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Healthy Parent sentence examples within Consanguineou Healthy Parent



A case of transient hyperphosphatasemia presenting with mild degree of bow legs



A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review


Healthy Parent sentence examples within Unrelated Healthy Parent



Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia



The Wrath of Severe Term Hypoxic-Ischemic Encephalopathy


Healthy Parent sentence examples within Support Healthy Parent



Indigenous Mothers’ Use of Web- and App-Based Information Sources to Support Healthy Parenting and Infant Health in Canada: Interpretive Description



CenteringParenting - Forming a Community Inside the Medical Home through the Group Well Child Visit




Healthy Parent sentence examples within Periodontally Healthy Parent



Parents with periodontitis impact the subgingival colonization of their offspring



Dynamics of colonization by Aggregatibacter actinomycetemcomitans in aggressive periodontitis families


Healthy Parent sentence examples within Her Healthy Parent



SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia.



A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia


Healthy Parent sentence examples within Two Healthy Parent



Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A



A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 - Review of the literature.


Healthy Parent sentence examples within healthy parent carer



Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children



Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children.


Healthy Parent sentence examples within healthy parent feeding



Regulatory parental feeding behaviors, emotion suppression, and emotional eating in the absence of hunger: Examining parent-adolescent dyadic associations



Family functioning mediates the relationship between child behavior problems and parent feeding practices in youth with overweight or obesity.


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10.1080/10410236.2021.1943891

Leveraging Upward Social Comparison in Social Media to Promote Healthy Parenting.


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10.1055/S-0041-1726282

Exome Sequencing Reveals De Novo Variants in Congenital Scoliosis


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10.4025/ACTASCIBIOLSCI.V43I1.53097

Strategies for vegetative propagation and viral cleaning of a miniature ornamental pineapple hybrid


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10.3389/fgene.2021.732002

Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs



Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1A.


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10.4038/SJDEM.V11I1.7432

A case of transient hyperphosphatasemia presenting with mild degree of bow legs


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10.1080/08039488.2021.1900389

A new measure of excessive parental worries about children’s health: Development of the Health Anxiety by Proxy Scale (HAPYS)


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10.3389/fgene.2021.652718

A Novel Germline Compound Heterozygous Mutation of BRCA2 Gene Associated With Familial Peripheral Neuroblastic Tumors in Two Siblings


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10.1177/1559827619849028

Parenting and Child Development: A Relational Health Perspective


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10.3389/fgene.2021.686993

Case Report: Identification of Maternal Low-Level Mosaicism in the Dystrophin Gene by Droplet Digital Polymerase Chain Reaction


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10.1007/s00223-021-00909-1

Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets.


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10.1016/j.aace.2021.01.007

A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review


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10.1016/j.childyouth.2020.105915

Child care institutions in India: Investigating issues and challenges in children’s rehabilitation and social integration


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10.1136/jmedgenet-2021-108114

SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum



A Novel BLOC1S5-Related HPS-11 Patient and Zebrafish with bloc1s5 Disruption.



High-Throughput Screen Detects Calcium Signaling Dysfunction in Hutchinson-Gilford Progeria Syndrome


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10.1016/j.jaac.2021.02.023

A Longitudinal Study of Psychiatric Disorders in Offspring of Parents With Bipolar Disorder From Preschool to Adolescence.


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10.1542/PEDS.147.3_MEETINGABSTRACT.52

Parenting in a Pandemic: An Innovative Virtual Support Forum for Families Living in Homeless Shelters


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10.1016/j.childyouth.2020.105751

Potential impacts, alleviating factors, and interventions for children of a parent with schizophrenia: A scoping review


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10.1186/s43045-021-00100-0

Autistic traits in offspring of schizophrenic patients in comparison to those of normal population: a case-control study


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10.4103/psychiatry.IndianJPsychiatry_107_20

Parenting skills of patients with chronic schizophrenia



Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy.


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10.1186/s40478-021-01121-w

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease


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10.1186/s40814-021-00881-5

Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children



Promoting mother-infant relationships and underlying neural correlates: Results from a randomized controlled trial of a home-visiting program for adolescent mothers in Brazil.


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10.1007/s10578-021-01229-z

Biased Maintenance of Attention on Sad Faces in Clinically Depressed Youth: An Eye-Tracking Study.



Indigenous Mothers’ Use of Web- and App-Based Information Sources to Support Healthy Parenting and Infant Health in Canada: Interpretive Description


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10.1016/J.MGENE.2021.100951

Tetrasomy 18p in one non-identical twin born to healthy parents: A case report



Barriers and facilitators to mood and confidence in pregnancy and early parenthood during COVID-19 in the UK: mixed-methods synthesis survey


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10.1007/978-3-030-73912-6_3

Child Development and Well-Being


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10.31249/rphil/2021.03.06

BIOETHICAL PROBLEMS OF THE DEVELOPMENT OF GENETICS


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10.1016/j.scr.2021.102178

Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A).



Child adjustment to parental cancer: A latent profile analysis.



Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors


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10.3389/fgene.2021.680838

Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia


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10.3390/ijerph18094709

Supporting Positive Parenting and Promoting Healthy Living through Family Cooking Classes


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10.1073/pnas.2023184118

Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies


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10.1016/j.jad.2021.07.086

Age related sex differences in maladaptive regulatory responses to sadness: A study of youths at high and low familial risk for depression.


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10.1016/j.appet.2021.105603

Regulatory parental feeding behaviors, emotion suppression, and emotional eating in the absence of hunger: Examining parent-adolescent dyadic associations


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10.5505/KPD.2020.87699

The evaluation of depression, anxiety and quality of life in children living with parental cancer: A case-control study (eng)


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10.1007/s00109-020-02033-3

Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant.


