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Content Provider : Psychology and Behavioral Sciences Collection Subject : ankle Subject : electric stimulation Subject : exercise Subject : glycogen storage disease type ii Subject : health surveys Subject : medical history taking Subject : quality of life Filter by : Subject

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Academic Journal

Risk factors and etiology of childhood hearing loss: a cohort review of 296 subjects.

Authors : Niu, Kai (AUTHOR); Brandström, Anni (AUTHOR); Skenbäck, Sara (AUTHOR)

Subjects: AUDITORY perception testing; CHROMOSOME abnormalities; HEARING impaired childrenSWEDEN

Source: Acta Oto-Laryngologica. Aug2020, Vol. 140 Issue 8, p668-674. 7p.

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Academic Journal

Screening for late‐onset Pompe disease in Poland.

Authors : Jastrzębska, Aleksandra (AUTHOR); Potulska‐Chromik, Anna (AUTHOR); Łusakowska, Anna (AUTHOR)

Subjects: GLYCOGEN storage disease type II; TANDEM mass spectrometry; MUSCLE weaknessPOLAND

Source: Acta Neurologica Scandinavica. Oct2019, Vol. 140 Issue 4, p239-243. 5p.

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Academic Journal

What do parents expect from a genetic diagnosis of their child with intellectual disability?

Authors : Dikow, Nicola (AUTHOR); Moog, Ute (AUTHOR); Karch, Stephanie (AUTHOR)

Subjects: ANXIETY diagnosis; COMPETENCY assessment (Law); DECISION making

Source: Journal of Applied Research in Intellectual Disabilities. Sep2019, Vol. 32 Issue 5, p1129-1137. 9p.

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Academic Journal

Psychosocial impact of BRCA testing in young Black breast cancer survivors.

Authors : Gonzalez, Brian D.; Hoogland, Aasha I.; Kasting, Monica L.

Subjects: BREAST cancer diagnosis; BREAST cancer patients; QUALITY of life

Source: Psycho-Oncology. Dec2018, Vol. 27 Issue 12, p2778-2785. 8p. 2 Charts, 2 Graphs.

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Academic Journal

Value of genetic testing for pediatric epilepsy: Driving earlier diagnosis of ceroid lipofuscinosis type 2 Batten disease.

Authors : Leal‐Pardinas, Fernanda (AUTHOR); Truty, Rebecca (AUTHOR); McKnight, Dianalee A. (AUTHOR)

Subjects: GENETIC testing; NEURONAL ceroid-lipofuscinosis; SYMPTOMS

Source: Epilepsia (Series 4). Jul2022, Vol. 63 Issue 7, pe68-e73. 6p.

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Academic Journal

Health Supervision for Children and Adolescents With Down Syndrome.

Authors : Bull, Marilyn J.; Trotter, Tracy; Santoro, Stephanie L.

Subjects: CHROMOSOME analysis; DIAGNOSIS of Down syndrome; COGNITION disorders

Source: Pediatrics. May2022, Vol. 149 Issue 5, p1-23. 24p.

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Academic Journal

Leukodystrophies in Children: Diagnosis, Care, and Treatment.

Authors : Bonkowsky, Joshua L.; Keller, Stephanie

Subjects: HEREDITARY central nervous system demyelinating diseases; NEWBORN screening; PEDIATRICS

Source: Pediatrics. Sep2021, Vol. 148 Issue 3, p1-15. 15p.

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Academic Journal

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS).

Authors : Usami, Shin-ichi (AUTHOR); Miyagawa, Maiko (AUTHOR); Nishio, Shin-ya (AUTHOR)

Subjects: SENSORY stimulation; TREATMENT of hearing disorders; MITOCHONDRIAL pathology

Source: Acta Oto-Laryngologica. Apr2012, Vol. 132 Issue 4, p377-384. 8p. 4 Diagrams, 1 Chart.

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Academic Journal

Prenatal genetic screening for intellectual disability.

Authors : Edwards, S. D. (AUTHOR)

Subjects: DIAGNOSIS of fetal diseases; PRENATAL genetic testing; MENTAL efficiency

Source: Journal of Intellectual Disability Research. Oct2003, Vol. 47 Issue 7, p526-532. 7p.

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Academic Journal

A 10-Month-Old With Intermittent Hypotonia and Paralysis.

Authors : Beinvogl, Beate C.; Rosman, N. Paul; Baumer, Fiona M.

Subjects: CHILD development; DIFFERENTIAL diagnosis; CLINICAL pathology

Source: Pediatrics. Jul2016, Vol. 138 Issue 1, p1-9. 9p.

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