Found: 26
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Kangaroo father care: A pilot feasibility study of physiologic, biologic, and psychosocial measures to capture the effects of father–infant and mother–infant skin‐to‐skin contact in the Neonatal Intensive Care Unit.
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- Developmental Psychobiology, 2021, v. 63, n. 5, p. 1521, doi. 10.1002/dev.22100
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- Article
ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.
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- 2018
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- Publication type:
- journal article
A Commentary on The importance of knowing from whence your PHOX2B mutation comes.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 6, p. 345, doi. 10.1038/jhg.2012.44
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- Article
Congenital central hypoventilation syndrome: Broader cognitive deficits revealed by parent controls.
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- Pediatric Pulmonology, 2018, v. 53, n. 4, p. 492, doi. 10.1002/ppul.23939
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- Article
Congenital central hypoventilation syndrome (CCHS): Circadian temperature variation.
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- Pediatric Pulmonology, 2016, v. 51, n. 3, p. 300, doi. 10.1002/ppul.23236
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- Article
Variable human phenotype associated with novel deletions of the PHOX2B gene.
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- Pediatric Pulmonology, 2012, v. 47, n. 2, p. 153, doi. 10.1002/ppul.21527
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- Article
Congenital central hypoventilation syndrome from past to future: Model for translational and transitional autonomic medicine.
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- Pediatric Pulmonology, 2009, v. 44, n. 6, p. 521, doi. 10.1002/ppul.21045
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- Article
A narrative review of the mechanisms and consequences of intermittent hypoxia and the role of advanced analytic techniques in pediatric autonomic disorders.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 287, doi. 10.1007/s10286-023-00958-6
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- Article
The future of rare autonomic disease research.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 211, doi. 10.1007/s10286-023-00957-7
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- Article
Apparently rare cases are worth studying because.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 209, doi. 10.1007/s10286-023-00956-8
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- Article
Neurocognition as a biomarker in the rare autonomic disorders of CCHS and ROHHAD.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 217, doi. 10.1007/s10286-022-00901-1
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- Article
Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndrome.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 231, doi. 10.1007/s10286-022-00908-8
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- Article
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD): a collaborative review of the current understanding.
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- Clinical Autonomic Research, 2023, v. 33, n. 3, p. 251, doi. 10.1007/s10286-023-00936-y
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- Article
Pupillometry measures of autonomic nervous system regulation with advancing age in a healthy pediatric cohort.
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- Clinical Autonomic Research, 2020, v. 30, n. 1, p. 43, doi. 10.1007/s10286-019-00639-3
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- Article
CLINICAL CASE ROUNDS IN CHILD AND ADOLESCENT PSYCHIATRY: Commentary: Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): Remember Your ABCs (Airway, Breathing, Circulation).
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- Journal of the Canadian Academy of Child & Adolescent Psychiatry, 2013, v. 22, n. 3, p. 238
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- Article
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours.
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- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0314-x
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- Article
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours.
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- 2015
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- Publication type:
- journal article
Cerebral Autoregulation during Orthostatic Challenge in Congenital Central Hypoventilation Syndrome.
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- 2022
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- Publication type:
- journal article
Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.
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- Acta Paediatrica, 2013, v. 102, n. 12, p. e546, doi. 10.1111/apa.12405
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- Article
HTR2A variation and sudden infant death syndrome: a case-control analysis.
- Published in:
- 2009
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- Publication type:
- journal article
HTR2A variation and sudden infant death syndrome: a case–control analysis.
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- Acta Paediatrica, 2009, v. 98, n. 1, p. 58, doi. 10.1111/j.1651-2227.2008.01018.x
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- Article
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene.
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- Acta Paediatrica, 2009, v. 98, n. 1, p. 192, doi. 10.1111/j.1651-2227.2008.01039.x
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- Article
Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®.
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- Pediatric Pulmonology, 2022, v. 57, n. 9, p. 2040, doi. 10.1002/ppul.25973
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- Article
Congenital central hypoventilation syndrome: Severe disease caused by co‐occurrence of two PHOX2B variants inherited separately from asymptomatic family members.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 503, doi. 10.1002/ajmg.a.61047
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- Article
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS).
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2297, doi. 10.1002/ajmg.a.35499
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- Article
Congenital Central Hypoventilation Syndrome.
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- American Journal of Respiratory & Critical Care Medicine, 2006, v. 174, n. 10, p. 1139, doi. 10.1164/rccm.200602-305OC
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- Publication type:
- Article