Hooper, Stephen R.
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Stephen R. Hooper researcher
VIAF ID: 5049220 (Personal)
Permalink: http://viaf.org/viaf/5049220
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Hooper
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Stephen R.
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Hooper, Stephen R
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100 1 _ ‡a Hooper, Stephen R
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100 1 _ ‡a Hooper, Stephen R (sparse)
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100 1 _ ‡a Hooper, Stephen R.
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Hooper, Stephen R.
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Hooper, Stephen R.
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100 1 _ ‡a Hooper, Stephen R.
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Hooper, Stephen R.
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100 1 _ ‡a Hooper, Stephen R.
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100 1 _ ‡a Hooper, Stephen R.
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100 1 _ ‡a Hooper, Stephen R.
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100 1 _ ‡a Hooper, Stephen R.
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Stephen R. Hooper
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researcher
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Works
| Title | Sources |
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| Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study |
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| Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome |
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| Assessment issues in child neuropsychology / ed. by Michael G. Tramontana and Stephen R. Hooper. - New York, 1988. |
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| Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians |
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| Association of Blood Pressure Level With Left Ventricular Mass in Adolescents |
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| Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome |
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| Basics of child neuropsychology : a primer for educators and clinicians |
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| Bicarbonate, blood pressure, and executive function in pediatric CKD-is there a link? |
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| Blood pressure and school performance |
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| The brain in pediatric chronic kidney disease-the intersection of cognition, neuroimaging, and clinical biomarkers |
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| Characteristics of undiagnosed diseases network applicants: implications for referring providers |
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| Child psychopathology : diagnostic criteria and clinical assessment |
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| Cognitive improvement in children with CKD after transplant |
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| Completing the puzzle: The search for pieces in the understanding of psychosis risk in 22q11.2 deletion syndrome |
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| Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference |
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| Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia. |
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| Duration of chronic kidney disease reduces attention and executive function in pediatric patients |
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| Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes |
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| Evaluation of Neurocognition in Youth with CKD Using a Novel Computerized Neurocognitive Battery |
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| Frontal Hypoactivation During a Working Memory Task in Children With 22q11 Deletion Syndrome |
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| Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion |
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| The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease |
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| Genomic Disorders and Neurocognitive Impairment in Pediatric CKD. |
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| Health Care Transition for Adolescents With CKD—The Journey From Pediatric to Adult Care |
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| Health care transition preparation in youth with chronic conditions: working towards translational evidence with a patient perspective |
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| Learning disability subtyping : neuropsychological foundations, conceptual models, and issues in clinical differentiation |
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| Longitudinal Self-Management and/or Transition Readiness per the TRxANSITION Index among Patients with Chronic Conditions in Pediatric or Adult Care Settings |
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| The nervous system and chronic kidney disease in children |
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| Neurocognitive Function in Children with Primary Hypertension after Initiation of Antihypertensive Therapy. |
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| Neurocognitive, Social-Behavioral, and Adaptive Functioning in Preschool Children with Mild to Moderate Kidney Disease |
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| Neurological basis of childhood psychopathology |
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| No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. |
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| Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders |
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| Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome |
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| Pediatric traumatic brain injury |
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| Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome |
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| Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? |
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| The relationship of health care transition readiness to disease-related characteristics, psychosocial factors, and health care outcomes: preliminary findings in adolescents with chronic kidney disease |
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| Self-Management and Transition Readiness Assessment: Concurrent, Predictive and Discriminant Validation of the STARx Questionnaire |
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| SHIP-AHOY (Study of High Blood Pressure in Pediatrics: Adult Hypertension Onset in Youth) |
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| Sleep disordered breathing as measured by SRBD-PSQ and neurocognition in children with hypertension. |
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| Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention |
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| Socioeconomic Status and Psychological Function in Children with Chromosome 22q11.2 Deletion Syndrome: Implications for Genetic Counseling |
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| STRANDS manual : survey of teenage readiness and neurodevelopment status, administration, scoring, and interpretation |
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| Subclinical Systolic and Diastolic Dysfunction Is Evident in Youth With Elevated Blood Pressure |
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| Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study |
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| Systematic review of structural and functional neuroimaging findings in children and adults with CKD. |
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| A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders. |
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| Target Organ Abnormalities in Pediatric Hypertension |
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| Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome |
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| A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network |
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| Young children with special needs |
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