Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mary P. Hamzik"'
Autor:
Carole A. Samango-Sprouse, Mary P. Hamzik, Kenneth Rosenbaum, Kosar Khaksari, Francie Mitchell, Ritika Kommareddi, Michaela R. Brooks, Elizabeth Tipton, Teresa Sadeghin, Andrea L. Gropman
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Pallister–Killian syndrome is an uncommon genetic disorder that has broad developmental and multisystemic effects. While medical complications are widely reported throughout the literature, research on the neurodevelopmental profile has been limite
Externí odkaz:
https://doaj.org/article/3e322b6a9d13490797006e3b3572b8e1
Autor:
Sophia Q. Song, Andrea Gropman, Robert W. Benjamin, Francie Mitchell, Michaela R. Brooks, Mary P. Hamzik, Kira Sampson, Ritika Kommareddi, Teresa Sadeghin, Carole A. Samango-Sprouse
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Congenital adrenal hyperplasia is a group of autosomal recessive disorders in which enzymes in the cortisol biosynthesis pathways are disrupted by gene mutations. The most common form of congenital adrenal hyperplasia, caused by 21-hydroxylase defici
Externí odkaz:
https://doaj.org/article/052e3e09f55845b3aa15aa9dfa52ee8c
Autor:
Samango-Sprouse, Mary P. Hamzik, Andrea L. Gropman, Michaela R. Brooks, Sherida Powell, Teresa Sadeghin, Carole A.
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1402
47,XXY, also known as Klinefelter syndrome, is the most commonly occurring sex chromosomal aneuploidy (SCA). Hormonal replacement therapy (HRT) has been associated with improved neurodevelopmental capabilities in boys with 47,XXY, although studies in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::2bfbae84a7de43012a9a9dc9950aeb46
Autor:
Carole A. Samango-Sprouse, Mary P. Hamzik, Eliana Gropman, Michaela R. Brooks, Sherida Powell, Alexa M. Taylor, Teresa Sadeghin, Andrea L. Gropman
Publikováno v:
Genetics in Medicine. 25:100847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5815dff0eac3ccc7a44eae9f17594253
https://doi.org/10.1016/j.gim.2023.100847
https://doi.org/10.1016/j.gim.2023.100847
Autor:
Carole A. Samango-Sprouse, Mary P. Hamzik, Kosar Khaksari, Michaela R. Brooks, Teresa Sadeghin, Andrea L. Gropman
Publikováno v:
Journal of developmental and behavioral pediatrics : JDBP. 43(9)
47,XXY, also known as Klinefelter syndrome, is the most commonly occurring sex chromosomal variation (1:660). The neurocognitive profile of boys with 47,XXY, in addition to verbal abilities, language skills, and general intelligence, has been explore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e005e033f74f3a13b6bd1db6a8e4f5ed
https://pubmed.ncbi.nlm.nih.gov/35947806
https://pubmed.ncbi.nlm.nih.gov/35947806