Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathy (Englisch)
- Neue Suche nach: Nevin, Suzanne M
- Neue Suche nach: Wakefield, Claire E
- Neue Suche nach: Barlow‐Stewart, Kristine
- Neue Suche nach: McGill, Brittany C
- Neue Suche nach: Bye, Ann
- Neue Suche nach: Palmer, Elizabeth E
- Neue Suche nach: Children's Hospital At Westmead Neurology Group
- Neue Suche nach: Cogenes Group
- Neue Suche nach: Nevin, Suzanne M
- Neue Suche nach: Wakefield, Claire E
- Neue Suche nach: Barlow‐Stewart, Kristine
- Neue Suche nach: McGill, Brittany C
- Neue Suche nach: Bye, Ann
- Neue Suche nach: Palmer, Elizabeth E
- Neue Suche nach: Dale, Russell C
- Neue Suche nach: Gill, Deepak
- Neue Suche nach: Kothur, Kavitha
- Neue Suche nach: Boggs, Kirsten
- Neue Suche nach: Le Marne, Fleur
- Neue Suche nach: Beavis, Erin
- Neue Suche nach: Macintosh, Rebecca
- Neue Suche nach: Sachdev, Rani
- Neue Suche nach: Children's Hospital At Westmead Neurology Group
- Neue Suche nach: Cogenes Group
In:
Developmental Medicine & Child Neurology
;
64
, 1
;
95-104
;
2022
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathy
-
Beteiligte:Nevin, Suzanne M ( Autor:in ) / Wakefield, Claire E ( Autor:in ) / Barlow‐Stewart, Kristine ( Autor:in ) / McGill, Brittany C ( Autor:in ) / Bye, Ann ( Autor:in ) / Palmer, Elizabeth E ( Autor:in ) / Dale, Russell C ( Mitwirkende:r ) / Gill, Deepak ( Mitwirkende:r ) / Kothur, Kavitha ( Mitwirkende:r ) / Boggs, Kirsten ( Mitwirkende:r )
-
Erschienen in:Developmental Medicine & Child Neurology ; 64, 1 ; 95-104
-
Verlag:
-
Erscheinungsdatum:01.01.2022
-
Format / Umfang:10 pages
-
ISSN:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Englisch
-
Datenquelle:
Inhaltsverzeichnis – Band 64, Ausgabe 1
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 1
-
Table of Contents| 2022
- 4
-
Developmental central hypotonia: implications for counselling, prognosis, and managementDan, Bernard et al. | 2022
- 5
-
Harnessing the power of neuroimaging and whole genome sequencing from fetus to adulthoodParker, Alasdair et al. | 2022
- 6
-
The way forward in medical and ethical antenatal counselling for neurological anomaliesFerrand, Amaryllis / Racine, Eric et al. | 2022
- 7
-
The difference rehabilitation can make after acquired brain injuryForsyth, Rob et al. | 2022
- 8
-
Hope, hype, cures, and persons with cerebral palsyTurner, Leigh et al. | 2022
- 9
-
Causation of cerebral palsy: the huge knowledge gap between populations and individualsGanesan, Vijeya et al. | 2022
- 10
-
Interference with prenatal, perinatal, and neonatal brain development is associated with a high risk for autism and attention‐deficit/hyperactivity disorderKraegeloh‐Mann, Ingeborg et al. | 2022
- 11
-
Promoting functional development for children with cerebral palsy in low‐income countriesTann, Cally J et al. | 2022
- 12
-
Overcoming the barriers to care for children with neurodevelopmental disordersBinagwaho, Agnes / Muvunyi, Raissa et al. | 2022
- 13
-
Unmet psychosocial needs of parents of children with rare, complex, and severe genetic diseasesTumiene, Birute et al. | 2022
- 14
-
Antenatal counselling for prospective parents whose fetus has a neurological anomaly: part 1, experiences and recommendations for service designHart, Anthony R / Vollmer, Brigitte / Howe, David / Boxall, Sally / Foulds, Nicola / de Lacy, Patricia / Vasudevan, Chakra / Griffiths, Paul D / Piercy, Hilary et al. | 2022
