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What do firms say in reporting on impacts of climate change? An approach to monitoring ESG actions and environmental policy.
- Published in:
- Corporate Social Responsibility & Environmental Management, 2023, v. 30, n. 5, p. 2664, doi. 10.1002/csr.2509
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- Publication type:
- Article
If so many are "few," how few are "many"?
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- Frontiers in Psychology, 2015, v. 6, p. 1, doi. 10.3389/fpsyg.2015.00441
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- Publication type:
- Article
Disparities in Routine Breast Cancer Screening for Medicaid Managed Care Members with a Work-Limiting Disability.
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- Medicare & Medicaid Research Review, 2011, v. 1, n. 4, p. E1, doi. 10.5600/mmrr.001.04.a02
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- Publication type:
- Article
Health Care Utilization and Expenditures of Homeless Family Members Before and After Emergency Housing.
- Published in:
- American Journal of Public Health, 2018, v. 108, n. 6, p. 808, doi. 10.2105/AJPH.2018.304370
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- Publication type:
- Article
CATEGORIZATION OF FREQUENT EMERGENCY DEPARTMENT USE IN AN INSURED HOMELESS POPULATION.
- Published in:
- 2016
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- Publication type:
- Letter to the Editor
Frequent Emergency Department Visits and Hospitalizations Among Homeless People With Medicaid: Implications for Medicaid Expansion.
- Published in:
- American Journal of Public Health, 2015, v. 105, p. S716, doi. 10.2105/AJPH.2015.302693
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- Publication type:
- Article
Health Care Utilization Patterns of Homeless Individuals in Boston: Preparing for Medicaid Expansion Under the Affordable Care Act.
- Published in:
- 2013
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- Publication type:
- Journal Article
Health Care Utilization Patterns of Homeless Individuals in Boston: Preparing for Medicaid Expansion Under the Affordable Care Act.
- Published in:
- American Journal of Public Health, 2013, v. 103, n. S2, p. S311, doi. 10.2105/AJPH.2013.301421
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- Publication type:
- Article
Unbalanced Whole-Arm Translocation der(18;21)(q10;q10) in Hematological Malignancies.
- Published in:
- Journal of the Association of Genetic Technologists, 2020, v. 46, n. 3, p. 141
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- Publication type:
- Article
50<sup>th</sup> Genetics Corner: A Patient with CHARGE Syndrome Illustrates the Parable of the Six Blind Men and the Elephant.
- Published in:
- Neonatology Today, 2022, v. 17, n. 6, p. 142, doi. 10.51362/neonatology.today/2022176142145
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- Publication type:
- Article
Genetics Corner: Klippel-Trenaunay Syndrome in an Infant with a Mosaic PIK3CA Variant, a Target for the Medical Treatment of Asymmetric Overgrowth.
- Published in:
- 2022
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- Publication type:
- Case Study
Genetics Corner: Syndromic Etiology of Apparently Isolated Clubfeet: a Child with Loeys-Dietz Syndrome.
- Published in:
- Neonatology Today, 2022, v. 17, n. 4, p. 127
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- Publication type:
- Article
Genetics Corner: Donohue Syndrome in a Small for Gestational Age Infant with Hyperinsulinemia.
- Published in:
- Neonatology Today, 2022, v. 17, n. 3, p. 146, doi. 10.51362/neonatology.today/2022173146150
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- Publication type:
- Article
Genetics Corner: Alpha Thalassemia X-Linked Intellectual Disability Syndrome in an Infant with Developmental Delay and DYS Recurrent Respiratory Failure Confirmed by Whole-Exome Sequencing.
- Published in:
- 2022
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- Publication type:
- Case Study
Genetics Corner: "Coat-hanger" ribs and Bell-Shaped Thorax in an Infant with Paternal Uniparental Disomy for Chromosome 14.
- Published in:
- 2022
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- Publication type:
- Case Study
Genetics Corner: Cat-Eye-Syndrome and Genetic Syndromes Associated with Ear Anomalies.
- Published in:
- 2021
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- Publication type:
- Case Study
Genetics Corner: A Newborn with a Disorder of Sex Development Caused by 45,X/46,X,idic(Y) Mosaicism.
- Published in:
- Neonatology Today, 2021, v. 16, n. 11, p. 133, doi. 10.51362/neonatology.today/2021111611133136
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- Publication type:
- Article
Atypical Williams Syndrome in a Child who Presented with Aortic Stenosis and Coarctation and a Positive Family History.
- Published in:
- 2021
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- Publication type:
- Case Study
Genetic Corner: Diaphragmatic Hernia in an Infant with a Type II Distal Deletion of 22q11.2 (LCR22E-F).
- Published in:
- 2021
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- Publication type:
- Case Study
The Genetics Corner: A Mother and Child with Cleft lip and Palate Have an Atypical 1p36 Deletion that Disrupts KIF1B, a Cause of Autosomal Dominant Charcot-Marie-Tooth Disease, Type 2A1.
- Published in:
- Neonatology Today, 2021, v. 16, n. 8, p. 118, doi. 10.51362/neonatology.today/20218168118121
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- Publication type:
- Article
The Genetics Corner: A Preterm Infant with Down Syndrome Complicated by Severe Transient Abnormal Myelopoiesis.
- Published in:
- Neonatology Today, 2021, v. 16, n. 7, p. 125, doi. 10.51362/neonatology.today/20217167124125
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- Publication type:
- Article
Genetics Corner: Multisuture Craniosynostosis Secondary to Intrauterine Constraint During Gestation in a Bicornuate Uterus.