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10.1007/s12519-021-00438-9

Mosaic trisomy 12 diagnosed in a female patient: clinical features, genetic analysis, and review of the literature


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10.1017/S2040174421000532

Newborns physiological differences in low- and high-altitude settings of Ecuador.



Loss of TANGO1 Leads to Absence of Bone Mineralization


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10.1186/s40814-021-00881-5

Healthy Parent Carers: feasibility randomised controlled trial of a peer-led group-based health promotion intervention for parent carers of disabled children.


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10.1016/j.isci.2021.102894

Genome-wide study of copy number variation implicates multiple novel loci for schizophrenia risk in Han Chinese family trios


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10.1136/bmjopen-2020-045570

Healthy Parent Carers programme: mixed methods process evaluation and refinement of a health promotion intervention



A FATAL OUTCOME OF A NEONATAL DILATED CARDIOMYOPATHY: EVOLUTIVE NEONATAL LUPUS OR EARLIER CHILDHOOD- ONSET SYSTEMIC LUPUS? A CASE REPORT


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10.1016/j.amsu.2021.102896

Possible autosomal recessive inheritance in a neonate with Nager syndrome: Case report



Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A


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10.1182/bloodadvances.2021005217

GATA2 deficiency phenotype associated with tandem duplication GATA2 and over-expression of GATA2-AS1.


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10.1080/00207454.2021.1967349

Chromosomal Microarray and Exome Sequencing in Unexplained Early Infantile Epileptic Encephalopathies in a Highly Consanguineous Population.


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10.4236/AASOCI.2021.114014

Parental Infertility: Impact of the Quality of the Relation between Parents and Adopted Children


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10.1556/2006.2021.00064

Associations between gaming disorder, parent-child relationship, parental supervision, and discipline styles: Findings from a school-based survey during the COVID-19 pandemic in Vietnam.


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10.1542/PEDS.147.3_MEETINGABSTRACT.68-A

Cuddle-Calm Intervention to Strengthen Emotional Connection


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10.1038/s10038-021-00975-1

SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia.


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10.1134/S1022795421070103

Estimation of the Prevalence and Parental Origin of Chromosomal Microdeletions and Microduplications Affecting the CNTN6 Gene in Patients with Neurodevelopmental Disorders and Healthy Individuals


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10.1038/s41598-020-80372-4

Parents with periodontitis impact the subgingival colonization of their offspring


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10.1038/s41386-021-01088-1

Differentiating white matter measures that protect against vs. predispose to bipolar disorder and other psychopathology in at-risk youth


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10.37547/TAJPSLC/VOLUME03ISSUE05-16

Considerations For The Prevention Of Crimes Against The Sexual Integrity Of Minors


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10.1136/jmedgenet-2020-107572

Biallelic GINS2 variant p.(Arg114Leu) causes Meier-Gorlin syndrome with craniosynostosis


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10.1007/s11920-019-0996-1

Parenting in Patients with Borderline Personality Disorder, Sequelae for the Offspring and Approaches to Treatment and Prevention


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10.1038/s41467-018-08135-4

A genome-wide CRISPR screen identifies N-acetylglucosamine-1-phosphate transferase as a potential antiviral target for Ebola virus



Case of Neonatal Fatality from Neuromuscular Variant of Glycogen Storage Disease Type IV.



[Association between time-appropriate vaccinations in early childhood and individual and community-level factors in Japan].



[Relationship between pregnancy factors and low birth weight infants, miscarriages, and stillbirths: A follow-up survey on birth conditions of pregnant women who received the maternal and child health handbook from public health nurses and midwives].


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10.1007/s12041-019-1057-6

Novel mutation in Cul7 gene in a family diagnosed with 3M syndrome


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10.1016/j.ejmg.2019.02.008

CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.


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10.1038/s41386-019-0339-2

Baseline and follow-up activity and functional connectivity in reward neural circuitries in offspring at risk for bipolar disorder


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10.1186/s13643-019-1215-1

Recruitment and retention of fathers with young children in early childhood health intervention research: a systematic review and meta-analysis protocol


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10.4103/jehp.jehp_397_18

Comparison of attachment styles of addicted parents and non-addicted parents in health-care referents


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10.1186/s12876-019-0929-9

Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report



National campaign to promote maternal and child health in 21st-century Japan Healthy Parents and Children 21


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10.1044/2018_LSHSS-CCJS-18-0030

Service and Learning at a Residential Parenting Program for Incarcerated Mothers: Speech-Language Pathology Student Outcomes and Maternal Perspectives.


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10.1016/J.MGENE.2018.10.003

Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation


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10.1136/practneurol-2019-002219

Progressive myelopathy in an adult


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10.1007/s12098-019-03053-9

The Wrath of Severe Term Hypoxic-Ischemic Encephalopathy


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10.1542/PEDS.144.2_MEETINGABSTRACT.68

The Parenting-Related Adverse Childhood Experiences Survey: A New Tool to Screen for Unhealthy Parenting in Pediatric Primary Care



Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report


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10.1177/0009922819884571

Investigating Parental Concerns at the First Well-Child Visit


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10.1186/s12881-019-0875-y

Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report


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10.3892/mmr.2019.10830

A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next-generation sequencing and Sanger sequencing


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10.21037/atm.2019.06.14

Whole exome sequencing identifies a rare variant in DAAM2 as a potential candidate in idiopathic pulmonary ossification.


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10.1007/s12519-019-00294-8

The clinical phenotype and genotype of NLRP12-autoinflammatory disease: a Chinese case series with literature review


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