- 23
-
Antenatal counselling for prospective parents whose fetus has a neurological anomaly: part 2, risks of adverse outcome in common anomaliesHart, Anthony R / Vasudevan, Chakra / Griffiths, Paul D / Foulds, Nicola / Piercy, Hilary / de Lacy, Patricia / Boxall, Sally / Howe, David / Vollmer, Brigitte et al. | 2022
- 40
-
Physical rehabilitation interventions in children with acquired brain injury: a scoping reviewGmelig Meyling, Christiaan / Verschuren, Olaf / Rentinck, Ingrid R / Engelbert, Raoul H H / Gorter, Jan Willem et al. | 2022
- 49
-
Is the search for cerebral palsy ‘cures’ a reasonable and appropriate goal in the 2020s?Honan, Ingrid / Finch‐Edmondson, Megan / Imms, Christine / Novak, Iona / Hogan, Amy / Clough, Shannon / Bonyhady, Bruce / McIntyre, Sarah / Elliott, Catherine / Wong, Shirley et al. | 2022
- 56
-
Perinatal arterial ischemic stroke and periventricular venous infarction in infants with unilateral cerebral palsyVitagliano, Melissa / Dunbar, Mary / Dyck Holzinger, Sasha / Letourneau, Nicole / Dewey, Deborah / Oskoui, Maryam / Shevell, Michael / Kirton, Adam et al. | 2022
- 63
-
Neuroimaging findings in children with cerebral palsy with autism and/or attention‐deficit/hyperactivity disorder: a population‐based studyPÅhlman, Magnus / Gillberg, Christopher / Himmelmann, Kate et al. | 2022
- 70
-
Functional development in children with cerebral palsy in Uganda: population‐based longitudinal cohort studyAndrews, Carin / Namaganda, Lukia / Eliasson, Ann‐Christin / Kakooza‐Mwesige, Angelina / Forssberg, Hans et al. | 2022
- 80
-
Health‐related quality of life and caregiver burden after hip reconstruction and spinal fusion in children with spastic cerebral palsyDiFazio, Rachel L / Vessey, Judith A / Miller, Patricia E / Snyder, Brian D / Shore, Benjamin J et al. | 2022
- 88
-
Organizational perspectives and diagnostic evaluations for children with neurodevelopmental disordersCloet, Eva / Jansen, Anna / Leys, Mark et al. | 2022
- 95
-
Psychosocial impact of genetic testing on parents of children with developmental and epileptic encephalopathyNevin, Suzanne M / Wakefield, Claire E / Barlow‐Stewart, Kristine / McGill, Brittany C / Bye, Ann / Palmer, Elizabeth E / Children's Hospital At Westmead Neurology Group / Cogenes Group et al. | 2022
- 105
-
Genotype–phenotype correlation of CACNA1A variants in children with epilepsyNiu, Xueyang / Yang, Ying / Chen, Yi / Cheng, Miaomiao / Liu, Ming / Ding, Changhong / Tian, Xiaojuan / Yang, Zhixian / Jiang, Yuwu / Zhang, Yuehua et al. | 2022
- 112
-
Mortality in pediatric hydrocephalusTully, Hannah M / Doherty, Dan / Wainwright, Mark et al. | 2022
- 118
-
Cerebral cortex maldevelopment in syndromic craniosynostosisWilson, Alexander T / Den Ottelander, Bianca K / Van Veelen, Marie‐Lise C / Dremmen, Marjolein HG / Persing, John A / Vrooman, Henri A / Mathijssen, Irene MJ / Tasker, Robert C et al. | 2022
- 125
-
Phenotype of heterozygous variants of dehydrodolichol diphosphate synthaseJiao, Xianru / Xue, Yinan / Yang, Sai / Gong, Pan / Niu, Yue / Wang, Qi / Yang, Hui / Xiong, Hui / Zhang, Yuehua / Yang, Zhixian et al. | 2022
- 135
-
Antenatal counselling families whose fetus has a neurological anomaly: one parent’s reflectionsTurner, Rachel et al. | 2022