- Published in:
- Neonatology Today, 2021, v. 16, n. 6, p. 131
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- Publication type:
- Article
The Genetics Corner: Pathogenic variants in DOCK6 mimic congenital viral infection in an SGA infant with VSD and intracranial calcifications.
- Published in:
- Neonatology Today, 2021, v. 16, n. 4, p. 124
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- Publication type:
- Article
The Genetics Corner: The Positive Predictive Value of NIPT for 22q11 Deletion Syndrome Varies with the Indication.
- Published in:
- 2021
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- Publication type:
- Case Study
Genetics Corner: An Infant with Amyoplasia Limited to the Upper Extremities.
- Published in:
- Neonatology Today, 2021, v. 16, n. 2, p. 113, doi. 10.51362/neonatology.today/20212162113116
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- Publication type:
- Article
Genetics Corner: Trichothiodystrophy 1 Causes Neutropenia in an Infant with Congenital ichthyosis and Brittle Hair.
- Published in:
- 2021
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- Publication type:
- Case Study
Genetics Corner: Risk of Epilepsy in an Asymptomatic Infant with Prenatally Diagnosed Tuberous Sclerosis.
- Published in:
- 2020
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- Publication type:
- Case Study
Genetics Corner: Townes-Brocks Syndrome in an Infant with Familial Imperforate Anus.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
The Genetics Corner: Hypophosphatasia.
- Published in:
- Neonatology Today, 2020, v. 15, n. 10, p. 99, doi. 10.51362/neonatology.today/202010151099103
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- Publication type:
- Article
The Genetics Corner: DiGeorge Anomaly Associated with Diabetic Embryopathy in an Infant without a Deletion on Chromosome 22q11.
- Published in:
- 2020
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- Publication type:
- Case Study
Fellow Column: An Unbalanced Translocation Involving Partial Duplication of Chromosome 6 and Partial Deletion of Chromosome 10 in a Premature Infant with Tetralogy of Fallot.
- Published in:
- Neonatology Today, 2020, v. 15, n. 9, p. 20, doi. 10.51362/neonatology.today/202091592025
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- Publication type:
- Article
The Genetics Corner: HNF1B-Related Bilateral Cystic Kidney Disease in an Infant and his Asymptomatic Mother.
- Published in:
- 2020
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- Publication type:
- Case Study
The Genetics Corner: Congenital Microcephaly and a Region of Homozygosity on Chromosome 1 that was not Reported on the Prenatal Chromosome Microarray.
- Published in:
- 2020
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- Publication type:
- Case Study
Kabuki Syndrome in a Newborn with a Complex Left-Sided Cardiac Lesion and Persistent Hypoglycemia due to Hyperinsulinism.
- Published in:
- 2020
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- Publication type:
- Case Study
Fellow Column: A Neonate with Fetal Brain Disruption Sequence.
- Published in:
- Neonatology Today, 2020, p. 41, doi. 10.51362/neonatology.today/202061564144
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- Publication type:
- Article
The Genetics Corner: A Consultation for Neonatal Diabetes Mellitus Reveals Uniparental Disomy 6.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
The Genetics Corner: Perisylvian Polymicrogyria and Seizures in One of Monochorionic Diamniotic Twins Following Twin-Twin-Transfusion Syndrome and in utero Laser Ablation Therapy.
- Published in:
- 2020
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- Publication type:
- Case Study
Genetics Corner: A Lethal Ciliopathy Affects Two Siblings with Renal Dysplasia and Oligohydramnios.
- Published in:
- Neonatology Today, 2020, v. 15, n. 3, p. 66
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- Publication type:
- Article
Genetics Corner: Alveolar Simplification and Down Syndrome.
- Published in:
- 2020
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- Publication type:
- Case Study
Genetics Corner: Prenatal Diagnosis of Klinefelter Syndrome.
- Published in:
- 2020
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- Publication type:
- Case Study
Genetics Corner: Genetic Counseling and Family Screening after Prenatal Diagnosis Of Hypoplastic Left Heart Syndrome: Is It Warranted?
- Published in:
- 2019
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- Publication type:
- Case Study
Genetics Corner: A Consultation for Wolf-Hirschhorn Syndrome.
- Published in:
- 2019
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- Publication type:
- Case Study
Genetics Corner: Translocation Down syndrome.
- Published in:
- 2019
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- Publication type:
- Case Study
Genetics Corner: Down Syndrome Tool Kit- a Resource for Physicians Taking Care of Neonates.
- Published in:
- Neonatology Today, 2019, v. 14, n. 9, p. 83
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- Publication type:
- Article
Frequently Asked Questions, Part II More about Copy number variants (CNVs), Variants of Uncertain Significance (VUS) in Chromosome Microarrays, with a special focus on Congenital Heart Defects (CHDs).
- Published in:
- Neonatology Today, 2019, v. 14, n. 8, p. 67
- By:
- Publication type:
- Article
The Genetics Corner: A Genetics consultation for a Family History of Permanent Neonatal-Onset Diabetes Mellitus.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
The Genetics Corner: A Consultation for Multiple Congenital Anomalies.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
The Genetics Corner: A Genetics Consultation for Agenesis Cutis Congenita and Methimazole Exposure.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
The Genetics Corner: A Genetics Evaluation for Chronic Diarrhea that Revealed Incest.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
The Genetics Corner: A Genetics Consultation for Agenesis of the Corpus Callosum and Poor Feeding.
- Published in:
- 2019
- By:
- Publication type:
- Case Study