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Intranasal Fentanyl for Pain Management in Children: A Systematic Review of the Literature

Journal of pediatric health care, 2011-09, Vol.25 (5), p.316-322

Mudd, Shawna, DNP, PNP-BC

2011

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Clinical Practice Guideline for the Treatment of Pediatric Acute Gastroenteritis in the Outpatient Setting

Journal of pediatric health care, 2016-11, Vol.30 (6), p.610-616

2016

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Violence prevention initiatives and resources

The Healthcare Forum journal, 1996-09, Vol.39 (5), p.33

1996

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The natural history of IgE-mediated cow's milk allergy

Journal of allergy and clinical immunology, 2007-11, Vol.120 (5), p.1172-1177

2007

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Common genetic susceptibility loci link PFAPA syndrome, Behçet’s disease, and recurrent aphthous stomatitis

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (25), p.14405-14411

2020

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A Nearly Obstructive Intratracheal Mass in a Pediatric Patient

JAMA otolaryngology-- head & neck surgery, 2023-04, Vol.149 (4), p.368

2023

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Parental decision making associated with pediatric emergency department use for asthma

Annals of allergy, asthma, & immunology, 2016-11, Vol.117 (5), p.490-494

2016

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The impact of food allergy on the daily activities of children and their families

Annals of allergy, asthma, & immunology, 2006-03, Vol.96 (3), p.415-421

2006

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Adaptive immune responses to SARS-CoV-2 persist in the pharyngeal lymphoid tissue of children

Nature immunology, 2023-01, Vol.24 (1), p.186-199

2023

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22q11.2 Deletion syndrome and obstructive sleep apnea

International journal of pediatric otorhinolaryngology, 2014-08, Vol.78 (8), p.1360-1364

2014

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Cognitive Function in Young Persons With and Without Perinatal HIV in the AALPHI Cohort in England: Role of Non–HIV-Related Factors

Clinical infectious diseases, 2016-11, Vol.63 (10), p.1380-1387

2016

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Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency

Metabolism, clinical and experimental, 2002-08, Vol.51 (8), p.981-988

2002

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Self-harm in young people with perinatal HIV and HIV negative young people in England: cross sectional analysis

BMC public health, 2019-08, Vol.19 (1), p.1165-1165, Article 1165

2019

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Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Journal of inherited metabolic disease, 2001-07, Vol.24 (4), p.448-464

2001

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Leisure-time physical activity during pregnancy and offspring size at 18 to 24 months

Journal of physical activity & health, 2011-07, Vol.8 (5), p.655-662

2011

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Retail Food Equivalents for Post–Oral Immunotherapy Dosing in the Omalizumab as Monotherapy and as Adjunct Therapy to Multi-Allergen Oral Immunotherapy in Food-Allergic Children and Adults (OUtMATCH) Clinical Trial

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2023-02, Vol.11 (2), p.572-580.e2

2023

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Association between second hand smoke (SHS) exposure and caregiver stress in children with poorly controlled asthma

The Journal of asthma, 2019-09, Vol.56 (9), p.915-926

2019

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Methionine adenosyltransferase I/III deficiency : Novel mutations and clinical variations

American journal of human genetics, 2000-02, Vol.66 (2), p.347-355

2000

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Clinical Handbook of Psychological Consultation in Pediatric Medical Settings

1st ed. 2020., 2020

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Isolated persistent hypermethioninemia

American journal of human genetics, 1995-10, Vol.57 (4), p.882-892

1995

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Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay

Human genetics, 1998-05, Vol.102 (5), p.591-597

1998

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Adulthood functioning : the joint effects of parental alcoholism, gender and childhood socio-economic stress

Addiction (Abingdon, England), 1997-05, Vol.92 (5), p.583-596

1997

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Asthma Management Practices at Home in Young Inner-City Children

The Journal of asthma, 2004-01, Vol.41 (4), p.433-444

2004

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Labile methyl group balances in the human: The role of sarcosine

Metabolism, clinical and experimental, 1980-08, Vol.29 (8), p.707-720

1980

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Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine β‐synthase (CBS) deficiency

American journal of medical genetics, 2002-02, Vol.108 (1), p.57-63

2002

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Intranasal Fentanyl for Pain Management in Children: A Systematic Review of the Literature

Clinical Practice Guideline for the Treatment of Pediatric Acute Gastroenteritis in the Outpatient Setting

Violence prevention initiatives and resources

The natural history of IgE-mediated cow's milk allergy

Common genetic susceptibility loci link PFAPA syndrome, Behçet’s disease, and recurrent aphthous stomatitis

A Nearly Obstructive Intratracheal Mass in a Pediatric Patient

Parental decision making associated with pediatric emergency department use for asthma

The impact of food allergy on the daily activities of children and their families

Adaptive immune responses to SARS-CoV-2 persist in the pharyngeal lymphoid tissue of children

22q11.2 Deletion syndrome and obstructive sleep apnea

Cognitive Function in Young Persons With and Without Perinatal HIV in the AALPHI Cohort in England: Role of Non–HIV-Related Factors

Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency

Self-harm in young people with perinatal HIV and HIV negative young people in England: cross sectional analysis

Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia

Leisure-time physical activity during pregnancy and offspring size at 18 to 24 months

Retail Food Equivalents for Post–Oral Immunotherapy Dosing in the Omalizumab as Monotherapy and as Adjunct Therapy to Multi-Allergen Oral Immunotherapy in Food-Allergic Children and Adults (OUtMATCH) Clinical Trial

Association between second hand smoke (SHS) exposure and caregiver stress in children with poorly controlled asthma

Methionine adenosyltransferase I/III deficiency : Novel mutations and clinical variations

Clinical Handbook of Psychological Consultation in Pediatric Medical Settings

Isolated persistent hypermethioninemia

Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay

Adulthood functioning : the joint effects of parental alcoholism, gender and childhood socio-economic stress

Asthma Management Practices at Home in Young Inner-City Children

Labile methyl group balances in the human: The role of sarcosine

Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine β‐synthase (CBS) deficiency

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