL-1 and IL-6 inhibitors (46 of 61) was associated with multiple LD features. By several indicators, severity of sJIA was comparable in drug-exposed subjects and published sJIA cohorts. MAS at sJIA onset was increased in the drug-exposed, but was not associated with LD features. CONCLUSIONS: A rare, life-threatening lung disease in sJIA is defined by a constellation of unusual clinical characteristics. The pathology, a PAP/ELP variant, suggests macrophage dysfunction. Inhibitor exposure may promote LD, independent of sJIA severity, in a small subset of treated patients. Treatment/prevention strategies are needed.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1136/annrheumdis-2019-216040" target="_blank" rel="noreferrer noopener">10.1136/annrheumdis-2019-216040</a>
PMID: 31562126
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2019
Abulaban Khalid
adult onset still's disease
Akron Children's Hospital
Annals of the rheumatic diseases
Balise Raymond
Baszis Kevin
Behrens Edward M
Bejerano Gill
Birgmeier Johannes
Birmingham James
Bouzoubaa Layla
Canna Scott
Casey Alicia
Chen Guangbo
Childhood Arthritis and Rheumatology Research Alliance Registry Investigators
Cidon Michal
Cron Randy Q
Davis Mark M
De Aliva
De Benedetti Fabrizio
Department of Pediatrics
Desai Tushar
Deterding Robin
Deutsch Gail H
DMARDs (biologic)
Ferguson Ian
Fishman Martha P
Goodman Steven I
Graham T Brent
Grom Alexei A
Guillerman R Paul
Haines Kathleen
Hazen Melissa
Henderson Lauren A
Ho Assunta
Ibarra Maria
Inflammation
Inman Christi J
Jagadeesh Karthik
Jerath Rita
Journal Article
juvenile idiopathic arthritis
Khatri Purvesh
Khawaja Khulood
Kingsbury Daniel J
Klein-Gitelman Marisa
Lai Khanh
Lapidus Sivia
Leung Ann N
Lin Clara
Lin Jenny
Liptzin Deborah R
Lu Ying
Mellins Elizabeth D
Milojevic Diana
Mombourquette Joy
NEOMED College of Medicine
November 2019 Update
Onel Karen
Ozen Seza
Perez Maria
Phillippi Kathryn
Prahalad Sampath
Radhakrishna Suhas
Reinhardt Adam
Riskalla Mona
Rosenwasser Natalie
Roth Johannes
Saper Vivian E
Schneider Rayfel
Schonenberg-Meinema Dieneke
Schulert Grant
Shenoi Susan
Smith Judith A
Sönmez Hafize Emine
Stoll Matthew L
Tian Lu
Towe Christopher
Treatment
Vargas Sara O
Vehe Richard K
Xu Jianpeng
Yang Jacqueline
Young Lisa R
-
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/10.3928/19382359-20190219-02" target="_blank" rel="noreferrer noopener">http://doi.org/10.3928/19382359-20190219-02</a>
Pages
E121–E127
Issue
3
Volume
48
ISSN
0090-4481
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Title
A name given to the resource
Exercise-Induced Dyspnea in Children and Adolescents: Differential Diagnosis
Publisher
An entity responsible for making the resource available
Pediatric Annals
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-03
Subject
The topic of the resource
Pediatrics; adults; asthma; induced bronchoconstriction; hyperventilation; vocal-cord dysfunction
Creator
An entity primarily responsible for making the resource
Bhatia R; Abu-Hasan M; Weinberger M
Description
An account of the resource
Exercise-induced dyspnea in children and adolescents can occur for many reasons. Although asthma is the common cause, failure to prevent exercise-induced asthma by pretreatment with a bronchodilator, such as albuterol, indicates that other etiologies should be considered. Other causes of exercise-induced dyspnea include exercise-induced vocal cord dysfunction, exercise-induced laryngomalacia, exercise-induced hyperventilation, chest wall restrictive abnormalities, cardiac causes, and normal physiologic limitation. When exercise-induced dyspnea is not from asthma, cardiopulmonary exercise testing with reproduction of the patient's dyspnea is the means to identify the other causes. Cardiopulmonary exercise testing monitors oxygen use, carbon-dioxide production, end-tidal pCO(2) (partial pressure of carbon dioxide), and electrocardiogram. Additional components to testing are measurement of blood pH and pCO(2) when symptoms are reproduced, and selective flexible laryngoscopy when upper airway obstruction is observed to specifically identify vocal cord dysfunction or laryngomalacia. This approach is a highly effective means to identify exercise-induced dyspnea that is not caused by asthma.
