Zobrazeno 1 - 10
of 313
pro vyhledávání: '"Helen D. Pratt"'
Publikováno v:
In Journal of Pediatric and Adolescent Gynecology 2010 23(1):e54-e57
Autor:
McClanahan, Kimberly K.
Publikováno v:
In Journal of Pediatric and Adolescent Gynecology 2007 20(6):367-369
Autor:
McClanahan, Kimberly K.
Publikováno v:
In Journal of Pediatric and Adolescent Gynecology 2007 20(3):215-217
Publikováno v:
Health Care for People with Intellectual and Developmental Disabilities across the Lifespan ISBN: 9783319180953
Sturge-Weber syndrome is a rare neurocutaneous syndrome (phakomatosis) due to a somatic activating mutation in GNAQ (guanine nucleotide binding protein [G protein], q polypeptide). Evaluation reveals a facial port-wine stain (nevus flammeus), ipsilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ae17e428ef6e8d2372e12b8ff4dfb7e
https://doi.org/10.1007/978-3-319-18096-0_76
https://doi.org/10.1007/978-3-319-18096-0_76
Publikováno v:
Health Care for People with Intellectual and Developmental Disabilities across the Lifespan ISBN: 9783319180953
Nager Syndrome is a rare autosomal dominant or recessive defect also called preaxial acrofacial dysostosis due to dysfunction of development of the first and second branchial arches. Nager syndrome is due to defect of the SF3B4 gene. These individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::369b37b90f0a37be80336b2782a664e6
https://doi.org/10.1007/978-3-319-18096-0_75
https://doi.org/10.1007/978-3-319-18096-0_75
Publikováno v:
Health Care for People with Intellectual and Developmental Disabilities across the Lifespan ISBN: 9783319180953
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc34acd649c2fefef00a952171fc65a9
https://doi.org/10.1007/978-3-319-18096-0_68
https://doi.org/10.1007/978-3-319-18096-0_68
Publikováno v:
Health Care for People with Intellectual and Developmental Disabilities across the Lifespan ISBN: 9783319180953
Lowe syndrome (oculocerebrorenal syndrome; OCRL) is a rare (i.e., 1 in 50,0000), X-linked disorder that was first described in 1952. Myriad medical problems arise including complex glaucoma, hypotonia, dental dysfunction, and renal compromise leading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5236dd4835c194b582f99e3732592ad
https://doi.org/10.1007/978-3-319-18096-0_74
https://doi.org/10.1007/978-3-319-18096-0_74
Publikováno v:
Disease-a-Month. 58:258-320
Sexual behavior is common in adolescents and young adults with or without chronic illness or disability, resulting in high levels of unplanned pregnancy and STDs. Individuals with chronic illness or disability should not receive suboptimal preventive
Publikováno v:
British Journal of Wellbeing. 2:39-42
Overview Overview This article discusses chronic illness in adolescents and suicide risk. The health professional's role in recognising the association will be explored. The article includes some self-assessment to test the reader's knowledge
Publikováno v:
Developmental Medicine & Child Neurology. 52:1083-1087
Suicide in adolescents is a global tragedy. Research-identified correlates of suicide in youth include depression, academic failure, loss of friends, social isolation, and substance abuse, among others. This review focuses on the potential link betwe