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Refinado por: Base de dados/Biblioteca: ClinicalKey remover assunto: Infant remover Family Health remover
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1
Guidance for the health sector to partner with parents and families for early childhood development
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Artigo
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Guidance for the health sector to partner with parents and families for early childhood development

Richter, Linda M ; Ghent, Liana ; Issa, Ghassan M ; Okengo, Lynette ; Santiago, Evelyn

The Lancet (British edition), 2020-03, Vol.395 (10226), p.766-768 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease
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Artigo
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Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease

Stone, Edwin M., MD, PhD ; Andorf, Jeaneen L., BA ; Whitmore, S. Scott, PhD ; DeLuca, Adam P., PhD ; Giacalone, Joseph C., BS ; Streb, Luan M., BA ; Braun, Terry A., PhD ; Mullins, Robert F., PhD ; Scheetz, Todd E., PhD ; Sheffield, Val C., MD, PhD ; Tucker, Budd A., PhD

Ophthalmology (Rochester, Minn.), 2017-09, Vol.124 (9), p.1314-1331 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Impact of childhood psoriasis on parents of affected children
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Artigo
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Impact of childhood psoriasis on parents of affected children

Tollefson, Megha M., MD ; Finnie, Dawn M., MPA ; Schoch, Jennifer J., MD ; Eton, David T., PhD

Journal of the American Academy of Dermatology, 2017-02, Vol.76 (2), p.286-289.e5 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Respiratory viruses transmission from children to adults within a household
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Artigo
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Respiratory viruses transmission from children to adults within a household

MacIntyre, Chandini Raina ; Ridda, Iman ; Seale, Holly ; Gao, Zhanhai ; Ratnamohan, Vigneswary Mala ; Donovan, Linda ; Zeng, Frank ; Dwyer, Dominic E

Vaccine, 2012-04, Vol.30 (19), p.3009-3014 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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5
Cardiac homeobox gene NKX2-5 Mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome
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Artigo
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Cardiac homeobox gene NKX2-5 Mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome

ELLIOTT, David A ; KIRK, Edwin P ; FENELEY, Michael ; HARVEY, Richard P ; YEOH, Thomas ; CHANDAR, Suchitra ; MCKENZIE, Fiona ; TAYLOR, Peter ; GROSSFELD, Paul ; FATKIN, Diane ; JONES, Owen ; HAYES, Peter

Journal of the American College of Cardiology, 2003-06, Vol.41 (11), p.2072-2076 [Periódico revisado por pares]

New York, NY: Elsevier Science

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6
Characteristics and patterns of health and social service use by families with babies and toddlers in Germany
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Artigo
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Characteristics and patterns of health and social service use by families with babies and toddlers in Germany

Ulrich, Susanne M. ; Walper, Sabine ; Renner, Ilona ; Liel, Christoph

Public health (London), 2022-02, Vol.203, p.83-90 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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7
Quality of life impacts from rotavirus gastroenteritis on children and their families in the UK
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Artigo
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Quality of life impacts from rotavirus gastroenteritis on children and their families in the UK

Marlow, Robin ; Finn, Adam ; Trotter, Caroline

Vaccine, 2015-09, Vol.33 (39), p.5212-5216 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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8
Family-Centered Service for Children With Cerebral Palsy and Their Families: A Review of the Literature
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Artigo
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Family-Centered Service for Children With Cerebral Palsy and Their Families: A Review of the Literature

King, Susanne ; Teplicky, Rachel ; King, Gillian ; Rosenbaum, Peter

Seminars in pediatric neurology, 2004-03, Vol.11 (1), p.78-86 [Periódico revisado por pares]

United States: Elsevier Inc

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9
The Impact on Family of Pediatric Chronic Respiratory Failure in the Home
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Artigo
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The Impact on Family of Pediatric Chronic Respiratory Failure in the Home

Graham, Robert J., MD ; Rodday, Angie Mae, PhD ; Weidner, Ruth Ann, MBA, MRP ; Parsons, Susan K., MD, MRP

The Journal of pediatrics, 2016-08, Vol.175, p.40-46 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
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Artigo
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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Van Driest, Sara L. ; Vasile, Vlad C. ; Ommen, Steve R. ; Will, Melissa L. ; Tajik, A.Jamil ; Gersh, Bernard J. ; Ackerman, Michael J.

Journal of the American College of Cardiology, 2004-11, Vol.44 (9), p.1903-1910 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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