Identifier
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<a href="http://doi.org/10.3928/19382359-20190219-02" target="_blank" rel="noreferrer noopener">10.3928/19382359-20190219-02</a>
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Information about rights held in and over the resource
Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).
2019
Abu-Hasan M
adults
asthma
Bhatia R
Department of Pediatrics
hyperventilation
induced bronchoconstriction
June 2019 Update
NEOMED College of Medicine
Pediatric Annals
Pediatrics
vocal-cord dysfunction
Weinberger M
-
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/10.1111/head.13681" target="_blank" rel="noreferrer noopener">http://doi.org/10.1111/head.13681</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
1871-1873
Issue
10
Volume
59
ISSN
1526-4610
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<a href="http://ezproxy.neomed.idm.oclc.org/login?url=http://doi.org/10.1111/head.13681" target="_blank" rel="noreferrer noopener">NEOMED Full-text Holding (if available) - Proxy DOI: 10.1111/head.13681</a>
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Dublin Core
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Title
A name given to the resource
Pediatric Migraine Action Plan (PedMAP)
Publisher
An entity responsible for making the resource available
Headache
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019-11
Creator
An entity primarily responsible for making the resource
Turner Scott B; Rende Elizabeth K; Pezzuto Tara; Weaver Samantha; Henderlong-Kropp Annmarie; Greene Kaitlin A; Bicknese Alma R; Dilts Jennifer J; Gautreaux Jennifer; Victorio M Cristina C; Strauss Lauren D; Lagman-Bartolome Ana Marissa; Szperka Christina L; Yonker Marcy; Hershey Andrew D; Gelfand Amy A
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1111/head.13681" target="_blank" rel="noreferrer noopener">10.1111/head.13681</a>
PMID: 31710105
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2019
Akron Children's Hospital
Bicknese Alma R
Department of Pediatrics
Dilts Jennifer J
Gautreaux Jennifer
Gelfand Amy A
Greene Kaitlin A
Headache
Henderlong-Kropp Annmarie
Hershey Andrew D
Journal Article
Lagman-Bartolome Ana Marissa
NEOMED College of Medicine
November 2019 Update
Pezzuto Tara
Rende Elizabeth K
Strauss Lauren D
Szperka Christina L
Turner Scott B
Victorio M Cristina C
Weaver Samantha
Yonker Marcy
-
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/10.1007/978-3-030-12771-8_46" target="_blank" rel="noreferrer noopener">http://doi.org/10.1007/978-3-030-12771-8_46</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
151
ISSN
3-030-12771-0
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<a href="http://ezproxy.neomed.idm.oclc.org/login?url=http://doi.org/10.1007/978-3-030-12771-8_46" target="_blank" rel="noreferrer noopener">NEOMED Full-text Holding (if available) - Proxy DOI: 10.1007/978-3-030-12771-8_46</a>
<p>Users with a NEOMED Library login can search for full-text journal articles at the following url: <a href="https://libraryguides.neomed.edu/home">https://libraryguides.neomed.edu/home</a></p>
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
Ugh
Publisher
An entity responsible for making the resource available
Health Disparities : Weaving A New Understanding Through Case Narratives
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
2019
Subject
The topic of the resource
Pediatrics; Mental health; Medicine; Social Work; Medicine & Public Health; Health Psychology; Medical Sociology; Premedical Education; Family support
Creator
An entity primarily responsible for making the resource
Sladjana Courson
Description
An account of the resource
Ugh. I am ashamed to say that is the first word that comes to my mind when I see Jake’s name on my schedule for the day. He is 10 and he has been my patient since he was born. He has an 8-year-old sister Annie and a 5-year-old brother Jimmy. They usually all come in together with their mother even if only one of them has an appointment that day.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1007/978-3-030-12771-8_46" target="_blank" rel="noreferrer noopener">10.1007/978-3-030-12771-8_46</a>
Format
The file format, physical medium, or dimensions of the resource
Journal Article
2019
Akron Children's Hospital
Department of Pediatrics
Family support
Health Disparities : Weaving A New Understanding Through Case Narratives
Health Psychology
Journal Article
Medical Sociology
Medicine
Medicine & Public Health
Mental Health
NEOMED College of Medicine
November 2019 Update
Pediatrics
Premedical Education
Sladjana Courson
Social Work